about
SMAD signaling drives heart and muscle dysfunction in a Drosophila model of muscular dystrophyReduced IGF signaling prevents muscle cell death in a Caenorhabditis elegans model of muscular dystrophyBiochemical and Functional Comparisons of mdx and Sgcg(-/-) Muscular Dystrophy Mouse Models.Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophy.Collagen content does not alter the passive mechanical properties of fibrotic skeletal muscle in mdx mice.Genetic background affects properties of satellite cells and mdx phenotypes.Restoration of gamma-sarcoglycan localization and mechanical signal transduction are independent in murine skeletal muscle.Influence of genetic background on ex vivo and in vivo cardiac function in several commonly used inbred mouse strainsNeonatal gene transfer of Serca2a delays onset of hypertrophic remodeling and improves function in familial hypertrophic cardiomyopathy.Distinct genetic regions modify specific muscle groups in muscular dystrophy.Transgenic expression of human S100A12 induces structural airway abnormalities and limited lung inflammation in a mouse model of allergic inflammationGenetic Modifiers for Neuromuscular DiseasesDistinct pathophysiological mechanisms of cardiomyopathy in hearts lacking dystrophin or the sarcoglycan complex.Cardiac function in muscular dystrophy associates with abdominal muscle pathology.Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal Muscle.Reengineering a transmembrane protein to treat muscular dystrophy using exon skippingMembrane-stabilizing copolymers confer marked protection to dystrophic skeletal muscle in vivo.Effect of genetic background on the dystrophic phenotype in mdx mice.A Common Variant of PROK1 (V67I) Acts as a Genetic Modifier in Early Human Pregnancy through Down-Regulation of Gene Expression.Plasma Membrane Repair in Health and DiseaseTowards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophyModifying muscular dystrophy through transforming growth factor-β.Isolation, characterization, and molecular regulation of muscle stem cells.Increased collagen cross-linking is a signature of dystrophin-deficient muscle.Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair.Identification and characterization of PDGFRα+ mesenchymal progenitors in human skeletal muscle.Modifiers of heart and muscle function: where genetics meets physiology.What do mouse models of muscular dystrophy tell us about the DAPC and its components?Magnetic Resonance Monitoring of Disease Progression in mdx Mice on Different Genetic Backgrounds.Intermittent Glucocorticoid Dosing Improves Muscle Repair and Function in Mice with Limb Girdle Muscular Dystrophy.Severe murine limb-girdle muscular dystrophy type 2C pathology is diminished by FTY720 treatment.Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy.The superhealing MRL background improves muscular dystrophy.Interplay between heart and skeletal muscle disease in heart failure: the 2011 George E. Brown Memorial Lecture.Genetic modifiers of muscular dystrophy act on sarcolemmal resealing and recovery from injury.Skeletal Muscle Metabolism in Duchenne and Becker Muscular Dystrophy-Implications for Therapies.Effect of genetic background on onset and disease progression in the SOD1-G93A model of amyotrophic lateral sclerosis
P2860
Q30498086-1AF8B539-03C3-4789-90F2-CA9A2583C503Q30557792-82EF8E51-B205-4FE7-9C04-A987F8907597Q30650746-11793C0A-6669-4E13-93C9-9295077A2342Q33281832-11BED0AD-1998-4A73-8217-D8F964025FF6Q33626503-874112DF-5F63-4917-9E87-2F892B0A99A6Q33816419-45D1FCD6-0711-4A26-8BA6-F546BAA9BB32Q33883334-196BFA69-6772-4419-B961-8A894F6F05DCQ34214799-3D3B14BD-C22D-4AE4-B67C-051082416DE7Q34313853-8DC883CA-3D22-400A-9918-041D5BCE9623Q34518008-5D65A11A-8F6B-4394-BD54-C30E5519AC37Q34977648-EA11EC0B-8744-44AD-ABA1-A7670734D3D3Q35119976-D8755BF0-34BF-4E80-B30A-4CDC251C8568Q35169510-F8A4AC3C-15C4-41CE-90A8-8E0FC627A280Q35660390-83557FD8-B8A3-4CAA-9156-F7387C5A46CAQ35760852-DFD2F3D7-8541-4397-846D-0E2AE34BB84AQ36266510-6EC65963-AA96-4365-8B33-B4999A0ED6EEQ36270889-35590880-AE13-47CD-93EB-332B2C7F068BQ36402584-1101111F-BD21-4D31-93C7-BECA635922E2Q36666959-1F248339-1FA0-49F1-8878-673CA66EAB07Q36785977-401985E2-18D6-4DB4-8FA4-42F3A4748347Q36841572-E938BE3F-7D48-400C-9E31-4E2B30DDFC1BQ37064241-0E8A8E9B-D787-45D1-9495-20C95E6B7972Q37298113-8F1531A5-D233-434D-BFAF-50460FB879A2Q37345809-147F3D38-FA2C-4356-B6AE-BB8DFE28D908Q37452338-813E21CD-4390-4BBC-87B3-912DFA41DC0AQ37725303-B0A5E97D-9B6D-4581-AB99-0FCC781BBB22Q37726150-56E86C0F-0F64-4918-A7BD-A8524B2A022CQ38161422-E4FFA33F-1E57-4B68-9677-DD1753CB56FAQ38255744-869FD8A7-098C-411D-A0E2-F533F0FFFEAAQ38615889-4308E869-E2B8-4539-8B6C-B0BCF0BE974EQ38617041-8B3D59DE-970F-4B54-9543-4718C32EC15AQ41019141-03A6D7E3-43E0-4241-859F-499A50D5A86DQ41902894-9C3E537A-18E8-429D-A68F-4BB78BADB69CQ42489265-05745B6D-57F9-483F-8537-F31704C62136Q42580068-27F3CFAE-B47C-4904-AFF2-76AEDB293339Q44907195-9A2E554F-4B9C-4AD2-8F2E-092E8023696EQ55515149-C25BAA05-76AB-4696-AAD9-38915A51D00AQ58264939-2E419BDE-5459-47D3-99F4-512581524A13
P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Genetic background influences muscular dystrophy.
@en
Genetic background influences muscular dystrophy.
@nl
type
label
Genetic background influences muscular dystrophy.
@en
Genetic background influences muscular dystrophy.
@nl
prefLabel
Genetic background influences muscular dystrophy.
@en
Genetic background influences muscular dystrophy.
@nl
P2093
P1476
Genetic background influences muscular dystrophy
@en
P2093
Ahlke Heydemann
Elizabeth M McNally
Jill M Huber
Michele Hadhazy
P304
P356
10.1016/J.NMD.2005.05.004
P577
2005-10-01T00:00:00Z