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Page last updated: 2024-08-17

lysine and Cardiomyopathy, Dilated

lysine has been researched along with Cardiomyopathy, Dilated in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (44.44)29.6817
2010's2 (22.22)24.3611
2020's3 (33.33)2.80

Authors

AuthorsStudies
Gillette, T; Girard, L; Gonzales, C; Liu, ZP; Martinez, ED; May, H; Tran, TA; Wang, L; Zhang, QJ1
Abnousi, A; Bazeley, P; Hu, M; Liu, CF; Moravec, CS; Morley, M; Ni, Y; Tang, WHW1
Boeckel, JN; Bordalo, DM; Drewe-Boss, P; Eger, N; Gaul, S; Ghanbari, M; Gotthardt, M; Haas, J; Katus, HA; Kneuer, JM; Kokot, KE; Lai, A; Laufs, U; Liss, M; Meder, B; Möbius-Winkler, M; Müller, M; Ohler, U; Rebs, S; Schoppe, L; Streckfuss-Bömeke, K; Tappu, R1
Blair, CA; Campbell, KS; Holewinski, RJ; Kirk, JA; Li, A; Martin, TG; Moravec, CS; Papadaki, M; Previs, SB; Stachowski, MJ; Van Eyk, JE; Warshaw, DM1
Avrova, SV; Borovikov, YS; Karpicheva, OE; Redwood, CS; Robinson, P1
Hui, R; Song, L; Wang, H; Wang, J; Wang, S; Wang, X; Yao, Y; Zheng, W; Zou, Y1
Ahmed, RP; Arteaga, GM; Rajan, S; Solaro, RJ; Warren, CM; Wieczorek, DF1
Assereto, S; Biancheri, R; Bruno, C; Donati, MA; Gazzerro, E; Giberti, L; Lisanti, MP; Minetti, C; Pasquini, E; Pedemonte, M; Scapolan, S; Sotgia, F; Stringara, S; Traverso, M; Wang, X; Zara, F1
Bousman, S; Coates, K; Dienel, NH; Hanson, EL; Hershberger, RE; Jakobs, PM; Keegan, H; Litt, M1

Other Studies

9 other study(ies) available for lysine and Cardiomyopathy, Dilated

ArticleYear
Inhibition of Jumonji demethylases reprograms severe dilated cardiomyopathy and prolongs survival.
    The Journal of biological chemistry, 2022, Volume: 298, Issue:2

    Topics: Animals; Cardiomyopathy, Dilated; Enzyme Inhibitors; Histone Demethylases; Histones; Humans; Jumonji Domain-Containing Histone Demethylases; Lysine; Mice; Small Molecule Libraries

2022
Global analysis of histone modifications and long-range chromatin interactions revealed the differential cistrome changes and novel transcriptional players in human dilated cardiomyopathy.
    Journal of molecular and cellular cardiology, 2020, Volume: 145

    Topics: Base Sequence; Cardiomyopathy, Dilated; Chromatin; DNA-Binding Proteins; Enhancer Elements, Genetic; Epigenesis, Genetic; Gene Ontology; Genome, Human; Heart Failure; Heart Ventricles; Histones; Humans; Lysine; Male; Methylation; Muscle Proteins; Nucleotide Motifs; Promoter Regions, Genetic; Protein Processing, Post-Translational; Transcription Factors

2020
SLM2 Is A Novel Cardiac Splicing Factor Involved in Heart Failure due to Dilated Cardiomyopathy.
    Genomics, proteomics & bioinformatics, 2022, Volume: 20, Issue:1

    Topics: Cardiomyopathy, Dilated; Connectin; Glutamates; Heart Failure; Humans; Lysine; Proline; RNA Splicing Factors; RNA-Binding Proteins; RNA, Messenger; Tropomyosin; Troponin I; Troponin T; Valine

2022
Diabetes with heart failure increases methylglyoxal modifications in the sarcomere, which inhibit function.
    JCI insight, 2018, 10-18, Volume: 3, Issue:20

    Topics: Actins; Adult; Animals; Arginine; Cardiomyopathy, Dilated; Diabetes Mellitus, Type 2; Disease Models, Animal; Female; Glycolysis; Heart Failure; Heart Ventricles; Humans; Lysine; Male; Mice; Middle Aged; Myosins; Pyruvaldehyde; Sarcomeres; Single-Cell Analysis

2018
The effect of the dilated cardiomyopathy-causing Glu40Lys TPM1 mutation on actin-myosin interactions during the ATPase cycle.
    Biochemical and biophysical research communications, 2011, Aug-05, Volume: 411, Issue:3

    Topics: Actins; Adenosine Triphosphatases; Cardiomyopathy, Dilated; Glutamic Acid; Humans; Lysine; Myosins; Tropomyosin

2011
Mutation Glu82Lys in lamin A/C gene is associated with cardiomyopathy and conduction defect.
    Biochemical and biophysical research communications, 2006, May-26, Volume: 344, Issue:1

    Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Asian People; Cardiomyopathy, Dilated; Cell Nucleus; Cells, Cultured; Child; Female; Glutamic Acid; Heart Block; Heart Conduction System; Humans; Lamin Type A; Lysine; Male; Membrane Proteins; Molecular Sequence Data; Nuclear Envelope; Nuclear Proteins; Pedigree; Point Mutation; Thymopoietins

2006
Use of 2-D DIGE analysis reveals altered phosphorylation in a tropomyosin mutant (Glu54Lys) linked to dilated cardiomyopathy.
    Proteomics, 2008, Volume: 8, Issue:1

    Topics: Amino Acid Substitution; Animals; Cardiomyopathy, Dilated; Electrophoresis, Gel, Two-Dimensional; Glutamic Acid; Immunoblotting; Lysine; Mice; Mice, Transgenic; Phosphorylation; Point Mutation; Tropomyosin

2008
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro.
    Laboratory investigation; a journal of technical methods and pathology, 2008, Volume: 88, Issue:3

    Topics: Adult; Alleles; Amino Acid Substitution; Animals; Cardiomyopathy, Dilated; Caveolin 3; Cell Membrane; Cell Nucleus; Chlorocebus aethiops; Codon; COS Cells; DNA; Electromyography; Female; Fluorescent Antibody Technique, Indirect; Genes, Dominant; Genes, Recessive; Green Fluorescent Proteins; Histocytochemistry; Homozygote; Humans; Immunohistochemistry; In Vitro Techniques; Lysine; Male; Methionine; Middle Aged; Muscle, Skeletal; Muscle, Smooth; Muscular Dystrophies; Mutation, Missense; Myocardium; Phenotype; Protein Isoforms; Transfection

2008
Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.
    Journal of cardiac failure, 2002, Volume: 8, Issue:1

    Topics: Cardiomyopathy, Dilated; Cardiomyopathy, Hypertrophic, Familial; Exons; Female; Gene Deletion; Humans; Lysine; Male; Middle Aged; Mutation; Pedigree; Troponin T

2002