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For: Nickolls AR, Bönnemann CG. The roles of dystroglycan in the nervous system: insights from animal models of muscular dystrophy. Dis Model Mech 2018;11:dmm035931. [PMID: 30578246 DOI: 10.1242/dmm.035931] [Cited by in Crossref: 23] [Cited by in F6Publishing: 19] [Article Influence: 5.8] [Reference Citation Analysis]
Number Citing Articles
1 Shi Y, Fu Y, Tao Z, Yong W, Peng H, Jian W, Chen G, Guo M, Zhao Y, Yao R, Guo D. A novel pathogenic deletion in ISPD causes Walker-Warburg syndrome in a Chinese family. Genes Genomics 2022. [PMID: 35951155 DOI: 10.1007/s13258-022-01296-z] [Reference Citation Analysis]
2 Dang K, Jiang S, Gao Y, Qian A. The role of protein glycosylation in muscle diseases. Mol Biol Rep. [DOI: 10.1007/s11033-022-07334-z] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Figiel I, Bączyńska E, Wójtowicz T, Magnowska M, Buszka A, Bijata M, Włodarczyk J. The cell adhesion protein dystroglycan affects the structural remodeling of dendritic spines. Sci Rep 2022;12:2506. [PMID: 35169214 DOI: 10.1038/s41598-022-06462-7] [Reference Citation Analysis]
4 Hang J, Wang J, Lu M, Xue Y, Qiao J, Tao L. Protein O-mannosylation across kingdoms and related diseases: From glycobiology to glycopathology. Biomed Pharmacother 2022;148:112685. [PMID: 35149389 DOI: 10.1016/j.biopha.2022.112685] [Reference Citation Analysis]
5 Wu WJ, Sun SZ, Li BG. Congenital muscular dystrophy caused by beta1,3-N-acetylgalactosaminyltransferase 2 gene mutation: Two case reports. World J Clin Cases 2022; 10(3): 1056-1066 [DOI: 10.12998/wjcc.v10.i3.1056] [Reference Citation Analysis]
6 Shalev I, Somekh J, Eran A. Multimodal bioinformatic analyses of the neurodegenerative disease-associated TECPR2 gene reveal its diverse roles. J Med Genet 2021:jmedgenet-2021-108193. [PMID: 34933910 DOI: 10.1136/jmedgenet-2021-108193] [Reference Citation Analysis]
7 Donkervoort S, Krause N, Dergai M, Yun P, Koliwer J, Gorokhova S, Geist Hauserman J, Cummings BB, Hu Y, Smith R, Uapinyoying P, Ganesh VS, Ghosh PS, Monaghan KG, Edassery SL, Ferle PE, Silverstein S, Chao KR, Snyder M, Ellingwood S, Bharucha-Goebel D, Iannaccone ST, Dal Peraro M, Foley AR, Savas JN, Bolduc V, Fasshauer D, Bönnemann CG, Schwake M. BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy. EMBO Mol Med 2021;13:e13787. [PMID: 34779586 DOI: 10.15252/emmm.202013787] [Reference Citation Analysis]
8 Taniguchi-Ikeda M, Koyanagi-Aoi M, Maruyama T, Takaori T, Hosoya A, Tezuka H, Nagase S, Ishihara T, Kadoshima T, Muguruma K, Ishigaki K, Sakurai H, Mizoguchi A, Novitch BG, Toda T, Watanabe M, Aoi T. Restoration of the defect in radial glial fiber migration and cortical plate organization in a brain organoid model of Fukuyama muscular dystrophy. iScience 2021;24:103140. [PMID: 34632335 DOI: 10.1016/j.isci.2021.103140] [Reference Citation Analysis]
9 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] [Reference Citation Analysis]
10 McGrath MJ, Eramo MJ, Gurung R, Sriratana A, Gehrig SM, Lynch GS, Lourdes SR, Koentgen F, Feeney SJ, Lazarou M, McLean CA, Mitchell CA. Defective lysosome reformation during autophagy causes skeletal muscle disease. J Clin Invest 2021;131:135124. [PMID: 33119550 DOI: 10.1172/JCI135124] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 7.0] [Reference Citation Analysis]
11 Zambon AA, Muntoni F. Congenital muscular dystrophies: What is new? Neuromuscul Disord 2021;31:931-42. [PMID: 34470717 DOI: 10.1016/j.nmd.2021.07.009] [Reference Citation Analysis]
12 Miller DS, Wright KM. Neuronal Dystroglycan regulates postnatal development of CCK/cannabinoid receptor-1 interneurons. Neural Dev 2021;16:4. [PMID: 34362433 DOI: 10.1186/s13064-021-00153-1] [Reference Citation Analysis]
13 Shelton GD, Minor KM, Guo LT, Friedenberg SG, Cullen JN, Hord JM, Venzke D, Anderson ME, Devereaux M, Prouty SJ, Handelman C, Campbell KP, Mickelson JR. Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation. Neuromuscul Disord 2021:S0960-8966(21)00203-0. [PMID: 34654610 DOI: 10.1016/j.nmd.2021.07.016] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Jing X, Liu B, Deng S, Du J, She Q. Agrin Yes-associated Protein Promotes the Proliferation of Epicardial Cells. J Cardiovasc Pharmacol 2021;77:94-9. [PMID: 33136763 DOI: 10.1097/FJC.0000000000000926] [Reference Citation Analysis]
15 Burger CA, Jiang D, Mackin RD, Samuel MA. Development and maintenance of vision's first synapse. Dev Biol 2021;476:218-39. [PMID: 33848537 DOI: 10.1016/j.ydbio.2021.04.001] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Klingler E, Francis F, Jabaudon D, Cappello S. Mapping the molecular and cellular complexity of cortical malformations. Science 2021;371:eaba4517. [PMID: 33479124 DOI: 10.1126/science.aba4517] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 9.0] [Reference Citation Analysis]
17 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: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Ortiz-Cordero C, Azzag K, Perlingeiro RCR. Fukutin-Related Protein: From Pathology to Treatments. Trends Cell Biol 2021;31:197-210. [PMID: 33272829 DOI: 10.1016/j.tcb.2020.11.003] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
19 El-dessouky SH, Hosny H, Elarab AE, Issa MY. Prenatal presentation of Walker–Warburg syndrome with a POMT2 mutation: an extended fetal phenotype. Egypt J Med Hum Genet 2020;21. [DOI: 10.1186/s43042-020-00093-1] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
20 Ferent J, Zaidi D, Francis F. Extracellular Control of Radial Glia Proliferation and Scaffolding During Cortical Development and Pathology. Front Cell Dev Biol 2020;8:578341. [PMID: 33178693 DOI: 10.3389/fcell.2020.578341] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
21 Żarski D, Le Cam A, Nynca J, Klopp C, Ciesielski S, Sarosiek B, Montfort J, Król J, Fontaine P, Ciereszko A, Bobe J. Domestication modulates the expression of genes involved in neurogenesis in high-quality eggs of Sander lucioperca. Mol Reprod Dev 2020;87:934-51. [PMID: 32864792 DOI: 10.1002/mrd.23414] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
22 Briatore F, Pregno G, Di Angelantonio S, Frola E, De Stefano ME, Vaillend C, Sassoè-Pognetto M, Patrizi A. Dystroglycan Mediates Clustering of Essential GABAergic Components in Cerebellar Purkinje Cells. Front Mol Neurosci 2020;13:164. [PMID: 32982691 DOI: 10.3389/fnmol.2020.00164] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
23 Nickolls AR, Lee MM, Zukosky K, Mallon BS, Bönnemann CG. Human embryoid bodies as a 3D tissue model of the extracellular matrix and α-dystroglycanopathies. Dis Model Mech 2020;13:dmm042986. [PMID: 32423971 DOI: 10.1242/dmm.042986] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
24 Mahjoub G, Faghihi MA, Taghdiri M. Reporting one very rare pathogenic variation c.1106G>A in POMT2 gene. Intractable Rare Dis Res 2020;9:104-8. [PMID: 32494558 DOI: 10.5582/irdr.2020.03013] [Reference Citation Analysis]
25 Kim DY, Zhang H, Park S, Kim Y, Bae CR, Kim YM, Kwon YG. CU06-1004 (endothelial dysfunction blocker) ameliorates astrocyte end-feet swelling by stabilizing endothelial cell junctions in cerebral ischemia/reperfusion injury. J Mol Med (Berl) 2020;98:875-86. [PMID: 32415357 DOI: 10.1007/s00109-020-01920-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
26 van Putten M, Hmeljak J, Aartsma-Rus A, Dowling JJ. Moving neuromuscular disorders research forward: from novel models to clinical studies. Dis Model Mech 2020;13:dmm044370. [PMID: 32224497 DOI: 10.1242/dmm.044370] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
27 Donkervoort S, Sabouny R, Yun P, Gauquelin L, Chao KR, Hu Y, Al Khatib I, Töpf A, Mohassel P, Cummings BB, Kaur R, Saade D, Moore SA, Waddell LB, Farrar MA, Goodrich JK, Uapinyoying P, Chan SHS, Javed A, Leach ME, Karachunski P, Dalton J, Medne L, Harper A, Thompson C, Thiffault I, Specht S, Lamont RE, Saunders C, Racher H, Bernier FP, Mowat D, Witting N, Vissing J, Hanson R, Coffman KA, Hainlen M, Parboosingh JS, Carnevale A, Yoon G, Schnur RE, Boycott KM, Mah JK, Straub V, Foley AR, Innes AM, Bönnemann CG, Shutt TE; Care4Rare Canada Consortium. MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. Acta Neuropathol 2019;138:1013-31. [PMID: 31463572 DOI: 10.1007/s00401-019-02059-z] [Cited by in Crossref: 21] [Cited by in F6Publishing: 13] [Article Influence: 7.0] [Reference Citation Analysis]
28 Bailey EC, Alrowaished SS, Kilroy EA, Crooks ES, Drinkert DM, Karunasiri CM, Belanger JJ, Khalil A, Kelley JB, Henry CA. NAD+ improves neuromuscular development in a zebrafish model of FKRP-associated dystroglycanopathy. Skelet Muscle 2019;9:21. [PMID: 31391079 DOI: 10.1186/s13395-019-0206-1] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]