The New England Journal of Medicine, ISSN 0028-4793, 11/2016, Volume 375, Issue 21, pp. 2023 - 2036
Decitabine produced responses in patients with acute myeloid leukemia or myelodysplastic syndromes who had cytogenetic abnormalities associated with a poor...
HYPOMETHYLATING AGENTS | MEDICINE, GENERAL & INTERNAL | THERAPY | RESPONSE CRITERIA | DNA METHYLATION | OLDER PATIENTS | TET2 MUTATIONS | CLONAL HEMATOPOIESIS | IN-VIVO | COMPLEX KARYOTYPE | INTERNATIONAL WORKING GROUP | Azacitidine - adverse effects | Prospective Studies | Humans | Middle Aged | Male | Tumor Suppressor Protein p53 - genetics | Antimetabolites, Antineoplastic - administration & dosage | Exome | Bone Marrow - chemistry | Aged, 80 and over | Leukemia, Myeloid, Acute - drug therapy | Adult | Female | Myelodysplastic Syndromes - drug therapy | Azacitidine - administration & dosage | 5-Methylcytosine - analysis | Biomarkers, Tumor - analysis | Risk Factors | Azacitidine - analogs & derivatives | Survival Rate | Leukemia, Myeloid, Acute - mortality | Bone Marrow - pathology | Antimetabolites, Antineoplastic - adverse effects | Myelodysplastic Syndromes - mortality | Aged | Myelodysplastic Syndromes - genetics | Mutation | Leukemia, Myeloid, Acute - genetics | Care and treatment | Research | Tumor proteins | Myelodysplastic syndromes | Myeloid leukemia | p53 Protein | Leukemia | Survival | Myelodysplastic syndrome | Risk factors | Clinical outcomes | Chemotherapy | Bone marrow | Biomarkers | Blood diseases | Acute myeloid leukemia | 5-aza-2'-deoxycytidine
HYPOMETHYLATING AGENTS | MEDICINE, GENERAL & INTERNAL | THERAPY | RESPONSE CRITERIA | DNA METHYLATION | OLDER PATIENTS | TET2 MUTATIONS | CLONAL HEMATOPOIESIS | IN-VIVO | COMPLEX KARYOTYPE | INTERNATIONAL WORKING GROUP | Azacitidine - adverse effects | Prospective Studies | Humans | Middle Aged | Male | Tumor Suppressor Protein p53 - genetics | Antimetabolites, Antineoplastic - administration & dosage | Exome | Bone Marrow - chemistry | Aged, 80 and over | Leukemia, Myeloid, Acute - drug therapy | Adult | Female | Myelodysplastic Syndromes - drug therapy | Azacitidine - administration & dosage | 5-Methylcytosine - analysis | Biomarkers, Tumor - analysis | Risk Factors | Azacitidine - analogs & derivatives | Survival Rate | Leukemia, Myeloid, Acute - mortality | Bone Marrow - pathology | Antimetabolites, Antineoplastic - adverse effects | Myelodysplastic Syndromes - mortality | Aged | Myelodysplastic Syndromes - genetics | Mutation | Leukemia, Myeloid, Acute - genetics | Care and treatment | Research | Tumor proteins | Myelodysplastic syndromes | Myeloid leukemia | p53 Protein | Leukemia | Survival | Myelodysplastic syndrome | Risk factors | Clinical outcomes | Chemotherapy | Bone marrow | Biomarkers | Blood diseases | Acute myeloid leukemia | 5-aza-2'-deoxycytidine
Journal Article
Leukemia, ISSN 0887-6924, 02/2013, Volume 27, Issue 2, pp. 430 - 440
Proteasome inhibitors (Pis), namely bortezomib, have become a cornerstone therapy for multiple myeloma (MM), potently reducing tumor burden and inhibiting...
MULTIPLE-MYELOMA | CELLS | multiple myeloma | ACTIVATION | OSTEOBLAST DIFFERENTIATION | TGF-BETA | proteasome inhibitors | osteoblast | BORTEZOMIB | MURINE MODEL | UNFOLDED PROTEIN RESPONSE | ONCOLOGY | bone lesions | IN-VIVO | osteoclast | HEMATOLOGY | IRREVERSIBLE INHIBITOR | Stromal Cells - pathology | Humans | Pyrazines - administration & dosage | Multiple Myeloma - drug therapy | Epoxy Compounds - pharmacology | Bone Marrow - metabolism | Stromal Cells - drug effects | Boronic Acids - administration & dosage | Tumor Cells, Cultured | Real-Time Polymerase Chain Reaction | Bone Marrow - drug effects | Tumor Microenvironment - drug effects | Bone Resorption - etiology | Osteoclasts - pathology | Bortezomib | Calcification, Physiologic - drug effects | Administration, Oral | Multiple Myeloma - complications | Mice, Inbred C57BL | Osteoblasts - drug effects | Osteogenesis - drug effects | RNA, Messenger - genetics | Stromal Cells - metabolism | Bone Resorption - drug therapy | Mice, SCID | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Proteasome Inhibitors - therapeutic use | Osteoblasts - pathology | Animals | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Cell Differentiation - drug effects | Bone Marrow - pathology | Mice, Inbred NOD | Cell Proliferation - drug effects | Mice | Oligopeptides - administration & dosage | Osteoclasts - drug effects | Usage | Enzyme inhibitors | Multiple myeloma | Carfilzomib | Drug therapy | Health aspects
MULTIPLE-MYELOMA | CELLS | multiple myeloma | ACTIVATION | OSTEOBLAST DIFFERENTIATION | TGF-BETA | proteasome inhibitors | osteoblast | BORTEZOMIB | MURINE MODEL | UNFOLDED PROTEIN RESPONSE | ONCOLOGY | bone lesions | IN-VIVO | osteoclast | HEMATOLOGY | IRREVERSIBLE INHIBITOR | Stromal Cells - pathology | Humans | Pyrazines - administration & dosage | Multiple Myeloma - drug therapy | Epoxy Compounds - pharmacology | Bone Marrow - metabolism | Stromal Cells - drug effects | Boronic Acids - administration & dosage | Tumor Cells, Cultured | Real-Time Polymerase Chain Reaction | Bone Marrow - drug effects | Tumor Microenvironment - drug effects | Bone Resorption - etiology | Osteoclasts - pathology | Bortezomib | Calcification, Physiologic - drug effects | Administration, Oral | Multiple Myeloma - complications | Mice, Inbred C57BL | Osteoblasts - drug effects | Osteogenesis - drug effects | RNA, Messenger - genetics | Stromal Cells - metabolism | Bone Resorption - drug therapy | Mice, SCID | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Proteasome Inhibitors - therapeutic use | Osteoblasts - pathology | Animals | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Cell Differentiation - drug effects | Bone Marrow - pathology | Mice, Inbred NOD | Cell Proliferation - drug effects | Mice | Oligopeptides - administration & dosage | Osteoclasts - drug effects | Usage | Enzyme inhibitors | Multiple myeloma | Carfilzomib | Drug therapy | Health aspects
Journal Article
Leukemia, ISSN 0887-6924, 07/2017, Volume 31, Issue 7, pp. 1648 - 1650
Journal Article
Bone Marrow Transplantation, ISSN 0268-3369, 2014, Volume 49, Issue 8, pp. 1009 - 1015
Despite tremendous advances in treatments for myeloma in the past decade, the disease remains incurable in the majority of patients. Here, we review recent...
WEIGHT-LOSS | IMMUNOLOGY | TRANSPLANTATION | BREAST-CANCER | ONCOLOGY | BODY-MASS INDEX | NON-HODGKIN-LYMPHOMA | PHYSICAL-ACTIVITY | ANTHROPOMETRIC CHARACTERISTICS | MONOCLONAL GAMMOPATHY | SMOLDERING MULTIPLE-MYELOMA | HEMATOLOGY | GROWTH-FACTOR-I | UNDETERMINED SIGNIFICANCE MGUS | Multiple Myeloma - epidemiology | Precancerous Conditions - etiology | Multiple Myeloma - etiology | Precancerous Conditions - epidemiology | Obesity - complications | Humans | Obesity - epidemiology | Risk Factors | Precancerous Conditions - metabolism | Multiple Myeloma - metabolism | Obesity - metabolism | Obesity | Complications and side effects | Evaluation | Multiple myeloma | Medicine, Preventive | Risk factors | Preventive health services
WEIGHT-LOSS | IMMUNOLOGY | TRANSPLANTATION | BREAST-CANCER | ONCOLOGY | BODY-MASS INDEX | NON-HODGKIN-LYMPHOMA | PHYSICAL-ACTIVITY | ANTHROPOMETRIC CHARACTERISTICS | MONOCLONAL GAMMOPATHY | SMOLDERING MULTIPLE-MYELOMA | HEMATOLOGY | GROWTH-FACTOR-I | UNDETERMINED SIGNIFICANCE MGUS | Multiple Myeloma - epidemiology | Precancerous Conditions - etiology | Multiple Myeloma - etiology | Precancerous Conditions - epidemiology | Obesity - complications | Humans | Obesity - epidemiology | Risk Factors | Precancerous Conditions - metabolism | Multiple Myeloma - metabolism | Obesity - metabolism | Obesity | Complications and side effects | Evaluation | Multiple myeloma | Medicine, Preventive | Risk factors | Preventive health services
Journal Article
ACS Symposium Series, ISSN 0097-6156, 2017, Volume 1271, pp. 189 - 209
Conference Proceeding
Bone Marrow Transplantation, ISSN 0268-3369, 05/2009, Volume 43, Issue 10, pp. 793 - 800
The appropriate induction therapy before and the role of maintenance therapy after auto-SCT for patients with multiple myeloma remain areas of active...
stem cell mobilization | multiple myeloma | LENALIDOMIDE PLUS DEXAMETHASONE | auto-SCT | IMPROVES SURVIVAL | THALIDOMIDE | IMMUNOLOGY | COMBINATION | VERSUS-HOST-DISEASE | CHEMOTHERAPY | RANDOMIZED TRIAL | TRANSPLANTATION | INTERFERON | ONCOLOGY | PROTEASOME INHIBITOR BORTEZOMIB | bortezomib | STEM-CELL TRANSPLANTATION | HEMATOLOGY | Peripheral Blood Stem Cell Transplantation - methods | Humans | Middle Aged | Pyrazines - administration & dosage | Boronic Acids - adverse effects | Male | Transplantation, Autologous | T-Lymphocytes, Cytotoxic - drug effects | Herpesvirus 3, Human - drug effects | Multiple Myeloma - drug therapy | Multiple Myeloma - therapy | Adult | Female | Boronic Acids - administration & dosage | Hematopoietic Stem Cell Mobilization | Bortezomib | Treatment Outcome | Remission Induction | Melphalan - administration & dosage | Virus Activation - drug effects | Lymphocyte Subsets | Pyrazines - adverse effects | Survival Analysis | Aged | Killer Cells, Natural - drug effects | Granulocyte Colony-Stimulating Factor - administration & dosage | Care and treatment | Patient outcomes | Multiple myeloma | Stem cells | Dosage and administration | Transplantation | Health aspects | Index Medicus
stem cell mobilization | multiple myeloma | LENALIDOMIDE PLUS DEXAMETHASONE | auto-SCT | IMPROVES SURVIVAL | THALIDOMIDE | IMMUNOLOGY | COMBINATION | VERSUS-HOST-DISEASE | CHEMOTHERAPY | RANDOMIZED TRIAL | TRANSPLANTATION | INTERFERON | ONCOLOGY | PROTEASOME INHIBITOR BORTEZOMIB | bortezomib | STEM-CELL TRANSPLANTATION | HEMATOLOGY | Peripheral Blood Stem Cell Transplantation - methods | Humans | Middle Aged | Pyrazines - administration & dosage | Boronic Acids - adverse effects | Male | Transplantation, Autologous | T-Lymphocytes, Cytotoxic - drug effects | Herpesvirus 3, Human - drug effects | Multiple Myeloma - drug therapy | Multiple Myeloma - therapy | Adult | Female | Boronic Acids - administration & dosage | Hematopoietic Stem Cell Mobilization | Bortezomib | Treatment Outcome | Remission Induction | Melphalan - administration & dosage | Virus Activation - drug effects | Lymphocyte Subsets | Pyrazines - adverse effects | Survival Analysis | Aged | Killer Cells, Natural - drug effects | Granulocyte Colony-Stimulating Factor - administration & dosage | Care and treatment | Patient outcomes | Multiple myeloma | Stem cells | Dosage and administration | Transplantation | Health aspects | Index Medicus
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2006, Volume 12, Issue 2, pp. 116 - 117
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2006, Volume 12, Issue 2, pp. 116 - 116
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2005, Volume 11, Issue 2, pp. 77 - 77
Journal Article
CANCER RESEARCH, ISSN 0008-5472, 06/2016, Volume 76, Issue 12, pp. 3484 - 3495
Integrin beta 3 is critical for tumor invasion, neoangiogenesis, and inflammation, making it a promising cancer target. However, preclinical and clinical data...
BETA-3-INTEGRIN | ANGIOGENESIS | ONCOLOGY | RANDOMIZED PHASE-II | NEWLY-DIAGNOSED GLIOBLASTOMA | MACROPHAGES | ALPHA-V-BETA-3 INTEGRIN | INHIBITOR CILENGITIDE | BONE | TUMOR-GROWTH | T-CELLS
BETA-3-INTEGRIN | ANGIOGENESIS | ONCOLOGY | RANDOMIZED PHASE-II | NEWLY-DIAGNOSED GLIOBLASTOMA | MACROPHAGES | ALPHA-V-BETA-3 INTEGRIN | INHIBITOR CILENGITIDE | BONE | TUMOR-GROWTH | T-CELLS
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 03/2019, Volume 25, Issue 3, pp. S399 - S400
Many studies showed that novel agent based regimens result in superior response rates and depth. Recommended practice prior to ASCT in TE, NDMM is novel...
Anthracyclines | Dexamethasone | Multiple myeloma | Etoposide | Transplantation | Cisplatin | Cyclophosphamide | Chemotherapy | Analysis | Central nervous system depressants | Stem cells | Steroids | Cancer
Anthracyclines | Dexamethasone | Multiple myeloma | Etoposide | Transplantation | Cisplatin | Cyclophosphamide | Chemotherapy | Analysis | Central nervous system depressants | Stem cells | Steroids | Cancer
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 06/2010, Volume 120, Issue 6, pp. 2109 - 2118
Antiapoptotic BCL2 family members have been implicated in the pathogenesis of acute myelogenous leukemia (AML), but the functional significance and relative...
SURVIVAL | MEDICINE, RESEARCH & EXPERIMENTAL | STEM-CELLS | INDUCED APOPTOSIS | IN-VIVO | C-MYC | RESISTANCE | CHRONIC LYMPHOCYTIC-LEUKEMIA | BCL-2 PROTEINS | BH3 MIMETIC ABT-737 | EXPRESSION | Proteins - genetics | Proto-Oncogene Proteins c-bcl-2 - metabolism | Animals | Proteins - metabolism | Humans | Mice, Inbred C57BL | Myeloid Cell Leukemia Sequence 1 Protein | Mice | Mice, Inbred BALB C | Genes, bcl-2 | Proto-Oncogene Proteins c-bcl-2 - genetics | Leukemia, Myeloid, Acute - genetics | Haplotypes | Prevention | Myelocytic leukemia | Physiological aspects | Nonlymphoid leukemia | Gene expression | Identification and classification | Risk factors
SURVIVAL | MEDICINE, RESEARCH & EXPERIMENTAL | STEM-CELLS | INDUCED APOPTOSIS | IN-VIVO | C-MYC | RESISTANCE | CHRONIC LYMPHOCYTIC-LEUKEMIA | BCL-2 PROTEINS | BH3 MIMETIC ABT-737 | EXPRESSION | Proteins - genetics | Proto-Oncogene Proteins c-bcl-2 - metabolism | Animals | Proteins - metabolism | Humans | Mice, Inbred C57BL | Myeloid Cell Leukemia Sequence 1 Protein | Mice | Mice, Inbred BALB C | Genes, bcl-2 | Proto-Oncogene Proteins c-bcl-2 - genetics | Leukemia, Myeloid, Acute - genetics | Haplotypes | Prevention | Myelocytic leukemia | Physiological aspects | Nonlymphoid leukemia | Gene expression | Identification and classification | Risk factors
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 08/2012, Volume 122, Issue 8, pp. 2793 - 2806
The histone methyltransferase WHSC1 (also known as MMSET) is overexpressed in multiple myeloma (MM) as a result of the t(4;14) chromosomal translocation and in...
MEDICINE, RESEARCH & EXPERIMENTAL | LYSINE 36 | SYNDROME CANDIDATE 1 | WOLF-HIRSCHHORN SYNDROME | DNA-DAMAGE | GROWTH-FACTOR RECEPTOR-3 | T(4/14) TRANSLOCATION | GENE-EXPRESSION | NUCLEAR EXPORT | HISTONE METHYLTRANSFERASE | STATISTICAL-MODEL | Translocation, Genetic | Cell Proliferation | Oxidative Stress | Humans | DNA, Complementary - genetics | Molecular Sequence Data | Gene Expression Profiling | Chromosomes, Human, Pair 4 - genetics | RNA, Neoplasm - metabolism | Ribosomal Proteins - metabolism | RNA, Small Nucleolar - metabolism | Base Sequence | Nucleic Acid Conformation | Repressor Proteins - metabolism | RNA, Neoplasm - chemistry | Introns | Ribosomal Proteins - genetics | Multiple Myeloma - metabolism | RNA, Small Nucleolar - genetics | RNA, Small Nucleolar - chemistry | Multiple Myeloma - pathology | Animals | Histone-Lysine N-Methyltransferase - metabolism | Cell Transformation, Neoplastic | RNA, Neoplasm - genetics | Mice | DNA, Neoplasm - genetics | Chromosomes, Human, Pair 14 - genetics | Multiple Myeloma - genetics | Proteins | Genetic aspects | RNA | Multiple myeloma | Cancer
MEDICINE, RESEARCH & EXPERIMENTAL | LYSINE 36 | SYNDROME CANDIDATE 1 | WOLF-HIRSCHHORN SYNDROME | DNA-DAMAGE | GROWTH-FACTOR RECEPTOR-3 | T(4/14) TRANSLOCATION | GENE-EXPRESSION | NUCLEAR EXPORT | HISTONE METHYLTRANSFERASE | STATISTICAL-MODEL | Translocation, Genetic | Cell Proliferation | Oxidative Stress | Humans | DNA, Complementary - genetics | Molecular Sequence Data | Gene Expression Profiling | Chromosomes, Human, Pair 4 - genetics | RNA, Neoplasm - metabolism | Ribosomal Proteins - metabolism | RNA, Small Nucleolar - metabolism | Base Sequence | Nucleic Acid Conformation | Repressor Proteins - metabolism | RNA, Neoplasm - chemistry | Introns | Ribosomal Proteins - genetics | Multiple Myeloma - metabolism | RNA, Small Nucleolar - genetics | RNA, Small Nucleolar - chemistry | Multiple Myeloma - pathology | Animals | Histone-Lysine N-Methyltransferase - metabolism | Cell Transformation, Neoplastic | RNA, Neoplasm - genetics | Mice | DNA, Neoplasm - genetics | Chromosomes, Human, Pair 14 - genetics | Multiple Myeloma - genetics | Proteins | Genetic aspects | RNA | Multiple myeloma | Cancer
Journal Article
Molecular Cancer Therapeutics, ISSN 1535-7163, 06/2015, Volume 14, Issue 6, pp. 1286 - 1294
Multiple myeloma pathogenesis is driven by the MYC oncoprotein, its dimerization with MAX, and the binding of this heterodimer to E-Boxes in the vicinity of...
VITRO | CELLS | THERAPY | ONCOLOGY | DRUG-DELIVERY | IN-VIVO | GENE-EXPRESSION | C-MYC/MAX DIMERIZATION | FUMAGILLIN PRODRUG | DIFFERENTIATION | CANCER | Small Molecule Libraries - pharmacology | Integrin alpha4beta1 - metabolism | Nanoparticles - chemistry | Apoptosis - drug effects | Humans | Small Molecule Libraries - metabolism | Integrin alphaVbeta3 - metabolism | Dose-Response Relationship, Drug | Multiple Myeloma - drug therapy | Disease Models, Animal | Integrin alphaVbeta3 - antagonists & inhibitors | Cell Survival - drug effects | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - chemistry | Proto-Oncogene Proteins c-myc - metabolism | Blotting, Western | Small Molecule Libraries - chemistry | Multiple Myeloma - pathology | Animals | Tumor Burden - drug effects | Integrin alpha4beta1 - antagonists & inhibitors | Proto-Oncogene Proteins c-myc - antagonists & inhibitors | Survival Analysis | Cell Line, Tumor | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Mice | Proto-Oncogene Proteins c-myc - chemistry | Prodrugs - pharmacology | Protein Multimerization - drug effects
VITRO | CELLS | THERAPY | ONCOLOGY | DRUG-DELIVERY | IN-VIVO | GENE-EXPRESSION | C-MYC/MAX DIMERIZATION | FUMAGILLIN PRODRUG | DIFFERENTIATION | CANCER | Small Molecule Libraries - pharmacology | Integrin alpha4beta1 - metabolism | Nanoparticles - chemistry | Apoptosis - drug effects | Humans | Small Molecule Libraries - metabolism | Integrin alphaVbeta3 - metabolism | Dose-Response Relationship, Drug | Multiple Myeloma - drug therapy | Disease Models, Animal | Integrin alphaVbeta3 - antagonists & inhibitors | Cell Survival - drug effects | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - chemistry | Proto-Oncogene Proteins c-myc - metabolism | Blotting, Western | Small Molecule Libraries - chemistry | Multiple Myeloma - pathology | Animals | Tumor Burden - drug effects | Integrin alpha4beta1 - antagonists & inhibitors | Proto-Oncogene Proteins c-myc - antagonists & inhibitors | Survival Analysis | Cell Line, Tumor | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Mice | Proto-Oncogene Proteins c-myc - chemistry | Prodrugs - pharmacology | Protein Multimerization - drug effects
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2012, Volume 44, Issue 1, pp. 53 - 57
Myelodysplastic syndromes (MDS) are hematopoietic stem cell disorders that often progress to chemotherapy-resistant secondary acute myeloid leukemia (sAML). We...
MESSENGER-RNA | RECOGNITION | METHYLTRANSFERASE GENE EZH2 | SMALL-SUBUNIT | GENETICS & HEREDITY | ACUTE MYELOID-LEUKEMIA | DNMT3A MUTATIONS | IDENTIFICATION | AU-RICH ELEMENT | CANCER | GENOME | Humans | Middle Aged | Molecular Sequence Data | Male | Mutation, Missense | Disease Progression | Splicing Factor U2AF | RNA Splicing | Base Sequence | Aged, 80 and over | Adult | Female | Ribonucleoproteins - genetics | Aged | Myelodysplastic Syndromes - genetics | Nuclear Proteins - genetics | Chemotherapy | Pathogenesis | Genetics | Genomes | Mutation | Genetic testing | Gene expression | Cancer
MESSENGER-RNA | RECOGNITION | METHYLTRANSFERASE GENE EZH2 | SMALL-SUBUNIT | GENETICS & HEREDITY | ACUTE MYELOID-LEUKEMIA | DNMT3A MUTATIONS | IDENTIFICATION | AU-RICH ELEMENT | CANCER | GENOME | Humans | Middle Aged | Molecular Sequence Data | Male | Mutation, Missense | Disease Progression | Splicing Factor U2AF | RNA Splicing | Base Sequence | Aged, 80 and over | Adult | Female | Ribonucleoproteins - genetics | Aged | Myelodysplastic Syndromes - genetics | Nuclear Proteins - genetics | Chemotherapy | Pathogenesis | Genetics | Genomes | Mutation | Genetic testing | Gene expression | Cancer
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 03/2008, Volume 118, Issue 3, pp. 946 - 955
A fundamental property of leukemic stem cells is clonal dominance of the bone marrow microenvironment. Truncation mutations of CSF3R, which encodes the G-CSF...
COLONY-STIMULATING-FACTOR | FACTOR-RECEPTOR | MEDICINE, RESEARCH & EXPERIMENTAL | BLAST-CRISIS | HEMATOPOIETIC STEM-CELLS | SEVERE CONGENITAL NEUTROPENIA | BONE-MARROW | GENE-EXPRESSION | SELF-RENEWAL | GRANULOCYTIC DIFFERENTIATION | ACUTE MYELOID-LEUKEMIA | Granulocyte Colony-Stimulating Factor - pharmacology | Animals | STAT3 Transcription Factor - physiology | Mice, Inbred C57BL | STAT5 Transcription Factor - physiology | Hematopoietic Stem Cells - physiology | Cell Proliferation - drug effects | Mice | Receptors, Granulocyte Colony-Stimulating Factor - genetics | Mutation | Neutropenia - congenital | Complications and side effects | Gene mutations | Stem cells | Genetic aspects | Research | Gene expression | Health aspects
COLONY-STIMULATING-FACTOR | FACTOR-RECEPTOR | MEDICINE, RESEARCH & EXPERIMENTAL | BLAST-CRISIS | HEMATOPOIETIC STEM-CELLS | SEVERE CONGENITAL NEUTROPENIA | BONE-MARROW | GENE-EXPRESSION | SELF-RENEWAL | GRANULOCYTIC DIFFERENTIATION | ACUTE MYELOID-LEUKEMIA | Granulocyte Colony-Stimulating Factor - pharmacology | Animals | STAT3 Transcription Factor - physiology | Mice, Inbred C57BL | STAT5 Transcription Factor - physiology | Hematopoietic Stem Cells - physiology | Cell Proliferation - drug effects | Mice | Receptors, Granulocyte Colony-Stimulating Factor - genetics | Mutation | Neutropenia - congenital | Complications and side effects | Gene mutations | Stem cells | Genetic aspects | Research | Gene expression | Health aspects
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2012, Volume 44, Issue 1, p. 53
Journal Article
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