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Mesodermal expression of Fgfr2 is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome

Developmental biology, 2012-08, Vol.368 (2), p.283-293

2012

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Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis

Cell reports (Cambridge), 2020-07, Vol.32 (1), p.107871-107871, Article 107871

2020

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Single-cell analysis identifies a key role for Hhip in murine coronal suture development

Nature communications, 2021-12, Vol.12 (1), p.7132-7132, Article 7132

2021

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Regulation of cranial morphogenesis and cell fate at the neural crest-mesoderm boundary by engrailed 1

Development (Cambridge), 2012-04, Vol.139 (7), p.1346-1358

2012

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Cleft Palate in Apert Syndrome

Journal of developmental biology, 2022-08, Vol.10 (3), p.33

2022

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Sox2 induction by FGF and FGFR2 activating mutations inhibits Wnt signaling and osteoblast differentiation

The Journal of cell biology, 2005-03, Vol.168 (7), p.1065-1076

2005

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C-type natriuretic peptide analog treatment of craniosynostosis in a Crouzon syndrome mouse model

PloS one, 2018-07, Vol.13 (7), p.e0201492-e0201492

2018

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The FaceBase Consortium: a comprehensive resource for craniofacial researchers

Development (Cambridge), 2016-07, Vol.143 (14), p.2677-2688

2016

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Fibroblast Growth Factor Signaling Uses Multiple Mechanisms To Inhibit Wnt-Induced Transcription in Osteoblasts

Molecular and Cellular Biology, 2008-08, Vol.28 (15), p.4759-4771

2008

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Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues

Bone (New York, N.Y.), 2014-06, Vol.63, p.101-109

2014

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p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice

The Journal of clinical investigation, 2012-06, Vol.122 (6), p.2153-2164

2012

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Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex

Journal of developmental biology, 2020-12, Vol.8 (4), p.30

2020

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The role of vertebrate models in understanding craniosynostosis

Child's nervous system, 2012-09, Vol.28 (9), p.1471-1481

Holmes, Greg

2012

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From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome

Disease models & mechanisms, 2013-05, Vol.6 (3), p.768-779

2013

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Therapy Discovery for Pharmacoresistant Epilepsy and for Disease‐modifying Therapeutics: Summary of the NIH/NINDS/AES Models II Workshop

Epilepsia, 2003-12, Vol.44 (12), p.1472-1478

2003

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Expression of slit‐2 and slit‐3 during chick development

Developmental dynamics, 2001-10, Vol.222 (2), p.301-307

2001

Volltextzugriff (PDF)

Mouse models of Apert syndrome

Child's nervous system, 2012-09, Vol.28 (9), p.1505-1510

Holmes, Greg

2012

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Processes and patterns: Insights on cranial covariation from an Apert syndrome mouse model

Developmental dynamics, 2022-10, Vol.251 (10), p.1684-1697

2022

Volltextzugriff (PDF)

Periodical cicadas (Magicicada spp.): Predator satiation, or too much of a good thing?

Great Lakes entomologist, 2023-09, Vol.56 (1)

2023

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Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome

Developmental biology, 2012-08, Vol.368 (2), p.283-293

2012

Volltextzugriff (PDF)

Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference

Pediatric neurology, 2013-10, Vol.49 (4), p.255-265

2013

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Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects

Development (Cambridge), 2018-10, Vol.145 (19)

2018

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Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology

Developmental biology, 2009-04, Vol.328 (2), p.273-284

2009

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Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis

Journal of visualized experiments, 2019-12 (154)

2019

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Mesodermal expression of Fgfr2 is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome

Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis

Single-cell analysis identifies a key role for Hhip in murine coronal suture development

Regulation of cranial morphogenesis and cell fate at the neural crest-mesoderm boundary by engrailed 1

Cleft Palate in Apert Syndrome

Sox2 induction by FGF and FGFR2 activating mutations inhibits Wnt signaling and osteoblast differentiation

C-type natriuretic peptide analog treatment of craniosynostosis in a Crouzon syndrome mouse model

The FaceBase Consortium: a comprehensive resource for craniofacial researchers

FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research

Fibroblast Growth Factor Signaling Uses Multiple Mechanisms To Inhibit Wnt-Induced Transcription in Osteoblasts

Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues

p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice

Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex

The role of vertebrate models in understanding craniosynostosis

From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome

Therapy Discovery for Pharmacoresistant Epilepsy and for Disease‐modifying Therapeutics: Summary of the NIH/NINDS/AES Models II Workshop

Expression of slit‐2 and slit‐3 during chick development

Mouse models of Apert syndrome

Processes and patterns: Insights on cranial covariation from an Apert syndrome mouse model

Periodical cicadas (Magicicada spp.): Predator satiation, or too much of a good thing?

Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome

Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference

Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects

Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology

Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis

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