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LPAR6 gene

Known as: P2Y5, LYSOPHOSPHATIDIC ACID RECEPTOR 6, LPAR6 
National Institutes of Health

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Related topics

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P2RY12 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Relative expression and regulation by short-term fasting of lysophosphatidic acid receptors and autotaxin in white and brown adipose tissue depots.
Lysophosphatidic acid (lysoPtdOH) levels have previously been reported to decrease in rodents with short-term fasting. We… 
2018
2018
Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families
Autosomal‐recessive woolly hair/hypotrichosis (ARWH/H) is a rare genetic disorder of hair caused by variants in the LIPH and… 
2015
2015
The effect of cyclic phosphatidic acid on the proliferation and differentiation of mouse cerebellar granule precursor cells during cerebellar development
2014
2014
Lysophosphatidic acid and sphingosine 1-phosphate metabolic pathways and their receptors are differentially regulated during decidualization of human endometrial stromal cells.
In the luteal phase, human endometrial stromal cells (HESCs) undergo proliferation, migration and differentiation during the… 
2014
2014
In Silico Analysis of Missense Mutations in LPAR6 Reveals Abnormal Phospholipid Signaling Pathway Leading to Hypotrichosis
Autosomal recessive hypotrichosis is a rare genetic irreversible hair loss disorder characterized by sparse scalp hair, sparse to… 
2013
2013
A novel mutation, c.699C>G (p.C233W), in the LIPH gene leads to a loss of the hydrolytic activity and the LPA6 activation ability of PA-PLA1α in autosomal recessive wooly hair/hypotrichosis.
2012
2012
Identification of an Alu‐mediated 12.2‐kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hair
Hypotrichosis is a rare form of progressive hair loss characterized by sparse and occasionally woolly hair that is curly and… 
2011
2011
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan
Background.  Autosomal recessive hypotrichosis/woolly hair is a rare genetic hair loss disorder characterized by sparse scalp… 
2008
2008
Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation.
2006
2006
Common variants in RB1 gene and risk of invasive ovarian cancer.
Somatic alteration of the RB1 gene is common in several types of cancer, and germ-line variants are implicated in others. We have… 
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