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1
المؤلفون: Ulke M, Niroshan Nadarajah, T Haferlach, Ulrike Bacher, Claudia Haferlach, Wolfgang Kern, Frank Dicker, Kuznia S, Susanne Schnittger, Maria Theresa Krauth, Christiane Eder, Tamara Alpermann
المصدر: Leukemia. 29:660-667
مصطلحات موضوعية: Adult, Male, Cancer Research, medicine.medical_specialty, Myeloid, Adolescent, Oncogene Proteins, Fusion, Antineoplastic Agents, Biology, Bioinformatics, Gastroenterology, DNA Methyltransferase 3A, Frameshift mutation, Sex Factors, Internal medicine, medicine, Humans, Missense mutation, DNA (Cytosine-5-)-Methyltransferases, WT1 Proteins, Survival analysis, Aged, Aged, 80 and over, Gene Expression Regulation, Leukemic, Hazard ratio, Age Factors, Myeloid leukemia, Wilms' tumor, Hematology, Middle Aged, Prognosis, medicine.disease, Survival Analysis, Axons, Repressor Proteins, Leukemia, Myeloid, Acute, Leukemia, medicine.anatomical_structure, fms-Like Tyrosine Kinase 3, Oncology, Mutation, CCAAT-Enhancer-Binding Proteins, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9099b41b94095ef19000166cb92f40f5Test
https://doi.org/10.1038/leu.2014.243Test -
2
المصدر: Blood. 128:2027-2027
مصطلحات موضوعية: 0301 basic medicine, Genetics, Mutation, In silico, Immunology, Cell Biology, Hematology, Biology, medicine.disease_cause, Biochemistry, DNA sequencing, Primer extension, 03 medical and health sciences, 030104 developmental biology, Consensus sequence, medicine, Missense mutation, Gene, Reference genome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::abf00229f1abf861dbd2b5dff3f595f6Test
https://doi.org/10.1182/blood.v128.22.2027.2027Test -
3
المؤلفون: Bhumika J. Patel, Manja Meggendorfer, Bartlomiej P Przychodzen, Torsten Haferlach, Hideki Makishima, Kassy E Kneen, Sean Hobson, Jaroslaw P. Maciejewski, Mikkael A. Sekeres, Mridul Mukherji, Tomas Radivoyevitch, Niroshan Nadarajah, Srinivasa R. Sanikommu, Aziz Nazha
المصدر: Blood. 126:1645-1645
مصطلحات موضوعية: Genetics, Mutation, dbSNP, Myeloid, Immunology, Single-nucleotide polymorphism, Cell Biology, Hematology, Biology, medicine.disease_cause, medicine.disease, Biochemistry, Germline, Frameshift mutation, Leukemia, medicine.anatomical_structure, hemic and lymphatic diseases, medicine, Missense mutation
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::57dcfcce485a6afb8fda8a335698010dTest
https://doi.org/10.1182/blood.v126.23.1645.1645Test -
4
المؤلفون: Jennifer Kienast, Sabine Denzel, Claudia Haferlach, Andreas Roller, Vera Grossmann, Alexander Kohlmann, Wolfgang Kern, Niroshan Nadarajah, Susanne Schnittger, Torsten Haferlach, Tamara Alpermann
المصدر: Blood. 122:2998-2998
مصطلحات موضوعية: Genetics, medicine.medical_specialty, Candidate gene, Immunology, Cytogenetics, Cell Biology, Hematology, Gene mutation, Biology, medicine.disease, BCL6, Biochemistry, Molecular biology, Leukemia, hemic and lymphatic diseases, medicine, Missense mutation, Mutation frequency, Burkitt's lymphoma
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::8d27eefb6b2658716248a3924f78915dTest
https://doi.org/10.1182/blood.v122.21.2998.2998Test -
5
المؤلفون: Alexander Kohlmann, Wolfgang Kern, Susanne Schnittger, Claudia Haferlach, Torsten Haferlach, Tamara Alpermann, Vera Grossmann, Niroshan Nadarajah
المصدر: Blood. 120:657-657
مصطلحات موضوعية: Oncology, medicine.medical_specialty, Mutation, Pathology, business.industry, medicine.medical_treatment, Immunology, Cytogenetics, Myeloid leukemia, Cell Biology, Hematology, medicine.disease, medicine.disease_cause, Biochemistry, Minimal residual disease, Leukemia, hemic and lymphatic diseases, Internal medicine, medicine, Missense mutation, Clinical significance, business, Neoadjuvant therapy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::34734637456ac81c1650e235d9981beeTest
https://doi.org/10.1182/blood.v120.21.657.657Test -
6
المؤلفون: Stefan Harbich, Vera Grossmann, Alexander Kohlmann, Wolfgang Kern, Susanne Schnittger, Frank Dicker, Niroshan Nadarajah, Claudia Haferlach, Torsten Haferlach, Tamara Alpermann
المصدر: Web of Science
مصطلحات موضوعية: Oncology, Sanger sequencing, medicine.medical_specialty, business.industry, Immunology, Cytogenetics, Myeloid leukemia, Cell Biology, Hematology, medicine.disease, Biochemistry, Minimal residual disease, Deep sequencing, Transplantation, Leukemia, symbols.namesake, hemic and lymphatic diseases, Internal medicine, medicine, symbols, Missense mutation, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0b3a61f651f01820081599bf1c55671Test
https://doi.org/10.1182/blood.v118.21.747.747Test -
7
المؤلفون: Wolfgang Kern, Claudia Haferlach, Torsten Haferlach, Susanne Schnittger, Niroshan Nadarajah
المصدر: Web of Science
مصطلحات موضوعية: Genetics, medicine.medical_specialty, NPM1, Mutation, Myeloid, Immunology, Cytogenetics, Cell Biology, Hematology, Biology, medicine.disease, medicine.disease_cause, Biochemistry, Gastroenterology, Frameshift mutation, Leukemia, medicine.anatomical_structure, hemic and lymphatic diseases, Internal medicine, CEBPA, medicine, Missense mutation
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b79ac1049bb3e59cc6defa7252e1be2fTest
https://publons.com/wos-op/publon/55589697Test/ -
8
المؤلفون: Manja Meggendorfer, Claudia Haferlach, Niroshan Nadarajah, Torsten Haferlach, Wolfgang Kern
المصدر: Web of Science
مصطلحات موضوعية: Genetics, education.field_of_study, dbSNP, Database, Immunology, Population, Cell Biology, Hematology, Gene mutation, Biology, computer.software_genre, Biochemistry, Minor allele frequency, CEBPA, SNP, Missense mutation, 1000 Genomes Project, education, computer
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de213af9ff62b3f576157553942b78ddTest
https://publons.com/wos-op/publon/55589662Test/ -
9The RUNX1 Gene Is Altered in 26% of AML Patients Either By Translocation, Mutation, Gain or Deletion
المؤلفون: Wolfgang Kern, Niroshan Nadarajah, Torsten Haferlach, Susanne Schnittger, Claudia Haferlach
المصدر: Web of Science
مصطلحات موضوعية: NPM1, medicine.medical_specialty, Immunology, Cytogenetics, Chromosomal translocation, Cell Biology, Hematology, Biology, medicine.disease, Biochemistry, Gastroenterology, Frameshift mutation, Fusion gene, Leukemia, hemic and lymphatic diseases, Internal medicine, embryonic structures, CEBPA, Cancer research, medicine, Missense mutation
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c8224b8e4f75891b9f0def482b7ac12Test
https://publons.com/wos-op/publon/55589688Test/ -
10
المؤلفون: Frank Dicker, Niroshan Nadarajah, Vera Grossmann, Stefan Harbich, Claudia Haferlach, Alexander Kohlmann, Wolfgang Kern, Susanne Schnittger, Torsten Haferlach, Tamara Alpermann
المصدر: Web of Science
مصطلحات موضوعية: Oncology, Cytopenia, medicine.medical_specialty, Pathology, business.industry, Myelodysplastic syndromes, Immunology, Cell Biology, Hematology, medicine.disease, Biochemistry, Transplantation, Leukemia, Dysplasia, hemic and lymphatic diseases, Internal medicine, Refractory anemia with ring sideroblasts, medicine, Missense mutation, Refractory cytopenia with multilineage dysplasia, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9f3461ed8ba76b285193ba5e4b9f9d8Test
https://publons.com/wos-op/publon/55589857Test/