{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,26]],"date-time":"2025-09-26T22:20:16Z","timestamp":1758925216610},"reference-count":12,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[1984,9,10]],"date-time":"1984-09-10T00:00:00Z","timestamp":463622400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Inher Metab Disea"],"published-print":{"date-parts":[[1985,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Type I glycogen storage disease (McKusick 23220), an inherited absence or deficiency of glucose\u20106\u2010phosphatase (EC 3.1.3.9) activity in the liver, kidney and intestine, is associated with the accumulation of glycogen in those organs. Previous reports have shown that glucose\u20106\u2010phosphatase exists in human placenta and that detection of a heterozygote for this disorder from placenta might be possible. Our finding of a normal glucose\u20106\u2010phosphatase activity in a placenta from a patient at risk for type Ia glycogen storage disease prompted us to examine in more detail placental glucose\u20106\u2010phosphatase. Unexpectedly, we found the properties of the placental enzyme differed from that in normal liver, and the placental enzyme hydrolyzed glucose\u20106\u2010phosphate, mannose\u20106\u2010phosphate, \u03b2\u2010glycerol phosphate and glucose\u20101\u2010phosphate equally well. Our data suggest the enzyme deficient in type I glycogen storage disease cannot be detected in placenta.<\/jats:p>","DOI":"10.1007\/bf01801675","type":"journal-article","created":{"date-parts":[[2005,6,27]],"date-time":"2005-06-27T23:55:39Z","timestamp":1119916539000},"page":"92-94","source":"Crossref","is-referenced-by-count":9,"title":["Liver\u2010specific glucose\u20106\u2010phosphatase is not present in human placenta"],"prefix":"10.1002","volume":"8","author":[{"given":"Y. T.","family":"Chen","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Division of Genetics and Metabolism Duke University Medical Center  Durham NC 27710 USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T.","family":"Kato","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Division of Genetics and Metabolism Duke University Medical Center  Durham NC 27710 USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[1984,9,10]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF01732001"},{"key":"e_1_2_1_3_1","first-page":"186S","article-title":"Prenatal diagnosis of glycogen storage disease","volume":"36","author":"Brown B. I.","year":"1984","journal-title":"Am. J. Human Genet."},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-0528.1967.tb03963.x"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1172\/JCI105230"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/B978-1-4831-6748-0.50006-9"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0021-9258(18)43502-8"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(77)92568-5"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1203\/00006450-197708000-00016"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/0009-8981(74)90096-5"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0021-9258(17)44560-1"},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.1016\/0006-291X(82)90643-X"},{"key":"e_1_2_1_13_1","doi-asserted-by":"publisher","DOI":"10.1002\/9780470110416.ch1"}],"container-title":["Journal of Inherited Metabolic Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/BF01801675","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/BF01801675","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,17]],"date-time":"2023-09-17T01:34:05Z","timestamp":1694914445000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1007\/BF01801675"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1984,9,10]]},"references-count":12,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1985,6]]}},"alternative-id":["10.1007\/BF01801675"],"URL":"https:\/\/doi.org\/10.1007\/bf01801675","archive":["Portico"],"relation":{},"ISSN":["0141-8955","1573-2665"],"issn-type":[{"value":"0141-8955","type":"print"},{"value":"1573-2665","type":"electronic"}],"subject":[],"published":{"date-parts":[[1984,9,10]]}}}