Literature DB >> 23438589

Filling in the gaps in cranial suture biology.

David R Fitzpatrick.   

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Year:  2013        PMID： 23438589     DOI： 10.1038/ng.2557

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  14 in total

1.  Molecular silencing of Twist1 enhances osteogenic differentiation of murine mesenchymal stem cells: implication of FGFR2 signaling.

Authors:  Hichem Miraoui; Nicolas Severe; Pascal Vaudin; Jean-Christophe Pagès; Pierre J Marie
Journal:  J Cell Biochem       Date:  2010-08-01       Impact factor: 4.429

2.  Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis.

Authors:  Andrew O M Wilkie; Jo C Byren; Jane A Hurst; Jayaratnam Jayamohan; David Johnson; Samantha J L Knight; Tracy Lester; Peter G Richards; Stephen R F Twigg; Steven A Wall
Journal:  Pediatrics       Date:  2010-07-19       Impact factor: 7.124

3.  A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.

Authors:  M Muenke; K W Gripp; D M McDonald-McGinn; K Gaudenz; L A Whitaker; S P Bartlett; R I Markowitz; N H Robin; N Nwokoro; J J Mulvihill; H W Losken; J B Mulliken; A E Guttmacher; R S Wilroy; L A Clarke; G Hollway; L C Adès; E A Haan; J C Mulley; M M Cohen; G A Bellus; C A Francomano; D M Moloney; S A Wall; A O Wilkie
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

4.  Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.

Authors:  T D Howard; W A Paznekas; E D Green; L C Chiang; N Ma; R I Ortiz de Luna; C Garcia Delgado; M Gonzalez-Ramos; A D Kline; E W Jabs
Journal:  Nat Genet       Date:  1997-01       Impact factor: 38.330

5.  Mutations of the TWIST gene in the Saethre-Chotzen syndrome.

Authors:  V el Ghouzzi; M Le Merrer; F Perrin-Schmitt; E Lajeunie; P Benit; D Renier; P Bourgeois; A L Bolcato-Bellemin; A Munnich; J Bonaventure
Journal:  Nat Genet       Date:  1997-01       Impact factor: 38.330

6.  A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.

Authors:  M Muenke; U Schell; A Hehr; N H Robin; H W Losken; A Schinzel; L J Pulleyn; P Rutland; W Reardon; S Malcolm
Journal:  Nat Genet       Date:  1994-11       Impact factor: 38.330

7.  Constitutive activation of fibroblast growth factor receptor-2 by a point mutation associated with Crouzon syndrome.

Authors:  K M Neilson; R E Friesel
Journal:  J Biol Chem       Date:  1995-11-03       Impact factor: 5.157

8.  Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome.

Authors:  W Reardon; R M Winter; P Rutland; L J Pulleyn; B M Jones; S Malcolm
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

9.  Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.

Authors:  Vikram P Sharma; Aimée L Fenwick; Mia S Brockop; Simon J McGowan; Jacqueline A C Goos; A Jeannette M Hoogeboom; Angela F Brady; Nu Owase Jeelani; Sally Ann Lynch; John B Mulliken; Dylan J Murray; Julie M Phipps; Elizabeth Sweeney; Susan E Tomkins; Louise C Wilson; Sophia Bennett; Richard J Cornall; John Broxholme; Alexander Kanapin; David Johnson; Steven A Wall; Peter J van der Spek; Irene M J Mathijssen; Robert E Maxson; Stephen R F Twigg; Andrew O M Wilkie
Journal:  Nat Genet       Date:  2013-01-27       Impact factor: 38.330

10.  Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis.

Authors:  Stephen R F Twigg; Elena Vorgia; Simon J McGowan; Ioanna Peraki; Aimée L Fenwick; Vikram P Sharma; Maryline Allegra; Andreas Zaragkoulias; Elham Sadighi Akha; Samantha J L Knight; Helen Lord; Tracy Lester; Louise Izatt; Anne K Lampe; Shehla N Mohammed; Fiona J Stewart; Alain Verloes; Louise C Wilson; Chris Healy; Paul T Sharpe; Peter Hammond; Jim Hughes; Stephen Taylor; David Johnson; Steven A Wall; George Mavrothalassitis; Andrew O M Wilkie
Journal:  Nat Genet       Date:  2013-01-27       Impact factor: 38.330
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  9 in total

1.  Activation of the IGF1 pathway mediates changes in cellular contractility and motility in single-suture craniosynostosis.

Authors:  Zeinab Al-Rekabi; Marsha M Wheeler; Andrea Leonard; Adriane M Fura; Ilsa Juhlin; Christopher Frazar; Joshua D Smith; Sarah S Park; Jennifer A Gustafson; Christine M Clarke; Michael L Cunningham; Nathan J Sniadecki
Journal:  J Cell Sci       Date:  2015-12-11       Impact factor: 5.285

2.  BCL11B regulates sutural patency in the mouse craniofacial skeleton.

Authors:  Kateryna Kyrylkova; Urszula T Iwaniec; Kenneth A Philbrick; Mark Leid
Journal:  Dev Biol       Date:  2015-10-09       Impact factor: 3.582

Review 3.  Understanding craniosynostosis as a growth disorder.

Authors:  Kevin Flaherty; Nandini Singh; Joan T Richtsmeier
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2016-03-22       Impact factor: 5.814

4.  A de novo substitution in BCL11B leads to loss of interaction with transcriptional complexes and craniosynostosis.

Authors:  Jacqueline A C Goos; Walter K Vogel; Hana Mlcochova; Christopher J Millard; Elahe Esfandiari; Wisam H Selman; Eduardo Calpena; Nils Koelling; Evan L Carpenter; Sigrid M A Swagemakers; Peter J van der Spek; Theresa M Filtz; John W R Schwabe; Urszula T Iwaniec; Irene M J Mathijssen; Mark Leid; Stephen R F Twigg
Journal:  Hum Mol Genet       Date:  2019-08-01       Impact factor: 6.150

5.  Signaling pathways in osteogenesis and osteoclastogenesis: Lessons from cranial sutures and applications to regenerative medicine.

Authors:  Justin B Maxhimer; James P Bradley; Justine C Lee
Journal:  Genes Dis       Date:  2015-01-09

6.  Characterization of distinct classes of differential gene expression in osteoblast cultures from non-syndromic craniosynostosis bone.

Authors:  Monica L Rojas-Peña; Rene Olivares-Navarrete; Sharon Hyzy; Dalia Arafat; Zvi Schwartz; Barbara D Boyan; Joseph Williams; Greg Gibson
Journal:  J Genomics       Date:  2014-08-01

7.  Bilambdoid and sagittal synostosis: Report of 39 cases.

Authors:  Nathalie Chivoret; Eric Arnaud; Kim Giraudat; Frazer O'Brien; Leslie Pamphile; Philippe Meyer; Dominique Renier; C Collet; Federico Di Rocco
Journal:  Surg Neurol Int       Date:  2018-10-11

8.  Dysregulation of the HOTAIR-miR-152-CAMKIIα Axis in Craniosynostosis Results in Impaired Osteoclast Differentiation.

Authors:  Chenbin Dong; Xiangqi Liu; Jun Li; Dongyi Lan; Shan Zheng
Journal:  Front Genet       Date:  2022-03-10       Impact factor: 4.599

9.  Identification of stiffness-induced signalling mechanisms in cells from patent and fused sutures associated with craniosynostosis.

Authors:  Sara Barreto; Arlyng González-Vázquez; Andrew R Cameron; Fergal J O'Brien; Dylan J Murray
Journal:  Sci Rep       Date:  2017-09-13       Impact factor: 4.379
  9 in total

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