Page last updated: 2024-10-18

glycine and Cardiomyopathies

glycine has been researched along with Cardiomyopathies in 14 studies

Cardiomyopathies: A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS).

Research Excerpts

ExcerptRelevanceReference
"Sivelestat was given for the complication of ARDS."1.42Elevation of pivaloylcarnitine by sivelestat sodium in two children. ( Bo, R; Hasegawa, Y; Ishige, N; Kobayashi, H; Nakamura, M; Takahashi, T; Yamada, K; Yamaguchi, S, 2015)
"Glycine has been shown to participate in protection from hypoxia/reoxygenation injury."1.39Effects of glycine supplementation on myocardial damage and cardiac function after severe burn. ( Liang, GP; Lv, SJ; Peng, X; Wan, QX; Wang, L; Yan, H; Zhang, Y, 2013)

Research

Studies (14)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's11 (78.57)29.6817
2010's3 (21.43)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ng, R1
Manring, H1
Papoutsidakis, N1
Albertelli, T1
Tsai, N1
See, CJ1
Li, X1
Park, J1
Stevens, TL1
Bobbili, PJ1
Riaz, M1
Ren, Y1
Stoddard, CE1
Janssen, PM1
Bunch, TJ1
Hall, SP1
Lo, YC1
Jacoby, DL1
Qyang, Y1
Wright, N1
Ackermann, MA1
Campbell, SG1
Yamada, K1
Kobayashi, H1
Bo, R1
Takahashi, T1
Hasegawa, Y1
Nakamura, M1
Ishige, N1
Yamaguchi, S1
Rajasekaran, NS2
Firpo, MA1
Milash, BA1
Weiss, RB1
Benjamin, IJ2
Zhang, Y1
Lv, SJ1
Yan, H1
Wang, L1
Liang, GP1
Wan, QX1
Peng, X1
Saint-Georges, Y1
Bonnefoy, N1
di Rago, JP1
Chiron, S1
Dujardin, G1
Schmidt, MR1
Birkebaek, N1
Gonzalez, I1
Sunde, L1
Jánosi, A1
Andrikovics, H1
Vas, K1
Bors, A1
Hubay, M1
Sápi, Z1
Tordai, A1
Holmgren, G1
Hellman, U1
Anan, I1
Lundgren, HE1
Jonasson, J1
Stafberg, C1
Fahoum, S1
Suhr, OB1
Stulc, T1
Ceska, R1
Rosenzweig, M1
Skinner, M1
Prokaeva, T1
Théberge, R1
Costello, C1
Drachman, BM1
Connors, LH1
Connell, P1
Christians, ES1
Yan, LJ1
Taylor, RP1
Orosz, A1
Zhang, XQ1
Stevenson, TJ1
Peshock, RM1
Leopold, JA1
Barry, WH1
Loscalzo, J1
Odelberg, SJ1
Bing, W1
Knott, A1
Redwood, C1
Esposito, G1
Purcell, I1
Watkins, H1
Marston, S1
Enjuto, M1
Francino, A1
Navarro-López, F1
Viles, D1
Paré, JC1
Ballesta, AM1
Hahner, A1
Erdmann, J1
Kallisch, H1
Fleck, E1
Regitz-Zagrosek, V1

Other Studies

14 other studies available for glycine and Cardiomyopathies

ArticleYear
Patient mutations linked to arrhythmogenic cardiomyopathy enhance calpain-mediated desmoplakin degradation.
    JCI insight, 2019, 06-13, Volume: 5

    Topics: Adult; Arrhythmias, Cardiac; Calpain; Cardiomyopathies; Desmoplakins; Female; Genetic Predisposition

2019
Elevation of pivaloylcarnitine by sivelestat sodium in two children.
    Molecular genetics and metabolism, 2015, Volume: 116, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Cardiomyopathies; Carnitine; Child, Preschool; Chromatography,

2015
Global expression profiling identifies a novel biosignature for protein aggregation R120GCryAB cardiomyopathy in mice.
    Physiological genomics, 2008, Oct-08, Volume: 35, Issue:2

    Topics: alpha-Crystallin B Chain; Animals; Arginine; Cardiomyopathies; Gene Expression Profiling; Glutathion

2008
Effects of glycine supplementation on myocardial damage and cardiac function after severe burn.
    Burns : journal of the International Society for Burn Injuries, 2013, Volume: 39, Issue:4

    Topics: Adenosine Triphosphate; Alanine; Analysis of Variance; Animals; Aspartate Aminotransferases; Biomark

2013
A pathogenic cytochrome b mutation reveals new interactions between subunits of the mitochondrial bc1 complex.
    The Journal of biological chemistry, 2002, Dec-20, Volume: 277, Issue:51

    Topics: Amino Acid Sequence; Animals; Cardiomyopathies; Catalytic Domain; Codon; Cytochrome b Group; Electro

2002
Barth syndrome without 3-methylglutaconic aciduria.
    Acta paediatrica (Oslo, Norway : 1992), 2004, Volume: 93, Issue:3

    Topics: Arginine; Cardiomyopathies; Chromosomes, Human, X; Fatal Outcome; Glutarates; Glycine; Humans; Infan

2004
Homozygosity for a novel nonsense mutation (G66X) of the HJV gene causes severe juvenile hemochromatosis with fatal cardiomyopathy.
    Blood, 2005, Jan-01, Volume: 105, Issue:1

    Topics: Adult; Age of Onset; Cardiomyopathies; Codon, Nonsense; Female; Glycine; GPI-Linked Proteins; Hemoch

2005
Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2005, Volume: 12, Issue:3

    Topics: Adipose Tissue; Aged; Arginine; Cardiomyopathies; Chromatography, High Pressure Liquid; Colon; DNA M

2005
Is it safe to combine PPAR agonists? A lesson from muraglitazar.
    Medical hypotheses, 2006, Volume: 67, Issue:3

    Topics: Cardiomyopathies; Drug Interactions; Glycine; Humans; Models, Biological; Oxazoles; PPAR alpha; PPAR

2006
A new transthyretin variant (Glu61Gly) associated with cardiomyopathy.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2007, Volume: 14, Issue:1

    Topics: Amino Acid Substitution; Amyloid Neuropathies, Familial; Base Sequence; Cardiomyopathies; DNA Mutati

2007
Human alpha B-crystallin mutation causes oxido-reductive stress and protein aggregation cardiomyopathy in mice.
    Cell, 2007, Aug-10, Volume: 130, Issue:3

    Topics: alpha-Crystallin B Chain; Animals; Arginine; Cardiomyopathies; Glucosephosphate Dehydrogenase; Gluta

2007
Effect of hypertrophic cardiomyopathy mutations in human cardiac muscle alpha -tropomyosin (Asp175Asn and Glu180Gly) on the regulatory properties of human cardiac troponin determined by in vitro motility assay.
    Journal of molecular and cellular cardiology, 2000, Volume: 32, Issue:8

    Topics: Animals; Asparagine; Aspartic Acid; Calcium; Cardiomegaly; Cardiomyopathies; Cell Movement; Dose-Res

2000
Malignant hypertrophic cardiomyopathy caused by the Arg723Gly mutation in beta-myosin heavy chain gene.
    Journal of molecular and cellular cardiology, 2000, Volume: 32, Issue:12

    Topics: Adult; Age Factors; Aged; Arginine; Cardiomyopathies; Electrocardiography; Female; Glycine; Humans;

2000
Identification of genetic variants (g789C>T and G111S) in the human HSPB2 gene.
    Human mutation, 2001, Volume: 17, Issue:1

    Topics: Amino Acid Substitution; Cardiomyopathies; Crystallins; Cytosine; Glycine; Heat-Shock Proteins; Huma

2001