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Anim."],"published-print":{"date-parts":[[2020]]},"DOI":"10.1538\/expanim.19-0088","type":"journal-article","created":{"date-parts":[[2019,9,25]],"date-time":"2019-09-25T22:03:26Z","timestamp":1569449006000},"page":"104-109","source":"Crossref","is-referenced-by-count":5,"title":["Genetic mutation of &lt;i&gt;Frem3&lt;\/i&gt; does not causeFraser syndrome in          mice"],"prefix":"10.1538","volume":"69","author":[{"given":"Daiji","family":"Kiyozumi","sequence":"first","affiliation":[{"name":"Research Institute for Microbial Diseases, 3-1              Yamadaoka, Suita, Osaka 565-0871, Japan"},{"name":"Immunology Frontier Research Center, 3-1 Yamadaoka,              Suita, Osaka 565-0871, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Masashi","family":"Mori","sequence":"additional","affiliation":[{"name":"Research Institute for Microbial Diseases, 3-1              Yamadaoka, Suita, Osaka 565-0871, Japan"},{"name":"Immunology Frontier Research Center, 3-1 Yamadaoka,              Suita, Osaka 565-0871, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mayo","family":"Kodani","sequence":"additional","affiliation":[{"name":"Research Institute for Microbial Diseases, 3-1              Yamadaoka, Suita, Osaka 565-0871, Japan"},{"name":"Graduate School of Pharmaceutical Sciences, 3-1              Yamadaoka, Suita, Osaka 565-0871, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Masahito","family":"Ikawa","sequence":"additional","affiliation":[{"name":"Research Institute for Microbial Diseases, 3-1              Yamadaoka, Suita, Osaka 565-0871, Japan"},{"name":"Immunology Frontier Research Center, 3-1 Yamadaoka,              Suita, Osaka 565-0871, Japan"},{"name":"Graduate School of Pharmaceutical Sciences, 3-1              Yamadaoka, Suita, Osaka 565-0871, Japan"},{"name":"Graduate School of Medicine, Osaka University, 3-1              Yamadaoka, Suita, Osaka 565-0871, Japan"},{"name":"The Institute of Medical Science, The University of              Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"439","reference":[{"key":"1","unstructured":"1. 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Jadeja              S., Smyth              I., Pitera              J.E., Taylor              M.S., van                Haelst              M., Bentley              E., McGregor              L., Hopkins              J.,                Chalepakis              G., Philip              N., Perez                Aytes              A., Watt              F.M., Darling              S.M., Jackson              I., Woolf              A.S. and                Scambler              P.J.          2005. Identification of a new gene mutated in Fraser syndrome            and mouse myelencephalic blebs. <i>Nat.            Genet.<\/i>          37: 520\u2013525.","DOI":"10.1038\/ng1549"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Kiyozumi              D., Sugimoto              N., Nakano              I. and                Sekiguchi              K.          2007. 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McGregor              L., Makela              V., Darling              S.M., Vrontou              S.,                Chalepakis              G., Roberts              C., Smart              N., Rutland              P., Prescott              N., Hopkins              J., Bentley              E., Shaw              A., Roberts              E., Mueller              R., Jadeja              S., Philip              N., Nelson              J.,                Francannet              C.,                Perez-Aytes              A., Megarbane              A., Kerr              B.,                Wainwright              B., Woolf              A.S., Winter              R.M. and                Scambler              P.J.          2003. Fraser syndrome and mouse blebbed phenotype caused by            mutations in FRAS1\/Fras1 encoding a putative extracellular matrix            protein. <i>Nat. Genet.<\/i>          34: 203\u2013208.","DOI":"10.1038\/ng1142"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Petrou              P., Pavlakis              E., Dalezios              Y. and                Chalepakis              G.          2007. Basement membrane localization of Frem3 is independent            of the Fras1\/Frem1\/Frem2 protein complex within the sublamina densa.              <i>Matrix Biol.<\/i>          26: 652\u2013658.","DOI":"10.1016\/j.matbio.2007.05.008"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Slavotinek              A.M. and                Tifft              C.J.          2002. Fraser syndrome and cryptophthalmos: review of the            diagnostic criteria and evidence for phenotypic modules in complex malformation            syndromes. <i>J. Med. Genet.<\/i>          39: 623\u2013633.","DOI":"10.1136\/jmg.39.9.623"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Slavotinek              A.M.,                Baranzini              S.E., Schanze              D.,                Labelle-Dumais              C., Short              K.M., Chao              R., Yahyavi              M., Bijlsma              E.K., Chu              C., Musone              S., Wheatley              A., Kwok              P.Y., Marles              S., Fryns              J.P., Maga              A.M., Hassan              M.G., Gould              D.B.,                Madireddy              L., Li              C., Cox              T.C., Smyth              I., Chudley              A.E. and                Zenker              M.          2011. Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by            mutations in FREM1. <i>J. Med. Genet.<\/i>          48: 375\u2013382.","DOI":"10.1136\/jmg.2011.089631"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. 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Vogel              M.J., van Zon              P., Brueton              L., Gijzen              M., van Tuil              M.C., Cox              P., Schanze              D.,                Kariminejad              A.,                Ghaderi-Sohi              S., Blair              E., Zenker              M., Scambler              P.J., Ploos van                Amstel              H.K. and van                Haelst              M.M.          2012. Mutations in GRIP1 cause Fraser          syndrome. <i>J. Med. Genet.<\/i>          49: 303\u2013306.","DOI":"10.1136\/jmedgenet-2011-100590"},{"key":"15","unstructured":"15. Vrontou              S., Petrou              P., Meyer              B.I.,                Galanopoulos              V.K., Imai              K., Yanagi              M., Chowdhury              K., Scambler              P.J. and                Chalepakis              G.          2003. Fras1 deficiency results in cryptophthalmos, renal            agenesis and blebbed phenotype in mice. <i>Nat.              Genet.<\/i>          34: 209\u2013214."}],"container-title":["Experimental Animals"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/expanim\/69\/1\/69_19-0088\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,2,1]],"date-time":"2020-02-01T03:32:21Z","timestamp":1580527941000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/expanim\/69\/1\/69_19-0088\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020]]},"references-count":15,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2020]]}},"URL":"https:\/\/doi.org\/10.1538\/expanim.19-0088","relation":{},"ISSN":["1341-1357","1881-7122"],"issn-type":[{"value":"1341-1357","type":"print"},{"value":"1881-7122","type":"electronic"}],"subject":[],"published":{"date-parts":[[2020]]}}}