BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 10331707)

  • 1. Cochlear histopathology associated with mitochondrial transfer RNA(Leu(UUR)) gene mutation.
    Yamasoba T; Tsukuda K; Oka Y; Kobayashi T; Kaga K
    Neurology; 1999 May; 52(8):1705-7. PubMed ID: 10331707
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial diabetes and deafness: possible dysfunction of strial marginal cells of the inner ear.
    Olmos PR; Borzone GR; Olmos JP; Diez A; Santos JL; Serrano V; Cataldo LR; Anabalón JL; Correa CH
    J Otolaryngol Head Neck Surg; 2011 Apr; 40(2):93-103. PubMed ID: 21453644
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region.
    Tsukuda K; Suzuki Y; Kameoka K; Osawa N; Goto Y; Katagiri H; Asano T; Yazaki Y; Oka Y
    Diabet Med; 1997 Dec; 14(12):1032-7. PubMed ID: 9455930
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pathologic Findings of the Cochlea in Labyrinthitis Ossificans Associated with the Round Window Membrane.
    Kaya S; Paparella MM; Cureoglu S
    Otolaryngol Head Neck Surg; 2016 Oct; 155(4):635-40. PubMed ID: 27221575
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Presence of mitochondrial tRNA(Leu(UUR)) A to G 3243 mutation in DNA extracted from serum and plasma of patients with type 2 diabetes mellitus.
    Zhong S; Ng MC; Lo YM; Chan JC; Johnson PJ
    J Clin Pathol; 2000 Jun; 53(6):466-9. PubMed ID: 10911806
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ; Mudde AH; 't Hart LM; Huygen PL; Cremers CW
    Otol Neurotol; 2006 Sep; 27(6):802-8. PubMed ID: 16788417
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Temporal bone histopathological and quantitative analysis of mitochondrial DNA in MELAS.
    Takahashi K; Merchant SN; Miyazawa T; Yamaguchi T; McKenna MJ; Kouda H; Iino Y; Someya T; Tamagawa Y; Takiyama Y; Nakano I; Saito K; Boyer P; Kitamura K
    Laryngoscope; 2003 Aug; 113(8):1362-8. PubMed ID: 12897560
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNA(Leu (UUR))) applied to a Norwegian family with diabetes mellitus and hearing loss.
    Akbari M; Skjelbred C; Følling I; Sagen J; Krokan HE
    Scand J Clin Lab Invest; 2004 Apr; 64(2):86-92. PubMed ID: 15115244
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene.
    Yamasoba T; Oka Y; Tsukuda K; Nakamura M; Kaga K
    Laryngoscope; 1996 Jan; 106(1 Pt 1):49-53. PubMed ID: 8544627
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heteroplasmy level of the mitochondrial tRNaLeu(UUR) A3243G mutation in a Chinese family is positively associated with earlier age-of-onset and increasing severity of diabetes.
    Zhang S; Tong AL; Zhang Y; Nie M; Li YX; Wang H
    Chin Med Sci J; 2009 Mar; 24(1):20-5. PubMed ID: 19382419
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Effects of type 2 diabetes mellitus on cochlear structure in humans.
    Fukushima H; Cureoglu S; Schachern PA; Paparella MM; Harada T; Oktay MF
    Arch Otolaryngol Head Neck Surg; 2006 Sep; 132(9):934-8. PubMed ID: 16982969
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Histopathology of the Human Inner Ear in a Patient With Sensorineural Hearing Loss Caused by a Variant in DFNA5.
    Nadol JB; Handzel O; Amr S
    Otol Neurotol; 2015 Dec; 36(10):1616-21. PubMed ID: 26496673
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hearing loss with a mitochondrial gene mutation is highly prevalent in Japan.
    Oshima T; Ueda N; Ikeda K; Abe K; Takasaka T
    Laryngoscope; 1999 Feb; 109(2 Pt 1):334-8. PubMed ID: 10890789
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial DNA [tRNA(Leu)(UUR)] mutation in a southern Italian diabetic population.
    Rigoli L; Di Benedetto A; Romano G; Corica F; Cucinotta D
    Diabetes Care; 1997 Apr; 20(4):674-5. PubMed ID: 9097002
    [No Abstract]   [Full Text] [Related]  

  • 17. Quantitative Assessment of Cochlear Histopathologic Findings in Patients With Suppurative Labyrinthitis.
    Kaya S; Tsuprun V; Hizli Ö; Paparella MM; Cureoglu S
    JAMA Otolaryngol Head Neck Surg; 2016 Apr; 142(4):364-9. PubMed ID: 26987015
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Temporal bone histopathologic abnormalities associated with mitochondrial mutation T7511C.
    Ishikawa K; Tamagawa Y; Takahashi K; Iino Y; Murakami Y; Kakizaki K; Kimura H; Kusakari J; Hara A; Ichimura K
    Laryngoscope; 2006 Nov; 116(11):1982-6. PubMed ID: 17075421
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cochlear changes in patients with type 1 diabetes mellitus.
    Fukushima H; Cureoglu S; Schachern PA; Kusunoki T; Oktay MF; Fukushima N; Paparella MM; Harada T
    Otolaryngol Head Neck Surg; 2005 Jul; 133(1):100-6. PubMed ID: 16025061
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.
    Jansen JJ; Maassen JA; van der Woude FJ; Lemmink HA; van den Ouweland JM; t' Hart LM; Smeets HJ; Bruijn JA; Lemkes HH
    J Am Soc Nephrol; 1997 Jul; 8(7):1118-24. PubMed ID: 9219161
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.