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

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description	articolo scientifico (it) artículu científicu espublizáu en 2000 (ast) vědecký článek publikovaný v roce 2000 (cs) 2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած (hyw) wüsseschaftlicher Artikel, wo im April 2000 veröffentlicht worden isch (gsw) مقالة علمية (نشرت في أبريل 2000) (ar) 2000 թվականի ապրիլին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована у квітні 2000 (uk) im April 2000 veröffentlichter wissenschaftlicher Artikel (de) wetenschappelijk artikel (gepubliceerd op 2000/04/01) (nl) vedecký článok (publikovaný 2000/04/01) (sk) scientific journal article (en) article scientifique publié en avril 2000 (fr)
publication date	wds:Q28511870-5B1368AD-B69A-483C-8169-8EC637237BC0
publication date	2000-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28511870-C93E54EC-9612-49DE-AAC9-1DE3CCF2AEDC
language of work or name	English
cites work	wds:Q28511870-028ABDE5-80F1-4288-AE11-BB444DE44738 wds:Q28511870-04076CB2-24C1-471E-BC21-DED3342CCBCC wds:Q28511870-085FEA70-E244-48A0-A0E8-C5AFDB4848AD wds:Q28511870-0F7EA2DE-B1AB-4702-A857-4DD2CDD0DC65 wds:Q28511870-11D85909-505F-47BB-B33E-EB773BADE646 wds:Q28511870-236AC26C-69D4-4792-9933-7CB83F2BD6C8 wds:Q28511870-3185259E-87C5-4092-B8A4-BA898EF61C14 wds:Q28511870-40FC37C6-254B-465C-B378-4428E814D6E8 wds:Q28511870-50FA845B-78CD-4C59-8E6E-E8F27288012E wds:Q28511870-564A9DE9-53D3-4A35-8AEE-4143137DBCB6 wds:Q28511870-5D552EF1-F36E-4124-A863-6DE454A76659 wds:Q28511870-6CE579C4-6248-405F-B210-1AECF770BD71 wds:Q28511870-96CE9280-1CD4-40DC-AD19-99F4235A26E3 wds:Q28511870-A5E552C0-2914-4B23-99C5-9B13F5F2F76C wds:Q28511870-AC67C90E-13DF-4412-A23F-FE0904CE15CC wds:Q28511870-B170B843-5972-42D4-A189-31600E1E4621 wds:Q28511870-B1EFD92D-A33E-4916-9A3D-319F8CE0B693 wds:Q28511870-B923079B-A0A2-4A9B-BF73-B3F3771DDE5D wds:Q28511870-BC273B07-6DAB-4DF1-B0AC-240DC9943A03 wds:Q28511870-D51CCC4B-9FA5-4D88-81C8-6A1ECE354B94 wds:Q28511870-D8A68CF7-4F34-43EA-B341-A004FB092511 wds:Q28511870-E3021B62-410C-479D-9F17-80C9099FA59B
cites work	Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene A comprehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia 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 Haploinsufficiency of parathyroid hormone-related peptide (PTHrP) results in abnormal postnatal bone development Hereditary cranium bifidum and symmetric parietal foramina are the same entity Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development Basal cell carcinomas in mice overexpressing sonic hedgehog Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice Syndromic foramina parietalia permagna Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family FGF5 as a regulator of the hair growth cycle: evidence from targeted and spontaneous mutations The cells and molecules that make a cerebellum. 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. Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice Reciprocal regulation of osteocalcin transcription by the homeodomain proteins Msx2 and Dlx5. Ectopic Msx2 overexpression inhibits and Msx2 antisense stimulates calvarial osteoblast differentiation Epithelial cytodifferentiation and extracellular matrix formation in enamel-free areas of the occlusal cusp during development of mouse molars: light and electron microscopic studies
author name string	wds:Q28511870-1678DC1F-546A-491E-8149-3476F19F631B wds:Q28511870-2D2BD3AE-3AF0-4F61-86E9-D51DA6E07212 wds:Q28511870-37D9948E-C017-4270-BBC8-7C39EA9897D2 wds:Q28511870-4316A3A3-BB48-4A2F-871D-1DF3F9E4CB24 wds:Q28511870-68394936-E8F0-478A-B995-4E2B0959AEB6 wds:Q28511870-6DCFA5BA-B43F-40F8-9E18-AC1E2C37145D wds:Q28511870-81F4899B-8EE9-4DCF-9CCB-AD35B6BBA553 wds:Q28511870-841B88D1-2FF7-4CD5-9756-63B17D19AAB0 wds:Q28511870-8E23439A-68F0-4FE0-933D-3CFFBB9DD9B8 wds:Q28511870-9962E6A9-7CFF-4A8D-9F15-BC067190F620 wds:Q28511870-9D25EC98-4630-4D8D-86DC-DFB0739E93CA wds:Q28511870-BC387478-72FD-4933-80B3-77A0E47ECE01 wds:Q28511870-DE0F8610-E48F-49E1-A2C2-3DEC46AE4FBB wds:Q28511870-EFB70045-5B5D-4A60-BB9F-D9F831CD36A7
OpenCitations bibliographic resource ID	wds:Q28511870-C98968E7-69CE-4FAF-A0FF-8D13504A49BC
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/1784916
author name string	R. Maas L. Ma M. Uchiyama R. Maxson K. Nishizawa T. Maeda Y. Takano H. Peters H. Ohshima Z. Tang I. Satokata I. Woo M. Bei S. Heaney
OpenCitations bibliographic resource ID	1784916
rdfs:label	Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation (en) Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation (nl) Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation (ast)
skos:prefLabel	Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation (en) Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation (nl) Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation (ast)
name	Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation (en)

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