Citations for
1HACD1, HACD2, HACD3, HACD4
The 3-hydroxyacyl-CoA dehydratases HACD1 and HACD2 exhibit functional redundancy and are active in a wide range of fatty acid elongation pathways.
Sawai M, Uchida Y, Ohno Y, Miyamoto M, Nishioka C, Itohara S, Sassa T, Kihara A.
J Biol Chem 292(37):15538-15551. doi: 10.1074/jbc.M117.803171. Epub 2017 Aug 7. 2017
2CNM7, HACD1
Progressive Structural Defects in Canine Centronuclear Myopathy Indicate a Role for HACD1 in Maintaining Skeletal Muscle Membrane Systems.
Walmsley GL, Blot S, Venner K, Sewry C, Laporte J, Blondelle J, Barthélémy I, Maurer M, Blanchard-Gutton N, Pilot-Storck F, Tiret L, Piercy RJ.
Am J Pathol 187(2):441-456. doi: 10.1016/j.ajpath.2016.10.002. Epub 2016 Dec 8. 2017
3CNM7, HACD1
HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth.
Blondelle J, Ohno Y, Gache V, Guyot S, Storck S, Blanchard-Gutton N, Barthélémy I, Walmsley G, Rahier A, Gadin S, Maurer M, Guillaud L, Prola A, Ferry A, Aubin-Houzelstein G, Demarquoy J, Relaix F, Piercy RJ, Blot S, Kihara A, Tiret L, Pilot-Storck F.
J Mol Cell Biol 7(5):429-40. doi: 10.1093/jmcb/mjv049. Epub 2015 Jul 9. 2015
4HACD1
Human recombinant cementum attachment protein (hrPTPLa/CAP) promotes hydroxyapatite crystal formation in vitro and bone healing in vivo.
Montoya G, Arenas J, Romo E, Zeichner-David M, Alvarez M, Narayanan AS, Velázquez U, Mercado G, Arzate H.
Bone 69:154-64. doi: 10.1016/j.bone.2014.09.014. Epub 2014 Sep 28. 2014
5CNM7, HACD1
Congenital myopathy is caused by mutation of HACD1.
Muhammad E, Reish O, Ohno Y, Scheetz T, Deluca A, Searby C, Regev M, Benyamini L, Fellig Y, Kihara A, Sheffield VC, Parvari R.
Hum Mol Genet 22(25):5229-36. doi: 10.1093/hmg/ddt380. Epub 2013 Aug 9. 2013
6HACD1
Protein tyrosine phosphatase-like A regulates myoblast proliferation and differentiation through MyoG and the cell cycling signaling pathway.
Lin X, Yang X, Li Q, Ma Y, Cui S, He D, Lin X, Schwartz RJ, Chang J.
Mol Cell Biol 32(2):297-308. doi: 10.1128/MCB.05484-11. Epub 2011 Nov 21. Erratum in: Mol Cell Biol. 2017 Jul 28;37(16):. 2012
7HACD1
Isolation of protein-tyrosine phosphatase-like member-a variant from cementum.
Valdés De Hoyos A, Hoz-Rodríguez L, Arzate H, Narayanan AS.
J Dent Res 91(2):203-9. doi: 10.1177/0022034511428155. Epub 2011 Nov 7. 2012
8HACD1, HACD2, HACD3, HACD4
Characterization of four mammalian 3-hydroxyacyl-CoA dehydratases involved in very long-chain fatty acid synthesis.
Ikeda M, Kanao Y, Yamanaka M, Sakuraba H, Mizutani Y, Igarashi Y, Kihara A.
FEBS Lett 582(16):2435-40. doi: 10.1016/j.febslet.2008.06.007. Epub 2008 Jun 11. 2008
9HACD1
SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs.
Pele M, Tiret L, Kessler JL, Blot S, Panthier JJ.
Hum Mol Genet 14(11):1417-27. Epub 2005 Apr 13. 2005
10HACD1
Molecular cloning, chromosomal mapping, and developmental expression of a novel protein tyrosine phosphatase-like gene.
Uwanogho DA, Hardcastle Z, Balogh P, Mirza G, Thornburg KL, Ragoussis J, Sharpe PT.
Genomics 62(3):406-16 1999