75 research outputs found
Relationship of Enhanced Liver Fibrosis Score with Pediatric Nonalcoholic Fatty Liver Disease Histology and Response to Vitamin E or Metformin
- Publication venue
- MOSBY-ELSEVIER
- Publication date
- 13/08/2021
- Field of study
OBJECTIVES:
To study the diagnostic performance of the enhanced liver fibrosis score (ELF) for detecting different stages of fibrosis and its usefulness in detecting histologic response to vitamin E or metformin in children with nonalcoholic fatty liver disease who participated in the Vitamin E or Metformin for the Treatment Of NAFLD In Children (TONIC) trial.
STUDY DESIGN:
ELF was measured at baseline and weeks 24, 48, and 96 on sera from 166 TONIC participants. Associations between ELF with baseline and end of trial (EOT) fibrosis stages and other histologic features were assessed using Ï2 tests and logistic regression models.
RESULTS:
ELF was significantly associated with severity of fibrosis at baseline and EOT. ELF areas under the curve for discriminating patients with clinically significant and advanced fibrosis were 0.70 (95% CI, 0.60-0.80) and 0.79 (95% CI, 0.69-0.89), respectively. A 1-unit decrease in ELF at EOT was associated with overall histologic improvement (OR, 1.86; 95% CI, 1.11-3.14; P = .02), resolution of steatohepatitis (OR, 1.88; 95% CI, 1.09-3.25; P = .02), improvement in steatosis grade (OR, 1.76; 95% CI, 1.06-2.82; P = .03), and hepatocellular ballooning (OR, 1.79; 95% CI, 1.06-3.00; P = .03), but not with improvement in fibrosis stage (OR, 1.26; 95% CI, 0.78-2.03; P = .34).
CONCLUSIONS:
ELF was associated with fibrosis stage in children who participated in TONIC. Although not associated with improvement in fibrosis, a decrease in ELF at EOT was associated with Nonalcoholic Steatohepatitis resolution and improvement in nonalcoholic fatty liver disease histology. ELF may be a useful noninvasive test to monitor treatment response in children with nonalcoholic fatty liver disease
Spermatocytic seminoma at the National Institute of Oncology in Morocco
- Author
- A Talerman
- AP Burke
- C Rosenberg
- E Dean
- Fellah Hel
- Ghizlane G Raiss
- H Steiner
- H Stoop
- Hassan H Errihani
- Hind H Mrabti
- I Verdorfer
- J Albores-Saavedra
- J Matoska
- J Rosai
- J Wolter Oosterhuis
- JC Manivel
- JN Eble
- JW Oosterhuis
- LD True
- LH Looijenga
- LHJ Looijenga
- M Lombardi
- Manrico Morroni
- Marwane M Benatiya Andaloussi
- Myriam Decaussin
- OW Cummings
- P Baldet
- P Camparo
- P Masson
- P Trivedi
- P Warde
- Pavel Dundra
- PW Chung
- S Pendlebury
- Soundouss S Raissouni
- T Gorecki
- T Gorecki
- T Horn
- TM Ulbright
- Publication venue
- BioMed Central
- Publication date
- 01/01/2011
- Field of study
Dynamic and influential interaction of cancer cells with normal epithelial cells in 3D culture
- Author
- A Hoeben
- A Orimo
- BC Spink
- BR Brinkley
- Brendan Cummings
- C Frezza
- C Hogan
- C Lehmann
- C Oliveras-Ferraros
- C Pinheiro
- C Pinheiro
- C Sheridan
- D Bani
- D Barkan
- D Whitaker-Menezes
- Darran OâConnor
- Dimitri Scholz
- F Sotgia
- Funke Owolabi
- GY Lee
- HS Koren
- IJ Fidler
- J Debnath
- J Monks
- J Pawelek
- JF Woessner Jr
- K Birsoy
- Katarzyna Welzel
- KB Hotary
- KJ Luzzi
- L Hegedus
- L Mathot
- Laura P Ivers
- M Ghoneum
- M Kajita
- M Nguyen
- MG Mendez
- MR Junttila
- N Elia
- NA Bhowmick
- Nobue Itasaki
- O Baum
- O Warburg
- OW Petersen
- P Schedin
- R Kalluri
- RA Toillon
- RA Toillon
- Rut Klinger
- S Howard
- S Leppa
- Sayaka Saitoh
- SM Gallagher
- T Nakanishi
- TN Seyfried
- VM Weaver
- X Dong-Le Bourhis
- Yasuyuki Fujita
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2014
- Field of study
BACKGROUND: The cancer microenvironment has a strong impact on the growth and dynamics of cancer cells. Conventional 2D culture systems, however, do not reflect in vivo conditions, impeding detailed studies of cancer cell dynamics. This work aims to establish a method to reveal the interaction of cancer and normal epithelial cells using 3D time-lapse. METHODS: GFP-labelled breast cancer cells, MDA-MB-231, were co-cultured with mCherry-labelled non-cancerous epithelial cells, MDCK, in a gel matrix. In the 3D culture, the epithelial cells establish a spherical morphology (epithelial sphere) thus providing cancer cells with accessibility to the basal surface of epithelia, similar to the in vivo condition. Cell movement was monitored using time-lapse analyses. Ultrastructural, immunocytochemical and protein expression analyses were also performed following the time-lapse study. RESULTS: In contrast to the 2D culture system, whereby most MDA-MB-231 cells exhibit spindle-shaped morphology as single cells, in the 3D culture the MDA-MB-231 cells were found to be single cells or else formed aggregates, both of which were motile. The single MDA-MB-231 cells exhibited both round and spindle shapes, with dynamic changes from one shape to the other, visible within a matter of hours. When co-cultured with epithelial cells, the MDA-MB-231 cells displayed a strong attraction to the epithelial spheres, and proceeded to surround and engulf the epithelial cell mass. The surrounded epithelial cells were eventually destroyed, becoming debris, and were taken into the MDA-MB-231 cells. However, when there was a relatively large population of normal epithelial cells, the MDA-MB-231 cells did not engulf the epithelial spheres effectively, despite repeated contacts. MDA-MB-231 cells co-cultured with a large number of normal epithelial cells showed reduced expression of monocarboxylate transporter-1, suggesting a change in the cell metabolism. A decreased level of gelatin-digesting ability as well as reduced production of matrix metaroproteinase-2 was also observed. CONCLUSIONS: This culture method is a powerful technique to investigate cancer cell dynamics and cellular changes in response to the microenvironment. The method can be useful for various aspects such as; different combinations of cancer and non-cancer cell types, addressing the organ-specific affinity of cancer cells to host cells, and monitoring the cellular response to anti-cancer drugs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12935-014-0108-6) contains supplementary material, which is available to authorized users
A Multi-Step Process of Viral Adaptation to a Mutagenic Nucleoside Analogue by Modulation of Transition Types Leads to Extinction-Escape
- Author
- A Airaksinen
- A Arias
- A Arias
- A Arias
- A Mas
- A Roussel
- AC Frank
- AM Di Bisceglie
- Armando Arias
- AS Perelson
- Bruno Canard
- C Crumpacker
- C EscarmĂs
- C EscarmĂs
- C EscarmĂs
- C Ferrer-Orta
- C Ferrer-Orta
- C Ferrer-Orta
- C Ferrer-Orta
- C Ferrer-Orta
- C Ferrer-Orta
- C Perales
- C Perales
- C Perales
- Celia Perales
- CK Biebricher
- CM Ruiz-Jarabo
- Cristina Ferrer-Orta
- CW Day
- D Maag
- DA Harki
- E Connor
- E Domingo
- E Domingo
- E Domingo
- E Domingo
- E Domingo
- Esteban Domingo
- F Sobrino
- G Ochoa
- GL Davis
- HC Wang
- I Jordan
- Ignacio de la Higuera
- J GarcĂa-Arriaza
- J GarcĂa-Arriaza
- J Swetina
- JD Graci
- JD Graci
- JD Graci
- JF Anderson
- JG McHutchison
- JJ Arnold
- JJ Holland
- JK Pfeiffer
- JK Pfeiffer
- JM Cuevas
- JP Anderson
- JR Coleman
- JW Ogle
- KJ Cummings
- KS Harris
- L Aragones
- LA Loeb
- LA Loeb
- LM Scheidel
- M Eigen
- M Eigen
- M Sanz-Ramos
- M Sierra
- M Sierra
- M Toja
- M Vignuzzi
- M Vignuzzi
- MS Freistadt
- N Charpentier
- N Galtier
- N Pariente
- N Tapia
- NJ Snell
- Nuria Verdaguer
- OW Sidwell
- P Schuster
- R Agudo
- RA Smith
- RE Lanford
- RM Pinto
- Rosa PĂ©rez-Luque
- Rubén Agudo
- S Chevaliez
- S Crotty
- S Crotty
- S Ojosnegros
- S Ojosnegros
- S Sierra
- WB Parker
- WE Severson
- WP Hofmann
- Y Asahina
- Z Hong
- Z Otwinowski
- Publication venue
- Public Library of Science
- Publication date
- 01/08/2010
- Field of study
Resistance of viruses to mutagenic agents is an important problem for the development of lethal mutagenesis as an antiviral strategy. Previous studies with RNA viruses have documented that resistance to the mutagenic nucleoside analogue ribavirin (1-ÎČ-D-ribofuranosyl-1-H-1,2,4-triazole-3-carboxamide) is mediated by amino acid substitutions in the viral polymerase that either increase the general template copying fidelity of the enzyme or decrease the incorporation of ribavirin into RNA. Here we describe experiments that show that replication of the important picornavirus pathogen foot-and-mouth disease virus (FMDV) in the presence of increasing concentrations of ribavirin results in the sequential incorporation of three amino acid substitutions (M296I, P44S and P169S) in the viral polymerase (3D). The main biological effect of these substitutions is to attenuate the consequences of the mutagenic activity of ribavirin âby avoiding the biased repertoire of transition mutations produced by this purine analogueâand to maintain the replicative fitness of the virus which is able to escape extinction by ribavirin. This is achieved through alteration of the pairing behavior of ribavirin-triphosphate (RTP), as evidenced by in vitro polymerization assays with purified mutant 3Ds. Comparison of the three-dimensional structure of wild type and mutant polymerases suggests that the amino acid substitutions alter the position of the template RNA in the entry channel of the enzyme, thereby affecting nucleotide recognition. The results provide evidence of a new mechanism of resistance to a mutagenic nucleoside analogue which allows the virus to maintain a balance among mutation types introduced into progeny genomes during replication under strong mutagenic pressure
Prognostic model to predict postoperative acute kidney injury in patients undergoing major gastrointestinal surgery based on a national prospective observational cohort study.
- Author
- Aamir A
- Abbas J
- Abbas N
- Abbott TEF
- Abdalla M
- Abdikadir H
- Abuhussein N
- Acquaah F
- Adamson R
- Adeleye O
- Adeogun A
- Adlan A
- Aftab R
- Afzal Z
- Agarwal M
- Aglan H
- Agnew CJF
- Agrawal R
- Ahern D
- Ahluwalia J
- Ahluwalia V
- Ahmad A
- Ahmad K
- Ahmed H
- Ahmed I
- Ahmed L
- Ahmed N
- Ahmed P
- Ainger E
- Ainsworth P
- Aishwarya G
- Ajibola-Taylor O
- Akhbari M
- Akhtar A
- Akhtar R
- Akpenyi O
- Al-Ausi M
- Al-Huneidi R
- Al-Khudairi R
- Al-Masri S
- Al-Mousawi A
- Al-Saadi N
- Alagappan A
- Alberts J
- Alfa-Wali M
- Ali A
- Ali B
- Ali I
- Ali M
- Ali Q
- Ali S
- Alturki N
- Alwandi A
- Amani L
- Amarnath T
- Amer M
- Amin H
- Amin MN
- Amoah R
- Amoah-Arko A
- Anandarajah C
- Ananthavarathan P
- Andah EJE
- Andrew K
- Andrews H
- Ang A
- Ang HL
- Ang JJ
- Ani C
- Anilkumar A
- Anto N
- Anwar S
- Apperley H
- Appleton S
- Aquilina T
- Archer M
- Arif T
- Arneill M
- Arnell S
- Arnold TJ
- Arshad A
- Arthur J
- Arulkumaran N
- Arya J
- Asad M
- Asemota N
- Ashaye T
- Ashdown T
- Ashour R
- Ashraf MR
- Ashwood J
- Asif U
- Atkin G
- Atkins B
- Attalla M
- Aubrey-Jones D
- Auckburally S
- Auld F
- Auluck I
- Azam S
- Aziz R
- Azizi A
- Azmi F
- Babatunde F
- Babu VS
- Bachi A
- Bagga R
- Bains H
- Bajwa DS
- Baker A
- Baker C
- Balai E
- Balian V
- Ball M
- Bamford M
- Bana R
- Banfield DA
- Bannard-Smith J
- Barai I
- Barclay J
- Barfi L
- Barker C
- Barker M
- Barmayehvar B
- Barnfield J
- Barnor-Ahiaku E
- Baron C
- Barr CJ
- Barraclough J
- Baryan HK
- Basra M
- Bassam N
- Bath MF
- Battle J
- Beasley W
- Beattie G
- Beattie S
- Beatty M
- Beghal G
- Begum F
- Behranwala K
- Belchos J
- Belgaid DR
- Belgaumkar A
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- Ben-Gal O
- Benchetrit S
- Bennett M
- Benons N
- Bernal TL
- Bertelli M
- Berthaume-Hawkins SD
- Best R
- Betts A
- Bevan K
- Bews-Hair M
- Bhambra R
- Bhamra N
- Bhangu A
- Bhatte S
- Bhatti A
- Bhide I
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- Bhudia R
- Bhullar S
- Bienias A
- Billyard C
- Bird C
- Birkinshaw F
- Black J
- Blake E
- Blazeby JM
- Bleakley A
- Bloom I
- Bogle R
- Bolton W
- Borakati A
- Boraluwe-Rallage H
- Borg CM
- Botha A
- Boualbanat Y
- Boulton APR
- Bountra K
- Bowley D
- Boyd G
- Boyles L
- Bradley P
- Brannick S
- Brayley J
- Brecher J
- Breen H
- Bristow S
- Britton N
- Broad J
- Brobbey P
- Brock E
- Brooke M
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- Budd E
- Bull K
- Burgin A
- Burke D
- Burke J
- Burnage S
- Burns N
- Burrows A
- Busti S
- Butler A
- Cabdi NMO
- Cadden F
- Cairns C
- Calabria C
- Calciu A
- Campbell A
- Campbell B
- Campbell G
- Campbell HS
- Cannon SP
- Cant M
- Capella S
- Cardus C
- Cardwell A
- Cargill Z
- Caroll P
- Carr G
- Carr R
- Carr W
- Carse S
- Carter N
- Carter R
- Castle A
- Cato L
- Cave D
- Cecil E
- Chadwick H
- Chadwick M
- Chan F
- Chan L
- Chan M
- Chan SSN
- Chan-lam N
- Chandler E
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- Chandramoorthy L
- Chandramoorthy S
- Chang A
- Chang LH
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- Chappelow I
- Chapple K
- Charnley R
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- Chaudhry S
- Chauhan P
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- Chin YR
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- Chitsabesan P
- Chohan K
- Choi JE
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- Choo S
- Chopada A
- Chouari T
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- Choudhry M
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- Fitzpatrick H
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- Hussain SF
- Hussain ST
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- Islam Y
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- Jackman T
- Jackson CES
- Jacob-Ramsdale B
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- Jamal S
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- Javaid NR
- Jawad L
- Jawad ZAR
- Jebakumar R
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- Ji C
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- Jiao LR
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- Kaminski F
- Kanabar S
- Kanapeckaite L
- Kandage D
- Kandhari N
- Kandiah K
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- Kapp J
- Kaptanis S
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- Karim MA
- Karim MJ
- Karmarkar A
- Karsan RB
- Karunatilleke AS
- Katira A
- Katsaiti I
- Kaur G
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- Keelan G
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- Kennedy ED
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- Keshvala C
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- Keyte A
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- Khaliq M
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- Khatri C
- Khaw J
- Khawaja H
- Khawar H
- Khawari S
- Khodatars K
- Khoo E
- Kiandee M
- Kidanu D
- Kiely A
- Killington K
- Kim P
- Kim S
- King J
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- Kinnersley H
- Kirby S
- Kirk S
- Kishore A
- Klimach S
- Knight C
- Knight JS
- Kokayi A
- Komolafe O
- Komoriyama A
- Kong C
- Kong CH
- Kong JTH
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- STARSurg Collaborative Writing Committee, Data analysis, Steering committee, Advisory group, Regional leads, Collaborators and validators
- STARSurg Collaborative Writing Committee, Data analysis, Steering committee, Advisory group, Regional leads, Collaborators and validators, Nepogodiev, D
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- Zanichelli D
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- Zubikarai G
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- Zuzarte L
- Publication venue
- 'Wiley'
- Publication date
- 18/05/2018
- Field of study
Background: Acute illness, existing co-morbidities and surgical stress response can all contribute to postoperative acute kidney injury (AKI) in patients undergoing major gastrointestinal surgery. The aim of this study was prospectively to develop a pragmatic prognostic model to stratify patients according to risk of developing AKI after major gastrointestinal surgery. Methods: This prospective multicentre cohort study included consecutive adults undergoing elective or emergency gastrointestinal resection, liver resection or stoma reversal in 2-week blocks over a continuous 3-month period. The primary outcome was the rate of AKI within 7 days of surgery. Bootstrap stability was used to select clinically plausible risk factors into the model. Internal model validation was carried out by bootstrap validation. Results: A total of 4544 patients were included across 173 centres in the UK and Ireland. The overall rate of AKI was 14·2 per cent (646 of 4544) and the 30-day mortality rate was 1·8 per cent (84 of 4544). Stage 1 AKI was significantly associated with 30-day mortality (unadjusted odds ratio 7·61, 95 per cent c.i. 4·49 to 12·90; P < 0·001), with increasing odds of death with each AKI stage. Six variables were selected for inclusion in the prognostic model: age, sex, ASA grade, preoperative estimated glomerular filtration rate, planned open surgery and preoperative use of either an angiotensin-converting enzyme inhibitor or an angiotensin receptor blocker. Internal validation demonstrated good model discrimination (c-statistic 0·65). Discussion: Following major gastrointestinal surgery, AKI occurred in one in seven patients. This preoperative prognostic model identified patients at high risk of postoperative AKI. Validation in an independent data set is required to ensure generalizability
Finishing the euchromatic sequence of the human genome
- Author
- . Haifeng
- . Magner
- . Yin
- Abbott Scott
- Abbott-Ozersky Amanda
- Abdellah Zahra
- Abouelleil Amr
- Abrajano Anne
- Adachi Tamami
- Adam Catherine
- Adams Charles Q.
- Adamson Aaron
- Adekoya Emmanuel
- Adio-Oduola Babajide
- Aerts Andrea
- Aggarwal Arun
- Ahmadi Alireza
- Ahmed Shahana
- Aimable Matthew
- Ainscough Rachael
- Ait-Zahra Mostafa
- Aizu Tomoyuki
- Alcivare Dana
- Alegria Michelle
- Ali Alla
- Ali Johar
- Allegria-hartmann Michelle
- Alleman Jennifer
- Allen Carlana C.
- Allen Heather
- Allen Nicole R.
- Allen Susan
- Allen Thaddeus
- Almeida Jeff
- Almond Claire
- Alsbrooks Stephen L.
- Altherr Michael R.
- Amaratunge Harshinie C.
- Ambler Andrew
- Ambrose Karen
- Ambrose Kerrie
- Amemiya Chris
- Amico-Keller Gina
- Amin Amita G.
- Anderson Mechele
- Anderson Scott
- Anderson Scott
- Andora Janice
- Andredesz Carol
- Andrew Robert
- Andrews Dan
- Andrews Daniel
- Andrews Neil
- Andrews Stephanie
- Andriese Tim
- Anthouard VĂ©ronique
- Antonarakis Stylianos E.
- Anyalebechi Vivian
- Aoki Norie
- Apostolou Sinoula
- Apweiler Eva
- Arachchi Harindra
- Arai Rie
- Arbery Hazel
- Arcaina Marlon
- Arcaina Terisita
- Archer Beth
- Arellano Andre
- Arellano-Jones Perry
- Armbruster Jeff
- Armstrong Jon
- Arredondo Dilrukshi P.
- Arredondo Heather Hope
- Artiguenave François
- Asakawa Shuichi
- Asakawa Teruyo
- Ash Gareth
- Ashcroft Kevin
- Ashurst Jennifer
- Ashwell Robert
- Ashworth Linda K.
- Aslanidis Cara
- Asomugha Chinwe O.
- Asuncion Lawreen
- Atkin Deborah
- Atkinson Andrea
- Atkinson Barry
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- Baptiste Pertrice
- Barbaria Joseph A.
- Barbe Valérie
- Bardill Simon
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- Barker Gary
- Barlow Karen
- Baron Laurent
- Barrett Anika
- Bartlett Rebecca
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- Bashman David
- Basu Suba
- Bateman Alex
- Bates Karen
- Battles John
- Batzer Mark
- Baumgart Cornelia
- Baumohl Jason
- Baynes Caroline
- Bayul Tashi
- Beall Keith
- Beard Lisa
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- Beare David
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- Beasley Oliver
- Beaucham Leslie
- Beaudet Arthur
- Beck Alfred
- Beck Stephen
- Becker Michael
- Bell Emma
- Bell George I.
- Bellard Terell M.
- Bellerby Damian
- Bellerby Tristram
- Belter Edward A., Jr.
- Bemrose Richard
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- BenKahla Alia
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- Benner William
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- Bensasson Douda
- Bentley Andrew
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- Berardinis VĂ©ronique de
- Bercovitz John
- Berghoff Amy
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- Berkowicz Nicolas
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- Bethel Graeme
- Beugelsdijk Tony J.
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- Bieri Tamberlyn
- Bimage Kesha E.
- Bird Christine
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- Birney Ewan
- Birren Bruce
- Bissell Helen
- Biswalo Kaneza
- Bituin Aleksandr
- Black Stacey
- Blackburne-Maze Suzanne
- Blair Jessica Anne
- Blakey Sarah
- Blanks Tia
- Blasiar Darin
- Blazej Robert
- Blitshsteyn Berta
- Blomstrom David B.
- Bloom Scott
- Bloom Toby
- Blumer Heather
- Blye Jason
- Blyth Peter R.
- Blöcker Helmut
- Boatright Elizabeth
- Boehm John
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- Boguslavskiy Leonid
- Bolton Christel
- Bolund Lars
- Bondoc Marnel
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- Bonnett Ralph
- Bonnin David
- Border Richard
- Borowsky Mark
- Borzym Katja
- Boukhgalter Boris
- Bowen Eric
- Bradley Amanda
- Bradshaw-Cordum Holly
- Brady Nicola
- Brandriff Brigitte F.
- Brannon Wade
- Branscomb Elbert
- Bray Jason
- Bray-Allen Sarah
- Brettin Thomas
- Bridgeman Anne
- Bridgers Michael
- Brimhall Angela K.
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- Brooking Shane
- Brottier Philippe
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- Brown Jacqui
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- Brown Nancy C.
- Bruce David D.
- Bruce Robert
- Bruno William J.
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- Buatsi Delali
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- Buckle Veronica
- Buczek Donald
- Budd Claire
- Buhay Christian J.
- Bulbul Kerem
- Buller Sarah
- Bunker Nathan
- Burberry Jill
- Burch Paula Ellen
- Burford Deborah
- Burgess Joanne
- Burgin Matt
- Burkett Carrie E.
- Burkhart-Schultz Karolyn
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- Cahill Patrick
- Cai Tianjing
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- Callen David F.
- Camarata Jody
- Camire David
- Camm Nick
- Campbell Christopher
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- Campbell Evelyn W.
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- Campo Kevin
- Canning Bruno
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- Caoile Chenier
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- Carder Carol
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- Carrano Anthony V.
- Carriere Jason
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- Ceasar Heather
- Cedroni Maria
- Cepeda Mario
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- Chain Patrick
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- Mercado George
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- Mercer Simon
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- 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 âŒ99% of the euchromatic genome and is accurate to an error rate of âŒ1 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
ICAR: endoscopic skullâbase surgery
- Author
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- Spaziante R
- Spear S
- Speelman JP
- Spiers AS
- Stamm AC
- Stamm AC
- Stangerup SE
- Stankiewicz JA
- Stapleton AL
- Stapleton AL
- Starke RM
- Starlinger V
- Stechison MT
- Steno J
- Stevens SM
- StevensâSimon C
- Stippler M
- Stokes WA
- Stokken J
- Strek P
- Stripp DC
- Strychowsky J
- Stummer W
- Su WF
- Su WF
- Subei AM
- Sugata S
- Sughrue ME
- Suh JD
- Suzuki K
- Sylvester PT
- Tabaee A
- Tabaee A
- Taggart MW
- Tahir MZ
- Tajudeen BA
- Tajudeen BA
- Tajudeen BA
- Tam S
- Tamasauskas A
- Tami TA.
- Tan G
- Tan NC
- Tanei T
- Taniguchi M
- Taniguchi M
- Tanzler ED
- Tavanaiepour D
- Tay HN
- Taylor RJ
- Teachey W
- Terranova P
- Thakar A
- Thaker A
- Thawani JP
- Thirumala P
- Thirumala PD
- Thirumala PD
- Thirumala PD
- Thirumala PD
- Thompson CF
- Thompson ED
- Thompson LD
- Thorp BD
- Thotakura AK
- Tien DA
- Tishler RB
- Tomazic PV
- Tomita T
- Tosaka M
- Tosun F
- Trautmann JC
- Trifanescu R
- Tsang RK
- Tsirbas A
- Tu GY
- Tu M
- Turan N
- Turel MK
- Turel MK
- Turner JH
- TurriâZanoni M
- Tyrrell JB
- Tzortzidis F
- Ulfarsson E
- Unsal AA
- Upadhyay S
- Vaezeafshar R
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- Valentine R
- Varlotto JM
- VazâGuimaraes F
- VazâGuimaraes F
- Veeravagu A
- Vellutini Ede A
- Velthoven V
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- Verstegen MJT
- Vescan AD
- Veyrat M
- Vikram B
- Villalobos T
- Virgin F
- Virk JS
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- Vohra ST
- Wadsworth B
- Waldbauer H
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- Wallace SA
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- Wang DH
- Wang EW
- Wang F
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- Wang Q
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- Wang X
- Wang YY
- Wang YY
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- Weber AL
- Wei M
- Wei WI
- Weidenbecher M
- Weiland DA
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- Wen YH
- Wendler O
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- Wessell A
- Wheless SA
- Wigand ME
- Wilson CB
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- Wilson PJ
- Wise SK
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- Wise SK
- Wiseman SM
- Witte O
- Wong EHC
- Wood JW
- Woodworth BA
- Woodworth BA
- Wormald PJ
- Wu JS
- Wu W
- Xie L
- Xie T
- Xie T
- Xiong L
- Xu CC
- Xu F
- Xu R
- Xu Z
- Yan CH
- Yang I
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- Yano S
- Yao WC
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- Yunoue S
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- Publication venue
- Publication date
- 01/07/2019
- Field of study
n/
Die Evaluation der Effekte der betrieblichen Bildungsarbeit mittels ökonomischer Grössen
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1992
- Field of study
Fluorescence in situ hybridization analysis of chromosome 12p in paraffin-embedded tissue is useful for establishing germ cell origin of metastatic tumors
- Publication venue
- Publication date
- 01/01/2004
- Field of study
Historical perspective: Two decades of progress in treating metastatic colorectal cancer
- Publication venue
- 'Wiley'
- Publication date
- Field of study
- âŠ