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1. Full Text Consistent in-frame internal tandem duplications of BCOR characterize clear cell sarcoma of the kidney
by Ueno-Yokohata, Hitomi and Okita, Hajime and Nakasato, Keiko and Akimoto, Shingo and Hata, Jun-Ichi and Koshinaga, Tsugumichi and Fukuzawa, Masahiro and Kiyokawa, Nobutaka
Nature Genetics, ISSN 1061-4036, 08/2015, Volume 47, Issue 8, pp. 861 - 863
Clear cell sarcoma of the kidney (CCSK) is one of the major pediatric renal neoplasms, but its associated genetic abnormalities are largely unknown. We... 
SUBTYPE | COMPLEX | THERAPY | GENETICS & HEREDITY | TUMOR STUDY-GROUP | WILMS-TUMOR | SOMATIC MUTATIONS | DURATION | SOCIETY | POLYCOMB GROUP | REVEALS | Immunohistochemistry | Proto-Oncogene Proteins - metabolism | Amino Acid Sequence | Kidney Neoplasms - genetics | Humans | Gene Expression Regulation, Neoplastic | Molecular Sequence Data | Repressor Proteins - genetics | Proto-Oncogene Proteins - genetics | Kidney Neoplasms - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Sequence Analysis, DNA | Sequence Homology, Nucleic Acid | Blotting, Western | Sequence Homology, Amino Acid | Base Sequence | HEK293 Cells | Female | Sarcoma, Clear Cell - metabolism | Sarcoma, Clear Cell - genetics | Child | Tandem Repeat Sequences - genetics | Repressor Proteins - metabolism | Sarcoma | Kidney cancer | Development and progression | Genetic aspects | Microsatellites (Genetics) | Disease susceptibility | Identification and classification | Health aspects | Genetics | Tumorigenesis | Kidneys | Genes | Tumors
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2. Analysis of gene expression and DNA methylation patterns in childhood acute lymphoblastic leukemia
by Iijima, Kazutoshi and Kiyokawa, Nobutaka
[Rinshō ketsueki] The Japanese journal of clinical hematology, ISSN 0485-1439, 04/2016, Volume 57, Issue 4, pp. 425 - 429
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3. Analysis of gene expression and DNA methylation patterns in childhood acute lymphoblastic leukemia
by Iijima, Kazutoshi and Kiyokawa, Nobutaka
[Rinsho ketsueki] The Japanese journal of clinical hematology, ISSN 0485-1439, 04/2016, Volume 57, Issue 4, p. 425
The 5-year survival rate of patients with childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL) now exceeds 90%, though there are still patients... 
Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Precursor Cell Lymphoblastic Leukemia-Lymphoma - metabolism | DNA Methylation | Prognosis | Humans | Gene Expression Regulation, Neoplastic | Antineoplastic Agents - therapeutic use | Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology | Child
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4. Full Text Negative CD19 expression is associated with inferior relapse‐free survival in children with RUNX1‐RUNX1T1–positive acute myeloid leukaemia: results from the Japanese Paediatric Leukaemia/Lymphoma Study Group AML‐05 study
by Sakamoto, Kenichi and Shiba, Norio and Deguchi, Takao and Kiyokawa, Nobutaka and Hashii, Yoshiko and Moriya‐Saito, Akiko and Tomizawa, Daisuke and Taga, Takashi and Adachi, Soichi and Horibe, Keizo and Imamura, Toshihiko
British Journal of Haematology, ISSN 0007-1048, 11/2019, Volume 187, Issue 3, pp. 372 - 376
Summary We performed a retrospective analysis of leukaemic surface antigen expression and genomic data from a total of 100 RUNX1‐RUNX1T1–positive paediatric... 
acute myeloid leukaemia | RUNX1‐RUNX1T1 | CD19 | Genetic research | Pediatrics | Gene mutations | Analysis | Confidence intervals | Antigens | CD19 antigen | Leukemia | Runx1 protein | Lymphomas | Mutation | Gene expression | Multivariate analysis | Risk analysis | Lymphoma | Risk factors
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5. Full Text Genotyping NUDT15 can predict the dose reduction of 6-MP for children with acute lymphoblastic leukemia especially at a preschool age
by Suzuki, Hisato and Fukushima, Hiroko and Suzuki, Ryoko and Hosaka, Sho and Yamaki, Yuni and Kobayashi, Chie and Sakai, Aiko and Imagawa, Kazuo and Iwabuchi, Atsushi and Yoshimi, Ai and Nakao, Tomohei and Kato, Keisuke and Tsuchida, Masahiro and Kiyokawa, Nobutaka and Koike, Kazutoshi and Noguchi, Emiko and Fukushima, Takashi and Sumazaki, Ryo
Journal of Human Genetics, ISSN 1434-5161, 09/2016, Volume 61, Issue 9, pp. 797 - 801
The pharmacokinetics among children has been altered dynamically. The difference between children and adults is caused by immaturity in things such as... 
RATES | METHYLTRANSFERASE | SUSCEPTIBILITY | GENETICS & HEREDITY | RISK | POLYMORPHISM | CANCER-STUDY-GROUP | JAPANESE CHILDREN | VARIANT | PREDNISOLONE | Pharmacogenetics | Age Factors | Genetic Association Studies | Gene Frequency | Humans | Mercaptopurine - administration & dosage | Methyltransferases - genetics | Pyrophosphatases - genetics | Child, Preschool | Genotype | Infant | Male | Antimetabolites, Antineoplastic - administration & dosage | Polymorphism, Genetic | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Alleles | Female | Child
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6. Full Text Appropriate dose reduction in induction therapy is essential for the treatment of infants with acute myeloid leukemia: a report from the Japanese Pediatric Leukemia/Lymphoma Study Group
by Tomizawa, Daisuke and Tawa, Akio and Watanabe, Tomoyuki and Saito, Akiko Moriya and Kudo, Kazuko and Taga, Takashi and Iwamoto, Shotaro and Shimada, Akira and Terui, Kiminori and Moritake, Hiroshi and Kinoshita, Akitoshi and Takahashi, Hiroyuki and Nakayama, Hideki and Kiyokawa, Nobutaka and Isoyama, Keiichi and Mizutani, Shuki and Hara, Junichi and Horibe, Keizo and Nakahata, Tatsutoshi and Adachi, Souichi
International Journal of Hematology, ISSN 0925-5710, 11/2013, Volume 98, Issue 5, pp. 578 - 588
Infants (<1 year old) with acute myeloid leukemia (AML) are particularly vulnerable to intensive cytotoxic therapy. Indeed, the mortality rate was high among... 
Acute respiratory distress syndrome | Medicine & Public Health | Hematology | Oncology | Early death | Infants | Acute myeloid leukemia | AML | TRIALS | CYTARABINE | HEMATOLOGY | CHILDREN | Antineoplastic Combined Chemotherapy Protocols - administration & dosage | Humans | Japan | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Child, Preschool | Induction Chemotherapy | Infant | Male | Treatment Outcome | Leukemia, Myeloid, Acute - mortality | Leukemia, Myeloid, Acute - diagnosis | Chromosome Aberrations | Leukemia, Myeloid, Acute - drug therapy | Female | Registries | Child | Infant, Newborn | Pediatrics | Reports | Research | Oncology, Experimental | Cancer
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7. Full Text EP300-ZNF384 fusion gene product up-regulates GATA3 gene expression and induces hematopoietic stem cell gene expression signature in B-cell precursor acute lymphoblastic leukemia cells
by Yaguchi, Akinori and Ishibashi, Takeshi and Terada, Kazuki and Ueno-Yokohata, Hitomi and Saito, Yuya and Fujimura, Junya and Shimizu, Toshiaki and Ohki, Kentaro and Manabe, Atsushi and Kiyokawa, Nobutaka
International Journal of Hematology, ISSN 0925-5710, 8/2017, Volume 106, Issue 2, pp. 269 - 281
ZNF384-related fusion genes are associated with a distinct subgroup of B-cell precursor acute lymphoblastic leukemias in childhood, with a frequency of... 
ZNF384 | Medicine & Public Health | Hematology | Transcription | Oncology | EP300 | GATA3 | CD33 | YOUNG-ADULTS | KINASE | LINEAGE SWITCH | RISK | TRANSCRIPTION FACTOR GATA-3 | REARRANGEMENT | PHENOTYPE ACUTE-LEUKEMIA | ADOLESCENTS | CIZ/NMP4 | HEMATOLOGY | SUBGROUP | GATA3 Transcription Factor - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - immunology | Gene Fusion - physiology | Gene Expression - genetics | Humans | E1A-Associated p300 Protein - genetics | E1A-Associated p300 Protein - physiology | Gene Expression Regulation, Developmental - genetics | Up-Regulation - genetics | Trans-Activators - physiology | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Gene Fusion - genetics | Leukemia, B-Cell - genetics | Trans-Activators - genetics | Cell Line, Tumor | Leukemia, B-Cell - immunology | Child | Hematopoietic Stem Cells | Medical colleges | Anopheles | DNA microarrays | Genes | Genetic research | Genetic aspects | Children | Acute lymphocytic leukemia | Genetic transcription | Health aspects | Hematopoietic stem cells | Cancer | Antigens | Acute lymphatic leukemia | Pathogenesis | Leukemia | CD13 antigen | Lymphatic leukemia | Gene expression | Kinases | Hemopoiesis | Biological effects | Lymphocytes B | Stem cells | GATA-3 protein | Aberration | Fusion protein
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8. Full Text Effect of protein adsorption layers and solution treatments on hydroxyapatite deposition on polystyrene plate surfaces in simulated body fluids
by Iijima, Kazutoshi and Iizuka, Ayako and Suzuki, Ryo and Ueno-Yokohata, Hitomi and Kiyokawa, Nobutaka and Hashizume, Mineo
Journal of Materials Science: Materials in Medicine, ISSN 0957-4530, 12/2017, Volume 28, Issue 12, pp. 1 - 10
We have developed a method to functionalize polystyrene (PS) cell culture plates with hydroxyapatite (HAp) via protein adsorption layers such as human serum... 
Biomedical Engineering | Polymer Sciences | Materials Science | Regenerative Medicine/Tissue Engineering | Ceramics, Glass, Composites, Natural Materials | Surfaces and Interfaces, Thin Films | Biomaterials | CARBOXYL GROUP | FUNCTIONALIZATION | ALTERNATE SOAKING PROCESS | CELLS | MATERIALS SCIENCE, BIOMATERIALS | APATITE-FORMING ABILITY | ENGINEERING, BIOMEDICAL | WOLLASTONITE | POLYMER SURFACES | BIOMIMETIC PROCESS | BONE | POLYAMIDE FILMS | Child development | Adsorption | Collagen | Stem cells | Albumin | Polystyrene | Glutamate | Lysozyme | Phosphates | Glutamic acid | Cell culture | Surgical implants | Collagen (type I) | Calcium | Mesenchyme | Surface chemistry | Tissue culture | Hydroxyapatite | Proteins | Biomedical materials | Biocompatibility | Deposition | Plates | Human serum albumin | Polystyrene resins | Albumen | Incubation | Serum albumin | Protein adsorption | Calcium phosphates | Body fluids | Bone | Coating | In vitro methods and tests | Calcium ions
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9. Full Text Risk-stratified therapy for children with FLT3-ITD-positive acute myeloid leukemia: results from the JPLSG AML-05 study
by Shimada, Akira and Iijima-Yamashita, Yuka and Tawa, Akio and Tomizawa, Daisuke and Yamada, Miho and Norio, Shiba and Watanabe, Tomoyuki and Taga, Takashi and Iwamoto, Shotaro and Terui, Kiminori and Moritake, Hiroshi and Kinoshita, Akitoshi and Takahashi, Hiroyuki and Nakayama, Hideki and Koh, Katsuyoshi and Goto, Hiroaki and Kosaka, Yoshiyuki and Saito, Akiko Moriya and Kiyokawa, Nobutaka and Horibe, Keizo and Hara, Yusuke and Oki, Kentaro and Hayashi, Yasuhide and Tanaka, Shiro and Adachi, Souichi
International Journal of Hematology, ISSN 0925-5710, 05/2018, Volume 107, Issue 5, pp. 586 - 595
Acute myeloid leukemia harboring internal tandem duplication of FMS-like tyrosine kinase 3 (AML (FLT3-ITD)) is associated with poor prognosis. We evaluated the... 
AML | Alleric ratio | FLT3-ITD | Childhood | NUP98-NSD1 | INTERNAL TANDEM DUPLICATION | FLT3 INHIBITORS | CELL TRANSPLANTATION | RELAPSE | IMPACT | POOR-PROGNOSIS | PROGNOSTIC-SIGNIFICANCE | MUTATIONS | HEMATOLOGY | EXPRESSION | NUP98/NSD1 | Research | Children | Health aspects | Oncology, Experimental | Cancer | Tyrosine | Myeloid leukemia | Leukemia | Stem cell transplantation | Transplantation | Multivariate analysis | Survival | Patients | Hematopoietic stem cells | Hemopoiesis | Medical prognosis | Remission | Flt3 protein | Mutation | Acute myeloid leukemia | Protein-tyrosine kinase
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10. Full Text Multiplex fusion gene testing in pediatric acute myeloid leukemia
by Iijima‐Yamashita, Yuka and Matsuo, Hidemasa and Yamada, Miho and Deguchi, Takao and Kiyokawa, Nobutaka and Shimada, Akira and Tawa, Akio and Takahashi, Hiroyuki and Tomizawa, Daisuke and Taga, Takashi and Kinoshita, Akitoshi and Adachi, Souichi and Horibe, Keizo
Pediatrics International, ISSN 1328-8067, 01/2018, Volume 60, Issue 1, pp. 47 - 51
Background Gene abnormalities, particularly chromosome rearrangements generating gene fusion, are associated with clinical characteristics and prognosis in... 
diagnosis | acute myeloid leukemia | fusion gene | multiplex polymerase chain reaction | Japanese Pediatric Leukemia/Lymphoma Study Group | SURVIVAL | AML | Japanese Pediatric Leukemia | CYTOGENETICS | CANCER | CHILDREN | TRANSCRIPTS | RELAPSE | POLYMERASE-CHAIN-REACTION | Lymphoma Study Group | PEDIATRICS | ACUTE PROMYELOCYTIC LEUKEMIA | Prognosis | Humans | Child, Preschool | Infant | Male | Multiplex Polymerase Chain Reaction | Reverse Transcriptase Polymerase Chain Reaction | Genetic Testing - methods | Leukemia, Myeloid, Acute - diagnosis | Oncogene Fusion | Oncogene Proteins, Fusion - genetics | Karyotyping | Adolescent | Female | Biomarkers, Tumor - genetics | Retrospective Studies | Child | Leukemia, Myeloid, Acute - genetics | Genetic research | Pediatrics | Genetic aspects | Genes | Genetic screening | Cancer | Multiplexing | Myeloid leukemia | Leukemia | Abnormalities | Karyotypes | Fluorescence | Reverse transcription | Runx1 protein | Chromosome rearrangements | Patients | Lymphoma | Polymerase chain reaction | Promyeloid leukemia | AML1 protein | Fluorescence in situ hybridization | Fusion protein | Acute myeloid leukemia | Acute promyeloid leukemia
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11. Full Text A Novel PAX5-KIDINS220 Fusion Protein Activates Multiple Signals Associated with Therapeutic Resistance
by Kanayama, Takuyo and Imamura, Toshihiko and Sakamoto, Kenichi and Hayakawa, Fumihiko and Tanizawa, Akihiko and Kiyokawa, Nobutaka and Hosoi, Hajime
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 3928 - 3928
Abstract Background: It is well known that PAX5 related fusion proteins are mainly associated with leukemogenesis of B cell precursor acute lymphoblastic... 
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12. Full Text Acute promyelocytic leukemia with a cryptic insertion of RARA into TBL1XR1
by Osumi, Tomoo and Watanabe, Akihiro and Okamura, Kohji and Nakabayashi, Kazuhiko and Yoshida, Masanori and Tsujimoto, Shin‐ichi and Uchiyama, Meri and Takahashi, Hiroyuki and Tomizawa, Daisuke and Hata, Kenichiro and Kiyokawa, Nobutaka and Kato, Motohiro
Genes, Chromosomes and Cancer, ISSN 1045-2257, 11/2019, Volume 58, Issue 11, pp. 820 - 823
Acute promyelocytic leukemia (APL) is cytogenetically characterized by the t(15;17) (q24;q21), although cases without this translocation exist. These cases are... 
acute promyelocytic leukemia | cryptic insertion | children | TBL1XR1/RARA | TRANS-RETINOIC ACID | IDENTIFICATION | REARRANGEMENT | RELAPSE | ONCOLOGY | TBL1XR1 | T(15/17) | GENETICS & HEREDITY | RARA | PCR | Chemotherapy | Chromosomes | Analysis | Genomics | Cancer | Translocation | Transcription | Pathogenesis | Leukemia | Karyotypes | Insertion | Case reports | Transplantation | Genomes | Girls | Gene sequencing | Promyeloid leukemia | Cord blood | Remission | Fusion protein | Retinoic acid | Acute promyeloid leukemia
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13. Full Text Monitoring of fusion gene transcripts to predict relapse in pediatric acute myeloid leukemia
by Matsuo, Hidemasa and Iijima‐Yamashita, Yuka and Yamada, Miho and Deguchi, Takao and Kiyokawa, Nobutaka and Shimada, Akira and Tawa, Akio and Tomizawa, Daisuke and Taga, Takashi and Kinoshita, Akitoshi and Adachi, Souichi and Horibe, Keizo
Pediatrics International, ISSN 1328-8067, 01/2018, Volume 60, Issue 1, pp. 41 - 46
Background In acute myeloid leukemia (AML), accurate detection of minimal residual disease (MRD) enables better risk‐stratified therapy. There are few studies,... 
minimal residual disease | acute myeloid leukemia | fusion gene | prognosis | polymerase chain reaction | AML | PROGNOSTIC IMPACT | CONTRIBUTE | MULTIPARAMETER FLOW-CYTOMETRY | RISK | REARRANGEMENT | THERAPY | RT-PCR | PEDIATRICS | STRATIFICATION | Recurrence | Oncogene Proteins, Fusion - metabolism | Prognosis | Humans | Leukemia, Myeloid, Acute - metabolism | Child, Preschool | Infant | Male | Neoplasm, Residual | Leukemia, Myeloid, Acute - diagnosis | Adolescent | Biomarkers, Tumor - metabolism | Female | Retrospective Studies | Child | Real-Time Polymerase Chain Reaction | Pediatrics | Relapse | RNA | Analysis | Genes | Genetic research | Genetic aspects | Diseases | Cancer | Myeloid leukemia | Leukemia | Health risks | Minimal residual disease | Runx1 protein | Ribonucleic acid--RNA | Lymphoma | Survival | Patients | Polymerase chain reaction | AML1 protein | Fusion protein | Acute myeloid leukemia | Monitoring
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14. Full Text Efficient Generation of Hepatoblasts From Human ES Cells and iPS Cells by Transient Overexpression of Homeobox Gene HEX
by Inamura, Mitsuru and Kawabata, Kenji and Takayama, Kazuo and Tashiro, Katsuhisa and Sakurai, Fuminori and Katayama, Kazufumi and Toyoda, Masashi and Akutsu, Hidenori and Miyagawa, Yoshitaka and Okita, Hajime and Kiyokawa, Nobutaka and Umezawa, Akihiro and Hayakawa, Takao and Furue, Miho K and Mizuguchi, Hiroyuki
Molecular Therapy, ISSN 1525-0016, 02/2011, Volume 19, Issue 2, pp. 400 - 407
Human embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) have the potential to differentiate into all cell lineages, including hepatocytes,... 
MEDICINE, RESEARCH & EXPERIMENTAL | MOUSE | PROLIFERATION | CULTURE | HEPATOCYTE-LIKE CELLS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ADENOVIRUS VECTOR | EMBRYONIC STEM-CELLS | GENETICS & HEREDITY | DIFFERENTIATION | LIVER DEVELOPMENT | EXPRESSION | FUNCTIONAL HEPATOCYTES | Embryonic Stem Cells - metabolism | Transcription Factors - physiology | Embryonic Stem Cells - cytology | Humans | Cytochrome P-450 Enzyme System - metabolism | Genes, Homeobox - genetics | Transcription Factors - genetics | Genetic Vectors - genetics | Homeodomain Proteins - genetics | Cell Differentiation - genetics | Hepatocytes - cytology | Adenoviridae - genetics | Cytochrome P-450 Enzyme System - genetics | Homeodomain Proteins - physiology | Induced Pluripotent Stem Cells - cytology | Cell Differentiation - physiology | Genes, Homeobox - physiology | Induced Pluripotent Stem Cells - metabolism | Original
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15. Full Text Dasatinib and low‐intensity chemotherapy for Philadelphia chromosome‐positive acute lymphoblastic leukemia in a child with Down syndrome
by Hirabayashi, Shinsuke and Hasegawa, Daisuke and Yamamoto, Kaoru and Nishimura, Akira and Hosoya, Yosuke and Shuo, Takuya and Kiyokawa, Nobutaka and Miura, Masatomo and Takahashi, Naoto and Manabe, Atsushi
Pediatric Blood & Cancer, ISSN 1545-5009, 05/2019, Volume 66, Issue 5, pp. e27612 - n/a
PEDIATRICS | INTERGROUP | ONCOLOGY | HEMATOLOGY | IMATINIB | Dasatinib | Chemotherapy | Genetic research | Disabled children | Genetic aspects | Down syndrome | Cancer | Acute lymphatic leukemia | Lymphatic leukemia | Down's syndrome | Leukemia | Philadelphia chromosome
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16. Full Text Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemia
by Seki, Masafumi and Kimura, Shunsuke and Isobe, Tomoya and Yoshida, Kenichi and Ueno, Hiroo and Nakajima-Takagi, Yaeko and Wang, Changshan and Lin, Lin and Kon, Ayana and Suzuki, Hiromichi and Shiozawa, Yusuke and Kataoka, Keisuke and Fujii, Yoichi and Shiraishi, Yuichi and Chiba, Kenichi and Tanaka, Hiroko and Shimamura, Teppei and Masuda, Kyoko and Kawamoto, Hiroshi and Ohki, Kentaro and Kato, Motohiro and Arakawa, Yuki and Koh, Katsuyoshi and Hanada, Ryoji and Moritake, Hiroshi and Akiyama, Masaharu and Kobayashi, Ryoji and Deguchi, Takao and Hashii, Yoshiko and Imamura, Toshihiko and Sato, Atsushi and Kiyokawa, Nobutaka and Oka, Akira and Hayashi, Yasuhide and Takagi, Masatoshi and Manabe, Atsushi and Ohara, Akira and Horibe, Keizo and Sanada, Masashi and Iwama, Atsushi and Mano, Hiroyuki and Miyano, Satoru and Ogawa, Seishi and Takita, Junko
Nature Genetics, ISSN 1061-4036, 08/2017, Volume 49, Issue 8, pp. 1274 - 1281
The outcome of treatment-refractory and/or relapsed pediatric T cell acute lymphoblastic leukemia (T-ALL) is extremely poor(1), and the genetic basis for this... 
ACTIVATION | INTEGRATED MOLECULAR ANALYSIS | NOTCH PATHWAY | GENETICS & HEREDITY | GENE-EXPRESSION | TUMOR-SUPPRESSOR | TRANSCRIPTION FACTOR PU.1 | NETWORKS | MUTATIONS | MLL | HEMATOPOIETIC PROGENITORS | T-Lymphocyte Subsets | Genetic Predisposition to Disease | Precursor Cell Lymphoblastic Leukemia-Lymphoma - immunology | Humans | Child, Preschool | Gene Fusion | Infant | Male | Proto-Oncogene Proteins - genetics | Gene Expression Profiling | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Adolescent | Survival Analysis | Trans-Activators - genetics | Female | Child | Physiological aspects | Genetic aspects | Research | Acute lymphocytic leukemia | T cells | Gene fusion | Risk factors | Cell proliferation | Pediatrics | Transcription factors | Profiling | Acute lymphatic leukemia | Transcription | Risk groups | Maturation | CD8 antigen | Leukemia | Genes | Lymphocytes T | Lymphatic leukemia | Gene expression | CD4 antigen | Gene sequencing | Proteins | PU.1 protein | Cell growth | Lymphocytes | Stem cells | Cells (biology) | Mutation | Cancer
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