نتائج البحث - "Niroshan Nadarajah"

المساهمون: Daniele, GIULIA MARIA, Simonetti, Giorgia, Fusilli, Caterina, Iacobucci, Ilaria, Lonoce, Angelo, Palazzo, Antonio, Lomiento, Mariana, Mammoli, Fabiana, Marsano, Renã Massimiliano, Marasco, Elena, Mantovani, Vilma, Quentmeier, Hilmar, Drexler, Hans G., Ding, Jie, Palumbo, Orazio, Carella, Massimo, Nadarajah, Niroshan, Perricone, Margherita, Ottaviani, Emanuela, Baldazzi, Carmen, Testoni, Nicoletta, Papayannidis, Cristina, Ferrari, Sergio, Mazza, Tommaso, Martinelli, Giovanni, Storlazzi, CLELIA TIZIANA

المصدر: Haematologica

مصطلحات موضوعية: 0301 basic medicine, Myeloid, Male, Cellular differentiation, Adult, Aged, Aged, 80 and over, Biomarkers, Tumor, Cell Differentiation, Cell Line, Tumor, Cell Proliferation, Computational Biology, DNA (Cytosine-5-)-Methyltransferases, DNA Methylation, Databases, Genetic, Female, Gene Expression Profiling, Genetic Association Studies, Homeodomain Proteins, Humans, Leukemia, Myeloid, Acute, Middle Aged, Mutation, Myeloid Cells, Translocation, Genetic, Young Adult, Ectopic Gene Expression, Epigenesis, Genetic, DNA Methyltransferase 3A, 80 and over, Tumor, Leukemia, Myeloid leukemia, Hematology, medicine.anatomical_structure, DNA methylation, Nucleophosmin, Acute promyelocytic leukemia, Acute Myeloid Leukemia, NPM1, Translocation, Biology, Acute, Article, Cell Line, 03 medical and health sciences, Databases, Genetic, medicine, medicine.disease, 030104 developmental biology, Immunology, Cancer research, Ectopic expression, Biomarkers, Epigenesis

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5921c973273cee723e9b3fbc945c418Test
https://pubmed.ncbi.nlm.nih.gov/28411256Test

9

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

المصدر: Leukemia
Leukemia, vol 28, iss 2

مصطلحات موضوعية: Neuroblastoma RAS viral oncogene homolog, Oncology, Male, Cancer Research, Leading Article, Gene mutation, Bioinformatics, Biochemistry, Somatic evolution in cancer, Risk groups, Gene Frequency, Mutation Rate, hemic and lymphatic diseases, 80 and over, Significant risk, Cancer, Aged, 80 and over, Univariate analysis, Myeloid leukemia, High-Throughput Nucleotide Sequencing, Single Nucleotide, Hematology, Middle Aged, Prognosis, myelodysplastic syndromes, prognostic score, Leukemia, Female, Biotechnology, Adult, Genetic Markers, medicine.medical_specialty, molecular markers, Clinical Sciences, Oncology and Carcinogenesis, Immunology, and over, Biology, Polymorphism, Single Nucleotide, Deep sequencing, DNA sequencing, Young Adult, Rare Diseases, Clinical Research, Internal medicine, Genetics, medicine, Humans, In patient, Genetic Testing, Polymorphism, Gene, Genetic Association Studies, Aged, Proportional Hazards Models, business.industry, Proportional hazards model, Myelodysplastic syndromes, Human Genome, Cell Biology, medicine.disease, ETV6, Mutation, next-generation sequencing, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e95fa5d62e1f292a1f85085b53ad4625Test
http://europepmc.org/articles/PMC3918868Test

10

Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant disease

المؤلفون: Niroshan Nadarajah, T Haferlach, Claudia Haferlach, Andreas Roller, Tamara Alpermann, Sonja Schindela, Frank Dicker, Susanne Schnittger, Alexander Kohlmann, Vera Grossmann, Wolfgang Kern

المصدر: Leukemia. 28:129-137

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20f0d82a86cdc06742f8595438050532Test
https://doi.org/10.1038/leu.2013.239Test

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