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Search results 1 to 100 out of 130 for Neb

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0.076s
Type Details Score
Gene
Type: gene
Organism: Homo sapiens
Gene
Type: gene
Organism: Drosophila melanogaster
Gene
Type: gene
Organism: Rattus norvegicus
Gene
Type: gene
Organism: Danio rerio
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Publication
First Author: Bang ML
Year: 2006
Journal: J Cell Biol
Title: Nebulin-deficient mice exhibit shorter thin filament lengths and reduced contractile function in skeletal muscle.
Volume: 173
Issue: 6
Pages: 905-16
Publication
First Author: Hughes DC
Year: 2015
Journal: Am J Physiol Endocrinol Metab
Title: Effects of aging, exercise, and disease on force transfer in skeletal muscle.
Volume: 309
Issue: 1
Pages: E1-E10
Publication
First Author: Bang ML
Year: 2009
Journal: FASEB J
Title: Nebulin plays a direct role in promoting strong actin-myosin interactions.
Volume: 23
Issue: 12
Pages: 4117-25
Publication
First Author: Mastrototaro G
Year: 2015
Journal: Cardiovasc Res
Title: Nebulette knockout mice have normal cardiac function, but show Z-line widening and up-regulation of cardiac stress markers.
Volume: 107
Issue: 2
Pages: 216-25
Publication
First Author: Bang ML
Year: 2017
Journal: J Cell Physiol
Title: Animal Models of Congenital Cardiomyopathies Associated With Mutations in Z-Line Proteins.
Volume: 232
Issue: 1
Pages: 38-52
Allele
Name: nebulin; targeted mutation 1, Ju Chen
Allele Type: Targeted
Attribute String: Null/knockout, Recombinase
Publication categories: ProxyCollection
Strain
Attribute String: mutant stock, targeted mutation
Genotype
Symbol: Neb/Neb
Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
Zygosity: hm
Has Mutant Allele: true
Publication  
First Author: Qiu B
Year: 2019
Journal: Biol Open
Title: Failure to identify modifiers of NEBULIN-related nemaline myopathy in two pre-clinical models of the disease.
Volume: 8
Issue: 9
Publication
First Author: Chandra M
Year: 2009
Journal: J Biol Chem
Title: Nebulin alters cross-bridge cycling kinetics and increases thin filament activation: a novel mechanism for increasing tension and reducing tension cost.
Volume: 284
Issue: 45
Pages: 30889-96
Publication
First Author: Li F
Year: 2015
Journal: Hum Mol Genet
Title: Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy.
Volume: 24
Issue: 18
Pages: 5219-33
Publication
First Author: Joureau B
Year: 2017
Journal: Neuromuscul Disord
Title: Muscle weakness in respiratory and peripheral skeletal muscles in a mouse model for nebulin-based nemaline myopathy.
Volume: 27
Issue: 1
Pages: 83-89
Publication
First Author: Kiss B
Year: 2018
Journal: Proc Natl Acad Sci U S A
Title: Nebulin stiffens the thin filament and augments cross-bridge interaction in skeletal muscle.
Volume: 115
Issue: 41
Pages: 10369-10374
Publication
First Author: Ottenheijm CA
Year: 2013
Journal: Brain
Title: Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy.
Volume: 136
Issue: Pt 6
Pages: 1718-31
Allele
Name: nebulin; targeted mutation 1, Siegfried Labeit
Allele Type: Targeted
Attribute String: Null/knockout
Publication categories: ProxyCollection
Publication
First Author: Wu HP
Year: 2014
Journal: Biochem Biophys Res Commun
Title: Transgenic mice expressing mutant Pinin exhibit muscular dystrophy, nebulin deficiency and elevated expression of slow-type muscle fiber genes.
Volume: 443
Issue: 1
Pages: 313-20
Publication  
First Author: Kolb J
Year: 2016
Journal: J Mol Cell Cardiol
Title: Thin filament length in the cardiac sarcomere varies with sarcomere length but is independent of titin and nebulin.
Volume: 97
Pages: 286-94
Publication
First Author: Lee EJ
Year: 2013
Journal: PLoS One
Title: Fast skeletal muscle troponin activation increases force of mouse fast skeletal muscle and ameliorates weakness due to nebulin-deficiency.
Volume: 8
Issue: 2
Pages: e55861
Publication
First Author: Müller-Seitz M
Year: 1993
Journal: Genomics
Title: Chromosomal localization of the mouse titin gene and its relation to "muscular dystrophy with myositis" and nebulin genes on chromosome 2.
Volume: 18
Issue: 3
Pages: 559-61
Publication
First Author: Rossi E
Year: 1994
Journal: Genomics
Title: Order of six loci at 2q24-q31 and orientation of the HOXD locus.
Volume: 24
Issue: 1
Pages: 34-40
Publication
First Author: Garg A
Year: 2014
Journal: J Clin Invest
Title: KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy.
Volume: 124
Issue: 8
Pages: 3529-39
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus caroli
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus musculus
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus pahari
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus spretus
Publication
First Author: Zhang JQ
Year: 1996
Journal: Eur J Biochem
Title: cDNA cloning of mouse nebulin. Evidence that the nebulin-coding sequence is highly conserved among vertebrates.
Volume: 239
Issue: 3
Pages: 835-41
Publication
First Author: Witt CC
Year: 2006
Journal: EMBO J
Title: Nebulin regulates thin filament length, contractility, and Z-disk structure in vivo.
Volume: 25
Issue: 16
Pages: 3843-55
Publication
First Author: Tonino P
Year: 2010
Journal: J Cell Sci
Title: Reduced myofibrillar connectivity and increased Z-disk width in nebulin-deficient skeletal muscle.
Volume: 123
Issue: Pt 3
Pages: 384-91
Publication
First Author: Ottenheijm CA
Year: 2009
Journal: Hum Mol Genet
Title: Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency.
Volume: 18
Issue: 13
Pages: 2359-69
Publication
First Author: Yamamoto DL
Year: 2013
Journal: J Cell Sci
Title: The nebulin SH3 domain is dispensable for normal skeletal muscle structure but is required for effective active load bearing in mouse.
Volume: 126
Issue: Pt 23
Pages: 5477-89
Publication
First Author: Kazmierski ST
Year: 2003
Journal: J Mol Biol
Title: The complete mouse nebulin gene sequence and the identification of cardiac nebulin.
Volume: 328
Issue: 4
Pages: 835-46
GXD Expression      
Probe: MGI:6315527
Assay Type: Immunohistochemistry
Annotation Date: 2019-06-30
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:3116917
Stage: TS17
Assay Id: MGI:6315528
Age: embryonic day 10.5
Detected: false
Specimen Num: 3
GXD Expression      
Probe: MGI:6315527
Assay Type: Immunohistochemistry
Annotation Date: 2019-06-30
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:3116915
Stage: TS15
Assay Id: MGI:6315528
Age: embryonic day 9.5
Detected: false
Specimen Num: 1
GXD Expression      
Probe: MGI:6315527
Assay Type: Immunohistochemistry
Annotation Date: 2019-06-30
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:3116916
Stage: TS16
Assay Id: MGI:6315528
Age: embryonic day 10.0
Detected: false
Specimen Num: 2
GXD Expression
Probe: MGI:1343413
Assay Type: Immunohistochemistry
Annotation Date: 1999-09-08
Strength: Present
Sex: Not Specified
Emaps: EMAPS:2969517
Pattern: Regionally restricted
Stage: TS17
Assay Id: MGI:1343442
Age: embryonic day 10.5
Image: 3G
Note: Expression is in the myotome.
Detected: true
Specimen Num: 2
GXD Expression    
Probe: MGI:1343413
Assay Type: Immunohistochemistry
Annotation Date: 1999-09-08
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1618417
Stage: TS17
Assay Id: MGI:1343442
Age: embryonic day 10.5
Image: 3H
Detected: false
Specimen Num: 1
Publication
First Author: Fülöp C
Year: 1997
Journal: Gene
Title: Coding sequence, exon-intron structure and chromosomal localization of murine TNF-stimulated gene 6 that is specifically expressed by expanding cumulus cell-oocyte complexes.
Volume: 202
Issue: 1-2
Pages: 95-102
Publication
First Author: Schurr E
Year: 1991
Journal: Cytogenet Cell Genet
Title: Mapping of the gene coding for the muscle protein nebulin (Neb) to the proximal region of mouse chromosome 2.
Volume: 57
Issue: 4
Pages: 214-6
Publication
First Author: Qureshi ST
Year: 1995
Journal: Genomics
Title: The murine endoglin gene (Eng) maps to chromosome 2.
Volume: 26
Issue: 1
Pages: 165-6
Publication
First Author: Takano K
Year: 2010
Journal: Science
Title: Nebulin and N-WASP cooperate to cause IGF-1-induced sarcomeric actin filament formation.
Volume: 330
Issue: 6010
Pages: 1536-40
Publication
First Author: Hinze F
Year: 2016
Journal: J Mol Med (Berl)
Title: Reducing RBM20 activity improves diastolic dysfunction and cardiac atrophy.
Volume: 94
Issue: 12
Pages: 1349-1358
Publication
First Author: Ottenheijm CA
Year: 2008
Journal: FASEB J
Title: Sarcoplasmic reticulum calcium uptake and speed of relaxation are depressed in nebulin-free skeletal muscle.
Volume: 22
Issue: 8
Pages: 2912-9
Publication
First Author: Kandli M
Year: 2000
Journal: Genomics
Title: Isolation and characterization of two evolutionarily conserved murine kinases (Nek6 and nek7) related to the fungal mitotic regulator, NIMA.
Volume: 68
Issue: 2
Pages: 187-96
Publication
First Author: Taketo M
Year: 1995
Journal: Genomics
Title: Homologs of Drosophila Fushi-Tarazu factor 1 map to mouse chromosome 2 and human chromosome 9q33.
Volume: 25
Issue: 2
Pages: 565-7
Publication    
First Author: Ramirez-Martinez A
Year: 2017
Journal: Elife
Title: KLHL41 stabilizes skeletal muscle sarcomeres by nonproteolytic ubiquitination.
Volume: 6
Publication
First Author: Witt SH
Year: 2005
Journal: J Mol Biol
Title: MURF-1 and MURF-2 target a specific subset of myofibrillar proteins redundantly: towards understanding MURF-dependent muscle ubiquitination.
Volume: 350
Issue: 4
Pages: 713-22
Publication
First Author: Malo D
Year: 1991
Journal: Genomics
Title: Three brain sodium channel alpha-subunit genes are clustered on the proximal segment of mouse chromosome 2.
Volume: 10
Issue: 3
Pages: 666-72
Publication
First Author: Askew DS
Year: 1991
Journal: Oncogene
Title: His-1 and His-2: identification and chromosomal mapping of two commonly rearranged sites of viral integration in a myeloid leukemia.
Volume: 6
Issue: 11
Pages: 2041-7
Publication
First Author: Beckers MC
Year: 1996
Journal: Genomics
Title: A new sodium channel alpha-subunit gene (Scn9a) from Schwann cells maps to the Scn1a, Scn2a, Scn3a cluster of mouse chromosome 2.
Volume: 36
Issue: 1
Pages: 202-5
Author
Publication
First Author: Klocke R
Year: 1997
Journal: Genomics
Title: Dynamin genes Dnm1 and Dnm2 are located on proximal mouse chromosomes 2 and 9, respectively.
Volume: 41
Issue: 2
Pages: 290-2
Publication
First Author: Gokhin DS
Year: 2010
Journal: J Cell Biol
Title: Tropomodulin isoforms regulate thin filament pointed-end capping and skeletal muscle physiology.
Volume: 189
Issue: 1
Pages: 95-109
Publication
First Author: Braun T
Year: 1994
Journal: Development
Title: MyoD expression marks the onset of skeletal myogenesis in Myf-5 mutant mice.
Volume: 120
Issue: 11
Pages: 3083-92
Publication
First Author: Kaul A
Year: 2000
Journal: Cell
Title: Myf-5 revisited: loss of early myotome formation does not lead to a rib phenotype in homozygous Myf-5 mutant mice.
Volume: 102
Issue: 1
Pages: 17-9
Publication
First Author: Rouger K
Year: 2002
Journal: Am J Physiol Cell Physiol
Title: Global/temporal gene expression in diaphragm and hindlimb muscles of dystrophin-deficient (mdx) mice.
Volume: 283
Issue: 3
Pages: C773-84
Publication
First Author: Mock B
Year: 1990
Journal: Genomics
Title: A genetic map of mouse chromosome 1 near the Lsh-Ity-Bcg disease resistance locus.
Volume: 7
Issue: 1
Pages: 57-64
Publication
First Author: Miner JH
Year: 1992
Journal: Development
Title: Skeletal muscle phenotypes initiated by ectopic MyoD in transgenic mouse heart.
Volume: 114
Issue: 4
Pages: 853-60
Publication
First Author: Li Z
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: Embryonic stem cell tumor model reveals role of vascular endothelial receptor tyrosine phosphatase in regulating Tie2 pathway in tumor angiogenesis.
Volume: 106
Issue: 52
Pages: 22399-404
Publication
First Author: Braun T
Year: 1995
Journal: EMBO J
Title: Inactivation of Myf-6 and Myf-5 genes in mice leads to alterations in skeletal muscle development.
Volume: 14
Issue: 6
Pages: 1176-86
Publication
First Author: Schiaffino S
Year: 1996
Journal: Physiol Rev
Title: Molecular diversity of myofibrillar proteins: gene regulation and functional significance.
Volume: 76
Issue: 2
Pages: 371-423
Publication
First Author: Siracusa LD
Year: 1991
Journal: Genetics
Title: Interspecific backcross mice show sex-specific differences in allelic inheritance.
Volume: 128
Issue: 4
Pages: 813-21
Publication
First Author: Ghazalpour A
Year: 2006
Journal: PLoS Genet
Title: Integrating genetic and network analysis to characterize genes related to mouse weight.
Volume: 2
Issue: 8
Pages: e130
Publication
First Author: Inagawa M
Year: 2013
Journal: Mech Dev
Title: Histone H3 lysine 9 methyltransferases, G9a and GLP are essential for cardiac morphogenesis.
Volume: 130
Issue: 11-12
Pages: 519-31
Publication
First Author: Lyssand JS
Year: 2008
Journal: J Biol Chem
Title: Blood pressure is regulated by an alpha1D-adrenergic receptor/dystrophin signalosome.
Volume: 283
Issue: 27
Pages: 18792-800
Publication  
First Author: Funato N
Year: 2018
Journal: Arch Oral Biol
Title: Deletion of the T-box transcription factor gene, Tbx1, in mice induces differential expression of genes associated with cleft palate in humans.
Volume: 95
Pages: 149-155
Publication
First Author: Harms MJ
Year: 2014
Journal: Cell Metab
Title: Prdm16 is required for the maintenance of brown adipocyte identity and function in adult mice.
Volume: 19
Issue: 4
Pages: 593-604
Publication
First Author: Chen JQ
Year: 2015
Journal: PLoS One
Title: Abnormal Mammary Development in 129:STAT1-Null Mice is Stroma-Dependent.
Volume: 10
Issue: 6
Pages: e0129895
Publication
First Author: Vaughan KT
Year: 1996
Journal: Genomics
Title: Multiple mouse chromosomal loci for dynein-based motility.
Volume: 36
Issue: 1
Pages: 29-38
Publication
First Author: Gómez-Del Arco P
Year: 2016
Journal: Cell Metab
Title: The Chromatin Remodeling Complex Chd4/NuRD Controls Striated Muscle Identity and Metabolic Homeostasis.
Volume: 23
Issue: 5
Pages: 881-92
Publication
First Author: Gineste C
Year: 2013
Journal: Neuromuscul Disord
Title: In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotype.
Volume: 23
Issue: 4
Pages: 357-69
Publication
First Author: Loo L
Year: 2019
Journal: Nat Commun
Title: Single-cell transcriptomic analysis of mouse neocortical development.
Volume: 10
Issue: 1
Pages: 134
Publication      
First Author: Wellcome Trust Sanger Institute
Year: 2009
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the Wellcome Trust Sanger Institute
Publication      
First Author: Lennon G
Year: 1999
Journal: Database Download
Title: WashU-HHMI Mouse EST Project
Publication      
First Author: Helmholtz Zentrum Muenchen GmbH
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu)
Publication
First Author: Skarnes WC
Year: 2011
Journal: Nature
Title: A conditional knockout resource for the genome-wide study of mouse gene function.
Volume: 474
Issue: 7351
Pages: 337-42
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Rat to Mouse ISO GO annotation transfer
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2003
Title: MGI Sequence Curation Reference
Publication          
First Author: MGD Nomenclature Committee
Year: 1995
Publication      
First Author: Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI)
Year: 2008
Journal: Database Download
Title: Mouse Gene Trap Data Load from dbGSS
Publication
First Author: Gaudet P
Year: 2011
Journal: Brief Bioinform
Title: Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Volume: 12
Issue: 5
Pages: 449-62