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TYR gene

Known as: TYROSINASE, TYR, OCAIA 
This gene is involved in sensory transduction and the biosynthesis of melanin.
National Institutes of Health

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Catechol OxidaseMONOPHENOL MONOOXYGENASEMelanogenesisOculocutaneous albinism type 1

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Caracterización molecular en individuos colombianos con albinismo Oculocutáneo (OCA)
El albinismo oculocutaneo (OCA, por sus siglas en ingles) es un grupo de desordenes hereditarios autosomicos recesivos que… 
2014
2014
A comprehensive study of oculocutaneous albinism type 1 reveals three previously unidentified alleles on the TYR gene
BackgroundOculocutaneous albinism (OCA) is a congenital genetic disorder characterized by defects in melanin production. OCA type… 
2013
2013
Table 1. [Summary of Molecular Genetic Testing Used in OCA1].
2011
2011
Phylogenetic and genetic linkage between novel atypical dual-specificity phosphatases from non-metazoan organisms
Dual-specificity phosphatases (DSPs) constitute a large protein tyrosine phosphatase (PTP) family, with examples in distant… 
2011
2011
A novel missense mutation of the TYR gene in a pedigree with oculocutaneous albinism type 1 from China.
BACKGROUND The mutation of the tyrosinase (TYR) gene results in oculocutaneous albinism type 1 (OCA1), an autosomal recessive… 
2011
2011
THE EFFECT OF CAABIS SATIVA LEAVES AQUEOUS AD ALCOHOLIC EXTRACTS OCA1 EUROAL DESITY IRATS
2010
2010
Systems Biology of Saccharomyces cerevisiae Physiology and its DNA Damage Response
The yeast Saccharomyces cerevisiae is a model organism in biology, being widely used in fundamental research, the first… 
2010
2010
Genetic Analysis of Oculocutaneous Albinism Type1A (OCA1A) in an Iranian Family
Background: Oculocutaneous albinism type1 (OCA1) is characterized by the absence of melanin pigmentation. The mutation on TYR… 
2006
2006
Is autosomal recessive deafness associated with oculocutaneous albinism a “coincidence syndrome”?
AbstractHearing impairment is frequently found associated with pigmentary disorders in many syndromes. However, total… 
2004
2004
Genetic analysis of oculocutaneous albinism type 1 (OCA1) in Indian families: two novel frameshift mutations in the TYR Gene.
PURPOSE Oculocutaneous albinism type 1 (OCA1) patients demonstrate a partial or total lack of melanin in the skin, hair and eye… 
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