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For: Brancaccio A. A molecular overview of the primary dystroglycanopathies. J Cell Mol Med 2019;23:3058-62. [PMID: 30838779 DOI: 10.1111/jcmm.14218] [Cited by in Crossref: 18] [Cited by in F6Publishing: 22] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Karas BF, Terez KR, Battula N, Gural BM, Flannery KP, Aboussleman G, Mubin N, Manzini MC. Removal ofpomt1in zebrafish leads to loss of α-dystroglycan glycosylation and dystroglycanopathy phenotypes.. [DOI: 10.1101/2022.10.15.512359] [Reference Citation Analysis]
2 Wilson DGS, Tinker A, Iskratsch T. The role of the dystrophin glycoprotein complex in muscle cell mechanotransduction. Commun Biol 2022;5:1022. [PMID: 36168044 DOI: 10.1038/s42003-022-03980-y] [Reference Citation Analysis]
3 Zago S, Silvestri E, Arcangeli T, Calisesi M, Romeo C, Parmeggiani G, Parrini E, Cetica V, Guerrini R, Palicelli A, Bonasoni MP. Fetal Presentation of Walker-Warburg Syndrome with Compound Heterozygous POMT2 Missense Mutations. Fetal Pediatr Pathol 2022;:1-8. [PMID: 36048137 DOI: 10.1080/15513815.2022.2116620] [Reference Citation Analysis]
4 Trotter JH, Wang CY, Zhou P, Südhof TC. A combinatorial code of neurexin-3 alternative splicing controls inhibitory synapses via a trans-synaptic dystroglycan signaling loop.. [DOI: 10.1101/2022.05.09.491206] [Reference Citation Analysis]
5 Skeffington KL, Jones FP, Suleiman MS, Caputo M, Brancaccio A, Bigotti MG. Determination of Agrin and Related Proteins Levels as a Function of Age in Human Hearts. Front Cardiovasc Med 2022;9:813904. [DOI: 10.3389/fcvm.2022.813904] [Reference Citation Analysis]
6 Falzarano MS, Rossi R, Grilli A, Fang M, Osman H, Sabatelli P, Antoniel M, Lu Z, Li W, Selvatici R, Al-Khalili C, Gualandi F, Bicciato S, Torelli S, Ferlini A. Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases. Front Physiol 2021;12:716471. [PMID: 34744760 DOI: 10.3389/fphys.2021.716471] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
7 Ganassi M, Muntoni F, Zammit PS. Defining and Identifying Satellite Cell-opathies within Muscular Dystrophies and Myopathies. Exp Cell Res 2021;:112906. [PMID: 34740639 DOI: 10.1016/j.yexcr.2021.112906] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 8.0] [Reference Citation Analysis]
8 Bigotti MG, Brancaccio A. High degree of conservation of the enzymes synthesizing the laminin-binding glycoepitope of α-dystroglycan. Open Biol 2021;11:210104. [PMID: 34582712 DOI: 10.1098/rsob.210104] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Lipiński P, Tylki-Szymańska A. Congenital Disorders of Glycosylation: What Clinicians Need to Know? Front Pediatr 2021;9:715151. [PMID: 34540767 DOI: 10.3389/fped.2021.715151] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
10 Valera IC, Wacker AL, Hwang HS, Holmes C, Laitano O, Landstrom AP, Parvatiyar MS. Essential roles of the dystrophin-glycoprotein complex in different cardiac pathologies. Adv Med Sci 2021;66:52-71. [PMID: 33387942 DOI: 10.1016/j.advms.2020.12.004] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
11 Yatsenko AS, Kucherenko MM, Xie Y, Urlaub H, Shcherbata HR. Exocyst-mediated membrane trafficking of the lissencephaly-associated ECM receptor dystroglycan is required for proper brain compartmentalization. Elife 2021;10:e63868. [PMID: 33620318 DOI: 10.7554/eLife.63868] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
12 Talenti G, Robson C, Severino MS, Alves CA, Chitayat D, Dahmoush H, Smith L, Muntoni F, Blaser SI, D'Arco F. Characteristic Cochlear Hypoplasia in Patients with Walker-Warburg Syndrome: A Radiologic Study of the Inner Ear in α-Dystroglycan-Related Muscular Disorders. AJNR Am J Neuroradiol 2021;42:167-72. [PMID: 33122211 DOI: 10.3174/ajnr.A6858] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
13 Geraldo AF, Rossi A, Severino M. Malformations of Cortical Development. Pediatric Neuroradiology 2021. [DOI: 10.1007/978-3-662-46258-4_6-1] [Reference Citation Analysis]
14 Zaganas I, Mastorodemos V, Spilioti M, Mathioudakis L, Latsoudis H, Michaelidou K, Kotzamani D, Notas K, Dimitrakopoulos K, Skoula I, Ioannidis S, Klothaki E, Erimaki S, Stavropoulos G, Vassilikos V, Amoiridis G, Efthimiadis G, Evangeliou A, Mitsias P. Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients. Mol Genet Metab Rep 2020;25:100682. [PMID: 33304817 DOI: 10.1016/j.ymgmr.2020.100682] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
15 Pilato CM, Walker MS, Nguyen AM, Hanna ME, Huang SL, Lutins EM, Meredith MA, Haar PJ, Thangarajh M, Richard HT, Chow WN. Dystrophic muscle distribution in late-stage muscular dystrophy. Autops Case Rep 2020;10:e2020221. [PMID: 33344329 DOI: 10.4322/acr.2020.221] [Reference Citation Analysis]
16 Bigotti MG, Skeffington KL, Jones FP, Caputo M, Brancaccio A. Agrin-Mediated Cardiac Regeneration: Some Open Questions. Front Bioeng Biotechnol 2020;8:594. [PMID: 32612983 DOI: 10.3389/fbioe.2020.00594] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
17 Castells-Ballester J, Rinis N, Kotan I, Gal L, Bausewein D, Kats I, Zatorska E, Kramer G, Bukau B, Schuldiner M, Strahl S. Translational Regulation of Pmt1 and Pmt2 by Bfr1 Affects Unfolded Protein O-Mannosylation. Int J Mol Sci 2019;20:E6220. [PMID: 31835530 DOI: 10.3390/ijms20246220] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
18 Castells-ballester J, Rinis N, Kotan I, Gal L, Bausewein D, Kats I, Zatorska E, Kramer G, Bukau B, Schuldiner M, Strahl S. Translational regulation of Pmt1 and Pmt2 by Bfr1 affects unfolded protein O-mannosylation.. [DOI: 10.1101/847095] [Reference Citation Analysis]
19 Vannoy CH, Leroy V, Broniowska K, Lu QL. Metabolomics Analysis of Skeletal Muscles from FKRP-Deficient Mice Indicates Improvement After Gene Replacement Therapy. Sci Rep 2019;9:10070. [PMID: 31296900 DOI: 10.1038/s41598-019-46431-1] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
20 Brancaccio A. A molecular overview of the primary dystroglycanopathies. J Cell Mol Med 2019;23:3058-62. [PMID: 30838779 DOI: 10.1111/jcmm.14218] [Cited by in Crossref: 18] [Cited by in F6Publishing: 22] [Article Influence: 6.0] [Reference Citation Analysis]