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Frontiers in Endocrinology|April 20, 2018
GATA4 Variants in Individuals With a 46,XY Disorder of Sex Development (DSD) May or May Not Be Associated With Cardiac Defects Depending on Second Hits in Other DSD GenesIdoia Martinez de LaPiscina, Carmen de Mingo, Stefan Riedl, et al.Molecular and Cellular Endocrinology|January 20, 2022
Whole exome sequencing reveals copy number variants in individuals with disorders of sex developmentRajini Sreenivasan, Katrina Bell, Jocelyn van den Bergen, et al.Journal of Thoracic Disease|April 10, 2019
Mechanical circulatory support for refractory cardiogenic shock post-acute myocardial infarction-a decade of lessonsSanjeet Singh Avtaar Singh, Sudeep Das De, Francesco Nappi, et al.Human Reproduction (Oxford, England)|September 2, 2024
Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesisHannes Syryn, Julie Van de Velde, Griet De Clercq, et al.Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 4, 2018
Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic ApproachesBrendan Backhouse, Chloe Hanna, Gorjana Robevska, et al.Maturitas|July 1, 2026
MSH4 and MSH5 variants in premature ovarian insufficiency: A literature review and case studyJaidah Fergus-Mackie, Brianna L Kline, Gorjana Robevska, et al.Frontiers in Nutrition|March 27, 2023
Demonstrating a link between diet, gut microbiota and brain: 14C radioactivity identified in the brain following gut microbial fermentation of 14C-radiolabeled tyrosine in a pig modelMargaret Murray, Christopher K Barlow, Scott Blundell, et al.Advanced Materials (Deerfield Beach, Fla.)|June 17, 2017
A Coating-Free Nonfouling Polymeric ElastomerHsiang-Chieh Hung, Priyesh Jain, Peng Zhang, et al.Human Molecular Genetics|October 25, 2022
Functional genomics analysis identifies loss of HNF1B function as a cause of Mayer-Rokitansky-Küster-Hauser syndromeElla Thomson, Minh Tran, Gorjana Robevska, et al.Plos Genetics|May 27, 2016
Heterogeneity of Human Neutrophil CD177 Expression Results from CD177P1 Pseudogene ConversionZuopeng Wu, Rong Liang, Thomas Ohnesorg, et al.Pageof 10