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Search results 101 to 200 out of 229 for Myl1

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Category: Publication
Type Details Score
Publication
First Author: Raben N
Year: 2010
Journal: Autophagy
Title: Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder--murine Pompe disease.
Volume: 6
Issue: 8
Pages: 1078-89
Publication
First Author: Zhang R
Year: 2019
Journal: FASEB J
Title: NDUFAB1 protects against obesity and insulin resistance by enhancing mitochondrial metabolism.
Volume: 33
Issue: 12
Pages: 13310-13322
Publication
First Author: Kim KH
Year: 2013
Journal: Nat Med
Title: Autophagy deficiency leads to protection from obesity and insulin resistance by inducing Fgf21 as a mitokine.
Volume: 19
Issue: 1
Pages: 83-92
Publication
First Author: Lyons GE
Year: 1991
Journal: Development
Title: Carbonic anhydrase III, an early mesodermal marker, is expressed in embryonic mouse skeletal muscle and notochord.
Volume: 111
Issue: 1
Pages: 233-44
Publication
First Author: Sartori R
Year: 2013
Journal: Nat Genet
Title: BMP signaling controls muscle mass.
Volume: 45
Issue: 11
Pages: 1309-18
Publication
First Author: Mammucari C
Year: 2007
Journal: Cell Metab
Title: FoxO3 controls autophagy in skeletal muscle in vivo.
Volume: 6
Issue: 6
Pages: 458-71
Publication
First Author: Kubalak SW
Year: 1994
Journal: J Biol Chem
Title: Chamber specification of atrial myosin light chain-2 expression precedes septation during murine cardiogenesis.
Volume: 269
Issue: 24
Pages: 16961-70
Publication
First Author: Sala D
Year: 2014
Journal: J Clin Invest
Title: Autophagy-regulating TP53INP2 mediates muscle wasting and is repressed in diabetes.
Volume: 124
Issue: 5
Pages: 1914-27
Publication
First Author: Song MY
Year: 2022
Journal: Nat Commun
Title: Sirt6 reprograms myofibers to oxidative type through CREB-dependent Sox6 suppression.
Volume: 13
Issue: 1
Pages: 1808
Publication
First Author: Hardy WR
Year: 2007
Journal: Science
Title: Combinatorial ShcA docking interactions support diversity in tissue morphogenesis.
Volume: 317
Issue: 5835
Pages: 251-6
Publication
First Author: Pfluger PT
Year: 2015
Journal: Cell Metab
Title: Calcineurin Links Mitochondrial Elongation with Energy Metabolism.
Volume: 22
Issue: 5
Pages: 838-50
Publication
First Author: Parsons SA
Year: 2004
Journal: J Biol Chem
Title: Genetic loss of calcineurin blocks mechanical overload-induced skeletal muscle fiber type switching but not hypertrophy.
Volume: 279
Issue: 25
Pages: 26192-200
Publication
First Author: Parsons SA
Year: 2007
Journal: J Biol Chem
Title: Genetic disruption of calcineurin improves skeletal muscle pathology and cardiac disease in a mouse model of limb-girdle muscular dystrophy.
Volume: 282
Issue: 13
Pages: 10068-78
Publication    
First Author: Tang Y
Year: 2022
Journal: Elife
Title: TIGAR deficiency enhances skeletal muscle thermogenesis by increasing neuromuscular junction cholinergic signaling.
Volume: 11
Publication
First Author: Chen H
Year: 2010
Journal: Cell
Title: Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.
Volume: 141
Issue: 2
Pages: 280-9
Publication
First Author: Mishra P
Year: 2015
Journal: Cell Metab
Title: Mitochondrial Dynamics is a Distinguishing Feature of Skeletal Muscle Fiber Types and Regulates Organellar Compartmentalization.
Volume: 22
Issue: 6
Pages: 1033-44
Publication  
First Author: Rhein P
Year: 2021
Journal: Mol Metab
Title: Compound- and fiber type-selective requirement of AMPKγ3 for insulin-independent glucose uptake in skeletal muscle.
Volume: 51
Pages: 101228
Publication
First Author: Bocco BM
Year: 2016
Journal: J Physiol
Title: Thyroid hormone activation by type 2 deiodinase mediates exercise-induced peroxisome proliferator-activated receptor-γ coactivator-1α expression in skeletal muscle.
Volume: 594
Issue: 18
Pages: 5255-69
Publication
First Author: Yamada M
Year: 2019
Journal: FASEB J
Title: p62/SQSTM1 and Nrf2 are essential for exercise-mediated enhancement of antioxidant protein expression in oxidative muscle.
Volume: 33
Issue: 7
Pages: 8022-8032
Publication
First Author: Bround MJ
Year: 2023
Journal: Sci Adv
Title: ANT-dependent MPTP underlies necrotic myofiber death in muscular dystrophy.
Volume: 9
Issue: 34
Pages: eadi2767
Publication
First Author: Nemazanyy I
Year: 2013
Journal: EMBO Mol Med
Title: Defects of Vps15 in skeletal muscles lead to autophagic vacuolar myopathy and lysosomal disease.
Volume: 5
Issue: 6
Pages: 870-90
Publication
First Author: Chung HK
Year: 2017
Journal: J Cell Biol
Title: Growth differentiation factor 15 is a myomitokine governing systemic energy homeostasis.
Volume: 216
Issue: 1
Pages: 149-165
Publication  
First Author: Milan G
Year: 2015
Journal: Nat Commun
Title: Regulation of autophagy and the ubiquitin-proteasome system by the FoxO transcriptional network during muscle atrophy.
Volume: 6
Pages: 6670
Publication
First Author: Hirata Y
Year: 2022
Journal: J Clin Invest
Title: A Piezo1/KLF15/IL-6 axis mediates immobilization-induced muscle atrophy.
Volume: 132
Issue: 10
Pages: 1-13
Publication  
First Author: Hirata Y
Year: 2019
Journal: JCI Insight
Title: Hyperglycemia induces skeletal muscle atrophy via a WWP1/KLF15 axis.
Volume: 4
Issue: 4
Publication
First Author: Arhzaouy K
Year: 2019
Journal: Autophagy
Title: VCP maintains lysosomal homeostasis and TFEB activity in differentiated skeletal muscle.
Volume: 15
Issue: 6
Pages: 1082-1099
Publication    
First Author: Moon JS
Year: 2020
Journal: Aging Cell
Title: Growth differentiation factor 15 protects against the aging-mediated systemic inflammatory response in humans and mice.
Pages: e13195
Publication
First Author: Patel S
Year: 2011
Journal: PLoS One
Title: Tissue-specific analysis of glycogen synthase kinase-3α (GSK-3α) in glucose metabolism: effect of strain variation.
Volume: 6
Issue: 1
Pages: e15845
Publication
First Author: Mitani Y
Year: 2017
Journal: FASEB J
Title: In vivo myomaker-mediated heterologous fusion and nuclear reprogramming.
Volume: 31
Issue: 1
Pages: 400-411
Publication
First Author: Hong S
Year: 2017
Journal: Nat Med
Title: Dissociation of muscle insulin sensitivity from exercise endurance in mice by HDAC3 depletion.
Volume: 23
Issue: 2
Pages: 223-234
Publication
First Author: Blaauw B
Year: 2008
Journal: Hum Mol Genet
Title: Akt activation prevents the force drop induced by eccentric contractions in dystrophin-deficient skeletal muscle.
Volume: 17
Issue: 23
Pages: 3686-96
Publication
First Author: Mock B
Year: 1989
Journal: Res Immunol
Title: A comparison of genetic linkage maps surrounding the Lsh/Ity/Bcg disease resistance locus.
Volume: 140
Issue: 8
Pages: 769-74
Publication
First Author: Cox RD
Year: 1990
Journal: Differentiation
Title: Transcriptional regulation of actin and myosin genes during differentiation of a mouse muscle cell line.
Volume: 43
Issue: 3
Pages: 183-91
Publication
First Author: Cerretti DP
Year: 1993
Journal: Genomics
Title: The murine homologue of the human interleukin-8 receptor type B maps near the Ity-Lsh-Bcg disease resistance locus.
Volume: 18
Issue: 2
Pages: 410-3
Publication
First Author: Chan CC
Year: 2021
Journal: Nat Commun
Title: A BAFF/APRIL axis regulates obesogenic diet-driven weight gain.
Volume: 12
Issue: 1
Pages: 2911
Publication
First Author: Matsushita Y
Year: 2023
Journal: J Biol Chem
Title: Hes1 marks peri-condensation mesenchymal cells that generate both chondrocytes and perichondrial cells in early bone development.
Volume: 299
Issue: 6
Pages: 104805
Publication
First Author: Acharyya S
Year: 2007
Journal: J Clin Invest
Title: Interplay of IKK/NF-kappaB signaling in macrophages and myofibers promotes muscle degeneration in Duchenne muscular dystrophy.
Volume: 117
Issue: 4
Pages: 889-901
Publication
First Author: Fujimaki S
Year: 2022
Journal: Nat Metab
Title: The endothelial Dll4-muscular Notch2 axis regulates skeletal muscle mass.
Volume: 4
Issue: 2
Pages: 180-189
Publication
First Author: Leduc-Gaudet JP
Year: 2023
Journal: Nat Commun
Title: MYTHO is a novel regulator of skeletal muscle autophagy and integrity.
Volume: 14
Issue: 1
Pages: 1199
Publication
First Author: Southard S
Year: 2014
Journal: Genesis
Title: A series of Cre-ER(T2) drivers for manipulation of the skeletal muscle lineage.
Volume: 52
Issue: 8
Pages: 759-70
Publication
First Author: Wissing ER
Year: 2014
Journal: Hum Mol Genet
Title: P38α MAPK underlies muscular dystrophy and myofiber death through a Bax-dependent mechanism.
Volume: 23
Issue: 20
Pages: 5452-63
Publication
First Author: Burr AR
Year: 2014
Journal: Mol Cell Biol
Title: Na+ dysregulation coupled with Ca2+ entry through NCX1 promotes muscular dystrophy in mice.
Volume: 34
Issue: 11
Pages: 1991-2002
Publication
First Author: Wang Y
Year: 1996
Journal: Nature
Title: Functional redundancy of the muscle-specific transcription factors Myf5 and myogenin.
Volume: 379
Issue: 6568
Pages: 823-5
Publication
First Author: Fulgenzi G
Year: 2020
Journal: Nat Commun
Title: Novel metabolic role for BDNF in pancreatic β-cell insulin secretion.
Volume: 11
Issue: 1
Pages: 1950
Publication  
First Author: Akkuratova N
Year: 2022
Journal: Front Endocrinol (Lausanne)
Title: Developmental heterogeneity of embryonic neuroendocrine chromaffin cells and their maturation dynamics.
Volume: 13
Pages: 1020000
Publication
First Author: Acharyya S
Year: 2010
Journal: PLoS One
Title: TNF inhibits Notch-1 in skeletal muscle cells by Ezh2 and DNA methylation mediated repression: implications in duchenne muscular dystrophy.
Volume: 5
Issue: 8
Pages: e12479
Publication
First Author: Cohen S
Year: 2009
Journal: J Cell Biol
Title: During muscle atrophy, thick, but not thin, filament components are degraded by MuRF1-dependent ubiquitylation.
Volume: 185
Issue: 6
Pages: 1083-95
Publication  
First Author: Fix DK
Year: 2019
Journal: Oxid Med Cell Longev
Title: Regulation of Skeletal Muscle DRP-1 and FIS-1 Protein Expression by IL-6 Signaling.
Volume: 2019
Pages: 8908457
Publication
First Author: Golding JP
Year: 2004
Journal: Dev Dyn
Title: Mouse myotomes pairs exhibit left-right asymmetric expression of MLC3F and alpha-skeletal actin.
Volume: 231
Issue: 4
Pages: 795-800
Publication
First Author: Franco D
Year: 2000
Journal: Circ Res
Title: Multiple transcriptional domains, with distinct left and right components, in the atrial chambers of the developing heart.
Volume: 87
Issue: 11
Pages: 984-91
Publication
First Author: Robert B
Year: 1985
Journal: Nature
Title: Investigation of genetic linkage between myosin and actin genes using an interspecific mouse back-cross.
Volume: 314
Issue: 6007
Pages: 181-3
Publication
First Author: Heidmann O
Year: 1986
Journal: Science
Title: Chromosomal localization of muscle nicotinic acetylcholine receptor genes in the mouse.
Volume: 234
Issue: 4778
Pages: 866-8
Publication
First Author: Skow LC
Year: 1988
Journal: Biochem Genet
Title: Mapping of mouse gamma crystallin genes on chromosome 1.
Volume: 26
Issue: 9-10
Pages: 557-70
Publication
First Author: Olson E
Year: 1990
Journal: Genomics
Title: Myogenin is in an evolutionarily conserved linkage group on human chromosome 1q31-q41 and unlinked to other mapped muscle regulatory factor genes.
Volume: 8
Issue: 3
Pages: 427-34
Publication
First Author: Lafuse WP
Year: 1992
Journal: Mamm Genome
Title: Assignment of the microtubule-associated protein 2 gene to mouse chromosome 1.
Volume: 3
Issue: 1
Pages: 48-51
Publication
First Author: Maddala R
Year: 2013
Journal: PLoS One
Title: L-type calcium channels play a critical role in maintaining lens transparency by regulating phosphorylation of aquaporin-0 and myosin light chain and expression of connexins.
Volume: 8
Issue: 5
Pages: e64676
Publication
First Author: Sasako T
Year: 2022
Journal: Nat Commun
Title: Deletion of skeletal muscle Akt1/2 causes osteosarcopenia and reduces lifespan in mice.
Volume: 13
Issue: 1
Pages: 5655
Publication    
First Author: Boyer JG
Year: 2019
Journal: JCI Insight
Title: ERK1/2 signaling induces skeletal muscle slow fiber-type switching and reduces muscular dystrophy disease severity.
Volume: 5
Publication
First Author: Moore KJ
Year: 1994
Journal: Genetics
Title: The murine dilute suppressor gene encodes a cell autonomous suppressor.
Volume: 138
Issue: 2
Pages: 491-7
Publication
First Author: Diaz F
Year: 2005
Journal: Hum Mol Genet
Title: Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency.
Volume: 14
Issue: 18
Pages: 2737-48
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: Lyons GE
Year: 1990
Journal: J Cell Biol
Title: The expression of myosin genes in developing skeletal muscle in the mouse embryo.
Volume: 111
Issue: 4
Pages: 1465-76
Publication
First Author: Ontell MP
Year: 1993
Journal: Dev Dyn
Title: Modulation of contractile protein gene expression in fetal murine crural muscles: emergence of muscle diversity.
Volume: 198
Issue: 3
Pages: 203-13
Publication
First Author: Ontell M
Year: 1995
Journal: Microsc Res Tech
Title: Muscle-specific gene expression during myogenesis in the mouse.
Volume: 30
Issue: 5
Pages: 354-65
Publication
First Author: Block NE
Year: 1996
Journal: Dev Dyn
Title: Acceleration of somitic myogenesis in embryos of myogenin promoter-MRF4 transgenic mice.
Volume: 207
Issue: 4
Pages: 382-94
Publication
First Author: Gambarotto L
Year: 2022
Journal: J Cachexia Sarcopenia Muscle
Title: Ambra1 deficiency impairs mitophagy in skeletal muscle.
Volume: 13
Issue: 4
Pages: 2211-2224
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: Petchey LK
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: Loss of Prox1 in striated muscle causes slow to fast skeletal muscle fiber conversion and dilated cardiomyopathy.
Volume: 111
Issue: 26
Pages: 9515-20
Publication
First Author: Ontell M
Year: 1993
Journal: Development
Title: Contractile protein gene expression in primary myotubes of embryonic mouse hindlimb muscles.
Volume: 117
Issue: 4
Pages: 1435-44
Publication
First Author: Issa LL
Year: 2006
Journal: Dev Biol
Title: MusTRD can regulate postnatal fiber-specific expression.
Volume: 293
Issue: 1
Pages: 104-15
Publication
First Author: Walther C
Year: 1991
Journal: Genomics
Title: Pax: a murine multigene family of paired box-containing genes.
Volume: 11
Issue: 2
Pages: 424-34
Publication
First Author: Niro C
Year: 2010
Journal: Dev Biol
Title: Six1 and Six4 gene expression is necessary to activate the fast-type muscle gene program in the mouse primary myotome.
Volume: 338
Issue: 2
Pages: 168-82
Publication
First Author: Delgado-Olguín P
Year: 2012
Journal: Nat Genet
Title: Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis.
Volume: 44
Issue: 3
Pages: 343-7
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: Swinehart IT
Year: 2013
Journal: Development
Title: Hox11 genes are required for regional patterning and integration of muscle, tendon and bone.
Volume: 140
Issue: 22
Pages: 4574-82
Publication
First Author: Vincent SD
Year: 2012
Journal: Mol Biol Evol
Title: Non conservation of function for the evolutionarily conserved prdm1 protein in the control of the slow twitch myogenic program in the mouse embryo.
Volume: 29
Issue: 10
Pages: 3181-91
Publication    
First Author: Cibi DM
Year: 2019
Journal: Elife
Title: Neural crest-specific deletion of Rbfox2 in mice leads to craniofacial abnormalities including cleft palate.
Volume: 8
Publication
First Author: Patapoutian A
Year: 1995
Journal: Development
Title: Disruption of the mouse MRF4 gene identifies multiple waves of myogenesis in the myotome.
Volume: 121
Issue: 10
Pages: 3347-58
Publication
First Author: Gerber SD
Year: 2020
Journal: Dev Biol
Title: Functional domains of the FgfrL1 receptor.
Volume: 461
Issue: 1
Pages: 43-54
Publication
First Author: Grote P
Year: 2013
Journal: Dev Cell
Title: The tissue-specific lncRNA Fendrr is an essential regulator of heart and body wall development in the mouse.
Volume: 24
Issue: 2
Pages: 206-14
Publication
First Author: Welcker JE
Year: 2013
Journal: Development
Title: Insm1 controls development of pituitary endocrine cells and requires a SNAG domain for function and for recruitment of histone-modifying factors.
Volume: 140
Issue: 24
Pages: 4947-58
Publication
First Author: Janssen L
Year: 2016
Journal: Angiogenesis
Title: ADAMTS3 activity is mandatory for embryonic lymphangiogenesis and regulates placental angiogenesis.
Volume: 19
Issue: 1
Pages: 53-65
Publication
First Author: Liu H
Year: 2024
Journal: iScience
Title: Epigenetic repression of Cend1 by lysine-specific demethylase 1 is essential for murine heart development.
Volume: 27
Issue: 1
Pages: 108722
Publication
First Author: Neidhardt L
Year: 2000
Journal: Mech Dev
Title: Large-scale screen for genes controlling mammalian embryogenesis, using high-throughput gene expression analysis in mouse embryos.
Volume: 98
Issue: 1-2
Pages: 77-94
Publication  
First Author: Tamplin OJ
Year: 2008
Journal: BMC Genomics
Title: Microarray analysis of Foxa2 mutant mouse embryos reveals novel gene expression and inductive roles for the gastrula organizer and its derivatives.
Volume: 9
Pages: 511
Publication
First Author: Hoffman BG
Year: 2008
Journal: Genome Biol
Title: Identification of transcripts with enriched expression in the developing and adult pancreas.
Volume: 9
Issue: 6
Pages: R99
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: RIKEN Data Curation in Mouse Genome Informatics
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Mouse Synonym Curation
Publication        
First Author: DDB, FB, MGI, GOA, ZFIN curators
Year: 2001
Title: Gene Ontology annotation through association of InterPro records with GO terms
Publication      
First Author: Shanghai Model Organisms Center
Year: 2017
Journal: MGI Direct Data Submission
Title: Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China
Publication        
First Author: GOA curators
Year: 2016
Title: Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Publication        
First Author: The Gene Ontology Consortium
Year: 2014
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2003
Title: MGI Sequence Curation Reference
Publication
First Author: Kawai J
Year: 2001
Journal: Nature
Title: Functional annotation of a full-length mouse cDNA collection.
Volume: 409
Issue: 6821
Pages: 685-90
Publication        
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
Publication        
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
Publication        
First Author: AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators
Year: 2011
Title: Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Publication
First Author: Okazaki Y
Year: 2002
Journal: Nature
Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Volume: 420
Issue: 6915
Pages: 563-73
Publication        
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
Publication
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582