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LIPH encodes a membrane-bound member of the mammalian triglyceride lipase family. Additionally we are shipping LIPH Antibodies (16) and LIPH Proteins (7) and many more products for this protein.
Showing 8 out of 13 products:
Human LIPH ELISA Kit for Sandwich ELISA - ABIN817452
Seki, Yoshida, Ishimine, Shinozaki-Ushiku, Ito, Sumitomo, Nakajima, Fukayama, Michiue, Asashima, Kurisaki: Lipase member H is a novel secreted protein selectively upregulated in human lung adenocarcinomas and bronchioloalveolar carcinomas. in Biochemical and biophysical research communications 2014
We finally isolate control and Enpp2 (show ENPP2 ELISA Kits)-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 ELISA Kits).
High LIPH (show LIPC ELISA Kits) expression is associated with metastasis in breast cancer.
Mutation patterns of LIPH (show LIPC ELISA Kits) might be associated with hypotrichosis severity in autosomal recessive woolly hair/hypotrichosis.
Immunohistochemistry detected LIPH (show LIPC ELISA Kits) expression in most of the adenocarcinomas and bronchioloalveolar carcinomas obtained from lung cancer patients. LIPH (show LIPC ELISA Kits) expression was also observed less frequently in the squamous lung cancer tissue samples.
Among South Indian subjects without diabetes, the rs1800588 C/T (C-480T) and rs6074 C/A (Thr479Thr) variants of the HL gene are associated with hypertriglyceridemia and low HDL (show HSD11B1 ELISA Kits)-C, respectively. The TGC (show TGM2 ELISA Kits) haplotype was significantly associated with low HDL (show HSD11B1 ELISA Kits)-C
A case of Japanese siblings with autosomal recessive woolly hair associated with LIPH (show LIPC ELISA Kits) gene homozygous mutation of c.736T > A is presented.
analysis of the LIPH (show LIPC ELISA Kits) gene revealed homozygosity for a novel truncating mutation, as well as three previously identified mutations in affected individuals with autosomal recessive hypotrichosis and woolly hair.
the c.659_660delTA mutation in the LIPH (show LIPC ELISA Kits) gene caused autosomal recessive wooly hair/hypotrichosis phenotype in the studied family.
A phosphatidic acid-phospholipase A1alpha-lysophosphatidic acid-P2Y5 (show LPAR6 ELISA Kits) axis regulates differentiation of hair follicles via a tumour necrosis factor alpha (show TNF ELISA Kits) converting enzyme-transforming growth factor alpha (show TGFA ELISA Kits)-epidermal growth factor receptor (show EGFR ELISA Kits) pathway.
Mutations identified in the present study extend the body of evidence implicating LPAR6 (show LPAR6 ELISA Kits) and LIPH (show LIPC ELISA Kits) genes in pathogenesis of human hereditary hair loss.
The results suggest defective activation of P2Y5 (show LPAR6 ELISA Kits) due to reduced 2-acyl lysophosphatidic acid production by the mutant PA-PLA1a (show PLA1A ELISA Kits) that are encoded by LIPH (show LIPC ELISA Kits) is involved in the pathogenesis of ARH (show LDLRAP1 ELISA Kits).
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