Compounds > tecnazene
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tecnazene and Muscular Dystrophies

tecnazene has been researched along with Muscular Dystrophies in 11 studies

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19909 (81.82)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (18.18)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arné-Bes, MC; Bieth, E; Cances, C; Cintas, P; Claustres, M; Cossée, M; Espil, C; Ferrer-Monasterio, X; Goizet, C; Juntas Morales, R; Koenig, M; Lacourt, D; Martin Negrier, ML; Pegeot, H; Renard, D; Rigau, V; Rivier, F; Sole, G; Theze, C; Uro-Coste, E; Walther-Louvier, U; Yauy, K; Zenagui, R1
Hsu, SY; Hu, JW; Ouyang, P; Wu, HP; Wu, WA1
Browning, K; Fischbeck, K; Oliver, N; Oronzi-Scott, M; Sarkar, S; Schmickel, R; Stedman, H; Sylvester, J; Wang, K1
Dubowitz, V; Dunn, MJ; Patel, K; Strong, PN; Voit, T1
Dubowitz, V; Dunn, MJ; Patel, K; Strong, PN1
Brown, RH; Hoffman, EP; Kunkel, LM1
Chafey, P; Chelly, J; Fardeau, M; Kaplan, JC; Pernelle, JJ; Tomé, F; Wahrmann, JP1
Betto, R; Bonilla, E; DiMauro, S; Miranda, AF; Prelle, A; Rowland, LP; Salviati, G; Schon, EA; Zeviani, M1
Feener, CC; Hoffman, EP; Kunkel, LM; Monaco, AP1
Archidiacono, N; Bardosi, A; Ferro, M; Fürst, D; Nave, R; Osborn, M; Romano, V; Romeo, G; Weber, K1
Bonilla, E; DiMauro, S; Miranda, AF; Prelle, A; Rowland, LP; Salviati, G; Wood, DS; Zeviani, M1

Other Studies

11 other study(ies) available for tecnazene and Muscular Dystrophies

ArticleYear
A Reliable Targeted Next-Generation Sequencing Strategy for Diagnosis of Myopathies and Muscular Dystrophies, Especially for the Giant Titin and Nebulin Genes.
    The Journal of molecular diagnostics : JMD, 2018, Volume: 20, Issue:4

    Topics: Computational Biology; Connectin; DNA; DNA Copy Number Variations; Exons; Heterozygote; High-Throughput Nucleotide Sequencing; Humans; INDEL Mutation; Muscle Proteins; Muscular Dystrophies; Reproducibility of Results

2018
Transgenic mice expressing mutant Pinin exhibit muscular dystrophy, nebulin deficiency and elevated expression of slow-type muscle fiber genes.
    Biochemical and biophysical research communications, 2014, Jan-03, Volume: 443, Issue:1

    Topics: Animals; Cell Adhesion Molecules; DNA-Binding Proteins; Drosophila Proteins; Gene Expression Profiling; Gene Expression Regulation; HeLa Cells; Humans; Mice; Mice, Transgenic; Muscle Fibers, Slow-Twitch; Muscle Proteins; Muscular Dystrophies; Nuclear Proteins; Protein Structure, Tertiary

2014
Nebulin cDNAs detect a 25-kilobase transcript in skeletal muscle and localize to human chromosome 2.
    Genomics, 1988, Volume: 2, Issue:1

    Topics: Chromosome Mapping; Chromosomes, Human, Pair 2; DNA; DNA Restriction Enzymes; Genes; Humans; Muscle Proteins; Muscles; Muscular Dystrophies; Nucleic Acid Hybridization; Transcription, Genetic

1988
Dystrophin and nebulin in the muscular dystrophies.
    Journal of the neurological sciences, 1988, Volume: 87, Issue:2-3

    Topics: Adolescent; Adult; Child; Child, Preschool; Dystrophin; Fetus; Humans; Infant, Newborn; Male; Middle Aged; Muscle Proteins; Muscular Dystrophies

1988
Calmodulin-binding profiles for nebulin and dystrophin in human skeletal muscle.
    FEBS letters, 1988, Jul-18, Volume: 234, Issue:2

    Topics: Calmodulin; Dystrophin; Humans; Molecular Weight; Muscle Proteins; Muscles; Muscular Dystrophies; Protein Binding; Reference Values

1988
Dystrophin: the protein product of the Duchenne muscular dystrophy locus.
    Cell, 1987, Dec-24, Volume: 51, Issue:6

    Topics: Animals; Disease Models, Animal; Dystrophin; Genes; Humans; Male; Mice; Molecular Weight; Muscle Proteins; Muscle, Smooth; Muscles; Muscular Dystrophies; Myocardium; Recombinant Fusion Proteins

1987
Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene.
    Human genetics, 1988, Volume: 78, Issue:3

    Topics: Chromosome Deletion; Electrophoresis, Polyacrylamide Gel; Humans; Male; Muscle Proteins; Muscles; Muscular Dystrophies

1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophy.
    Neurology, 1988, Volume: 38, Issue:10

    Topics: Child; Child, Preschool; Chromosome Deletion; Humans; Immunohistochemistry; Muscle Proteins; Muscular Dystrophies; X Chromosome

1988
Conservation of the Duchenne muscular dystrophy gene in mice and humans.
    Science (New York, N.Y.), 1987, Oct-16, Volume: 238, Issue:4825

    Topics: Amino Acid Sequence; Animals; Base Sequence; DNA; DNA, Recombinant; Exons; Humans; Male; Mice; Molecular Sequence Data; Muscle Proteins; Muscles; Muscular Dystrophies; Muscular Dystrophy, Animal; Myocardium; Nucleic Acid Hybridization; RNA, Messenger; X Chromosome

1987
Nebulin and titin expression in Duchenne muscular dystrophy appears normal.
    FEBS letters, 1987, Nov-16, Volume: 224, Issue:1

    Topics: Antibodies, Monoclonal; Child; Child, Preschool; Chromosome Deletion; Connectin; Humans; Male; Muscle Proteins; Muscles; Muscular Dystrophies; Protein Kinases; X Chromosome

1987
Is nebulin the defective gene product in Duchenne muscular dystrophy?
    The New England journal of medicine, 1987, Jan-08, Volume: 316, Issue:2

    Topics: Child; Child, Preschool; Humans; Infant; Male; Muscle Proteins; Muscles; Muscular Dystrophies

1987