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 *

113 related articles for article (PubMed ID: 10331707)

  • 41. Unpleasant alcohol effect in diabetes associated with 3243 bp mitochondrial tRNALeu(UUR) mutation.
    Suzuki Y; Atsumi Y; Hosokawa K; Taniyama M; Kadowaki T; Oka Y; Tanaka Y; Asahina T; Matsuoka K
    Diabetes Care; 1995 Jun; 18(6):880-1. PubMed ID: 7555519
    [No Abstract]   [Full Text] [Related]  

  • 42. A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy.
    Fu K; Hartlen R; Johns T; Genge A; Karpati G; Shoubridge EA
    Hum Mol Genet; 1996 Nov; 5(11):1835-40. PubMed ID: 8923013
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Cardiomyopathies and mitochondrial DNA mutations.
    Takeda N
    Mol Cell Biochem; 1997 Nov; 176(1-2):287-90. PubMed ID: 9406174
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [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]  

  • 45. Study of systemic lupus erythematosus in temporal bones.
    Sone M; Schachern PA; Paparella MM; Morizono N
    Ann Otol Rhinol Laryngol; 1999 Apr; 108(4):338-44. PubMed ID: 10214779
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Stria vascularis and cochlear hair cell changes in syphilis: A human temporal bone study.
    Hızlı Ö; Kaya S; Hızlı P; Paparella MM; Cureoglu S
    Auris Nasus Larynx; 2016 Dec; 43(6):614-9. PubMed ID: 26860231
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Histopathological observations of presbycusis.
    Suga F; Lindsay JR
    Ann Otol Rhinol Laryngol; 1976; 85(2 pt.1):169-84. PubMed ID: 1267323
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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; 113(2):111-6. PubMed ID: 11775531
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [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; 112(3):99-101. PubMed ID: 10074618
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Diabetes mellitus with mitochondrial DNA tRNA(Leu)(UUR) mutation at 3264(T-->C)].
    Suzuki Y; Suzuki S
    Nihon Rinsho; 1998 Jan; 56 Suppl 3():534-8. PubMed ID: 9513475
    [No Abstract]   [Full Text] [Related]  

  • 51. Cochlear degeneration in leigh disease: histopathologic features.
    Ulualp SO; Wright CG; Pawlowski K; Roland PS
    Laryngoscope; 2004 Dec; 114(12):2239-42. PubMed ID: 15564853
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Endolymphatic deafness: a particular variety of cochlear disorder.
    Tran BH
    ORL J Otorhinolaryngol Relat Spec; 2002; 64(2):120-4. PubMed ID: 12021503
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Age-related histopathologic changes in the human cochlea: a temporal bone study.
    Kusunoki T; Cureoglu S; Schachern PA; Baba K; Kariya S; Paparella MM
    Otolaryngol Head Neck Surg; 2004 Dec; 131(6):897-903. PubMed ID: 15577787
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.
    Nagata H; Kumahara K; Tomemori T; Arimoto Y; Isoyama K; Yoshida K; Konno A
    J Hum Genet; 2001; 46(10):595-9. PubMed ID: 11587074
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA(Leu)(UUR) 3254C-to-G.
    Kawarai T; Kawakami H; Kozuka K; Izumi Y; Matsuyama Z; Watanabe C; Kohriyama T; Nakamura S
    Neurology; 1997 Aug; 49(2):598-600. PubMed ID: 9270605
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Quantitative cellular level analysis of mitochondrial DNA 3243A > G mutations in individual tissues from the archival temporal bones of a MELAS patient.
    Koda H; Kimura Y; Ishige I; Eishi Y; Iino Y; Kitamura K
    Acta Otolaryngol; 2010 Mar; 130(3):344-50. PubMed ID: 19685357
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Audiological findings of sensorineural deafness associated with a mutation in the mitochondrial DNA.
    Sawada S; Takeda T; Kakigi A; Saito H; Suehiro T; Nakauchi Y; Chikamori K
    Am J Otol; 1997 May; 18(3):332-5. PubMed ID: 9149827
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
    Iwasaki N; Babazono T; Tsuchiya K; Tomonaga O; Suzuki A; Togashi M; Ujihara N; Sakka Y; Yokokawa H; Ogata M; Nihei H; Iwamoto Y
    J Hum Genet; 2001; 46(6):330-4. PubMed ID: 11393536
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Otopathology in Mohr-Tranebjaerg syndrome.
    Bahmad F; Merchant SN; Nadol JB; Tranebjaerg L
    Laryngoscope; 2007 Jul; 117(7):1202-8. PubMed ID: 17471106
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.