Kết quả tìm kiếm - Benjamin Challis
- Đang hiển thị 1 - 20 kết quả của 20
-
1
Minireview: Human Obesity—Lessons from Monogenic Disorders Bằng Stephen O’Rahilly, I. Sadaf Farooqi, Giles S.H. Yeo, Benjamin Challis
Được phát hành 2003Revisão -
2
-
3
-
4
Proopiomelanocortin and Energy Balance: Insights from Human and Murine Genetics Bằng Anthony P. Coll, I. Sadaf Farooqi, Benjamin Challis, Giles S.H. Yeo, Stephen O’Rahilly
Được phát hành 2004Revisão -
5
Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms Bằng Giles S.H. Yeo, Emma Lank, I. Sadaf Farooqi, Julia M. Keogh, Benjamin Challis, Stephen O’Rahilly
Được phát hành 2003Artigo -
6
-
7
-
8
A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: Beyond phaeochromocytoma and paraganglioma Bằng James MacFarlane, Keat Cheah Seong, Chad Bisambar, Basetti Madhu, Kieren Allinson, Alison Marker, Anne Y. Warren, Soo‐Mi Park, Olivier Giger, Benjamin Challis, Eamonn R. Maher, Ruth Casey
Được phát hành 2020Revisão -
9
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank Bằng Abhishek Nag, Ryan S. Dhindsa, Lawrence Middleton, Xiao Jiang, Dimitrios Vitsios, Eleanor M. Wigmore, Erik L. Allman, Anna Reznichenko, Keren Carss, Katherine R. Smith, Quanli Wang, Benjamin Challis, Dirk S. Paul, Andrew R. Harper, Slavé Petrovski
Được phát hành 2023Artigo -
10
A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechani... Bằng Benjamin Challis, Lynn E. Pritchard, John W.M. Creemers, Jérôme Delplanque, Julia M. Keogh, Jian’an Luan, Nicholas J. Wareham, Giles S.H. Yeo, Sumit Bhattacharyya, Philippe Froguel, Anne White, I. Sadaf Farooqi, Stephen O’Rahilly
Được phát hành 2002Artigo -
11
Inhibition of Interleukin-33 to Reduce Glomerular Endothelial Inflammation in Diabetic Kidney Disease Bằng Alexis Hofherr, Elena Liarte Marin, Barbara Musiał, Asha Seth, Tim Slidel, James Conway, David Baker, Pernille Hansen, Benjamin Challis, Stefano Bartesaghi, Maria Bhat, Roberto Pecoits–Filho, Tu Xiao, Viknesh Selvarajah, Kevin Woollard, Hiddo J.L. Heerspink
Được phát hành 2024Artigo -
12
#5413 FRONTIER-1: A PHASE 2B STUDY OF IL-33 BLOCKADE IN DIABETIC KIDNEY DISEASE Bằng Elena Liarte Marin, Barbara Musiał, Asha Seth, Timothy Slidel, James Conway, David H. Baker, Pernille Laerkegaard Hansen, Benjamin Challis, Maria Bhat, Stefano Bartesaghi, Roberto Pecoits–Filho, Tu Xiao, Viknesh Selvarajah, Kevin Woollard, Hiddo J.L. Heerspink, Alexis Hofherr
Được phát hành 2023Artigo -
13
An Activating Mutation of <i>AKT2</i> and Human Hypoglycemia Bằng Khalid Hussain, Benjamin Challis, Nuno Rocha, Felicity Payne, Marina Minic, Alastair Thompson, Allan Daly, Clare L. Scott, Jeffrey R. Harris, B. J. L. Smillie, David B. Savage, Uma Ramaswami, Pascale de Lonlay, Stephen O’Rahilly, Inês Barroso, Robert K. Semple
Được phát hành 2011Artigo -
14
Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY <sub>3-36</sub> Bằng Benjamin Challis, Anthony P. Coll, Giles S.H. Yeo, Scarlett B. Pinnock, Suzanne L. Dickson, Rosemary R. Thresher, John B. Dixon, Dirk Zahn, Justin J. Rochford, Anne White, R. L. Oliver, G. W. M. Millington, Samuel Aparício, William H Colledge, A. P. Russ, Mark Carlton, Stephen O’Rahilly
Được phát hành 2004Artigo -
15
Influences of rare protein-coding genetic variants on the human plasma proteome in 50,829 UK Biobank participants Bằng Ryan S. Dhindsa, Oliver S. Burren, Benjamin B. Sun, Bram P. Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Erin Oerton, Ventzislava A. Hristova, Katherine R. Smith, Keren Carss, Sebastian Wasilewski, Andrew R. Harper, Dirk S. Paul, Margarete A. Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, Dimitrios Vitsios, Euan A. Ashley, Christopher D. Whelan, Menelas N. Pangalos, Quanli Wang, Slavé Petrovski
Được phát hành 2022Pré-impressão -
16
CT Characteristics of Pheochromocytoma: Relevance for the Evaluation of Adrenal Incidentaloma Bằng Letizia Canu, Janna A W Van Hemert, Michiel N. Kerstens, Robert P. Hartman, Aakanksha Khanna, Ivana Kraljević, Darko Kaštelan, Corin Badiu, Urszula Ambroziak, Antoine Tabarin, Magalie Haissaguerre, Edward Buitenwerf, Anneke Visser, Massimo Mannelli, Wiebke Arlt, Vasileios Chortis, Isabelle Bourdeau, Nadia Gagnon, Marie Buchy, Françoise Borson‐Chazot, Timo Deutschbein, Martin Faßnacht, Alicja Hubalewska‐Dydejczyk, Marcin Motyka, Ewelina Rzepka, Ruth Casey, Benjamin Challis, Marcus Quinkler, Laurent Vroonen, Ariadni Spyroglou, Felix Beuschlein, Cristina Lamas, William F. Young, Irina Bancos, Henri Timmers
Được phát hành 2018Artigo -
17
Rare variant contribution to human disease in 281,104 UK Biobank exomes Bằng Quanli Wang, Ryan S. Dhindsa, Keren Carss, Andrew R. Harper, Abhishek Nag, Ioanna Tachmazidou, Dimitrios Vitsios, Sri V. V. Deevi, Alex Mackay, Daniel Muthas, Michael Hühn, Susan J. Monkley, Henric Olsson, Bastian R. Angermann, Ronen Artzi, Carl Barrett, Maria G. Belvisi, Mohammad Bohlooly‐Y, Oliver S. Burren, Lisa Buvall, Benjamin Challis, Sophia Cameron‐Christie, E. Suzanne Cohen, Andrew Davis, Regina Fritsche Danielson, Brian Dougherty, Benjamin Georgi, Zara Ghazoui, Pernille Hansen, Fengyuan Hu, Magda Jeznach, Xiao Jiang, Chanchal Kumar, Zhongwu Lai, Glenda Lassi, Samuel H. Lewis, Bolan Linghu, Kieren Lythgow, Peter Maccallum, Carla Martins, Athena Matakidou, Erik Michaëlsson, Sven Moosmang, Sean M. O’Dell, Yoichiro Ohne, Joel Okae, Amanda O’Neill, Dirk S. Paul, Anna Reznichenko, Michael Snowden, Anna Walentinsson, Jorge Zeron, Menelas N. Pangalos, Sebastian Wasilewski, Katherine R. Smith, Ruth March, Adam Platt, Carolina Haefliger, Slavé Petrovski
Được phát hành 2021Artigo -
18
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection Bằng Seyedeh M. Zekavat, Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri, Chen Wang, Md Mesbah Uddin, Yixuan Ye, Zhaolong Yu, Xiaoxi Liu, Yoichiro Kamatani, Romit Bhattacharya, James P. Pirruccello, Akhil Pampana, Po‐Ru Loh, Puja Kohli, Steven A. McCarroll, Krzysztof Kiryluk, Benjamin M. Neale, Iuliana Ionita‐Laza, Eric A. Engels, Derek W. Brown, Jordan W. Smoller, Robert C. Green, Elizabeth W. Karlson, Matthew S. Lebo, Patrick T. Ellinor, Scott T. Weiss, Mark J. Daly, Satoshi Koyama, Kaoru Ito, Yukihide Momozawa, Koichi Matsuda, Yuji Yamanashi, Yoichi Furukawa, Takayuki Morisaki, Yoshinori Murakami, Kaori Muto, Akiko Nagai, Wataru Obara, Ken Yamaji, Kazuhisa Takahashi, Satoshi Asai, Yasuo Takahashi, Takao Suzuki, Nobuaki Sinozaki, Hiroki Yamaguchi, Shiro Minami, Shigeo Murayama, Kozo Yoshimori, Satoshi Nagayama, Daisuke Obata, Masahiko Higashiyama, Akihide Masumoto, Yukihiro Koretsune, Aarno Palotie, Adam Ziemann, Adele A. Mitchell, Adriana Huertas‐Vázquez, Aino Salminen, Airi Jussila, Aki S. Havulinna, Alex Mackay, Ali Abbasi, Amanda Elliott, Amy L. Cole, Anastasia Shcherban, Anders Mälarstig, Andrea Ganna, Andrey Loboda, Anna Podgornaia, Anne Lehtonen, Anne Pitkäranta, Anne M. Remes, Annika Auranen, Antti Hakanen, Antti Palomäki, Anu Jalanko, Anu Loukola, Aparna Chhibber, Apinya Lertratanakul, Arto Lehistö, Graham J. Mann, Åsa K. Hedman, Audrey Y. Chu, Aviv Madar, Awaisa Ghazal, Benjamin Challis, Benjamin B. Sun, Beryl B. Cummings, Bridget Riley‐Gillis, Caroline S. Fox, Chia‐Yen Chen, Clarence Wang, Clément Chatelain, Daniel Gordin, Danjuma Quarless, Danny Oh, David F. Choy, David A. Close
Được phát hành 2021Artigo -
19
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy Bằng Hanna M. Ollila, Eilon Sharon, Ling Lin, Nasa Sinnott-Armstrong, Aditya Ambati, Selina Yogeshwar, Ryan P. Hillary, Otto Jolanki, Juliette Faraco, Mali Einen, Guo Luo, Jing Zhang, Fang Han, Han Yan, Xiao Song Dong, Jing Li, Jun Zhang, Seung‐Chul Hong, Tae Won Kim, Yves Dauvilliers, Lucie Barateau, Gert Jan Lammers, Rolf Fronczek, Geert Mayer, Joan Santamaría, Isabelle Arnulf, Stine Knudsen, May Kristin Lyamouri Bredahl, Per Medbøe Thorsby, Giuseppe Plazzi, Fabio Pizza, Monica Moresco, Catherine Crowe, Stephen K. Van Den Eeden, Michel Lecendreux, Patrice Bourgin, Takashi Kanbayashi, F Martínez-Orozco, Rosa Peraita‐Adrados, Antonio Benetó, Jacques Montplaisir, Alex Désautels, Yu‐Shu Huang, Thomas D. Als, Adam Ziemann, Ali Abbasi, Anne Lehtonen, Apinya Lertratanakul, Bridget Riley‐Gillis, Fedik Rahimov, Howard J. Jacob, Jeffrey F. Waring, Mengzhen Liu, Nizar Smaoui, Relja Popovic, Adam Platt, Athena Matakidou, Benjamin Challis, Dirk S. Paul, Glenda Lassi, Ioanna Tachmazidou, Antti Hakanen, Johanna Schleutker, Nina Pitkänen, Perttu Terho, Petri Virolainen, Arto Mannermaa, Veli‐Matti Kosma, Chia‐Yen Chen, Heiko Runz, Sally John, Sanni Lahdenperä, Stephanie Loomis, Susan Eaton, George Okafo, Heli Salminen‐Mankonen, Marc Jung, Nathan Lawless, Zhihao Ding, Joseph Maranville, Marla Hochfeld, Robert Plenge, Shameek Biswas, Masahiro Kanai, Mutaamba Maasha, Wei Zhou, Outi Tuovila, Raimo Pakkanen, Jari A. Laukkanen, Teijo Kuopio, Kristiina Aittomäki, Antti Mäkitie, Natalia Pujol, Triin Laisk, Katriina Aalto‐Setälä, Johanna Mäkelä, Marco Hautalahti, Sarah Smith, Tom Southerington, Eeva Kangasniemi
Được phát hành 2023Artigo -
20
Rare variant associations with plasma protein levels in the UK Biobank Bằng Ryan S. Dhindsa, Oliver S. Burren, Benjamin B. Sun, Bram P. Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Erin Oerton, Ventzislava A. Hristova, Katherine R. Smith, Keren Carss, Sebastian Wasilewski, Andrew R. Harper, Dirk S. Paul, Margarete A. Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, Rasmus Ågren, Lauren Anderson-Dring, Santosh S. Atanur, David H. Baker, Carl Barrett, Maria G. Belvisi, Mohammad Bohlooly‐Y, Lisa Buvall, Niedzica Camacho, Lisa H. Cazares, Sophia Cameron‐Christie, Morris Chen, E. Suzanne Cohen, Regina Fritsche Danielson, Shikta Das, Andrew Davis, Sri Vishnu Vardhan Deevi, Wei Ding, Brian Dougherty, Zammy Fairhurst-Hunter, Manik Garg, Benjamin Georgi, Carmen Guerrero Rangel, Carolina Haefliger, Mårten Hammar, Richard N. Hanna, Pernille Hansen, Jennifer Harrow, Ian Henry, Sonja Hess, Ben Hollis, Fengyuan Hu, Xiao Jiang, Kousik Kundu, Zhongwu Lai, Mark Lal, Glenda Lassi, Yupu Liang, Margarida Lopes, Kieren Lythgow, Stewart MacArthur, Meeta Maisuria-Armer, Ruth March, Carla Martins, Karyn Mégy, Robert Menzies, Erik Michaëlsson, Fiona K. Middleton, Bill Mowrey, Daniel Muthas, Abhishek Nag, Sean M. O’Dell, Yoichiro Ohne, Henric Olsson, Amanda O’Neill, Kristoffer Ostridge, Benjamin Pullman, William Rae, Arwa Bin Raies, Anna Reznichenko, Xavier Romero Ros, Maria Ryaboshapkina, Hitesh J. Sanganee, Ben S. Sidders, Mike Snowden, Stasa Stankovic, Helen Stevens, Ioanna Tachmazidou, Haeyam Taiy, Lifeng Tian, Christina Underwood, Anna Walentinsson, Qing‐Dong Wang, Ahmet Zehir, Zoe Zou, Dimitrios Vitsios, Euan A. Ashley, Christopher D. Whelan, Menelas N. Pangalos, Quanli Wang, Slavé Petrovski
Được phát hành 2023Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Medicine
Internal medicine
Biology
Gene
Endocrinology
Genetics
Genotype
Genome-wide association study
Mutation
Single-nucleotide polymorphism
Biobank
Biochemistry
Exome
Exome sequencing
Genetic association
Obesity
Phenotype
Bioinformatics
Chemistry
Computational biology
Disease
Hormone
Immunology
Prohormone
Proteomics
Receptor
Albuminuria
Allele
Chromatography
Diabetes mellitus