Structure and function of the mammalian fibrillin gene family: implications for human connective tissue diseases.
about
Large animal models of cardiovascular diseaseRare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosisGenetic determinants of arterial stiffness.Transcriptional profiling of the human fibrillin/LTBP gene family, key regulators of mesenchymal cell functions.Live imaging of follicle stimulating hormone receptors in gonads and bones using near infrared II fluorophoreMarfanoid-progeroid-lipodystrophy syndrome: a newly recognized fibrillinopathy.Expression of FBN1 during adipogenesis: Relevance to the lipodystrophy phenotype in Marfan syndrome and related conditionsGWAS of 972 autologous stem cell recipients with multiple myeloma identifies 11 genetic variants associated with chemotherapy-induced oral mucositisEarly Impairment of Lung Mechanics in a Murine Model of Marfan Syndrome.Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome SequencingDecreased Desmin expression in the developing diaphragm of the nitrofen-induced congenital diaphragmatic hernia rat model.Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactylyAn Evaluation of Lysyl Oxidase-Derived Cross-Linking in Keratoconus by Liquid Chromatography/Mass Spectrometry.VE-statin/Egfl7 expression in malignant glioma and its relevant molecular networkDevelopment and pathologies of the arterial wall.Agonists and Antagonists of TGF-β Family Ligands.Vascular smooth muscle cells in Marfan syndrome aneurysm: the broken bricks in the aortic wall.Disruption of fibronectin matrix affects type IV collagen, fibrillin and laminin deposition into extracellular matrix of human trabecular meshwork (HTM) cells.Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome.Patients with non-tuberculous mycobacterial lung disease have elevated transforming growth factor-beta following ex vivo stimulation of blood with live Mycobacterium intracellulare.Fibrillin 2 is upregulated in the ascending aorta of patients with bicuspid aortic valve.Association study of common variations of FBN1 gene and essential hypertension in Han Chinese population.Exfoliation syndrome: assembling the puzzle pieces.Truncated C-terminus of fibrillin-1 induces Marfanoid-progeroid-lipodystrophy (MPL) syndrome in rabbit.Analysis of TGFBR1*6A variant in individuals evaluated for Marfan syndrome.
P2860
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P2860
Structure and function of the mammalian fibrillin gene family: implications for human connective tissue diseases.
description
2012 nî lūn-bûn
@nan
2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Structure and function of the ...... an connective tissue diseases.
@ast
Structure and function of the ...... an connective tissue diseases.
@en
Structure and function of the ...... an connective tissue diseases.
@nl
type
label
Structure and function of the ...... an connective tissue diseases.
@ast
Structure and function of the ...... an connective tissue diseases.
@en
Structure and function of the ...... an connective tissue diseases.
@nl
prefLabel
Structure and function of the ...... an connective tissue diseases.
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Structure and function of the ...... an connective tissue diseases.
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Structure and function of the ...... an connective tissue diseases.
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P1476
Structure and function of the ...... man connective tissue diseases
@en
P2093
Margaret R Davis
P304
P356
10.1016/J.YMGME.2012.07.023
P577
2012-08-03T00:00:00Z