Modeling autosomal recessive cutis laxa type 1C (ARCL1C) in mice reveals distinct functions of Ltbp-...
Modeling autosomal recessive cutis laxa type 1C (ARCL1C) in mice reveals distinct functions of Ltbp-4 isoforms
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Bultmann-Mellin, Insa , Conradi, Anne , Maul, Alexandra C. , Dinger, Katharina , Wempe, Frank , Wohl, Alexander P. , Imhof, Thomas , Wunderlich, F. Thomas , Bunck, Alexander C. , Nakamura, Tomoyuki , Koli, Katri , Bloch, Wilhelm , Ghanem, Alexander , Heinz, Andrea , von Melchner, Harald , Sengle, Gerhard and Sterner-Kock, Anja
Publisher
England: The Company of Biologists Ltd
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English
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England: The Company of Biologists Ltd
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Recent studies revealed an important role for LTBP-4 in elastogenesis. Its mutational inactivation in humans causes autosomal recessive cutis laxa type 1C (ARCL1C), which is a severe disorder caused by defects of the elastic fiber network. Although the mechanisms underlying the disease were discovered based on similar elastic fiber abnormalities ex...
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Modeling autosomal recessive cutis laxa type 1C (ARCL1C) in mice reveals distinct functions of Ltbp-4 isoforms
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TN_cdi_doaj_primary_oai_doaj_org_article_a4bd9f218f2d4e76a01d420ae7b52376
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a4bd9f218f2d4e76a01d420ae7b52376
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ISSN
1754-8403
E-ISSN
1754-8411
DOI
10.1242/dmm.018960