141 related articles for article (PubMed ID: 19185523)
41. Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutations.
Levin L; Blumberg A; Barshad G; Mishmar D
Front Genet; 2014; 5():448. PubMed ID: 25566330
[TBL] [Abstract][Full Text] [Related]
42. New MT-ND6 and NDUFA1 mutations in mitochondrial respiratory chain disorders.
Uehara N; Mori M; Tokuzawa Y; Mizuno Y; Tamaru S; Kohda M; Moriyama Y; Nakachi Y; Matoba N; Sakai T; Yamazaki T; Harashima H; Murayama K; Hattori K; Hayashi J; Yamagata T; Fujita Y; Ito M; Tanaka M; Nibu K; Ohtake A; Okazaki Y
Ann Clin Transl Neurol; 2014 May; 1(5):361-9. PubMed ID: 25356405
[TBL] [Abstract][Full Text] [Related]
43. Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health.
Gershoni M; Levin L; Ovadia O; Toiw Y; Shani N; Dadon S; Barzilai N; Bergman A; Atzmon G; Wainstein J; Tsur A; Nijtmans L; Glaser B; Mishmar D
Genome Biol Evol; 2014 Sep; 6(10):2665-80. PubMed ID: 25245408
[TBL] [Abstract][Full Text] [Related]
44. Mitochondrial disease associated with complex I (NADH-CoQ oxidoreductase) deficiency.
Scheffler IE
J Inherit Metab Dis; 2015 May; 38(3):405-15. PubMed ID: 25224827
[TBL] [Abstract][Full Text] [Related]
45. Mitochondrial DNA variation and virologic and immunological HIV outcomes in African Americans.
Aissani B; Shrestha S; Wiener HW; Tang J; Kaslow RA; Wilson CM
AIDS; 2014 Aug; 28(13):1871-8. PubMed ID: 24932613
[TBL] [Abstract][Full Text] [Related]
46. Mitonuclear interactions: evolutionary consequences over multiple biological scales.
Wolff JN; Ladoukakis ED; Enríquez JA; Dowling DK
Philos Trans R Soc Lond B Biol Sci; 2014 Jul; 369(1646):20130443. PubMed ID: 24864313
[TBL] [Abstract][Full Text] [Related]
47. Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease.
Wallace DC; Chalkia D
Cold Spring Harb Perspect Biol; 2013 Nov; 5(11):a021220. PubMed ID: 24186072
[TBL] [Abstract][Full Text] [Related]
48. The impact of darwinian evolution on medicine: the maternal side of the story.
Mishmar D
Rambam Maimonides Med J; 2010 Jul; 1(1):e0010. PubMed ID: 23908782
[TBL] [Abstract][Full Text] [Related]
49. XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
Piton A; Redin C; Mandel JL
Am J Hum Genet; 2013 Aug; 93(2):368-83. PubMed ID: 23871722
[TBL] [Abstract][Full Text] [Related]
50. A mitochondrial bioenergetic etiology of disease.
Wallace DC
J Clin Invest; 2013 Apr; 123(4):1405-12. PubMed ID: 23543062
[TBL] [Abstract][Full Text] [Related]
51. Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup.
Strauss KA; DuBiner L; Simon M; Zaragoza M; Sengupta PP; Li P; Narula N; Dreike S; Platt J; Procaccio V; Ortiz-González XR; Puffenberger EG; Kelley RI; Morton DH; Narula J; Wallace DC
Proc Natl Acad Sci U S A; 2013 Feb; 110(9):3453-8. PubMed ID: 23401503
[TBL] [Abstract][Full Text] [Related]
52. Impaired mitochondrial metabolism and mammary carcinogenesis.
Yadava N; Schneider SS; Jerry DJ; Kim C
J Mammary Gland Biol Neoplasia; 2013 Mar; 18(1):75-87. PubMed ID: 23269521
[TBL] [Abstract][Full Text] [Related]
53. Genetic counseling in mitochondrial disease.
Vento JM; Pappa B
Neurotherapeutics; 2013 Apr; 10(2):243-50. PubMed ID: 23264099
[TBL] [Abstract][Full Text] [Related]
54. Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases.
Koene S; Rodenburg RJ; van der Knaap MS; Willemsen MA; Sperl W; Laugel V; Ostergaard E; Tarnopolsky M; Martin MA; Nesbitt V; Fletcher J; Edvardson S; Procaccio V; Slama A; van den Heuvel LP; Smeitink JA
J Inherit Metab Dis; 2012 Sep; 35(5):737-47. PubMed ID: 22644603
[TBL] [Abstract][Full Text] [Related]
55. Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile.
Crobu F; Latini V; Marongiu MF; Sogos V; Scintu F; Porcu S; Casu C; Badiali M; Sanna A; Manchinu MF; Ristaldi MS
Mol Biol Rep; 2012 Apr; 39(4):3995-4007. PubMed ID: 21773948
[TBL] [Abstract][Full Text] [Related]
56. The pathophysiology of mitochondrial disease as modeled in the mouse.
Wallace DC; Fan W
Genes Dev; 2009 Aug; 23(15):1714-36. PubMed ID: 19651984
[TBL] [Abstract][Full Text] [Related]
57. A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease.
Potluri P; Davila A; Ruiz-Pesini E; Mishmar D; O'Hearn S; Hancock S; Simon M; Scheffler IE; Wallace DC; Procaccio V
Mol Genet Metab; 2009 Apr; 96(4):189-95. PubMed ID: 19185523
[TBL] [Abstract][Full Text] [Related]
58. Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy.
Malfatti E; Bugiani M; Invernizzi F; de Souza CF; Farina L; Carrara F; Lamantea E; Antozzi C; Confalonieri P; Sanseverino MT; Giugliani R; Uziel G; Zeviani M
Brain; 2007 Jul; 130(Pt 7):1894-904. PubMed ID: 17535832
[TBL] [Abstract][Full Text] [Related]
59. An X-chromosome linked mouse model (Ndufa1
Kim C; Potluri P; Khalil A; Gaut D; McManus M; Compton S; Wallace DC; Yadava N
Neurochem Int; 2017 Oct; 109():78-93. PubMed ID: 28506826
[TBL] [Abstract][Full Text] [Related]
60. Adaptive selection of mitochondrial complex I subunits during primate radiation.
Mishmar D; Ruiz-Pesini E; Mondragon-Palomino M; Procaccio V; Gaut B; Wallace DC
Gene; 2006 Aug; 378():11-8. PubMed ID: 16828987
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]