{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,15]],"date-time":"2025-12-15T13:35:27Z","timestamp":1765805727248},"reference-count":22,"publisher":"Springer Science and Business Media LLC","issue":"10","license":[{"start":{"date-parts":[[2001,11,1]],"date-time":"2001-11-01T00:00:00Z","timestamp":1004572800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Endocrinol Invest"],"published-print":{"date-parts":[[2001,11]]},"DOI":"10.1007\/bf03343931","type":"journal-article","created":{"date-parts":[[2014,4,10]],"date-time":"2014-04-10T18:41:05Z","timestamp":1397155265000},"page":"806-810","source":"Crossref","is-referenced-by-count":10,"title":["Multiple endocrine neoplasia type 1Burin from Mauritius: A novel MEN 1 mutation1"],"prefix":"10.1007","volume":"24","author":[{"given":"C.","family":"Kong","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Ellard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Johnston","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nadir R.","family":"Farid","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2014,3,11]]},"reference":[{"key":"BF03343931_CR1","doi-asserted-by":"crossref","first-page":"874","DOI":"10.1016\/S0002-9343(80)80013-1","volume":"69","author":"NR Farid","year":"1980","unstructured":"Farid N.R., Buehler S., Russell N.A., Maroun F.B., Allerdice P., Smith H.S. Prolactinomas in familial multiple endocrine neoplasia syndrome type 1. Am. J. Med. 1980, 69: 874\u2013880.","journal-title":"Am. J. Med."},{"key":"BF03343931_CR2","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1159\/000153508","volume":"35","author":"JC Bear","year":"1985","unstructured":"Bear J.C., Briones-Urbina R., Fahey J.F., Farid N.R. Variant multiple endocrine neoplasia type I (MEN IBurin): further studies and non-linkage to HLA. Hum. Hered. 1985, 35: 15\u201320.","journal-title":"Hum. Hered."},{"key":"BF03343931_CR3","volume-title":"Memorial University of Newfoundland","author":"JS Green","year":"1995","unstructured":"Green J.S. Development, implementation and evaluation of clinical and genetic programs for hereditary tumor syndromes, Ph.D. thesis. Memorial University of Newfoundland, St John\u2019s, Newfoundland, Canada, 1995."},{"key":"BF03343931_CR4","first-page":"1060","volume":"54","author":"EM Petty","year":"1994","unstructured":"Petty E.M., Green J.S., Marx S.J., Taggart R.T., Farid N., Bale A.E. Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: Evidence for a founder effect in patients from Newfoundland. Am. J. Hum. Genet. 1994, 54: 1060\u20131066.","journal-title":"Am. J. Hum. Genet."},{"key":"BF03343931_CR5","doi-asserted-by":"crossref","first-page":"713","DOI":"10.1016\/0002-9343(83)91032-X","volume":"74","author":"KS Hershon","year":"1983","unstructured":"Hershon K.S., Kelly W.A., Shaw C.M., Schwartz R., Bierman E.L. Prolactinomas as part of the multiple endocrine neo-plastic syndrome type 1. Am. J. Med. 1983, 74: 713\u2013720.","journal-title":"Am. J. Med."},{"key":"BF03343931_CR6","doi-asserted-by":"crossref","first-page":"404","DOI":"10.1126\/science.276.5311.404","volume":"276","author":"SC Chandrasekharappa","year":"1997","unstructured":"Chandrasekharappa S.C., Guru S.C., Manickam P., Olufemi S.E., Collins F.S., Emmert-Buck M.R., Debelenko L.V., Zhuang Z., Lubensky I.A., Liotta, L.A., Crabtree J.S., Wang Y., Roe B.A., Weisemann J., Boguski M.S., Agarwal S.K., Kester M.B., Kim Y.S., Heppner C., Dong Q., Spiegel A.M., Burns A.L., Marx S.J. Positional cloning of the gene for multiple endocrine neoplasia type 1. Science 1997, 276: 404\u2013407.","journal-title":"Science"},{"key":"BF03343931_CR7","doi-asserted-by":"crossref","first-page":"1177","DOI":"10.1093\/hmg\/6.7.1177","volume":"6","author":"The European Consortium on MEN 1.","year":"1997","unstructured":"The European Consortium on MEN 1. Identification of the multiple endocrine neoplasia type 1 (MEN 1) gene. Hum. Mol. Genet. 1997, 6: 1177\u20131183.","journal-title":"Hum. Mol. Genet."},{"key":"BF03343931_CR8","doi-asserted-by":"crossref","first-page":"1169","DOI":"10.1093\/hmg\/6.7.1169","volume":"6","author":"SK Agarwal","year":"1997","unstructured":"Agarwal S.K., Kester M.B., Debelenko L.V., Heppner C., Emmert-Buck M.R., Skarulis M.C., Doppman J.L., Kim Y.S., Lubensky I.A., Zhaung Z., Green J.S., Guru S.C., Manickam P., Olufemi S.E., Liotta L.A., Chandrasekharappa S.C., Collins F.S., Burns A.L., Marx S.J. Germline mutations of the MEN 1 gene in familial multiple endocrine neoplasia type 1 and related states. Hum. Mol. Genet. 1997, 6: 1169\u20131175.","journal-title":"Hum. Mol. Genet."},{"key":"BF03343931_CR9","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1002\/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V","volume":"11","author":"SE Olufemi","year":"1998","unstructured":"Olufemi S.E., Green J.S., Manickam P., Guru S.C., Argawal S.K., Kester M.B., Dong Q., Burns A.L., Speigel A.M., Marx S.J., Collins F.S., Chandra-sekharappa S.C. Common ancestral mutation in the MEN I gene is likely responsible for the prolactinoma variant of MEN I (MEN IBurin) in four kindreds from Newfoundland. Hum. Mutat. 1998, 11: 264\u2013269.","journal-title":"Hum. Mutat."},{"key":"BF03343931_CR10","first-page":"397","volume":"54","author":"SJ Marx","year":"1999","unstructured":"Marx S.J., Agarwal S.K., Kester M.B., Heppner C., Kim Y.S., Skarulis M.C., James L.A., Goldsmith P.K., Saggar S.K., Park S.Y., Spiegel A.M., Burns A.L., Debelenko L.V., Zhuang Z., Lubensky I.A., Liotta L.A., Emmert-Buck M.R., Guru S.C., Manickam P., Crabtree J.S., Erdos M.R., Collins F.S., Chanra-sekharappa S.C. Multiple endocrine neoplasia type I: Clinical and genetic features of the hereditary endocrine neoplasia. Recent Prog. Horm. Res. 1999, 54: 397\u2013439.","journal-title":"Horm. Res."},{"key":"BF03343931_CR11","doi-asserted-by":"crossref","first-page":"853","DOI":"10.1001\/archderm.1997.03890430067009","volume":"133","author":"TN Darling","year":"1997","unstructured":"Darling T.N., Skarulis M.C., Steinberg S.M., Marx S.J., Spiegel A.M., Turner M. Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type I. Arch. Dermatol. 1997, 133: 853\u2013857.","journal-title":"Arch. Dermatol."},{"key":"BF03343931_CR12","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1046\/j.1365-2265.1999.00747.x","volume":"51","author":"C Waterlot","year":"1999","unstructured":"Waterlot C., Porchet N., Bauters C., Decoulx M., Wemeau J.L., Proye C., Degrand P.M., Aubert J.P., Cortet C., Dewailly D. Type 1 multiple endocrine neoplasia (MEN1): contribution of genetic screening and follow-up of a large French kindred. Clin. Endocrinol. (Oxf.) 1999, 51: 101\u2013107.","journal-title":"Clin. Endocrinol. (Oxf.)"},{"key":"BF03343931_CR13","doi-asserted-by":"crossref","first-page":"1630","DOI":"10.1073\/pnas.95.4.1630","volume":"95","author":"SC Guru","year":"1998","unstructured":"Guru S.C., Goldsmith P.K., Burns A.L., Marx S.J., Spiegel A.M., Collins F.S., Chandrasekharappa S.C. Menin, the product of the MEN1 gene, is a nuclear protein. Proc. Natl. Acad. Sci. USA 1998, 95: 1630\u20131634.","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"BF03343931_CR14","first-page":"51","volume":"1447","author":"AE Gobl","year":"1999","unstructured":"Gobl A.E., Berg M., Lopez-Egido J.R., Oberg K., Skogseid B., Westin G. Menin represses JunD-activated transcription by a histone deacetylase-dependent mechanism. Biochem. Biophys. Acta 1999, 1447: 51\u201356.","journal-title":"Biochem. Biophys. Acta"},{"key":"BF03343931_CR15","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1016\/S0092-8674(00)80967-8","volume":"96","author":"SK Agarwal","year":"1999","unstructured":"Agarwal S.K., Guru S.C., Heppner C., Erdos M.R., Collins F.S., Park S.Y., Saggar S., Chandrasekharappa S.C., Collins F.S., Spiegel A.M., Marx S.J., Burns A.L. Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription. Cell 1999, 96: 143\u2013152.","journal-title":"Cell"},{"key":"BF03343931_CR16","doi-asserted-by":"crossref","first-page":"5936","DOI":"10.1038\/sj.onc.1203005","volume":"18","author":"YS Kim","year":"1999","unstructured":"Kim Y.S., Burns A.L., Goldsmith P.K., Heppner C., Park Y.S., Chandrasekharappa S.C., Collins F.S., Spiegel A.M., Marx S.J. Stable overexpression of MEN1 suppresses tumorigenicity of RAS. Oncogene 1999, 18: 5936\u20135942.","journal-title":"Oncogene"},{"key":"BF03343931_CR17","first-page":"5097","volume":"59","author":"H Kaji","year":"1999","unstructured":"Kaji H., Canaff L., Goltzman D., Hendy G.N. Cell cycle regulation of menin gene expression. Cancer Res. 1999, 59: 5097\u20135101.","journal-title":"Cancer Res."},{"key":"BF03343931_CR18","doi-asserted-by":"crossref","first-page":"1088","DOI":"10.1111\/j.1349-7006.1999.tb00682.x","volume":"90","author":"Y Ikeo","year":"1999","unstructured":"Ikeo Y., Sakurai A., Hashizume K. Characterization of the MEN1 gene product, menin, by site-specific polyclonal antibodies. Jpn. J. Cancer Res. 1999, 90: 1088\u20131095.","journal-title":"Jpn. J. Cancer Res."},{"key":"BF03343931_CR19","doi-asserted-by":"crossref","first-page":"877","DOI":"10.1002\/(SICI)1097-0215(20000315)85:6<877::AID-IJC23>3.0.CO;2-F","volume":"85","author":"V Waulot","year":"2000","unstructured":"Waulot V., Khodaei S., Frappart L., Buisson N., Baro E., Lenoir G.M., Calender A., Zhang C.X., Weber G. Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type I gene, in cell lines and human tissues. Int. J. Cancer 2000, 85: 877\u2013881.","journal-title":"Int. J. Cancer"},{"key":"BF03343931_CR20","first-page":"113","volume":"9","author":"AG Knudson","year":"1973","unstructured":"Knudson A.G., Strong L.C., Anderson D.E. Heredity and cancer in man. Prog. Med. Genet. 1973, 9: 113\u2013158.","journal-title":"Prog. Med. Genet."},{"key":"BF03343931_CR21","first-page":"221","volume":"1","author":"S Benvenga","year":"2000","unstructured":"Benvenga S., Bartolone L., Facchiano A., Trimarchi F. Homologies of Menin with tumor suppressor gene products and other proteins. J. Endocr. Genet. 2000, 1: 221\u2013230.","journal-title":"J. Endocr. Genet."},{"key":"BF03343931_CR22","doi-asserted-by":"crossref","first-page":"325","DOI":"10.1006\/geno.1997.4751","volume":"42","author":"JB Williams","year":"1997","unstructured":"Williams J.B., Rexer B., Sirripurapu S., John S., Goldstein R., Phillips J.A. III, Haley L.L., Sait S.N., Shows T.B., Smith C.M., Gerhard D.S. The human HNP36 is localized to chromosome 11q13 and produces alternative transcripts that are not mutated in multiple endocrine neoplasia type 1 (MEN I) syndrome. Genomics 1997, 42: 325\u2013330.","journal-title":"Genomics"}],"container-title":["Journal of Endocrinological Investigation"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF03343931.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF03343931\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF03343931","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,22]],"date-time":"2019-05-22T10:26:17Z","timestamp":1558520777000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF03343931"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2001,11]]},"references-count":22,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2001,11]]}},"alternative-id":["BF03343931"],"URL":"https:\/\/doi.org\/10.1007\/bf03343931","relation":{},"ISSN":["0391-4097","1720-8386"],"issn-type":[{"value":"0391-4097","type":"print"},{"value":"1720-8386","type":"electronic"}],"subject":[],"published":{"date-parts":[[2001,11]]}}}