TYRP1 gene

Known as: TYRP, Tyrosinase-Related Protein 1 Gene, OCA3 
This gene plays a role in melanogenesis and sensory transduction/vision.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1980-2018
010203019802018

Papers overview

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2011
2011
Brown coat colour has been described in Chinese-Tibetan, Kele, and Dahe pigs. Here, we report the identification of a causal… (More)
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2009
2009
Temperature-activated transient receptor potential ion channels (thermoTRPs) are polymodal detectors of various stimuli including… (More)
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2007
2007
Identifying the genes that underlie phenotypic variation in natural populations is a central objective of evolutionary genetics… (More)
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2006
2006
Non-syndromic oculocutaneous albinism (OCA) is a clinically and genetically heterogeneous autosomal recessive disorder with… (More)
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Highly Cited
2002
Highly Cited
2002
Rationale. Cognitive impairment is a common feature of depressive illness. While accumulating evidence suggests that brain… (More)
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Highly Cited
2001
Highly Cited
2001
Coat color genetics, when successfully adapted and applied to different mammalian species, provides a good demonstration of the… (More)
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1999
1999
BACKGROUND Rapid and transient depletion of tryptophan (TRP) causes a brief depressive relapse in most patients successfully… (More)
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1998
1998
One aim of current research into talk-in-interaction is to identify the resources that enable recipients to monitor the course of… (More)
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1997
1997
Oculocutaneous albinism (OCA) is the most common autosomal recessive disorder among southern African Blacks. There are three… (More)
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1996
1996
Most types of human oculocutaneous albinism (OCA) result from mutations in the gene for tyrosinase (OCA1) or the P protein (OCA2… (More)
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