Literature DB >> 9611066

Toward understanding the pathogenesis of craniosynostosis through clinical and molecular correlates.

E W Jabs1.   

Abstract

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Year:  1998        PMID： 9611066     DOI： 10.1111/j.1399-0004.1998.tb02648.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  10 in total

1.  In vivo modulation of FGF biological activity alters cranial suture fate.

Authors:  J A Greenwald; B J Mehrara; J A Spector; S M Warren; P J Fagenholz; L E Smith; P J Bouletreau; F E Crisera; H Ueno; M T Longaker
Journal:  Am J Pathol       Date:  2001-02       Impact factor: 4.307

2.  A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.

Authors:  Simeon A Boyadjiev; Cristina M Justice; Wafaa Eyaid; Victor A McKusick; Ralph S Lachman; Arnab B Chowdry; Monzer Jabak; Johan Zwaan; Alexander F Wilson; Ethylin Wang Jabs
Journal:  Hum Genet       Date:  2003-04-03       Impact factor: 4.132

3.  A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes.

Authors:  M K Hajihosseini; S Wilson; L De Moerlooze; C Dickson
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-27       Impact factor: 11.205

Review 4.  Genetic advances in craniosynostosis.

Authors:  Wanda Lattanzi; Marta Barba; Lorena Di Pietro; Simeon A Boyadjiev
Journal:  Am J Med Genet A       Date:  2017-02-04       Impact factor: 2.802

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

6.  Pictorial essay: The many faces of craniosynostosis.

Authors:  Paritosh C Khanna; Mahesh M Thapa; Ramesh S Iyer; Shashank S Prasad
Journal:  Indian J Radiol Imaging       Date:  2011-01

7.  Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis.

Authors:  Araceli Cuellar; Krithi Bala; Lorena Di Pietro; Marta Barba; Garima Yagnik; Jia Lie Liu; Christina Stevens; David J Hur; Roxann G Ingersoll; Cristina M Justice; Hicham Drissi; Jinoh Kim; Wanda Lattanzi; Simeon A Boyadjiev
Journal:  Bone       Date:  2020-04-30       Impact factor: 4.398

8.  Actual concepts in scaphocephaly : (an experience of 98 cases).

Authors:  A V Ciurea; C Toader; C Mihalache
Journal:  J Med Life       Date:  2011-11-24

9.  Apert syndrome: A case report and review of the literature.

Authors:  Tuba Tulay Koca
Journal:  North Clin Istanb       Date:  2016-05-14

Review 10.  Genetics of craniosynostosis: review of the literature.

Authors:  Alexandru Vlad Ciurea; Corneliu Toader
Journal:  J Med Life       Date:  2009 Jan-Mar
  10 in total

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