Page last updated: 2024-10-16

adenine and Muscular Dystrophies

adenine has been researched along with Muscular Dystrophies in 11 studies

Muscular Dystrophies: A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS.

Research Excerpts

ExcerptRelevanceReference
" In particular, we show that systemic injection of 3-methyladenine (3-MA) reduces muscle fibrosis, atrophy, apoptosis and increases muscle regeneration and muscle mass."3.77Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A. ( Allamand, V; Carmignac, V; Durbeej, M; Elowsson, L; Gawlik, KI; Körner, Z; Matsumura, C; Svensson, M, 2011)

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19907 (63.64)18.7374
1990's3 (27.27)18.2507
2000's0 (0.00)29.6817
2010's1 (9.09)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Carmignac, V1
Svensson, M1
Körner, Z1
Elowsson, L1
Matsumura, C1
Gawlik, KI1
Allamand, V1
Durbeej, M1
Müller, MM3
Kuzmits, R1
Frass, M3
Mamoli, B2
Willers, I1
Singh, S1
Goedde, HW1
Toifl, K1
Leixnering, W1
Kulakowski, S2
Renoirte, P2
de Bruyn, CH2
van Bennekom, CA1
Kaneko, K1
Igarashi, S1
Miyatake, T1
Tsuji, S1
Lasa, A1
Gallano, P1
Colomer, J1
Baiget, M1
Comi, GP1
Ciafaloni, E1
de Silva, HA1
Prelle, A1
Bardoni, A1
Rigoletto, C1
Robotti, M1
Bresolin, N1
Moggio, M1
Fortunato, F1
Banerji, AP1
Khopkar, PP1
Deshpande, DH1
Desai, AD1

Other Studies

11 other studies available for adenine and Muscular Dystrophies

ArticleYear
Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.
    Human molecular genetics, 2011, Dec-15, Volume: 20, Issue:24

    Topics: Adenine; Animals; Apoptosis; Autophagy; Behavior, Animal; Disease Models, Animal; Drug Therapy, Comb

2011
Purine metabolism of erythrocytes in myotonic dystrophy.
    Journal of neurology, 1980, Volume: 223, Issue:1

    Topics: Adenine; Adenosine; Adenosine Diphosphate; Adenosine Monophosphate; Adenosine Triphosphate; Erythroc

1980
Purine metabolism in fibroblasts of patients with Duchenne's muscular dystrophy.
    Human heredity, 1982, Volume: 32, Issue:4

    Topics: Adenine; Adenine Phosphoribosyltransferase; Adenosine Monophosphate; Cells, Cultured; Fibroblasts; H

1982
Adenine metabolism in erythrocytes of patients with Duchenne muscular dystrophy.
    European neurology, 1983, Volume: 22, Issue:5

    Topics: Adenine; Adenosine Triphosphate; Adolescent; Adult; Allopurinol; Child; Erythrocytes; Humans; Male;

1983
Dynamometric and biochemical observations in Duchenne patients receiving allopurinol.
    Neuropediatrics, 1981, Volume: 12, Issue:1

    Topics: Adenine; Allopurinol; Child; Creatine Kinase; Erythrocytes; Humans; Muscle Contraction; Muscular Dys

1981
Purine metabolism in Duchenne muscular dystrophy.
    Advances in experimental medicine and biology, 1980, Volume: 122A

    Topics: Adenine; Allopurinol; Biological Transport; Creatine Kinase; Erythrocyte Membrane; Female; Humans; M

1980
Metabolism of adenine and adenosine in erythrocytes of patients with myotonic muscular dystrophy (MMD).
    Advances in experimental medicine and biology, 1980, Volume: 122A

    Topics: Adenine; Adenine Nucleotides; Adenosine; Biological Transport; Carbon Radioisotopes; Erythrocytes; H

1980
Hypertrophic cardiomyopathy and increased number of CAG repeats in the androgen receptor gene.
    American heart journal, 1993, Volume: 126, Issue:1

    Topics: Adenine; Aged; Cardiomyopathy, Hypertrophic; Cytosine; Guanine; Humans; Male; Muscular Dystrophies;

1993
A novel insertional mutation of a single base on exon 12 of the dystrophin gene.
    Clinical genetics, 1995, Volume: 48, Issue:3

    Topics: Adenine; Base Sequence; Child; Dystrophin; Exons; Humans; Male; Molecular Sequence Data; Muscular Dy

1995
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient.
    Human molecular genetics, 1995, Volume: 4, Issue:11

    Topics: Adenine; Base Sequence; Child; DNA; Dystrophin; Guanine; Humans; Introns; Male; Molecular Sequence D

1995
Study of creatine phosphokinase isoenzymes of serum and cerebrospinal fluid in a patient with duchenne muscular dystrophy.
    Clinica chimica acta; international journal of clinical chemistry, 1973, Feb-12, Volume: 43, Issue:3

    Topics: Adenine; Creatine Kinase; Electrophoresis, Disc; Electrophoresis, Polyacrylamide Gel; Humans; Isoenz

1973