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Search results 1 to 100 out of 164 for Neb

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1.169s
Type Details Score
Gene
Type: gene
Organism: human
Gene
Type: gene
Organism: cattle
Gene
Type: gene
Organism: zebrafish
Gene
Type: gene
Organism: macaque, rhesus
Gene
Type: gene
Organism: chicken
Gene
Type: gene
Organism: frog, western clawed
Gene
Type: gene
Organism: dog, domestic
Gene
Type: gene
Organism: rat
Gene
Type: gene
Organism: chimpanzee
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Publication
First Author: Ranu N
Year: 2022
Journal: Acta Neuropathol Commun
Title: NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy.
Volume: 10
Issue: 1
Pages: 185
Publication
First Author: Slick RA
Year: 2023
Journal: Am J Pathol
Title: Aberrations in Energetic Metabolism and Stress-Related Pathways Contribute to Pathophysiology in the Neb Conditional Knockout Mouse Model of Nemaline Myopathy.
Volume: 193
Issue: 10
Pages: 1528-1547
Publication  
First Author: Kiss B
Year: 2020
Journal: Sci Adv
Title: Nebulin and Lmod2 are critical for specifying thin-filament length in skeletal muscle.
Volume: 6
Issue: 46
Publication
First Author: Lindqvist J
Year: 2020
Journal: Nat Commun
Title: Triggering typical nemaline myopathy with compound heterozygous nebulin mutations reveals myofilament structural changes as pathomechanism.
Volume: 11
Issue: 1
Pages: 2699
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: Gineste C
Year: 2020
Journal: Muscle Nerve
Title: In vivo characterization of skeletal muscle function in nebulin-deficient mice.
Volume: 61
Issue: 3
Pages: 416-424
Publication
First Author: Tinklenberg JA
Year: 2019
Journal: J Neuropathol Exp Neurol
Title: Myostatin Inhibition Using ActRIIB-mFc Does Not Produce Weight Gain or Strength in the Nebulin Conditional KO Mouse.
Volume: 78
Issue: 2
Pages: 130-139
Allele
Name: nebulin; targeted mutation 1, Siegfried Labeit
Allele Type: Targeted
Attribute String: Null/knockout
Publication
First Author: Laitila JM
Year: 2020
Journal: Acta Neuropathol Commun
Title: Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb.
Volume: 8
Issue: 1
Pages: 18
Publication
First Author: Gokhin DS
Year: 2009
Journal: Am J Physiol Cell Physiol
Title: Reduced thin filament length in nebulin-knockout skeletal muscle alters isometric contractile properties.
Volume: 296
Issue: 5
Pages: C1123-32
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: 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: Lindqvist J
Year: 2019
Journal: PLoS One
Title: Omecamtiv mecarbil lowers the contractile deficit in a mouse model of nebulin-based nemaline myopathy.
Volume: 14
Issue: 11
Pages: e0224467
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: Winter JM
Year: 2016
Journal: Ann Neurol
Title: Mutation-specific effects on thin filament length in thin filament myopathy.
Volume: 79
Issue: 6
Pages: 959-69
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: 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
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: 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: 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: 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: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
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: 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: Lindqvist J
Year: 2023
Journal: Int J Mol Sci
Title: Pharmacological Inhibition of Myostatin in a Mouse Model of Typical Nemaline Myopathy Increases Muscle Size and Force.
Volume: 24
Issue: 20
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: 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: 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: 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: 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:7505648
Assay Type: RT-PCR
Annotation Date: 2023-07-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3604827
Stage: TS27
Assay Id: MGI:7505664
Age: postnatal day 0
Image: 4-S2
Specimen Label: WT
Detected: true
Specimen Num: 1
GXD Expression    
Probe: MGI:7505648
Assay Type: RT-PCR
Annotation Date: 2023-07-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3604827
Stage: TS27
Assay Id: MGI:7505664
Age: postnatal day 0
Image: 4-S2
Specimen Label: KO
Detected: true
Specimen Num: 2
GXD Expression    
Probe: MGI:7505655
Assay Type: Western blot
Annotation Date: 2023-07-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3604827
Stage: TS27
Assay Id: MGI:7505670
Age: postnatal day 0
Image: 2
Specimen Label: WT
Detected: true
Specimen Num: 1
GXD Expression    
Probe: MGI:7505655
Assay Type: Western blot
Annotation Date: 2023-07-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3604827
Stage: TS27
Assay Id: MGI:7505670
Age: postnatal day 0
Image: 2
Specimen Label: WT
Detected: true
Specimen Num: 2
GXD Expression    
Probe: MGI:7505655
Assay Type: Western blot
Annotation Date: 2023-07-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3604827
Stage: TS27
Assay Id: MGI:7505670
Age: postnatal day 0
Image: 2
Specimen Label: WT
Detected: true
Specimen Num: 3
GXD Expression    
Probe: MGI:7505655
Assay Type: Western blot
Annotation Date: 2023-07-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3604827
Stage: TS27
Assay Id: MGI:7505670
Age: postnatal day 0
Image: 2
Specimen Label: KO
Detected: true
Specimen Num: 4
GXD Expression    
Probe: MGI:7505655
Assay Type: Western blot
Annotation Date: 2023-07-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3604827
Stage: TS27
Assay Id: MGI:7505670
Age: postnatal day 0
Image: 2
Specimen Label: KO
Detected: true
Specimen Num: 5
GXD Expression    
Probe: MGI:7505655
Assay Type: Western blot
Annotation Date: 2023-07-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3604827
Stage: TS27
Assay Id: MGI:7505670
Age: postnatal day 0
Image: 2
Specimen Label: KO
Detected: true
Specimen Num: 6
GXD Expression      
Probe: MGI:7462474
Assay Type: RT-PCR
Annotation Date: 2023-04-25
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1736221
Stage: TS21
Assay Id: MGI:7466239
Age: embryonic day 13.5
Specimen Label: Wild-type
Detected: true
Specimen Num: 1
GXD Expression      
Probe: MGI:7462474
Assay Type: RT-PCR
Annotation Date: 2023-04-25
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1736221
Stage: TS21
Assay Id: MGI:7466239
Age: embryonic day 13.5
Specimen Label: Tbx1<-/->
Detected: true
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.
Specimen Label: 3G
Detected: true
Specimen Num: 2
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
Specimen Label: E10.0
Detected: false
Specimen Num: 2
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
Specimen Label: E9.5
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:3116917
Stage: TS17
Assay Id: MGI:6315528
Age: embryonic day 10.5
Specimen Label: E10.5
Detected: false
Specimen Num: 3
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
Specimen Label: 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: 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: 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: 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: Li F
Year: 2019
Journal: Hum Mol Genet
Title: Deleting nebulin's C-terminus reveals its importance to sarcomeric structure and function and is sufficient to invoke nemaline myopathy.
Volume: 28
Issue: 10
Pages: 1709-1725
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: 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: 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: 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: Ramirez-Martinez A
Year: 2017
Journal: Elife
Title: KLHL41 stabilizes skeletal muscle sarcomeres by nonproteolytic ubiquitination.
Volume: 6
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: 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: 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: 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: 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: 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
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: 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: 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: 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: 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