Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome.

Teraishi, Mika; Takaishi, Mikiro; Nakajima, Kimiko; Ikeda, Mitsunori; Higashi, Yujiro; Shimoda, Shinji; Asada, Yoshinobu; Hijikata, Atsushi; Ohara, Osamu; Hiraki, Yoko; Mizuno, Seiji; Fukada, Toshiyuki; Furukawa, Takahisa; Wakamatsu, Nobuaki; Sano, Shigetoshi

Teraishi, Mika; Takaishi, Mikiro; Nakajima, Kimiko; Ikeda, Mitsunori; Higashi, Yujiro; Shimoda, Shinji; Asada, Yoshinobu; Hijikata, Atsushi; Ohara, Osamu; Hiraki, Yoko; Mizuno, Seiji; Fukada, Toshiyuki; Furukawa, Takahisa; Wakamatsu, Nobuaki; Sano, Shigetoshi.

Afiliação

Teraishi M; Department of Dermatology, Kochi Medical School, Nankoku 783-8505, Japan.
Takaishi M; Department of Dermatology, Kochi Medical School, Nankoku 783-8505, Japan.
Nakajima K; Department of Dermatology, Kochi Medical School, Nankoku 783-8505, Japan.
Ikeda M; Department of Dermatology, Kochi Medical School, Nankoku 783-8505, Japan.
Higashi Y; Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai 480-0392, Japan.
Shimoda S; Department of Anatomy, Tsurumi University School of Dental Medicine, Yokohama 230-8501, Japan.
Asada Y; Department of Pediatric Dentistry, Tsurumi University School of Dental Medicine, Yokohama 230-8501, Japan.
Hijikata A; Department of Bioscience, Nagahama Institute of Bio-Science and Technology, Nagahama 526-0829, Japan.
Ohara O; Laboratory for Integrative Genomics, RIKEN IMS, Yokohama 230-0045, Japan.
Hiraki Y; Hiroshima Municipal Center for Child Health and Development, Hiroshima 732-0052, Japan.
Mizuno S; Department of Pediatrics, Central Hospital, Aichi Human Service Center, Kasugai 480-0392, Japan.
Fukada T; Department of Molecular and Cellular Physiology, Faculty of Pharmaceutical Science, Tokushima Bunri University, Tokushima 770-8514, Japan.
Furukawa T; Laboratory for Molecular and Developmental Biology, Institute for Protein Research, Osaka University, Suita 565-0871, Japan.
Wakamatsu N; Department of Genetics, Institute for Developmental Research, Aichi Human Service Center, Kasugai 480-0392, Japan.
Sano S; Department of Dermatology, Kochi Medical School, Nankoku 783-8505, Japan.

Sci Rep ; 7: 46565, 2017 04 19.

Article em En | MEDLINE | ID: mdl-28422173

Assuntos

Colágeno; Derme; Síndrome de Ehlers-Danlos; Fácies; Doença de Hirschsprung; Deficiência Intelectual; Microcefalia; Homeobox 2 de Ligação a E-box com Dedos de Zinco; Animais; Criança; Pré-Escolar; Colágeno/genética; Colágeno/metabolismo; Derme/metabolismo; Derme/patologia; Síndrome de Ehlers-Danlos/genética; Síndrome de Ehlers-Danlos/metabolismo; Síndrome de Ehlers-Danlos/patologia; Matriz Extracelular/genética; Matriz Extracelular/metabolismo; Feminino; Fibroblastos/metabolismo; Fibroblastos/patologia; Doença de Hirschsprung/genética; Doença de Hirschsprung/metabolismo; Doença de Hirschsprung/patologia; Humanos; Deficiência Intelectual/genética; Deficiência Intelectual/metabolismo; Deficiência Intelectual/patologia; Masculino; Camundongos; Camundongos Knockout; Microcefalia/genética; Microcefalia/metabolismo; Microcefalia/patologia; Proteólise; Homeobox 2 de Ligação a E-box com Dedos de Zinco/genética; Homeobox 2 de Ligação a E-box com Dedos de Zinco/metabolismo

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Colágeno / Fácies / Derme / Síndrome de Ehlers-Danlos / Homeobox 2 de Ligação a E-box com Dedos de Zinco / Doença de Hirschsprung / Deficiência Intelectual / Microcefalia Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article

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