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1دورية أكاديمية
المؤلفون: Stenzel, P., Yu, Z., Morimoto, M., Clewing, J.M., Najafian, B., Mayfield, C., Hendson, G.
مصطلحات موضوعية: Pulmonary emphysema, autopsy, autosomal recessive disorder, child, emphysema, female, fibroblast, gene expression profiling, gene expression regulation, gene mutation, gene sequence, histopathology, human, human cell, Elastin, Schimke immuno-osseous dysplasia, SMARCAL1, Vascular disease, binding protein, elastin binding protein, genomic DNA, messenger RNA, nuclear protein, osteopontin, SWI SNF related matrix associated actin dependent regulator of chromatin subfamily a like 1, unclassified drug, adult, aorta, arteriosclerosis, artery
العلاقة: Orphanet Journal of Rare Diseases; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/8473Test; https://doi.org/10.1186/1750-1172-7-70Test; 2-s2.0-84866491739; WOS:000312257000001
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2
المؤلفون: François Nobili, Lawrence R. Shoemaker, David V. Milford, Mitra Basiratnia, Anna Buck, Georges Deschênes, Isabel Cordeiro, Jorge M. Saraiva, Helen Fryssira, Anja Stein, Behzad Najafian, Natasa Stajic, Laura Massella, Joel Charrow, Glenda Hendson, Umakumaran Ponniah, Thomas Lücke, M. Semin Fenkçi, Doris Taha, Elena Levtchenko, J. Marietta Clewing, Pierre Frange, Yumi Asakura, Christine Kobelka, Jean Luc André, David M. Parham, Jonathan Zonana, Radovan Bogdanovic, Justin Weinkauf, Zhongxin Yu, C. Nur Semerci, Stefan Fründ, Arend Bökenkamp, Cornelius F. Boerkoel, Salman Kirmani, Dorothea Wand, Peter Stenzel, Kory Keller, David B. Lewis, Pierre Cochat, Marie Morimoto, Christy Mayfield, Encarna Guillén-Navarro, D. Ross McLeod, Andrew K. Gormley, Petra Lamfers, Dominique Bonneau
المساهمون: Pediatric surgery, ICaR - Circulation and metabolism
المصدر: Orphanet Journal of Rare Diseases, 7:70. BioMed Central
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 70 (2012)
Morimoto, M, Yu, Z X, Stenzel, P, Clewing, J M, Najafian, B, Mayfield, C, Hendson, G, Weinkauf, J G, Gormley, A K, Parham, D M, Ponniah, U, Andre, J L, Asakura, Y, Basiratnia, M, Bogdanovic, R, Bokenkamp, A, Bonneau, D, Buck, A, Charrow, J, Cochat, P, Cordeiro, I, Deschenes, G, Fenkci, M S, Frange, P, Frund, S, Fryssira, H, Guillen-Navarro, E, Keller, K, Kirmani, S, Kobelka, C, Lamfers, P, Levtchenko, E, Lewis, D B, Massella, L, Mcleod, D R, Milford, D V, Nobili, F, Saraiva, J M, Semerci, C N, Shoemaker, L, Stajic, N, Stein, A, Taha, D, Wand, D, Zonana, J, Lucke, T & Boerkoel, C F 2012, ' Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia? ', Orphanet Journal of Rare Diseases, vol. 7, 70 . https://doi.org/10.1186/1750-1172-7-70Test
Orphanet Journal of Rare Diseasesمصطلحات موضوعية: Male, Pathology, Nephrotic Syndrome, Arteriosclerosis, Gene mutation, Research & Experimental Medicine, GENETIC-DISEASES, fibroblast, medical record review, 0302 clinical medicine, MOUSE MODELS, nuclear protein, Genetics(clinical), Pharmacology (medical), Child, COSTELLO-SYNDROME, Genetics & Heredity, 0303 health sciences, adult, gene expression regulation, General Medicine, Hyperplasia, elastin binding protein, Immunohistochemistry, 3. Good health, emphysema, Medicine, Research & Experimental, SUPRAVALVULAR AORTIC-STENOSIS, Child, Preschool, histopathology, Autopsy, medicine.medical_specialty, gene sequence, Osteochondrodysplasias, Vascular disease, Schimke immuno-osseous dysplasia, CELL-PROLIFERATION, 03 medical and health sciences, Humans, human, protein expression, Science & Technology, autosomal recessive disorder, MUTATIONS, human cell, lcsh:R, DNA Helicases, Immunologic Deficiency Syndromes, Schimke immunoosseous dysplasia, school child, medicine.disease, major clinical study, myofibroblast, Elastin, aorta, vascular smooth muscle, smooth muscle fiber, Immunology, umbilical cord, Pulmonary Embolism, Nephrotic syndrome, 030217 neurology & neurosurgery, lung disease, genomic DNA, osteopontin, Medizin, lcsh:Medicine, preschool child, artery intima proliferation, single nucleotide polymorphism, SMARCAL1, gene mutation, Genetics (clinical), Medicine(all), messenger RNA, ELASTIN-BINDING-PROTEIN, article, artery, hyperplasia, unclassified drug, DEFICIENCY, female, Female, Life Sciences & Biomedicine, Adult, EXPRESSION, Pulmonary emphysema, Primary Immunodeficiency Diseases, binding protein, protein localization, lung parenchyma, gene expression profiling, medicine, IMMUNOOSSEOUS DYSPLASIA, 030304 developmental biology, Emphysema, business.industry, Research, human tissue, SWI SNF related matrix associated actin dependent regulator of chromatin subfamily a like 1, Dysplasia, business
وصف الملف: Electronic; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aff0e0995712e817e2e461d654ddc339Test
https://lirias.kuleuven.be/handle/123456789/653703Test