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 *

121 related articles for article (PubMed ID: 21491618)

  • 41. Molecular bases of tyrosinase-negative oculocutaneous albinism: a single base insertion or a missense point mutation in the tyrosinase gene.
    Tomita Y; Takeda A; Matsunaga J; Okinaga S; Shibahara S; Tagami H
    Pigment Cell Res; 1992; Suppl 2():96-100. PubMed ID: 1409445
    [TBL] [Abstract][Full Text] [Related]  

  • 42. P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome.
    Garrison NA; Yi Z; Cohen-Barak O; Huizing M; Hartnell LM; Gahl WA; Brilliant MH
    J Med Genet; 2004 Jun; 41(6):e86. PubMed ID: 15173252
    [No Abstract]   [Full Text] [Related]  

  • 43. Molecular basis of albinism in the rhesus monkey.
    Ding B; Ryder OA; Wang X; Bai SC; Zhou SQ; Zhang Y
    Mutat Res; 2000 Apr; 449(1-2):1-6. PubMed ID: 10751629
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1).
    Oetting WS; King RA
    Pigment Cell Res; 1994 Oct; 7(5):285-90. PubMed ID: 7886000
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Molecular basis of type IA (tyrosinase negative) oculocutaneous albinism.
    King RA; Oetting WS
    Pigment Cell Res; 1992; Suppl 2():249-53. PubMed ID: 1409426
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [An overview of oculocutaneous albinism: TYR gene mutations in five Colombian individuals].
    Sanabria D; Groot H; Guzmán J; Lattig MC
    Biomedica; 2012 Jun; 32(2):269-76. PubMed ID: 23242301
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism.
    King RA; Mentink MM; Oetting WS
    Mol Biol Med; 1991 Feb; 8(1):19-29. PubMed ID: 1943686
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Identification of a Homozygous Missense Mutation in the TYR Gene in a Chinese Family with OCA1.
    Wang Y; Zhou YF; Shen N; Zhu YW; Tan K; Wang X
    Curr Med Sci; 2018 Oct; 38(5):932-936. PubMed ID: 30341532
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
    Ray K; Chaki M; Sengupta M
    Hum Genet; 2007 Dec; 122(5):556. PubMed ID: 18383611
    [No Abstract]   [Full Text] [Related]  

  • 50. Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
    Ray K; Chaki M; Sengupta M
    Hum Genet; 2007 Dec; 122(5):556. PubMed ID: 18383610
    [No Abstract]   [Full Text] [Related]  

  • 51. Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.
    Ray K; Chaki M; Sengupta M
    Hum Genet; 2007 Dec; 122(5):555. PubMed ID: 18383609
    [No Abstract]   [Full Text] [Related]  

  • 52. Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism.
    Lee ST; Nicholls RD; Bundey S; Laxova R; Musarella M; Spritz RA
    N Engl J Med; 1994 Feb; 330(8):529-34. PubMed ID: 8302318
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Single-strand conformation polymorphism analysis of point mutation in a tyrosinase-negative oculocutaneous albinism.
    Park KC; Kim KH; Lee YS; Kwon BS
    J Inherit Metab Dis; 1994; 17(1):123-6. PubMed ID: 8051921
    [No Abstract]   [Full Text] [Related]  

  • 54. Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism.
    Oetting WS; King RA
    Hum Genet; 1992 Nov; 90(3):258-62. PubMed ID: 1487241
    [TBL] [Abstract][Full Text] [Related]  

  • 55. One-allele system in the Korean for MboI-RFLP in exon 1 of the human tyrosinase (TYR) gene.
    Kim DK; Kang KH; Choi IJ
    J Dermatol Sci; 2000 Sep; 24(1):1-3. PubMed ID: 10960773
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Cloning and sequence analysis of the tyrosinase gene from a patient with tyrosinase-positive oculocutaneous albinism.
    Matsunaga J; Takeda A; Tomita Y; Hara M; Shibahara S; Tagami H
    J Dermatol Sci; 1992 May; 3(3):181-5. PubMed ID: 1498098
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Tyrosinase gene mutations causing oculocutaneous albinisms.
    Tomita Y
    J Invest Dermatol; 1993 Feb; 100(2 Suppl):186S-190S. PubMed ID: 8433007
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [New nonsense mutation (p.E250X) in the tyrosinase gene of a patient with oculocutaneous albinism type 1A].
    Aquaron R; Hesse S; Badens C; Bonerandi JJ
    Ann Dermatol Venereol; 2009 Jan; 136(1):57-9. PubMed ID: 19171234
    [No Abstract]   [Full Text] [Related]  

  • 59. Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism.
    Forshew T; Khaliq S; Tee L; Smith U; Johnson CA; Mehdi SQ; Maher ER
    Clin Genet; 2005 Aug; 68(2):182-4. PubMed ID: 15996218
    [No Abstract]   [Full Text] [Related]  

  • 60. Mutations of the tyrosinase gene in three Korean patients with type I oculocutaneous albinism.
    Park KC; Park SK; Lee YS; Youn SW; Park BS; Kim KH; Lee ST
    Jpn J Hum Genet; 1996 Sep; 41(3):299-305. PubMed ID: 8996965
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.