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International Journal of Molecular Sciences|November 18, 2016
SEPT12-NDC1 Complexes Are Required for Mammalian SpermiogenesisTsung-Hsuan Lai, Ying-Yu Wu, Ya-Yun Wang, et al.Plos One|April 6, 2012
SEPTIN12 genetic variants confer susceptibility to teratozoospermiaYing-Hung Lin, Ya-Yun Wang, Hau-Inh Chen, et al.Bioorganic Chemistry|December 20, 2024
The first attempt in synthesis, identification, and evaluation of SEPT9 inhibitors on human oral squamous carcinomasHsuan-Yu Lai, Ko-Hua Yu, Keng-Chang Tsai, et al.Scientific Reports|February 3, 2016
Human X-linked Intellectual Disability Factor CUL4B Is Required for Post-meiotic Sperm Development and Male FertilityChien-Yu Lin, Chun-Yu Chen, Chih-Hsiang Yu, et al.Journal of Cellular Biochemistry|June 2, 2017
LRWD1 Regulates Microtubule Nucleation and Proper Cell Cycle Progression in the Human Testicular Embryonic Carcinoma CellsChia-Yih Wang, Yu-Han Hong, Jhih-Siang Syu, et al.Biochimie|December 5, 2018
Identification of SEPTIN12 as a novel target of the androgen and estrogen receptors in human testicular cellsPao-Lin Kuo, Jie-Yun Tseng, Hau-Inh Chen, et al.Journal of Assisted Reproduction and Genetics|February 21, 2013
Characterization of 3-hydroxyisobutyrate dehydrogenase, HIBADH, as a sperm-motility markerYung-Chieh Tasi, Hsin-Chih Albert Chao, Chia-Ling Chung, et al.Human Mutation|January 26, 2012
SEPT12 mutations cause male infertility with defective sperm annulusYung-Che Kuo, Ying-Hung Lin, Hau-Inh Chen, et al.Acta Paediatrica (Oslo, Norway : 1992)|June 1, 2007
Genotype and phenotype in patients with Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.Biomedicines|June 2, 2021
Variants in Maternal Effect Genes and Relaxed Imprinting Control in a Special Placental Mesenchymal Dysplasia Case with Mild Trophoblast HyperplasiaTien-Chi Huang, Kung-Chao Chang, Jen-Yun Chang, et al.Pageof 17