139 related articles for article (PubMed ID: 9163730)
21. Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism (OCA1). Mutations in brief no. 204. Online.
Oetting WS; Fryer JP; King RA
Hum Mutat; 1998; 12(6):433-4. PubMed ID: 10671066
[TBL] [Abstract][Full Text] [Related]
22. Tyrosinase gene mutations in type I (tyrosinase-deficient) oculocutaneous albinism define two clusters of missense substitutions.
Tripathi RK; Strunk KM; Giebel LB; Weleber RG; Spritz RA
Am J Med Genet; 1992 Jul; 43(5):865-71. PubMed ID: 1642278
[TBL] [Abstract][Full Text] [Related]
23. Sequence analysis of tyrosinase gene in ocular and oculocutaneous albinism patients: introducing three novel mutations.
Khordadpoor-Deilamani F; Akbari MT; Karimipoor M; Javadi G
Mol Vis; 2015; 21():730-5. PubMed ID: 26167114
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Mutations of the tyrosinase gene in oculocutaneous albinism.
Shibahara S
Pigment Cell Res; 1992 Nov; 5(5 Pt 2):279-83. PubMed ID: 1292010
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. [Early prenatal genetic diagnosis of oculocutaneous albinism type I in seven families].
Wu Q; Shi HR; Liu N; Lu N; Jiang M; Zhao ZH; Kong XD
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):377-81. PubMed ID: 22875490
[TBL] [Abstract][Full Text] [Related]
28. OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene.
Chaki M; Sengupta M; Mukhopadhyay A; Subba Rao I; Majumder PP; Das M; Samanta S; Ray K
Ann Hum Genet; 2006 Sep; 70(Pt 5):623-30. PubMed ID: 16907708
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene.
Oetting WS; King RA
Hum Mutat; 1993; 2(1):1-6. PubMed ID: 8477259
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinism.
Oetting WS; Mentink MM; Summers CG; Lewis RA; White JG; King RA
Am J Hum Genet; 1991 Jul; 49(1):199-206. PubMed ID: 1905879
[TBL] [Abstract][Full Text] [Related]
33. Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase gene.
Chaki M; Mukhopadhyay A; Chatterjee S; Das M; Samanta S; Ray K
Mol Vis; 2005 Jul; 11():531-4. PubMed ID: 16056219
[TBL] [Abstract][Full Text] [Related]
34. A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinism.
Giebel LB; Musarella MA; Spritz RA
J Med Genet; 1991 Jul; 28(7):464-7. PubMed ID: 1832718
[TBL] [Abstract][Full Text] [Related]
35. Diverse mutations of the P gene among African-Americans with type II (tyrosinase-positive) oculocutaneous albinism (OCA2).
Lee ST; Nicholls RD; Schnur RE; Guida LC; Lu-Kuo J; Spinner NB; Zackai EH; Spritz RA
Hum Mol Genet; 1994 Nov; 3(11):2047-51. PubMed ID: 7874125
[TBL] [Abstract][Full Text] [Related]
36. Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism.
Spritz RA; Strunk KM; Hsieh CL; Sekhon GS; Francke U
Am J Hum Genet; 1991 Feb; 48(2):318-24. PubMed ID: 1899321
[TBL] [Abstract][Full Text] [Related]
37. Mutational Analysis of TYR, OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism.
Lin Y; Chen X; Yang Y; Che F; Zhang S; Yuan L; Wu Y
Mol Genet Genomic Med; 2019 Jul; 7(7):e00687. PubMed ID: 31199599
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Genetic analysis of oculocutaneous albinism type 1 (OCA1) in Indian families: two novel frameshift mutations in the TYR Gene.
Sundaresan P; Sil AK; Philp AR; Randolph MA; Natchiar G; Namperumalsamy P
Mol Vis; 2004 Dec; 10():1005-10. PubMed ID: 15635296
[TBL] [Abstract][Full Text] [Related]
40. Molecular basis of tyrosinase-negative oculocutaneous albinism. A single base mutation in the tyrosinase gene causing arginine to glutamine substitution at position 59.
Takeda A; Tomita Y; Matsunaga J; Tagami H; Shibahara S
J Biol Chem; 1990 Oct; 265(29):17792-7. PubMed ID: 2120217
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
