192 related articles for article (PubMed ID: 22678792)
1. [Mitochondrial genetics and human essential hypertension].
Chen H; Guan MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Jun; 29(3):293-5. PubMed ID: 22678792
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial DNA mutations: an overview of clinical and molecular aspects.
Craigen WJ
Methods Mol Biol; 2012; 837():3-15. PubMed ID: 22215537
[TBL] [Abstract][Full Text] [Related]
3. Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations.
Da Pozzo P; Cardaioli E; Radi E; Federico A
Biochem Biophys Res Commun; 2004 Nov; 324(1):360-4. PubMed ID: 15465027
[TBL] [Abstract][Full Text] [Related]
4. The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement.
Wallace DC
Gene; 2005 Jul; 354():169-80. PubMed ID: 16024186
[TBL] [Abstract][Full Text] [Related]
5. Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family.
Wang S; Li R; Fettermann A; Li Z; Qian Y; Liu Y; Wang X; Zhou A; Mo JQ; Yang L; Jiang P; Taschner A; Rossmanith W; Guan MX
Circ Res; 2011 Apr; 108(7):862-70. PubMed ID: 21454794
[TBL] [Abstract][Full Text] [Related]
6. The Role of Mitochondrial DNA Mutations in Cardiovascular Diseases.
Dabravolski SA; Khotina VA; Sukhorukov VN; Kalmykov VA; Mikhaleva LM; Orekhov AN
Int J Mol Sci; 2022 Jan; 23(2):. PubMed ID: 35055137
[TBL] [Abstract][Full Text] [Related]
7. Insight into mammalian mitochondrial DNA segregation.
Jokinen R; Battersby BJ
Ann Med; 2013 Mar; 45(2):149-55. PubMed ID: 22775146
[TBL] [Abstract][Full Text] [Related]
8. Prospects for DNA-based prenatal diagnosis of mitochondrial disorders.
Poulton J; Marchington DR
Prenat Diagn; 1996 Dec; 16(13):1247-56. PubMed ID: 9061755
[TBL] [Abstract][Full Text] [Related]
9. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
Mao YJ; Qu J; Guan MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial DNA mutations in human disease.
Greaves LC; Taylor RW
IUBMB Life; 2006 Mar; 58(3):143-51. PubMed ID: 16766381
[TBL] [Abstract][Full Text] [Related]
11. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
Lévêque M; Marlin S; Jonard L; Procaccio V; Reynier P; Amati-Bonneau P; Baulande S; Pierron D; Lacombe D; Duriez F; Francannet C; Mom T; Journel H; Catros H; Drouin-Garraud V; Obstoy MF; Dollfus H; Eliot MM; Faivre L; Duvillard C; Couderc R; Garabedian EN; Petit C; Feldmann D; Denoyelle F
Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
[TBL] [Abstract][Full Text] [Related]
12. Transmission of mitochondrial DNA--playing favorites?
Boore JL
Bioessays; 1997 Sep; 19(9):751-3. PubMed ID: 9297965
[TBL] [Abstract][Full Text] [Related]
13. [Inheritance and evolution of plant mtDNA: Overview].
Sugiyama Y
Tanpakushitsu Kakusan Koso; 2005 Nov; 50(14 Suppl):1780-1. PubMed ID: 16318315
[No Abstract] [Full Text] [Related]
14. Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family.
Li Z; Liu Y; Yang L; Wang S; Guan MX
Biochem Biophys Res Commun; 2008 Mar; 367(4):906-11. PubMed ID: 18177739
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial DNA variants influence mitochondrial bioenergetics in Drosophila melanogaster.
Correa CC; Aw WC; Melvin RG; Pichaud N; Ballard JW
Mitochondrion; 2012 Jul; 12(4):459-64. PubMed ID: 22735574
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial genome variation and the origin of modern humans.
Ingman M; Kaessmann H; Pääbo S; Gyllensten U
Nature; 2000 Dec; 408(6813):708-13. PubMed ID: 11130070
[TBL] [Abstract][Full Text] [Related]
17. No evidence for paternal inheritance of mtDNA in patients with sporadic mtDNA mutations.
Schwartz M; Vissing J
J Neurol Sci; 2004 Mar; 218(1-2):99-101. PubMed ID: 14759640
[TBL] [Abstract][Full Text] [Related]
18. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.
Holt IJ; Harding AE; Morgan-Hughes JA
Nature; 1988 Feb; 331(6158):717-9. PubMed ID: 2830540
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial DNA mutations and essential hypertension (Review).
Ding Y; Xia B; Yu J; Leng J; Huang J
Int J Mol Med; 2013 Oct; 32(4):768-74. PubMed ID: 23900616
[TBL] [Abstract][Full Text] [Related]
20. Obtaining mice that carry human mitochondrial DNA transmitted to the progeny.
Sokolova VA; Kustova ME; Arbuzova NI; Sorokin AV; Moskaliova OS; Bass MG; Vasilyev VB
Mol Reprod Dev; 2004 Jul; 68(3):299-307. PubMed ID: 15112322
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
