Page last updated: 2024-08-18

tecnazene and Muscle Disorders

tecnazene has been researched along with Muscle Disorders in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (10.00)18.2507
2000's5 (50.00)29.6817
2010's3 (30.00)24.3611
2020's1 (10.00)2.80

Authors

AuthorsStudies
Chang, X; Hu, Z; Lv, H; Wang, Q; Wang, Z; Xie, Z; Xiong, H; Yu, M; Yuan, Y; Zhang, W1
Barth, PG; Beggs, AH; Clarke, NF; den Dunnen, JT; Donner, K; Frey, JA; Kiiski, K; Laing, NG; Laporte, J; Lehtokari, VL; Marttila, M; North, KN; Pelin, K; Repo, P; Romero, NB; Sandaradura, SA; Saunders, C; Wallgren-Pettersson, C; Winder, TL1
Arumilli, M; Evilä, A; Hackman, P; Udd, B1
Beggs, AH; Bönnemann, CG; Clarke, NF; Donkervoort, S; Edvardson, S; Engelen, BG; Granzier, H; Gregorio, CC; Gupta, VA; Joureau, B; Kiss, B; Lee, EJ; Lehtokari, VL; Malfatti, E; Ottenheijm, CA; Pappas, CT; Pelin, K; Romero, NB; Stienen, GJ; Voermans, NC; Wallgren-Pettersson, C; Winter, JM; Yuen, M1
Ochala, J1
Conover, GM; Gregorio, CC; Henderson, SN1
Ackermann, MA; Bloch, RJ; Bowman, AL; Kontrogianni-Konstantopoulos, A; Yap, SV1
Gregorio, CC; Kazmierski, ST; Labeit, S; McElhinny, AS1
Clarkson, E; Costa, CF; Machesky, LM1
Barth, PG; Jap, PH; Nonaka, I; Ramaekers, FC; Sengers, RC; Stadhouders, AM; ter Laak, HJ; van der Ven, PF1

Reviews

4 review(s) available for tecnazene and Muscle Disorders

ArticleYear
Thin filament proteins mutations associated with skeletal myopathies: defective regulation of muscle contraction.
    Journal of molecular medicine (Berlin, Germany), 2008, Volume: 86, Issue:11

    Topics: Actins; Animals; Humans; Muscle Contraction; Muscle Proteins; Muscle, Skeletal; Muscular Diseases; Mutation; Troponin T

2008
Muscle giants: molecular scaffolds in sarcomerogenesis.
    Physiological reviews, 2009, Volume: 89, Issue:4

    Topics: Animals; Connectin; Guanine Nucleotide Exchange Factors; Humans; Muscle Proteins; Muscles; Muscular Diseases; Myofibrils; Protein Kinases; Protein Serine-Threonine Kinases; Rho Guanine Nucleotide Exchange Factors; Sarcomeres

2009
Nebulin: the nebulous, multifunctional giant of striated muscle.
    Trends in cardiovascular medicine, 2003, Volume: 13, Issue:5

    Topics: Actin Cytoskeleton; Animals; Humans; Mice; Muscle Proteins; Muscle, Skeletal; Muscular Diseases; Mutation; Sarcomeres

2003
Congenital myopathies: diseases of the actin cytoskeleton.
    The Journal of pathology, 2004, Volume: 204, Issue:4

    Topics: Actins; Cytoskeleton; Humans; Muscle Proteins; Muscle, Skeletal; Muscular Diseases; Mutation; Phenotype; Tropomyosin

2004

Other Studies

6 other study(ies) available for tecnazene and Muscle Disorders

ArticleYear
Mutational and clinical spectrum in a cohort of Chinese patients with hereditary nemaline myopathy.
    Clinical genetics, 2020, Volume: 97, Issue:6

    Topics: Actins; Adolescent; Adult; Child; Child, Preschool; DNA Mutational Analysis; Exons; Female; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Humans; Male; Middle Aged; Muscle Proteins; Muscular Diseases; Mutation; Myopathies, Nemaline; Phenotype; Protein Isoforms; RNA Splicing; Troponin T; Young Adult

2020
Mutation update: the spectra of nebulin variants and associated myopathies.
    Human mutation, 2014, Volume: 35, Issue:12

    Topics: Alternative Splicing; Animals; Chromosomes, Human, Pair 2; Databases, Genetic; Exons; Genotype; Humans; Models, Animal; Muscle Proteins; Muscular Diseases; Mutation; Phenotype

2014
Targeted next-generation sequencing assay for detection of mutations in primary myopathies.
    Neuromuscular disorders : NMD, 2016, Volume: 26, Issue:1

    Topics: Exons; Family Health; Female; Genetic Linkage; Humans; International Cooperation; Male; Membrane Proteins; Muscle Proteins; Muscular Diseases; Mutation; Sequence Analysis, DNA; Tenascin

2016
Mutation-specific effects on thin filament length in thin filament myopathy.
    Annals of neurology, 2016, Volume: 79, Issue:6

    Topics: Actins; Animals; Case-Control Studies; Cytoskeleton; Humans; Mice, Knockout; Muscle Contraction; Muscle Proteins; Muscle, Skeletal; Muscular Diseases; Mutation; Sarcomeres

2016
A myopathy-linked desmin mutation perturbs striated muscle actin filament architecture.
    Molecular biology of the cell, 2009, Volume: 20, Issue:3

    Topics: Actin Cytoskeleton; Amino Acid Substitution; Animals; Chick Embryo; Cytoplasm; Desmin; Green Fluorescent Proteins; Humans; Mice; Muscle Proteins; Muscle, Striated; Muscular Diseases; Mutant Proteins; Mutation; Myocytes, Cardiac; Myosins; Protein Binding; Protein Structure, Quaternary; Protein Structure, Secondary; Rats; Recombinant Fusion Proteins

2009
Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteins.
    Journal of the neurological sciences, 1995, Volume: 129, Issue:2

    Topics: Adolescent; Adult; Child; Collagen; Connectin; Cytoskeletal Proteins; Desmin; Extracellular Matrix Proteins; Female; Fluorescent Antibody Technique; Humans; Immunophenotyping; Infant; Infant, Newborn; Laminin; Male; Muscle Proteins; Muscular Diseases; Myosins; Protein Kinases; Sarcomeres; Vimentin

1995