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LIPH encodes a membrane-bound member of the mammalian triglyceride lipase family. Additionally we are shipping LIPH Kits (32) and LIPH Antibodies (32) and many more products for this protein.
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We finally isolate control and Enpp2 (show ENPP2 Proteins)-null dermal pipilla precursors and identify the expression and upregulation of LIPH, an alternative LPA-producing enzyme, suggesting that this gene could functionally compensate for the absence of Enpp2 (show ENPP2 Proteins).
Novel sequence variants in the LIPH (show LIPC Proteins) and LPAR6 (show LPAR6 Proteins) genes underlies autosomal recessive woolly hair/hypotrichosis in three consanguineous Pakistani families.
The present study shows 93% of Japanese patients with ARWH had at least one of the two founder mutations in exon 6 of LIPH (show LIPC Proteins). Highly prevalent founder mutations in LIPH (show LIPC Proteins).
The authors report no apparent decrease in total hair count but remarkable miniaturization and increased telogen/anagen hair ratio in patients homozygous mutations in LIPH (show LIPC Proteins).
This meta-analysis demonstrates that the T allele in the LIPC (show LIPC Proteins) rs493258 polymorphism was significantly associated with the risk of any and late age related macular degeneration
Our data suggest that LIPH (show LIPC Proteins) may have prognostic value for esophageal cancer.
sequencing LIPH (show LIPC Proteins) identi fi ed a novel non-sense mutation (c.328C>T; p.Arg110*) in one and a previously reported 2-bp deletion mutation (c.659_660delTA, p.Ile220ArgfsX29) in three other families.
A heterozygous missense mutation c.736T>A (p.Cys246Ser) in exon 6 of the LIPH (show LIPC Proteins) gene of both the affected individuals was identified. In addition, we also found that both patients carried heterozygous sequences in exon 5 of the LIPH (show LIPC Proteins) gene.
The study further extends the body of evidence that sequence variants in the LIPH (show LIPC Proteins) gene result in hypotrichosis and woolly hair phenotype.
High LIPH (show LIPC Proteins) expression is associated with metastasis in breast cancer.
Mutation patterns of LIPH (show LIPC Proteins) might be associated with hypotrichosis severity in autosomal recessive woolly hair/hypotrichosis.
Results show the LIPH mode of action and confirm the crucial role of LIPH in hair production.
association between a deletion of a single nucleotide in LIPH exon and rex phenotype
This gene encodes a membrane-bound member of the mammalian triglyceride lipase family. It catalyzes the production of 2-acyl lysophosphatidic acid (LPA), which is a lipid mediator with diverse biological properties that include platelet aggregation, smooth muscle contraction, and stimulation of cell proliferation and motility.
, lipase member H
, LPD lipase-related protein
, mPA-PLA1 alpha
, membrane-associated phosphatidic acid-selective phospholipase A1-alpha
, membrane-bound phosphatidic acid-selective phospholipase A1
, phospholipase A1 member B
, lacrimal lipase