FoxD1-driven CCN2 deletion causes axial skeletal deformities, pulmonary hypoplasia, and neonatal asphyctic death.

Falke, Lucas L; He, Nannan; Chuva de Sousa Lopes, Susana M; Broekhuizen, Roel; Lyons, Karen; Nguyen, Tri Q; Goldschmeding, Roel

Falke, Lucas L; He, Nannan; Chuva de Sousa Lopes, Susana M; Broekhuizen, Roel; Lyons, Karen; Nguyen, Tri Q; Goldschmeding, Roel.

Afiliação

Falke LL; Deparment Pathology, University Medical Centre Utrecht, Heidelberglaan 100, 3584, CX, Utrecht, The Netherlands.
He N; Department Internal medicine, Diakonessenhuis, Utrecht, the Netherlands.
Chuva de Sousa Lopes SM; Department Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Broekhuizen R; Department Anatomy and Embryology, Leiden University Medical Center, Leiden, the Netherlands.
Lyons K; Deparment Pathology, University Medical Centre Utrecht, Heidelberglaan 100, 3584, CX, Utrecht, The Netherlands.
Nguyen TQ; Department Orthopedic Surgery, University of California, Berkeley, CA, USA.
Goldschmeding R; Department Molecular Cell and Developmental Biology, University of California, Berkeley, CA, USA.

J Cell Commun Signal ; 13(4): 573-577, 2019 Dec.

Article em En | MEDLINE | ID: mdl-32020419

Palavras-chave

CCN2; CTGF; FoxD1; Hypoplasia; Lung; Skeletogenesis

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies Idioma: En Revista: J Cell Commun Signal Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda País de publicação: Holanda

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