المؤلفون: Arezou Sayad, Mir Davood Omrani, Ghasem Solgi, Rezvan Noroozi, Shahram Arsang-Jang, Hidetoshi Inoko, Mohammad Taheri

المصدر: Iranian Journal of Allergy, Asthma and Immunology, Vol 16, Iss 4 (2017)

مصطلحات موضوعية: Gene expression, IL7Rα gene, Multiple sclerosis, Polymorphism, Medicine

وصف الملف: electronic resource

Relation: https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1024; https://doaj.org/toc/1735-1502; https://doaj.org/toc/1735-5249

URL الوصول: https://doaj.org/article/82f81183b61a4489a498d0e652f323a3

المؤلفون: Arend Bökenkamp, Kira Y. Dionis-Petersen, Lan Xiang Liu, Neeraja Kambham, Helen Fryssira, Ayşe İpek Polat, Mattia Gentile, C. Nur Semerci, Tracy E. Hunley, Katarina Mitrovic, Behzad Najafian, Radovan Bogdanovic, Mrinmoy Sanyal, Uluç Yiş, Encarna Guillen-Navarro, Katie Felix, Marie Morimoto, Christy Mayfield, Alireza Baradaran-Heravi, Thomas Lücke, Susan A. Berry, Cornelius F. Boerkoel, David B. Lewis, Kent P. Jensen, Kunho Choi, Lydia Najera, Giuliana Lama, Suparna Dutt, Michel Tsimaratos, Ann Haskins Olney, Benjamin Dekel, Milena Brugnara

المساهمون: Pediatric surgery, ICaR - Circulation and metabolism

المصدر: Clinical Immunology, 161(2), 355-365. Academic Press Inc.
Sanyal, M, Morimoto, M, Baradaran-Heravi, A, Choi, K, Kambham, N, Jensen, K, Dutt, S, Dionis-Petersen, K Y, Liu, L X, Felix, K, Mayfield, C, Dekel, B, Bokenkamp, A, Fryssira, H, Guillen-Navarro, E, Lama, G, Brugnara, M, Lucke, T, Olney, A H, Hunley, T E, Polat, A I, Yis, U, Bogdanovic, R, Mitrovic, K, Berry, S, Najera, L, Najafian, B, Gentile, M, Semerci, C N, Tsimaratos, M, Lewis, D B & Boerkoel, C F 2015, ' Lack of IL7R alpha expression in T cells is a hallmark of T-cell immunodeficiency in Schimke immuno-osseous dysplasia (SIOD) ', Clinical Immunology, vol. 161, no. 2, pp. 355-365 . https://doi.org/10.1016/j.clim.2015.10.005

مصطلحات موضوعية: Nephrotic Syndrome, SMARCAL1 protein, human, Arteriosclerosis, T-Lymphocytes, interleukin 7 receptor alpha, Gene Expression, Gene mutation, SIOD, preschool child, T-cell immunodeficiency, 0302 clinical medicine, chondrodysplasia, mononuclear cell, T lymphocyte, Immunology and Allergy, genetics, exon, gene mutation, Child, Promoter Regions, Genetic, Immunodeficiency, Cells, Cultured, 0303 health sciences, clinical article, DNA methylation, messenger RNA, Reverse Transcriptase Polymerase Chain Reaction, adult, Interleukin-17, Flow Cytometry, Immunohistochemistry, IL7R?, 3. Good health, Adolescent, Adult, Arteriosclerosis/*genetics/metabolism/pathology, Child, Preschool, DNA Helicases/genetics, DNA Methylation, Humans, Immunologic Deficiency Syndromes/*genetics/metabolism/pathology, Interleukin-17/pharmacology, Leukocytes, Mononuclear/drug effects/metabolism, Mutation, Nephrotic Syndrome/*genetics/metabolism/pathology, Osteochondrodysplasias/*genetics/metabolism/pathology, Primary Immunodeficiency Di, priority journal, young adult, Interleukin 17, schimke immuno osseous dysplasia, T-Cell Immunodeficiency, IL7Rα, lung embolism, Primary Immunodeficiency Diseases, Immunology, interleukin-7 receptor, alpha chain, DNA sequence, DNA helicase, Biology, interleukin 7, Osteochondrodysplasias, Article, Promoter DNA methylation, reverse transcription polymerase chain reaction, 03 medical and health sciences, promoter region, CpG, medicine, controlled study, human, Interleukin-7 receptor, protein expression, 030304 developmental biology, cell culture, Receptors, Interleukin-7, autosomal recessive disorder, human cell, Schimke immuno-osseous dysplasia, DNA Helicases, Immunologic Deficiency Syndromes, Sequence Analysis, DNA, immune deficiency, medicine.disease, school child, human tissue, CD127, Dysplasia, interleukin 7 receptor, drug effects, Leukocytes, Mononuclear, pathology, interleukin 17, Pulmonary Embolism, metabolism, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f50c6086f08104dec7b390962062b36b
https://doi.org/10.1016/j.clim.2015.10.005

المؤلفون: Sayad, Arezou, Omrani, Mir Davood, Solgi, Ghasem, Rezvan Noroozi, Arsang-Jang, Shahram, Inoko, Hidetoshi, Taheri, Mohammad

المصدر: Scopus-Elsevier
Iranian Journal of Allergy, Asthma and Immunology, Vol 16, Iss 4 (2017)
Web of Science

مصطلحات موضوعية: Adult, Male, Receptors, Interleukin-7, Genotype, lcsh:R, Genetic Variation, lcsh:Medicine, Polymorphism, Single Nucleotide, IL7Rα gene, Multiple sclerosis, Young Adult, Multiple Sclerosis, Relapsing-Remitting, Case-Control Studies, Odds Ratio, Humans, Female, Genetic Predisposition to Disease, Gene expression, Polymorphism, Alleles, Genetic Association Studies

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::723d0ac7c366a6804d8be881824c2622
http://www.scopus.com/inward/record.url?eid=2-s2.0-85027365929&partnerID=MN8TOARS