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Standardized definitions of molecular response in chronic myeloid leukemia
by
Saglio, G
, Müller, M C
, White, H E
, Hochhaus, A
, Cross, N C P
in
631/67/1059/602
/ 692/699/67/1990/283/1896
/ BCR-ABL protein
/ Biological and medical sciences
/ Biological response modifiers
/ Biomarkers, Tumor - genetics
/ Cancer Research
/ Care and treatment
/ Chromosome aberrations
/ Chronic myeloid leukemia
/ Critical Care Medicine
/ Cytogenetics
/ Enzyme inhibitors
/ Fusion protein
/ Genes, abl
/ Genetic aspects
/ Genetic transcription
/ Health aspects
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Imatinib
/ Intensive
/ Interferon
/ Internal Medicine
/ Kinases
/ Laboratories
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical genetics
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Myeloid leukemia
/ Oncology
/ Patients
/ Protein Kinase Inhibitors - therapeutic use
/ Protein-tyrosine kinase
/ Protein-Tyrosine Kinases - antagonists & inhibitors
/ review
/ Standardization
/ Stem cell transplantation
/ Transcription
/ Tyrosine
2012
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Standardized definitions of molecular response in chronic myeloid leukemia
by
Saglio, G
, Müller, M C
, White, H E
, Hochhaus, A
, Cross, N C P
in
631/67/1059/602
/ 692/699/67/1990/283/1896
/ BCR-ABL protein
/ Biological and medical sciences
/ Biological response modifiers
/ Biomarkers, Tumor - genetics
/ Cancer Research
/ Care and treatment
/ Chromosome aberrations
/ Chronic myeloid leukemia
/ Critical Care Medicine
/ Cytogenetics
/ Enzyme inhibitors
/ Fusion protein
/ Genes, abl
/ Genetic aspects
/ Genetic transcription
/ Health aspects
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Imatinib
/ Intensive
/ Interferon
/ Internal Medicine
/ Kinases
/ Laboratories
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical genetics
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Myeloid leukemia
/ Oncology
/ Patients
/ Protein Kinase Inhibitors - therapeutic use
/ Protein-tyrosine kinase
/ Protein-Tyrosine Kinases - antagonists & inhibitors
/ review
/ Standardization
/ Stem cell transplantation
/ Transcription
/ Tyrosine
2012
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Do you wish to request the book?
Standardized definitions of molecular response in chronic myeloid leukemia
by
Saglio, G
, Müller, M C
, White, H E
, Hochhaus, A
, Cross, N C P
in
631/67/1059/602
/ 692/699/67/1990/283/1896
/ BCR-ABL protein
/ Biological and medical sciences
/ Biological response modifiers
/ Biomarkers, Tumor - genetics
/ Cancer Research
/ Care and treatment
/ Chromosome aberrations
/ Chronic myeloid leukemia
/ Critical Care Medicine
/ Cytogenetics
/ Enzyme inhibitors
/ Fusion protein
/ Genes, abl
/ Genetic aspects
/ Genetic transcription
/ Health aspects
/ Hematologic and hematopoietic diseases
/ Hematology
/ Humans
/ Imatinib
/ Intensive
/ Interferon
/ Internal Medicine
/ Kinases
/ Laboratories
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medical genetics
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Myeloid leukemia
/ Oncology
/ Patients
/ Protein Kinase Inhibitors - therapeutic use
/ Protein-tyrosine kinase
/ Protein-Tyrosine Kinases - antagonists & inhibitors
/ review
/ Standardization
/ Stem cell transplantation
/ Transcription
/ Tyrosine
2012
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Standardized definitions of molecular response in chronic myeloid leukemia
Journal Article
Standardized definitions of molecular response in chronic myeloid leukemia
2012
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Overview
The International Randomized Study of Interferon and STI571 (IRIS) demonstrated long-term cytogenetic responses in patients with chronic-phase chronic myeloid leukemia (CML-CP) treated with the tyrosine kinase inhibitor (TKI) imatinib. However, deep molecular responses (MRs), as measured by reductions in
BCR-ABL
transcript levels below the threshold of major MR, were achieved only by a small proportion of patients. With the advent of the second-generation TKIs nilotinib and dasatinib for the treatment of patients with newly diagnosed CML-CP, the proportion of patients who achieve the deepest levels of MR is likely to increase significantly. With these changes, the potential for patient eligibility in TKI cessations studies is becoming a more widely discussed topic and area for research. These developments highlight the need for robust, standardized and workable definitions of deep MRs. Specifically, it is critical that the measurement of MR is standardized in a manner to withstand both intra- and inter-laboratory variability, as well as new methodological developments. This review summarizes the relevant clinical background and proposes a framework within which standardization of MR can be taken forward.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Biological and medical sciences
/ Biological response modifiers
/ Biomarkers, Tumor - genetics
/ Hematologic and hematopoietic diseases
/ Humans
/ Imatinib
/ Kinases
/ Leukemia
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy
/ Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics
/ Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
/ Medicine
/ Oncology
/ Patients
/ Protein Kinase Inhibitors - therapeutic use
/ Protein-Tyrosine Kinases - antagonists & inhibitors
/ review
/ Tyrosine
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