66 research outputs found
Establishing engineering S-curves to evaluate supervision engineer allocations for highway construction projects
- Publication venue
- 'Vilnius Gediminas Technical University'
- Publication date
- 01/07/2016
- Field of study
An engineering consultant firm needs to allocate engineers to supervise a highway construction project in each month during the construction phase. Properly assigning the supervision engineers under a cost-plus-fixed-fee contract has been a key factor affecting the profitability of the firm and the quality assurance of the project. Assigning too many engineers will be a waste, while allocating too few engineers may harm the supervision quality. This work proposes a two-stage model to develop engineering S-curves (called ES-curves) for planning and controlling the engineering supervision schedule. In the planning stage, a predictive ES-curve model is established based on historical ES-curves. In the controlling stage, an ES-curve is built according to the relationships between the engineering progress and construction progress. A cluster analysis and regression analysis are applied to the model development. A case study demonstrates that the produced ES-curves can help management in planning and evaluating when to increase or decrease the number of supervision engineers assigned to a project
Large-Scale Comparative Analyses of Tick Genomes Elucidate Their Genetic Diversity and Vector Capacities
- Author
- Bell-Sakyi Lesley
- Cao Wu-Chun
- Chang Qiao-Cheng
- Chen Hai-Ying
- Chen Shen-En
- Cheng Jing Xia
- Consortium Tick Genome Microbiome
- Cui Xiao-Ming
- Dai Pei-Fang
- Ding Shu-Jun
- Du Chun-Hong
- Du Lifeng
- Gao Yu-Chi
- Guo Wen-Bin
- Han Xiao-Hu
- Huang En-Jiong
- Huo Qiu-Bo
- Ji Peifeng
- Jia Na
- Jiang Bao-Gui
- Jiang Jia-Fu
- Lam Tommy Tsan-Yuk
- Li Jie
- Li Lian-Feng
- Li Wei
- Liu Jing-Ze
- Liu Tao
- Ni Xue-Bing
- Pan Yu-Sheng
- Que Teng Cheng
- Ruan Xiang-Dong
- Shao Hong-Ze
- Sheng Yue
- Shi Wenqiang
- Sun Yi
- Tian Jun-Hua
- Wang Chong-Cai
- Wang Jinfeng
- Wang Qian
- Wang Xian-Jun
- Wang Xin
- Wei Jia-Te
- Wei Wei
- Xia Luo-Yuan
- Yang Tian-Ci
- Yang Wei-Fei
- Ye Run-Ze
- Yuan Ting-Ting
- Zhan Wei
- Zhang Bing
- Zhao Fangqing
- Zhao Lin
- Zhou Ling-Guo
- Zhou Yu-Hao
- Zhu Jin-Guo
- Publication venue
- 'Elsevier BV'
- Publication date
- 03/09/2020
- Field of study
Robust estimation of bacterial cell count from optical density
- Author
- Aarnio Tiu
- Aaron Leow Chung Yong
- Abbas Anser
- Abduraimova Aiganym
- Abraham Doris
- Acar Beliz Leyla
- Acosta Joaquin
- Adler Nina
- Adulyanukosol Natthawut
- Agena Ejouan
- Agena Ethan
- Aggarwal Priya
- Aguirre Adriana Lizeth Rubio
- Ahlgren Christopher
- Ahuja Janvi
- Aizik Dror
- Akbary Mina
- Akinfenwa Akinwumi
- Akingbesote Ngozi D.
- Akova Umut
- Aldo Ferdinan
- Alexopoulos Ioannis
- Allen Lucy
- Alonso Alejandro
- Altarawneh Dina
- Alvarado Andres Benjamin Sanchez
- Ambre Sanika
- Ameziane Annissa
- Amheine Khadija
- Amin Ihya Fakhrurizal
- Amir Sayeda Sakina
- Amstel Chiel van
- An Yongyan
- Anand Nithishwer Mouroug
- Ananthakrishnan Sathvik
- Anderson Karl
- Angel Sagi
- Annem Vidhya
- Anson Chung Tsun Ho
- Anwar Mariam
- Appel Alana
- Araya Lucas
- Armstrong Alexander
- Arora Neha
- Arora Vasu
- Arruda Beck
- Ashwin F Amal Jude
- Astapenka Artur
- Astles Ben
- Astorino Gabe
- Aubry Celine
- Avileli Rebecca
- Azad Mahnaz Sabeta
- Babar Rehmat
- Babu Priyanka
- Badalli Turan
- Badash Lior
- Baichman-Kass Amichai
- Baldwin Geoff S.
- Baltensperger Oliver Andreas
- Bao Guanke
- Bao Minyue
- Baronaite Ugne
- Barrat Leon Michael
- Barrington Seth
- Barshap Alon
- Bartzoka Natalia
- Basu Anubhav
- Basulto Cynthia
- Bath Scott
- Battina Rohith
- Bauersachs Daniel
- Beal Jacob
- Beale Renee
- Beard Eleanor
- Beck Selina
- Becker Evan
- Benavides Samantha Ayde Pena
- Bennis Nicole
- Bete Anna
- Bhatt Darshak
- Bhowmick Shilpa
- Bian Weixin
- Bijman Eline Yafele
- Bindt Felix
- Blas Karla Soto
- Bo Tang
- Boada Yadira
- Boer Meine
- Bohner Ariel
- Borovko Irina
- Bott Amie
- Bouwmeester Susan
- Bowman Kyle
- Boxem Mike
- Boxuan Cheng
- Boyce Kira
- Boyer Jess
- Brasas Valentas
- Brewer Mathew
- Briand William
- Brink Matilda
- Browne Emily
- Buckley-Taylor Russell
- Budhan Stephanie
- Buller Lisa
- Burckhardt Nele
- Burgland Zachary
- Burns Frank
- Burridge Matt
- Burud Hanna Nedreberg
- Buson Felipe Xavier
- Butterfield Tom
- Byagathvalli Gaurav
- Byatt Gabriel
- Byun Sumin
- Caballero Amalia
- Cai Fu
- Cai Niangui
- Caldwell Sarah
- Camacho Yazmin
- Camille Monteil
- Campbell Robert
- Cao Qinhao
- Cao Yixin
- Cao Yuze
- Carrillo Leo
- Carter Jonah
- Casas Alexis
- Castillo Nora Esther Torres
- Castillo Sandra
- Cave John
- Chai Ruochen
- Chamiec-Case Elizabeth
- Chan Janice
- Chan Yuan-Yao
- Chandramouli Priyanka
- Chang Annabel
- Chang Catherine
- Chang Kevin
- Chang Thomas
- Chang Ting-Chen
- Chang Yu-Ci
- Chapman Tyler
- Chater Dounia
- Chau Anthony
- Chavez Benjamin
- Chavez Francisco
- Chehade Ibrahim
- Chen Carmen
- Chen Chih-Chiang
- Chen Ching-Wei
- Chen Janice
- Chen Junhong
- Chen Junyang
- Chen Junyu
- Chen Pei-Hong
- Chen Ryan
- Chen Weixuan
- Chen Yan
- Chen Yi-Cian
- Chen Yifei
- Chen Zhuoyang
- Cheng Cheng
- Cheng Haolun
- Cheng Hsuan
- Cheng Yu-Hong
- Cheng Yu-Hsuan
- Chenxi Liang
- Cherupalla Arjun
- Chi Jordi
- Chi Shumei
- Chiang Jason
- Chiang Woody
- Ching Lai Tsz
- Ching Lam Kai
- Ching Law Hiu
- Ching Luk Hau
- Chinnathambi Sathivel
- Cho Sungwoo
- Choi Lee Sze
- Choi Youngeun
- Chou Ryan
- Chou Ryan
- Chu Wai Yan
- Chua Yah Tse Sabrina
- Chuang Yi-Chien
- Chulkova Nadezhda
- Chun Cheung Man
- Chun Emily
- Chun Ng Tsz
- Cifuentes Rodrigo Hernandez
- Clapper Jude
- Clapper Jude
- Clark Brittany
- Clemente Borja Sanchez
- Clerc Valerian
- Clodomir Christina
- Coates Ryan
- Cohen Katherine
- Colant Noelle
- Coleman Sarah
- Colgan Cian
- Cone Eli
- Corre Christophe
- Costa Ben
- Cott Rachel Van
- Craw Darilyn
- Crispim Larissa de Souza
- Crone Michael Andrew
- Crooijmans Marjolein
- Crosby Laurel Constanti
- Crowley Peter
- Cruz Frida
- Cubukcu Hande
- Culfogienis Dylan
- Czekster Clarissa
- Dai Leijie
- Dalangin Rochelin
- Daniel Benjamin
- Daniels Lea
- Das Neves Laura
- Das Diptatanu
- Davis Christina
- De Silva Nimaya
- Deb Shalini S.
- Deepak Kumar S.
- Deibel Emilie
- Dejoie Julianne
- Dejoux Alice
- DeKloe Jackson
- Del Toro Mariano
- Delalez Nicolas
- Delgadillo Sabrina
- Delhomme Jean
- Demchuk Aubrey
- Deng Nian Ruei
- Deng Rui
- Denter Jennifer
- Deshmukh-Reeves Ed
- Despres Philippe C.
- Devi Velvizhi
- Dhaliwal Gurpreet
- Diaz Fernanda
- Ding Shizhi
- Ding Yiming
- Ding Zhipeng
- Dingyue Tang
- Dirven Yvette
- Dissmann Jil-Sophie
- Do Stephanie
- Dogra Arushi
- Dominguez Viana Isabel Perez
- Dong Dongyang
- Dong Haitao
- Dong Jason
- Dong Shan
- Dong Shan
- Dong Shan
- Dong Shangzhi
- Dong Shangzhi
- Doyle David
- Doyle Shannon
- Dube Alexandre
- Dubuc Emilien
- Dunstan Izzy
- Dusseaux Theodore A.
- Dvorkin Steve
- Edelmayer Marco
- Ehrenworth Amy
- Eidloth Franziska
- Eijkens Bruno
- Eilers Keno
- El Moubayed Yorgo
- Elcin Evrim
- Elias Noel
- Elikan Max
- Ellermeier Craig
- Elliott Hannah
- Elsa Yeung Hoi Lam
- Emilov Kristian
- Espinoza Diego
- Evans Rhys
- Faidh Mohammed
- Falgenhauer Elisabeth
- Fan Catherine
- Fang Chengzhu
- Fang Choco
- Fang Xiangyi
- Farhi Einan
- Farias Sebastian
- Farny Natalie
- Farny Natalie G.
- Farrell Jennifer
- Fassler Jan
- Faurdal David
- Faustova Ilona
- Feng Xinhua
- Fernandez Cesar Ibrahym Rodriguez
- Fierro Daniela Olono
- Figueroa Ana Cristina
- Figueroa Jose Arnulfo Juarez
- Fikry Clara
- Filzen Rachael
- Fischer Matthew
- Fitzgerald Kevin
- Fitzgerald Liza
- Flores Vinicius
- Foda Asmaa
- Fong Yuhui Deborah
- Forman Victor
- Frank Stefanie
- Frankel Eva
- Freire Paulo J. C.
- Friedman Yonatan
- Frohlich Lisa
- Fu Wenhan
- Fu Yousi
- Fuentes Ernie
- Fulton Leah
- Fung Ip Ning
- Fung Yam Shing
- Gabrielli Jacopo
- Gahagan Maddison
- Gaitt Tobias
- Gaizauskaite Aukse
- Gallegos Isabella
- Gamoneda Diego
- Gandhi Rishi
- Gao Cecily
- Garavito Paula
- Garcia Chrismar
- Garcia David
- Garrido Delia
- Garulli Elisa
- Gaspar Camila
- Gaudi Alex
- Ge Gao
- Ge Yubin
- George Stephan
- Gerard Antoine
- Gershater Markus
- Ghosh Souvik
- Giannopoulos Alexandros Dimitriou
- Giannoula Yvoni
- Gilman Daniel Barber James
- Glockner Eleanor
- Goenka Anushya
- Goetz Marley
- Gogineni Namrata
- Gokul [NO FIRST NAME IN SCOPUS]
- Gonzalo Gonzalo Saiz
- Goodson Michael
- Gopaul Deshmukh
- Gou Yanchen
- Govers Jolijn
- Graaf Floor de
- Grace Tsui Shing Yan
- Graves Daniel
- Grazulyte Inga
- Greenwald Matthew
- Gu Jiajun
- Gu Yiheng
- Gu Yining
- Guadagnino Brett
- Guenther James
- Guerassimoff Lea
- Guo Jintao
- Gupta Shreya
- Guptil Chris
- Guseva Anna
- Ha Jacqueline
- Haddock-Angelli Traci
- Haight Travis
- Hale Mitch
- Hamady Carla
- Han Wang
- Han Weitang
- Handal Paola
- Hanrong Zhu
- Hansen Cecilie
- Hao Junyao
- Hao Mei
- Hao Zhengguo
- Haoran Xu
- Haralsvik Anne Kristin
- Hariyani Imtiyaz
- Hartley Zach
- Hassan Sondoss
- Hau Sion
- He Fa
- He Hanker
- He Henry
- He Karen
- He Lindong
- He Menglan
- He Peixiang
- He Yuna
- He Zhien
- Healy Liam
- Heath Emily
- Heger Theresa
- Hei Chan Yick
- Heijningen Franca van
- Heintze Maxime
- Hemmings Sam
- Heng Heng
- Heng Mary
- Henras Anthony
- Herbert Heydy
- Hernandez Ivan Martin
- Hernandez Laura Armero
- Herrmann Max
- Heux Stephanie
- Hewitt Amy
- Hiesinger Marlene
- Hill Kurt
- Hin Chan Lok
- Hin Wong Chung
- Hin Yu Man
- Ho Anthony
- Ho Ng Sze
- Ho Tim
- Hodson Sophie
- Hofer Sebastian
- Holman Olivor
- Holmedal Ingebjorg
- Hong Lai Tsz
- Hong Lee Chi
- Hong Yiquan
- Hong Yirui
- Horz Philip
- Hoskan Mehmet Ali
- Hosseini Reza
- Hou Ali
- Houmani Moustafa
- Hsiao Chia-Yi
- Hsieh Yi Da
- Hsu Chia-Wei
- Hsu Yi-Hsuan
- Hu Miao
- Hu Shi
- Hu Vivian
- Hu Wenyue
- Hu Xinyi
- Hu Yunyun
- Hu Zhaoqing
- Hu Zhiyuan
- Huang Fangliang
- Huang Jiaxi
- Huang Morris
- Huang Ray
- Huang William
- Huang Yansong
- Huang Yaohua
- Huang Yilin
- Huang Yinpin
- Huanying He
- HuaYue Zhang
- Huerta Ana Laura Torres
- Humphreys Christopher
- Hung Chia
- Husnatter Kai
- Huuki Liz
- Huynh Juilanne
- Hwang Michael
- Ibrahim Ahmed
- Ikagawa Yuichiro
- Ikhsan Muhammad
- Ikwuagwu Bon
- Imgold Markus
- Inanc Tugba
- Inckemann Rene
- Isaac Ashley
- Isaacs Farren
- Isogai Tatsuki
- Iwuogo Amanda
- Iyer Aditya
- Iyer Tvarita Shivakumar
- Izzati Nurul
- Jacq Annick
- Jain Rishabh
- Jain Shubham
- Jainarayanan Ashwin Kumar
- Jakutis Gabrielius
- Jaoui Samuel
- Japranata Valdi Ven
- Jaramillo Alfonso
- Jasiunas Simas
- Jasti Naveen
- Jay Leung Chung Yin
- Jayaraman Guhan
- Jayaraman Srimathi
- Jenakendran Jenaagan
- Jensen Joen Haahr
- Jesse Hayley
- Jha Aryaman
- Ji Peicheng
- Jiacheng Wu
- Jiahe Zhang
- Jiamiao Liu
- Jian Liu
- Jiang Nannan
- Jiang Zhenyu
- Jianzhao Yang
- Jiaqi Hu
- Jiaqi Xiao
- Jimenez Carlene
- Jin Kaifeng
- Jingjing Zhao
- Jinyu Zhu
- Jo Kyuhee
- Joe Lam Kai Ching
- Johnson Elizabeth
- Johnson Michael
- Jones Ari
- Jones Cara
- Jones Ethan
- Jones Megan
- Jones Melissa
- Jongkees Seino
- Jonsson Martin
- Jude Marcia Smiti
- Jung Younji
- Juskaite Ieva
- Justice Isaac
- Kabbara Ismat
- Kadimi Sricharan
- Kailash B.P.
- Kalinowski Jorn
- Kalinowski Jorn
- Kalson Pranshu
- Kamble Yash Laxman
- Kanata Eleni
- Kanaya Toshihiro
- Kang Han
- Kang Xu
- Kang Ziqi
- Kantas Gamze
- Kantor Nicole
- Kapsokefalou Maria
- Karpauskaite Laura
- Karpus Laurynas
- Karshenas Arman
- Karumanchi Pranathi
- Katherine Lai Man Wai
- Katopodi Xanthi Leda
- Kawasaki Yusuke
- Kayihan Ceyhun
- Keating Collin
- Kehan Tao
- Keidar Nitzan
- Keij Sander
- Kelly Ellis
- Kelly Julia
- Kennedy Fiona
- Kenneth Ng Tsz Chun
- Khaimani Jatin
- Khalid Alizah
- Khenwar Arundhati
- Kiga Daisuke
- Kim Anna
- Kim Christine
- Kim Dong Ju
- Kim Ellie
- Kim Gloria
- Kim Goeun
- Kim Grace
- Kim Sean
- Kin-ning Wong Carol
- King Stefanie
- Kittur M. Sagar
- Kiu Lee Hong
- Kiu Wong Hoi
- Kivisto Samu
- Klaas Liz
- Klopprogge Bjarne
- Ko LiangYu
- Kofoed Selma
- Kohabir Kavish
- Kolosova Anastasia
- Kong Cheng Chak
- Kong Linzhen
- Kortus Drew
- Koski Jessica
- Kostadima Eleni
- Kostopoulos Ioannis V.
- Kotzastratis Stylianos
- Kou Senhao
- Koutelidakis Antonios E.
- Kozhevnikov Adrian
- Krabacher Rachel
- Krainer Birgit
- Krauss Elisha
- Kristy Brandon
- Krokos Vasilios
- Kruger Dustin
- Krusemann Jan Lukas
- Kryukova Jhanna
- Ku Chi-Yao
- Kuang Yi
- Kuangyi Wei
- Kuebler Nadine
- Kugathasan Luxcia
- Kumar Adarsh
- Kumar Vignesh
- Kumbhojkar Ninad
- Kurian Jacob
- Kwasniak Dominika
- Kyrpizidis Grigorios
- Labecka Nikol
- Lahad Divangana
- Lai Evelyn
- Lai Evelyn
- Lam Chan Wing
- Lam Kendrick
- Lam Kevin
- Lam Yiu Choi
- Lang Jacob
- Lang Yusen
- Lassel Nicole
- Latham Michael
- Laun Sarah
- Laurel Ralph
- Laurentius Andrea
- Laury Jessica
- Lautru Sylvie
- Lawrence Jack
- Leach Cass
- Leal Luis Mario
- Ledalla Karthik
- Lee James
- Lee Jordan
- Lee Matthew
- Lee Meixuan
- Lee Meng-Zhan
- Lee Yeonjae
- leelahakorn Nattawut
- Leeuw Monique de
- Lefevre Marine
- Lehtonen Leevi
- Leitner Karl
- Lekshmi Hema
- Lemieux Pascale
- Leon Karen De
- Lepetit Florian
- Levrier Antoine
- Li Caidian
- Li Changyu
- Li Hailong
- Li Haocong
- Li Jiadong
- Li Kevin
- Li Nuonan
- Li Peilin
- Li Sophie Ruojia
- Li Tingting
- Li Tingting
- Li Tingyue
- Li Xuecheng
- Li Yanyan
- Li Yuanyuan
- Li Yuqi
- Li Zihao
- Li Zonghao
- Liang Tommy
- Liang Yuteng
- Liang Zhihan
- Liangjian Yang
- Liao Chin-Hsuan
- Liaoqi Du
- Lichi Fang
- Lim Sangwu
- Lim Yan Ping
- Lima Guilherme Meira
- Lin Beatrix Tung Xue
- Lin Chenyi
- Lin Junliang
- Lin Weifeng
- Lin Yasmin
- Lin Yu-Chun
- Lind Andrea Clausen
- Linke Dirk
- Litsa Maria
- Liu Fangqi
- Liu Huan
- Liu Jiangyuan
- Liu Jiezheng
- Liu Jingang
- Liu Ting
- Liu Wei-Ting
- Liu Weijia
- Liu Wukun
- Liu Xiaolong
- Liu Xutong
- Liu Yiheng
- Liu Yuansheng
- Liu Zhaoyu
- Liu Zhihao
- Liu Zhixiang
- Liu Zi
- Liya Devang Haresh
- Lo Natalie
- Lockwood Savannah
- Loeffler Frank
- Logel Dominic
- Loke Chun Kit
- Lombardero Francisco Javier Quero
- Longo Ylenia
- Loog Mart
- Lopez-Grado Guillem
- Lorch Kevin
- Lortie Louis-Andre
- Lotz Thea
- Louis Simon
- Lu Chenyu
- Lu Yinjing
- Luan Lin
- Luo Chenfei
- Luo Claire
- Luo Fang
- Luo Linda
- Luo Liudong
- Luo Mingyue
- Luo Xiaofan
- Luo Zhi
- Luque Ana Cecilia
- Luzuriaga Juan Carlos
- Lykkegaard Magnus Ronne
- Ma Guanghui
- Ma Jiaxin
- Ma Liang
- Ma Lingling
- Ma Yingqi
- Ma Yuan
- Maddiboina Dhanyasri
- Madelenat Manon
- Madrid Micah
- Magzoub Mazin
- Mahapatra Nitish R.
- Maljavin Artemi
- Mancinotti Davide
- Mangkusaputra Venda
- Mansfield Laura
- Mao Jiangjiao
- Marcoleta Andres
- Marinovic Adrian
- Marken John
- Markiv Anatoliy
- Marquina D.
- Marta Britany
- Marti Marcos Vega-Hazas
- Martin Michael
- Martinelli Adriano
- Martinez Antonio
- Martinez Victor Javier Robledo
- Maruo Tatuya
- Matheis Anna
- Matiyevskaya Frida
- Mattens Jard
- Matthew Cheah
- Maupu Clemence
- Mayer Julia
- Mazelis Ignas
- McConnell Kelton
- McDonald Dallas
- McDonough Matt
- McShane Evie
- Meas Catherosette
- Medina Maria Jose Ramos
- Meerbrei Tanja
- Meirkhanova Ayagoz
- Mejlsted Jacob
- Mellou Areti-Efremia
- Menart Peter
- Mendoza Adrian Federico Hernandez
- Meneu Lea
- Menghan Gao
- Mengtao Du
- Menon Sarvesh
- Mertes Verena
- Meyer Lasse
- Meyfarth Oda-Emilia
- Miao Xinyi
- Miao Zhoudi
- Michelsen Stephanie
- Milano Fiona
- Mills Channah
- Milshtein Eliya
- Ming Shaw Kar
- Mingge Li
- Mishler Dennis M.
- Mishra Vibhu
- Mitropoulos Alex
- Mo Yilin
- Mohan Kumar B.S.
- Moncayo Eduardo
- Moreira Natalia Torres
- Mori Yuya
- Morrison Shikei
- Moscoso Ricardo
- Mota Mariana Santana da
- Mubeen Sara
- Mueller Julia
- Mukhanova Assel
- Mulikova Tomiris
- Mullin Matthew
- Munoz Felipe
- Murugan Santosh
- Muthukrishnan Anantha Barathi
- Myers Karl
- Neda Andrei
- Ngo Cheng Tsz
- Nguyen Aerilynn
- Nguyen Judy Van
- Ni Haochen
- Nianlong Li
- Nicholson Kyle
- Nickels Elena
- Nieberding-Swanberg Jolee
- Nielsen Lina
- Nijenhuis Janine
- Ning Hsiu Ou
- Niu Wei
- Niu Xubo
- Niwa Ryo
- Norberg Axel
- Norvaisaite Ieva
- Notheisen Jan
- Ntekas Ioannis
- Nunez Anna Karen Aguilar
- Nurachman Luthfian Aby
- Obaji Daniel
- Obrvan Marko
- Oetelaar Maxime van den
- Oliveira Nina De Sousa
- Oliver Adam
- Ollessa-Daragon Xavier
- Olmin Amanda
- Ong June
- Oropeza Carlos Javier Cordero
- Oser Eden
- Oswald Andreas
- Otto Matthias
- Otto Matthias
- O’Brien James
- O’Leary Travis
- Paez Timmy
- Pageni Aroma
- Pai Sveekruth Sheshagiri
- Palo Sara
- Pan Catherine
- Pan Lin Yu
- Pan Luyao
- Pan Yuyao
- Pang Chung Him
- Pang Yibo
- Pange Nishtha
- Papadopoulo Kenn
- Parab Komal
- Park Kevin
- Park Mikyung
- Park Seunghyun
- Parmar Jasmeen
- Parmentier Mathieu
- Parr Lillian
- Parry Geraint
- Partridge Daniel
- Pasi Mor
- Pate Kaylee
- Patel Abhilash
- Patel Bhargav
- Patel Jaymin
- Patel Vainav
- Patel Varun
- Patil Mitali
- Pattiradjawane Lorenzo
- Paul Ahavi
- Pavelek Tucker
- Pearce Camille
- Pedamallu Havisha
- Pedersen Hege Hetland
- Pedrolli Danielle Biscaro
- Pehlivan Meryem
- Pei Yifei
- Pei Yuanzhe
- Peiyao Fan
- Pena Thevenet Esteban de la
- Peng Jiarong
- Peng Jiarong
- Peng Yue
- Peng Zhao
- Penny Leo
- Peras Marie
- Perera Dylan
- Perez Jose Pablo Rascon
- Petracchini Serena
- Pezzutto Denise
- Phelan Cam
- Pinheiro Vitor
- Pinto Elizabeth
- Pitaliya Madhav
- Polanka Laura
- Pollitt Chynna
- Poole Andrea
- Portillo Roberto
- Powis Simon
- Praditya Albert
- Prakash Satya
- Prakash Supriya
- Pratama Muhammad Iqbal Adi
- Preetha R.
- Premo Jacob
- Prins Rianne
- Pruneski James
- Ptak Jeffrey
- Putthoff Lisa
- Qi Ariel
- Qian Ling
- Qiang Ye
- Qiaochu Jiang
- Qin Zichen
- Qipeng Zhang
- Qiu Hao
- Qu Jingting
- Qu Mingbo
- Quinn Katherine
- Raadam Morten
- Rai Hrishika
- Rajagopal Varshni
- Raju Deeksha
- Rajurkar Aishwarya
- Rakhimov Jennifer
- Rambhatla Rahul
- Ramstrom Elin
- Ramzeen Aaron
- Ran Guozheng
- Ran Yuncong
- Rana Yash
- Rao Achala
- Rao Xichen
- Rasheed Moiz
- Rashid Khadija
- Rasmussen Tenna
- Rasmussen Victoria Svaerke
- Rastogi Tashi
- Raut Sandeep
- Rautanen Pauliina
- Reaney Bethany
- Rebello Alex
- Rege Mayuri
- Ren Haotian
- Ren Wenan
- Rentouli Stamatina
- Resendiz Armando Cortes
- Reshamwala Shamlan M. S.
- Rettedal Neil
- Ribeiro Nathan Vinicius
- Ries Anna
- Rigon Luca
- Ripp Steven
- Ritmejeris Justas
- Rivas Paula
- Rivera Mario Loya
- Roberts Luc
- Robin Marina
- Rodriguez Guillermo Fernandez
- Roige Biel Badia
- Rokaitis Irmantas
- Rolfsnes Rebekka Rekkedal
- Romeo Yves
- Rong Ziyue
- Rosa Caio Gomes Tavares
- Rouleau Francois D.
- Ruhnau Johannes
- Ruhnau Johannes
- Run Zhouyan
- Ruscher David
- Ruzic Robert
- Ruzicka Alex
- Ryan Sean
- Ryu Bo Sun
- Saade Ursula
- Sabandal Angelica
- Sabuwala Burhanuddin
- Sackey Juliana
- Saha Margaret
- Saini Karandip
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- Zhao Peng
- Zhao Tianyan
- Zhao Wenxue
- Zhao Yihang
- Zhaoting Li
- Zhecheng Huang
- Zheng Daniel
- Zheng Jiyang
- Zhiwei Song
- Zhong Yanling
- Zhou Hanmi
- Zhou Jiajie
- Zhou Jianan
- Zhou Rui
- Zhou Shuyao
- Zhou Xuanhao
- Zhou Yanjun
- Zhou Yi
- Zhou Yinchi
- Zhou Yineng
- Zhou Yuezhang
- Zhou Yuxin
- Zhou Zhiyu
- Zhu Chushu
- Zhu Ke
- Zhu Xueqian
- Zi Lihan
- Zilinskaite Nemira
- Zimmermann Andreas
- Zimmermann Jennifer
- Zirong Zeng
- Ziwei Zhou
- Ziyi Zhao
- Zorrilla Francisco
- Zou Jiahua
- Zukauskaite Kristina
- Zulueta Patricia
- Zvirblyte Justina
- Publication venue
- Publication date
- 01/01/2020
- Field of study
Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data
New genetic loci link adipose and insulin biology to body fat distribution.
- Author
- Aalto Ville
- Aasarød Knut
- Abecasis Goncalo R
- Abecasis Gonçalo
- Absher Devin
- Adair Linda S
- Adam Martin
- Adeyemo Adebowale
- Ahlqvist Emma
- Ahmadi Kourosh R
- Ahola Aila
- Ainali Chrysanthi
- Akylbekova Ermeg
- Ala-Korpela Mika
- Alavere Helen
- Albagha Omar M E
- Albrecht Eva
- Alen Markku
- Alexander Myriam
- Alhenc-Gelas François
- Alizadeh Behrooz Z
- Allison Matthew A
- Alonso Nerea
- Altshuler David
- Ambite Jose Luis
- Amin Najaf
- Amouyel Philippe
- An Ping
- Anderson Carl A
- Anderson Denise
- Anderson Garnet
- Andrews Jeanette S
- Antonella Mulas
- Antti Jula
- Aragaki Aaron K
- Arking Dan E
- Arnold Alice
- Arnold Alice M
- Arora Pankaj
- Arscott Gillian M
- Artigas Maria Soler
- Arveiler Dominique
- Asiki Gershim
- Aspelund Thor
- Assimes Themistocles L
- Atalay Mustafa
- Atkinson Elizabeth J
- Aulchenko Yurii
- Avery Christy
- Bain Stephen C
- Bakker Stephan J L
- Balcells Susana
- Balkau Beverley
- Ballantyne Christie M
- Balmforth Anthony J
- Bandinelli Stefania
- Barbalic Maja
- Barrett Amy
- Barroso Ines
- Barroso Inês
- Basart Hanneke
- Basart Hanneke V
- Bataille Veronique
- Baumert Jens
- Beckmann Jacques S
- Beekman Marian
- Been Latonya F
- Beilby John
- Beilby John P
- Bell Jordana T
- Bellis Claire
- Bennett Amanda J
- Bennett Franklyn
- Berenson Gerald S
- Bergman Richard N
- Bergmann Sven
- Berndt Sonja I
- Berne Christian
- Bidulescu Aurelian
- Bielak Lawrence F
- Bierut Laura J
- Biffar Reiner
- Bis Joshua C
- Blackburn Hannah
- Blangero John
- Blankenberg Stefan S
- Blüher Matthias
- Boban Mladen
- Bochud Murielle
- Boehm Bernhard O
- Boehnke Michael
- Boerwinkle Eric
- Boezen H Marike
- Bolton Jennifer L
- Bolton Judith A Hoffman
- Bonnet Fabrice
- Bonnycastle Lori L
- Boomsma Dorret I
- Borecki Ingrid
- Boright Andrew P
- Borja Judith B
- Bornstein Stefan R
- Boston Jonathan
- Bots Michiel L
- Bouatia-Naji Nabila
- Bouchard Claude
- Bovet Pascal
- Boyd Heather A
- Bragg-Gresham Jennifer L
- Brambilla Paolo
- Brand Eva
- Brand Stefan-Martin
- Brandi Maria Luisa
- Braund Peter S
- Brennan Eoin P
- Brismar Kerstin
- Brody Jennifer
- Broekmans Frank J
- Broer Linda
- Brown Matthew A
- Brown Morris J
- Brown-Gentry Kristin
- Bruinenberg Marcel
- Buchkovich Martin L
- Buckley Brendan M
- Buil Alfonso
- Bull Shelley B
- Burgdorf Christof
- Buring Julie E
- Burnett Mary S
- Burnier Michel
- Burri Andrea
- Burton Paul R
- Bush William S
- Busonero Fabio
- Buxbaum Sarah G
- Buyske Steve
- Buzkova Petra
- Byrne Enda M
- Böger Carsten A
- Böhringer Stefan
- Böttcher Yvonne
- Cambien Francois
- Campbell Harry
- Campbell Susan
- Carba Delia B
- Carlson Chris
- Carlson Olga D
- Carty Cara
- Casas Juan P
- Caspersen Ida H
- Castano-Betancourt Martha
- Cauchi Stéphane
- Cauley Jane A
- Caulfield Mark
- Cavalieri Margherita
- Cazier Jean-Baptiste
- Center Jacqueline R
- Cesana Giancarlo
- Chakravarti Aravinda
- Chambers John
- Chandak Giriraj R
- Chang Hsing-Yi
- Chang Yen-Pei C
- Chanock Stephen J
- Charchar Fadi J
- Chasman Dan
- Chaturvedi Nish
- Chen Constance
- Chen Han
- Chen Ida
- Chen Jin
- Chen Ming-Huei
- Chen Wei
- Chen Yii-Der Ida
- Cheng Iona
- Cheng Sulin
- Chines Peter S
- Cho Yoon Shin
- Choi Murim
- Chouraki Vincent
- Christiansen Claus
- Chu Audrey Y
- Cimponeriu Dan
- Ciullo Marina
- Clark Graeme R
- Clarke Robert
- Claudi-Boehm Simone
- Coassin Stefan
- Cochran Barbara
- Cole Shelley
- Colhoun Helen
- Colhoun Helen M
- Collins Francis S
- Collins Rory
- Connell John M
- Cooper Cyrus
- Cooper Jackie A
- Cooper Matthew N
- Cooper Richard S
- Coresh Josef
- Cornelis Marilyn C
- Corre Tanguy
- Corsi Anna Maria
- Couper David
- Cousminer Diana L
- Coviello Andrea D
- Cox David
- Crawford Dana
- Crisponi Laura
- Croteau-Chonka Damien C
- Cucca Francesco
- Cummings Steven R
- Cupples Adrienne L
- Cupples L Adrienne
- Curhan Gary
- d'Adamo Pio
- Dahgam Santosh
- Dailiana Zoe
- Danesh John
- Danoy Patrick
- Dastani Zari
- Davies Gail
- Daw E Warwick
- Day Felix R
- Day Ian N M
- de Andrade Mariza
- de Boer Ian H
- de Boer Rudolf A
- de Faire Ulf
- de Geus Eco J C
- Deary Ian J
- Dedoussis George
- Dedoussis George V
- Dedoussis George V Z
- Deelen Joris
- Deelman Ewa
- Dehghan Abbas
- Delgado Graciela
- Deloukas Panagiotis
- Deloukas Panos
- Demerath Ellen W
- Demirkan Ayse
- Demirkan Ayşe
- Den Hertog Heleen M
- Denniff Matthew
- Dennison Elaine M
- Dermitzakis Emmanouil T
- Deshmukh Harshal
- Deshmukh Harshal A
- Devuyst Olivier
- di Meglio Paola
- Diemert Patrick
- Dimas Antigone S
- Dimitriou Maria
- Ding Jingzhong
- Do Ron
- Dominiczak Anna F
- Doney Alex
- Dong Yanbin
- Donnelly Louise A
- Doumatey Ayo
- Dreisbach Albert W
- Drong Alexander W
- Duggan David
- Dumitrescu Logan
- Duncan Bruce B
- Duncan Emma L
- Dupuis Josee
- Dupuis Josée
- Durbin Richard
- Durda Peter
- Döring Angela
- Dörr Marcus
- Eastell Richard
- Easton Douglas F
- Ebrahim Shah
- Econs Michael J
- Edkins Sarah
- Egan Josephine
- Ehret Georg
- Eiriksdottir Gudny
- Eisman John A
- Eklund Niina
- El Mokhtari NourEddine
- Elks Cathy E
- Ellinghaus David
- Elliott Paul
- Elosua Roberto
- Emilsson Valur
- Endlich Karlhans
- Epstein Stephen E
- Erbel Raimund
- Erdmann Jeanette
- Erdos Michael R
- Eriksson Joel
- Eriksson Johan
- Eriksson Niclas
- Eriksson Per
- Ernst Florian
- Esko Tonu
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- Esko Tönu
- Estrada Karol
- Eury Elodie
- Evangelou Evangelos
- Evans Alun
- Evans David M
- Eyheramendy Susana
- Eyjolfsson Gudmundur Ingi
- Fagerholm Emma
- Falhammar Henrik
- Fall Tove
- Farrall Martin
- Fauser Bart C J M
- Fava Cristiano
- Feenstra Bjarke
- Fehrmann Rudolf
- Feitosa Mary
- Feranil Alan B
- Ferrannini Ele
- Ferrario Marco M
- Ferreira Teresa
- Ferreli Liana
- Ferrières Jean
- Ferrucci Luigi
- Fischer Krista
- Florez Jose C
- Folkersen Lasse
- Folsom Aaron R
- Fontanillas Pierre
- Ford Ian
- Fornage Myriam
- Foroud Tatiana
- Forouhi Nita G
- Forrester Terrence
- Forsblom Carol
- Foster Meredith C
- Fowke Jay
- Fowkes F Gerald R
- Fowkes Gerard R
- Fox Caroline S
- Fox Ervin R
- Franceschini Nora
- Franco Oscar H
- Franco-Cereceda Anders
- Franke Andre
- Franke Lude
- Franks Paul W
- Frants Rune
- Fraser Ross M
- Frayling Timothy M
- Freedman Barry I
- Freimer Nelson B
- Freitag Daniel F
- Friedrich Nele
- Froguel Philippe
- Frost Morten
- Fuchsberger Christian
- Galan Pilar
- Ganesh Santhi K
- Ganna Andrea
- Gansevoort Ron T
- Gao Xiaoyi
- Garcia Melissa
- Garcia-Giralt Natàlia
- Garnaas Maija
- Gasparini Paolo
- Gauguier Dominique
- Gaunt Tom R
- Gautvik Kaare M
- Geller Frank
- Gharavi Ali G
- Giedraitis Vilmantas
- Gieger Christian
- Gierman Hinco J
- Gigante Bruna
- Gill Geoffrey V
- Giroux Sylvie
- Giulianini Franco
- Glass Daniel
- Glazer Nicole
- Glazer Nicole L
- Glenn Kim
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- Go Min Jin
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- Goessling Wolfram
- Golay Alain
- Goldstein Benjamin A
- Goltzman David
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- Goodall Alison H
- Goodarzi Mark O
- Goodloe Robert
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- Gorski Mathias
- Grabe Hans-Jörgen
- Graff Misa
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- Grammer Tanja B
- Gravito Martha L
- Greenwood Celia M T
- Grewal Jagvir
- Grimsby Jonna
- Grobbee Diederick E
- Groop Leif
- Groop Per-Henrik
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- Grundberg Elin
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- Gräßler Jürgen
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- Gudnason Villi
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- Gyllensten Ulf B
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- Hall Per
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- Hallmans Göran
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- Han Bok-Ghee
- Hankinson Susan E
- Hanson Robert L
- Hardy Rebecca
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- Harjutsalo Valma
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- Hartman Catharina A
- Hass Merli
- Hassanali Neelam
- Hassinen Maija
- Hastie Nicholas D
- Hastie Nick
- Hattersley Andrew T
- Haun Margot
- Havulinna Aki S
- Hayward Caroline
- Hazen Stanley L
- He Bing
- He Chunyan
- Heard-Costa Nancy L
- Heath Andrew C
- Heath Simon
- Heckbert Susan R
- Hedblad Bo
- Hedman Åsa K
- Heid Iris M
- Heikkilä Kauko
- Heikkilä Outi
- Heiss Gerardo
- Heliövaara Markku
- Helmer Catherine
- Helmer Quinta
- Henders Anjali K
- Henderson Brian
- Hengstenberg Christian
- Henneman Peter
- Hercberg Serge
- Herder Christian
- Hernandez Dena
- Hernandez Dena G
- Herrera Lizbeth
- Herzig Karl-Heinz
- Hicks Andrew A
- Hietala Kustaa
- Higashio Julia
- Hillege Hans L
- Hilton Gina
- Hindorff Lucia
- Hingorani Aroon
- Hirschhorn Joel N
- Hivert Marie-France
- Ho Weang K
- Hocking Lynne J
- Hoffmann Wolfgang
- Hofman Albert
- Holliday Elizabeth G
- Holm Hilma
- Holmen Oddgeir
- Homuth Georg
- Hopewell Jemma C
- Horikoshi Momoko
- Hosseini Mohsen
- Hottenga Jouke-Jan
- Hovingh G Kees
- Howard Philip
- Hsiung Chao Agnes
- Hsu Yi-Hsiang
- Hu Frank B
- Huang Huateng
- Huang Jinyan
- Hui Jennie
- Humphries Steve E
- Hundertmark Claudia
- Hung Yi-Jen
- Hunt Sarah E
- Hunt Steven C
- Hunter David J
- Husted Lise Bjerre
- Hveem Kristian
- Hwang Shih-Jen
- Hyppönen Elina
- Igl Wilmar
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- Iribarren Carlos
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- Islam Muhammad
- Ittermann Till
- Iwai Naoharu
- Jackson Anne U
- Jackson Rebecca
- Jacobs Gunnar
- Jafar Tazeen H
- James Alan L
- Jameson Karen A
- Jang Yangsoo
- Janipalli Charles S
- Jansen Hanneke
- Janssens A Cecile J W
- Jarvelin Marjo-Riitta
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- Jousilahti Pekka
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- Kanaya Alka
- Kang Hyun M
- Kang Hyun Min
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- Keller Benjamin J
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- Komulainen Pirjo
- Kong Augustine
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- Witteman Jacqueline C M
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- Wolffenbuttel Bruce H R
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- Wong Tien Y
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- Wood Andy
- Workalemahu Tsegaselassie
- Wright Alan F
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- Wu Joseph M W
- Wu Ying
- Würtz Peter
- Xiao Su-Mei
- Yajnik Chittaranjan S
- Yang Jian
- Yang Qiong
- Yang Tsun-Po
- Yao Jie
- Yengo Loïc
- Yerges-Armstrong Laura M
- Young Alicia
- Young Elizabeth H
- Young J H
- Young Lauren
- Yuan Xin
- Zaboli Ghazal
- Zalloua Pierre A
- Zarrabeitia María T
- Zelenika Diana
- Zemunik Tatijana
- Zerbini Gianpaolo
- Zgaga Lina
- Zhai Guangju
- Zhang Feng
- Zhang Qunyuan
- Zhang Weihua
- Zhao Jing Hua
- Zhao Wei
- Zheng Hou-Feng
- Zheng Wei
- Zhou Yanhua
- Zhu Haidong
- Zhu Kun
- Zhu Xiaofeng
- Zhuang Wei V
- Zhuang Wei Vivian
- Ziegler Andreas
- Zillikens M Carola
- Zimmermann Martina E
- Zitting Paavo
- Zondervan Krina T
- Zukowska-Szczechowska Ewa
- Zygmunt Marek
- Ärnlöv Johan
- Österholm Anne-May
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
Body fat distribution is a heritable trait and a well-established predictor of adverse metabolic outcomes, independent of overall adiposity. To increase our understanding of the genetic basis of body fat distribution and its molecular links to cardiometabolic traits, here we conduct genome-wide association meta-analyses of traits related to waist and hip circumferences in up to 224,459 individuals. We identify 49 loci (33 new) associated with waist-to-hip ratio adjusted for body mass index (BMI), and an additional 19 loci newly associated with related waist and hip circumference measures (P < 5 × 10(-8)). In total, 20 of the 49 waist-to-hip ratio adjusted for BMI loci show significant sexual dimorphism, 19 of which display a stronger effect in women. The identified loci were enriched for genes expressed in adipose tissue and for putative regulatory elements in adipocytes. Pathway analyses implicated adipogenesis, angiogenesis, transcriptional regulation and insulin resistance as processes affecting fat distribution, providing insight into potential pathophysiological mechanisms
Global baryon number conservation encoded in net-proton fluctuations measured in Pb–Pb collisions at √sNN = 2.76 TeV
- Author
- Acharya S.
- Adamova D.
- Adler A.
- Adolfsson J.
- Aggarwal M. M.
- Agnello M.
- Agrawal N.
- Ahammed Z.
- Ahmad S.
- Ahn S. U.
- Akindinov A.
- Al-Turany M.
- Alam S. N.
- Alba J. L. Bazo
- Albuquerque D. S. D.
- Aleksandrov D.
- Alessandro B.
- Alfanda H. M.
- Alfaro Molina R.
- Ali B.
- Ali Y.
- Alici A.
- Alkin A.
- Alme J.
- Alt T.
- Altenkamper L.
- Altsybeev I
- Anaam M. N.
- Andrei C.
- Andreou D.
- Andrews H. A.
- Andronic A.
- Angeletti M.
- Anguelov V
- Anson C.
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- Arcelli S.
- Arnaldi R.
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- Augustinus A.
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- Baek Y. W.
- Bagnasco S.
- Bai X.
- Bailhache R.
- Baillie O. Villalobos
- Bala R.
- Balbastre G. Conesa
- Baldisseri A.
- Ball M.
- Balouza S.
- Barbera R.
- Barioglio L.
- Barnafoldi G. G.
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- Barroso V. Chibante
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- Basu S.
- Batigne G.
- Batyunya B.
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- Buhler P.
- Buncic P.
- Bustamante R. T. Jimenez
- Buthelezi Z.
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- Camerini P.
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- Caron R.
- Castellanos J. Castillo
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- Chakraborty P.
- Chandra S.
- Chang W.
- Chapeland S.
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- Yoon J. H.
- Yuan S.
- Yuncu A.
- Yurchenko V
- Zaccolo V
- Zaman A.
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- Zanoli H. J. C.
- Zardoshti N.
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- Zaviyalov N.
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2020
- Field of study
Experimental results are presented on event-by-event net-proton fluctuation measurements in Pb–Pb collisions at √SNN=2.76 TeV, recorded by the ALICE detector at the CERN LHC. These measurements have as their ultimate goal an experimental test of Lattice QCD (LQCD) predictions on second and higher order cumulants of net-baryon distributions to search for critical behavior near the QCD phase boundary. Before confronting them with LQCD predictions, account has to be taken of correlations stemming from baryon number conservation as well as fluctuations of participating nucleons. Both effects influence the experimental measurements and are usually not considered in theoretical calculations. For the first time, it is shown that event-by-event baryon number conservation leads to subtle long-range correlations arising from very early interactions in the collisions.publishedVersio
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- Zhu B
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- Zhu Y
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- Zhuang H
- Zhuang X
- Zientara-Rytter K
- Zimmermann CM
- Ziviani E
- Zoladek T
- Zong W-X
- Zorov DB
- Zorzano A
- Zou W
- Zou Z
- Zou Z
- Zuryn S
- Zwerschke W
- Álvarez ÉMC
- Ávalos Y
- Önal G
- Üstün S
- Čolić M
- Đokić J
- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Iron Behaving Badly: Inappropriate Iron Chelation as a Major Contributor to the Aetiology of Vascular and Other Progressive Inflammatory and Degenerative Diseases
- Author
- A Abbott
- A Abou-Raya
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- The Long-Term Intervention with Pravastatin in Ischaemic Disease (LIPID) Study Group
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- ZZ Chong
- ZZ Chong
- Publication venue
- Publication date
- 09/08/2008
- Field of study
The production of peroxide and superoxide is an inevitable consequence of
aerobic metabolism, and while these particular "reactive oxygen species" (ROSs)
can exhibit a number of biological effects, they are not of themselves
excessively reactive and thus they are not especially damaging at physiological
concentrations. However, their reactions with poorly liganded iron species can
lead to the catalytic production of the very reactive and dangerous hydroxyl
radical, which is exceptionally damaging, and a major cause of chronic
inflammation. We review the considerable and wide-ranging evidence for the
involvement of this combination of (su)peroxide and poorly liganded iron in a
large number of physiological and indeed pathological processes and
inflammatory disorders, especially those involving the progressive degradation
of cellular and organismal performance. These diseases share a great many
similarities and thus might be considered to have a common cause (i.e.
iron-catalysed free radical and especially hydroxyl radical generation). The
studies reviewed include those focused on a series of cardiovascular, metabolic
and neurological diseases, where iron can be found at the sites of plaques and
lesions, as well as studies showing the significance of iron to aging and
longevity. The effective chelation of iron by natural or synthetic ligands is
thus of major physiological (and potentially therapeutic) importance. As
systems properties, we need to recognise that physiological observables have
multiple molecular causes, and studying them in isolation leads to inconsistent
patterns of apparent causality when it is the simultaneous combination of
multiple factors that is responsible. This explains, for instance, the
decidedly mixed effects of antioxidants that have been observed, etc...Comment: 159 pages, including 9 Figs and 2184 reference
A LASSO-Based Prediction Model for Child Influenza Epidemics: A Case Study of Shanghai, China
- Publication venue
- 'Hindawi Limited'
- Publication date
- 01/01/2022
- Field of study
Child influenza is an acute infectious disease that places substantial burden on children and their families. Real-time accurate prediction of child influenza epidemics can aid scientific and timely decision-making that may reduce the harm done to children infected with influenza. Several models have been proposed to predict influenza epidemics. However, most existing studies focus on adult influenza prediction. This study demonstrates the feasibility of using the LASSO (least absolute shrinkage and selection operator) model to predict influenza-like illness (ILI) levels in children between 2017 and 2020 in Shanghai, China. The performance of the LASSO model was compared with that of other statistical influenza-prediction techniques, including autoregressive integrated moving average (ARIMA), random forest (RF), ordinary least squares (OLS), and long short-term memory (LSTM). The LASSO model was observed to exhibit superior performance compared to the other candidate models. Owing to the variable shrinkage and low-variance properties of LASSO, it eliminated unimportant features and avoided overfitting. The experimental results suggest that the LASSO model can provide useful guidance for short-term child influenza prevention and control for schools, hospitals, and governments
Primary Central Nervous System Lymphoma
- Publication venue
- Wolters Kluwer
- Publication date
- 01/01/2016
- Field of study
Two Unique Ligand-Binding Clamps of <em>Rhizopus oryzae</em> Starch Binding Domain for Helical Structure Disruption of Amylose
- Author
- Publication venue
- Publication date
- 17/07/2012
- Field of study
<div><p>The <em>N</em>-terminal starch binding domain of <em>Rhizopus oryzae</em> glucoamylase (<em>Ro</em>SBD) has a high binding affinity for raw starch. <em>Ro</em>SBD has two ligand-binding sites, each containing a ligand-binding clamp: a polyN clamp residing near binding site I is unique in that it is expressed in only three members of carbohydrate binding module family 21 (CBM21) members, and a Y32/F58 clamp located at binding site II is conserved in several CBMs. Here we characterized different roles of these sites in the binding of insoluble and soluble starches using an amylose-iodine complex assay, atomic force microscopy, isothermal titration calorimetry, site-directed mutagenesis, and structural bioinformatics. <em>Ro</em>SBD induced the release of iodine from the amylose helical cavity and disrupted the helical structure of amylose type III, thereby significantly diminishing the thickness and length of the amylose type III fibrils. A point mutation in the critical ligand-binding residues of sites I and II, however, reduced both the binding affinity and amylose helix disruption. This is the first molecular model for structure disruption of the amylose helix by a non-hydrolytic CBM21 member. <em>Ro</em>SBD apparently twists the helical amylose strands apart to expose more ligand surface for further SBD binding. Repeating the process triggers the relaxation and unwinding of amylose helices to generate thinner and shorter amylose fibrils, which are more susceptible to hydrolysis by glucoamylase. This model aids in understanding the natural roles of CBMs in protein-glycan interactions and contributes to potential molecular engineering of CBMs.</p> </div
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