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Human Genetics|September 6, 2025
Genetic burden and multidimensional predictors in prenatal diagnosis of fetal congenital diaphragmatic herniaRuibin Huang, Fang Fu, Shanshan Mei, et al.
Elife|August 15, 2022
Tissue-specific modifier alleles determine Mertk loss-of-function traitsYemsratch T Akalu, Maria E Mercau, Marleen Ansems, et al.
Plos One|November 9, 2013
Steroid-associated hip joint collapse in bipedal emusLi-Zhen Zheng, Zhong Liu, Ming Lei, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2014
Establishment and characterization of novel human primary and metastatic anaplastic thyroid cancer cell lines and their genomic evolution over a year as a primagraftManoj Garg, Ryoko Okamoto, Yasunobu Nagata, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2013
Genomic and functional characterizations of phosphodiesterase subtype 4D in human cancersDe-Chen Lin, Liang Xu, Ling-Wen Ding, et al.
Human Molecular Genetics|July 21, 2016
An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinomaQian Cui, Qi-Sheng Feng, Hao-Yuan Mo, et al.
Oncotarget|July 28, 2015
NOP14 suppresses breast cancer progression by inhibiting NRIP1/Wnt/β-catenin pathwayJin-Ju Lei, Rou-Jun Peng, Bo-Hua Kuang, et al.
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