Citations for
1CCL18, NFKB1, PITPNM3
CCL18/PITPNM3 enhances migration, invasion, and EMT through the NF-κB signaling pathway in hepatocellular carcinoma.
Lin Z, Li W, Zhang H, Wu W, Peng Y, Zeng Y, Wan Y, Wang J, Ouyang N.
Tumour Biol 37(3):3461-8. doi: 10.1007/s13277-015-4172-x. 2016
2CCL18, PITPNM3, PTK2B
Pyk2 and Src mediate signaling to CCL18-induced breast cancer metastasis.
Li HY, Cui XY, Wu W, Yu FY, Yao HR, Liu Q, Song EW, Chen JQ.
J Cell Biochem 115(3):596-603. doi: 10.1002/jcb.24697. 2014
3PITPNM1, PITPNM2, PITPNM3
Pitpnm1 is expressed in hair cells during development but is not required for hearing.
Carlisle FA, Pearson S, Steel KP, Lewis MA.
Neuroscience 248:620-5. doi: 10.1016/j.neuroscience.2013.06.045. 2013
4CCL18, PITPNM3
The Activity of CCL18 is Principally Mediated through Interaction with Glycosaminoglycans.
Krohn S, Garin A, Gabay C, Proudfoot AE.
Front Immunol 4:193. doi: 10.3389/fimmu.2013.00193. 2013
5CORD5, PITPNM3
Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation.
Reinis A, Golovleva I, Köhn L, Sandgren O.
Acta Ophthalmol 91(3):259-66. doi: 10.1111/j.1755-3768.2011.02381.x. 2013
6CCL18, PITPNM3
CCL18 from tumor-associated macrophages promotes breast cancer metastasis via PITPNM3.
Chen J, Yao Y, Gong C, Yu F, Su S, Chen J, Liu B, Deng H, Wang F, Lin L, Yao H, Su F, Anderson KS, Liu Q, Ewen ME, Yao X, Song E.
Cancer Cell 19(4):541-55. doi: 10.1016/j.ccr.2011.02.006. Erratum in: Cancer Cell. 2011 Jun 14;19(6):814-6. 2011
7PITPNM3
PITPNM3 is an uncommon cause of cone and cone-rod dystrophies.
Köhn L, Kohl S, Bowne SJ, Sullivan LS, Kellner U, Daiger SP, Sandgren O, Golovleva I.
Ophthalmic Genet 31(3):139-40. doi: 10.3109/13816810.2010.486776. 2010
8CORD5,PITPNM3
Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.
Kohn L, Kadzhaev K, Burstedt MS, Haraldsson S, Hallberg B, Sandgren O, Golovleva I.
Eur J Hum Genet 15(6):664-71. Epub 2007 Mar 21. 2007
9PITPNM1, PITPNM2, PITPNM3
Chromosomal localization, genomic organization and evolution of the genes encoding human phosphatidylinositol transfer protein membrane-associated (PITPNM) 1, 2 and 3.
Ocaka L, Spalluto C, Wilson DI, Hunt DM, Halford S.
Cytogenet Genome Res 108(4):293-302. 2005
10PITPNM3
Cellular and developmental distribution of human homologues of the Drosophilia rdgB protein in the rat retina.
Tian D, Lev S.
Invest Ophthalmol Vis Sci 43(6):1946-53. 2002
11PITPNM1, PITPNM2, PITPNM3
Identification of a novel family of targets of PYK2 related to Drosophila retinal degeneration B (rdgB) protein.
Lev S, Hernandez J, Martinez R, Chen A, Plowman G, Schlessinger J.
Mol Cell Biol 19(3):2278-88. 1999