(Q28511870)

25 January 2017

title

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation (English)

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25 January 2017

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GOA release 2020-03-11

Msh homeobox 1

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GOA release 2020-03-11

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I. Satokata

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25 January 2017

L. Ma

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25 January 2017

H. Ohshima

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25 January 2017

M. Bei

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25 January 2017

I. Woo

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25 January 2017

K. Nishizawa

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25 January 2017

T. Maeda

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25 January 2017

Y. Takano

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25 January 2017

M. Uchiyama

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25 January 2017

S. Heaney

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25 January 2017

H. Peters

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25 January 2017

Z. Tang

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25 January 2017

R. Maxson

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25 January 2017

R. Maas

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25 January 2017

language of work or name

English

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publication date

1 April 2000

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25 January 2017

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25 January 2017

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25 January 2017

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25 January 2017

page(s)

391–395

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

25 January 2017

cites work

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7 January 2021

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

1 reference

7 January 2021

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

1 reference

7 January 2021

Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans.

1 reference

7 January 2021

Ectopic Msx2 overexpression inhibits and Msx2 antisense stimulates calvarial osteoblast differentiation

1 reference

7 January 2021

Reciprocal regulation of osteocalcin transcription by the homeodomain proteins Msx2 and Dlx5.

1 reference

7 January 2021

Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein

1 reference

7 January 2021

Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene

1 reference

7 January 2021

PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth

1 reference

7 January 2021

Haploinsufficiency of parathyroid hormone-related peptide (PTHrP) results in abnormal postnatal bone development

1 reference

7 January 2021

Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice

1 reference

7 January 2021

The cells and molecules that make a cerebellum.

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7 January 2021

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

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7 January 2021

FGF5 as a regulator of the hair growth cycle: evidence from targeted and spontaneous mutations

1 reference

7 January 2021

Hereditary cranium bifidum and symmetric parietal foramina are the same entity

1 reference

7 January 2021

Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family

1 reference

7 January 2021

Syndromic foramina parietalia permagna

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7 January 2021

Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia

1 reference

7 January 2021

Epithelial cytodifferentiation and extracellular matrix formation in enamel-free areas of the occlusal cusp during development of mouse molars: light and electron microscopic studies

1 reference

7 January 2021

A comprehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis

1 reference

7 January 2021

Basal cell carcinomas in mice overexpressing sonic hedgehog

1 reference

7 January 2021

Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice

1 reference

7 January 2021