FGFs, their receptors, and human limb malformations: clinical and molecular correlations. - sprookjes - yvandenbroek - TriplyDB

FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

http://www.wikidata.org/entity/Q34926833

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Cbl-mediated degradation of Lyn and Fyn induced by constitutive fibroblast growth factor receptor-2 activation supports osteoblast differentiation A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23 A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome Paternal age effect mutations and selfish spermatogonial selection: causes and consequences for human disease Molecular mechanisms of fibroblast growth factor signaling in physiology and pathology Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis Prox1 promotes lineage-specific expression of fibroblast growth factor (FGF) receptor-3 in lymphatic endothelium: a role for FGF signaling in lymphangiogenesis Developmental and Evolutionary Significance of the Zygomatic Bone Development and evolution of the amniote integument: current landscape and future horizon Patterns of somatic mutation in human cancer genomes Looking at cerebellar malformations through text-mined interactomes of mice and humans Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.Gain-of-function amino acid substitutions drive positive selection of FGFR2 mutations in human spermatogonia Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk.A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities.Analysis of the biochemical mechanisms for the endocrine actions of fibroblast growth factor-23 Serial homology and the evolution of mammalian limb covariation structure.Molecular basis of cranial suture biology and disease: Osteoblastic and osteoclastic perspectives Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.Pictorial essay: The many faces of craniosynostosis.Defective osteogenic differentiation in the development of osteosarcoma.PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption Inducible suppression of Fgfr2 and Survivin in ES cells using a combination of the RNA interference (RNAi) and the Cre-LoxP system.FGF signalling restricts haematopoietic stem cell specification via modulation of the BMP pathway.Positional plasticity in regenerating Amybstoma mexicanum limbs is associated with cell proliferation and pathways of cellular differentiation.FGF signaling in the developing endochondral skeleton.Fibroblast growth factor receptor 1 signaling in the osteo-chondrogenic cell lineage regulates sequential steps of osteoblast maturation Urothelial tumorigenesis: a tale of divergent pathways.A case of Pfeiffer syndrome The Current and Future Therapies for Human Osteosarcoma.Osteosarcoma development and stem cell differentiation Negative regulation of fibroblast growth factor 10 (FGF-10) by polyoma enhancer activator 3 (PEA3).FGFR2 as a molecular target in endometrial cancer.Whole exome sequencing of adenoid cystic carcinoma.Interdigital cell death function and regulation: new insights on an old programmed cell death model.P-15 cell-binding domain derived from collagen: analysis of MG63 osteoblastic-cell response by means of a microarray technology.The two domain hypothesis of limb prepattern and its relevance to congenital limb anomalies.Bone marker gene expression in calvarial bones: different bone microenvironments.

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P2860

FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

http://www.wikidata.org/entity/Q34926833

description

2002 nî lūn-bûn

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2002 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2002年の論文

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name

FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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type

label

FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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American Journal of Medical Genetics Part A

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FGFs, their receptors, and human limb malformations: clinical and molecular correlations.

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Ans M W van den Ouweland

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Ben C J Hamel

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Shih-Hsin Kan

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Susannah J Patey

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P2860

Structural basis for FGF receptor dimerization and activation

Structural interactions of fibroblast growth factor receptor with its ligands

Crystal structures of two FGF-FGFR complexes reveal the determinants of ligand-receptor specificity

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

Crystal structure of fibroblast growth factor receptor ectodomain bound to ligand and heparin

Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

Receptor specificity of the fibroblast growth factor family

Fibroblast growth factors

Structure of the FGF receptor tyrosine kinase domain reveals a novel autoinhibitory mechanism

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3

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Andrew Oliver Mungo Wilkie

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2002-10-01T00:00:00Z

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11100973

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