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Notch regulation of bone development and remodeling and related skeletal disorders

Notch regulation of bone development and remodeling and related skeletal disorders

http://www.wikidata.org/entity/Q27021132

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Cilia/Ift protein and motor -related bone diseases and mouse models Current insights on the regenerative potential of the periosteum: molecular, cellular, and endogenous engineering approaches Notch signaling in osteocytes differentially regulates cancellous and cortical bone remodeling Identification and characterization of regulatory elements in the promoter of ACVR1, the gene mutated in Fibrodysplasia Ossificans Progressiva.Pathological fracture of the femur in Alagille syndrome that was treated with low-intensity pulsed ultrasound stimulation and an Ilizarov ring fixator: a case report.Vitamin D: direct effects of vitamin D metabolites on bone: lessons from genetically modified mice.Hajdu-Cheney syndrome: a review.Jagged1 is essential for osteoblast development during maxillary ossification.Function and regulation of primary cilia and intraflagellar transport proteins in the skeleton Dkk1 haploinsufficiency requires expression of Bmp2 for bone anabolic activity Notch signaling in skeletal health and disease.Osteocytes and Skeletal Pathophysiology Hajdu Cheney Mouse Mutants Exhibit Osteopenia, Increased Osteoclastogenesis, and Bone Resorption.Notch signaling in chondrocytes modulates endochondral ossification and osteoarthritis development.Cisplatin selects for stem-like cells in osteosarcoma by activating Notch signaling.Notch signaling in skeletal stem cells.Hajdu-Cheney Syndrome, a Disease Associated with NOTCH2 Mutations.Transcriptional Networks in Single Perivascular Cells Sorted from Human Adipose Tissue Reveal a Hierarchy of Mesenchymal Stem Cells.How rare bone diseases have informed our knowledge of complex diseases.Loss of Notch3 Signaling Enhances Osteogenesis of Mesenchymal Stem Cells from Mandibular Torus.Rho/ROCK-dependent inhibition of 3T3-L1 adipogenesis by G-protein-deamidating dermonecrotic toxins: differential regulation of Notch1, Pref1/Dlk1, and β-catenin signaling.An unusual presentation of diabetic ketoacidosis in familial hajdu-cheney syndrome: a case report.Report of the CCFA pediatric bone, growth and muscle health workshop, New York City, November 11-12, 2011, with updates.Notch signaling negatively regulates BMP9-induced osteogenic differentiation of mesenchymal progenitor cells by inhibiting JunB expression.Alagille syndrome case report: implications for forensic pathology and anthropology.Clinical consequences in truncating mutations in exon 34 of NOTCH2: report of six patients with Hajdu-Cheney syndrome and a patient with serpentine fibula polycystic kidney syndrome.Effects of microgravity simulation on zebrafish transcriptomes and bone physiology-exposure starting at 5 days post fertilization.NOTCH3 expression is linked to breast cancer seeding and distant metastasis

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Notch regulation of bone development and remodeling and related skeletal disorders

http://www.wikidata.org/entity/Q27021132

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2012 nî lūn-bûn

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2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2012 թվականի փետրվարին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Notch regulation of bone development and remodeling and related skeletal disorders

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Notch regulation of bone development and remodeling and related skeletal disorders

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Notch regulation of bone development and remodeling and related skeletal disorders

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Notch regulation of bone development and remodeling and related skeletal disorders

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Notch regulation of bone development and remodeling and related skeletal disorders

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Notch regulation of bone development and remodeling and related skeletal disorders

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Notch regulation of bone development and remodeling and related skeletal disorders

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Notch regulation of bone development and remodeling and related skeletal disorders

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Notch regulation of bone development and remodeling and related skeletal disorders

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P2860

Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome

NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway

Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss

Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis

Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signaling

Mutation of the fucose-specific beta1,3 N-acetylglucosaminyltransferase LFNG results in abnormal formation of the spine

Mutated MESP2 causes spondylocostal dysostosis in humans.

Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype

Direct inhibition of the NOTCH transcription factor complex

Osteoclasts: what do they do and how do they do it?

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