Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice. (Q52195908)

26 April 2018

title

Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice. (English)

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26 April 2018

11

Semenza GL

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26 April 2018

Winograd J

1

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26 April 2018

Reilly MP

2

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26 April 2018

Roe R

3

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26 April 2018

Lutz J

4

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26 April 2018

Laughner E

5

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26 April 2018

Xu X

6

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26 April 2018

Hu L

7

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26 April 2018

Asakura T

8

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26 April 2018

vander Kolk C

9

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26 April 2018

Strandberg JD

10

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26 April 2018

publication date

1 March 1997

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26 April 2018

published in

Human Molecular Genetics

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26 April 2018

volume

6

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26 April 2018

issue

3

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26 April 2018

page(s)

369-379

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26 April 2018

A distinct Hox code for the branchial region of the vertebrate head

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Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression

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Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest

21 January 2018

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A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene

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Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5

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Differential and overlapping expression domains of Dlx-2 and Dlx-3 suggest distinct roles for Distal-less homeobox genes in craniofacial development.

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Cloning and characterization of two members of the vertebrate Dlx gene family

21 January 2018

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A new family of mouse homeo box-containing genes: molecular structure, chromosomal location, and developmental expression of Hox-7.1.

21 January 2018

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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

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The membranous skeleton: the role of cell condensations in vertebrate skeletogenesis

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Newly recognized autosomal dominant disorder with craniosynostosis

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DNA binding and transcriptional properties of wild-type and mutant forms of the homeodomain protein Msx2

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A human MSX1 homeodomain missense mutation causes selective tooth agenesis

21 January 2018

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Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

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The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome.

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Regulation of the Msx2 homeobox gene during mouse embryogenesis: a transgene with 439 bp of 5' flanking sequence is expressed exclusively in the apical ectodermal ridge of the developing limb

21 January 2018

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Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull

21 January 2018

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Comparison of MSX-1 and MSX-2 suggests a molecular basis for functional redundancy

21 January 2018

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Position-dependent expression of two related homeobox genes in developing vertebrate limbs

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The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages

21 January 2018

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Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain

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Functional analysis of activins during mammalian development.

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Different phenotypes for mice deficient in either activins or activin receptor type II

21 January 2018

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Multiple defects and perinatal death in mice deficient in follistatin

21 January 2018

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Activin/inhibin beta B subunit gene disruption leads to defects in eyelid development and female reproduction.

21 January 2018

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Chondrodystrophic mice with coincidental agnathia: evidence for the tongue obstruction hypothesis in cleft palate

21 January 2018

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Homeotic transformation of the occipital bones of the skull by ectopic expression of a homeobox gene

21 January 2018

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Transcription factor AP-2 essential for cranial closure and craniofacial development

21 January 2018

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Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2

21 January 2018

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Experimental fetal alcohol syndrome: proposed pathogenic basis for a variety of associated facial and brain anomalies

21 January 2018

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Patterns of ethanol-induced cell death in the developing nervous system of mice; neural fold states through the time of anterior neural tube closure

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Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

21 January 2018

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Experimental analysis of Msx-1 and Msx-2 gene expression during chick mandibular morphogenesis

21 January 2018

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12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/6.3.369

Genomic structure, chromosomal location, and evolution of the mouse Hox 8 gene

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/6.3.369

MHox: a mesodermally restricted homeodomain protein that binds an essential site in the muscle creatine kinase enhancer

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12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/6.3.369

Ethanol-induced teratogenesis: free radical damage as a possible mechanism

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12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1093/HMG/6.3.369

Identifiers

DOI

10.1093/HMG/6.3.369

1 reference

26 April 2018

PubMed ID

9147639

1 reference

26 April 2018