Showing results (491-500 of 603) with videos related to

Sort By:
Pageof 61
Endocrine-Related Cancer|September 9, 2010
Role of PTPRJ genotype in papillary thyroid carcinoma riskRodolfo Iuliano, Dario Palmieri, Huiling He, et al.
The New England Journal of Medicine|May 6, 2005
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)Heather Hampel, Wendy L Frankel, Edward Martin, et al.
Nature Structural & Molecular Biology|July 19, 2011
Transcription initiation platforms and GTF recruitment at tissue-specific enhancers and promotersFrederic Koch, Romain Fenouil, Marta Gut, et al.
Thyroid : Official Journal of the American Thyroid Association|April 9, 2019
Identification of Rare Variants Predisposing to Thyroid CancerYanqiang Wang, Sandya Liyanarachchi, Katherine E Miller, et al.
Thyroid : Official Journal of the American Thyroid Association|May 11, 2013
Cumulative risk impact of five genetic variants associated with papillary thyroid carcinomaSandya Liyanarachchi, Anna Wojcicka, Wei Li, et al.
Nature Medicine|February 1, 1996
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patientsB Liu, R Parsons, N Papadopoulos, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Search for copy number alterations in the MEFV gene using multiplex ligation probe amplification, experience from three diagnostic centresMarielle E van Gijn, Stéphan Soler, Claire de la Chapelle, et al.
ACS Applied Materials & Interfaces|March 12, 2025
Single-Bacterium Diagnosis via Terahertz Near-Field Dielectric NanoimagingJie Zhou, Xiaoqiuyan Zhang, Xingxing Xu, et al.
Nature Genetics|August 1, 1996
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane proteinJ Kere, A K Srivastava, O Montonen, et al.
American Journal of Human Genetics|May 6, 2003
Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transportJuha Kolehmainen, Graeme C M Black, Anne Saarinen, et al.
Pageof 61