218 related articles for article (PubMed ID: 9302261)
1. Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease.
Hofmann S; Jaksch M; Bezold R; Mertens S; Aholt S; Paprotta A; Gerbitz KD
Hum Mol Genet; 1997 Oct; 6(11):1835-46. PubMed ID: 9302261
[TBL] [Abstract][Full Text] [Related]
2. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD
Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481
[TBL] [Abstract][Full Text] [Related]
3. Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndrome.
Hofmann S; Bezold R; Jaksch M; Kaufhold P; Obermaier-Kusser B; Gerbitz KD
Mol Cell Biochem; 1997 Sep; 174(1-2):209-13. PubMed ID: 9309689
[TBL] [Abstract][Full Text] [Related]
4. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P
Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
[TBL] [Abstract][Full Text] [Related]
5. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
Brown MD; Sun F; Wallace DC
Am J Hum Genet; 1997 Feb; 60(2):381-7. PubMed ID: 9012411
[TBL] [Abstract][Full Text] [Related]
6. The sudden infant death syndrome gene: does it exist?
Opdal SH; Rognum TO
Pediatrics; 2004 Oct; 114(4):e506-12. PubMed ID: 15466077
[TBL] [Abstract][Full Text] [Related]
7. Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans.
Collins DW; Gudiseva HV; Trachtman B; Bowman AS; Sagaser A; Sankar P; Miller-Ellis E; Lehman A; Addis V; O'Brien JM
Mol Vis; 2016; 22():454-71. PubMed ID: 27217714
[TBL] [Abstract][Full Text] [Related]
8. The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS.
Pulkes T; Eunson L; Patterson V; Siddiqui A; Wood NW; Nelson IP; Morgan-Hughes JA; Hanna MG
Ann Neurol; 1999 Dec; 46(6):916-9. PubMed ID: 10589546
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction.
Lertrit P; Kapsa RM; Jean-Francois MJ; Thyagarajan D; Noer AS; Marzuki S; Byrne E
Hum Mol Genet; 1994 Nov; 3(11):1973-81. PubMed ID: 7874114
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!
Hassani-Kumleh H; Houshmand M; Panahi MS; Riazi GH; Sanati MH; Gharagozli K; Ghabaee M
Cell Mol Neurobiol; 2006 Mar; 26(2):119-25. PubMed ID: 16763779
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
Tharaphan P; Chuenkongkaew WL; Luangtrakool K; Sanpachudayan T; Suktitipat B; Suphavilai R; Srisawat C; Sura T; Lertrit P
J Neuroophthalmol; 2006 Dec; 26(4):264-7. PubMed ID: 17204919
[TBL] [Abstract][Full Text] [Related]
12. Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutations.
Ohlenbusch A; Wilichowski E; Hanefeld F
Neuropediatrics; 1998 Aug; 29(4):175-9. PubMed ID: 9762692
[TBL] [Abstract][Full Text] [Related]
13. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
Brown MD; Starikovskaya E; Derbeneva O; Hosseini S; Allen JC; Mikhailovskaya IE; Sukernik RI; Wallace DC
Hum Genet; 2002 Feb; 110(2):130-8. PubMed ID: 11935318
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD).
Pilz D; Quarrell OW; Jones EW
J Med Genet; 1994 Apr; 31(4):328-30. PubMed ID: 8071960
[TBL] [Abstract][Full Text] [Related]
15. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.
Torroni A; Petrozzi M; D'Urbano L; Sellitto D; Zeviani M; Carrara F; Carducci C; Leuzzi V; Carelli V; Barboni P; De Negri A; Scozzari R
Am J Hum Genet; 1997 May; 60(5):1107-21. PubMed ID: 9150158
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial DNA variability in Poles and Russians.
Malyarchuk BA; Grzybowski T; Derenko MV; Czarny J; Woźniak M; Miścicka-Sliwka D
Ann Hum Genet; 2002 Jul; 66(Pt 4):261-83. PubMed ID: 12418968
[TBL] [Abstract][Full Text] [Related]
17. Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors.
Shafa Shariat Panahi M; Houshmand M; Tabassi AR
Arch Med Res; 2006 Nov; 37(8):1028-33. PubMed ID: 17045122
[TBL] [Abstract][Full Text] [Related]
18. Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J.
Moilanen JS; Finnila S; Majamaa K
Mol Biol Evol; 2003 Dec; 20(12):2132-42. PubMed ID: 12949126
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
Dogulu CF; Kansu T; Seyrantepe V; Ozguc M; Topaloglu H; Johns DR
Eye (Lond); 2001 Apr; 15(Pt 2):183-8. PubMed ID: 11339587
[TBL] [Abstract][Full Text] [Related]
20. Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes.
Wilichowski E; Ohlenbusch A; Hanefeld F
Neuropediatrics; 1998 Dec; 29(6):307-12. PubMed ID: 10029350
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]