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Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome

Scientific reports, 2018-08, Vol.8 (1), p.12824-11, Article 12824

2018

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Long-term outcome of 6-month maintenance chemotherapy for acute lymphoblastic leukemia in children

Leukemia, 2017-03, Vol.31 (3), p.580-584

2017

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Image Gallery: Palmoplantar hyperkeratosis in dermatomyositis with anti‐PM/Scl antibodies

British journal of dermatology (1951), 2017-05, Vol.176 (5), p.e94-e94

2017

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A patient with bullous pemphigoid with mucosal involvement serologically positive for anti‐BP230 autoantibodies only

British journal of dermatology (1951), 2020-01, Vol.182 (1), p.221-223, Article bjd.18343

2020

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Image Gallery: Unilaterally dominant acrokeratoelastoidosis (punctate palmoplantar keratoderma type 3)

British journal of dermatology (1951), 2017-10, Vol.177 (4), p.e157-e157

2017

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Mutational analysis of 29 patients with autosomal‐recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal‐recessive woolly hair and hypotrichosis in Japan

British journal of dermatology (1951), 2017-07, Vol.177 (1), p.290-292

2017

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Characterization of pediatric Philadelphia-negative B-cell precursor acute lymphoblastic leukemia with kinase fusions in Japan

Blood cancer journal (New York), 2016-05, Vol.6 (5), p.e419-e419

2016

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Usefulness of chemoradiotherapy for inoperable gastric cancer

Annals of the Royal College of Surgeons of England, 2017-04, Vol.99 (4), p.332-336

2017

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Prognostic significance of angiogenesis in human pancreatic cancer

British journal of cancer, 1999-03, Vol.79 (9-10), p.1553-1563

1999

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Prognostic implications of CEBPA mutations in pediatric acute myeloid leukemia: a report from the Japanese Pediatric Leukemia/Lymphoma Study Group

Blood cancer journal (New York), 2014-07, Vol.4 (7), p.e226-e226

2014

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Clinical significance of transmembrane 4 superfamily in colon cancer

British journal of cancer, 2003-07, Vol.89 (1), p.158-167

2003

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High frequencies of simultaneous FLT3-ITD, WT1 and KIT mutations in hematological malignancies with NUP98-fusion genes

Leukemia, 2010-11, Vol.24 (11), p.1975-1977

2010

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Mixed-lineage-leukemia (MLL) fusion protein collaborates with Ras to induce acute leukemia through aberrant Hox expression and Raf activation

Leukemia, 2009-12, Vol.23 (12), p.2197-2209

2009

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Randomised study of adjuvant chemotherapy for completely resected p-stage I-IIIA non-small cell lung cancer

British journal of cancer, 2006-10, Vol.95 (7), p.817-821

2006

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The mouse and human homologs of DMC1, the yeast meiosis-specific homologous recombination gene, have a common unique form of exon-skipped transcript in meiosis

Nucleic acids research, 1996-02, Vol.24 (3), p.470-477

1996

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The MYO1F, unconventional myosin type 1F, gene is fused to MLL in infant acute monocytic leukemia with a complex translocation involving chromosomes 7, 11, 19 and 22

Oncogene, 2005-08, Vol.24 (33), p.5191-5197

2005

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New Serials“ Mitsumeru, Mitsumoru” (0), Special event to launch the serials: "Estimation in Planetary Science Research" roundtable discussion

Planetary People - The Japanese Society for Planetary Sciences, 2023/09/25, Vol.32(3), pp.244-259

2023

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802 Whole-exome sequencing reveals a retinitis pigmentosa-causative PRPH2 variant as a secondary finding in a patient with pseudoxanthoma elasticum

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S138-S138

2023

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Identification of the novel AML1 fusion partner gene, LAF4, a fusion partner of MLL, in childhood T-cell acute lymphoblastic leukemia with t(2;21)(qll;q22) by bubble PCR method for cDNA

Oncogene, 2008-04, Vol.27 (15), p.2249-2256

2008

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Isoscalar giant dipole resonance in [formula omitted]Pb via inelastic α scattering at 400 MeV and nuclear incompressibility

Physics letters. B, 2003-03, Vol.557 (1-2), p.12-19

2003

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CBL mutation in childhood therapy-related leukemia

Leukemia, 2011-08, Vol.25 (8), p.1356-1358

2011

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Tandem duplication of the FLT3 gene is found in acute lymphoblastic leukaemia as well as acute myeloid leukaemia but not in myelodysplastic syndrome or juvenile chronic myelogenous leukaemia in children

British journal of haematology, 1999-04, Vol.105 (1), p.155-162

1999

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N822 mutation of KIT gene was frequent in pediatric acute myeloid leukemia patients with t(8;21) in Japan: a study of the Japanese childhood AML cooperative study group

Leukemia, 2007-10, Vol.21 (10), p.2218-2219

2007

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Better-resolution measurement of vertical scattering angle in a new ion-optical mode of spectrometer “Grand Raiden”

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2001-08, Vol.469 (1), p.55-62

2001

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No nucleophosmin mutations in pediatric acute myeloid leukemia with normal karyotype: a study of the Japanese Childhood AML Cooperative Study Group

Leukemia, 2007-06, Vol.21 (6), p.1307-1307

2007

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Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome

Long-term outcome of 6-month maintenance chemotherapy for acute lymphoblastic leukemia in children

Image Gallery: Palmoplantar hyperkeratosis in dermatomyositis with anti‐PM/Scl antibodies

A patient with bullous pemphigoid with mucosal involvement serologically positive for anti‐BP230 autoantibodies only

Image Gallery: Unilaterally dominant acrokeratoelastoidosis (punctate palmoplantar keratoderma type 3)

Mutational analysis of 29 patients with autosomal‐recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal‐recessive woolly hair and hypotrichosis in Japan

Characterization of pediatric Philadelphia-negative B-cell precursor acute lymphoblastic leukemia with kinase fusions in Japan

Usefulness of chemoradiotherapy for inoperable gastric cancer

Prognostic significance of angiogenesis in human pancreatic cancer

Prognostic implications of CEBPA mutations in pediatric acute myeloid leukemia: a report from the Japanese Pediatric Leukemia/Lymphoma Study Group

Clinical significance of transmembrane 4 superfamily in colon cancer

High frequencies of simultaneous FLT3-ITD, WT1 and KIT mutations in hematological malignancies with NUP98-fusion genes

Mixed-lineage-leukemia (MLL) fusion protein collaborates with Ras to induce acute leukemia through aberrant Hox expression and Raf activation

Randomised study of adjuvant chemotherapy for completely resected p-stage I-IIIA non-small cell lung cancer

The mouse and human homologs of DMC1, the yeast meiosis-specific homologous recombination gene, have a common unique form of exon-skipped transcript in meiosis

The MYO1F, unconventional myosin type 1F, gene is fused to MLL in infant acute monocytic leukemia with a complex translocation involving chromosomes 7, 11, 19 and 22

New Serials“ Mitsumeru, Mitsumoru” (0), Special event to launch the serials: "Estimation in Planetary Science Research" roundtable discussion

802 Whole-exome sequencing reveals a retinitis pigmentosa-causative PRPH2 variant as a secondary finding in a patient with pseudoxanthoma elasticum

Identification of the novel AML1 fusion partner gene, LAF4, a fusion partner of MLL, in childhood T-cell acute lymphoblastic leukemia with t(2;21)(qll;q22) by bubble PCR method for cDNA

Isoscalar giant dipole resonance in [formula omitted]Pb via inelastic α scattering at 400 MeV and nuclear incompressibility

CBL mutation in childhood therapy-related leukemia

Tandem duplication of the FLT3 gene is found in acute lymphoblastic leukaemia as well as acute myeloid leukaemia but not in myelodysplastic syndrome or juvenile chronic myelogenous leukaemia in children

N822 mutation of KIT gene was frequent in pediatric acute myeloid leukemia patients with t(8;21) in Japan: a study of the Japanese childhood AML cooperative study group

Better-resolution measurement of vertical scattering angle in a new ion-optical mode of spectrometer “Grand Raiden”

No nucleophosmin mutations in pediatric acute myeloid leukemia with normal karyotype: a study of the Japanese Childhood AML Cooperative Study Group

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