Related references
Note: Only part of the references are listed.Quantitative Morphologic Analysis of Cranial Vault in Twist1+/- Mice: Implications in Craniosynostosis
Takashi Nuri et al.
PLASTIC AND RECONSTRUCTIVE SURGERY (2022)
Mechanical loading of cranial joints minimizes the craniofacial phenotype in Crouzon syndrome
Mehran Moazen et al.
SCIENTIFIC REPORTS (2022)
Cranial Suture Regeneration Mitigates Skull and Neurocognitive Defects in Craniosynostosis
Mengfei Yu et al.
CELL (2021)
PIN1 Attenuation Improves Midface Hypoplasia in a Mouse Model of Apert Syndrome
B. Kim et al.
JOURNAL OF DENTAL RESEARCH (2020)
Mouse Models of Syndromic Craniosynostosis
Kevin K. L. Lee et al.
MOLECULAR SYNDROMOLOGY (2019)
Predicting calvarial growth in normal and craniosynostotic mice using a computational approach
Arsalan Marghoub et al.
JOURNAL OF ANATOMY (2018)
Intracranial Volume and Head Circumference in Children with Unoperated Syndromic Craniosynostosis
Richard William Francis Breakey et al.
PLASTIC AND RECONSTRUCTIVE SURGERY (2018)
Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes
Susan M. Motch Perrine et al.
FRONTIERS IN HUMAN NEUROSCIENCE (2017)
Modelling human skull growth: a validated computational model
Joseph Libby et al.
JOURNAL OF THE ROYAL SOCIETY INTERFACE (2017)
Postnatal Craniofacial Skeletal Development of Female C57BL/6NCrl Mice
Xiaoxi Wei et al.
FRONTIERS IN PHYSIOLOGY (2017)
Size, shape, and form: concepts of allometry in geometric morphometrics
Christian Peter Klingenberg
DEVELOPMENT GENES AND EVOLUTION (2016)
Developmental Regulation of the Growth Plate and Cranial Synchondrosis
X. Wei et al.
JOURNAL OF DENTAL RESEARCH (2016)
Understanding craniosynostosis as a growth disorder
Kevin Flaherty et al.
WILEY INTERDISCIPLINARY REVIEWS-DEVELOPMENTAL BIOLOGY (2016)
Postnatal Ontogeny of the Cranial Base and Craniofacial Skeleton in Male C57BL/6J Mice: A Reference Standard for Quantitative Analysis
Siddharth R. Vora et al.
FRONTIERS IN PHYSIOLOGY (2016)
The Fibroblast Growth Factor signaling pathway
David M. Ornitz et al.
WILEY INTERDISCIPLINARY REVIEWS-DEVELOPMENTAL BIOLOGY (2015)
Craniofacial Shape Variation in Twist1+/- Mutant Mice
Trish E. Parsons et al.
ANATOMICAL RECORD-ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY (2014)
Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice
Susan M. Motch Perrine et al.
BMC DEVELOPMENTAL BIOLOGY (2014)
Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome
Aimee L. Fenwick et al.
BMC MEDICAL GENETICS (2014)
Premature Closure of the Spheno-occipital Synchondrosis in Pfeiffer Syndrome: A Link to Midface Hypoplasia
James Thomas Paliga et al.
JOURNAL OF CRANIOFACIAL SURGERY (2014)
The Spheno-Occipital Synchondrosis Fuses Prematurely in Patients With Crouzon Syndrome and Midface Hypoplasia Compared With Age- and Gender-Matched Controls
Youssef Tahiri et al.
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY (2014)
Molecular basis of cranial suture biology and disease: Osteoblastic and osteoclastic perspectives
Maureen Beederman et al.
GENES & DISEASES (2014)
Hand in glove: brain and skull in development and dysmorphogenesis
Joan T. Richtsmeier et al.
ACTA NEUROPATHOLOGICA (2013)
Postnatal brain and skull growth in an Apert syndrome mouse model
Cheryl A. Hill et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2013)
Further Analysis of the Crouzon Mouse: Effects of the FGFR2C342Y Mutation Are Cranial Bone-Dependent
Jin Liu et al.
CALCIFIED TISSUE INTERNATIONAL (2013)
Tissue-specific responses to aberrant FGF signaling in complex head phenotypes
Neus Martinez-Abadias et al.
DEVELOPMENTAL DYNAMICS (2013)
Interrelationship of Cranial Suture Fusion, Basicranial Development, and Resynostosis Following Suturectomy in Twist1+/- Mice, a Murine Model of Saethre-Chotzen Syndrome
Christopher D. Hermann et al.
CALCIFIED TISSUE INTERNATIONAL (2012)
Differential Closure of the Spheno-occipital Synchondrosis in Syndromic Craniosynostosis
Jennifer McGrath et al.
PLASTIC AND RECONSTRUCTIVE SURGERY (2012)
Facial Suture Synostosis of Newborn Fgfr1P250R/+ and Fgfr2S252W/+ Mouse Models of Pfeiffer and Apert Syndromes
Roopa Purushothaman et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2011)
The primary site of the acrocephalic feature in Apert syndrome is a dwarf cranial base with accelerated chondrocytic differentiation due to aberrant activation of the FGFR2 signaling
Masaki Nagata et al.
BONE (2011)
Effect of Three Types of Mixed Anesthetic Agents Alternate to Ketamine in Mice
Sumiko KAWAI et al.
EXPERIMENTAL ANIMALS (2011)
MorphoJ: an integrated software package for geometric morphometrics
Christian Peter Klingenberg
MOLECULAR ECOLOGY RESOURCES (2011)
Beyond the Closed Suture in Apert Syndrome Mouse Models: Evidence of Primary Effects of FGFR2 Signaling on Facial Shape at Birth
Neus Martinez-Abadias et al.
DEVELOPMENTAL DYNAMICS (2010)
Pivotal role of Twist in skeletal biology and pathology
Hichem Miraoui et al.
GENE (2010)
Evolution and development of shape: integrating quantitative approaches
Christian Peter Klingenberg
NATURE REVIEWS GENETICS (2010)
A twist of insight - the role of Twist-family bHLH factors in development
Ralston M. Barnes et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY (2009)
A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003
Sheree L. Boulet et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
Liangjun Yin et al.
BONE (2008)
Twist1 homodimers enhance FGF responsiveness of the cranial sutures and promote suture closure
Jeannette Connerney et al.
DEVELOPMENTAL BIOLOGY (2008)
Cranial Sutures: A Brief Review
Bethany J. Slater et al.
PLASTIC AND RECONSTRUCTIVE SURGERY (2008)
Twist1 dimer selection regulates cranial suture patterning and fusion
Jeannette Connerney et al.
DEVELOPMENTAL DYNAMICS (2006)
Abnormalities in cartilage and bone development in the Apert syndrome FGFR2+/S252W mouse
YL Wang et al.
DEVELOPMENT (2005)
Progressive postnatal craniosynostosis and increased intracranial pressure
JP Connolly et al.
PLASTIC AND RECONSTRUCTIVE SURGERY (2004)
A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis
VP Eswarakumar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Geometric morphometrics: ten years of progress following the 'revolution'
DC Adams et al.
ITALIAN JOURNAL OF ZOOLOGY (2004)
A Ser250Trp substitution in mouse fibroblast growth factor receptor 2 (Fgfr2) results in craniosynostosis
L Chen et al.
BONE (2003)
Morphological relationship between the cranial base and dentofacial complex obtained by reconstructive computer tomographic images
I Hayashi
EUROPEAN JOURNAL OF ORTHODONTICS (2003)
Fgfr mRNA isoforms in craniofacial bone development
DPC Rice et al.
BONE (2003)
Craniosynostosis in Twist heterozygous mice:: A model for Saethre-Chotzen syndrome
EA Carver et al.
ANATOMICAL RECORD (2002)
FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease
DM Ornitz et al.
GENES & DEVELOPMENT (2002)
Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome
OA Ibrahimi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Crystal structures of two FGF-FGFR complexes reveal the determinants of ligand-receptor specificity
AN Plotnikov et al.
CELL (2000)