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Scholar Results 1 - 10 of about 20 citing Choo-Kang: Defining the importance of mitochondrial gene defects in maternally inherited.... (0.10 sec) 

Mitochondrial disorders


M Zeviani, A Spinazzola - Current Neurology and Neuroscience Reports, 2003 - Springer
Introduction Mitochondrial disorders are clinical phenotypes associated with
abnormalities of the terminal component of mito- chondrial energy metabolism
(ie, oxidative phosphoryla- tion [OXPHOS]). OXPHOS is carried out in the ...
Cited by 373 - Related articles - BL Direct - All 20 versions

Mitochondrial DNA mutations in human disease


RW Taylor, DM Turnbull - Nature reviews. Genetics, 2005 - pubmedcentral.nih.gov
Cited by 248 - Related articles - All 12 versions

Genetics of type 2 diabetes and insulin resistance: knowledge from human studies


EA McIntyre, M Walker - Clinical endocrinology, 2002 - interscience.wiley.com
Both type 2 diabetes mellitus (T2DM) and insulin resistance are complex traits
in which multiple gene effects and metabolic and environmental factors combine
to contribute to the overall pathogenesis of these conditions. This ...
Cited by 47 - Related articles - BL Direct - All 5 versions

Molecular mechanisms of mitochondrial diabetes (MIDD)


JA Maassen, GMC Janssen, LM 't Hart - Annals of Medicine, 2005 - informahealthcare.com
Abstract Mitochondria provide cells with most of the energy in the form of
adenosine triphosphate (ATP). Mitochondria are complex organelles encoded both
by nuclear and mtDNA. Only a few mitochondrial components are encoded by ...
Cited by 38 - Related articles - All 6 versions

Variation of mitochondrial gene and the association with type 2 diabetes mellitus in a …


DL Tang, X Zhou, X Li, L Zhao, F Liu - Diabetes research and clinical practice, 2006 - Elsevier
Mitochondrial DNA (mtDNA) variants have been implicated in many diseases
including diabetes mellitus. To explore whether these genetic variants
contribute to the susceptibility for type 2 diabetes mellitus (T2DM) in a ...
Cited by 11 - Related articles - All 13 versions

Clinical features, diagnosis and management of maternally inherited diabetes and deafness …


R Murphy, DM Turnbull, M Walker, AT … - Diabetic Medicine, 2008 - pt.wkhealth.com
Cited by 11 - Related articles - BL Direct - All 5 versions

Novel mutations found in mitochondrial diabetes in Chinese Han population


SM Liu, X Zhou, F Zheng, X Li, F Liu, HM … - Diabetes research and clinical practice, 2007 - Elsevier
Mitochondria provide cells with most of the energy in the form of ATP. Mutations
in mitochondrial DNA (mtDNA) are associated with type 2 diabetes mellitus (T2DM)
because ATP plays a critical role in the production and the release of ...
Cited by 8 - Related articles - All 11 versions

[CITATION] Mitochondrial diabetes.


M Walker, RW Taylor, DM Turnbull - Diabetic medicine: a journal of the British Diabetic …, 2005 - ncbi.nlm.nih.gov
1: Diabet Med. 2005 Sep;22 Suppl 4:18-20. Mitochondrial diabetes. Walker
M, Taylor RW, Turnbull DM. Diabetes Research Group, School ...
Cited by 6 - Related articles - BL Direct - All 4 versions

The G1888A variant in the mitochondrial 16S rRNA gene may be associated with Type 2 …


D Crispim, LH Canani, JL Gross, RM Carlessi, … - Diabetic Medicine, 2005 - interscience.wiley.com
Methods We analysed 520 Type 2 diabetic patients (389 Caucasian– and 131
African–Brazilians) and 530 control subjects (400 Caucasian– and 130
African–Brazilians). DNA samples were amplified by polymerase chain ...
Cited by 7 - Related articles - BL Direct - All 4 versions

Infantile cardiomyopathy caused by the T14709C mutation in the mitochondrial tRNA …


JLK Van Hove, C Freehauf, S Miyamoto, GD … - European Journal of Pediatrics, 2008 - Springer
Abstract A 6-week-old child presented with hypotonia, myopathy, and a rapidly
worsening dilated cardiomyopathy with severe atrial and ventricular arrhythmias
and pulmo- nary hypertension, which proved fatal at age 3 months. ...
Cited by 3 - Related articles - BL Direct - All 3 versions


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