Arama Sonuçları - Vladimı́r Saudek
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GDF15: A Hormone Conveying Somatic Distress to the Brain Yazar: Sam Lockhart, Vladimı́r Saudek, Stephen O’Rahilly
Baskı/Yayın Bilgisi 2020Revisão -
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FICD acts bifunctionally to AMPylate and de-AMPylate the endoplasmic reticulum chaperone BiP Yazar: Steffen Preißler, Cláudia Rato, Luke A. Perera, Vladimı́r Saudek, David Ron
Baskı/Yayın Bilgisi 2016Artigo -
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Human Frame Shift Mutations Affecting the Carboxyl Terminus of Perilipin Increase Lipolysis by Failing to Sequester the Adipose Triglyceride Lipase (ATGL) Coactivator AB-hydrolase-... Yazar: Sheetal Gandotra, Koini Lim, Amandine Girousse, Vladimı́r Saudek, Stephen O’Rahilly, David B. Savage
Baskı/Yayın Bilgisi 2011Artigo -
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The human lipodystrophy protein seipin is an ER membrane adaptor for the adipogenic PA phosphatase lipin 1 Yazar: M. F. Michelle Sim, Rowena J. Dennis, Évelyne Aubry, Nardev Ramanathan, Hiroshi Sembongi, Vladimı́r Saudek, Daisuke Ito, Stephen O’Rahilly, Symeon Siniossoglou, Justin J. Rochford
Baskı/Yayın Bilgisi 2012Artigo -
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Conserved Amphipathic Helices Mediate Lipid Droplet Targeting of Perilipins 1–3 Yazar: Emily R. Rowe, Michael L. Mimmack, António Daniel Barbosa, Afreen Haider, Iona Isaac, Myriam Ouberaï, Abdou Rachid Thiam, Satish Patel, Vladimı́r Saudek, Symeon Siniossoglou, David B. Savage
Baskı/Yayın Bilgisi 2016Artigo -
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Dual binding motifs underpin the hierarchical association of perilipins1–3 with lipid droplets Yazar: Dalila Ajjaji, Kalthoum Ben M’Barek, Michael L. Mimmack, Cheryl England, Haya Herscovitz, Dong Liang, Richard G. Kay, Satish Patel, Vladimı́r Saudek, Donald Small, David B. Savage, Abdou Rachid Thiam
Baskı/Yayın Bilgisi 2019Artigo -
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Clinical and Molecular Characterization of a Novel PLIN1 Frameshift Mutation Identified in Patients With Familial Partial Lipodystrophy Yazar: Kristina Kozusko, Venessa Tsang, William Bottomley, Yoon Hi Cho, Sheetal Gandotra, Michael L. Mimmack, Koini Lim, Iona Isaac, Satish Patel, Vladimı́r Saudek, Stephen O’Rahilly, Shubha Srinivasan, Jerry R. Greenfield, Inês Barroso, Lesley V. Campbell, David B. Savage
Baskı/Yayın Bilgisi 2014Artigo -
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Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance Yazar: Felicity Payne, Rita Colnaghi, Nuno Rocha, Asha Seth, J. Ieuan Harris, Gillian Carpenter, William Bottomley, Eleanor Wheeler, Stephen Q. Wong, Vladimı́r Saudek, David B. Savage, Stephen O’Rahilly, Jean‐Claude Carel, Inês Barroso, Mark O’Driscoll, Robert K. Semple
Baskı/Yayın Bilgisi 2014Artigo -
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Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations Yazar: Sarah Boissel, Orit Reish, Karine Proulx, Hiroko Kawagoe-Takaki, Barbara Sedgwick, Giles S.H. Yeo, Stephen Eyre, Christelle Golzio, Florence Molinari, Noman Kadhom, Heather Etchevers, Vladimı́r Saudek, I. Sadaf Farooqi, Philippe Froguel, Tomas Lindahl, Stephen O’Rahilly, Arnold Münnich, Laurence Colleaux
Baskı/Yayın Bilgisi 2009Artigo -
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Obesity-associated gene <i>TMEM18</i> has a role in the central control of appetite and body weight regulation Yazar: Rachel Larder, M. F. Michelle Sim, Pawan Gulati, Robin Antrobus, Y.C. Loraine Tung, Debra Rimmington, Eduard Ayuso, Joseph Polex-Wolf, Brian Lam, Cristina Dias, Darren W. Logan, Sam Virtue, Fátima Bosch, Giles S.H. Yeo, Vladimı́r Saudek, Stephen O’Rahilly, Anthony P. Coll
Baskı/Yayın Bilgisi 2017Artigo -
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Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease Yazar: Felicity Payne, Koini Lim, Amandine Girousse, Rebecca J. Brown, Nora Kory, Ann L. Robbins, Yali Xue, Alison Sleigh, Elaine Cochran, Claire Adams, Arundhati Dev Borman, David L. Russel‐Jones, Phillip Görden, Robert K. Semple, Vladimı́r Saudek, Stephen O’Rahilly, Tobias C. Walther, Inês Barroso, David B. Savage
Baskı/Yayın Bilgisi 2014Artigo -
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PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress Yazar: Afreen Haider, Yu‐Chen Wei, Koini Lim, António Daniel Barbosa, Che Liu, Ursula Weber, Marek Mlodzik, Kadri Oras, Simon Collier, M. Mahmood Hussain, Dong Liang, Satish Patel, Anna Álvarez-Guaita, Vladimı́r Saudek, Benjamin Jenkins, Albert Koulman, Marcus K. Dymond, Roger Hardie, Symeon Siniossoglou, David B. Savage
Baskı/Yayın Bilgisi 2018Artigo -
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Prevalence of Loss-of-Function <i>FTO</i> Mutations in Lean and Obese Individuals Yazar: Stephen Eyre, Karine Proulx, Hiroko Kawagoe-Takaki, Vincent Vatin, Ruth Gutiérrez‐Aguilar, Debbie Lyon, Marcella Ma, Hélène Choquet, Fritz Horber, Wim Van Hul, Luc Van Gaal, Beverley Balkau, Sophie Visvikis‐Siest, François Pattou, I. Sadaf Farooqi, Vladimı́r Saudek, Stephen O’Rahilly, Philippe Froguel, Barbara Sedgwick, Giles S.H. Yeo
Baskı/Yayın Bilgisi 2009Artigo -
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Partial lipodystrophy and insulin resistant diabetes in a patient with a homozygous nonsense mutation in <i>CIDEC</i> Yazar: Oscar Rubio‐Cabezas, Vishwajeet Puri, Incoronata Murano, Vladimı́r Saudek, Robert K. Semple, Satya Dash, Caroline S. S. Hyden, William Bottomley, Corinne Vigouroux, Jocelyne Magré, Philippa Raymond‐Barker, Peter R. Murgatroyd, Anil Chawla, Jeremy N. Skepper, Krishna Chatterjee, Sara Suliman, Ann‐Marie Patch, Anil Agarwal, Abhimanyu Garg, Inês Barroso, Saverio Cinti, Michael Czech, Jesús Argente, Stephen O’Rahilly, David B. Savage
Baskı/Yayın Bilgisi 2009Artigo -
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The Obesity-Associated<i>FTO</i>Gene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase Yazar: Thomas Gerken, Christophe A. Girard, Yi‐Chun Loraine Tung, Celia J. Webby, Vladimı́r Saudek, Kirsty S. Hewitson, Giles S.H. Yeo, M.A. McDonough, Sharon L. Cunliffe, Luke A. McNeill, Juris Galvanovskis, Patrik Rorsman, Peter Robins, Xavier Prieur, Anthony P. Coll, Marcella Ma, Z Jovanović, I. Sadaf Farooqi, Barbara Sedgwick, Inês Barroso, Tomas Lindahl, Chris P. Ponting, Frances M. Ashcroft, Stephen O’Rahilly, Christopher J. Schofield
Baskı/Yayın Bilgisi 2007Artigo -
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Mechanistic basis for protection against fatty liver disease by CIDEB loss-of-function mutations Yazar: Qiyu Zeng, Satish Patel, Xun Wang, Meng-Hsiung Hsieh, Zhijie Li, Xuejun Ren, Jingjing Wang, Dohun Kim, Shili Li, Xinping Gu, Gaia Chiara Mannino, Giuseppe Maggiore, Xiangyi Fang, Lin Li, Min Zhu, Mengmeng Wang, Boyuan Li, Amaey Bellary, Koini Lim, Zhetuo Qi, Pushpa Pushpa, Mandour O Mandour, Vladimı́r Saudek, Tripti Sharma, Yu Zhang, Gerta Hoxhaj, Prashant Mishra, Purva Gopal, Peter Campbell, Matthew Hoare, David B. Savage, Hao Zhu
Baskı/Yayın Bilgisi 2025Pré-impressão -
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Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression Yazar: Nuno Rocha, David A. Bulger, Andrea Frontini, Hannah Titheradge, Sigrid Bjerge Gribsholt, Rachel Knox, Matthew Page, Julie Harris, Felicity Payne, Claire Adams, Alison Sleigh, John R. Crawford, Anette P. Gjesing, Jette Bork‐Jensen, Oluf Pedersen, Inês Barroso, Torben Hansen, Helen Cox, Mary M. Reilly, Alexander M. Rossor, Rebecca J. Brown, Simeon I. Taylor, Duncan McHale, Martin Armstrong, Elif A Oral, Vladimı́r Saudek, Stephen O’Rahilly, Eamonn R. Maher, Bjørn Richelsen, David B. Savage, Robert K. Semple
Baskı/Yayın Bilgisi 2017Artigo
Arama Araçları:
İlgili Konular
Biology
Gene
Genetics
Cell biology
Medicine
Endocrinology
Internal medicine
Biochemistry
Adipose tissue
Lipid droplet
Chemistry
Mutation
Antiretroviral therapy
Lipodystrophy
Lipolysis
Loss function
Perilipin
Phenotype
Viral load
Virus
Endoplasmic reticulum
Function (biology)
Membrane
Mutant
Adipocyte
Adipogenesis
Adipose triglyceride lipase
Biophysics
Disease
Fatty liver