Literature DB >> 10602123

Epidemiology and genetics of craniosynostosis.

A O Wilkie.   

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Year:  2000        PMID: 10602123     DOI: 10.1002/(sici)1096-8628(20000103)90:1<82::aid-ajmg15>3.0.co;2-5

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


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  10 in total

1.  Effects of thyroxine exposure on the Twist 1 +/- phenotype: A test of gene-environment interaction modeling for craniosynostosis.

Authors:  Emily L Durham; R Nicole Howie; Laurel Black; Grace Bennfors; Trish E Parsons; Mohammed Elsalanty; Jack C Yu; Seth M Weinberg; James J Cray
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2016-07-20

2.  Quantification of Head Shape from Three-Dimensional Photography for Presurgical and Postsurgical Evaluation of Craniosynostosis.

Authors:  Antonio R Porras; Liyun Tu; Deki Tsering; Esperanza Mantilla; Albert Oh; Andinet Enquobahrie; Robert Keating; Gary F Rogers; Marius George Linguraru
Journal:  Plast Reconstr Surg       Date:  2019-12       Impact factor: 4.730

3.  Bone morphogenetic protein is required for fibroblast growth factor 2-dependent later-stage osteoblastic differentiation in cranial suture cells.

Authors:  Taoran Jiang; Shengfang Ge; Yoong Hoon Shim; Ce Zhang; Dejun Cao
Journal:  Int J Clin Exp Pathol       Date:  2015-03-01

4.  Executive Function and Adaptive Behavior in Muenke Syndrome.

Authors:  Colin M P Yarnell; Yonit A Addissie; Donald W Hadley; Maria J Guillen Sacoto; Nneamaka B Agochukwu; Rachel A Hart; Edythe A Wiggs; Petra Platte; Yvonne Paelecke; Hartmut Collmann; Tilmann Schweitzer; Paul Kruszka; Maximilian Muenke
Journal:  J Pediatr       Date:  2015-05-28       Impact factor: 4.406

5.  Leucine-rich repeat, immunoglobulin-like and transmembrane domain 3 (LRIT3) is a modulator of FGFR1.

Authors:  Sun-Don Kim; Jia Lie Liu; Tony Roscioli; Michael F Buckley; Garima Yagnik; Simeon A Boyadjiev; Jinoh Kim
Journal:  FEBS Lett       Date:  2012-04-20       Impact factor: 4.124

Review 6.  Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling.

Authors:  Anna Kutkowska-Kaźmierczak; Monika Gos; Ewa Obersztyn
Journal:  J Appl Genet       Date:  2018-02-01       Impact factor: 3.240

7.  A combined series of Fgf9 and Fgf18 mutant alleles identifies unique and redundant roles in skeletal development.

Authors:  Irene H Hung; Gary C Schoenwolf; Mark Lewandoski; David M Ornitz
Journal:  Dev Biol       Date:  2016-01-16       Impact factor: 3.582

8.  FGF9 regulates early hypertrophic chondrocyte differentiation and skeletal vascularization in the developing stylopod.

Authors:  Irene H Hung; Kai Yu; Kory J Lavine; David M Ornitz
Journal:  Dev Biol       Date:  2007-05-06       Impact factor: 3.582

9.  Isolation and Characterization of Human Suture Mesenchymal Stem Cells In Vitro.

Authors:  Liangliang Kong; Yuan Wang; Yi Ji; Jianbing Chen; Jie Cui; Weimin Shen
Journal:  Int J Stem Cells       Date:  2020-11-30       Impact factor: 2.500

10.  Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis.

Authors:  Anna K Coussens; Christopher R Wilkinson; Ian P Hughes; C Phillip Morris; Angela van Daal; Peter J Anderson; Barry C Powell
Journal:  BMC Genomics       Date:  2007-12-12       Impact factor: 3.969

  10 in total

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