Søgeresultater - Naila Haq
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1
Transcriptome-guided GLP-1 receptor therapy rescues metabolic and behavioral disruptions in a Bardet-Biedl Syndrome mouse model af Arashdeep Singh, Naila Haq, Mingxin Yang, Shelby Luckey, Samira Mansouri, Martha Campbell‐Thompson, Lei Jin, Sofia Christou‐Savina, Guillaume de Lartigue
Udgivet 2025Artigo -
2
Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer af Rebecca A. Barnetson, Nicola Cartwright, Annelot van Vliet, Naila Haq, Kate Drew, Susan M. Farrington, Nicola Williams, Jon Warner, Harry Campbell, Mary Porteous, Malcolm G. Dunlop
Udgivet 2007Artigo -
3
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21 af Albert Tenesa, Susan M. Farrington, James Prendergast, Mary Porteous, Marion Walker, Naila Haq, Rebecca A. Barnetson, Evropi Τheodoratou, Roseanne Cetnarskyj, Nicola Cartwright, Colin A. Semple, Andrew J. Clark, Fiona Jane Reid, Lorna Smith, Kostas Kavoussanakis, Thibaud Koessler, Paul D.P. Pharoah, Stephan Buch, Clemens Schafmayer, Jürgen Tepel, Stefan Schreiber, Henry Völzke, Carsten Oliver Schmidt, Jochen Hampe, Jenny Chang‐Claude, Michael Hoffmeister, Hermann Brenner, Stefan Wilkening, Federico Canzian, Gabriel Capellà, Vı́ctor Moreno, Ian J. Deary, John M. Starr, Ian Tomlinson, Zoe Kemp, Kimberley Howarth, Luis G. Carvajal–Carmona, Emily L. Webb, Peter Broderick, Jayaram Vijayakrishnan, Richard S. Houlston, Gad Rennert, Dennis G. Ballinger, Laura S. Rozek, Stephen B. Gruber, Koichi Matsuda, Tomohide Kidokoro, Yusuke Nakamura, Brent W. Zanke, Celia M.T. Greenwood, Jagadish Rangrej, Rafal Kustra, Alexandre Montpetit, Thomas J. Hudson, Steven Gallinger, Harry Campbell, Malcolm G. Dunlop
Udgivet 2008Artigo
Søgeredskaber:
Relaterede emner
Biology
Gene
Genetics
Cancer
Colorectal cancer
Medicine
Allele
Bardet–Biedl syndrome
Bioinformatics
Cancer research
DNA mismatch repair
Endocrinology
Environmental health
Gene expression
Genome-wide association study
Genotype
Germline mutation
Locus (genetics)
Lynch syndrome
MLH1
MSH2
MSH6
Metabolic syndrome
Microsatellite
Microsatellite instability
Mutation
Obesity
Phenotype
Population
Receptor