Cargando…

A dysmorphic mouse model reveals developmental interactions of chondrocranium and dermatocranium

The cranial endo and dermal skeletons, which comprise the vertebrate skull, evolved independently over 470 million years ago and form separately during embryogenesis. In mammals, much of the cartilaginous chondrocranium is transient, undergoing endochondral ossification or disappearing, so its role...

Descripción completa

Detalles Bibliográficos
Autores principales:	Motch Perrine, Susan M, Pitirri, M Kathleen, Durham, Emily L, Kawasaki, Mizuho, Zheng, Hao, Chen, Danny Z, Kawasaki, Kazuhiko, Richtsmeier, Joan T
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	eLife Sciences Publications, Ltd 2022
Materias:	Developmental Biology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259032/ https://www.ncbi.nlm.nih.gov/pubmed/35704354 http://dx.doi.org/10.7554/eLife.76653

Ejemplares similares

Meckel’s Cartilage in Mandibular Development and Dysmorphogenesis
por: Pitirri, M. Kathleen, et al.
Publicado: (2022)

Quantification of gene expression patterns to reveal the origins of abnormal morphogenesis
por: Martínez-Abadías, Neus, et al.
Publicado: (2018)

Evolution and development of the bird chondrocranium
por: Hüppi, Evelyn, et al.
Publicado: (2021)

Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
por: Motch Perrine, Susan M., et al.
Publicado: (2020)

Developmental and Evolutionary Significance of the Zygomatic Bone
por: Heuzé, Yann, et al.
Publicado: (2016)

Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes
por: Motch Perrine, Susan M., et al.
Publicado: (2017)

The biomechanical role of the chondrocranium and sutures in a lizard cranium
por: Jones, Marc E. H., et al.
Publicado: (2017)

On the development of the chondrocranium and the histological anatomy of the head in perinatal stages of marsupial mammals
por: Sánchez-Villagra, Marcelo R., et al.
Publicado: (2017)

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice
por: Motch Perrine, Susan M, et al.
Publicado: (2014)

Mouse Model of Congenital Heart Defects, Dysmorphic Facial Features and Intellectual Developmental Disorders as a Result of Non-functional CDK13
por: Nováková, Monika, et al.
Publicado: (2019)

Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice
por: Motch Perrine, Susan M., et al.
Publicado: (2019)

Ontogeny and phylogeny of the mammalian chondrocranium: the cupula nasi anterior and associated structures of the anterior head region
por: Hüppi, Evelyn, et al.
Publicado: (2018)

Acute upregulation of hedgehog signaling in mice causes differential effects on cranial morphology
por: Singh, Nandini, et al.
Publicado: (2015)

Biallelic Mutations in ACACA Cause a Disruption in Lipid Homeostasis That Is Associated With Global Developmental Delay, Microcephaly, and Dysmorphic Facial Features
por: Lou, Xiaoting, et al.
Publicado: (2021)

Single-cell analysis identifies a key role for Hhip in murine coronal suture development
por: Holmes, Greg, et al.
Publicado: (2021)

Developmental variability channels mouse molar evolution
por: Hayden, Luke, et al.
Publicado: (2020)

Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features
por: BERTOK, Sara, et al.
Publicado: (2015)

Phelan-McDermid syndrome presenting with developmental delays and facial dysmorphisms
por: Kim, Yoon-Myung, et al.
Publicado: (2016)

Total hip arthroplasty in an adult patient with pelvic dysmorphism, unilateral sacroiliac joint autofusion, and developmental hip dysplasia
por: Fassihi, Safa C., et al.
Publicado: (2019)

Developmental Stage-Specific Distribution of Macrophages in Mouse Mammary Gland
por: Stewart, Teneale A., et al.
Publicado: (2019)

A Computational Analysis of Bone Formation in the Cranial Vault in the Mouse
por: Lee, Chanyoung, et al.
Publicado: (2015)

Developmental, cellular, and behavioral phenotypes in a mouse model of congenital hypoplasia of the dentate gyrus
por: Rattner, Amir, et al.
Publicado: (2020)

Integration of mouse ovary morphogenesis with developmental dynamics of the oviduct, ovarian ligaments, and rete ovarii
por: McKey, Jennifer, et al.
Publicado: (2022)

Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
por: Seo, Go Hun, et al.
Publicado: (2016)

De novo PHIP-predicted deleterious variants are associated with developmental delay, intellectual disability, obesity, and dysmorphic features
por: Webster, Emily, et al.
Publicado: (2016)

Body dysmorphic disorder
por: Bjornsson, Andri S., et al.
Publicado: (2010)

Validation of Spanish Language Evaluation Instruments for Body Dysmorphic Disorder and the Dysmorphic Concern Construct
por: Senín-Calderón, Cristina, et al.
Publicado: (2017)

Functions of Oxysterol-Binding Proteins at Membrane Contact Sites and Their Control by Phosphoinositide Metabolism
por: Nakatsu, Fubito, et al.
Publicado: (2021)

Differential Regenerative Capacity of the Optic Tectum of Adult Medaka and Zebrafish
por: Shimizu, Yuki, et al.
Publicado: (2021)

Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features
por: Hu, Jie, et al.
Publicado: (2011)

Non-mosaic partial duplication 12p in a patient with dysmorphic characteristics and developmental delay
por: Oliveira, Jakeline Santos, et al.
Publicado: (2020)

Novel cell types and developmental lineages revealed by single-cell RNA-seq analysis of the mouse crista ampullaris
por: Wilkerson, Brent A, et al.
Publicado: (2021)

Developmental biology
por: Browder, Leon W.
Publicado: (1991)

The Developmental Basis of Quantitative Craniofacial Variation in Humans and Mice
por: Martínez-Abadías, Neus, et al.
Publicado: (2012)

Developmental Functions of the Dynamic DNA Methylome and Hydroxymethylome in the Mouse and Zebrafish: Similarities and Differences
por: Jessop, Peter, et al.
Publicado: (2018)

Hypoparathyroidism-retardation-dysmorphism syndrome
por: Kumar, Kalenahalli Jagadish, et al.
Publicado: (2013)

Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search
por: Vrachnis, Nikolaos, et al.
Publicado: (2021)

Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations
por: Sirisena, Nirmala D., et al.
Publicado: (2013)

A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms
por: Hladilkova, Eva, et al.
Publicado: (2015)

A Review of the Genomic Analysis of Children Presenting with Developmental Delay/Intellectual Disability and Associated Dysmorphic Features
por: Vickers, Ramiah R, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_e1jv66eodl5pnq2cvdbovlkkb4