Calpainopathy (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Calpainopathy" in English language version.

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curecalpain3.org

Levy, Jennifer (21 January 2020). "Dufour Lab to investigate the biological role of calpain 3 in muscle". Coalition to Cure Calpain 3. Archived from the original on 6 May 2020. Retrieved 6 May 2020.

Pollitt, C; Anderson, LV; Pogue, R; Davison, K; Pyle, A; Bushby, KM (April 2001). "The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach". Neuromuscular Disorders. 11 (3): 287–96. doi:10.1016/s0960-8966(00)00197-8. PMID 11297944. S2CID 20081475.
Lasa-Elgarresta, J; Mosqueira-Martín, L; Naldaiz-Gastesi, N; Sáenz, A; López de Munain, A; Vallejo-Illarramendi, A (13 September 2019). "Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations". International Journal of Molecular Sciences. 20 (18): 4548. doi:10.3390/ijms20184548. PMC 6770289. PMID 31540302.
Dowling, JJ; Weihl, CC; Spencer, MJ (November 2021). "Molecular and cellular basis of genetically inherited skeletal muscle disorders". Nature Reviews. Molecular Cell Biology. 22 (11): 713–732. doi:10.1038/s41580-021-00389-z. PMC 9686310. PMID 34257452. S2CID 235822532.
Guha, TK; Pichavant, C; Calos, MP (13 December 2019). "Plasmid-Mediated Gene Therapy in Mouse Models of Limb Girdle Muscular Dystrophy". Molecular Therapy: Methods & Clinical Development. 15: 294–304. doi:10.1016/j.omtm.2019.10.002. PMC 6923511. PMID 31890729.

Angelini, C; Fanin, M; Adam, MP; Ardinger, HH; Pagon, RA; Wallace, SE; Bean, LJH; Stephens, K; Amemiya, A (1993). Calpainopathy in GeneReviews. PMID 20301490.
Pollitt, C; Anderson, LV; Pogue, R; Davison, K; Pyle, A; Bushby, KM (April 2001). "The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach". Neuromuscular Disorders. 11 (3): 287–96. doi:10.1016/s0960-8966(00)00197-8. PMID 11297944. S2CID 20081475.
Lasa-Elgarresta, J; Mosqueira-Martín, L; Naldaiz-Gastesi, N; Sáenz, A; López de Munain, A; Vallejo-Illarramendi, A (13 September 2019). "Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations". International Journal of Molecular Sciences. 20 (18): 4548. doi:10.3390/ijms20184548. PMC 6770289. PMID 31540302.
Dowling, JJ; Weihl, CC; Spencer, MJ (November 2021). "Molecular and cellular basis of genetically inherited skeletal muscle disorders". Nature Reviews. Molecular Cell Biology. 22 (11): 713–732. doi:10.1038/s41580-021-00389-z. PMC 9686310. PMID 34257452. S2CID 235822532.
Guha, TK; Pichavant, C; Calos, MP (13 December 2019). "Plasmid-Mediated Gene Therapy in Mouse Models of Limb Girdle Muscular Dystrophy". Molecular Therapy: Methods & Clinical Development. 15: 294–304. doi:10.1016/j.omtm.2019.10.002. PMC 6923511. PMID 31890729.

Lasa-Elgarresta, J; Mosqueira-Martín, L; Naldaiz-Gastesi, N; Sáenz, A; López de Munain, A; Vallejo-Illarramendi, A (13 September 2019). "Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations". International Journal of Molecular Sciences. 20 (18): 4548. doi:10.3390/ijms20184548. PMC 6770289. PMID 31540302.
Dowling, JJ; Weihl, CC; Spencer, MJ (November 2021). "Molecular and cellular basis of genetically inherited skeletal muscle disorders". Nature Reviews. Molecular Cell Biology. 22 (11): 713–732. doi:10.1038/s41580-021-00389-z. PMC 9686310. PMID 34257452. S2CID 235822532.
Guha, TK; Pichavant, C; Calos, MP (13 December 2019). "Plasmid-Mediated Gene Therapy in Mouse Models of Limb Girdle Muscular Dystrophy". Molecular Therapy: Methods & Clinical Development. 15: 294–304. doi:10.1016/j.omtm.2019.10.002. PMC 6923511. PMID 31890729.

Levy, Jennifer (21 January 2020). "Dufour Lab to investigate the biological role of calpain 3 in muscle". Coalition to Cure Calpain 3. Archived from the original on 6 May 2020. Retrieved 6 May 2020.