Defective neural crest migration revealed by a Zebrafish model of Alx1-related frontonasal dysplasia (Q45768286)

15 December 2017

title

Defective neural crest migration revealed by a Zebrafish model of Alx1-related frontonasal dysplasia (English)

1 reference

15 December 2017

main subject

ALX homeobox 1

1 reference

GOA release 2020-03-11

Tokiharu Takahashi

4

0 references

author name string

Chris T Dee

series ordinal

1

1 reference

15 December 2017

Christoph R Szymoniuk

series ordinal

2

1 reference

15 December 2017

Peter E D Mills

series ordinal

3

1 reference

15 December 2017

publication date

11 October 2012

1 reference

15 December 2017

published in

Human Molecular Genetics

1 reference

15 December 2017

volume

22

1 reference

15 December 2017

issue

2

1 reference

15 December 2017

page(s)

239-251

1 reference

15 December 2017

Cranial neural crest and development of the head skeleton

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

The eye as an organizer of craniofacial development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Palatogenesis: morphogenetic and molecular mechanisms of secondary palate development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Evolving maps in craniofacial development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Cleft lip and palate: understanding genetic and environmental influences

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Frontonasal malformation as a field defect and in syndromic associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

21 January 2018

Frontonasal dysplasia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

ALX4 dysfunction disrupts craniofacial and epidermal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Clinical and genetic characterization of frontorhiny: report of 3 novel cases and discussion of the surgical management

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

The gene for the homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Mouse Alx3: an aristaless-like homeobox gene expressed during embryogenesis in ectomesenchyme and lateral plate mesoderm

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Expression patterns of group-I aristaless-related genes during craniofacial and limb development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Alx3-deficient mice exhibit folic acid-resistant craniofacial midline and neural tube closure defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Regulation of facial morphogenesis by endothelin signaling: insights from mice and fish.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Early Hedgehog signaling from neural to oral epithelium organizes anterior craniofacial development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Hedgehog signaling is required for cranial neural crest morphogenesis and chondrogenesis at the midline in the zebrafish skull.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Examination of a palatogenic gene program in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Neural crest derivatives in ocular and periocular structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Genetics of shoulder girdle formation: roles of Tbx15 and aristaless-like genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Function and regulation of Alx4 in limb development: complex genetic interactions with Gli3 and Shh.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Mechanisms driving neural crest induction and migration in the zebrafish and Xenopus laevis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

A gene regulatory network orchestrates neural crest formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

A zebrafish model of axenfeld-rieger syndrome reveals that pitx2 regulation by retinoic acid is essential for ocular and craniofacial development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

pitx2 Deficiency results in abnormal ocular and craniofacial development in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

tp53 mutant zebrafish develop malignant peripheral nerve sheath tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

p53 activation by knockdown technologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Sox10 is required for the early development of the prospective neural crest in Xenopus embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Tfap2a and Foxd3 regulate early steps in the development of the neural crest progenitor population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Zebrafish Foxd3 is required for development of a subset of neural crest derivatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Zebrafish foxd3 is selectively required for neural crest specification, migration and survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Disc1 regulates foxd3 and sox10 expression, affecting neural crest migration and differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Overexpression of the transcriptional repressor FoxD3 prevents neural crest formation in Xenopus embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

FOXD3 regulates migration properties and Rnd3 expression in melanoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

The contribution of both forebrain and midbrain crest cells to the mesenchyme in the frontonasal mass of mouse embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Subtypes of frontonasal dysplasia are useful in determining clinical prognosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Frontonasal dysplasia in two successive generations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Duplication of the EFNB1 gene in familial hypertelorism: imbalance in ephrin-B1 expression and abnormal phenotypes in humans and mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

EphA receptor signaling--complexity and emerging themes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Ephrin-B1 forward and reverse signaling are required during mouse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

The EphA4 and EphB1 receptor tyrosine kinases and ephrin-B2 ligand regulate targeted migration of branchial neural crest cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

ADAM13 induces cranial neural crest by cleaving class B Ephrins and regulating Wnt signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Frontonasal dysplasia in 3H1 Br/Br mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Neural crest cell survival is dependent on Rho kinase and is required for development of the mid face in mouse embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

The eye organizes neural crest cell migration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Genetics of anterior segment dysgenesis disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Development of the vertebrate central nervous system: formation of the neural tube.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Cellular mechanisms of posterior neural tube morphogenesis in the zebrafish.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

N-cadherin is required for the polarized cell behaviors that drive neurulation in the zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Frontonasal dysplasia: analysis of 21 cases and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Genetically altered mouse models: the good, the bad, and the ugly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Molecular mechanisms of cranial neural crest cell migration and patterning in craniofacial development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Molecular bases of human neurocristopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

Stages of embryonic development of the zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

A two-color acid-free cartilage and bone stain for zebrafish larvae.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS423

21 January 2018

Identifiers

DOI

10.1093/HMG/DDS423

1 reference

15 December 2017

PubMed ID

23059813

1 reference

15 December 2017