Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Wendi A. Roscoe"'
Publikováno v:
Biology of Reproduction. 65:829-838
Connexin43 (Cx43), a gap junction protein encoded by the Gja1 gene, is expressed in several cell types of the testis. Cx43 gap junctions couple Sertoli cells with each other, Leydig cells with each other, and spermatogonia/spermatocytes with Sertoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c0ffa48ebc4cef1fa6f8ad63292c378
https://doi.org/10.1095/biolreprod65.3.829
https://doi.org/10.1095/biolreprod65.3.829
Publikováno v:
Canadian journal of physiology and pharmacology. 90(7)
Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system, in which the release of reactive oxygen species by infiltrating immune cells contributes to demyelination. American ginseng ( Panax quinquefolius ) is a natural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f36c747d8873b4114f744743d090cb7d
https://pubmed.ncbi.nlm.nih.gov/22720838
https://pubmed.ncbi.nlm.nih.gov/22720838
Publikováno v:
Central Nervous System Agents in Medicinal Chemistry
Central Nervous System Agents in Medicinal Chemistry, Bentham Science Publishers, 2012, ⟨10.2174/187152412800229125⟩
Central Nervous System Agents in Medicinal Chemistry, Bentham Science Publishers, 2012, ⟨10.2174/187152412800229125⟩
What is the origin of the complex vascular changes that exist in the CNS lesions of Multiple Sclerosis (MS)? From the beginning of the study of the pathological changes in MS in the 19th century, lesions were seen to be associated with veins. On a mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93596e1385686f4f531f0963f0a284eb
https://pubmed.ncbi.nlm.nih.gov/22280405
https://pubmed.ncbi.nlm.nih.gov/22280405
Publikováno v:
Cell communicationadhesion. 14(2-3)
Alterations in the expression of gap junction proteins (connexins) have previously been observed in experimental allergic encephalomyelitis (EAE). Demyelinating lesions have significantly decreased Cx43, while recovering lesions have greatly increase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc6c6c028fd7faae4d621a7debf5ecce
https://pubmed.ncbi.nlm.nih.gov/17668350
https://pubmed.ncbi.nlm.nih.gov/17668350
Autor:
Donglin Bai, Xiang-Qun Gong, Gerald M. Kidder, Dale W. Laird, Qing Shao, Gregory I.L. Veitch, Emily M. Pellegrino, Elizabeth McLachlan, Wendi A. Roscoe
Publikováno v:
The Journal of biological chemistry. 280(12)
Oculodentodigital dysplasia, a rare condition displaying congenital craniofacial deformities and limb abnormalities, has been associated with over 20 known human connexin43 (Cx43) mutations. The localization of two of these mutants, G21R and G138R, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::987a2090c4050057782a820a95b47f86
https://pubmed.ncbi.nlm.nih.gov/15644317
https://pubmed.ncbi.nlm.nih.gov/15644317