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注意:仅列出部分参考文献,下载原文获取全部文献信息。Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease
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Loss of fibulin-4 results in abnormal collagen fibril assembly in bone, caused by impaired lysyl oxidase processing and collagen cross-linking
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Emilin3 is required for notochord sheath integrity and interacts with Scube2 to regulate notochord-derived Hedgehog signals
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Inactivation of Anoctamin-6/Tmem16f, a Regulator of Phosphatidylserine Scrambling in Osteoblasts, Leads to Decreased Mineral Deposition in Skeletal Tissues
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EMILIN-3, Peculiar Member of Elastin Microfibril Interface-located Protein (EMILIN) Family, Has Distinct Expression Pattern, Forms Oligomeric Assemblies, and Serves as Transforming Growth Factor β (TGF-β) Antagonist
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JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
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EMILIN1-α4/α9 integrin interaction inhibits dermal fibroblast and keratinocyte proliferation
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JOURNAL OF CELL BIOLOGY (2011)
Fibulin-2 and Fibulin-5 Cooperatively Function to Form the Internal Elastic Lamina and Protect From Vascular Injury
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Latent Transforming Growth Factor β-binding Proteins and Fibulins Compete for Fibrillin-1 and Exhibit Exquisite Specificities in Binding Sites
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JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Fibulin-4 conducts proper elastogenesis via interaction with cross-linking enzyme lysyl oxidase
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Emilin1 deficiency causes structural and functional defects of lymphatic vasculature
Carla Danussi et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
Regulation of the extrinsic apoptotic pathway by the extracellular matrix glycoprotein EMILIN2
Maurizio Mongiat et al.
MOLECULAR AND CELLULAR BIOLOGY (2007)
A comparative analysis of the fibulin protein family -: Biochemical characterization, binding interactions, and tissue localization
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JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
EMILIN1 represents a major stromal element determining human trophoblast invasion of the uterine wall
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Fibulin-4:: A novel gene for an autosomal recessive cutis laxa syndrome
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AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Regulation of bone mass by Wnt signaling
V Krishnan et al.
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Emilin1 links TGF-β maturation to blood pressure homeostasis
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Targeted disruption of fibulin-4 abolishes elastogenesis and causes perinatal lethality in mice
PJ McLaughlin et al.
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Fibronectin regulates latent transforming growth factor-β (TGFβ) by controlling matrix assembly of latent TGFβ-binding protein-1
SL Dallas et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Molecular cloning and characterization of a novel gene, EMILIN-5, and its possible involvement in skeletal development
M Doi et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2004)
EMILIN-1 deficiency induces elastogenesis and vascular cell defects
M Zanetti et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Overlapping, complementary and site-specific expression pattern of genes of the EMILIN/Multimerin family
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MATRIX BIOLOGY (2004)
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R Timpl et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2003)
β1 integrin-dependent cell adhesion to EMILIN-1 is mediated by the gC1q domain
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JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Developmental expression and biochemical characterization of Emu family members
C Leimeister et al.
DEVELOPMENTAL BIOLOGY (2002)
Cbfa1-independent decrease in osteoblast proliferation, osteopenia, and persistent embryonic eye vascularization in mice deficient in Lrp5, a Wnt coreceptor
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JOURNAL OF CELL BIOLOGY (2002)
Fibulin-5/DANCE is essential for elastogenesis in vivo
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Interactions of fibrillin-1 with heparin/heparan sulfate, implications for microfibrillar assembly
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Isolation and characterization of EMILIN-2, a new component of the growing EMILINs family and a member of the EMI domain-containing superfamily
R Doliana et al.
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Self-assembly and supramolecular organization of EMILIN
M Mongiat et al.
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