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Human Genomics|January 12, 2019
Germline TP53 and MSH6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary studyDandan Yi, Lei Xu, Jiaqi Luo, et al.Human Genomics|February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsAnna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.Human Genomics|December 5, 2019
Genetics and functions of the retinoic acid pathway, with special emphasis on the eyeBrian Thompson, Nicholas Katsanis, Nicholas Apostolopoulos, et al.Human Genomics|November 30, 2019
Transcriptomic analysis of monocytes from HIV-positive men on antiretroviral therapy reveals effects of tobacco smoking on interferon and stress response systems associated with depressive symptomsDavid R Lorenz, Vikas Misra, Dana GabuzdaHuman Genomics|January 15, 2020
Re-analysis of whole blastocysts after trophectoderm biopsy indicated chromosome aneuploidyZhanhui Ou, Zhiheng Chen, Minna Yin, et al.Human Genomics|January 10, 2020
Investigating diagnostic sequencing techniques for CADASIL diagnosisP J Dunn, N Maksemous, R A Smith, et al.Human Genomics|February 1, 2020
Identification and characterization of methylation-mediated transcriptional dysregulation dictate methylation roles in preeclampsiaShuyu Zhao, Nan Lv, Yan Li, et al.Human Genomics|February 14, 2019
Toward a clinical diagnostic pipeline for SPINK1 intronic variantsXin-Ying Tang, Jin-Huan Lin, Wen-Bin Zou, et al.Human Genomics|April 6, 2006
Human SNPs resulting in premature stop codons and protein truncationSevtap Savas, Sukru Tuzmen, Hilmi OzcelikHuman Genomics|April 6, 2006
Fabry disease: identification of 50 novel alpha-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutationsJunaid Shabbeer, Makiko Yasuda, Stacy D Benson, et al.Pageof 112