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TYRP1 gene
Known as:
TYRP
, Tyrosinase-Related Protein 1 Gene
, OCA3
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This gene plays a role in melanogenesis and sensory transduction/vision.
National Institutes of Health
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Related topics
Related topics
8 relations
ALBINISM, OCULOCUTANEOUS, TYPE III
Melanogenesis
Oxidation-Reduction
Recombinant Tyrosinase-Related Protein-1
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Narrower (1)
TYRP1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigree.
J. Hawkes
,
P. Cassidy
,
+5 authors
S. Leachman
Journal of dermatological science (Amsterdam)
2013
Corpus ID: 3973335
2011
2011
Genome Sequence of Paracoccus sp. Strain TRP, a Chlorpyrifos Biodegrader
Kang Li
,
Shenghui Wang
,
+8 authors
Yanchun Yan
Journal of Bacteriology
2011
Corpus ID: 31214797
ABSTRACT Paracoccus sp. strain TRP, isolated from activated sludge, could completely biodegrade chlorpyrifos and 3,5,6-trichloro…
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2011
2011
Oculocutaneous Albinism Type 3 (OCA3): Analysis of Two Novel Mutations in TYRP1 Gene in Two Chinese Patients
Kai Zhang
,
Zhuo Li
,
+4 authors
Hong-yi Li
Cell Biochemistry and Biophysics
2011
Corpus ID: 207359705
Oculocutaneous albinism (OCA) is a genetic disease characterized by the reduction or deficiency of melanin in eyes, skin, and…
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2006
2006
Is autosomal recessive deafness associated with oculocutaneous albinism a “coincidence syndrome”?
Karina Lezirovitz
,
F. S. Nicastro
,
+5 authors
R. Mingroni-Netto
Journal of Human Genetics
2006
Corpus ID: 220224
AbstractHearing impairment is frequently found associated with pigmentary disorders in many syndromes. However, total…
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Review
2005
Review
2005
Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism
T. Forshew
,
S. Khaliq
,
+4 authors
E. Maher
Clinical Genetics
2005
Corpus ID: 10341700
To the Editor: Four genes have been implicated in non-syndromic oculocutaneous albinism (OCA1–4; MIM 203100, 203200, 203290…
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Highly Cited
2002
Highly Cited
2002
Multiple HLA Class II-Restricted Melanocyte Differentiation Antigens Are Recognized by Tumor-Infiltrating Lymphocytes from a Patient with Melanoma
P. Robbins
,
M. El-Gamil
,
Yong F Li
,
G. Zeng
,
M. Dudley
,
S. Rosenberg
Journal of Immunology
2002
Corpus ID: 13780947
Dramatic clinical responses were observed in patient 888 following the adoptive transfer of autologous tumor-infiltrating…
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2002
2002
DNA sequence variants in the tyrosinase-related protein 1 (TYRP1) gene are not associated with human pigmentary glaucoma.
S. Lynch
,
G. Yanagi
,
E. Delbono
,
J. Wiggs
Molecular Vision
2002
Corpus ID: 40489948
PURPOSE Pigmentary glaucoma is a common form of glaucoma affecting young adults. Previous studies have suggested that multiple…
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Highly Cited
1993
Highly Cited
1993
The mouse brown (b) locus protein has dopachrome tautomerase activity and is located in lysosomes in transfected fibroblasts.
A. Winder
,
A. Wittbjer
,
E. Rosengren
,
H. Rorsman
Journal of Cell Science
1993
Corpus ID: 16327925
Many genes mapping to pigmentation loci are involved in the regulation of melanin synthesis in the mouse. The brown (b) locus…
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1993
1993
Growth Suppression of Normal Mammary Epithelial Cells by Wild‐Type p53
G. Merlo
,
T. Venesio
,
D. Taverna
,
R. Callahan
,
N. Hynes
Annals of the New York Academy of Sciences
1993
Corpus ID: 7596658
We examined the status of the p53 gene in the HC11 normal mammary epithelial cells. Two mutations were identified: a Cys to Trp…
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1992
1992
Assignment of the human TYRP (brown) locus to chromosome region 9p23 by nonradioactive in situ hybridization.
V. Murty
,
B. Bouchard
,
S. Mathew
,
S. Vijayasaradhi
,
A. Houghton
Genomics
1992
Corpus ID: 36394943
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