Cargando…

Characterization of a hypercontraction-induced myopathy in Drosophila caused by mutations in Mhc

The Myosin heavy chain (Mhc) locus encodes the muscle-specific motor mediating contraction in Drosophila. In a screen for temperature-sensitive behavioral mutants, we have identified two dominant Mhc alleles that lead to a hypercontraction-induced myopathy. These mutants are caused by single point m...

Descripción completa

Detalles Bibliográficos
Autores principales:	Montana, Enrico S., Littleton, J. Troy
Formato:	Texto
Lenguaje:	English
Publicado:	The Rockefeller University Press 2004
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172052/ https://www.ncbi.nlm.nih.gov/pubmed/15051736 http://dx.doi.org/10.1083/jcb.200308158

Ejemplares similares

Hypercontractivity in group Von Neumann algebras
por: Junge, Marius, et al.
Publicado: (2017)

Inhibition of As(III) and Hg(II) caused aortic hypercontraction by eugenol, linalool and carvone
por: Kundu, Swati, et al.
Publicado: (2015)

Elevated Expression of the Integrin-Associated Protein PINCH Suppresses the Defects of Drosophila melanogaster Muscle Hypercontraction Mutants
por: Pronovost, Stephen M., et al.
Publicado: (2013)

Characterization of axonal transport defects in Drosophila Huntingtin mutants
por: Weiss, Kurt R., et al.
Publicado: (2016)

Role of calcium channels and endothelial factors in nickel induced aortic hypercontraction in Wistar rats
por: WANI, Shahnawaz Ahmad, et al.
Publicado: (2018)

Tensor Hypercontraction Form of the Perturbative Triples Energy in Coupled-Cluster Theory
por: Jiang, Andy, et al.
Publicado: (2023)

Overexpression of miRNA-9 Generates Muscle Hypercontraction Through Translational Repression of Troponin-T in Drosophila melanogaster Indirect Flight Muscles
por: Katti, Prasanna, et al.
Publicado: (2017)

A Genomic Analysis of Membrane Trafficking and Neurotransmitter Release in Drosophila
por: Littleton, J. Troy
Publicado: (2000)

Quercetin and resveratrol ameliorate nickel-mediated hypercontraction in isolated Wistar rat aorta
por: Wani, Shahnawaz Ahmad, et al.
Publicado: (2022)

Mutations in the cell-binding motif of lam-3/laminin α reveal hypercontraction behavior and defective sensitivity to levamisole in Caenorhabditis elegans
por: Wang, Lianzijun, et al.
Publicado: (2021)

Characterization of developmental and molecular factors underlying release heterogeneity at Drosophila synapses
por: Akbergenova, Yulia, et al.
Publicado: (2018)

Function of Drosophila Synaptotagmins in membrane trafficking at synapses
por: Quiñones-Frías, Mónica C., et al.
Publicado: (2021)

Synaptic Plasticity Induced by Differential Manipulation of Tonic and Phasic Motoneurons in Drosophila
por: Aponte-Santiago, Nicole A., et al.
Publicado: (2020)

Tensor-Hypercontracted MP2 First Derivatives: Runtime and Memory Efficient Computation of Hyperfine Coupling Constants
por: Bangerter, Felix H., et al.
Publicado: (2022)

Hypercontractive Inequalities for the Second Norm of Highly Concentrated Functions, and Mrs. Gerber’s-Type Inequalities for the Second Rényi Entropy
por: Levhari, Niv, et al.
Publicado: (2022)

Congenital myopathy is caused by mutation of HACD1
por: Muhammad, Emad, et al.
Publicado: (2013)

Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1
por: Tasca, Giorgio, et al.
Publicado: (2015)

Misato underlies visceral myopathy in Drosophila
por: Min, Soohong, et al.
Publicado: (2017)

Dominant collagen XII mutations cause a distal myopathy
por: Mohassel, Payam, et al.
Publicado: (2019)

Basal wall hypercontraction of Takotsubo cardiomyopathy in a patient who had been diagnosed with dilated cardiomyopathy: a case report
por: Ichihara, Noboru, et al.
Publicado: (2017)

The Inhibitory Effect of Extra Virgin Olive Oil and Its Active Compound Oleocanthal on Prostaglandin-Induced Uterine Hypercontraction and Pain—Ex Vivo and In Vivo Study
por: Chiang, Yi-Fen, et al.
Publicado: (2020)

Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy
por: Biancalana, Valérie, et al.
Publicado: (2018)

Homozygous mutation in HSPB1 causing distal vacuolar myopathy and motor neuropathy
por: Bugiardini, Enrico, et al.
Publicado: (2017)

Skeletal muscle fiber hypercontraction induced by Bothrops asper myotoxic phospholipases A(2) ex vivo does not involve a direct action on the contractile apparatus
por: López-Dávila, Alfredo Jesús, et al.
Publicado: (2023)

Drosophila Synaptotagmin 7 negatively regulates synaptic vesicle release and replenishment in a dosage-dependent manner
por: Guan, Zhuo, et al.
Publicado: (2020)

Loss of the extracellular matrix protein Perlecan disrupts axonal and synaptic stability during Drosophila development
por: Guss, Ellen J, et al.
Publicado: (2023)

The Molecular Mechanisms of Mutations in Actin and Myosin that Cause Inherited Myopathy
por: Marston, Steven
Publicado: (2018)

Nemaline myopathy caused byTNNT1 mutations in a Dutch pedigree
por: van der Pol, W Ludo, et al.
Publicado: (2014)

Biallelic LINE insertion mutation in HACD1 causing congenital myopathy
por: Al Amrani, Fatema, et al.
Publicado: (2020)

Novel Desmin Mutation Causing Myofibrillar Myopathy in a Hmong Family
por: Nicolau, Stefan, et al.
Publicado: (2020)

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy
por: Konersman, Chamindra G., et al.
Publicado: (2017)

South Asian-Specific MYBPC3(Δ25bp) Deletion Carriers Display Hypercontraction and Impaired Diastolic Function Under Exercise Stress
por: Bazrafshan, Sholeh, et al.
Publicado: (2021)

Novel HSPB1 mutation causes both motor neuronopathy and distal myopathy
por: Lewis-Smith, D.J., et al.
Publicado: (2016)

Novel Splicing Mutation in MTM1 Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy
por: Bosco, Luca, et al.
Publicado: (2022)

Case report: Mutation in NPPA gene as a cause of fibrotic atrial myopathy
por: Silva Cunha, Pedro, et al.
Publicado: (2023)

Drosophila Homolog of Human KIF22 at the Autism-Linked 16p11.2 Loci Influences Synaptic Connectivity at Larval Neuromuscular Junctions
por: Park, Sang Mee, et al.
Publicado: (2016)

Vacuolar Myopathy Associated to CACNA1S Mutation as a Rare Cause of Late-Onset Limb-Girdle Myopathy: A Case Report
por: López-Hernández, Juan Carlos, et al.
Publicado: (2021)

Tubular aggregate myopathy caused by a novel mutation in the cytoplasmic domain of STIM1
por: Okuma, Hidehiko, et al.
Publicado: (2016)

Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsy
por: Hardy, Steven A., et al.
Publicado: (2016)

A novel recessive mutation affecting DNAJB6a causes myofibrillar myopathy
por: Qian, Fang-Yuan, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_ikg0kt1gcn838tm31q37vpdabm