- LIPH
Lipase, member H, also known as LIPH, is a human
gene .cite web | title = Entrez Gene: LIPH lipase, member H| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=200879| accessdate = ]PBB_Summary
section_title =
summary_text = 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.cite web | title = Entrez Gene: LIPH lipase, member H| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=200879| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Sonoda H, Aoki J, Hiramatsu T, "et al." |title=A novel phosphatidic acid-selective phospholipase A1 that produces lysophosphatidic acid. |journal=J. Biol. Chem. |volume=277 |issue= 37 |pages= 34254–63 |year= 2002 |pmid= 12063250 |doi= 10.1074/jbc.M201659200
*cite journal | author=Jin W, Broedl UC, Monajemi H, "et al." |title=Lipase H, a new member of the triglyceride lipase family synthesized by the intestine. |journal=Genomics |volume=80 |issue= 3 |pages= 268–73 |year= 2003 |pmid= 12213196 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Wen XY, Hegele RA, Wang J, "et al." |title=Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans. |journal=Hum. Mol. Genet. |volume=12 |issue= 10 |pages= 1131–43 |year= 2004 |pmid= 12719377 |doi=
*cite journal | author=Hiramatsu T, Sonoda H, Takanezawa Y, "et al." |title=Biochemical and molecular characterization of two phosphatidic acid-selective phospholipase A1s, mPA-PLA1alpha and mPA-PLA1beta. |journal=J. Biol. Chem. |volume=278 |issue= 49 |pages= 49438–47 |year= 2004 |pmid= 12963729 |doi= 10.1074/jbc.M213018200
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Aslam M, Chahrour MH, Razzaq A, "et al." |title=A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3. |journal=J. Med. Genet. |volume=41 |issue= 11 |pages= 849–52 |year= 2005 |pmid= 15520410 |doi= 10.1136/jmg.2004.019729
*cite journal | author=Kazantseva A, Goltsov A, Zinchenko R, "et al." |title=Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH. |journal=Science |volume=314 |issue= 5801 |pages= 982–5 |year= 2006 |pmid= 17095700 |doi= 10.1126/science.1133276
*cite journal | author=Ali G, Chishti MS, Raza SI, "et al." |title=A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis. |journal=Hum. Genet. |volume=121 |issue= 3-4 |pages= 319–25 |year= 2007 |pmid= 17333281 |doi= 10.1007/s00439-007-0344-0PBB_Controls
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