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1دورية أكاديمية
المؤلفون: Bello, Luca, Sabbatini, Daniele, Fusto, Aurora, Gorgoglione, Domenico, Borin, Giovanni, Penzo, Martina, Riguzzi, Pietro, Villa, Matteo, Vianello, Sara, Calore, Chiara, Melacini, Paola, Vio, Riccardo, Barp, Andrea, DAngelo, Grazia, Gandossini, Sandra, Politano, Luisa, Berardinelli, Angela, Messina, Sonia, Vita, Gian, Pedemonte, Marina, Bruno, Claudio, Albamonte, Emilio, Sansone, Valeria, Baranello, Giovanni, Masson, Riccardo, Astrea, Guja, DAmico, Adele, Bertini, Enrico, Pane, Marika, Lucibello, Simona, Mercuri, Eugenio, Spurney, Christopher, Clemens, Paula, Morgenroth, Lauren, Gordish-Dressman, Heather, Hoffman, Eric, Pegoraro, Elena, McDonald, Craig
المصدر: Journal of Neuromuscular Diseases. 11(2)
مصطلحات موضوعية: Duchenne muscular dystrophy, LTBP4, dilated cardiomyopathy, genetic modifiers, glucocorticoid treatment, Humans, Dystrophin, Haplotypes, Retrospective Studies, Stroke Volume, Ventricular Function, Left, Muscular Dystrophy, Duchenne, Cardiomyopathies, Protein Isoforms, Latent TGF-beta Binding Proteins
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/5v7247q8
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2دورية أكاديمية
المؤلفون: Liu, Ya-nan, Lv, Xue, Chen, Xin, Yan, Meng, Guo, Ling-chuan, Liu, GangAff4, IDs12265022102781_cor6, Yao, LiuAff1, IDs12265022102781_cor7, Jiang, Hong-fengAff5, IDs12265022102781_cor8
المصدر: Journal of Cardiovascular Translational Research. 16(1):65-76
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3دورية أكاديمية
المصدر: Medicinski Podmladak, Vol 74, Iss 3, Pp 33-38 (2023)
مصطلحات موضوعية: duchenne muscular dystrophy, gene modifiers, spp1, ltbp4, cd40, Medicine
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Ingrid Yali Ibarra-Tapia, Ariadna Juárez-Sandoval, Itzel Torres Pérez, Luis Javier Cano-Martínez, Sergio Sánchez-García, Juana Marlen Ruiz-Batalla, Irma Angélica Aroche-Reyes, Silvia García, Patricia Canto, David-Rojano Mejía, Ramón Mauricio Coral-Vázquez
المصدر: Annals of Human Biology, Vol 49, Iss 7-8, Pp 311-316 (2022)
مصطلحات موضوعية: type 2 diabetes mellitus, ltbp4, polymorphisms, sarcopenia, mexican patients, Biology (General), QH301-705.5, Human anatomy, QM1-695, Physiology, QP1-981
وصف الملف: electronic resource
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5دورية أكاديمية
المؤلفون: Mazaheri, MahtaAff1, Aff2, Aff3, IDs11033022074546_cor1, Jahantigh, Hamid RezaAff4, Aff5, Yavari, Mahdie, Mirjalili, Seyed Reza, Vahidnezhad, HassanAff6, Aff7
المصدر: Molecular Biology Reports: An International Journal on Molecular and Cellular Biology. 49(5):4135-4140
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6دورية أكاديمية
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7كتاب إلكتروني
المؤلفون: Beyens, AudeAff8, Pottie, LoreAff9, Aff10, Sips, PatrickAff9, Aff10, Callewaert, BertAff11
المساهمون: Crusio, Wim E., Series EditorAff1, Dong, Haidong, Series EditorAff2, Radeke, Heinfried H., Series EditorAff3, Rezaei, Nima, Series EditorAff4, Steinlein, Ortrud, Series EditorAff5, Xiao, Junjie, Series EditorAff6, Halper, Jaroslava, editorAff7
المصدر: Progress in Heritable Soft Connective Tissue Diseases. 1348:273-309
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8دورية أكاديمية
المؤلفون: Simonetta Andrea Licandro, Luca Crippa, Roberta Pomarico, Raffaella Perego, Gianluca Fossati, Flavio Leoni, Christian Steinkühler
المصدر: Skeletal Muscle, Vol 11, Iss 1, Pp 1-22 (2021)
مصطلحات موضوعية: Duchenne nuscular dystrophy, Givinostat, mdx, D2.B10, LTBP4, HDAC inhibitor, Diseases of the musculoskeletal system, RC925-935
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2044-5040
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9
المؤلفون: Aartsma-Rus, A., Ferlini, A., McNally, E. M., Spitali, P., Sweeney, H. L., Al-Khalili Szigyarto, Cristina, Bello, L., Bronson, A., Brown, K., Buccella, F., Chadwick, J., Frank, D., Hoffman, E., Larkindale, J., McClorey, G., Munschauer, R., Muntoni, F., Owens, J., Schara, U., Straub, V., Tinsley, J., Versnel, J., Vroom, E., Welch, E.
المصدر: Neuromuscular Disorders. 28(1):77-86
مصطلحات موضوعية: Biobank, Biomarker, Duchenne muscular dystrophy, Dystrophin, MRI, alanine aminotransferase, aspartate aminotransferase, biological marker, carbonate dehydratase III, corticosteroid, dysferlin, enolase, fukutin related protein, glucocorticoid receptor, glutamate dehydrogenase, immunoglobulin enhancer binding protein, microRNA, microRNA 133a, microRNA 133b, osteopontin, protein enolase 3, stromelysin, unclassified drug, utrophin, vamorolone, alanine aminotransferase level, aspartate aminotransferase blood level, Becker muscular dystrophy, blood analysis, blood sampling, Conference Paper, corticosteroid therapy, CRISPR-CAS9 system, DNA modification, drug design, exon, exon skipping, gene, gene expression, human, lipidomics, LTBP4 gene, Netherlands, nonhuman, nuclear magnetic resonance imaging, priority journal, protein expression, real time polymerase chain reaction, single nucleotide polymorphism, SPP1 gene, urinalysis, urine sampling, workshop, animal, information dissemination, male, metabolism, non profit organization, validation study, Animals, Biomarkers, Humans, Muscular Dystrophy, Duchenne, Organizations, Nonprofit, Validation Studies as Topic
وصف الملف: print
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10دورية أكاديمية
المؤلفون: Qiang Zhang, Zailong Qin, Shang Yi, Hao Wei, Xun Zhao Zhou, Jiasun Su
المصدر: BMC Medical Genomics, Vol 13, Iss 1, Pp 1-9 (2020)
مصطلحات موضوعية: ARCL IC, LTBP4 gene, Mutation, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1755-8794