36 research outputs found
Proteolysis-Dependent Remodeling of the Tubulin Homolog FtsZ at the Division Septum in \u3ci\u3eEscherichia coli\u3c/i\u3e
- Author
- A Khlebnikov
- A Roll-Mecak
- A Roll-Mecak
- AJ Egan
- B Geissler
- B Shen
- B Shen
- B Soderstrom
- B Soderstrom
- B Williams
- BS Marteyn
- C Lu
- C Ortiz
- CA Hale
- CA Hale
- Christopher J. LaBreck
- D Bramhill
- D RayChaudhuri
- DE Anderson
- DP Haeusser
- DW Adams
- E Galli
- E Small
- Eric Cascales
- FR Blattner
- G Fu
- H Cho
- HA Arjes
- HP Erickson
- J Buss
- J Buss
- J Stricker
- JL Camberg
- JL Camberg
- JL Camberg
- JM Flynn
- JM Gonzalez
- Jodi L. Camberg
- Joseph Conti
- K Dai
- KA Datsenko
- L Ling
- M Jacq
- M Pazos
- MA Oliva
- Marissa G. Viola
- MP Strauss
- MR Maurizi
- MR Maurizi
- MS Buczek
- N Monroe
- N Sharma
- NK Tonthat
- P de Boer
- P Szwedziak
- P Szwedziak
- PJ Buske
- PP Cherepanov
- R Dziedzic
- R Grimaud
- RB Weart
- RM Teather
- S Du
- S Pichoff
- S Sugimoto
- SB Neher
- SC Smith
- SD Redick
- SJ Holden
- T Baba
- T Eckert
- TA Baker
- TG Bernhardt
- TG Bernhardt
- X Ma
- XC Yu
- YL Shih
- Z Li
- Z Liu
- Publication venue
- DigitalCommons@URI
- Publication date
- 01/01/2017
- Field of study
During bacterial cell division a dynamic protein structure called the Z-ring assembles at the septum. The major protein in the Z-ring in Escherichia coli is FtsZ, a tubulin homolog that polymerizes with GTP. FtsZ is degraded by the two-component ATP-dependent protease ClpXP. Two regions of FtsZ, located outside of the polymerization domain in the unstructured linker and at the C-terminus, are important for specific recognition and degradation by ClpXP. We engineered a synthetic substrate containing green fluorescent protein (Gfp) fused to an extended FtsZ C-terminal tail (residues 317–383), including the unstructured linker and the C-terminal conserved region, but not the polymerization domain, and showed that it is sufficient to target a non-native substrate for degradation in vitro. To determine if FtsZ degradation regulates Z-ring assembly during division, we expressed a full length Gfp-FtsZ fusion protein in wild type and clp deficient strains and monitored fluorescent Z-rings. In cells deleted for clpX or clpP, or cells expressing protease-defective mutant protein ClpP(S97A), Z-rings appear normal; however, after photobleaching a region of the Z-ring, fluorescence recovers ~70% more slowly in cells without functional ClpXP than in wild type cells. Gfp-FtsZ(R379E), which is defective for degradation by ClpXP, also assembles into Z-rings that recover fluorescence ~2-fold more slowly than Z-rings containing Gfp-FtsZ. In vitro, ClpXP cooperatively degrades and disassembles FtsZ polymers. These results demonstrate that ClpXP is a regulator of Z-ring dynamics and that the regulation is proteolysis-dependent. Our results further show that FtsZ-interacting proteins in E. coli fine-tune Z-ring dynamics
Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries.
- Author
- Ab Majid MA
- Ab Rahman AS
- Ab Rahman R
- Abayasinghe C
- Abbott T
- Abdullah NH
- Abdur-Rahman L
- Abeloos J
- Abernethy C
- Abidin UN
- Abrunhosa A
- Absar M
- Adam S
- Adams D
- Adams G
- Adamson M
- Adekola O
- Adelaja Y
- Ademola A
- Adenekan A
- Adenike O
- Adeolu AA
- Adetoye A
- Adewale B
- Adigun T
- Adolfsson A
- Aflori L
- Africander C
- Afshari A
- Agarwal V
- Agodirin O
- Aguero Vera M
- Aguzzoli C
- Ahmad A
- Ahmad N
- Ahmad T
- Ahmad T
- Ahmad Y
- Ahmed A
- Ahmed J
- Ai Y
- Aignatoaie M
- Aimoniotou-Georgiou E
- Akanmu O
- Akerman N
- Akinwale M
- Akring I
- Al 'Amri K
- Al Anizi M
- Al hussaini S
- Al-Soudaine Y
- Aladin H
- Alagbe-Briggs O
- Alaman Laguarda G
- Albaj S
- Alcock D
- Alcock L
- Aldecoa C
- Aldecoa C
- Aleixo FB
- Alexander H
- Alexander M
- Alexander-Sefre F
- Alherz F
- Ali H
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- Zou X
- Zoulamoglou M
- Zsisku L
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2016
- Field of study
BACKGROUND: As global initiatives increase patient access to surgical treatments, there remains a need to understand the adverse effects of surgery and define appropriate levels of perioperative care. METHODS: We designed a prospective international 7-day cohort study of outcomes following elective adult inpatient surgery in 27 countries. The primary outcome was in-hospital complications. Secondary outcomes were death following a complication (failure to rescue) and death in hospital. Process measures were admission to critical care immediately after surgery or to treat a complication and duration of hospital stay. A single definition of critical care was used for all countries. RESULTS: A total of 474 hospitals in 19 high-, 7 middle- and 1 low-income country were included in the primary analysis. Data included 44 814 patients with a median hospital stay of 4 (range 2-7) days. A total of 7508 patients (16.8%) developed one or more postoperative complication and 207 died (0.5%). The overall mortality among patients who developed complications was 2.8%. Mortality following complications ranged from 2.4% for pulmonary embolism to 43.9% for cardiac arrest. A total of 4360 (9.7%) patients were admitted to a critical care unit as routine immediately after surgery, of whom 2198 (50.4%) developed a complication, with 105 (2.4%) deaths. A total of 1233 patients (16.4%) were admitted to a critical care unit to treat complications, with 119 (9.7%) deaths. Despite lower baseline risk, outcomes were similar in low- and middle-income compared with high-income countries. CONCLUSIONS: Poor patient outcomes are common after inpatient surgery. Global initiatives to increase access to surgical treatments should also address the need for safe perioperative care. STUDY REGISTRATION: ISRCTN5181700
The global burden of cancer attributable to risk factors, 2010-19 : a systematic analysis for the Global Burden of Disease Study 2019
- Author
- Aali Amirali
- Abbas Qamar
- Abbasi Behzad
- Abbasi-Kangevari Mohsen
- Abbasi-Kangevari Zeinab
- Abbastabar Hedayat
- Abd-Elsalam Sherief
- Abdelmasseh Michael
- Abdelwahab Ahmed Abdelwahab
- Abdoli Gholamreza
- Abdulkader Rizwan Suliankatchi
- Abdulkadir Hanan Abdulkadir
- Abedi Aidin
- Abegaz Kedir Hussein
- Abidi Hassan
- Aboagye Richard Gyan
- Abolhassani Hassan
- Absalan Abdorrahim
- Abtew Yonas Derso
- Abu-Gharbieh Eman
- Achappa Basavaprabhu
- Acheson Alistair R
- Acuna Juan Manuel
- Addison Daniel
- Addo Isaac Yeboah
- Adegboye Oyelola A
- Adesina Miracle Ayomikun
- Adnan Mohammad
- Adnani Qorinah Estiningtyas Sakilah
- Advani Shailesh M
- Afrin Sumia
- Afzal Muhammad Sohail
- Aggarwal Manik
- Ahinkorah Bright Opoku
- Ahmad Araz Ramazan
- Ahmad Rizwan
- Ahmad Sajjad
- Ahmad Sohail
- Ahmadi Sepideh
- Ahmed Haroon
- Ahmed Luai A
- Ahmed Muktar Beshir
- Aiman Wajeeha
- Ajami Marjan
- Akalu Gizachew Taddesse
- Akbarzadeh-Khiavi Mostafa
- Aklilu Addis
- Akonde Maxwell
- Akunna Chisom Joyqueenet
- Al-Hanawi Mohammed Khaled
- Al-Maweri Sadeq Ali Ali
- Al-Raddadi Rajaa M
- Al-Rifai Rami H Hani
- Al-Sabah Salman Khalifah
- Al-Tammemi Ala'a B
- Alahdab Fares
- Alanezi Fahad Mashhour
- Alanzi Turki M
- Alessy Saleh Ali
- Algammal Abdelazeem M
- Alhassan Robert Kaba
- Ali Adel Hajj
- Ali Beriwan Abdulqadir
- Ali Hiwa Abubaker
- Ali Liaqat
- Ali Syed Shujait
- Alimohamadi Yousef
- Alipour Vahid
- Aljunid Syed Mohamed
- Alkhayyat Motasem
- Almustanyir Sami
- Alonso Nivaldo
- Alqalyoobi Shehabaldin
- Altawalah Haya
- Alvis-Guzman Nelson
- Amare Firehiwot
- Ameyaw Edward Kwabena
- Amirzade-Iranaq Mohammad Hosein
- Amu Hubert
- Amusa Ganiyu Adeniyi
- Ancuceanu Robert
- Anderson Jason A
- Animut Yaregal Animut
- Anoushiravani Amir
- Anoushirvani Ali Arash
- Ansari-Moghaddam Alireza
- Ansha Mustafa Geleto
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- Anwar Sumadi Lukman
- Anwer Razique
- Anyasodor Anayochukwu Edward
- Arab-Zozani Morteza
- Arabloo Jalal
- Aremu Olatunde
- Argaw Ayele Mamo
- Ariffin Hany
- Aripov Timur
- Arshad Muhammad
- Artaman Al
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- Aruleba Raphael Taiwo
- Aryannejad Armin
- Asaad Malke
- Asemahagn Mulusew A
- Asemi Zatollah
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- Ashraf Tahira
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- Athar Mohammad
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- Aujayeb Avinash
- Ausloos Marcel
- Avila-Burgos Leticia
- Avval Atlas Haddadi
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- Awoke Mamaru Ayenew
- Awoke Tewachew
- Ayana Tegegn Mulatu
- Ayen Solomon Shitu
- Azadi Davood
- Azadnajafabad Sina
- Azami-Aghdash Saber
- Azanaw Melkalem Mamuye
- Azangou-Khyavy Mohammadreza
- Azizi Hosein
- Azzam Ahmed YY
- Babajani Amirhesam
- Badar Muhammad
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- Baghcheghi Nayereh
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- Bagherieh Sara
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- Bardhan Mainak
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- Bashir Nasir Z
- Bashiri Azadeh
- Basu Saurav
- Batiha Abdul-Monim Mohammad
- Begum Aeysha
- Bekele Alehegn Bekele
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- Bermudez Amiel Nazer C
- Bernabe Eduardo
- Bhagavathula Akshaya Srikanth
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- Boloor Archith
- Bosetti Cristina
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- Conde Joao
- Cortés Sandra
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- Cámera Luis Alberto
- Dadras Omid
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- Dehkordi Javad Javad Aminian
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- Demisse Fitsum Wolde
- Denova-Gutiérrez Edgar
- Derakhshani Afshin
- Dereje Diriba
- Deribe Kalkidan Solomon
- Desai Rupak
- Desalegn Markos Desalegn
- Desideri Lorenzo Ferro
- Dessalegn Fikadu Nugusu
- Dessalegni Samuel Abebe A
- Dessie Gashaw
- Desta Abebaw Alemayehu
- Dewan Syed Masudur Rahman
- Dharmaratne Samath Dhamminda
- Dhimal Meghnath
- Dianatinasab Mostafa
- Diao Nancy
- Diaz Daniel
- Digesa Lankamo Ena
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- Doaei Saeid
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- Doku Paul Narh
- Dongarwar Deepa
- dos Santos Florentino Luciano Caetano
- dos Santos Wendel Mombaque
- Driscoll Tim Robert
- Dsouza Haneil Larson
- Durojaiye Oyewole Christopher
- Edalati Sareh
- Eghbalian Fatemeh
- Ehsani-Chimeh Elham
- Eini Ebrahim
- Ekholuenetale Michael
- Ekundayo Temitope Cyrus
- Ekwueme Donatus U
- El-Huneidi Waseem
- Elbahnasawy Mostafa Ahmed
- Elbarazi Iffat
- Elghazaly Hesham
- Elhadi Muhammed
- Emamian Mohammad Hassan
- Enyew Daniel Berhanie
- Erkhembayar Ryenchindorj
- Eshetu Tegegne
- Eshrati Babak
- Eskandarieh Sharareh
- Esmaeili Elham Davtalab
- Espinosa-Montero Juan
- Etaee Farshid
- Etemadimanesh Azin
- Eyayu Tahir
- Ezeonwumelu Ifeanyi Jude
- Ezzikouri Sayeh
- Fagbamigbe Adeniyi Francis
- Fahimi Saman
- Fakhradiyev Ildar Ravisovich
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- Farrokhpour Hossein
- Fasanmi Abidemi Omolara
- Fatehizadeh Ali
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- Ghafourifard Mansour
- Ghamari Seyyed-Hadi
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- Goulart Bárbara Niegia Garcia
- Grosso Giuseppe
- Guadie Habtamu Alganeh
- Gubari Mohammed Ibrahim Mohialdeen
- Gudayu Temesgen Worku
- Guerra Maximiliano Ribeiro
- Gunawardane Damitha Asanga
- Gupta Bhawna
- Gupta Sapna
- Gupta Veer Bala
- Gupta Vivek Kumar
- Gurara Mekdes Kondale
- Guta Alemu
- Habibzadeh Parham
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- Haj-Mirzaian Arvin
- Halboub Esam S
- Halimi Aram
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- Hameed Sajid
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- Hasan SM Mahmudul
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- Hassanipour Soheil
- Hay Simon I
- Hayat Khezar
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- Henrikson Hannah Jacqueline
- Herrera-Serna Brenda Yuliana
- Herteliu Claudiu
- Hezam Kamal
- Hiraike Yuta
- Hlongwa Mbuzeleni Mbuzeleni
- Holla Ramesh
- Holm Marianne
- Horita Nobuyuki
- Hoseini Mohammad
- Hossain Mahbub
- Hossain Mohammad Bellal Hossain
- Hosseini Mohammad-Salar
- Hosseinzadeh Ali
- Hosseinzadeh Mehdi
- Hostiuc Mihaela
- Hostiuc Sorin
- Househ Mowafa
- Huang Junjie
- Hugo Fernando N
- Humayun Ayesha
- Hussain Salman
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- Iftikhar Pulwasha Maria
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- Ilesanmi Olayinka Stephen
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- Immurana Mustapha
- Innos Kaire
- Iranpour Pooya
- Irham Lalu Muhammad
- Isfahani Haleh Mousavi
- Islam Rakibul M
- Islam Shariful
- Islami Farhad
- Ismail Nahlah Elkudssiah
- Isola Gaetano
- Iwagami Masao
- J Linda Merin
- Jabbari Seyed Hossein Yahyazadeh
- Jafari Amirhossein Azari
- Jaiswal Abhishek
- Jakovljevic Mihajlo
- Jalili Mahsa
- Jalilian Shahram
- Jamshidi Elham
- Jang Sung-In
- Jani Chinmay T
- Javaheri Tahereh
- Jayarajah Umesh Umesh
- Jayaram Shubha
- Jazayeri Seyed Behzad
- Jebai Rime
- Jemal Bedru
- Jeong Wonjeong
- Jha Ravi Prakash
- Jindal Har Ashish
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- Jonas Jost B
- Jonasson Junmei Miao
- Joo Tamas
- Joseph Nitin
- Joukar Farahnaz
- Jozwiak Jacek Jerzy
- Julian Guilherme Silva
- Jürisson Mikk
- Kabir Ali
- Kacimi Salah Eddine Oussama
- Kadashetti Vidya
- Kahe Farima
- Kakodkar Pradnya Vishal
- Kalankesh Laleh R
- Kalankesh Leila R
- Kalhor Rohollah
- Kamal Vineet Kumar
- Kamangar Farin
- Kamath Ashwin
- Kanchan Tanuj
- Kandaswamy Eswar
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- Kandel Sandhya Neupane
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- Karch André
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- Kashani Hamid Reza Khayat
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- Katoto Patrick DMC
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- Kaur Harkiran
- Kebede Abinet Gebremickael
- Keikavoosi-Arani Leila
- Kejela Gemechu Gemechu
- Keramati Maryam
- Keykhaei Mohammad
- Khajuria Himanshu
- Khan Abbas
- Khan Abdul Aziz Khan
- Khan Ejaz Ahmad
- Khan Gulfaraz
- Khan Moien AB
- Khan Nuruzzaman
- Khanali Javad
- Khaneghah Amin Mousavi
- Khatab Khaled
- Khatatbeh Moawiah Mohammad
- Khatib Mahalaqua Nazli
- Khayamzadeh Maryam
- Khezeli Mehdi
- Khodadost Mahmoud
- Kim Min Seo
- Kim Yun Jin
- Kisa Adnan
- Kisa Sezer
- Klugar Miloslav
- Klugarová Jitka
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- Kolahi Ali-Asghar
- Kolkhir Pavel
- Kompani Farzad
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- Krishnamoorthy Yuvaraj
- Kugbey Nuworza
- Kulimbet Mukhtar
- Kumar Akshay
- Kumar G Anil
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- La Vecchia Carlo
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- Larijani Bagher
- Lasrado Savita
- Lau Jerrald
- Lauriola Paolo
- Laxminarayana Sindhura Lakshmi Koulmane
- Ledda Caterina
- Lee Sang-woong
- Lee Shaun Wen Huey
- Lee Wei-Chen
- Lee Yeong Yeh
- Lee Yo Han
- Legesse Samson Mideksa
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- Li Ming-Chieh
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- Majeed Azeem
- Majidpoor Jamal
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- Makris Konstantinos Christos
- Malekpour Mohammad-Reza
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- Michalek Irmina Maria
- Mijena Gelana Fekadu Worku
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- Mirinezhad Seyed Kazem
- Mirmoeeni Seyyedmohammadsadeq
- Mirza-Aghazadeh-Attari Mohammad
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- Misganaw Abay Sisay
- Misra Sanjeev
- Mohammad Karzan Abdulmuhsin
- Mohammadi Esmaeil
- Mohammadi Mokhtar
- Mohammadian-Hafshejani Abdollah
- Mohammadpourhodki Reza
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- Mohammed Shafiu
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- Moosavi Mohammad Amin
- Moradi Abdolvahab
- Moradi Yousef
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- Morawska Lidia
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- Morze Jakub
- Mosapour Abbas
- Mostafavi Ebrahim
- Mousavi Seyyed Meysam
- Mpundu-Kaambwa Christine
- Mubarik Sumaira
- Mulita Francesk
- Munblit Daniel
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- Rafiei Alireza
- Raheem Nasiru
- Rahim Fakher
- Rahman Mosiur
- Rahman Muhammad Aziz
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- Thavamani Aravind
- Thomas Nihal
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- Ticoalu Jansje Henny Vera
- Tiyuri Amir
- Tollosa Daniel Nigusse
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- Woldemariam Melat
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- Xiao Hong
- Xu Rixing
- Xu Suowen
- Xu Xiaoyue
- Yadav Lalit
- Yang Lin
- Yazdanpanah Fereshteh
- Yeshaw Yigizie
- Yismaw Yazachew
- Yonemoto Naohiro
- Younis Mustafa Z
- Yousefi Zabihollah
- Yousefian Fatemeh
- Yu Chuanhua
- Yu Yong
- Yunusa Ismaeel
- Zahir Mazyar
- Zaki Nazar
- Zaman Burhan Abdullah
- Zangiabadian Moein
- Zare Fariba
- Zare Iman
- Zareshahrabadi Zahra
- Zarrintan Armin
- Zastrozhin Mikhail Sergeevich
- Zeineddine Mohammad A
- Zhang Dongyu
- Zhang Jianrong
- Zhang Yunquan
- Zhang Zhi-Jiang
- Zhou Linghui
- Zodpey Sanjay
- Zoladl Mohammad
- Šekerija Mario
- Publication venue
- Publication date
- 01/01/2022
- Field of study
Background Understanding the magnitude of cancer burden attributable to potentially modifiable risk factors is crucial for development of effective prevention and mitigation strategies. We analysed results from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 to inform cancer control planning efforts globally. Methods The GBD 2019 comparative risk assessment framework was used to estimate cancer burden attributable to behavioural, environmental and occupational, and metabolic risk factors. A total of 82 risk-outcome pairs were included on the basis of the World Cancer Research Fund criteria. Estimated cancer deaths and disability-adjusted life-years (DALYs) in 2019 and change in these measures between 2010 and 2019 are presented. Findings Globally, in 2019, the risk factors included in this analysis accounted for 4.45 million (95% uncertainty interval 4.01-4.94) deaths and 105 million (95.0-116) DALYs for both sexes combined, representing 44.4% (41.3-48.4) of all cancer deaths and 42.0% (39.1-45.6) of all DALYs. There were 2.88 million (2.60-3.18) risk-attributable cancer deaths in males (50.6% [47.8-54.1] of all male cancer deaths) and 1.58 million (1.36-1.84) risk-attributable cancer deaths in females (36.3% [32.5-41.3] of all female cancer deaths). The leading risk factors at the most detailed level globally for risk-attributable cancer deaths and DALYs in 2019 for both sexes combined were smoking, followed by alcohol use and high BMI. Risk-attributable cancer burden varied by world region and Socio-demographic Index (SDI), with smoking, unsafe sex, and alcohol use being the three leading risk factors for risk-attributable cancer DALYs in low SDI locations in 2019, whereas DALYs in high SDI locations mirrored the top three global risk factor rankings. From 2010 to 2019, global risk-attributable cancer deaths increased by 20.4% (12.6-28.4) and DALYs by 16.8% (8.8-25.0), with the greatest percentage increase in metabolic risks (34.7% [27.9-42.8] and 33.3% [25.8-42.0]). Interpretation The leading risk factors contributing to global cancer burden in 2019 were behavioural, whereas metabolic risk factors saw the largest increases between 2010 and 2019. Reducing exposure to these modifiable risk factors would decrease cancer mortality and DALY rates worldwide, and policies should be tailored appropriately to local cancer risk factor burden. Copyright (C) 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.Peer reviewe
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- Author
- . Haifeng
- . Magner
- . Yin
- Abbott Scott
- Abbott-Ozersky Amanda
- Abdellah Zahra
- Abouelleil Amr
- Abrajano Anne
- Adachi Tamami
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- Adams Charles Q.
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- Ellington Andrew
- Elliot David
- Elliot Glendoria
- Elliot Jeffrey
- Ellwood Matthew
- Emberson Becky
- Emelianenko Natalia
- Emery-Cohen Alexandra J.
- Endrizzi Matthew
- Engh Ger van den
- Engle David
- Erickson Jeffery
- Erler Anne Marie
- Errington Helen
- Escobar Julio
- Escotto Michael
- Eugene Craig S.
- Evans Gareth
- Evans John
- Evans Katie
- Evans Richard
- Eveleth Gerald
- Eyras Eduardo
- Fan Hongyuan
- Fan Keke
- Fang Jianqiu
- Farina Abderrahim
- Faro Susan
- Faulkner Louisa
- Fawcett Joseph J.
- Fechtel Kim
- Fellingham Charlotte
- Felming Claire
- Felsenfeld Adam
- Feltwell Theresa
- Feng Guodong
- Feng Haiyan
- Feng Jie
- Feng Xiaoli
- Fennell Stephen
- Ferguson Alicia
- Fernandez Sonia
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- Fernando Pushpa Ranjani
- Ferriera Pat
- Fertitta Anne
- Fey Jim
- Fidel Patrick
- Fields Elizabeth
- Fink Marie
- Finley Maria C.
- Finn Robert
- Fischer Heather
- Fischer Laurice
- Fisher Shelia
- Fitch Pat
- Fitzgerald Mike
- Flack Tina
- Flagg Nicole
- Flanagan J.
- Fleming Kerry
- Flint Jonathan
- Flint Mark
- Flowers Dave
- Floyd Yvonne
- Foley Karen
- Folta Peg
- Fong Jonathan
- Fonknechten Núrua
- Footman Simon
- Forbes Lisa D.
- Ford Amanda F.
- Foster Myre J.
- Fotopulos Dea
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- Fowler John
- Fox Jessica
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- Fu Gang
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- Fu Gang
- Fu Qiushi
- Fujioka Michiru
- Fujiyama Asao
- Fukawa Rintaro
- Fuller Liam
- Fuller Sharin
- Fullerton Kathryn
- Fulton Lucinda A.
- Fulton Robert S.
- Furey Terrence S.
- Furuhashi Mie
- Förste Silke
- Gabisi Abdul M.
- Gage Diane
- Gaige Tony
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- Garcia Carmen
- Garcia Emilio
- Garcia Marvin
- Garcia Ricardo M, III
- Garcia-Martinez Antonio
- Gardner Alison
- Gardner Alison
- Garduno Consuelo
- Gardyna Steph
- Garner Patrick
- Garner Toni T.
- Garnes Jeffrey A.
- Garnett Jane
- Garza Melissa
- Gatewood Joseph M.
- Gatland Leigh
- Gatland Lindsay
- Gattung Stacie
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- Gearin Gary
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- Gelein Cynthia
- Gelpke Maartin
- Gench Stephanie L.
- Geng Jianing
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- Ghori Jilur
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- Gibbs Ben
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- Gibson Diane
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- Gong Guanghui
- Gong Jinying
- Gonzales Eidelyn
- Gonzalez Guillermo B.
- Gooderham April
- Goodstadt Leo
- Goodstein David
- Goodwin Lynne A.
- Gordon Catherine
- Gordon Laurie A.
- Gordon Seth
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- Gorvad Ann
- Gould Christine
- Goyea Ernest
- Goyette Audra
- Grady Deborah I.
- Grady Michelle L.
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- Grandbois Edward
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- Grant Michael
- Grant Susan
- Graves Tina A.
- Gray Bruce
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- Gray Lain
- Green Lisa
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- Gribble Susan
- Griffith Jeffrey K.
- Griffiths Coline
- Griffiths Ed
- Griffiths Mark
- Griffiths-Jones Sam
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- Gu Wenyi
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- Guevara Whitney V.
- Gui Qi
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- Hamada Junko
- Hamilton Cerissa
- Hamilton Keelan A.
- Hamilton Matt
- Hamlett John
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- Hammon Nancy
- Hammond Martin
- Hammond Sha
- Hammond Sian
- Hamza Khalid
- Han Guiqing
- Han Shunsheng
- Han Xurong
- Hanak Vincent A.
- Hancock Julie
- Harbes Brandy A.
- Harding Adam
- Harkins C. Richard
- Harley Joanne
- Harper David
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- Hashimoto Wakako
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- Haugen Eric
- Haussler David
- Havlak Paul
- Hawes Alicia C.
- Hawkins Ebere Sylvia Onyirioha
- Hawkins Natalie
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- Heyen Joshua
- Higgs Douglas
- Hildebrand Carl E.
- Hillier LaDeana
- Hillyard Guy
- Hines Sandra
- Hinkins Russell
- Hinrichs Angela S.
- Hitchens Matthew Edward
- Ho Issac
- Ho Sara-Jane
- Hodgson Anne V.
- Hodgson David
- Hoffman Susan M.G.
- Hoffs Michael
- Hogues Marilyn E.
- Holden Jane
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- Holtzer Caleb
- Homsi Deana K.
- Homsi Farah J.
- Honan Tracy
- Hood Leroy
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- Howden Philip
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- Howell Latoya Lynette
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- Hubbard Timothy
- Huber James W.
- Huckle Elizabeth
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- Hupman Matt
- Huynh Sandy
- Hyde David
- Hynds Christopher
- Idlebird Devincent G.
- Iliev Ilian
- Imbro Paula
- Imo Kelvin C.
- Inacio Nicole
- Inagaki Naomi
- Ince Michael
- Ingram Drew
- Inoue Shuuji
- Isak Amber
- Isherwood Judith
- Ishibashi Akiko
- Ishikawa Sabine K.
- Ishizaki Hinako
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- Ito Fumiaki
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- Itoh Takehiko
- Iwakawa Shinobu
- Iwatate Mariko
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- Izumiyama Tomohiro
- Jacintho Mark
- Jackson Laronda R.
- Jackson Terri
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- Jaeger Sara
- Jaffe David B.
- Jahn Niels
- Jaklevic Joseph
- Jaklevic Michael
- James Kent W.
- Jareborg Niclas
- Jarek Michael
- Jassal Bijay
- Jeffery Grant
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- Jekosch Kerstin
- Jenkins Lee
- Jett Jamie
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- Jia Jia
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- Jia Xingchang
- Jiang Lu
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- Jones Myrna D.
- Jones Steven
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- Keenan Stephen
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- Kegg Lisa
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- Kelly Shayna P.
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- Kershaw Joanna
- Kettleborough Ross
- Keys David
- Khan Arsi
- Khan Umer F.
- Khan Ziad Mohid
- Khine Susu
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- Kohlberg Sara
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- Kong Yi
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- Kosiura Anna
- Kou Zhaohui
- Kovar Christie L.
- Krawczyk Marie-Claude
- Kremitzki Colin
- Kremmidiotis Gabriel
- Krogh Anders
- Kronmiller Brent
- Kruchowski Scott S.
- Kube Michael
- Kubischta Duane
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- Kulish Larissa
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- Lamerdin Jane E.
- Lander Eric S.
- Landers Tom
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- Lapidus Alla
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- Leversha Margaret
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- Lewis Keith
- Lewis Lakeshia C.
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- Lim Meng K.
- Lindblad-Toh Kerstin
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- Lorensuhewa Lorna M.
- Lou Yunian
- Loulseged Hermela
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- Lovell Jamie
- Lovett Demetria A.
- Lowenstein Michael G.
- Lowry Stephen
- Lozado Ryan J.
- Lu Lingfeng
- Lu Tao
- Lu Xiuhua
- Lu Yongxiang
- Lu Yontao T.
- Lu Yue
- Lucas Robert
- Lucas Susan
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- Lucier Raymond L.
- Ludeman Thom
- Lui Annie
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- Machrus Migdad
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- MacLean Christine
- Madabhushi Ramki
- Madu Renita C.
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- Maheshwari Manjula
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- Maltbie Mary I.
- Mangum Brian
- Manning Jonathan
- Manohar Chitra
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- Mardis Elaine R.
- Mareth David
- Mariano Marisa
- Marinelli Lisa
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- Marquis-Homeyer Catherine
- Marr Thomas G.
- Marra Marco
- Marriott Neil
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- Matthews Lucy
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- Matthews Sterling D.
- Mauceli Evan
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- Maupin Rachel
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- McLeod Michael P.
- McMurdo John
- McMurray Amanda
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- McMurray Kimberly
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- McNinch Jenny
- McPherson John
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- Meidi Patrick
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- Mercado Iracema C.
- Mercer Simon
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- Mesirov Jill P.
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- Miller Christie
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- Minja Emmanuel
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- Morgan Margaret B.
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- Mundt Mark O.
- Mungall Andy
- Munidasa Mala
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- Munson Glen
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- Murayama Yuji
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- Murphy Michael
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- Nagao Syunsuke
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- Nair Latha
- Nair Seema R.
- Naka Maho
- Nakagawa Masayo
- Nakagawa Saori
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- Nelson Joanne
- Nelson Kathryn
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- Nesbitt Ryan
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- Ng Bee
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- Nguyen Natalie M.
- Nguyen Ngoc Bich
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- Norbu Nyima
- Nordsiek Gabriele
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- Nowlin Larry
- Nusbaum Chad
- Nwaokelemeh Ogechi O.
- Nwokenkwo Stanley
- O\u27Donnell Paula
- O\u27Donovan Daniel
- O\u27Leary Sinead
- O\u27Loughlin Jennifer
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- Obayashi Izumi
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- Ohtsubo Masafumi
- Oinn Tom
- Okoawo Ose
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- Olson Maynard V.
- Omotosho Bamidele
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- Oomori Nobuhiro
- Ooshima Kenshiro
- Oragunye Njideka
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- Ovcharenko Ivan
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- Oviedo Rodolfo J.
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- Parks Kenya L.
- Parry-Brown Ginny
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- Pasternak Shiran
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- Patel Ritesh
- Patel Shripa
- Patel Vishal V.
- Patrick James
- Paul Heidie A.
- Paul Shelia
- Paulson Edward
- Payton Brett A.
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- Pearman Charlene
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- Pecherer Robert M.
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- Pedan John
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- Pelletier Eric
- Peng Vivian
- Peng Vivian
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- Pennacchio Len A.
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- Percy Chantel
- Perez Agapito
- Perez Lesette M.
- Perito Andrew
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- Peters Leonard G.
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- Phillips Kim
- Phillips Samantha
- Phulchung Tenzin
- Phunkang Pema
- Pickens Adam
- Pieper Natasha
- Pierre Nadia
- Piqani Bruno
- Piscia C.
- Pitesky Maurice
- Pitluck Sam
- Plajzer-Frick Ingrid
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- Playford Emma
- Plopper Farah Jo Homsi
- Plumb Bob
- Pocock Matthew
- Pohl Craig
- Poindexter Alan
- Poliakov Alex
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- Polman Jos
- Ponting Chris P.
- Porter Aaron
- Porter Keith
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- Posada Martha
- Potter Christopher
- Potter Simon
- Poundstone Pat
- Pourrajabi Nima M.
- Powell Don
- Powell Jason
- Prado Daisy
- Prange Christa
- Prathalingham Radhika
- Predki Paul
- Prigmore Elena
- Primus Eltrick L.
- Primus Jennifer
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- Pruitt Kim
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- Qi Xiaohua
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- Qiang Boqin
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- Quail Michael
- Quan Glenda
- Quarrie Hannah
- Quiles Miyo M.
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- Quiroz Juana B.
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- Rachlin Eric K.
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- Sonaike Titilola
- Song Liping
- Song Liping
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- Sonnhammer Erik
- Sonnhammer Erik
- Sorelle Richard P.
- Sotheran Elizabeth
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- Spainhower Corey
- Sparks Anastasia L.
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- Stallings Raymond I.
- Stalvey Malinda
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- Steffen David
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- Su Xiaohu
- Subramanian Sandhya
- Subramanian Sandhya
- Sudbrak Ralf
- Sugnet Charles W.
- Sulston John
- Summers Leslie J.
- Sun Hui
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- Sun Jiu Qin
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- Sun Yu
- Sun Yue
- Sutherland Grant R.
- Sutherland Robert D.
- Sutton Angelica E.
- Svatek Amanda F.
- Svetz Jessica
- Svetz Leah Anne
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- Sycamore Neil
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- Tabor Paul E.
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- Tam Serena
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- Tan Olivia
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- Tan Xinyu
- Tang Hongli
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- Tatsuyama Miho
- Tatum Owatha I.
- Taudien Stefan
- Taylor Amy
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- Taylor Kate
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- Taylor Tineace R.
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- Tchuinga Pierre
- Tee Louise
- Telford Ethan Brett
- Tenzin Pema
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- Tesfaye Senait
- Tesmer Judith G.
- Tester Julieanne
- Thayer Nina
- Theaker Andrew
- Theil James
- Theodore Joumathe
- Thexton David
- Thies Stephanie
- Thomas Craig
- Thomas Daniel
- Thomas Daryl J.
- Thomas Karen
- Thomas Nicole
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- Thomas Ruth
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- Thommai Roselin
- Thompson Linda S.
- Thorne Rachel Diane
- Thorpe Andrea
- Thorpe Karen
- Thoulutsang Yama
- Threadgold Glen
- Thurston Scott
- Tian Chaoguang
- Tian Chaoguang
- Tian Wei
- Tian Yan
- Tian Yong
- Tian Yuqing
- Tice Hope
- Tighe Damon
- Tin-Wollam Aye M.
- Tinsley Emma
- Tochigi Miwako
- Togashi Naoko
- Tomizawa Iori
- Tomlinson Chad
- Tong Jingli
- Topham Kerri
- Torcaso Bill
- Torney David C.
- Totoki Yasushi
- Towey Sarah
- Toyoda Atsushi
- Tracey Alan
- Tran Ly Thanh
- Tran-Gyamfi Mary
- Trani Lee
- Trankiem Margie
- Trask Barbara J.
- Travers Johnathan
- Trejos Zulma Y.
- Treuhaft Marianne
- Trevino Brenda Kaye
- Tromans Anthony
- Trong Stephan
- Trumbower Heather
- Tsai Ming
- Tsamla Tsamla
- Tsolas Jason
- Tsomo Nawang
- Tsujimoto Susan
- Tsukamoto Yumi
- Tsuruoka Hiromi
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- Tu Yuefeng
- Tu Yuefeng
- Tubby Ben
- Tufarelli Cristina
- Turner Heidi
- Turney Kathryn
- Tynan Katherine
- Ueland Stephanie
- Ueng Samantha
- Ukegbu Ogechi Nkemdirim
- Ulanovsky Levy E.
- Un Chun
- Ung Quyen
- Upson Darren
- Urban Jeremy B.
- Ureta-Vidal Abel
- Ureta-Vidal Abel
- Usmani Kamran
- Ustaszewska Anna
- Uyama Nozomi
- Valas Ruben E.
- Valdez Michelle
- Valle Duane
- Valles Yvonne
- Van Brunt Andrew
- Van Dilla Marvin
- Van Helmond Zoe
- Van Luchene Ryan
- Vardanian Zachary
- Vargas Michelle
- Vargo Charles E.
- Vartanian Steffan
- Vasquez Lydia I.
- Vassiliev Helen
- Vastrik Imre
- Vaudin Mark
- Veil Rose
- Veklerov Eugene
- Velasco Nelson
- Velasquez Lisa
- Venkataranan Vijay
- Vera Virginia A.
- Verduzco Daniel
- Vergez Lisa
- Vico Virginie
- Viknaraja Ramya
- Villasana Donna M.
- Vine Wendy
- Viswanathan Vijay
- Vo Andy
- Vo Nu
- Voak Paul
- Vollenhoven David
- Wada Hiromi
- Wagner Mark
- Wagner-McPherson Caryn
- Waldron Lenee
- Waligorski Jason E.
- Walker Davian L.
- Walker Keya
- Walker Sarah
- Wall Melanie
- Wall Randy E.
- Wallace John
- Wallis Justine
- Wallis Michelle
- Walsh Jennifer
- Walsham Natalie
- Wan Ma
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- Wang Guihai
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- Wang Huifeng
- Wang Jian
- Wang Jian
- Wang Jian
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- Wang Jun
- Wang Jun
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- Wang Lijie
- Wang Lijuan
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- Wang Liqun
- Wang Mei
- Wang Qiaoyan
- Wang Shifen
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- Wang Suzhen
- Wang Wenjun
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- Wang Xuegang
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- Wang Yimin
- Wang Ying
- Wang Ying
- Wang Yuanyuan
- Wangchuck Tsering
- Wangdi Tsering
- Ward-Moore Stephanie
- Warren Graham
- Warren James T.
- Warry Georgina
- Watanabe Hidemi
- Watanabe Saki
- Waterston Robert H.
- Watson Andy
- Watt Nicola
- Webb Anthony
- Webb Jeannette
- Webber Caleb
- Weber Ryan J.
- Wehri Edward
- Wei Shulin
- Wei Xuehong
- Weidenbach Richard
- Weinstock George
- Weinstock Keith
- Weir John
- Weissenbach Jean
- Wells Alan
- Wells Sarah
- Welton Robert
- Wen Gaiping
- Wendi Mike
- Weng Li
- Wenning Sarah
- Wentz Sara
- Werler Daniela
- Wesley Mary Melissa
- West Paul
- West Tony
- Wetterstrand Kris
- Wheatley Angela
- Wheatley Carl
- Wheeler David A.
- Wheeler Gideon
- Wheeler Jeremy
- Whitaker Hayley
- White Adam
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- White Jennifer
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- White Scott P.
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- Whitmore Scott
- Whittaker Adam
- Whittaker Charles
- Whittaker Pamela
- Wickremasinghe Manosha I.
- Widaa Sara
- Wiegel Sarah
- Wild Anna
- Wilkinson Jane
- Wilkinson Jane
- Wilkinson Paul
- Willey David
- Williams Albert L.
- Williams Andy
- Williams Bill
- Williams Gabrielle A.
- Williams Leanne
- Williamson Angela L.
- Williamson Helen
- Wills Patricia L.
- Wills Richard
- Wilmer Tamsin
- Wilming Laurens
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- Wilson Gareth
- Wilson Margaret
- Wilson Nyree
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- Wilson Richard K.
- Wilson Siobhan
- Wilson Steve
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- Wincker Patrick
- Window Philip
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- Winzar Claire
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- Wleczyk Regina
- Wobus Fred
- Woessner Jeffrey
- Wohldmann Patty
- Wollard Jessica
- Womack Andrew W.
- Wong Benjamin
- Wong Gane K-S
- Wood Diane
- Wood Emma
- Wood Joe
- Wooden Hailey S.
- Wooden Steven H.
- Woodeson Sharon
- Woodfine Kathryn
- Woodmansey Rebecca
- Woods Eric
- Woodwark Cara
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- Wray Matthew
- Wray Paul
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- Wright Debbie
- Wright Kathrine
- Wright Kristin
- Wright Rita A.
- Wu Chungen
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- Wu Qingfa
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- Wyatt Julia
- Wycoff-Montenegro Melissa
- Wylie Kris
- Wyman Dudley
- Wyman Stacia
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- Xi Yingying
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- Xie Gary
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- Xu Jing
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- Xu Yuning
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- Xu Zuyuan
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- Yada Tetsushi
- Yadav Shailendra
- Yakub Syed
- Yamamoto Lynn
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- Yamamoto Yuko
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- Yang Huanming
- Yang Huanming
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- Yang Shiaw-Pyng
- Yang Shudong
- Yang Xiaonan
- Yang Xiaonan
- Yang Xiaoping
- Yang Yongkui
- Yano Candance
- Yao Zhijian
- Yao Zhijian
- Yaspo Marie-Laure
- Ye Chen
- Yeager Shane
- Yeh Mimi
- Yen Jennifer
- Yeshitela Rahel Retta
- Yoakum Martin
- Yokobata Kathy
- Yokoyama Jennifer
- Yonezawa Miho
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- Yu Jun
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- Yue Shujie
- Yumae Brian
- Yun Rui
- Zainoun Joanne
- Zembeck Lisa
- Zeng Yixin
- Zhai Dong
- Zhan Guoping
- Zhang Bo
- Zhang Caimin
- Zhang Fengmei
- Zhang Guangyu
- Zhang Guohua
- Zhang Guohua
- Zhang Haiqing
- Zhang Haiqing
- Zhang Haiqing
- Zhang Hongbo
- Zhang Hongbo
- Zhang Jingjing
- Zhang Jingjing
- Zhang Jingkun
- Zhang Jiuchun
- Zhang Jiuchun
- Zhang Lanzhi
- Zhang Li
- Zhang Li
- Zhang Meihua
- Zhang Meng
- Zhang Ming
- Zhang Qing
- Zhang Ruhua
- Zhang Shaojie
- Zhang Tiezhen
- Zhang Wei
- Zhang Wei
- Zhang Xianglin
- Zhang Xianglin
- Zhang Xiaoliang
- Zhang Xiuqing
- Zhang Yan
- Zhang Yi
- Zhang Yilin
- Zhang Yilin
- Zhang Ying
- Zhang Yuansen
- Zhang Yuzhi
- Zhang Zhengdong
- Zhao Hongmei
- Zhao Lijian
- Zhao Shenru
- Zhao Zhijing
- Zhen Zhicheng
- Zheng Haibo
- Zhong Ming
- Zhou Carol
- Zhou Haixia
- Zhou Jianling
- Zhou Nannan
- Zhou Xinfeng
- Zhou Yan
- Zhou Yang
- Zhou Yi
- Zhu Bingying
- Zhu Bofeng
- Zhu Fenghua
- Zhu Genfeng
- Zhu Genfeng
- Zhu Miao
- Zhu Ning
- Zhu Yongge
- Zhu Zhen
- Zhuang Shitao
- Zierten Deborah
- Zimmer Andrew
- Zody Michael C.
- Zollo Massimo
- Zorrilla Sara E.
- Zuo Lin
- Publication venue
- LSU Digital Commons
- Publication date
- 21/10/2004
- Field of study
The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead
Embodied and Situated: Kerry James Marshall’s Formulations of Blackness in the Garden Project Series
- Publication venue
- Publication date
- 07/12/2012
- Field of study
Kerry James Marshall’s Garden Project paintings (1994-95) refer to the ways dual mechanisms of racialized subject production and racialized spatialization compound and work to define blackness as an invisible other within the urban landscape. Marshall engages multiple historical modes of painting to disrupt the visual field and refuse an easy legibility of public housing as a racialized space. Marshall investigates the intense ambiguity to the legacy of public housing projects in the history of black America.
Marshall’s life experiences and artistic development in relation to black cultural and political history in America have informed the production of his artwork. The paintings emerged in the 1990s amidst the debates regarding the emergence of identity politics in the art world and the critical response to the controversial 1993 Whitney Biennial. The five Garden Project paintings are analyzed of them in relation to the historical traditions of painting. They are significant for their evocations of an embodied and situated blackness in the visualization of black figuration, and in relation to the historical circumstances of public housing in Chicago, its role in the history of black class mobility, and the ways that many representations of public housing have presented it as a charged symbol of societal regression despite the complexity of its history
Reflection on the Role of Artists: A Case Study on the Hidden Visual Curriculum of the School of the Art Institute of Chicago
- Author
- Publication venue
- 'Informa UK Limited'
- Publication date
- Field of study
Transforming Growth Factor α Expression Drives Constitutive Epidermal Growth Factor Receptor Pathway Activation and Sensitivity to Gefitinib (Iressa) in Human Pancreatic Cancer Cell Lines
- Author
- Publication venue
- 'American Association for Cancer Research (AACR)'
- Publication date
- Field of study
Blood Manganese as an Exposure Biomarker: State of the Evidence
- Author
- Publication venue
- 'Informa UK Limited'
- Publication date
- Field of study
Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouse
- Author
- Publication venue
- 'Cambridge University Press (CUP)'
- Publication date
- 01/01/2005
- Field of study
We performed genome-wide mutagenesis of C57BL/6J mice using the mutagen N-ethyl-N-nitrosourea (ENU) and screened the third generation (G3) offspring for visual system alterations using electroretinography and fundus photography. Several mice in one pedigree showed characteristics of retinal degeneration when tested at 12–14 weeks of age: no recordable electroretinogram (ERG), attenuation of retinal vessels, and speckled pigmentation of the fundus. Histological studies showed that the retinas undergo a photoreceptor degeneration with apoptotic loss of outer nuclear layer nuclei but visual acuity measured using the optomotor response under photopic conditions persists in spite of considerable photoreceptor loss. The Noerg-1 mutation showed an autosomal dominant pattern of inheritance in progeny. Studies in early postnatal mice showed degeneration to occur after formation of partially functional rods. The Noerg-1 mutation was mapped genetically to chromosome 6 by crossing C57BL/6J mutants with DBA/2J or BALB/cJ mice to produce an N2 generation and then determining the ERG phenotypes and the genotypes of the N2 offspring at multiple loci using SSLP and SNP markers. Fine mapping was accomplished with a set of closely spaced markers. A nonrecombinant region from 112.8 Mb to 115.1 Mb was identified, encompassing the rhodopsin (Rho) coding region. A single nucleotide transition from G to A was found in the Rho gene that is predicted to result in a substitution of Tyr for Cys at position 110, in an intradiscal loop. This mutation has been found in patients with autosomal dominant retinitis pigmentosa (RP) and results in misfolding of rhodopsin expressed in vitro. Thus, ENU mutagenesis is capable of replicating mutations that occur in human patients and is useful for generating de novo models of human inherited eye disease. Furthermore, the availability of the mouse genomic sequence and extensive DNA polymorphisms made the rapid identification of this gene possible, demonstrating that the use of ENU-induced mutations for functional gene identification is now practical for individual laboratories