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 *

133 related articles for article (PubMed ID: 7732778)

  • 1. Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNA.
    Campos Y; Bautista J; Gutiérrez-Rivas E; Chinchón D; Cabello A; Segura D; Arenas J
    Acta Neurol Scand; 1995 Jan; 91(1):62-5. PubMed ID: 7732778
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM; Lemkes HH; Trembath RC; Ross R; Velho G; Cohen D; Froguel P; Maassen JA
    Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
    Campos Y; Martin MA; Lorenzo G; Aparicio M; Cabello A; Arenas J
    Muscle Nerve; 1996 Feb; 19(2):187-90. PubMed ID: 8559168
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P; Lee HC; Pang CY; Jeng CM; Huang SF; Wei YH
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
    Fabrizi GM; Cardaioli E; Grieco GS; Cavallaro T; Malandrini A; Manneschi L; Dotti MT; Federico A; Guazzi G
    J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):47-51. PubMed ID: 8676159
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.
    Remes AM; Majamaa K; Herva R; Hassinen IE
    Neurology; 1993 May; 43(5):1015-20. PubMed ID: 8492919
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Muscle histopathology in diabetes mellitus associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243.
    Suzuki Y; Goto Y; Taniyama M; Nonaka I; Murakami N; Hosokawa K; Asahina T; Atsumi Y; Matsuoka K
    J Neurol Sci; 1997 Jan; 145(1):49-53. PubMed ID: 9073028
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
    Hammans SR; Sweeney MG; Hanna MG; Brockington M; Morgan-Hughes JA; Harding AE
    Brain; 1995 Jun; 118 ( Pt 3)():721-34. PubMed ID: 7600089
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 families.
    Vilarinho L; Santorelli FM; Coelho I; Rodrigues L; Maia M; Barata I; Cabral P; Dionísio A; Costa A; Guimarães A; DiMauro S
    J Neurol Sci; 1999 Mar; 163(2):168-74. PubMed ID: 10371079
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy.
    Hsieh RH; Li JY; Pang CY; Wei YH
    J Biomed Sci; 2001; 8(4):328-35. PubMed ID: 11455195
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
    Suzuki S; Hinokio Y; Hirai S; Onoda M; Matsumoto M; Ohtomo M; Kawasaki H; Satoh Y; Akai H; Abe K
    Diabetologia; 1994 Aug; 37(8):818-25. PubMed ID: 7988784
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene.
    Vialettes B; Paquis-Fluckinger V; Silvestre-Aillaud P; Ben Dahan D; Pelissier JF; Etchary-Bouyx F; Raccah D; Gin H; Guillausseau PJ; Vanuxen D
    Diabetes Care; 1995 Jul; 18(7):1023-8. PubMed ID: 7555536
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: molecular genetic analysis and family study.
    Onishi H; Inoue K; Osaka H; Kimura S; Nagatomo H; Hanihara T; Kawamoto S; Okuda K; Yamada Y; Kosaka K
    J Neurol Sci; 1993 Feb; 114(2):205-8. PubMed ID: 8445402
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription.
    Suomalainen A; Majander A; Pihko H; Peltonen L; Syvänen AC
    Hum Mol Genet; 1993 May; 2(5):525-34. PubMed ID: 8518790
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family.
    Huang CC; Chen RS; Chen CM; Wang HS; Lee CC; Pang CY; Hsu HS; Lee HC; Wei YH
    J Neurol Neurosurg Psychiatry; 1994 May; 57(5):586-9. PubMed ID: 8201329
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autoimmune IDDM in a sporadic MELAS patient with mitochondrial tRNA(Leu(UUR)) mutation.
    Huang CN; Jee SH; Hwang JJ; Kuo YF; Chuang LM
    Clin Endocrinol (Oxf); 1998 Aug; 49(2):265-70. PubMed ID: 9828917
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.
    Katagiri H; Asano T; Ishihara H; Inukai K; Anai M; Yamanouchi T; Tsukuda K; Kikuchi M; Kitaoka H; Ohsawa N
    Diabetologia; 1994 May; 37(5):504-10. PubMed ID: 8056189
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.
    Moraes CT; Ricci E; Bonilla E; DiMauro S; Schon EA
    Am J Hum Genet; 1992 May; 50(5):934-49. PubMed ID: 1315123
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diabetes associated with a novel 3264 mitochondrial tRNA(Leu)(UUR) mutation.
    Suzuki Y; Suzuki S; Hinokio Y; Chiba M; Atsumi Y; Hosokawa K; Shimada A; Asahina T; Matsuoka K
    Diabetes Care; 1997 Jul; 20(7):1138-40. PubMed ID: 9203451
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Sato W; Hayasaka K; Shoji Y; Takahashi T; Takada G; Saito M; Fukawa O; Wachi E
    Biochem Mol Biol Int; 1994 Aug; 33(6):1055-61. PubMed ID: 7804130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.