Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice. - Wikidata - wikimedia - TriplyDB

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

http://www.wikidata.org/entity/Q37452338

about

Overexpression of Latent TGFβ Binding Protein 4 in Muscle Ameliorates Muscular Dystrophy through Myostatin and TGFβ Abnormal Activation of BMP Signaling Causes Myopathy in Fbn2 Null Mice Marginal level dystrophin expression improves clinical outcome in a strain of dystrophin/utrophin double knockout mice Myofibroblasts: trust your heart and let fate decide.Modifier genes and their effect on Duchenne muscular dystrophy The super super-healing MRL mouse strain SMAD signaling drives heart and muscle dysfunction in a Drosophila model of muscular dystrophy Biochemical and Functional Comparisons of mdx and Sgcg(-/-) Muscular Dystrophy Mouse Models.LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophy.Mechanisms of muscle weakness in muscular dystrophy Influence of genetic background on ex vivo and in vivo cardiac function in several commonly used inbred mouse strains Transforming growth factor-beta (TGF- β) signaling in paravertebral muscles in juvenile and adolescent idiopathic scoliosis.Distinct genetic regions modify specific muscle groups in muscular dystrophy.The Murphy Roths Large (MRL) mouse strain is naturally resistant to high fat diet-induced hyperglycemia Duchenne muscular dystrophy gene therapy: Lost in translation?Genetic Modifiers for Neuromuscular Diseases Role of TGF-β signaling in inherited and acquired myopathies.mdx(⁵cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx Mice Genetic modifiers of ambulation in the Cooperative International Neuromuscular Research Group Duchenne Natural History Study Latent transforming growth factor binding protein 4 regulates transforming growth factor beta receptor stability.Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.Enhanced Muscular Dystrophy from Loss of Dysferlin Is Accompanied by Impaired Annexin A6 Translocation after Sarcolemmal Disruption.Deletion of periostin reduces muscular dystrophy and fibrosis in mice by modulating the transforming growth factor-β pathway.Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants.The matrix protein Fibulin-5 is at the interface of tissue stiffness and inflammation in fibrosis.Effect of genetic background on the dystrophic phenotype in mdx mice.Genetic mutations and mechanisms in dilated cardiomyopathy Congenic mice provide in vivo evidence for a genetic locus that modulates intrinsic transforming growth factor β1-mediated signaling and bone acquisition.Role of Transforming Growth Factor-β1 and Smads Signaling Pathway in Intrauterine Adhesion.Modifying muscular dystrophy through transforming growth factor-β.Conditional expression of TGF-β1 in skeletal muscles causes endomysial fibrosis and myofibers atrophy Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy.Targeting fibrosis in Duchenne muscular dystrophy.δ-Sarcoglycan-deficient muscular dystrophy: from discovery to therapeutic approaches.Pathophysiology and therapy of cardiac dysfunction in Duchenne muscular dystrophy.Cross talk among TGF-β signaling pathways, integrins, and the extracellular matrix Modifiers of heart and muscle function: where genetics meets physiology.Prospect for pharmacological therapies to treat skeletal muscle dysfunction.Magnetic Resonance Monitoring of Disease Progression in mdx Mice on Different Genetic Backgrounds.

P2860

Q27308903-158AEC9C-E243-4619-BA8F-8F240B9BE0D7 Q27310854-78C42581-9C67-4DCA-9298-90879455DF51 Q27312780-C6E5EDDB-A031-48FD-BBA1-8680F577BC31 Q27692541-2A8E3834-C875-4E45-AA26-8E169BBBF044 Q28083441-1D39A8D8-B446-4227-8F2D-17C1078A06AF Q29542636-622EF9BE-B5D3-484A-B735-4CBB3DC5485D Q30498086-9361413B-EAE1-490B-909D-1E4CDC23B612 Q30650746-EE7B606C-34FA-4B99-B555-DEB833ECB92E Q33931637-35616138-B1C7-4183-A627-C265D7F8325E Q33950716-CB2BE404-EF94-4A46-823F-7EFC7958C101 Q34214799-278DE99D-7C55-46B6-93F1-D61EC82B74CD Q34275449-4AEB2009-C7EF-4722-8FE8-B35B0F1D67BC Q34518008-3F16E2CE-C5FE-48EF-B6C4-6795B1624AEC Q34614691-61264409-F86E-4A1F-B83E-850475ACADBB Q35052506-92EFC6D2-7412-4E83-8634-FFAAC3D62F4E Q35119976-95CE243B-0B38-403B-AF7F-CDF56DE8B32E Q35166254-BC001AA1-827D-419B-B7DD-33503A4C4D6C Q35474357-DA2BA1CB-7C8F-46CF-9A4D-8B1910FF60D1 Q35495274-8CA32741-FFFB-44E1-A474-E39C1B3EF377 Q35766401-68775EFA-0DC0-409A-9795-4BAE69285A50 Q35826211-11276322-DDD2-4463-B64A-905F76020E99 Q35987272-EB9114DB-1E86-4135-B3A6-A5B11AF55B64 Q36079434-2E67803F-5180-4F0D-9B2E-3F6EF979606F Q36150125-8B740349-65BD-4BC1-88B7-7EA4D1255307 Q36251455-0F17C6B5-2383-4B0E-B968-A2087CF7F896 Q36402584-D39AD63F-2B92-444D-A2DD-CD13394409CA Q36497170-702AC5AD-6233-46A7-9411-31E548F6609A Q36510130-A27A1541-6E39-4371-AB80-EC32DBF123B5 Q36655274-D9FFB6B9-A689-477C-AAE4-35EE1CC14C45 Q37064241-617E1400-3F7A-41A0-A7C9-2632CD9FCAC2 Q37309267-84C01D45-A2B7-4721-8354-8681674298CB Q37374329-64F94CDC-AADC-4D23-A40B-B11411F7109A Q37396900-663FF916-240A-4F04-9B01-DAAE45253E3F Q37770947-CB455B3D-3E21-4187-95C7-CAB9D0DA499E Q37907409-55A5024E-C8E2-4604-B463-95AF8FA5C9C1 Q37910906-C452F010-424D-408C-AC87-E794599FFE7F Q37928833-88642B8E-B755-45F7-BBB3-80BEE159D92D Q38161422-04A02ED7-F5F9-4BBE-A8E6-63CC219F0B6F Q38264369-A1CF3F9F-FEB2-4188-BF41-CE7F2C803DE1 Q38615889-8D1DC4A3-5E5D-4D6B-A1F1-F82B3EB3E9EC

P2860

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

http://www.wikidata.org/entity/Q37452338

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh

2009年學術文章

@zh-hant

name

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

@en

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

@nl

type

label

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

@en

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

@nl

prefLabel

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

@en

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

@nl

P1433

Q37452338-B8F86E46-E4C7-41DE-B25C-B3CEDF187D0A

P1476

Q37452338-6D3D7DCB-8E25-4103-9995-163C9559D5A7

P2093

Q37452338-14DE714E-8BDC-4797-8C9D-E84DBFF620CA

Q37452338-54C0E6B2-2DBA-435A-80C0-B3380DF319C6

Q37452338-6CE2F2B8-9298-44CF-9D51-919BAAC16F40

Q37452338-945C0619-4A12-4956-9B89-63EFC42F1B29

Q37452338-AD5EC009-B895-4A6C-93EC-8EAD64A0A061

Q37452338-D1B35C5D-81EA-4F2A-8CD2-C6463F52C4DF

Q37452338-E3D335A4-2F72-403E-B8BB-07D9B6F92ACF

Q37452338-E7F76BA4-A9AC-42EC-99F1-8F42B963FF5A

P2860

Q37452338-05737661-D14B-4F06-81D6-FDB82BC1D9A9

Q37452338-09ADCAB6-0FF6-455B-BE65-EF9C09773C92

Q37452338-146C1013-87CA-415C-9E9F-EE276F6E624E

Q37452338-1AF357F7-63D4-4A32-B155-F7E6F5EF24C3

Q37452338-1CC2E31D-F7B4-4BA4-A3F6-529405A1ABBD

Q37452338-1E9197DE-72B0-43DA-9FDD-7526FA99508E

Q37452338-2011DE09-97EF-4B21-A3D0-D443A2BC82E5

Q37452338-281B5EE6-4D27-4E30-A9C0-3C9A1ADD73B8

Q37452338-324B0CD6-78FA-44FA-8CFC-F9FB442C1268

Q37452338-37CF7706-50A6-4907-A80E-05CC717BCB7C

P304

Q37452338-C4AF9D70-F9CC-4500-B7C7-D6C6C15FAF90

P31

Q37452338-17068B5A-EBB5-4CA6-8B5C-3838336804A5

P356

Q37452338-7236DB35-892E-4217-9B56-5EEB560C4E85

P407

Q37452338-165F1D2A-9F99-4286-B6A4-B6392081A5BF

P433

Q37452338-F3AF5637-FBA6-43E4-9013-F9016FE1C69D

P478

Q37452338-62B85D7B-7BB9-43E3-AD3F-743263F8C6CB

P50

Q37452338-22FE84D8-9AD2-442F-A204-4C5058B85465

P577

Q37452338-F6A5D762-8B32-436C-ACAA-319549A44983

P698

Q37452338-C35B970F-20A4-4B24-A89A-6900487BC6F6

P932

Q37452338-A97ECCF8-D4FA-47CE-913C-0DE5BBBFF0C6

P356

P1433

Journal of Clinical Investigation

P1476

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.

@en

P2093

Abraham A Palmer

http://www.w3.org/2001/XMLSchema#string

Ahlke Heydemann

http://www.w3.org/2001/XMLSchema#string

David R Beier

http://www.w3.org/2001/XMLSchema#string

Elizabeth M McNally

http://www.w3.org/2001/XMLSchema#string

Ermelinda Ceco

http://www.w3.org/2001/XMLSchema#string

Jackie E Lim

http://www.w3.org/2001/XMLSchema#string

Michele Hadhazy

http://www.w3.org/2001/XMLSchema#string

Pearl Ryder

http://www.w3.org/2001/XMLSchema#string

P2860

Specific sequence motif of 8-Cys repeats of TGF-beta binding proteins, LTBPs, creates a hydrophobic interaction surface for binding of small latent TGF-beta

Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle

Identification and characterization of a new latent transforming growth factor-beta-binding protein, LTBP-4

Sequential deposition of latent TGF-beta binding proteins (LTBPs) during formation of the extracellular matrix in human lung fibroblasts

Disruption of the gene encoding the latent transforming growth factor-beta binding protein 4 (LTBP-4) causes abnormal lung development, cardiomyopathy, and colorectal cancer

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation

Sequence and expression of a novel member (LTBP-4) of the family of latent transforming growth factor-beta binding proteins

The dystrophin complex forms a mechanically strong link between the sarcolemma and costameric actin

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

Smad transcription factors

P304

3703-3712

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1172/JCI39845

http://www.w3.org/2001/XMLSchema#string

P407

P433

12

http://www.w3.org/2001/XMLSchema#string

P478

119

http://www.w3.org/2001/XMLSchema#string

P50

Jennifer L. Moran

P577

2009-11-02T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

19884661

http://www.w3.org/2001/XMLSchema#string

P932

2786802

http://www.w3.org/2001/XMLSchema#string