Mitochondrial inheritance and disease
Yasuda, N.
No to Hattatsu 19(2): 150-156
1987
ISSN/ISBN: 0029-0831 PMID: 3103657 Document Number: 295391
Document emailed within 1 workday
Related Documents
Holliday, P.L.; Gilroy, J. 1983: Mitochondrial inheritance New England Journal of Medicine 309(25): 1583-1584Schwartz, M.; Vissing, J. 2003: Paternal inheritance of mitochondrial DNA Ugeskrift for Laeger 165(38): 3627-3630
Wikström, M. 1981: The inner mitochondrial membrane--inheritance from ancient bacteria Duodecim; Laaketieteellinen Aikakauskirja 97(18): 1546-1553
Hintz, W.; Anderson, J.B.; Horgen, P.A. 1988: Nuclear migration and mitochondrial inheritance in the mushroom agaricus bitorquis Genetics 119(1): 35-41
Goto, Y.-i. 2002: Classification of mitochondrial diseases based on inheritance pattern and genetic counseling Nihon Rinsho. Japanese Journal of Clinical Medicine 60(Suppl 4): 693-697
Fu, W.-p.; Zhao, Z.-h.; Zhong, L.; Liu, L.; Zhao, Y.-l.; Wang, X.-m.; Qiu, Y.-h.; Dai, L.-m. 2013: Relationship between mitochondrial cytochrome oxidase mRNA expression and maternal inheritance of asthma Zhonghua Yi Xue Za Zhi 93(28): 2191-2194
Kawai, H.; Akaike, M.; Yokoi, K.; Tamaki, Y.; Saito, S. 1993: Mitochondrial myopathy with autosomal dominant inheritance--report of a family and review of the literature Rinsho Shinkeigaku 33(2): 162-168
Johnson, D.R.; O'Higgins, P.; McAndrew, T.J.; Kida, M.Y. 1992: The inheritance of vertebral shape in the mouse. I. a study using Fourier analysis to examine patterns of inheritance in the morphology of cervical and upper thoracic vertebrae Journal of Anatomy 180: 507-514
Ohta, S. 1995: Mitochondrial diseases caused by mitochondrial DNA mutants and their related regulation of mitochondrial biogenesis Seikagaku. Journal of Japanese Biochemical Society 67(1): 15-32
Marsac, C.; Degoul, F.; Bonne, G.; Romero, N.; Nelson, I.; Fardeau, M.; François, D.; Ponsot, G.; Harpey, J.P.; Eymard, B. 1991: Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy Revue Neurologique (Paris) 147(6-7): 462-466
Inamori, M.; Ishigami, T.; Takahashi, N.; Hibi, K.; Ashino, K.; Sumita, S.; Tamura, K.; Ochiai, H.; Umemura, S.; Ishii, M.; Tanaka, S.; Sekihara, H.; Inayama, Y. 1997: A case of mitochondrial cardiomyopathy with heart failure, sick sinus syndrome and diabetes mellitus: mitochondrial DNA adenine-to-guanine transition at 3243 of mitochondrial tRNA(LEU)(UUR) gene Journal of Cardiology 30(6): 341-347
Yao, J.; Li, H. 2000: Evidence for inheritance of Alzheimer disease in families Zhonghua Yu Fang Yi Xue Za Zhi 34(2): 122-123
Dassler, A.; Allen, P.J. 2014: Mitochondrial disease in children and adolescents Pediatric Nursing 40(3): 150-154
Hattori, N. 2004: Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease Rinsho Shinkeigaku 44(4-5): 241-262
Goto, Y. 1997: Mitochondrial DNA mutations and three major forms of mitochondrial myopathies: CPEO, MELAS and MERRF Nihon Rinsho. Japanese Journal of Clinical Medicine 55(12): 3259-3264
Song, D.; Zhang, Y.; Shi, J. 2001: The study of point mutation of muscular mitochondrial DNA from patients with mitochondrial encephalomyopathies Zhonghua Yi Xue Za Zhi 81(11): 659-661
Rábano, J.A.; Playan, A.; Guirado, F.; Montoya, J.; Baldellou, A.; López-Pisón, J. 1998: Acute presentation of leukodystrophy due to mitochondrial cytopathology and multiple deletions of mitochondrial DNA Revista de Neurologia 27(160): 1005-1007
Yamamoto, M.; Shimokawa, M.; Hamada, K. 1997: Application of long PCR method to detection of mitochondrial DNA deletions in mitochondrial encephalomyopathies Nihon Rinsho. Japanese Journal of Clinical Medicine 55(12): 3282-3285
Nonaka, I. 2002: Approach for a final diagnosis of mitochondrial disease Nihon Rinsho. Japanese Journal of Clinical Medicine 60(Suppl 4): 224-228
Nakada, K.; Inoue, K.; Hayashi, J.-I.; Nakada, K.; Hayashi, J.-I.; Inoue, K. 2002: Mitochondrial DNA-based disease model mice Nihon Rinsho. Japanese Journal of Clinical Medicine 60(Suppl 4): 688-692