From Wikipedia, the free encyclopedia
Interphotoreceptor matrix proteoglycan 1 is a protein that in humans is encoded by the IMPG1 gene .[5]
References [ ]
Further reading [ ]
Felbor U, Gehrig A, Sauer CG, et al. (1998). "Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies". Cytogenet. Cell Genet . 81 (1): 12–7. doi :10.1159/000015001 . PMID 9691169 . S2CID 46766267 .
Gehrig A, Felbor U, Kelsell RE, et al. (1998). "Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)" . J. Med. Genet . 35 (8): 641–5. doi :10.1136/jmg.35.8.641 . PMC 1051388 . PMID 9719369 .
Acharya S, Rayborn ME, Hollyfield JG (1998). "Characterization of SPACR, a sialoprotein associated with cones and rods present in the interphotoreceptor matrix of the human retina: immunological and lectin binding analysis" . Glycobiology . 8 (10): 997–1006. doi :10.1093/glycob/8.10.997 . PMID 9719680 .
Acharya S, Rodriguez IR, Moreira EF, et al. (1998). "SPACR, a novel interphotoreceptor matrix glycoprotein in human retina that interacts with hyaluronan" . J. Biol. Chem . 273 (47): 31599–606. doi :10.1074/jbc.273.47.31599 . PMID 9813076 .
Kuehn MH, Hageman GS (2000). "Expression and characterization of the IPM 150 gene (IMPG1) product, a novel human photoreceptor cell-associated chondroitin-sulfate proteoglycan". Matrix Biol . 18 (5): 509–18. doi :10.1016/S0945-053X(99)00043-8 . PMID 10601738 .
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences" . Proc. Natl. Acad. Sci. U.S.A . 99 (26): 16899–903. doi :10.1073/pnas.242603899 . PMC 139241 . PMID 12477932 .
Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6" . Nature . 425 (6960): 805–11. Bibcode :2003Natur.425..805M . doi :10.1038/nature02055 . PMID 14574404 .
van Lith-Verhoeven JJ, Hoyng CB, van den Helm B, et al. (2004). "The benign concentric annular macular dystrophy locus maps to 6p12.3-q16" . Invest. Ophthalmol. Vis. Sci . 45 (1): 30–5. doi :10.1167/iovs.03-0392 . PMID 14691150 .
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)" . Genome Res . 14 (10B): 2121–7. doi :10.1101/gr.2596504 . PMC 528928 . PMID 15489334 .
Abd El-Aziz MM, El-Ashry MF, Barragan I, et al. (2006). "Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus". Curr. Eye Res . 30 (12): 1081–7. doi :10.1080/02713680500351039 . PMID 16354621 . S2CID 26204316 .
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Genes on human chromosome 6 Human chromosome 6 gene stubs