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For: Paco S, Casserras T, Rodríguez MA, Jou C, Puigdelloses M, Ortez CI, Diaz-Manera J, Gallardo E, Colomer J, Nascimento A, Kalko SG, Jimenez-Mallebrera C. Transcriptome Analysis of Ullrich Congenital Muscular Dystrophy Fibroblasts Reveals a Disease Extracellular Matrix Signature and Key Molecular Regulators. PLoS One 2015;10:e0145107. [PMID: 26670220 DOI: 10.1371/journal.pone.0145107] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 2.6] [Reference Citation Analysis]
Number Citing Articles
1 Castroflorio E, Pérez Berná AJ, López-márquez A, Badosa C, Loza-alvarez P, Roldán M, Jiménez-mallebrera C. The Capillary Morphogenesis Gene 2 Triggers the Intracellular Hallmarks of Collagen VI-Related Muscular Dystrophy. IJMS 2022;23:7651. [DOI: 10.3390/ijms23147651] [Reference Citation Analysis]
2 Parker E, Mendhe B, Ruan L, Marshall B, Zhi W, Liu Y, Fulzele S, Tang Y, McGee-Lawrence M, Lee TJ, Sharma A, Johnson M, Chen J, Hamrick M. MicroRNA cargo of extracellular vesicles from skeletal muscle fibro-adipogenic progenitor cells is altered with disuse atrophy and IL-1β deficiency. Physiol Genomics 2022. [PMID: 35759450 DOI: 10.1152/physiolgenomics.00177.2021] [Reference Citation Analysis]
3 Jiménez‐mallebrera C. The importance of verifying the novelty of a finding and the value of combining results. Ann Clin Transl Neurol. [DOI: 10.1002/acn3.51572] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Almici E, Chiappini V, López-márquez A, Badosa C, Blázquez B, Caballero D, Montero J, Natera-de Benito D, Nascimento A, Roldán M, Lagunas A, Jiménez-mallebrera C, Samitier J. Personalized in vitro Extracellular Matrix Models of Collagen VI-Related Muscular Dystrophies. Front Bioeng Biotechnol 2022;10:851825. [DOI: 10.3389/fbioe.2022.851825] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 López-Márquez A, Morín M, Fernández-Peñalver S, Badosa C, Hernández-Delgado A, Natera-de Benito D, Ortez C, Nascimento A, Grinberg D, Balcells S, Roldán M, Moreno-Pelayo MÁ, Jiménez-Mallebrera C. CRISPR/Cas9-Mediated Allele-Specific Disruption of a Dominant COL6A1 Pathogenic Variant Improves Collagen VI Network in Patient Fibroblasts. Int J Mol Sci 2022;23:4410. [PMID: 35457228 DOI: 10.3390/ijms23084410] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Koutsoulidou A, Koutalianos D, Georgiou K, Kakouri AC, Oulas A, Tomazou M, Kyriakides TC, Roos A, Papadimas GK, Papadopoulos C, Kararizou E, Spyrou GM, Papanicolaou EZ, Lochmüller H, Phylactou LA. Serum miRNAs as biomarkers for the rare types of muscular dystrophy. Neuromuscular Disorders 2022. [DOI: 10.1016/j.nmd.2022.03.003] [Reference Citation Analysis]
7 Guadagnin E, Mohassel P, Johnson KR, Yang L, Santi M, Uapinyoying P, Dastgir J, Hu Y, Dillmann A, Cookson MR, Foley AR, Bönnemann CG. Transcriptome analysis of collagen VI-related muscular dystrophy muscle biopsies. Ann Clin Transl Neurol 2021;8:2184-98. [PMID: 34729958 DOI: 10.1002/acn3.51450] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
8 Zhang W, Liu Y, Zhang H. Extracellular matrix: an important regulator of cell functions and skeletal muscle development. Cell Biosci 2021;11:65. [PMID: 33789727 DOI: 10.1186/s13578-021-00579-4] [Cited by in Crossref: 14] [Cited by in F6Publishing: 18] [Article Influence: 14.0] [Reference Citation Analysis]
9 Castells AA, Balada R, Tristán-Noguero A, O'Callaghan M, Cortès-Saladelafont E, Pascual-Alonso A, Garcia-Cazorla À, Armstrong J, Alcántara S. Unraveling Molecular Pathways Altered in MeCP2-Related Syndromes, in the Search for New Potential Avenues for Therapy. Biomedicines 2021;9:148. [PMID: 33546327 DOI: 10.3390/biomedicines9020148] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Zevallos RAC, Reis EM. Noncoding Gene Families of the Human Genome. Human Genome Structure, Function and Clinical Considerations 2021. [DOI: 10.1007/978-3-030-73151-9_5] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Koutsoulidou A, Phylactou LA. Circulating Biomarkers in Muscular Dystrophies: Disease and Therapy Monitoring. Mol Ther Methods Clin Dev 2020;18:230-9. [PMID: 32637452 DOI: 10.1016/j.omtm.2020.05.017] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 4.5] [Reference Citation Analysis]
12 Trifunov S, Natera-de Benito D, Exposito Escudero JM, Ortez C, Medina J, Cuadras D, Badosa C, Carrera L, Nascimento A, Jimenez-Mallebrera C. Longitudinal Study of Three microRNAs in Duchenne Muscular Dystrophy and Becker Muscular Dystrophy. Front Neurol 2020;11:304. [PMID: 32373058 DOI: 10.3389/fneur.2020.00304] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
13 Finotti A, Fabbri E, Lampronti I, Gasparello J, Borgatti M, Gambari R. MicroRNAs and Long Non-coding RNAs in Genetic Diseases. Mol Diagn Ther 2019;23:155-71. [PMID: 30610665 DOI: 10.1007/s40291-018-0380-6] [Cited by in Crossref: 35] [Cited by in F6Publishing: 29] [Article Influence: 11.7] [Reference Citation Analysis]
14 Delbaere S, Dhooge T, Syx D, Petit F, Goemans N, Destrée A, Vanakker O, De Rycke R, Symoens S, Malfait F. Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers-Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix. Genet Med 2020;22:112-23. [PMID: 31273343 DOI: 10.1038/s41436-019-0599-6] [Cited by in Crossref: 19] [Cited by in F6Publishing: 22] [Article Influence: 6.3] [Reference Citation Analysis]
15 Bao M, Mao F, Zhao Z, Ma G, Xu G, Xu W, Chen H, Zhu M. COL6A1 mutation leading to Bethlem myopathy with recurrent hematuria: a case report. BMC Neurol 2019;19:32. [PMID: 30808312 DOI: 10.1186/s12883-019-1263-0] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 1.7] [Reference Citation Analysis]
16 Cury SS, Freire PP, Martinucci B, Dos Santos VC, de Oliveira G, Ferretti R, Dal-Pai-Silva M, Pacagnelli FL, Delella FK, Carvalho RF. Fractal dimension analysis reveals skeletal muscle disorganization in mdx mice. Biochem Biophys Res Commun 2018;503:109-15. [PMID: 29852164 DOI: 10.1016/j.bbrc.2018.05.189] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]
17 Butterfield RJ, Dunn DM, Hu Y, Johnson K, Bönnemann CG, Weiss RB. Transcriptome profiling identifies regulators of pathogenesis in collagen VI related muscular dystrophy. PLoS One 2017;12:e0189664. [PMID: 29244830 DOI: 10.1371/journal.pone.0189664] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 1.8] [Reference Citation Analysis]
18 Chen Y, Marotti JD, Jenson EG, Onega TL, Johnson KC, Christensen BC. Concordance of DNA methylation profiles between breast core biopsy and surgical excision specimens containing ductal carcinoma in situ (DCIS). Exp Mol Pathol 2017;103:78-83. [PMID: 28711544 DOI: 10.1016/j.yexmp.2017.07.001] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
19 Llano-diez M, Ortez CI, Gay JA, Álvarez-cabado L, Jou C, Medina J, Nascimento A, Jimenez-mallebrera C. Digital PCR quantification of miR-30c and miR-181a as serum biomarkers for Duchenne muscular dystrophy. Neuromuscular Disorders 2017;27:15-23. [DOI: 10.1016/j.nmd.2016.11.003] [Cited by in Crossref: 22] [Cited by in F6Publishing: 20] [Article Influence: 4.4] [Reference Citation Analysis]