203 related articles for article (PubMed ID: 16828917)
1. Mitochondrial complex I activity is significantly decreased in a patient with maternally inherited type 2 diabetes mellitus and hypertrophic cardiomyopathy associated with mitochondrial DNA C3310T mutation: a cybrid study.
Chen J; Hattori Y; Nakajima K; Eizawa T; Ehara T; Koyama M; Hirai T; Fukuda Y; Kinoshita M; Sugiyama A; Hayashi J; Onaya T; Kobayashi T; Tawata M
Diabetes Res Clin Pract; 2006 Nov; 74(2):148-53. PubMed ID: 16828917
[TBL] [Abstract][Full Text] [Related]
2. A heteroplasmic mitochondrial DNA 3310 mutation in the ND1 gene in a patient with type 2 diabetes, hypertrophic cardiomyopathy, and mental retardation.
Hattori Y; Takeoka M; Nakajima K; Ehara T; Koyama M
Exp Clin Endocrinol Diabetes; 2005 Jun; 113(6):318-23. PubMed ID: 15977098
[TBL] [Abstract][Full Text] [Related]
3. Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy.
Mariotti C; Tiranti V; Carrara F; Dallapiccola B; DiDonato S; Zeviani M
J Clin Invest; 1994 Mar; 93(3):1102-7. PubMed ID: 8132749
[TBL] [Abstract][Full Text] [Related]
4. A patient with type 2 diabetes mellitus associated with mutations in calcium sensing receptor gene and mitochondrial DNA.
Ohkubo E; Aida K; Chen J; Hayashi JI; Isobe K; Tawata M; Onaya T
Biochem Biophys Res Commun; 2000 Nov; 278(3):808-13. PubMed ID: 11095989
[TBL] [Abstract][Full Text] [Related]
5. Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction.
Raha S; Merante F; Shoubridge E; Myint AT; Tein I; Benson L; Johns T; Robinson BH
Hum Mutat; 1999; 13(3):245-54. PubMed ID: 10090480
[TBL] [Abstract][Full Text] [Related]
6. A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness.
Chen FL; Liu Y; Song XY; Hu HY; Xu HB; Zhang XM; Shi JH; Hu J; Shen Y; Lu B; Wang XC; Hu RM
Mutat Res; 2006 Dec; 602(1-2):26-33. PubMed ID: 16949108
[TBL] [Abstract][Full Text] [Related]
7. A new mitochondrial DNA mutation at 14577 T/C is probably a major pathogenic mutation for maternally inherited type 2 diabetes.
Tawata M; Hayashi JI; Isobe K; Ohkubo E; Ohtaka M; Chen J; Aida K; Onaya T
Diabetes; 2000 Jul; 49(7):1269-72. PubMed ID: 10909988
[TBL] [Abstract][Full Text] [Related]
8. Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.
Bonora E; Porcelli AM; Gasparre G; Biondi A; Ghelli A; Carelli V; Baracca A; Tallini G; Martinuzzi A; Lenaz G; Rugolo M; Romeo G
Cancer Res; 2006 Jun; 66(12):6087-96. PubMed ID: 16778181
[TBL] [Abstract][Full Text] [Related]
9. Sequence and functional analyses of mtDNA in a maternally inherited family with bipolar disorder and depression.
Munakata K; Fujii K; Nanko S; Kunugi H; Kato T
Mutat Res; 2007 Apr; 617(1-2):119-24. PubMed ID: 17320116
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial DNA oxidation and manganese superoxide dismutase activity in peripheral blood mononuclear cells from type 2 diabetic patients.
García-Ramírez M; Francisco G; García-Arumí E; Hernández C; Martínez R; Andreu AL; Simó R
Diabetes Metab; 2008 Apr; 34(2):117-24. PubMed ID: 18291700
[TBL] [Abstract][Full Text] [Related]
11. Cytoplasmic transfer of platelet mtDNA from elderly patients with Parkinson's disease to mtDNA-less HeLa cells restores complete mitochondrial respiratory function.
Aomi Y; Chen CS; Nakada K; Ito S; Isobe K; Murakami H; Kuno SY; Tawata M; Matsuoka R; Mizusawa H; Hayashi JI
Biochem Biophys Res Commun; 2001 Jan; 280(1):265-73. PubMed ID: 11162509
[TBL] [Abstract][Full Text] [Related]
12. Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family.
Swerdlow RH; Parks JK; Davis JN; Cassarino DS; Trimmer PA; Currie LJ; Dougherty J; Bridges WS; Bennett JP; Wooten GF; Parker WD
Ann Neurol; 1998 Dec; 44(6):873-81. PubMed ID: 9851431
[TBL] [Abstract][Full Text] [Related]
13. Novel mitochondrial DNA length variants and genetic instability in a family with diabetes and deafness.
Janssen GM; Neu A; 't Hart LM; van de Sande CM; Antonie Maassen J
Exp Clin Endocrinol Diabetes; 2006 Apr; 114(4):168-74. PubMed ID: 16705548
[TBL] [Abstract][Full Text] [Related]
14. A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy.
Jonckheere AI; Hogeveen M; Nijtmans LG; van den Brand MA; Janssen AJ; Diepstra JH; van den Brandt FC; van den Heuvel LP; Hol FA; Hofste TG; Kapusta L; Dillmann U; Shamdeen MG; Smeitink JA; Rodenburg RJ
J Med Genet; 2008 Mar; 45(3):129-33. PubMed ID: 17954552
[TBL] [Abstract][Full Text] [Related]
15. [Mitochondrial DNA 3243, 3316 point mutations and type 2 diabetes mellitus].
Tang J; Li J; Tian X; Kong Q; Zhang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):198-200. PubMed ID: 15793785
[TBL] [Abstract][Full Text] [Related]
16. Biochemical analysis of cybrids expressing mitochondrial DNA from Contursi kindred Parkinson's subjects.
Swerdlow RH; Parks JK; Cassarino DS; Binder DR; Bennett JP; Di Iorio G; Golbe LI; Parker WD
Exp Neurol; 2001 Jun; 169(2):479-85. PubMed ID: 11358461
[TBL] [Abstract][Full Text] [Related]
17. A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy.
Mahjoub S; Sternberg D; Boussaada R; Filaut S; Gmira F; Mechmech R; Jardel C; Arab SB
Diagn Mol Pathol; 2007 Dec; 16(4):238-42. PubMed ID: 18043288
[TBL] [Abstract][Full Text] [Related]
18. Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma.
Mayr JA; Meierhofer D; Zimmermann F; Feichtinger R; Kögler C; Ratschek M; Schmeller N; Sperl W; Kofler B
Clin Cancer Res; 2008 Apr; 14(8):2270-5. PubMed ID: 18413815
[TBL] [Abstract][Full Text] [Related]
19. Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndrome.
De Joanna G; Santorelli FM; Casali C; Brescia-Morra V; Perretti A; Santoro L
J Hum Genet; 2000; 45(2):109-11. PubMed ID: 10721677
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial diabetes and its lessons for common Type 2 diabetes.
Maassen JA; 't Hart LM; Janssen GM; Reiling E; Romijn JA; Lemkes HH
Biochem Soc Trans; 2006 Nov; 34(Pt 5):819-23. PubMed ID: 17052206
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]