{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,12]],"date-time":"2026-05-12T03:54:15Z","timestamp":1778558055647,"version":"3.51.4"},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"4","license":[{"start":{"date-parts":[[1997,8,1]],"date-time":"1997-08-01T00:00:00Z","timestamp":870393600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1997,8,1]]},"abstract":"<jats:p>It has previously been shown that abnormal placental development, i.e., hyper- and hypoplasia, occurs in crosses and backcrosses between different mouse (Mus) species. These defects are caused mainly by abnormal growth of the spongiotrophoblast. The precise genetic basis for these placental malformations has not been determined. However, a locus that contributes to the abnormal development (Ihpd: interspecific hybrid placental dysplasia) has been mapped to the X chromosome. The X-chromosomal location of Ihpd and its site of action, that is the spongiotrophoblast, mean that normally only the maternally inherited Ihpd locus is active even in female fetuses. However, by making use of the X-chromosomal inversion In(X)1H, we have produced interspecific hybrid Xp0, in which the active X chromosome was inherited from Mus macedonicus males. In contrast to XX female and XY male conceptuses from this cross, which have hypoplastic placentas, the Xp0 female conceptuses have hyperplastic placentas. This finding supports the view that it is expression of the M. macedonicus Ihpd locus in the spongiotrophoblast that leads to hyperplasia due to an abnormal interaction with M. musculus autosomal loci.<\/jats:p>","DOI":"10.1093\/genetics\/146.4.1399","type":"journal-article","created":{"date-parts":[[2021,1,13]],"date-time":"2021-01-13T17:48:09Z","timestamp":1610560089000},"page":"1399-1405","source":"Crossref","is-referenced-by-count":26,"title":["Paternal Transmission of <i>X<\/i>-Linked Placental Dysplasia in Mouse Interspecific Hybrids"],"prefix":"10.1093","volume":"146","author":[{"given":"Ulrich","family":"Zechner","sequence":"first","affiliation":[{"name":"Max-Planck-Institut f\u00fcr Molekulare Genetik, Berlin, Germany"},{"name":"Abteilung Medizinische Genetik der Universit\u00e4t Ulm, Ulm, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Matthias","family":"Reule","sequence":"additional","affiliation":[{"name":"Max-Planck-Institut f\u00fcr Molekulare Genetik, Berlin, Germany"},{"name":"Institut f\u00fcr Biologie III der Universit\u00e4t Freiburg, Freiburg, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paul S","family":"Burgoyne","sequence":"additional","affiliation":[{"name":"Laboratory of Developmental Genetics, National Institute for Medical Research, London, United Kingdom"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alexis","family":"Schubert","sequence":"additional","affiliation":[{"name":"Institut f\u00fcr Biologie III der Universit\u00e4t Freiburg, Freiburg, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Annie","family":"Orth","sequence":"additional","affiliation":[{"name":"Laboratoire G\u00e9nome et Populations, Universit\u00e9 de Montpellier, Montpellier, France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Horst","family":"Hameister","sequence":"additional","affiliation":[{"name":"Abteilung Medizinische Genetik der Universit\u00e4t Ulm, Ulm, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Reinald","family":"Fundele","sequence":"additional","affiliation":[{"name":"Max-Planck-Institut f\u00fcr Molekulare Genetik, Berlin, Germany"},{"name":"Institut f\u00fcr Biologie III der Universit\u00e4t Freiburg, Freiburg, Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[1997,8,1]]},"container-title":["Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/academic.oup.com\/genetics\/article-pdf\/146\/4\/1399\/35202316\/genetics1399.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"http:\/\/academic.oup.com\/genetics\/article-pdf\/146\/4\/1399\/35202316\/genetics1399.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,4,27]],"date-time":"2021-04-27T15:02:23Z","timestamp":1619535743000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/genetics\/article\/146\/4\/1399\/6053944"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1997,8,1]]},"references-count":0,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1997,8,1]]}},"URL":"https:\/\/doi.org\/10.1093\/genetics\/146.4.1399","relation":{},"ISSN":["1943-2631"],"issn-type":[{"value":"1943-2631","type":"electronic"}],"subject":[],"published-other":{"date-parts":[[1997,8,1]]},"published":{"date-parts":[[1997,8,1]]}}}