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For: Ohlendieck K, Swandulla D. Complexity of skeletal muscle degeneration: multi-systems pathophysiology and organ crosstalk in dystrophinopathy. Pflugers Arch 2021;473:1813-39. [PMID: 34553265 DOI: 10.1007/s00424-021-02623-1] [Cited by in Crossref: 5] [Cited by in F6Publishing: 10] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Khairullin AE, Grishin SN, Ziganshin AU. P2 Receptor Signaling in Motor Units in Muscular Dystrophy. Int J Mol Sci 2023;24. [PMID: 36675094 DOI: 10.3390/ijms24021587] [Reference Citation Analysis]
2 Zweyer M, Ohlendieck K, Swandulla D. Verification of Protein Changes Determined by 2D-DIGE Based Proteomics Using Immunofluorescence Microscopy. Methods in Molecular Biology 2023. [DOI: 10.1007/978-1-0716-2831-7_30] [Reference Citation Analysis]
3 Vu Hong A, Bourg N, Sanatine P, Poupiot J, Charton K, Gicquel E, Massourides E, Spinazzi M, Richard I, Israeli D. Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophy. Life Sci Alliance 2023;6:e202201506. [PMID: 36265896 DOI: 10.26508/lsa.202201506] [Reference Citation Analysis]
4 Murphy S, Zweyer M, Swandulla D, Ohlendieck K. Bioinformatic Analysis of the Subproteomic Profile of Cardiomyopathic Tissue. Methods in Molecular Biology 2023. [DOI: 10.1007/978-1-0716-2831-7_26] [Reference Citation Analysis]
5 Zweyer M, Ohlendieck K, Swandulla D. Histological and Histochemical Microscopy Used to Verify 2D-DIGE Pathoproteomics. Methods in Molecular Biology 2023. [DOI: 10.1007/978-1-0716-2831-7_31] [Reference Citation Analysis]
6 Gargan S, Dowling P, Zweyer M, Henry M, Meleady P, Swandulla D, Ohlendieck K. Proteomic Identification of Markers of Membrane Repair, Regeneration and Fibrosis in the Aged and Dystrophic Diaphragm. Life 2022;12:1679. [DOI: 10.3390/life12111679] [Reference Citation Analysis]
7 Eraslan G, Drokhlyansky E, Anand S, Fiskin E, Subramanian A, Slyper M, Wang J, Van Wittenberghe N, Rouhana JM, Waldman J, Ashenberg O, Lek M, Dionne D, Win TS, Cuoco MS, Kuksenko O, Tsankov AM, Branton PA, Marshall JL, Greka A, Getz G, Segrè AV, Aguet F, Rozenblatt-Rosen O, Ardlie KG, Regev A. Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function. Science 2022;376:eabl4290. [PMID: 35549429 DOI: 10.1126/science.abl4290] [Cited by in Crossref: 36] [Cited by in F6Publishing: 30] [Article Influence: 36.0] [Reference Citation Analysis]
8 Stefano ME, Ferretti V, Mozzetta C. Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy. Neurobiol Dis 2022;:105718. [PMID: 35390481 DOI: 10.1016/j.nbd.2022.105718] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Bourg N, Vu Hong A, Lostal W, Jaber A, Guerchet N, Tanniou G, Bordier F, Bertil-Froidevaux E, Georger C, Daniele N, Richard I, Israeli D. Co-Administration of Simvastatin Does Not Potentiate the Benefit of Gene Therapy in the mdx Mouse Model for Duchenne Muscular Dystrophy. Int J Mol Sci 2022;23:2016. [PMID: 35216132 DOI: 10.3390/ijms23042016] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Dowling P, Gargan S, Zweyer M, Sabir H, Swandulla D, Ohlendieck K. Proteomic profiling of carbonic anhydrase CA3 in skeletal muscle. Expert Rev Proteomics 2021;:1-14. [PMID: 34890519 DOI: 10.1080/14789450.2021.2017776] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]