Literature DB >> 15358727

Genetic disorders influencing lung formation and function at birth.

Jeffrey A Whitsett1, Susan E Wert, Bruce C Trapnell.   

Abstract

Adaptation to air breathing at birth is dependent on formation and function of the lung. Lung morphogenesis is a complex process dependent on precise temporal-spatial control of cell proliferation, differentiation and behavior mediated by autocrine-paracrine signaling that instructs transcriptional processes during organogenesis. Mutations in genes causing severe, and often lethal, lung malformations include those in the sonic hedgehog, fibroblast growth factor and thyroid transcription factor-1 pathways. Mutations in genes regulating surfactant homeostasis, necessary for reduction of surface tension in the alveoli, cause lethal respiratory distress at birth or interstitial lung disease in childhood. Inherited disorders of the surfactant system that affect neonatal respiratory adaptation at birth include hereditary surfactant protein B deficiency, mutations in surfactant protein C and the ABCA3 transporter.

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Year:  2004        PMID: 15358727     DOI: 10.1093/hmg/ddh252

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  52 in total

1.  Smad1 and its target gene Wif1 coordinate BMP and Wnt signaling activities to regulate fetal lung development.

Authors:  Bing Xu; Cheng Chen; Hui Chen; Song-Guo Zheng; Pablo Bringas; Min Xu; Xianghong Zhou; Di Chen; Lieve Umans; An Zwijsen; Wei Shi
Journal:  Development       Date:  2011-01-26       Impact factor: 6.868

Review 2.  The molecular basis of pulmonary alveolar proteinosis.

Authors:  Brenna Carey; Bruce C Trapnell
Journal:  Clin Immunol       Date:  2010-03-25       Impact factor: 3.969

3.  Cited2 is required for fetal lung maturation.

Authors:  Bing Xu; Xiaoling Qu; Shi Gu; Yong-Qiu Doughman; Michiko Watanabe; Sally L Dunwoodie; Yu-Chung Yang
Journal:  Dev Biol       Date:  2008-02-26       Impact factor: 3.582

Review 4.  Antenatally diagnosed lung malformations: a plea for long-term outcome studies.

Authors:  Muhammad Choudhry; David Drake
Journal:  Pediatr Surg Int       Date:  2015-01-04       Impact factor: 1.827

5.  Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapy.

Authors:  Takuji Suzuki; Takuro Sakagami; Lisa R Young; Brenna C Carey; Robert E Wood; Maurizio Luisetti; Susan E Wert; Bruce K Rubin; Katharine Kevill; Claudia Chalk; Jeffrey A Whitsett; Carrie Stevens; Lawrence M Nogee; Ilaria Campo; Bruce C Trapnell
Journal:  Am J Respir Crit Care Med       Date:  2010-07-09       Impact factor: 21.405

Review 6.  An overview of pulmonary surfactant in the neonate: genetics, metabolism, and the role of surfactant in health and disease.

Authors:  Paul O Nkadi; T Allen Merritt; De-Ann M Pillers
Journal:  Mol Genet Metab       Date:  2009-02-04       Impact factor: 4.797

7.  Macrophage dysfunction and susceptibility to pulmonary Pseudomonas aeruginosa infection in surfactant protein C-deficient mice.

Authors:  Stephan W Glasser; Albert P Senft; Jeffrey A Whitsett; Melissa D Maxfield; Gary F Ross; Theresa R Richardson; Daniel R Prows; Yan Xu; Thomas R Korfhagen
Journal:  J Immunol       Date:  2008-07-01       Impact factor: 5.422

8.  Characteristics of a large cohort of patients with autoimmune pulmonary alveolar proteinosis in Japan.

Authors:  Yoshikazu Inoue; Bruce C Trapnell; Ryushi Tazawa; Toru Arai; Toshinori Takada; Nobuyuki Hizawa; Yasunori Kasahara; Koichiro Tatsumi; Masaaki Hojo; Toshio Ichiwata; Naohiko Tanaka; Etsuro Yamaguchi; Ryosuke Eda; Kazunori Oishi; Yoshiko Tsuchihashi; Chinatsu Kaneko; Toshihiro Nukiwa; Mitsunori Sakatani; Jeffrey P Krischer; Koh Nakata
Journal:  Am J Respir Crit Care Med       Date:  2008-01-17       Impact factor: 21.405

9.  Antenatally diagnosed congenital cystic adenomatoid malformations (CCAM): Research Review.

Authors:  Fosca Antonia Francesca Di Prima; Adriano Bellia; Genny Inclimona; Francesco Grasso; Maria Teresa; Meli Nazario Cassaro
Journal:  J Prenat Med       Date:  2012-04

10.  The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesis.

Authors:  Laura L Yates; Carsten Schnatwinkel; Jennifer N Murdoch; Debora Bogani; Caroline J Formstone; Stuart Townsend; Andy Greenfield; Lee A Niswander; Charlotte H Dean
Journal:  Hum Mol Genet       Date:  2010-03-10       Impact factor: 6.150

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