Literature DB >> 26589935

From Bench to Bedside and Back: Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models.

Alice F Goodwin1, Rebecca Kim1, Jeffrey O Bush2, Ophir D Klein3.   

Abstract

Craniofacial anomalies are among the most common birth defects and are associated with increased mortality and, in many cases, the need for lifelong treatment. Over the past few decades, dramatic advances in the surgical and medical care of these patients have led to marked improvements in patient outcomes. However, none of the treatments currently in clinical use address the underlying molecular causes of these disorders. Fortunately, the field of craniofacial developmental biology provides a strong foundation for improved diagnosis and for therapies that target the genetic causes of birth defects. In this chapter, we discuss recent advances in our understanding of the embryology of craniofacial conditions, and we focus on the use of animal models to guide rational therapies anchored in genetics and biochemistry.
© 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cleft lip and palate; Craniofacial anomalies; Craniosynostosis; Developmental biology; Ectodermal dysplasia; RASopathies; Treacher Collins; XLHED

Mesh:

Year:  2015        PMID: 26589935      PMCID: PMC7398124          DOI: 10.1016/bs.ctdb.2015.07.003

Source DB:  PubMed          Journal:  Curr Top Dev Biol        ISSN: 0070-2153            Impact factor:   4.897


  196 in total

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Journal:  Nat Immunol       Date:  2001-03       Impact factor: 25.606

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Journal:  J Hered       Date:  1997 Nov-Dec       Impact factor: 2.645

5.  Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras.

Authors:  B D Galvin; K C Hart; A N Meyer; M K Webster; D J Donoghue
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-23       Impact factor: 11.205

6.  Indirect modulation of Shh signaling by Dlx5 affects the oral-nasal patterning of palate and rescues cleft palate in Msx1-null mice.

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Journal:  Development       Date:  2009-12       Impact factor: 6.868

7.  Germline KRAS mutations cause Noonan syndrome.

Authors:  Suzanne Schubbert; Martin Zenker; Sara L Rowe; Silke Böll; Cornelia Klein; Gideon Bollag; Ineke van der Burgt; Luciana Musante; Vera Kalscheuer; Lars-Erik Wehner; Hoa Nguyen; Brian West; Kam Y J Zhang; Erik Sistermans; Anita Rauch; Charlotte M Niemeyer; Kevin Shannon; Christian P Kratz
Journal:  Nat Genet       Date:  2006-02-12       Impact factor: 38.330

8.  Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

Authors:  Shinji Kondo; Brian C Schutte; Rebecca J Richardson; Bryan C Bjork; Alexandra S Knight; Yoriko Watanabe; Emma Howard; Renata L L Ferreira de Lima; Sandra Daack-Hirsch; Achim Sander; Donna M McDonald-McGinn; Elaine H Zackai; Edward J Lammer; Arthur S Aylsworth; Holly H Ardinger; Andrew C Lidral; Barbara R Pober; Lina Moreno; Mauricio Arcos-Burgos; Consuelo Valencia; Claude Houdayer; Michel Bahuau; Danilo Moretti-Ferreira; Antonio Richieri-Costa; Michael J Dixon; Jeffrey C Murray
Journal:  Nat Genet       Date:  2002-09-03       Impact factor: 38.330

Review 9.  Molecular and cellular bases of syndromic craniosynostoses.

Authors:  Jacky Bonaventure; Vincent El Ghouzzi
Journal:  Expert Rev Mol Med       Date:  2003-01-29       Impact factor: 5.600

10.  Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair.

Authors:  Viviana Cordeddu; Elia Di Schiavi; Len A Pennacchio; Avi Ma'ayan; Anna Sarkozy; Valentina Fodale; Serena Cecchetti; Alessio Cardinale; Joel Martin; Wendy Schackwitz; Anna Lipzen; Giuseppe Zampino; Laura Mazzanti; Maria C Digilio; Simone Martinelli; Elisabetta Flex; Francesca Lepri; Deborah Bartholdi; Kerstin Kutsche; Giovanni B Ferrero; Cecilia Anichini; Angelo Selicorni; Cesare Rossi; Romano Tenconi; Martin Zenker; Daniela Merlo; Bruno Dallapiccola; Ravi Iyengar; Paolo Bazzicalupo; Bruce D Gelb; Marco Tartaglia
Journal:  Nat Genet       Date:  2009-08-16       Impact factor: 38.330

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  3 in total

Review 1.  Feedback regulation of RTK signaling in development.

Authors:  Cynthia L Neben; Megan Lo; Natalia Jura; Ophir D Klein
Journal:  Dev Biol       Date:  2017-10-26       Impact factor: 3.582

2.  Prenatal retinoic acid exposure reveals candidate genes for craniofacial disorders.

Authors:  Marie Berenguer; Muriel Darnaudery; Stéphane Claverol; Marc Bonneu; Didier Lacombe; Caroline Rooryck
Journal:  Sci Rep       Date:  2018-11-30       Impact factor: 4.379

3.  An Irf6-Esrp1/2 regulatory axis controls midface morphogenesis in vertebrates.

Authors:  Shannon H Carroll; Claudio Macias Trevino; Edward B Li; Kenta Kawasaki; Nikita Myers; Shawn A Hallett; Nora Alhazmi; Justin Cotney; Russ P Carstens; Eric C Liao
Journal:  Development       Date:  2020-12-23       Impact factor: 6.862

  3 in total

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