Mitochondrial DNA A3243G variant-associated retinopathy: current perspectives and clinical implications
Cellular function and survival are critically dependent on the proper functionality of the
mitochondrion. Neurodegenerative cellular processes including cellular adenosine …
mitochondrion. Neurodegenerative cellular processes including cellular adenosine …
Meta-Analysis of Association of Mitochondrial DNA Mutations with Type 2 Diabetes and Gestational Diabetes Mellitus
SP Alexandar, I Dhinakaran, V Ravi… - … Journal of Human …, 2017 - Taylor & Francis
Type 2 diabetes mellitus (TIIDM) and Gestational diabetes mellitus (GDM) are two most
prevalent metabolic diseases affecting humans. These two diseases are characterised by …
prevalent metabolic diseases affecting humans. These two diseases are characterised by …
The first concurrent detection of mitochondrial DNA m. 3243A> G mutation, deletion, and depletion in a family with mitochondrial diabetes
M Tabebi, W Safi, R Felhi, O Alila Fersi… - … Genetics & Genomic …, 2020 - Wiley Online Library
Background Mitochondrial diabetes (MD) is a rare monogenic form of diabetes and divided
into type l and type 2. It is characterized by a strong familial clustering of diabetes with the …
into type l and type 2. It is characterized by a strong familial clustering of diabetes with the …
Mitochondrial haplogroups are not associated with diabetic retinopathy in a large Australian and British Caucasian sample
E Liu, G Kaidonis, MC Gillies, S Abhary, RW Essex… - Scientific Reports, 2019 - nature.com
Mitochondrial haplogroups H1, H2 and UK have previously been reported to be associated
with proliferative diabetic retinopathy (PDR) in Caucasian patients with diabetes. We aimed …
with proliferative diabetic retinopathy (PDR) in Caucasian patients with diabetes. We aimed …
线粒体DNA4977bp 大片缺失突变与喉癌的相关性研究..
张姝， 孙娟， 徐凌， 王博谦， 赵斐斐… - Progress in Modern …, 2020 - search.ebscohost.com
摘要目的: 探讨线粒体DNA4977bp 大片缺失突变与喉癌的相关性. 方法: 选择2016 年1 月~
2017 年6 月我院收治的喉乳头状瘤, 喉癌患者, 分别纳入良性肿瘤组, 恶性肿瘤组, 每组各150 例 …
2017 年6 月我院收治的喉乳头状瘤, 喉癌患者, 分别纳入良性肿瘤组, 恶性肿瘤组, 每组各150 例 …
Computational Analysis of Structural Differences Between Wildtype Human Mitochondrial tRNA Leucine (UUR) and the A3243G Mutant
T Nguyen - 2023 - search.proquest.com
Maternally inherited diabetes and deafness (MIDD), a subtype of mitochondrial
encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), is caused by the …
encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), is caused by the …
Genetics of diabetic retinopathy
H Isildak, SG Schwartz, MA Brantley Jr - Genetics and Genomics of Eye …, 2020 - Elsevier
Diabetic retinopathy is a complex disease, with both genetic and environmental contributing
factors. Several approaches have been used to identify genetic determinants, including …
factors. Several approaches have been used to identify genetic determinants, including …
[PDF][PDF] Risk Factors for Diabetic Retinopathy Blindness and Its Treatment
E Liu - 2021 - flex.flinders.edu.au
Risk factors for diabetic retinopathy blindness and its treatment Page 1 Risk factors for diabetic
retinopathy blindness and its treatment By Ebony Liu Thesis Submitted to Flinders University for …
retinopathy blindness and its treatment By Ebony Liu Thesis Submitted to Flinders University for …