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Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2019
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humansYue-Qiu Tan, Chaofeng Tu, Lanlan Meng, et al.
Journal of Medical Genetics|August 16, 2019
Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformationsWeili Wang, Chaofeng Tu, Hongchuan Nie, et al.
Human Reproduction (Oxford, England)|February 25, 2022
Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and miceYing Shen, Jing Guo, Xueguang Zhang, et al.
ESC Heart Failure|April 9, 2020
Age-related longitudinal change in cardiac structure and function in adults at increased cardiovascular riskFei Fei Gong, Jennifer M Coller, Michele McGrady, et al.
Frontiers in Endocrinology|September 15, 2022
25(OH)VitD and human endocrine and functional fertility parameters in women undergoing IVF/ICSIMei Tian, Suimin Zeng, Sufen Cai, et al.
Bioactive Materials|August 21, 2023
Manganese molybdate nanodots with dual amplification of STING activation for "cycle" treatment of metalloimmunotherapyHuali Lei, Quguang Li, Guangqiang Li, et al.
BMC Nephrology|April 27, 2021
Kidney age - chronological age difference (KCD) score provides an age-adapted measure of kidney functionDuncan J Campbell, Jennifer M Coller, Fei Fei Gong, et al.
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