Hirofumi Kobayashi

发表

Cloning and characterization of the human BAZF gene, a homologue of the BCL6 oncogene.

N. Miyasaka, T. Tokuhisa, S. Okabe, 2002, Biochemical and biophysical research communications.

Biology of neuroblastomas that were found by mass screening at 6 months of age in Japan

A. Nakagawara, Y. Kaneko, Hirofumi Kobayashi, 2006, Pediatric blood & cancer.

Chromosomes that show partial loss or gain in near‐diploid tumors coincide with chromosomes that show whole loss or gain in near‐triploid tumors: Evidence suggesting the involvement of the same genes in the tumorigenesis of high‐ and low‐risk neuroblastomas

M. Ohira, Yohko Nakamura, A. Nakagawara, 2003, Genes, chromosomes & cancer.

High expression of Survivin, mapped to 17q25, is significantly associated with poor prognostic factors and promotes cell survival in human neuroblastoma

M. Ohira, E. Isogai, A. Nakagawara, 2000, Oncogene.

R‐CHOP‐14 versus R‐CHOP‐14/CHASER for upfront autologous transplantation in diffuse large B‐cell lymphoma: JCOG0908 study

Y. Kagami, M. Ogura, J. Kuroda, 2020, Cancer science.

R‐High‐CHOP/CHASER/LEED with autologous stem cell transplantation in newly diagnosed mantle cell lymphoma: JCOG0406 STUDY

I. Hanamura, M. Taniwaki, Y. Matsuno, 2018, Cancer science.

Analysis of deletions of the long arm of chromosome 11 in hematologic malignancies with fluorescence in situ hybridization

J. Rowley, M. L. Beau, R. Espinosa, 1993, Genes, chromosomes & cancer.

Clonal, nonconstitutional rearrangements of the MLL gene in infant twins with acute lymphoblastic leukemia: in utero chromosome rearrangement of 11q23

J. Rowley, P. Rothberg, M. Diaz, 1994 .

Inversion of chromosome 11, inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: Identification of a P1 clone spanning the 11q22 breakpoint

F. Hosoda, Y. Hayashi, Y. Arai, 1997, Genes, chromosomes & cancer.

Hematologic malignancies with the t(10;11)(p13;q21) have the same molecular event and a variety of morphologic or immunologic phenotypes

F. Hosoda, M. Ohki, Y. Kaneko, 1997, Genes, chromosomes & cancer.

Minimal residual disease with TEL‐AML1 fusion transcript in childhood acute lymphoblastic leukaemia with t(12;21)

Y. Tsunematsu, Y. Kaneko, N. Satake, 1997, British journal of haematology.

Disappearance of AML1 ‐MTG8(ETO) fusion transcript in acute myeloid leukaemia patients with t(8;21) in long‐term remission

M. Ohki, Y. Kaneko, N. Satake, 1995, British journal of haematology.

The der(21)t(12;21) chromosome is always formed in a 12;21 translocation associated with childhood acute lymphoblastic leukaemia

Y. Kaneko, N. Satake, Hirofumi Kobayashi, 1996, British journal of haematology.

Molecular assignment of a translocation breakpoint in acute myeloid leukemia with t(8;21)

M. Ohki, Y. Kaneko, H. Ichikawa, 1991, Genes, chromosomes & cancer.

Waldenstrom Macroglobulinemia/Lymphoplasmacytic Lymphoma Associated with Nephrotic Syndrome during Hemodialysis, Treated Successfully with Tirabrutinib

M. Kawamura, Kazuhiko Kobayashi, Hirofumi Kobayashi, 2022, Internal medicine.

Extracellular NM23 protein promotes the growth and survival of primary cultured human acute myelogenous leukemia cells

Y. Kaneko, Y. Honma, Hirofumi Kobayashi, 2009, Cancer science.

Extracellular NM23-H1 protein inhibits the survival of primary cultured normal human peripheral blood mononuclear cells and activates the cytokine production

Y. Kaneko, Y. Honma, Hirofumi Kobayashi, 2009, International journal of hematology.

Cryptic t(12;15)(p13;q26) producing the ETV6-NTRK3 fusion gene and no loss of IGF2 imprinting in congenital mesoblastic nephroma with trisomy 11: fluorescence in situ hybridization and IGF2 allelic expression analysis.

Y. Kaneko, Hirofumi Kobayashi, A. Kikuta, 2002, Cancer genetics and cytogenetics.

Frequent Increase of DNA Copy Number in the 2q24 Chromosomal Region and Its Association with a Poor Clinical Outcome in Hepatoblastoma: Cytogenetic and Comparative Genomic Hybridization Analysis

Y. Tsunematsu, Y. Kaneko, Y. Horikoshi, 2001, Japanese journal of cancer research : Gann.

Histochemical study of colonic cancer in experimental colitis of rats

F. Shimamoto, G. Kajiyama, W. Brown, 1993, Digestive Diseases and Sciences.

Disomy 1 with terminal 1 p deletion is frequent in mass‐screening‐negative/late‐presenting neuroblastomas in young children, but not in mass‐screening‐positive neuroblastomas in infants

A. Nakagawara, Y. Kaneko, Hirofumi Kobayashi, 1999, International journal of cancer.

Clinical and Genetic Characteristics of Japanese Burkitt Lymphomas with or without Leukemic Presentation

Y. Kaneko, M. Kikuchi, Y. Komada, 2003, International journal of hematology.

A novel chromosomal translocation t(1;14)(q25;q32) in pre-B acute lymphoblastic leukemia involves the LIM homeodomain protein gene, Lhx4

K. Oshimi, N. Kawamata, S. Sakajiri, 2002, Oncogene.

Consistent detection of CALM‐AF10 chimaeric transcripts in haematological malignancies with t(10;11)(p13;q14) and identification of novel transcripts

F. Hosoda, T. Taki, M. Taniwaki, 1999, British journal of haematology.

Novel MLL‐CBP fusion transcript in therapy‐related chronic myelomonocytic leukemia with a t(11;16) (q23;p13) chromosome translocation

Y. Kaneko, N. Satake, Hirofumi Kobayashi, 1997, Genes, chromosomes & cancer.

Changes of colonic vasoactive intestinal peptide and cholinergic activity in rats with chemical colitis

K. Haruma, G. Kajiyama, Hirofumi Kobayashi, 1992, Digestive Diseases and Sciences.

Fusion of TEL/ETV6 to a novel ACS2 in myelodysplastic syndrome and acute myelogenous leukemia with t(5;12)(q31;p13)

N Asou, I. Jinnai, A. Matsuda, 1999, Genes, chromosomes & cancer.

Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization

J. Rowley, R. Espinosa, M. L. Le Beau, 1993, Genes, chromosomes & cancer.

Analysis of the t(6;11)(q27;q23) in leukemia shows a consistent breakpoint in AF6 in three patients and in the ML‐2 cell line

J. Rowley, N. Zeleznik-Le, R. Espinosa, 1996, Genes, chromosomes & cancer.

The inv ( 11 ) ( p 15 q 22 ) Chromosome Translocation of De Novo and Therapy-Related Myeloid Malignancies Results in Fusion of the Nucleoporin Gene , NUP 98 , With the Putative RNA Helicase Gene

F. Hosoda, Y. Hayashi, N. Kamada, 1997 .

Outcomes after R-CHOP in patients with newly diagnosed advanced follicular lymphoma: a 10-year follow-up analysis of the JCOG0203 trial.

M. Taniwaki, T. Yoshino, M. Ogura, 2018, The Lancet. Haematology.

Radiotherapy for localized gastric mucosa–associated lymphoid tissue lymphoma: long-term outcomes over 10 years

M. Kurosumi, J. Saitoh, Hirofumi Kobayashi, 2017, Journal of radiation research.

Identification of cytogenetically undetected 12p13 translocations and associated deletions with fluorescence in situ hybridization

J. Rowley, Hirofumi Kobayashi, H. Kobayashi, 1995, Genes, chromosomes & cancer.

11p15 translocations involving the NUP98 gene in childhood therapy‐related acute myeloid leukemia/myelodysplastic syndrome

Y. Arai, M. Ohki, Y. Tsunematsu, 1999, Genes, chromosomes & cancer.

Mixed‐lineage leukemia with t(10;11)(p13;q21): An analysis of AF10‐CALM and CALM‐AF10 fusion mRNAs and clinical features

Y. Kaneko, Hirofumi Kobayashi, N. Maseki, 1999, Genes, chromosomes & cancer.

EWS‐ERG fusion transcript produced by chromosomal insertion in a Ewing sarcoma

Y. Kaneko, N. Satake, Hirofumi Kobayashi, 1997, Genes, chromosomes & cancer.

Amplification of IGH/CCND1 fusion gene in a primary plasma cell leukemia case.

S. Toyota, Hirofumi Kobayashi, S. Tohda, 2010, Cancer genetics and cytogenetics.

Long‐term follow‐up after R‐High CHOP/CHASER/LEED with Auto‐PBSCT in untreated mantle cell lymphoma—Final analysis of JCOG0406

I. Hanamura, M. Taniwaki, Y. Matsuno, 2023, Cancer science.

Rearrangement of the MLL gene in acute lymphoblastic and acute myeloid leukemias with 11q23 chromosomal translocations.

J. Rowley, R. Larson, M. L. Le Beau, 1993, The New England journal of medicine.

Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases.

R. Kucherlapati, J. Rowley, S. Bohlander, 1994, Blood.

Cryptic insertion and translocation or nondividing leukemic cells disclosed by FISH analysis in infant acute leukemia with discrepant molecular and cytogenetic findings

Y. Tsunematsu, Y. Kaneko, M. Yoshida, 2003, Leukemia.

LAPTM5: a novel lysosomal-associated multispanning membrane protein preferentially expressed in hematopoietic cells.

J. Rowley, J. Lélias, T. Horiuchi, 1996, Genomics.

Cloning of ELL, a gene that fuses to MLL in a t(11;19)(q23;p13.1) in acute myeloid leukemia.

J. Rowley, M. Simon, M. Thirman, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Chromosomal and immunophenotypic patterns in T cell acute lymphoblastic leukemia (T ALL) and lymphoblastic lymphoma (LBL).

Y. Kaneko, Hirofumi Kobayashi, G. Frizzera, 1989, Leukemia.

The inv(11)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase gene, DDX10.

F. Hosoda, Y. Hayashi, N. Kamada, 1997, Blood.

Extracellular NM23 protein promotes the growth and survival of primary cultured human acute myelogenous leukemia cells

Y. Kaneko, Y. Honma, Hirofumi Kobayashi, 2009, Cancer science.