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541 related items for PubMed ID: 16949108

  • 1. 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 01; 602(1-2):26-33. PubMed ID: 16949108
    [Abstract] [Full Text] [Related]

  • 2. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM.
    Ophthalmology; 1999 Jun 01; 106(6):1101-8. PubMed ID: 10366077
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  • 3. [Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA. Apropos a case].
    Biarnés J, Barrientos A, Ricart W, Nunes V, Fernández-Castañer M, Soler J.
    Med Clin (Barc); 1999 Jan 30; 112(3):99-101. PubMed ID: 10074618
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  • 4. Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?
    Holmes-Walker DJ, Mitchell P, Boyages SC.
    Diabet Med; 1998 Nov 30; 15(11):946-52. PubMed ID: 9827849
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  • 5. 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 30; 113(2):111-6. PubMed ID: 11775531
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  • 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 30; 22(2):198-200. PubMed ID: 15793785
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  • 7. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.
    van den Ouweland JM, Lemkes HH, Ruitenbeek W, Sandkuijl LA, de Vijlder MF, Struyvenberg PA, van de Kamp JJ, Maassen JA.
    Nat Genet; 1992 Aug 30; 1(5):368-71. PubMed ID: 1284550
    [Abstract] [Full Text] [Related]

  • 8. Sequence analysis of the mitochondrial genome from a large family with maternally inherited nonsyndromic deafness.
    Zhang HJ, Xu CH, Zhan YJ, Zhao SY, Shan YF, Geng XX, Shan XN.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug 30; 22(4):368-71. PubMed ID: 16086269
    [Abstract] [Full Text] [Related]

  • 9. Search for mitochondrial A3243G tRNA(Leu) mutation in Polish patients with type 2 diabetes mellitus.
    Małecki M, Klupa T, Wanic K, Frey J, Cyganek K, Sieradzki J.
    Med Sci Monit; 2001 Aug 30; 7(2):246-50. PubMed ID: 11257730
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  • 11. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.
    Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC.
    Nat Genet; 1992 Apr 30; 1(1):11-5. PubMed ID: 1301992
    [Abstract] [Full Text] [Related]

  • 12. Novel mitochondrial DNA length variants and genetic instability in a family with diabetes and deafness.
    Janssen GM, Neu A, 't Hart LM, van de Sande CM, Antonie Maassen J.
    Exp Clin Endocrinol Diabetes; 2006 Apr 30; 114(4):168-74. PubMed ID: 16705548
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  • 14. Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.
    Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C.
    Biochem Biophys Res Commun; 2000 Nov 02; 277(3):771-5. PubMed ID: 11062027
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  • 15. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.
    Kameoka K, Isotani H, Tanaka K, Azukari K, Fujimura Y, Shiota Y, Sasaki E, Majima M, Furukawa K, Haginomori S, Kitaoka H, Ohsawa N.
    Biochem Biophys Res Commun; 1998 Apr 17; 245(2):523-7. PubMed ID: 9571188
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  • 17. A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy.
    Tabebi M, Mkaouar-Rebai E, Mnif M, Kallabi F, Ben Mahmoud A, Ben Saad W, Charfi N, Keskes-Ammar L, Kamoun H, Abid M, Fakhfakh F.
    Biochem Biophys Res Commun; 2015 Apr 10; 459(3):353-60. PubMed ID: 25701779
    [Abstract] [Full Text] [Related]

  • 18. Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation.
    Thorns C, Widjaja A, Boeck N, Skamira C, Zühlke H.
    Exp Clin Endocrinol Diabetes; 1998 Apr 10; 106(5):384-8. PubMed ID: 9831303
    [Abstract] [Full Text] [Related]

  • 19. Nonrandom tissue distribution of mutant mtDNA.
    Chinnery PF, Zwijnenburg PJ, Walker M, Howell N, Taylor RW, Lightowlers RN, Bindoff L, Turnbull DM.
    Am J Med Genet; 1999 Aug 27; 85(5):498-501. PubMed ID: 10405450
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