343 related articles for article (PubMed ID: 19065528)
1. [The mitochondrial DNA mutation in spinocerebellar ataxia type 3].
Wang J; Luo M; Yuan Z; Yang X; Li G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):667-9. PubMed ID: 19065528
[TBL] [Abstract][Full Text] [Related]
2. [Aberrance analysis of mitochondrial DNA in a family with hereditary ataxia in Guangxi province].
Wang J; Liu HH; Luo SG
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):323-5. PubMed ID: 16767675
[TBL] [Abstract][Full Text] [Related]
3. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
Ma L; Wang H; Chen J; Jin W; Liu L; Ban B; Shen J; Hua Z; Chai J
Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
[TBL] [Abstract][Full Text] [Related]
4. [Mutation analysis of mitochondrial DNA of children with Rett syndrome].
Tang J; Qi Y; Bao X
Zhonghua Yi Xue Za Zhi; 1996 Sep; 76(9):684-7. PubMed ID: 9275552
[TBL] [Abstract][Full Text] [Related]
5. [Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].
Zhang XA; Wu HC; Zhang BF; Yu W; Fan QS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):18-21. PubMed ID: 15696472
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. [Mitochondrial DNA mutations in patients with myocardial diseases].
Li YY; Xu J; Zhang JN
Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):345-8, 350. PubMed ID: 7994642
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial DNA point mutations and a novel deletion induced by direct low-LET radiation and by medium from irradiated cells.
Murphy JE; Nugent S; Seymour C; Mothersill C
Mutat Res; 2005 Aug; 585(1-2):127-36. PubMed ID: 16002327
[TBL] [Abstract][Full Text] [Related]
9. Detection of mitochondrial DNA deletion by a modified PCR method in a 60Co radiation-exposed patient.
Wang ZC; Wang XM; Jiao BH; Jin YX; Miao MY; Zhu KJ; Ni QG
IUBMB Life; 2003 Mar; 55(3):133-7. PubMed ID: 12822889
[TBL] [Abstract][Full Text] [Related]
10. Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia.
Houshmand M; Panahi MS; Nafisi S; Soltanzadeh A; Alkandari FM
Mitochondrion; 2006 Apr; 6(2):82-8. PubMed ID: 16581313
[TBL] [Abstract][Full Text] [Related]
11. [Relationship between human age and mtDNA 4977 deletions in human blood cells].
Li CT; Li L; Liu Y
Fa Yi Xue Za Zhi; 2006 Oct; 22(5):346-8. PubMed ID: 17190146
[TBL] [Abstract][Full Text] [Related]
12. Familial gene analysis for Wilson disease from north-west Indian patients.
Kumar S; Thapa BR; Kaur G; Prasad R
Ann Hum Biol; 2006; 33(2):177-86. PubMed ID: 16684691
[TBL] [Abstract][Full Text] [Related]
13. [Mitochondrial DNA mutations and non-syndromic sensorineural hearing loss].
Kong W; Wang Q; Zheng X; Cheng H
Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Oct; 37(5):338-42. PubMed ID: 12772452
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Detecting the DNA polymorphism of human complement component C8A by PCR-SSCP analysis].
Yang ZH; Zhang L; Zhou B; Wang C; Jia J
Sichuan Da Xue Xue Bao Yi Xue Ban; 2006 May; 37(3):471-3. PubMed ID: 16761437
[TBL] [Abstract][Full Text] [Related]
16. [The application of polymerase chain reaction-single strain conformation polymorphism in the pedigree analysis of familial hypercholerolemia patients].
Zhu D; Chen Z; Chen B; Lu Z; Lu X; Kou W; Xu Y; Sun G; Zeng W; Yang Y; Chen J; Gao R; Du H; Ma X; Xu H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Apr; 17(2):108-11. PubMed ID: 10751533
[TBL] [Abstract][Full Text] [Related]
17. Rapid detection of sequence polymorphisms in the human mitochondrial DNA control region by polymerase chain reaction and single-strand conformation analysis in mutation detection enhancement gels.
Alonso A; Martin P; Albarran C; Garcia O; Sancho M
Electrophoresis; 1996 Aug; 17(8):1299-301. PubMed ID: 8874053
[TBL] [Abstract][Full Text] [Related]
18. [Study on the mitochondrial DNA variation in patients with type 2 diabetes mellitus].
Ji JZ; Lu JX; Ye W; Hu X; Wang DW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Apr; 24(2):167-72. PubMed ID: 17407074
[TBL] [Abstract][Full Text] [Related]
19. Somatic D-loop mitochondrial DNA mutations are frequent in uterine serous carcinoma.
Pejovic T; Ladner D; Intengan M; Zheng K; Fairchild T; Dillon D; Easley S; Dillon D; Marchetti D; Schwartz P; Lele S; Costa J; Odunsi K
Eur J Cancer; 2004 Nov; 40(16):2519-24. PubMed ID: 15519528
[TBL] [Abstract][Full Text] [Related]
20. [Mutation analysis of neurofilament-light gene in Chinese Charcot-Marie-Tooth disease].
Luo W; Tang B; Zhao G; Li Q; Xiao J; Yang Q; Xia J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):169-70. PubMed ID: 12673592
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
