Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles. - Wikidata - thesis-toulmin - TriplyDB

Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles.

Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles.

http://www.wikidata.org/entity/Q35088026

about

Emerin-prelamin A interplay in human fibroblasts The nuclear envelope LEM-domain protein emerin Lamina-associated polypeptide 1: protein interactions and tissue-selective functions Building up the nucleus: nuclear organization in the establishment of totipotency and pluripotency during mammalian development Nuclear envelope structural proteins facilitate nuclear shape changes accompanying embryonic differentiation and fidelity of gene expression Loss of GATA6 leads to nuclear deformation and aneuploidy in ovarian cancer.Emerin organizes actin flow for nuclear movement and centrosome orientation in migrating fibroblasts.Linker of nucleoskeleton and cytoskeleton complex proteins in cardiac structure, function, and disease.MAPK signaling pathways and HDAC3 activity are disrupted during differentiation of emerin-null myogenic progenitor cells.Genome-wide analysis links emerin to neuromuscular junction activity in Caenorhabditis elegans.Lamin-binding Proteins Nuclear envelope structural defects cause chromosomal numerical instability and aneuploidy in ovarian cancer.Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan."Laminopathies": a wide spectrum of human diseases.Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy.Emerin in health and disease.Nuclear lamins: key regulators of nuclear structure and activities Networking in the nucleus: a spotlight on LEM-domain proteins Mouse models of the laminopathies.Emerin is hyperphosphorylated and redistributed in herpes simplex virus type 1-infected cells in a manner dependent on both UL34 and US3.Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy Drosophila male and female germline stem cell niches require the nuclear lamina protein Otefin.Till disassembly do us part: a happy marriage of nuclear envelope and chromatin.Muscle development, regeneration and laminopathies: how lamins or lamina-associated proteins can contribute to muscle development, regeneration and disease.Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins.Lamina-associated polypeptide-1 interacts with the muscular dystrophy protein emerin and is essential for skeletal muscle maintenance Nuclear positioning in muscle development and disease.Laminopathies: the molecular background of the disease and the prospects for its treatment.Nuclear autophagy: An evolutionarily conserved mechanism of nuclear degradation in the cytoplasm.Diseases of the Nucleoskeleton.The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C-LAP2α complex in mice.Depletion of lamina-associated polypeptide 1 from cardiomyocytes causes cardiac dysfunction in mice.Expression Profiling of Differentiating Emerin-Null Myogenic Progenitor Identifies Molecular Pathways Implicated in Their Impaired Differentiation.Phenotype of matrin-3-related distal myopathy in 16 German patients.Linker of nucleoskeleton and cytoskeleton complex proteins in cardiomyopathy The Pathogenesis and Therapies of Striated Muscle Laminopathies

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P2860

Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles.

http://www.wikidata.org/entity/Q35088026

description

2006 nî lūn-bûn

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2006 թուականի Մարտին հրատարակուած գիտական յօդուած

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2006 թվականի մարտին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Emerin-lacking mice show minim ...... h nuclear-associated vacuoles.

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Emerin-lacking mice show minim ...... h nuclear-associated vacuoles.

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type

label

Emerin-lacking mice show minim ...... h nuclear-associated vacuoles.

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Emerin-lacking mice show minim ...... h nuclear-associated vacuoles.

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prefLabel

Emerin-lacking mice show minim ...... h nuclear-associated vacuoles.

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Emerin-lacking mice show minim ...... h nuclear-associated vacuoles.

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AJPATH.2006.050564

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The American Journal of Pathology

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Emerin-lacking mice show minim ...... h nuclear-associated vacuoles.

@en

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Hiroshi Matsumoto

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

Ichizo Nishino

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

Ikuya Nonaka

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Megumu Ogawa

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

Ritsuko Ozawa

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

Rumi Kurokawa

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

Satoru Noguchi

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

Yukiko K Hayashi

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

P2860

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle

Emerin caps the pointed end of actin filaments: evidence for an actin cortical network at the nuclear inner membrane

Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro

Emerin binding to Btf, a death-promoting transcriptional repressor, is disrupted by a missense mutation that causes Emery-Dreifuss muscular dystrophy

Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy

Emery-Dreifuss syndrome

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy

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10.2353/AJPATH.2006.050564

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3

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168

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7269715

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16507906

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1606524

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