These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

552 related articles for article (PubMed ID: 9748738)

  • 21. A pilot study of mitochondrial DNA point mutation A3243G in a sample of Croatian patients having type 2 diabetes mellitus associated with maternal inheritance.
    Martin-Kleiner I; Pape-Medvidović E; Pavlić-Renar I; Metelko Z; Kusec R; Gabrilovac J; Boranić M
    Acta Diabetol; 2004 Dec; 41(4):179-84. PubMed ID: 15660201
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 1(5):368-71. PubMed ID: 1284550
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes.
    Kawakami Y; Sakuta R; Hashimoto K; Fujino O; Fujita T; Hida M; Horai S; Goto Y; Nonaka I
    Ann Neurol; 1994 Mar; 35(3):370-3. PubMed ID: 8122892
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [A case of mitochondrial encephalomyopathy showing ophthalmoplegia, diabetes mellitus and hearing loss associated with the A3243G mutation of mitochondrial DNA].
    Hoshino S; Tamaoka A; Ohkoshi N; Shoji S; Goto Y
    Rinsho Shinkeigaku; 1997 Apr; 37(4):326-30. PubMed ID: 9248343
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA; Wang N
    Arch Pathol Lab Med; 1998 Nov; 122(11):978-81. PubMed ID: 9822126
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Melas with point mutations involving tRNALeu (A3243G) and tRNAGlu(A14693g).
    Tzen CY; Thajeb P; Wu TY; Chen SC
    Muscle Nerve; 2003 Nov; 28(5):575-81. PubMed ID: 14571459
    [TBL] [Abstract][Full Text] [Related]  

  • 27. MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletions.
    Aharoni S; Traves TA; Melamed E; Cohen S; Silver EL
    J Neurol Sci; 2010 Sep; 296(1-2):101-3. PubMed ID: 20655066
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].
    Zhang Y; Wang ZX; Niu SL; Xu YF; Pei P; Yuan Y; Yang YL; Qi Y
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb; 27(1):77-80. PubMed ID: 15782498
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M; Mita S; Murakami T; Kumamoto T; Uchino M; Nonaka I; Ando M
    Ann Neurol; 1994 Apr; 35(4):413-9. PubMed ID: 8154867
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Rapid and noninvasive screening of patients with mitochondrial myopathy.
    Kotsimbos N; Jean-Francois MJ; Huizing M; Kapsa RM; Lertrit P; Siregar NC; Marzuki S; Sue C; Byrne E
    Hum Mutat; 1994; 4(2):132-5. PubMed ID: 7981717
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation.
    Mancuso M; Ferraris S; Nishigaki Y; Azan G; Mauro A; Sammarco P; Krishna S; Tay SK; Bonilla E; Romansky SG; Hirano M; DiMauro S
    J Neurol Sci; 2005 Jan; 228(1):93-7. PubMed ID: 15607216
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution.
    Hirata K; Nakagawa M; Higuchi I; Hashimoto K; Hanada K; Takahashi K; Niiyama T; Izumi K; Sakoda S; Yamada H; Osame M
    J Hum Genet; 1999; 44(3):210-4. PubMed ID: 10319590
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Mitochondrial encephalomyopathy associated with parkinsonism and a point mutation in the mitochondrial tRNA(Leu)(UUR)) gene].
    Hara K; Yamamoto M; Anegawa T; Sakuta R; Nakamura M
    Rinsho Shinkeigaku; 1994 Apr; 34(4):361-5. PubMed ID: 8026131
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Reduction of mitochondrial tRNALeu(UUR) aminoacylation by some MELAS-associated mutations.
    Hao R; Yao YN; Zheng YG; Xu MG; Wang ED
    FEBS Lett; 2004 Dec; 578(1-2):135-9. PubMed ID: 15581630
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].
    Mitsuoka T; Kawarai T; Watanabe C; Katayama S; Nakamura S
    No To Shinkei; 1998 Dec; 50(12):1089-92. PubMed ID: 9989353
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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; 106(6):1101-8. PubMed ID: 10366077
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [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; 22(2):198-200. PubMed ID: 15793785
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 602(1-2):26-33. PubMed ID: 16949108
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 7(2):246-50. PubMed ID: 11257730
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Search for difference in aminoacylation of mitochondrial DNA-encoded wild-type and mutant human tRNALeu (UUR).
    Wang ZC; Wang XM; Jin YX; Jiao BH; Xu F; Miao MY; Zhu KJ
    IUBMB Life; 2003 Mar; 55(3):139-44. PubMed ID: 12822890
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 28.