- GLB1
Galactosidase, beta 1, also known as GLB1, is a human
beta-galactosidase .In
corn ("Zea mays "), "Glb1" is a gene coding for the storage proteinglobulin .PBB_Summary
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summary_text =Further reading
PBB_Further_reading
citations =
*cite journal | author=Hinek A |title=Biological roles of the non-integrin elastin/laminin receptor. |journal=Biol. Chem. |volume=377 |issue= 7-8 |pages= 471–80 |year= 1997 |pmid= 8922281 |doi=
*cite journal | author=Kaye EM, Shalish C, Livermore J, "et al." |title=beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosis. |journal=J. Child Neurol. |volume=12 |issue= 4 |pages= 242–7 |year= 1997 |pmid= 9203065 |doi=
*cite journal | author=Callahan JW |title=Molecular basis of GM1 gangliosidosis and Morquio disease, type B. Structure-function studies of lysosomal beta-galactosidase and the non-lysosomal beta-galactosidase-like protein. |journal=Biochim. Biophys. Acta |volume=1455 |issue= 2-3 |pages= 85–103 |year= 1999 |pmid= 10571006 |doi=
*cite journal | author=Shows TB, Scrafford-Wolff L, Brown JA, Meisler M |title=Assignment of a beta-galactosidase gene (beta GALA) to chromosome 3 in man. |journal=Cytogenet. Cell Genet. |volume=22 |issue= 1-6 |pages= 219–22 |year= 1979 |pmid= 110522 |doi=
*cite journal | author=Shows TB, Scrafford-Wolff LR, Brown JA, Meisler MH |title=GM1-gangliosidosis: chromosome 3 assignment of the beta-galactosidase-A gene (beta GALA). |journal=Somatic Cell Genet. |volume=5 |issue= 2 |pages= 147–58 |year= 1979 |pmid= 113895 |doi=
*cite journal | author=Yoshida K, Oshima A, Sakuraba H, "et al." |title=GM1 gangliosidosis in adults: clinical and molecular analysis of 16 Japanese patients. |journal=Ann. Neurol. |volume=31 |issue= 3 |pages= 328–32 |year= 1992 |pmid= 1353343 |doi= 10.1002/ana.410310316
*cite journal | author=Mosna G, Fattore S, Tubiello G, "et al." |title=A homozygous missense arginine to histidine substitution at position 482 of the beta-galactosidase in an Italian infantile GM1-gangliosidosis patient. |journal=Hum. Genet. |volume=90 |issue= 3 |pages= 247–50 |year= 1993 |pmid= 1487238 |doi=
*cite journal | author=Oshima A, Yoshida K, Ishizaki A, "et al." |title=GM1-gangliosidosis: tandem duplication within exon 3 of beta-galactosidase gene in an infantile patient. |journal=Clin. Genet. |volume=41 |issue= 5 |pages= 235–8 |year= 1992 |pmid= 1606711 |doi=
*cite journal | author=Yoshida K, Oshima A, Shimmoto M, "et al." |title=Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases. |journal=Am. J. Hum. Genet. |volume=49 |issue= 2 |pages= 435–42 |year= 1991 |pmid= 1907800 |doi=
*cite journal | author=Nishimoto J, Nanba E, Inui K, "et al." |title=GM1-gangliosidosis (genetic beta-galactosidase deficiency): identification of four mutations in different clinical phenotypes among Japanese patients. |journal=Am. J. Hum. Genet. |volume=49 |issue= 3 |pages= 566–74 |year= 1991 |pmid= 1909089 |doi=
*cite journal | author=Morreau H, Bonten E, Zhou XY, D'Azzo A |title=Organization of the gene encoding human lysosomal beta-galactosidase. |journal=DNA Cell Biol. |volume=10 |issue= 7 |pages= 495–504 |year= 1991 |pmid= 1909871 |doi=
*cite journal | author=Oshima A, Yoshida K, Shimmoto M, "et al." |title=Human beta-galactosidase gene mutations in morquio B disease. |journal=Am. J. Hum. Genet. |volume=49 |issue= 5 |pages= 1091–3 |year= 1991 |pmid= 1928092 |doi=
*cite journal | author=Yamamoto Y, Hake CA, Martin BM, "et al." |title=Isolation, characterization, and mapping of a human acid beta-galactosidase cDNA. |journal=DNA Cell Biol. |volume=9 |issue= 2 |pages= 119–27 |year= 1990 |pmid= 2111707 |doi=
*cite journal | author=Morreau H, Galjart NJ, Gillemans N, "et al." |title=Alternative splicing of beta-galactosidase mRNA generates the classic lysosomal enzyme and a beta-galactosidase-related protein. |journal=J. Biol. Chem. |volume=264 |issue= 34 |pages= 20655–63 |year= 1990 |pmid= 2511208 |doi=
*cite journal | author=Hoogeveen AT, Reuser AJ, Kroos M, Galjaard H |title=GM1-gangliosidosis. Defective recognition site on beta-galactosidase precursor. |journal=J. Biol. Chem. |volume=261 |issue= 13 |pages= 5702–4 |year= 1986 |pmid= 3084469 |doi=
*cite journal | author=Verheijen FW, Palmeri S, Galjaard H |title=Purification and partial characterization of lysosomal neuraminidase from human placenta. |journal=Eur. J. Biochem. |volume=162 |issue= 1 |pages= 63–7 |year= 1987 |pmid= 3102233 |doi=
*cite journal | author=Oshima A, Tsuji A, Nagao Y, "et al." |title=Cloning, sequencing, and expression of cDNA for human beta-galactosidase. |journal=Biochem. Biophys. Res. Commun. |volume=157 |issue= 1 |pages= 238–44 |year= 1988 |pmid= 3143362 |doi=
*cite journal | author=Sips HJ, de Wit-Verbeek HA, de Wit J, "et al." |title=The chromosomal localization of human beta-galactosidase revisited: a locus for beta-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22. |journal=Hum. Genet. |volume=69 |issue= 4 |pages= 340–4 |year= 1985 |pmid= 3921454 |doi=
*cite journal | author=Verheijen FW, Palmeri S, Hoogeveen AT, Galjaard H |title=Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein. |journal=Eur. J. Biochem. |volume=149 |issue= 2 |pages= 315–21 |year= 1985 |pmid= 3922758 |doi=
*cite journal | author=Goldman JE, Katz D, Rapin I, "et al." |title=Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features. |journal=Ann. Neurol. |volume=9 |issue= 5 |pages= 465–75 |year= 1981 |pmid= 6791574 |doi= 10.1002/ana.410090509PBB_Controls
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