IMPG1


IMPG1

Interphotoreceptor matrix proteoglycan 1, also known as IMPG1, is a human gene.cite web | title = Entrez Gene: IMPG1 interphotoreceptor matrix proteoglycan 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3617| accessdate = ]

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References

Further reading

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*cite journal | author=Felbor U, Gehrig A, Sauer CG, "et al." |title=Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies. |journal=Cytogenet. Cell Genet. |volume=81 |issue= 1 |pages= 12–7 |year= 1998 |pmid= 9691169 |doi=
*cite journal | author=Gehrig A, Felbor U, Kelsell RE, "et al." |title=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). |journal=J. Med. Genet. |volume=35 |issue= 8 |pages= 641–5 |year= 1998 |pmid= 9719369 |doi=
*cite journal | author=Acharya S, Rayborn ME, Hollyfield JG |title=Characterization of SPACR, a sialoprotein associated with cones and rods present in the interphotoreceptor matrix of the human retina: immunological and lectin binding analysis. |journal=Glycobiology |volume=8 |issue= 10 |pages= 997–1006 |year= 1998 |pmid= 9719680 |doi=
*cite journal | author=Acharya S, Rodriguez IR, Moreira EF, "et al." |title=SPACR, a novel interphotoreceptor matrix glycoprotein in human retina that interacts with hyaluronan. |journal=J. Biol. Chem. |volume=273 |issue= 47 |pages= 31599–606 |year= 1998 |pmid= 9813076 |doi=
*cite journal | author=Kuehn MH, Hageman GS |title=Expression and characterization of the IPM 150 gene (IMPG1) product, a novel human photoreceptor cell-associated chondroitin-sulfate proteoglycan. |journal=Matrix Biol. |volume=18 |issue= 5 |pages= 509–18 |year= 2000 |pmid= 10601738 |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=Mungall AJ, Palmer SA, Sims SK, "et al." |title=The DNA sequence and analysis of human chromosome 6. |journal=Nature |volume=425 |issue= 6960 |pages= 805–11 |year= 2003 |pmid= 14574404 |doi= 10.1038/nature02055
*cite journal | author=van Lith-Verhoeven JJ, Hoyng CB, van den Helm B, "et al." |title=The benign concentric annular macular dystrophy locus maps to 6p12.3-q16. |journal=Invest. Ophthalmol. Vis. Sci. |volume=45 |issue= 1 |pages= 30–5 |year= 2004 |pmid= 14691150 |doi=
*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=Abd El-Aziz MM, El-Ashry MF, Barragan I, "et al." |title=Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus. |journal=Curr. Eye Res. |volume=30 |issue= 12 |pages= 1081–7 |year= 2006 |pmid= 16354621 |doi= 10.1080/02713680500351039

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