المؤلفون: Xiao, Sheng

المساهمون: Brigham and Women's Hospital, Boston, MA 02215

مصطلحات موضوعية: eosinophilia, PDGFRA, PDGFRB, FGFR1, PCM1/JAK2, Leukaemia Section, Biomarkers, Tumor/*genetics, Bone Marrow Cells/metabolism/pathology, Chromosomes, Human, Pair 2/genetics, Pair 5/genetics, Golgi Matrix Proteins/*genetics, Humans, Hypereosinophilic Syndrome/*genetics/pathology, Leukemia/*genetics/pathology, Male, Middle Aged, Oncogene Fusion, Oncogene Proteins, Fusion/*genetics, Receptor, Platelet-Derived Growth Factor beta/*genetics, Translocation, Genetic, Blood Cell Count, Pair 9/genetics, Hypereosinophilic Syndrome/blood/drug therapy/*genetics, Imatinib Mesylate/therapeutic use

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/PDGFRAPDGFRBFGFR1PCM1-JAK2ID1855.htmlTest; Sheng, Xiao. Myeloid/lymphoid neoplasms with eosinophilia and rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2: Overview 2019. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2020, 4, p. 174-179; http://hdl.handle.net/2042/70698Test; https://doi.org/10.4267/2042/70698Test

الإتاحة: https://doi.org/10.4267/2042/70698Test
http://hdl.handle.net/2042/70698Test

المؤلفون: Salcedo, Luis Miguel Juárez, Conde Royo, Diego, Dalia, Samir

المساهمون: Guadalajara University Hospital, Guadalajara, Spain (LMJS), Principe de Asturias University Hospital, Madrid, Spain (DCR), Oncology and Hematology, Mercy Clinic Joplin, Joplin, MO, USA (SD)

مصطلحات موضوعية: Extranodal NK/T-cell lymphoma nasal type, Angiocentric T-cell lymphoma, Malignant reticulosis, Leukaemia Section, Adult, Aged, 80 and over, Chromosome Aberrations, Chromosomes, Human, Pair 1/genetics, Drug Resistance, Neoplasm/*genetics, Female, Hematologic Neoplasms/*genetics/pathology, Humans, Karyotyping, Leukemia, Myeloid, Acute/*genetics/pathology, Male, Middle Aged, Myelodysplastic Syndromes/*genetics/pathology, Myeloproliferative Disorders/*genetics/pathology, Prognosis, Translocation, Genetic/*genetics, Bone Marrow Cells/metabolism/pathology, Chromosome Deletion

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/ExtranodalNKTLNHID1689.htmlTest; Luis Miguel Juárez, Salcedo; Diego, Conde Royo; Samir, Dalia. Extranodal NK/T-cell lymphoma, nasal type (ENKL). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 6, p. 146-148; http://hdl.handle.net/2042/70457Test; https://doi.org/10.4267/2042/70457Test

الإتاحة: https://doi.org/10.4267/2042/70457Test
http://hdl.handle.net/2042/70457Test

المؤلفون: Zamecnikova, Adriana, al Bahar, Soad

المساهمون: Kuwait Cancer Control Center, Department of Hematology

مصطلحات موضوعية: Leukaemia Section, Bone Marrow Cells/metabolism/pathology, Chromosome Deletion, Chromosomes, Human, Pair 1/*genetics, Pair 17/*genetics, Cytogenetic Analysis, Disease Progression, Humans, In Situ Hybridization, Fluorescence, Interspersed Repetitive Sequences, Karyotype, Multiple Myeloma/*genetics/pathology, Risk, Translocation, Genetic, Base Sequence, CCCTC-Binding Factor, Cell Cycle Proteins/genetics, Cell Proliferation

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/der0109q11q34ID1648.htmlTest; Adriana, Zamecnikova; Soad, al Bahar. der(9)t(1;9)(q11-12;q34). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 10, p. 531-533; http://hdl.handle.net/2042/66087Test; https://doi.org/10.4267/2042/66087Test

الإتاحة: https://doi.org/10.4267/2042/66087Test
http://hdl.handle.net/2042/66087Test

المؤلفون: Lima, Keli, Machado-Neto, Joao Agostinho

المساهمون: Department of Clinical Pathology, School of Medical Sciences, University of Campinas - UNICAMP, Campinas, Sao Paulo, Brazil (KL), Hematology and Hemotherapy Center, University of Campinas - UNICAMP, Instituto Nacional de Ciencia e Tecnologia do Sangue, Campinas, Sao Paulo, Brazil (JAMN), Department of Internal Medicine, University of Sao Paulo at Ribeirao Preto Medical School, Ribeirao Preto, Sao Paulo, Brazil (JAMN)

مصطلحات موضوعية: PIP4K2A, cell proliferation, clonogenicity, cell cycle, apoptosis, phosphatidylinositol signaling, Genes Section, Apoptosis/genetics, Bone Marrow Cells/metabolism/pathology, Cell Count, Cell Line, Tumor, Cell Proliferation/genetics, Cell Survival/genetics, Gene Expression Regulation, Neoplastic, Gene Silencing, Hematologic Neoplasms/*metabolism/pathology, Humans, Myelodysplastic Syndromes/metabolism/pathology

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Genes/PIP4K2AID43943ch10p12.htmlTest; Keli, Lima; Joao Agostinho, Machado-Neto. PIP4K2A (phosphatidylinositol-5-phosphate 4-kinase, type II, alpha). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 7, p. 380-384; http://hdl.handle.net/2042/66053Test; https://doi.org/10.4267/2042/66053Test

الإتاحة: https://doi.org/10.4267/2042/66053Test
http://hdl.handle.net/2042/66053Test

المؤلفون: Zamecnikova, Adriana, Al Bahar, Soad

المساهمون: Kuwait Cancer Control Center, Laboratory of Cancer Genetics, Department of Hematology, Shuwaikh, 70653, Kuwait

مصطلحات موضوعية: t(1, 20)(q10-21, q11-13), Leukaemia Section, Bone Marrow Cells/metabolism/pathology, Chromosome Deletion, Chromosomes, Human, Pair 1/*genetics, Pair 17/*genetics, Cytogenetic Analysis, Disease Progression, Humans, In Situ Hybridization, Fluorescence, Interspersed Repetitive Sequences, Karyotype, Multiple Myeloma/*genetics/pathology, Risk, Translocation, Genetic, Adult, Aged, 80 and over, Antineoplastic Agents/adverse effects, Cells, Cultured, Chromosome Aberrations/chemically induced, Comparative Genomic Hybridization/methods, DNA Copy Number Variations/physiology

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t0120q10q11ID1657.htmlTest; Adriana, Zamecnikova; Soad, Al Bahar. der(20)t(1;20)(q10-21;q11-13). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 7, p. 426-428; http://hdl.handle.net/2042/66059Test; https://doi.org/10.4267/2042/66059Test

الإتاحة: https://doi.org/10.4267/2042/66059Test
http://hdl.handle.net/2042/66059Test

المؤلفون: Zamecnikova, Adriana, Al Bahar, Soad

المساهمون: Kuwait Cancer Control Center, Laboratory of Cancer Genetics, Department of Hematology, Shuwaikh, 70653, Kuwait

مصطلحات موضوعية: Leukaemia Section, Bone Marrow Cells/metabolism/pathology, Chromosome Deletion, Chromosomes, Human, Pair 1/*genetics, Pair 17/*genetics, Cytogenetic Analysis, Disease Progression, Humans, In Situ Hybridization, Fluorescence, Interspersed Repetitive Sequences, Karyotype, Multiple Myeloma/*genetics/pathology, Risk

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t118q10q11ID1655.htmlTest; Adriana, Zamecnikova; Soad, Al Bahar. der(18)t(1;18)(q10-25;q11-23). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 6, p. 347-351; http://hdl.handle.net/2042/62944Test; https://doi.org/10.4267/2042/62944Test

الإتاحة: https://doi.org/10.4267/2042/62944Test
http://hdl.handle.net/2042/62944Test

المؤلفون: Zamecnikova, Adriana, Al Bahar, Soad

المساهمون: Kuwait Cancer Control Center, Department of Hematology, Laboratory of Cancer Genetics, Kuwait

مصطلحات موضوعية: chromosome 1, chromosome 13, translocation, hematologic malignancies, Leukaemia Section, Bone Marrow Cells/metabolism/pathology, Chromosome Deletion, Chromosomes, Human, Pair 1/*genetics, Pair 17/*genetics, Cytogenetic Analysis, Disease Progression, Humans, In Situ Hybridization, Fluorescence, Interspersed Repetitive Sequences, Karyotype, Multiple Myeloma/*genetics/pathology, Risk, Translocation, Genetic, Adolescent, Adult, Bone Marrow/physiology, Child, Preschool, Core Binding Factor Alpha 2 Subunit/*genetics, Fanconi Anemia/complications/*genetics, Fem

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/der0113q10q10ID1653.htmlTest; Adriana, Zamecnikova; Soad, Al Bahar. Unbalanced whole-arm translocation der(1;13) in hematologic malignancies. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 1, p. 48-51; http://hdl.handle.net/2042/62510Test; https://doi.org/10.4267/2042/62510Test

الإتاحة: https://doi.org/10.4267/2042/62510Test
http://hdl.handle.net/2042/62510Test