Page last updated: 2024-10-18

glycine and Cardiomyopathy, Congestive

glycine has been researched along with Cardiomyopathy, Congestive in 8 studies

Research Excerpts

ExcerptRelevanceReference
"The genetic factors that underlie idiopathic dilated cardiomyopathy (IDCM) have not yet been elucidated."2.69Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group. ( Amouyel, P; Cambien, F; Charron, P; Desnos, M; Dorent, R; Jullières, Y; Komajda, M; Nicaud, V; Peuchmaurd, M; Poirier, O; Roizès, G; Schwartz, K; Tesson, F; Tiret, L, 1999)
"Genetic dilated cardiomyopathy (DCM) is a leading cause of heart failure."1.72Serine biosynthesis as a novel therapeutic target for dilated cardiomyopathy. ( Ameen, M; Arthur Ataam, J; Bharucha, N; Bruyneel, AAN; Diecke, S; Feyen, DAM; Furihata, T; Gavidia, AA; Karakikes, I; Kaur, B; Lim, EW; Martinez-Amador, N; Mercola, M; Metallo, CM; Monte, E; Nair, P; Perea-Gil, I; Seeger, T; Serrano, R; Snyder, MP; Termglinchan, V; Vadgama, N, 2022)
"Familial dilated cardiomyopathy can be caused by mutations in the proteins of the muscle thin filament."1.35Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle. ( Burch, M; Dyer, EC; Gallon, CE; Hoskins, AC; Jacques, AM; Kaski, JP; Kentish, JC; Marston, SB; Messer, AE; Ward, DG, 2009)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (12.50)18.2507
2000's4 (50.00)29.6817
2010's1 (12.50)24.3611
2020's2 (25.00)2.80

Authors

AuthorsStudies
Perea-Gil, I1
Seeger, T1
Bruyneel, AAN1
Termglinchan, V1
Monte, E1
Lim, EW1
Vadgama, N1
Furihata, T1
Gavidia, AA1
Arthur Ataam, J1
Bharucha, N1
Martinez-Amador, N1
Ameen, M1
Nair, P1
Serrano, R1
Kaur, B1
Feyen, DAM1
Diecke, S1
Snyder, MP1
Metallo, CM1
Mercola, M1
Karakikes, I1
Kong, Q1
Gu, J1
Lu, R1
Huang, C1
Chen, L1
Wu, W1
Lin, D1
Dyer, EC1
Jacques, AM1
Hoskins, AC1
Ward, DG1
Gallon, CE1
Messer, AE1
Kaski, JP1
Burch, M1
Kentish, JC1
Marston, SB1
Małek, LA1
Labib, S1
Mazurkiewicz, L1
Saj, M1
Płoski, R1
Tesson, F3
Bilińska, ZT2
Iwai, C1
Akita, H1
Shiga, N1
Takai, E1
Miyamoto, Y1
Shimizu, M1
Kawai, H1
Takarada, A1
Kajiya, T1
Yokoyama, M1
Magnusson, Y1
Levin, MC1
Eggertsen, R1
Nyström, E1
Mobini, R1
Schaufelberger, M1
Andersson, B1
Fidziańska, A1
Wagner, T1
Walski, M1
Grzybowski, J1
Ruzyłło, W1
Hausmanowa-Petrusewicz, I1
Charron, P1
Peuchmaurd, M1
Nicaud, V1
Cambien, F1
Tiret, L1
Poirier, O1
Desnos, M1
Jullières, Y1
Amouyel, P1
Roizès, G1
Dorent, R1
Schwartz, K1
Komajda, M1

Trials

1 trial available for glycine and Cardiomyopathy, Congestive

ArticleYear
Characterization of a unique genetic variant in the beta1-adrenoceptor gene and evaluation of its role in idiopathic dilated cardiomyopathy. CARDIGENE Group.
    Journal of molecular and cellular cardiology, 1999, Volume: 31, Issue:5

    Topics: Adult; Alleles; Arginine; Cardiomyopathy, Dilated; Evaluation Studies as Topic; Female; Genetic Code

1999

Other Studies

7 other studies available for glycine and Cardiomyopathy, Congestive

ArticleYear
Serine biosynthesis as a novel therapeutic target for dilated cardiomyopathy.
    European heart journal, 2022, 09-21, Volume: 43, Issue:36

    Topics: Activating Transcription Factor 4; Adenosine Triphosphate; Anti-Inflammatory Agents, Non-Steroidal;

2022
NMR-Based Metabolomic Analysis of Cardiac Tissues Clarifies Molecular Mechanisms of CVB3-Induced Viral Myocarditis and Dilated Cardiomyopathy.
    Molecules (Basel, Switzerland), 2022, Sep-19, Volume: 27, Issue:18

    Topics: Alanine; Animals; Aspartic Acid; Biomarkers; Cardiomyopathy, Dilated; Coxsackievirus Infections; Ent

2022
Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle.
    Circulation. Heart failure, 2009, Volume: 2, Issue:5

    Topics: Actins; Aspartic Acid; Calcium; Cardiomyopathy, Dilated; Child, Preschool; Cytoskeleton; Genotype; G

2009
A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlation.
    Journal of human genetics, 2011, Volume: 56, Issue:1

    Topics: Amino Acid Substitution; Arginine; Cardiomyopathy, Dilated; Dyskinesias; Family; Genetic Association

2011
Suppressive effect of the Gly389 allele of the beta1-adrenergic receptor gene on the occurrence of ventricular tachycardia in dilated cardiomyopathy.
    Circulation journal : official journal of the Japanese Circulation Society, 2002, Volume: 66, Issue:8

    Topics: Alleles; Cardiomyopathy, Dilated; Female; Gene Dosage; Gene Frequency; Genotype; Glycine; Humans; Ma

2002
Ser49Gly of beta1-adrenergic receptor is associated with effective beta-blocker dose in dilated cardiomyopathy.
    Clinical pharmacology and therapeutics, 2005, Volume: 78, Issue:3

    Topics: Adrenergic beta-Antagonists; Aged; Amino Acid Substitution; Cardiomyopathy, Dilated; Codon; Cohort S

2005
Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation.
    Journal of the neurological sciences, 2008, Aug-15, Volume: 271, Issue:1-2

    Topics: Adult; Aspartic Acid; Cardiomyopathy, Dilated; Cell Nucleus; DNA Mutational Analysis; Glycine; Human

2008
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