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1Academic Journal
المؤلفون: Lew-Derivry, Lucille, Marceau-Renaut, Alice, Fenwarth, Laurène, Cuccuini, Wendy, Ballerini, Paola, Ferreboeuf, Maxime, Guilmatre, Audrey, Petit, Arnaud, Gandemer, Virginie, Rialland, Fanny, Schneider, Pascale, Robert, Bruno, Gérard, Michel, B.G.M., Bertrand, Yves, Baruchel, André, Preudhomme, Claude, Leverger, Guy, Lapillonne, Helene
المساهمون: CHU Trousseau APHP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille), Lille Neurosciences & Cognition - U 1172 (LilNCog), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille), Hopital Saint-Louis AP-HP (AP-HP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Centre de Recherche Saint-Antoine (CRSA), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Centre Hospitalier Universitaire de Rennes CHU Rennes = Rennes University Hospital Ponchaillou, Institut de Génétique et Développement de Rennes (IGDR), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes), Hôpital de la Timone CHU - APHM (TIMONE), Hospices Civils de Lyon (HCL), ELAM02 national tumor Bank, Société Française de lutte contre les Cancers et les leucémies de l'Enfant et de l'Adolescent, SFCE, Fondation de France, Ministère des Affaires Sociales et de la Santé, (03142, PHRC-K 2003), Association Laurette Fugain, (ALF2015/12), Institut National Du Cancer, INCa, (INCA-DGOS_5797)
المصدر: ISSN: 0887-6924.
مصطلحات موضوعية: Child, Core Binding Factor Alpha 2 Subunit, Humans, Leukemia, Myeloid, Acute, Mutation, Prognosis, transcription factor RUNX1, RUNX1 protein, human, acute myeloid leukemia, adolescent, Article, cancer mortality, cancer prognosis, controlled study, cytogenetics, cytology, event free survival, female, frameshift mutation, France, gene deletion, gene frequency, gene mutation, leukemia remission, major clinical study, male, missense mutation
Relation: info:eu-repo/semantics/altIdentifier/pmid/37328541; hal-04283874; https://hal.science/hal-04283874; https://hal.science/hal-04283874/document; https://hal.science/hal-04283874/file/s41375-023-01931-y.pdf; PUBMED: 37328541
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2Academic Journal
المؤلفون: Masuda, Tatsuya, Maeda, Shintaro, Shimada, Sae, Sakuramoto, Naoya, Morita, Ken, Koyama, Asami, Suzuki, Kensho, Mitsuda, Yoshihide, Matsuo, Hidemasa, Kubota, Hirohito, Kato, Itaru, Tanaka, Kuniaki, Takita, Junko, Hirata, Masahiro, Kataoka, Tatsuki R, Nakahata, Tatsutoshi, Adachi, Souichi, Hirai, Hideyo, Mizuta, Shuichi, Naka, Kazuhito, Imai, Yoichi, Kimura, Shinya, Sugiyama, Hiroshi, Kamikubo, Yasuhiko
المساهمون: 増田, 達哉, 前田, 信太郎, 嶌田, 紗英, 櫻本, 直也, 森田, 剣, 小山, 朝美, 鈴木, 健聖, 光田, 吉秀, 松尾, 英将, 窪田, 博仁, 加藤, 格, 田中, 邦昭, 滝田, 順子, 平田, 勝啓, 片岡, 竜貴, 中畑, 龍俊, 足立, 壯一, 平位, 秀世, 杉山, 弘, 上久保, 靖彦, 10610454, 00359621, 50183843
مصطلحات موضوعية: bcr-abl, fusion proteins, gene expression regulation, leukemia, lymphoid, Philadelphia chromosome, RUNX1 protein, human
Relation: http://hdl.handle.net/2433/278380; Cancer Science; 113; 529; 539
الاتاحة: http://hdl.handle.net/2433/278380
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3
المؤلفون: Tatsuya Masuda, Shintaro Maeda, Sae Shimada, Naoya Sakuramoto, Ken Morita, Asami Koyama, Kensho Suzuki, Yoshihide Mitsuda, Hidemasa Matsuo, Hirohito Kubota, Itaru Kato, Kuniaki Tanaka, Junko Takita, Masahiro Hirata, Tatsuki R Kataoka, Tatsutoshi Nakahata, Souichi Adachi, Hideyo Hirai, Shuichi Mizuta, Kazuhito Naka, Yoichi Imai, Shinya Kimura, Hiroshi Sugiyama, Yasuhiko Kamikubo
المصدر: Cancer Science. 113(2):529-539
مصطلحات موضوعية: Cancer Research, Cell Death, bcr-abl, lymphoid, Fusion Proteins, bcr-abl, leukemia, Antineoplastic Agents, General Medicine, gene expression regulation, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Philadelphia chromosome, Gene Expression Regulation, Neoplastic, Mice, Oncology, RUNX1 protein, human, Drug Resistance, Neoplasm, Cell Line, Tumor, Core Binding Factor Alpha 2 Subunit, Mutation, Imatinib Mesylate, Animals, Humans, Protein Kinase Inhibitors, fusion proteins, Cell Proliferation
وصف الملف: application/pdf
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4Academic Journal
المؤلفون: Marsman, J, Thomas, A, Osato, M, O'sullivan, J.M, Horsfield, J.A
المساهمون: CANCER SCIENCE INSTITUTE OF SINGAPORE
المصدر: Unpaywall 20201031
مصطلحات موضوعية: protein binding, RUNX1 protein, human, transcription factor RUNX1, animal, biological model, chromatin, chromatin immunoprecipitation, cytology, enhancer region, gene expression regulation, gene locus, genetics, hematopoiesis, hematopoietic stem cell, high throughput sequencing, metabolism, mouse, phenotype, promoter region, reporter gene, Animals, Core Binding Factor Alpha 2 Subunit, Enhancer Elements, Genetic, Developmental, Genes, Reporter, Genetic Loci, Hematopoietic Stem Cells
Relation: Marsman, J, Thomas, A, Osato, M, O'sullivan, J.M, Horsfield, J.A (2017). A DNA contact map for the mouse runx1 gene identifies novel haematopoietic enhancers. Scientific Reports 7 (1) : 13347. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-017-13748-8; https://scholarbank.nus.edu.sg/handle/10635/178568
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5Academic Journal
المؤلفون: Regha, K, Assi, S.A, Tsoulaki, O, Gilmour, J, Lacaud, G, Bonifer, C
المساهمون: MECHANOBIOLOGY INSTITUTE
المصدر: Unpaywall 20201031
مصطلحات موضوعية: hybrid protein, RUNX1 ETO protein, transcription factor RUNX1, unclassified drug, DNA binding protein, messenger RNA, MTG8 protein, mouse, oncoprotein, Runx1 protein, transcription factor, transcriptome, blood, developmental stage, gene expression, genetic differentiation, germ cell, molecular analysis, acute myeloblastic leukemia, animal cell, Article, binding site, blood cell, cell differentiation, cell expansion, cell population, cell selection, chromatin immunoprecipitation, controlled study, down regulation
Relation: Regha, K, Assi, S.A, Tsoulaki, O, Gilmour, J, Lacaud, G, Bonifer, C (2015). Developmental-stage-dependent transcriptional response to leukaemic oncogene expression. Nature Communications 6 : 7203. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms8203; https://scholarbank.nus.edu.sg/handle/10635/180469
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6Academic Journal
المؤلفون: Ampatzidou Μ., Papadhimitriou S.I., Paterakis G., Pavlidis D., Tsitsikas Κ., Kostopoulos I.V., Papadakis V., Vassilopoulos G., Polychronopoulou S.
المصدر: Cancer Genetics ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045106431&doi=10.1016%2fj.cancergen.2018.03.001&partnerID=40&md5=0f017e5767af35b3ff49d0952e155984
مصطلحات موضوعية: transcription factor ETV6, transcription factor RUNX1, repressor protein, RUNX1 protein, human, transcription factor Ets, acute lymphoblastic leukemia, adolescent, Article, cancer prognosis, child, chromosome 21q, chromosome 9p, clinical feature, cohort analysis, disease association, female, flow cytometry, follow up, genetic disorder, genetic heterogeneity, human cell, human tissue, long term care, major clinical study, male, minimal residual disease, priority journal, treatment outcome, treatment response
Relation: http://hdl.handle.net/11615/81056
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7
المؤلفون: Gerd Kempermann, Frank Buchholz, Hirokazu Fukui, Annette E. Rünker, Klaus Fabel
المصدر: PLoS ONE, Vol 13, Iss 1, p e0190789 (2018)
PLOS ONE 13(1), e0190789 (2018). doi:10.1371/journal.pone.0190789
PLoS ONEمصطلحات موضوعية: 0301 basic medicine, Volition, Neural precursor cell proliferation, Gene Expression, lcsh:Medicine, Apoptosis, metabolism [Hippocampus], metabolism [Neural Stem Cells], Hippocampal formation, Biochemistry, Hippocampus, Running, chemistry.chemical_compound, 0302 clinical medicine, physiology [Running], Neural Stem Cells, Animal Cells, hemic and lymphatic diseases, Hippocampal Neurogenesis, Medicine and Health Sciences, Protein Isoforms, cytology [Neural Stem Cells], administration & dosage [Transforming Growth Factor beta1], lcsh:Science, Cells, Cultured, Multidisciplinary, Stem Cells, Systems Biology, Neurogenesis, Brain, Cell Differentiation, physiology [Neurogenesis], Cell biology, metabolism [Transforming Growth Factor beta1], RUNX1, Mice, Inbred DBA, Core Binding Factor Alpha 2 Subunit, embryonic structures, Cellular Types, Anatomy, Stem cell, Neuronal Differentiation, genetics [Core Binding Factor Alpha 2 Subunit], Research Article, Precursor Cells, Cell Survival, physiology [Cell Survival], Biology, metabolism [Core Binding Factor Alpha 2 Subunit], Transfection, metabolism [RNA, Messenger], Transforming Growth Factor beta1, 03 medical and health sciences, Developmental Neuroscience, Species Specificity, Precursor cell, DNA-binding proteins, Genetics, Animals, Gene Regulation, metabolism [Dendrites], ddc:610, RNA, Messenger, Transcription factor, Runx1 protein, mouse, lcsh:R, Adult Neurogenesis, Biology and Life Sciences, Proteins, Cell Biology, Dendrites, Regulatory Proteins, Mice, Inbred C57BL, Alternative Splicing, 030104 developmental biology, physiology [Apoptosis], chemistry, Cellular Neuroscience, cytology [Hippocampus], Neuron differentiation, lcsh:Q, Transcriptome, 030217 neurology & neurosurgery, Developmental Biology, Transcription Factors, Neuroscience
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8
المؤلفون: Fiedler, Hannah
مصطلحات موضوعية: Chromosom 7-Veränderung, RUNX1, protein, human, Akute myeloische Leukämie, Chromosomes, human, pair 7, Chromosone 7, monosomy, Monosomie 7, RUNX1, Leukemia, myeloid, acute, hemic and lymphatic diseases, embryonic structures, Chromosom 7, ddc:610, DDC 610 / Medicine & health
وصف الملف: application/pdf
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9Academic Journal
المؤلفون: Mailer R.K.W., Falk K., Rötzschke O.
المساهمون: MICROBIOLOGY AND IMMUNOLOGY
المصدر: Unpaywall 20200320
مصطلحات موضوعية: cytotoxic T lymphocyte antigen 4, immunoglobulin enhancer binding protein, interleukin 2 receptor alpha, isoprotein, leucine zipper protein, transcription factor FOXP3, transcription factor NFAT, transcription factor RUNX1, forkhead transcription factor, FOXP3 protein, human, primer DNA, RUNX1 protein, animal cell, animal experiment, article, cancer cell, carcinogenesis, CD4+ T lymphocyte, cell function, controlled study, dimerization, exon, gene mutation, gene repression, gene transfer, genetic transcription, human cell, immunoprecipitation, IPEX syndrome
Relation: Mailer R.K.W., Falk K., Rötzschke O. (2009). Absence of leucine zipper in the natural FOXP3Delta2Delta7 isoform does not affect dimerization but abrogates suppressive capacity. PLoS ONE 4 (7) : e6104. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0006104; https://scholarbank.nus.edu.sg/handle/10635/165604
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10
المؤلفون: Huret, JL
المساهمون: Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
مصطلحات موضوعية: Chromosome 7, Chromosome 21, Leukemia Section, ANLL (class disease), RUNX1 protein, human, Chromosome Aberrations, Leukemia, Myeloid, Acute, Translocation, Genetic
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Anomalies/t0721p22q22ID1449.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2008, Vol. 12, N° 6; p. 456; http://hdl.handle.net/2042/38606; https://doi.org/10.4267/2042/38606
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11
المؤلفون: Huret, JL
المساهمون: Genetics, Dept Medical Information, UMR 8125 CNRS, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
مصطلحات موضوعية: Chromosome 6, Chromosome 21, Leukemia Section, MDS (class disease), t-ANLL (class disease), RUNX1 protein, human, Anemia, Refractory, with Excess of Blasts, Bone Marrow Diseases, Chromosome Aberrations, Myelodysplastic Syndromes, Translocation, Genetic
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Anomalies/t0621p22q22ID1266.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2003, Vol. 7, N° 2; p. 121; http://hdl.handle.net/2042/37965; https://doi.org/10.4267/2042/37965
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12Academic Journal
المؤلفون: Huret, JL
المساهمون: Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
مصطلحات موضوعية: Transcription factor, PEBPaB (alias), Chromosome 21, CBFA2 (alias), RUNX1 gene, Genes Section, RUNX1 protein, human, Core Binding Factors, Translocation, Genetic, Myelodysplastic Syndromes, Lymphoproliferative Disorders, Leukemia, T-Cell, Myeloid, Acute, Lymphoid, Chromosome Aberrations, Transcription Factors
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Genes/AML1.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 1997, Vol. 1, N° 2; p. 59-61; http://hdl.handle.net/2042/32051; https://doi.org/10.4267/2042/32051
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13Academic Journal
المؤلفون: Huret, JL
المساهمون: Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
مصطلحات موضوعية: Chromosome 8, Chromosome 21, ANLL (class disease), t-ANLL (class disease), Leukemia Section, Leukemia, Chromosome Aberrations, RUNX1 protein, human, Translocation, Genetic
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Anomalies/t0821.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 1997, Vol. 1, N° 1; p. 23-25; http://hdl.handle.net/2042/32034; https://doi.org/10.4267/2042/32034
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14Review
المؤلفون: Moorman, AV, Harrison, CJ
المساهمون: Leukaemia Research Cytogenetics Group, Cancer Sciences Division, University of Southampton, MP822, Duthie Building, Southampton General Hospital, Tremona Road, Southampton, SO16 6YD, UK
مصطلحات موضوعية: Chromosome 21, Duplication of 21q with amplification of RUNX1 (AML1) in acute lymphoblastic leukaemia (alias), Leukemia Section, B-ALL (class disease), RUNX1 protein, human, Gene Duplication
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Anomalies/dup21qID1382.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2006, Vol. 10, N° 2; p. 112-113; http://hdl.handle.net/2042/38300; https://doi.org/10.4267/2042/38300
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15
المؤلفون: Huret, JL
المساهمون: Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
مصطلحات موضوعية: Chromosome 17, Chromosome 21, Leukemia Section, ANLL (class disease), t-ANLL (class disease), RUNX1 protein, human, Chromosome Aberrations, Leukemia, Translocation, Genetic
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Anomalies/t1721ID1181.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2000, Vol. 4, N° 1; p. 37; http://hdl.handle.net/2042/37597; https://doi.org/10.4267/2042/37597
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16Academic Journal
المؤلفون: Recouvreux, M.S., Grasso, E.N., Echeverria, P.C., Rocha-Viegas, L., Castilla, L.H., Schere-Levy, C., Tocci, J.M., Kordon, E.C., Rubinstein, N.
مصطلحات موضوعية: Foxp3, Gene expression regulation, GJA1, Rspo3, Runx1, transcription factor FOXP3, transcription factor RUNX1, connexin 43, forkhead transcription factor, FOXP3 protein, human, GJA1 protein, RSPO3 protein, RUNX1 protein, thrombospondin, animal cell, Article, breast cancer, breast cell, breast epithelium cell, cell migration, controlled study, down regulation, FOXP3 gene, gene activity, gene expression, gene interaction, genetic transcription, GJA1 gene, in vitro study
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17Review
المؤلفون: Huret, JL
المساهمون: Genetics, Dept Medical Information, UMR 8125 CNRS, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
مصطلحات موضوعية: Chromosome 21, Leukemia Section, t-ANLL (class disease), RUNX1 protein, human, Chromosome Aberrations
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Anomalies/21q22TreatRelLeukID1296.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2004, Vol. 8, N° 1; p. 20-21; http://hdl.handle.net/2042/38045; https://doi.org/10.4267/2042/38045
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18Review
المؤلفون: Bangs, CD
المساهمون: Cytogenetics Laboratory, Rm. H1517, Stanford Hospital and Clinics, 300 Pasteur Dr. Stanford, CA 94305, USA
مصطلحات موضوعية: Chromosome 1, Chromosome 21, Leukemia Section, RUNX1 protein, human, Chromosome Aberrations, Translocation, Genetic
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Anomalies/t0121p32q22ID1259.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2003, Vol. 7, N° 3; p. 183-184; http://hdl.handle.net/2042/37990; https://doi.org/10.4267/2042/37990
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19Review
المساهمون: Genetics, Dept Medical Information, UMR 8125 CNRS, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
مصطلحات موضوعية: Chromosome 21, RUNX1 gene, PEBPaB (polyomavirus enhancer binding protein aB) (alias), Genes Section, Core Binding Factors, RUNX1 protein, human, Transcription Factors, Chromosome Aberrations, Leukemia, Lymphoid, Myeloid, Acute, T-Cell, Lymphoproliferative Disorders, Myelodysplastic Syndromes, Translocation, Genetic
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Genes/AML1.html; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 2003, Vol. 7, N° 2; p. 98-101; http://hdl.handle.net/2042/37948; https://doi.org/10.4267/2042/37948
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20
المؤلفون: Echeverría, Pablo Christian, Rocha Viegas, Luciana, Schere Levy, Carolina P., Tocci, Johanna Melisa, Kordon, Edith Claudia, Rubinstein, Natalia
مصطلحات موضوعية: Foxp3, Gene expression regulation, GJA1, Rspo3, Runx1, transcription factor FOXP3, transcription factor RUNX1, connexin 43, forkhead transcription factor, FOXP3 protein, human, GJA1 protein, RSPO3 protein, RUNX1 protein, thrombospondin, animal cell, Article, breast cancer, breast cell, breast epithelium cell, cell migration, controlled study, down regulation, FOXP3 gene, gene activity, gene expression, gene interaction, genetic transcription, GJA1 gene, in vitro study
Relation: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19492553_v7_n6_p6552_Recouvreux; http://hdl.handle.net/20.500.12110/paper_19492553_v7_n6_p6552_Recouvreux
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