Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Qinxian, Guo"'
Autor:
Qinxian Guo, Gideon1,2,3 lionhopetherapy@gmail.com
Publikováno v:
Asian Journal of Interdisciplinary Research (AJIR). 2023, Vol. 6 Issue 3, p15-25. 11p.
Publikováno v:
Biomolecules, Vol 13, Iss 6, p 907 (2023)
Type 2 diabetes mellitus (T2DM) is a common endocrine disorder which remains a large challenge for clinicians. Previous studies have suggested that mitochondrial dysfunction plays an active role in T2DM progression, but a detailed mechanism is still
Externí odkaz:
https://doaj.org/article/15603a7726d84b518c38f4ea375f49be
Publikováno v:
Biomolecules; Volume 13; Issue 6; Pages: 907
Type 2 diabetes mellitus (T2DM) is a common endocrine disorder which remains a large challenge for clinicians. Previous studies have suggested that mitochondrial dysfunction plays an active role in T2DM progression, but a detailed mechanism is still
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::2db5c5ea6d61a2424fb6fc99e6d69323
Publikováno v:
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 15:1687-1701
Yu Ding,1 Shunrong Zhang,2 Qinxian Guo,1 Hui Zheng1 1Central Laboratory, Hangzhou First Peopleâs Hospital, Hangzhou, 310006, Zhejiang, Peopleâs Republic of China; 2Department of Geriatrics, Hangzhou First Peopleâs Hospital, Hangzhou, 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1f54a0be3644ac9b52c67401d381763
https://doi.org/10.2147/dmso.s363978
https://doi.org/10.2147/dmso.s363978
Publikováno v:
Genes; Volume 13; Issue 10; Pages: 1794
The mitochondrial 1555A>G mutation plays a critical role in aminoglycoside-induced and non-syndromic hearing loss (AINSHL). Previous studies have suggested that mitochondrial secondary variants may modulate the clinical expression of m.1555A>G-induce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1db76edabdebbd63eca3dc7c1458750
Publikováno v:
Genes. 13(10)
The mitochondrial 1555Agt;G mutation plays a critical role in aminoglycoside-induced and non-syndromic hearing loss (AINSHL). Previous studies have suggested that mitochondrial secondary variants may modulate the clinical expression of m.1555Agt;G-in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46e171db0574916febe4cf6c60de081a
https://pubmed.ncbi.nlm.nih.gov/36292680
https://pubmed.ncbi.nlm.nih.gov/36292680
Publikováno v:
Journal of Clinical Laboratory Analysis. 36
Background Mitochondrial dysfunctions caused by mitochondrial DNA (mtDNA) pathogenic mutations play putative roles in type 2 diabetes mellitus (T2DM) progression. But the underlying mechanism remains poorly understood. Methods A large Chinese family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7c5aadcc16a6140fc2acbb50354858a
https://doi.org/10.1002/jcla.24102
https://doi.org/10.1002/jcla.24102
Publikováno v:
Journal of Clinical Laboratory Analysis
Background Mitochondrial dysfunctions caused by mitochondrial DNA (mtDNA) pathogenic mutations play putative roles in type 2 diabetes mellitus (T2DM) progression. But the underlying mechanism remains poorly understood. Methods A large Chinese family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2c0532534522b89d68c8c274161526f
https://pubmed.ncbi.nlm.nih.gov/34811812
https://pubmed.ncbi.nlm.nih.gov/34811812
Publikováno v:
The journal of gene medicineREFERENCES. 23(4)
BACKGROUND Mutations in mitochondrial tRNA (mt-tRNA) genes are associated with hypertension, although their pathogenic mechanisms remain poorly understood. METHODS In the present study, two Han Chinese families with maternally transmitted hypertensio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14ade0e8924a097f1cb6d9afe17eaa12
https://pubmed.ncbi.nlm.nih.gov/33625761
https://pubmed.ncbi.nlm.nih.gov/33625761