Zobrazeno 1 - 10
of 1 248
pro vyhledávání: '"Gap junction protein"'
Publikováno v:
Reproductive Biology and Endocrinology, Vol 22, Iss 1, Pp 1-14 (2024)
Abstract Background At present, a number of clinical trials have been carried out on GLP-1 receptor agonist liraglutide in the treatment of polycystic ovary syndrome (PCOS). However, the effect of liraglutide on follicle development and its specific
Externí odkaz:
https://doaj.org/article/0a87cf99b9174367991edf9b5e9b910a
Autor:
Yongsheng Huang, Wenyi Guo, Yuan Zeng, Xinrong Wang, Bohao Fan, Ying Zhang, Lei Yan, Gangli Gu, Zhao Liu
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
BackgroundGap junction proteins (GJPs) are a class of channel proteins that are closely related to cell communication and tumor development. The objective of this study was to screen out GJPs related prognostic signatures (GRPS) associated with clear
Externí odkaz:
https://doaj.org/article/1979ec99b3b14452adc65f5adce7d28d
Akademický článek
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Publikováno v:
Frontiers in Cellular Neuroscience, Vol 17 (2023)
Hearing loss is the most common congenital sensory impairment. Mutations or deficiencies of the GJB2 gene are the most common genetic cause of congenital non-syndromic deafness. Pathological changes such as decreased potential in the cochlea, active
Externí odkaz:
https://doaj.org/article/15cbf16934fd47eb9f165841ddddf24b
Publikováno v:
Journal of Inflammation Research, Vol Volume 15, Pp 2461-2476 (2022)
Yuan-jie Liu,1,2,* Mei Han,1,* Jie-pin Li,1– 3 Shu-hong Zeng,1,2 Qian-wen Ye,1,2 Zhong-hua Yin,1,2 Shen-lin Liu,1,2 Xi Zou1,2,4 1Department of Oncology, Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospita
Externí odkaz:
https://doaj.org/article/3758cf23af49415697d4b0069aa89a12
Akademický článek
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Autor:
Joern Pascal Laubach, Michael Ludwig, Tabea Horn, Olaf Eickmeier, Christina Smaczny, Ralf Schubert, Stefan Zielen, Christof Majoor, Malik Aydin, Alexander Schnell, Sabina Schmitt-Grohé
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 28, Iss 7, p 138 (2023)
Background: High TGFβ1-producing variants cause severe clinical disease in F508del homozygous patients. Lately, we showed that a single nucleotide polymorphism (SNP), rs41266431, in the GJA4 gene modifies the disease severity of cystic fibrosis (CF)
Externí odkaz:
https://doaj.org/article/16d181019809414886fb939000eab2b6
Publikováno v:
Cancer Management and Research, Vol Volume 13, Pp 1967-1979 (2021)
Shanshan Li1 *,* Yize Liu2 *,* Guanzhen Qiu,2 Yinzhou Luo,2 Lan Luan,3 Tiance Xu,4 Yong Wang,2,5 Shuyue Xia1,6 1Respiratory Department, Central Hospital Affiliated to Shenyang Medical College, Shenyang, Liaoning, 110024, People’s Republic of China;
Externí odkaz:
https://doaj.org/article/92168fbf121342599b1a12742d6565de
Publikováno v:
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-13 (2020)
Abstract Background Gap junction protein alpha 3 (GJA3), an important pathogenic gene of congenital cataracts, encodes the transmembrane protein connexin46, which functions as an intercellular channel for voltage and chemical gating by forming dodeca
Externí odkaz:
https://doaj.org/article/c3d46cc6260d4894b865bdee18890382
Genotype-phenotype Correlation in Pelizaeus Merzbacher Disease and Pelizaeus Merzbacher-like Disease
Publikováno v:
Bezmiâlem Science, Vol 7, Iss 3, Pp 215-220 (2019)
Objective:Among the hypomyelinating diseases of childhood, Pelizaeus Merzbacher disease (PMD) is caused by X-linked proteolipid protein (PLP) gene mutations, whereas patients without mutations of PLP gene-called Pelizaues Merzbacher-like disease (PML
Externí odkaz:
https://doaj.org/article/5c6310c0d99248609049ab22057db45f