المؤلفون: Vasily V. Grinev, Farnaz Barneh, Ilya M. Ilyushonak, Sirintra Nakjang, Job Smink, Anita van Oort, Richard Clough, Michael Seyani, Hesta McNeill, Mojgan Reza, Natalia Martinez-Soria, Salam A. Assi, Tatsiana V. Ramanouskaya, Constanze Bonifer, Olaf Heidenreich

المصدر: Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2041-1723Test

الوصول الحر: https://doaj.org/article/5eec00d838bf48d7a8a72e936547e1a8Test

المؤلفون: Chiara Passarelli, Rita Selvatici, Alberto Carrieri, Francesca Romana Di Raimo, Maria Sofia Falzarano, Fernanda Fortunato, Rachele Rossi, Volker Straub, Katie Bushby, Mojgan Reza, Irina Zharaieva, Adele D’Amico, Enrico Bertini, Luciano Merlini, Patrizia Sabatelli, Paola Borgiani, Giuseppe Novelli, Sonia Messina, Marika Pane, Eugenio Mercuri, Mireille Claustres, Sylvie Tuffery-Giraud, Annemieke Aartsma-Rus, Pietro Spitali, Peter A. C. T’Hoen, Hanns Lochmüller, Kristin Strandberg, Cristina Al-Khalili, Ekaterina Kotelnikova, Michael Lebowitz, Elena Schwartz, Francesco Muntoni, Chiara Scapoli, Alessandra Ferlini

المصدر: Frontiers in Genetics, Vol 11 (2020)

مصطلحات موضوعية: biomarker, corticosteroid (betamethasone), receptor, TNFR, Duchenne, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/article/10.3389/fgene.2020.00605/fullTest; https://doaj.org/toc/1664-8021Test

الوصول الحر: https://doaj.org/article/b81fc57f071f44379d499b268e34d2ebTest

المؤلفون: Benedicte Neven, Preeti Singh, Rachel E. Dickinson, Mojgan Reza, Aneta Mikulasova, Laetitia Largeaud, Venetia Bigley, Anastasia Resteu, Eric Delabesse, Jacinta Bustamante, Matthew Collin, Maninder Heer, Daniel Rico, Marlène Pasquet, Stephanie Dufrechou, Naïs Prade

المصدر: Blood Advances

مصطلحات موضوعية: GATA2 Deficiency, DNA Copy Number Variations, Hematology, Biology, Molecular biology, Monocytes, Frameshift mutation, GATA2 Transcription Factor, Phenotype, Transcription (biology), Chimeric RNA, Child, Preschool, Gene duplication, Humans, Exceptional Case Report, Female, Tandem exon duplication, Copy-number variation, Allele, Alleles

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec3fc2caa75946d9eaa5c3b25d4d5e50Test
https://doi.org/10.1182/bloodadvances.2021005217Test

المؤلفون: Salam A. Assi, Michael Seyani, Vasily V. Grinev, Mojgan Reza, N Martinez-Soria, Tatsiana V. Ramanouskaya, Anita van Oort, Hesta McNeill, Sirintra Nakjang, Job Smink, Constanze Bonifer, Olaf Heidenreich, Richard Clough, Ilya M. Ilyushonak, Farnaz Barneh

المصدر: Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)

مصطلحات موضوعية: 0301 basic medicine, Oncogene Proteins, Fusion, Science, General Physics and Astronomy, Biology, General Biochemistry, Genetics and Molecular Biology, Article, Acute myeloid leukaemia, Gene regulatory networks, 03 medical and health sciences, Exon, chemistry.chemical_compound, 0302 clinical medicine, RUNX1 Translocation Partner 1 Protein, RNA Isoforms, hemic and lymphatic diseases, Cell Line, Tumor, Transcriptional regulation, Humans, Transcriptomics, Gene, Regulation of gene expression, Multidisciplinary, Models, Genetic, Gene Expression Regulation, Leukemic, Gene Expression Profiling, Alternative splicing, General Chemistry, Oncogenes, Cell biology, Alternative Splicing, 030104 developmental biology, RUNX1, chemistry, Leukemia, Myeloid, 030220 oncology & carcinogenesis, RNA splicing, Acute Disease, Core Binding Factor Alpha 2 Subunit, RNA Interference, Transcription Initiation Site

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dace14325547570ede9ed3dad87f4b89Test
http://europepmc.org/articles/PMC7822815Test

المؤلفون: Chiara Passarelli, Rita Selvatici, Alberto Carrieri, Francesca Romana Di Raimo, Maria Sofia Falzarano, Fernanda Fortunato, Rachele Rossi, Volker Straub, Katie Bushby, Mojgan Reza, Irina Zharaieva, Adele D’Amico, Enrico Bertini, Luciano Merlini, Patrizia Sabatelli, Paola Borgiani, Giuseppe Novelli, Sonia Messina, Marika Pane, Eugenio Mercuri, Mireille Claustres, Sylvie Tuffery-Giraud, Annemieke Aartsma-Rus, Pietro Spitali, Peter A. C. T’Hoen, Hanns Lochmüller, Kristin Strandberg, Cristina Al-Khalili, Ekaterina Kotelnikova, Michael Lebowitz, Elena Schwartz, Francesco Muntoni, Chiara Scapoli, Alessandra Ferlini

مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, biomarker, corticosteroid (betamethasone), receptor, TNFR, Duchenne

العلاقة: https://figshare.com/articles/figure/Image_1_Tumor_Necrosis_Factor_Receptor_SF10A_TNFRSF10A_SNPs_Correlate_With_Corticosteroid_Response_in_Duchenne_Muscular_Dystrophy_pdf/12609104Test

الإتاحة: https://doi.org/10.3389/fgene.2020.00605.s001Test
https://figshare.com/articles/figure/Image_1_Tumor_Necrosis_Factor_Receptor_SF10A_TNFRSF10A_SNPs_Correlate_With_Corticosteroid_Response_in_Duchenne_Muscular_Dystrophy_pdf/12609104Test

المؤلفون: Natalia Martinez-Soria, Lynsey McKenzie, Julia Draper, Anetta Ptasinska, Hasan Issa, Sandeep Potluri, Helen J. Blair, Anna Pickin, Asmida Isa, Paulynn Suyin Chin, Ricky Tirtakusuma, Daniel Coleman, Sirintra Nakjang, Salam Assi, Victoria Forster, Mojgan Reza, Ed Law, Philip Berry, Dorothee Mueller, Cameron Osborne, Alex Elder, Simon N. Bomken, Deepali Pal, James M. Allan, Gareth J. Veal, Peter N. Cockerill, Christian Wichmann, Josef Vormoor, Georges Lacaud, Constanze Bonifer, Olaf Heidenreich

المصدر: Martinez-Soria, N, McKenzie, L, Draper, J, Ptasinska, A, Issa, H, Potluri, S, Blair, H J, Pickin, A, Isa, A, Chin, P S, Tirtakusuma, R, Coleman, D, Nakjang, S, Assi, S, Forster, V, Reza, M, Law, E, Berry, P, Mueller, D, Osborne, C, Elder, A, Bomken, S N, Pal, D, Allan, J M, Veal, G J, Cockerill, P N, Wichmann, C, Vormoor, J, Lacaud, G, Bonifer, C & Heidenreich, O 2018, ' The Oncogenic Transcription Factor RUNX1/ETO Corrupts Cell Cycle Regulation to Drive Leukemic Transformation ', Cancer Cell, vol. 34, no. 4, pp. 705 . https://doi.org/10.1016/j.ccell.2018.08.015Test, https://doi.org/10.1016/j.ccell.2019.03.012Test
Cancer Cell
Martinez-Soria, N, McKenzie, L, Draper, J, Ptasinska, A, Issa, H, Potluri, S, Blair, H J, Pickin, A, Isa, A, Chin, P S, Tirtakusuma, R, Coleman, D, Nakjang, S, Assi, S, Forster, V, Reza, M, Law, E, Berry, P, Mueller, D, Elder, A, Bomken, S N, Pal, D, Allan, J M, Veal, G J, Cockerill, P N, Wichmann, C, Vormoor, J, Lacaud, G, Bonifer, C & Heidenreich, O 2018, ' The Oncogenic Transcription Factor RUNX1/ETO Corrupts Cell Cycle Regulation to Drive Leukemic Transformation ', Cancer Cell, vol. 34, no. 4, pp. 626-642.e8 . https://doi.org/10.1016/j.ccell.2018.08.015Test

مصطلحات موضوعية: Male, Cancer Research, endocrine system, Oncogene Proteins, Fusion, palbociclib, Chromosomes, Human, Pair 21, KIT mutation, acute myeloid leukemia, Translocation, Genetic, Article, CCND2, Mice, Cell Line, Tumor, hemic and lymphatic diseases, Animals, Cyclin D2, Humans, RNAi screen, Manchester Cancer Research Centre, Gene Expression Regulation, Leukemic, ResearchInstitutes_Networks_Beacons/mcrc, Cell Cycle Checkpoints, Oncogenes, Cell Biology, C400, cell-cycle control, CDK6 inhibition, B900, RUNX1/ETO, Leukemia, Myeloid, Acute, Oncology, fusion gene, imatinib, Core Binding Factor Alpha 2 Subunit, embryonic structures

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acacb6b896402d3704032615136e9045Test
https://research.manchester.ac.uk/en/publications/c8ac0ff2-d9af-420f-aa3b-957c35c55420Test

المؤلفون: Mojgan Rezakhani, Sung-Ah Kim

المصدر: Buildings, Vol 14, Iss 4, p 1086 (2024)

مصطلحات موضوعية: genetic algorithm, façade optimization, pattern, visual of occupants, Building construction, TH1-9745

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2075-5309/14/4/1086Test; https://doaj.org/toc/2075-5309Test

الوصول الحر: https://doaj.org/article/a4606614df184e9c90414ad570207a59Test

المؤلفون: S. de Kimpe, D. de Klerk, Monika Hiller, Jan J.G.M. Verschuuren, Annemieke Aartsma-Rus, R. Jean-Baptiste, Francesco Muntoni, Mar Tulinius, Afrodite Lourbakos, Peter Nilsson, Zaïda Koeks, K. Kozaczynska, G. Campion, Nathalie Goemans, Pietro Spitali, Burcu Ayoglu, Ron Wolterbeek, Vishna Devi Nadarajah, N. Yau, Peter A C 't Hoen, Erik H. Niks, Mojgan Reza, Hanns Lochmüller, P. de Bruijn, C. Al-Khalili Szigyarto, Irina Zaharieva

المصدر: Scientific Reports
Scientific Reports, 7
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)

مصطلحات موضوعية: 0301 basic medicine, Oncology, Adult, Male, medicine.medical_specialty, Adolescent, government.form_of_government, Duchenne muscular dystrophy, Placebo-controlled study, lcsh:Medicine, Muscle disorder, Article, Dystrophin, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Double-Blind Method, Internal medicine, Medicine, Humans, Longitudinal Studies, Muscular dystrophy, lcsh:Science, Child, Drisapersen, Randomized Controlled Trials as Topic, Antisense therapy, Multidisciplinary, biology, business.industry, lcsh:R, Exons, Oligonucleotides, Antisense, medicine.disease, Clinical trial, Muscular Dystrophy, Duchenne, 030104 developmental biology, Clinical Trials, Phase III as Topic, Matrix Metalloproteinase 9, Child, Preschool, government, biology.protein, lcsh:Q, Female, business, 030217 neurology & neurosurgery, Biomarkers

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e00690df27119c632541d5bb3e76d3aTest
https://hdl.handle.net/1887/115152Test

المؤلفون: Hanns Lochmüller, Stephanie Carr, Mojgan Reza, Andreas Roos, Steve Laval

المصدر: Human gene therapy methods. 27(5)

مصطلحات موضوعية: musculoskeletal diseases, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, DNA, Complementary, Duchenne muscular dystrophy, Transgene, Genetic Vectors, Gene Expression, Mice, Transgenic, Nitric Oxide Synthase Type I, Gene delivery, Applied Microbiology and Biotechnology, Dystrophin, 03 medical and health sciences, Mice, 0302 clinical medicine, Complementary DNA, Gene expression, Genetics, medicine, Animals, Humans, Muscle, Skeletal, Genetics (clinical), Pharmacology, biology, Genetic Therapy, musculoskeletal system, medicine.disease, Cell biology, Muscular Dystrophy, Duchenne, 030104 developmental biology, biology.protein, Mice, Inbred mdx, Molecular Medicine, Stem cell, 030217 neurology & neurosurgery, Ex vivo

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e16e241713213244f13ef33c0f9e6548Test
https://pubmed.ncbi.nlm.nih.gov/27477497Test

المؤلفون: Jinhong Meng, John R. Counsell, Mojgan Reza, Steven H. Laval, Olivier Danos, Adrian Thrasher, Hanns Lochmüller, Francesco Muntoni, Jennifer E. Morgan

المصدر: Scientific Reports

مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Recombinant Fusion Proteins, Genetic Vectors, Lentivirus, Muscle Fibers, Skeletal, Cell- and Tissue-Based Therapy, Gene Expression, Mice, Nude, Cell Differentiation, Genetic Therapy, Nitric Oxide Synthase Type I, musculoskeletal system, Article, Dystrophin, Muscular Dystrophy, Duchenne, Myoblasts, Disease Models, Animal, Mice, Transduction, Genetic, Mice, Inbred mdx, Animals, Humans, Pericytes, Protein Binding

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b5813467a6d55b63c627ec64108a230bTest
https://pubmed.ncbi.nlm.nih.gov/26813695Test