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

1

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25 January 2017

L. Ma

2

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H. Ohshima

3

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M. Bei

4

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I. Woo

5

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K. Nishizawa

6

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T. Maeda

7

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Y. Takano

8

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M. Uchiyama

9

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S. Heaney

10

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H. Peters

11

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Z. Tang

12

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R. Maxson

13

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R. Maas

14

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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

volume

24

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25 January 2017

issue

4

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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

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7 January 2021

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

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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.

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7 January 2021

Ectopic Msx2 overexpression inhibits and Msx2 antisense stimulates calvarial osteoblast differentiation

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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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

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7 January 2021

Hereditary cranium bifidum and symmetric parietal foramina are the same entity

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7 January 2021

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

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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

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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

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7 January 2021

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

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7 January 2021

Basal cell carcinomas in mice overexpressing sonic hedgehog

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7 January 2021

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

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7 January 2021