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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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Phosphotungstic acid‐enhanced microCT: Optimized protocols for embryonic and early postnatal mice

Developmental dynamics, 2020-04, Vol.249 (4), p.573-585

2020

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A dysmorphic mouse model reveals developmental interactions of chondrocranium and dermatocranium

eLife, 2022-06, Vol.11

2022

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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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Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes

Frontiers in human neuroscience, 2017-07, Vol.11, p.369-369

2017

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Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice

Disease models & mechanisms, 2019-05, Vol.12 (5)

2019

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Quantification of gene expression patterns to reveal the origins of abnormal morphogenesis

eLife, 2018-09, Vol.7

2018

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Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

BMC developmental biology, 2014-02, Vol.14 (1), p.8-8, Article 8

2014

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Altered metabolism and resistance to obesity in long-lived mice producing reduced levels of IGF-I

American journal of physiology: endocrinology and metabolism, 2015-04, Vol.308 (7), p.E545-E553

2015

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Cartilage Segmentation in High-Resolution 3D Micro-CT Images via Uncertainty-Guided Self-training with Very Sparse Annotation

Medical Image Computing and Computer Assisted Intervention – MICCAI 2020, 2020-10, p.802-812

2020

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Meckel's Cartilage in Mandibular Development and Dysmorphogenesis

Frontiers in genetics, 2022-05, Vol.13, p.871927-871927

2022

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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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Meckel’s Cartilage and Mandibles: Effects of the Fgfr2 C342Y mutation on development of the lower jaw in a Crouzon syndrome mouse model

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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Small Brains, Small Skulls: Effect of Cortex Specific Overexpression of BAF170 on the Mouse Cranium

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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Cortex Specific Overexpression of BAF170 and Growth of the Cranial Base, Cranial Vault, and Facial Skeleton in Mice

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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Embryonic cranial cartilage defects in the Fgfr3 Y367C /+ mouse model of achondroplasia

Anatomical record (Hoboken, N.J. : 2007), 2023-09

2023

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Embryonic cranial cartilage defects in the Fgfr3Y367C /+ mouse model of achondroplasia

Anatomical record (Hoboken, N.J. : 2007), 2023-09

2023

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Postnatal Cranial Characterization in a Mouse Model of Cortex‐Specific Overexpression of BAF170

The FASEB journal, 2021-05, Vol.35 (S1), p.n/a, Article fasebj.2021.35.S1.03647

2021

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Abnormalities in Cartilage in Embryonic Fgfr2cC342Y/+ Crouzon Syndrome Mice

The FASEB journal, 2021-05, Vol.35, p.n/a

2021

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Abnormalities in Cartilage in Embryonic Fgfr2c C342Y/+ Crouzon Syndrome Mice

The FASEB journal, 2021-05, Vol.35 (S1), Article fasebj.2021.35.S1.01830

2021

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Late embryonic skull anomalies in mice carrying the Fgfr2 W290R Crouzon mutation

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1

2020

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Assessing Gene Expression Patterns in Mouse Models to Test Hypotheses About Human Head Evolution

The FASEB journal, 2021-05, Vol.35 (S1), p.n/a, Article fasebj.2021.35.S1.03594

2021

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Identification of a Novel Vomer Phenotype in the Fgfr2c C342Y/+ Mouse Model of Crouzon Syndrome

The FASEB journal, 2018-04, Vol.32 (S1), p.776.12-776.12

2018

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Three‐dimensional visualization of cranial soft tissues in embryonic and early postnatal mice using phosphotungstic acid enhanced microCT

The FASEB journal, 2019-04, Vol.33 (S1), p.453.1-453.1

2019

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Come together over me: Cells that form the dermatocranium and chondrocranium in mice

Anatomical record (Hoboken, N.J. : 2007), 2023-07

2023

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

Phosphotungstic acid‐enhanced microCT: Optimized protocols for embryonic and early postnatal mice

A dysmorphic mouse model reveals developmental interactions of chondrocranium and dermatocranium

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

Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes

Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice

Quantification of gene expression patterns to reveal the origins of abnormal morphogenesis

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice

Altered metabolism and resistance to obesity in long-lived mice producing reduced levels of IGF-I

Cartilage Segmentation in High-Resolution 3D Micro-CT Images via Uncertainty-Guided Self-training with Very Sparse Annotation

Meckel's Cartilage in Mandibular Development and Dysmorphogenesis

Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex

Meckel’s Cartilage and Mandibles: Effects of the Fgfr2 C342Y mutation on development of the lower jaw in a Crouzon syndrome mouse model

Small Brains, Small Skulls: Effect of Cortex Specific Overexpression of BAF170 on the Mouse Cranium

Cortex Specific Overexpression of BAF170 and Growth of the Cranial Base, Cranial Vault, and Facial Skeleton in Mice

Embryonic cranial cartilage defects in the Fgfr3 Y367C /+ mouse model of achondroplasia

Embryonic cranial cartilage defects in the Fgfr3Y367C /+ mouse model of achondroplasia

Postnatal Cranial Characterization in a Mouse Model of Cortex‐Specific Overexpression of BAF170

Abnormalities in Cartilage in Embryonic Fgfr2cC342Y/+ Crouzon Syndrome Mice

Abnormalities in Cartilage in Embryonic Fgfr2c C342Y/+ Crouzon Syndrome Mice

Late embryonic skull anomalies in mice carrying the Fgfr2 W290R Crouzon mutation

Assessing Gene Expression Patterns in Mouse Models to Test Hypotheses About Human Head Evolution

Identification of a Novel Vomer Phenotype in the Fgfr2c C342Y/+ Mouse Model of Crouzon Syndrome

Three‐dimensional visualization of cranial soft tissues in embryonic and early postnatal mice using phosphotungstic acid enhanced microCT

Come together over me: Cells that form the dermatocranium and chondrocranium in mice

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