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American Journal of Human Genetics|December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and miceChen Tan, Lanlan Meng, Mingrong Lv, et al.Mitochondrion|September 10, 2018
Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell linesDan Li, Yaping Sun, Qianqian Zhuang, et al.Iscience|October 27, 2022
A novel NF2 splicing mutant causes neurofibromatosis type 2 via liquid-liquid phase separation with large tumor suppressor and Hippo pathwayZexiao Jia, Shuxu Yang, Mengyao Li, et al.Journal of Assisted Reproduction and Genetics|February 18, 2026
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnosticsChen Tan, Tiantian Wang, Chaofeng Tu, et al.Biological & Pharmaceutical Bulletin|February 5, 2014
Berberine inhibits fluphenazine-induced up-regulation of CDR1 in Candida albicansShao-Long Zhu, Lan Yan, Yan-Xia Zhang, et al.Biochemical Pharmacology|October 26, 2017
Identification of new shikonin derivatives as STAT3 inhibitorsHan-Yue Qiu, Jiang-Yan Fu, Min-Kai Yang, et al.Neuroimage|December 5, 2024
Exploring the impact of APOE ɛ4 on functional connectivity in Alzheimer's disease across cognitive impairment levelsKangli Dong, Wei Liang, Ting Hou, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 10, 2025
METTL5 deficiency induces oligoasthenoteratozoospermia via impaired 18S rRNA m<sup>6</sup>A methylation in humans and miceMengya Zhang, Xueguang Zhang, Chen Tan, et al.The Journal of Pediatrics|July 5, 2016
High-Throughput Sequencing Reveals Immunological Characteristics of the TRB-/IgH-CDR3 Region of Umbilical Cord BloodChanglong Guo, Qidi Wang, Xiaofang Cao, et al.Clinical Rheumatology|June 10, 2025
LncRNA PVT1 regulates CD4 + T cell dysregulation in systemic lupus erythematosus: insights from human patients and MRL/lpr mouseJiali Zhang, Ying Yuan, Shuangying Ni, et al.Pageof 94