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Molecular Medicine Reports|May 12, 2018
A novel PNPLA6 compound heterozygous mutation identified in a Chinese patient with Boucher‑Neuhäuser syndromeRuizhi Zheng, Yaguang Zhao, Jiayu Wu, et al.
Environmental Pollution (Barking, Essex : 1987)|November 29, 2023
Triclocarban exhibits higher adipogenic activity than triclosan through peroxisome proliferator-activated receptors pathwaysJia-Da Zhang, Sen He, Ting-Ting He, et al.
JCI Insight|March 17, 2026
Reciprocal regulation between autism risk gene POGZ and circadian clockTing Wu, Jiao He, Chu-Jun Xu, et al.
Biochemical and Biophysical Research Communications|December 5, 2012
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosisWen-Juan Guan, Jun-Ling Wang, Yu-Tao Liu, et al.
Cell Death & Disease|February 5, 2020
Locus-specific DNA methylation of Mecp2 promoter leads to autism-like phenotypes in miceZongyang Lu, Zhen Liu, Wei Mao, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 26, 2007
Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadismNelly Pitteloud, Chengkang Zhang, Duarte Pignatelli, et al.
Biochemical and Biophysical Research Communications|June 27, 2013
Transglutaminase 6 interacts with polyQ proteins and promotes the formation of polyQ aggregatesWen-Juan Guan, Kai-De Xia, Yan-Tao Ma, et al.
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