{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,2]],"date-time":"2022-04-02T08:02:06Z","timestamp":1648886526424},"reference-count":24,"publisher":"Springer Science and Business Media LLC","issue":"10","license":[{"start":{"date-parts":[[1989,10,1]],"date-time":"1989-10-01T00:00:00Z","timestamp":623203200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["In Vitro Cell Dev Biol"],"published-print":{"date-parts":[[1989,10]]},"DOI":"10.1007\/bf02624012","type":"journal-article","created":{"date-parts":[[2007,5,3]],"date-time":"2007-05-03T17:41:38Z","timestamp":1178214098000},"page":"971-976","source":"Crossref","is-referenced-by-count":4,"title":["The ornithine aminotransferase gene in gyrate, atrophy of the retina: Analysis of expression and gross structure of this gene in cultured fibroblasts"],"prefix":"10.1007","volume":"25","author":[{"given":"James D.","family":"Shull","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Henry C.","family":"Pitot","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF02624012_CR1","first-page":"1037","volume":"28","author":"D. J. Barrett","year":"1987","unstructured":"Barrett, D. J.; Bateman, J. B.; Sparkes, R. S., et al. Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2. Invest. Opthal. Vis. Sci. 28:1037\u20131042; 1987.","journal-title":"Invest. Opthal. Vis. Sci."},{"key":"BF02624012_CR2","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1016\/0003-2697(83)90418-9","volume":"132","author":"A. P. Feinberg","year":"1983","unstructured":"Feinberg, A. P.; Vogelstein, B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 132:6\u201313; 1983.","journal-title":"Anal. Biochem."},{"key":"BF02624012_CR3","doi-asserted-by":"crossref","first-page":"1203","DOI":"10.1073\/pnas.83.5.1203","volume":"83","author":"G. Inana","year":"1986","unstructured":"Inana, G.; Totsuka, S.; Redmond, M., et al. Molecular cloning of human ornithine aminotransferase mRNA. Proc. Natl. Acad. Sci. USA 83:1203\u20131207; 1986.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"BF02624012_CR4","first-page":"1001","volume":"29","author":"G. Inana","year":"1988","unstructured":"Inana, G.; Hotta, Y.; Zintz, C., et al. Expression defect of ornithine aminotransferase gene in gyrate atrophy. Invest. Opthal. Vis. Sci. 29:1001\u20131005; 1988.","journal-title":"Invest. Opthal. Vis. Sci."},{"key":"BF02624012_CR5","first-page":"1180","volume":"297","author":"N. G. Kennaway","year":"1977","unstructured":"Kennaway, N. G.; Weleber, R. G.; Buist, N. R. M. Gyrate atrophy of choroid and retina: Deficient activity of ornithine ketoacid aminotransferase in cultured skin fibroblasts. N. Engl. J. Med. 297:1180; 1977.","journal-title":"N. Engl. J. Med."},{"key":"BF02624012_CR6","doi-asserted-by":"crossref","first-page":"4743","DOI":"10.1021\/bi00640a033","volume":"16","author":"H. Lehrach","year":"1977","unstructured":"Lehrach, H.; Diamond, D.; Wozney, J. M., et al. RNA molecular weight determinations by gel electrophoresis under denaturing conditions, a critical reexamination. Biochemistry 16:4743\u20134750; 1977.","journal-title":"Biochemistry"},{"key":"BF02624012_CR7","volume-title":"Molecular Cloning: A Laboratory Manual","author":"T. Maniatis","year":"1982","unstructured":"Maniatis, T.; Fritsch, E. F.; Sambrook, J. Molecular Cloning: A Laboratory Manual. Gold Spring Harbor, New York: Cold Spring Harbor Laboratory; 1982."},{"key":"BF02624012_CR8","doi-asserted-by":"crossref","first-page":"630","DOI":"10.1172\/JCI113365","volume":"81","author":"G. A. Mitchell","year":"1988","unstructured":"Mitchell, G. A.; Brody, L. C.; Looney, J. E., et al. An initiator codon mutationin ornithine-\u03c3-aminotransferase causing gyrate atrophy of the choroid and retina. J. Clin. Invest. 81:630\u2013633; 1988.","journal-title":"J. Clin. Invest."},{"key":"BF02624012_CR9","doi-asserted-by":"crossref","first-page":"14288","DOI":"10.1016\/S0021-9258(18)68219-5","volume":"263","author":"G. A. Mitchell","year":"1988","unstructured":"Mitchell, G. A.; Looney, J. E.; Brody, L. C., et al. Human ornithine-\u03c3-aminotransferase cDNA cloning and analysis of the structural gene. J. Biol. Chem. 263:14288\u201314295; 1988.","journal-title":"J. Biol. Chem."},{"key":"BF02624012_CR10","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1073\/pnas.86.1.197","volume":"86","author":"G. A. Mitchell","year":"1989","unstructured":"Mitchell, G. A.; Brody, L. C.; Sipila, I., et al. At least two mutant alleles of ornithine-\u03c3-aminotransferase cause gyrate atrophy of the choroid and retina in Finns. Proc. Natl. Acad. Sci. USA 86:197\u2013201; 1989.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"BF02624012_CR11","doi-asserted-by":"crossref","first-page":"12993","DOI":"10.1016\/S0021-9258(17)38826-9","volume":"260","author":"M. M. Mueckler","year":"1985","unstructured":"Mueckler, M. M.; Pitot, H. C. Sequence of the precursor to ornithine aminotransferase deduced from a cDNA clone. J. Biol. Chem. 260:12993\u201312997; 1985.","journal-title":"J. Biol. Chem."},{"key":"BF02624012_CR12","doi-asserted-by":"crossref","first-page":"396","DOI":"10.1016\/0006-291X(77)90170-X","volume":"79","author":"J. J. O'Donnell","year":"1977","unstructured":"O'Donnell, J. J.; Sandman, R. P.; Martin, S. R. Deficient Lornithine: 2-oxoacid aminotransferase activity in cultured fibroblasts from a patient with gyrate atrophy of the retina. Biochem. Biophys. Res. Commun. 79:396\u2013399; 1977.","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"BF02624012_CR13","doi-asserted-by":"crossref","first-page":"200","DOI":"10.1126\/science.635581","volume":"200","author":"J. J. O'Donnell","year":"1978","unstructured":"O'Donnell, J. J.; Sandman, R. P.; Martin, S. R. Gyrate atrophy of the retina: Inborn error of L-ornithine: 2-oxoacid aminitransferase. Science 200:200\u2013201; 1978.","journal-title":"Science"},{"key":"BF02624012_CR14","doi-asserted-by":"crossref","first-page":"493","DOI":"10.1089\/dna.1.1986.5.493","volume":"5","author":"V. Ramesh","year":"1986","unstructured":"Ramesh, V.; Shaffer, M. M.; Allaire, J. M., et al. Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase. DNA 5:493\u2013501; 1986.","journal-title":"DNA"},{"key":"BF02624012_CR15","first-page":"365","volume":"42","author":"V. Ramesh","year":"1988","unstructured":"Ramesh, V.; Benoit, L. A.; Crawford, P., et al. The ornithine anminotransferase (OAT) locus: Analysis of RFLPs in gyrate atrophy. Am. J. Hum. Gen. 42:365\u2013372; 1988.","journal-title":"Am. J. Hum. Gen."},{"key":"BF02624012_CR16","doi-asserted-by":"crossref","first-page":"3777","DOI":"10.1073\/pnas.85.11.3777","volume":"85","author":"V. Ramesh","year":"1988","unstructured":"Ramesh, V.; McClatchey, A. I.; Ramesh, N., et al. Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and-nonresponsive forms of gyrate atrophy. Proc. Natl. Acad. Sci. USA 85:3777\u20133780; 1988.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"BF02624012_CR17","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1016\/0022-2836(77)90052-3","volume":"113","author":"P. W. J. Rigby","year":"1977","unstructured":"Rigby, P. W. J.; Dieckman, M.; Rhodes, C., et al. Labeling deoxyribonucleic acid to high specific activity,in vitro by nick translation with DNA polymerase I. J. Mol. Biol. 113:237\u2013242; 1977.","journal-title":"J. Mol. Biol."},{"key":"BF02624012_CR18","doi-asserted-by":"crossref","first-page":"659","DOI":"10.1016\/0092-8674(86)90341-7","volume":"46","author":"G. Shaw","year":"1986","unstructured":"Shaw, G.; Kamen, R. A conserved AU sequence from the 3\u2032 untranslated reion of GM-CSF mRNA mediates selective mRNA degradation. Cell 46:659\u2013667; 1986.","journal-title":"Cell"},{"key":"BF02624012_CR19","first-page":"174","volume":"30","author":"V. E. Shih","year":"1978","unstructured":"Shih, V. E.; Berson, E. L.; Mandell, R., et al. Ornithine ketoacid transaminase deficiency in gyrate atrophy of the choroid and retina. Am. J. Hum. Genet. 30:174\u2013179; 1978.","journal-title":"Am. J. Hum. Genet."},{"key":"BF02624012_CR20","first-page":"1950","volume":"46","author":"J. D. Shull","year":"1987","unstructured":"Shull, J. D.; Pitot, H. C. Structure and expression of ornithine aminotransferase (OAT) gene and related genes in various rat tissues and fibroblasts from humans with gyrate atrophy. Fed. Proc. 46:1950; 1987.","journal-title":"Fed. Proc."},{"key":"BF02624012_CR21","doi-asserted-by":"crossref","first-page":"1031","DOI":"10.1016\/S0140-6736(73)90667-3","volume":"1","author":"O. Simell","year":"1973","unstructured":"Simell, O.; Takki, K. Raised plasma ornithine and gyrate atrophy of the choroid and retina. Lancet 1:1031; 1973.","journal-title":"Lancet"},{"key":"BF02624012_CR22","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1016\/0014-5793(86)81219-4","volume":"199","author":"M. Simmaco","year":"1986","unstructured":"Simmaco, M.; John, R. A.; Barra, D., et al. The primary structure of ornithine aminotransferase. FEBS 199:39\u201342; 1986.","journal-title":"FEBS"},{"key":"BF02624012_CR23","doi-asserted-by":"crossref","first-page":"5159","DOI":"10.1073\/pnas.74.11.5159","volume":"74","author":"D. Valle","year":"1977","unstructured":"Valle, D.; Kaiser-Kupfer, M. I.; Del Valle, L. A. Gyrate atrophy of the choroid and retina: Deficiency of ornithine aminotransferase in transformed lymphocytes. Proc. Natl. Acad. Sci. USA 74:5159\u20135161; 1977.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"BF02624012_CR24","first-page":"219","volume":"18","author":"R. G. Weleber","year":"1982","unstructured":"Weleber, R. G.; Wirtz, M. K.; Kennaway, N. G. Gyrate atrophy of the choroid and retina: Clinical and biochemical heterogeneity and response to vitamin B6. Birth Defects: Original Article Series 18:219\u2013230; 1982.","journal-title":"Birth Defects: Original Article Series"}],"container-title":["In Vitro Cellular & Developmental Biology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02624012.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02624012\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02624012","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,8,13]],"date-time":"2021-08-13T02:58:53Z","timestamp":1628823533000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02624012"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1989,10]]},"references-count":24,"journal-issue":{"issue":"10","published-print":{"date-parts":[[1989,10]]}},"alternative-id":["BF02624012"],"URL":"https:\/\/doi.org\/10.1007\/bf02624012","relation":{},"ISSN":["0883-8364","1475-2689"],"issn-type":[{"value":"0883-8364","type":"print"},{"value":"1475-2689","type":"electronic"}],"subject":[],"published":{"date-parts":[[1989,10]]}}}