J. Furuyama

发表

The Escherichia coli ldcC gene encodes another lysine decarboxylase, probably a constitutive enzyme.

Y. Yamamoto, Y. Miwa, K. Miyoshi, 1997, Genes & genetic systems.

Suppression of growth of hepatocellular carcinoma by sodium butyrate in vitro and in vivo

J. Fujimoto, H. Yamamoto, T. Tamaoki, 1998, International journal of cancer.

Founder effect of a prevalent phenylketonuria mutation in the Oriental population.

M. Harvey, W. H. Lo, S. Huang, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Frequency and distribution of phenylketonuric mutations in orientals

Dong-hwan Lee, G. Isshiki, H. Shintaku, 1992, Human mutation.

Molecular characterization of phenylketonuric mutations in Japanese by analysis of phenylalanine hydroxylase mRNA from lymphoblasts.

G. Isshiki, H. Shintaku, J. Furuyama, 1994, Human molecular genetics.

Association between genetic variants of mast-cell chymase and eczema

T. Shirakawa, J. Furuyama, M. Kawai, 1996, The Lancet.

Characterization of the three genotypes of low Km aldehyde dehydrogenase in a Japanese population

T. Takeshita, K. Morimoto, J. Furuyama, 1994, Human Genetics.

Molecular and clinical study of familial adenomatous polyposis for genetic testing and management.

K. Tamura, J. Utsunomiya, J. Furuyama, 1999, Journal of experimental & clinical cancer research : CR.

HVJ-liposome-mediated transfection of HSVtk gene driven by AFP promoter inhibits hepatic tumor growth of hepatocellular carcinoma in SCID mice

Y. Kaneda, S. Kaneko, K. Kobayashi, 2001, Gene Therapy.

Hepatocyte growth factor promotes migration of human hepatocellular carcinoma via phosphatidylinositol 3-kinase

Y. Sasaki, J. Fujimoto, J. Furuyama, 1999, Clinical & Experimental Metastasis.

Expressions of matrilysin and stromelysin in human glioma cells.

J. Furuyama, K. Miyazaki, A. Nakano, 1993, Biochemical and biophysical research communications.

Fas antigen mRNA induction in postischemic murine brain

Yoshihiro Yamamoto, R. Hata, M. Tagaya, 1994, Brain Research.

Japanese siblings with missense mutation (717Val right arrow Ile) in amyloid precursor protein of early-onset Alzheimer's disease

T. Sugihara, E. Kitamura, K. Miyoshi, 1996, Neurology.

B cell response pathways regulated by IL-5 and IL-2. Secretory microH chain-mRNA and J chain mRNA expression are separately controlled events.

T. Hada, K. Higashino, K. Nakanishi, 1989, Journal of immunology.

Linkage between severe atopy and chromosome 11q13 in Japanese families

T. Takeshita, J. Furuyama, T. Shirakawa, 1994, Clinical genetics.

Direct assessment of triploid cells in mosaic human fetuses by fluorescence in-situ hybridization.

J. Furuyama, K. Koyama, Y. Tsuji, 1997, Molecular human reproduction.

DNA repair characteristics and skin cancers of xeroderma pigmentosum patients in Japan.

K. Tanaka, H. Takebe, J. Furuyama, 1977, Cancer research.

Usefulness of K-ras gene mutation at codon 12 in bile for diagnosing biliary strictures.

K. Tamura, J. Utsunomiya, Joji Utsunomiya, 1998, International journal of oncology.

Analysis of Wallace mutation in patients with Leber's hereditary optic neuropathy: familial study and tissue distribution

J. Furuyama, M. Shimo-oku, S. Miyazaki, 1996 .

Levels of Superoxide Dismutases, Glutathione, and Poly(ADP‐ribose) Polymerase in Radioresistant Human KB Carcinoma Cell Line

Yoshihiro Yamamoto, J. Furuyama, T. Yanagisawa, 1997, Japanese journal of cancer research : Gann.

Differential hypersensitivity of xeroderma pigmentosum lymphoblastoid cell lines to ultraviolet light mutagenesis.

H. Takebe, J. Furuyama, T. Kurihara, 1987, Carcinogenesis.

A hypotetraploid human T lymphoid cell line established by cell fusion

J. Yodoi, J. Furuyama, M. Hanaoka, 1978, Journal of cellular physiology.

Characterization of anti-sperm antibodies and their coding cDNA sequences by Epstein-Barr virus transformed B cell lines from lymphocytes of infertile women possessing anti-sperm antibodies.

J. Furuyama, H. Shibahara, K. Koyama, 1996, Journal of reproductive immunology.

Purification and some properties of the fast migrating alkaline phosphatase in FL-amnion cells (the Kasahara isoenzyme) and its cDNA cloning.

Y. Yamamoto, K. Higashino, J. Furuyama, 1990, Clinica chimica acta; international journal of clinical chemistry.

Simple, rapid, and accurate determination of deletion mutations by automated dna sequencing of heteroduplex fragments of the adenomatous polyposis coli (APC) gene generated by PCR amplification

K. Tamura, Y. Saeki, Joji Utsunomiya, 1993, Human mutation.

Hypersialyloligosacchariduria in mucolipidoses: a method for diagnosis.

T. Kato, A. Kobata, J. Furuyama, 1978, Clinica chimica acta; international journal of clinical chemistry.

Clonal analysis of hematopoietic cells using a novel polymorphic site of the X chromosome

J. Furuyama, M. Okada, A. Kanamaru, 1998, American journal of hematology.

Dual antitumor effects of 5-fluorouracil on the cell cycle in colorectal carcinoma cells: a novel target mechanism concept for pharmacokinetic modulating chemotherapy.

M. Kusunoki, J. Furuyama, R Yoshikawa, 2001, Cancer research.

Are human herpes viruses or measles virus associated with esophageal achalasia?

Yoshihiro Yamamoto, J. Fujimoto, J. Furuyama, 1995, Digestive Diseases and Sciences.

[Rapid diagnosis of cytomegalovirus interstitial pneumonitis by the polymerase chain reaction method--comparison of four diagnostic procedures].

J. Furuyama, Y. Eizuru, M. Okada, 1993, Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases.

Physiological and biochemical studies of effects of mitomycin C on strain HeLa cells in cell culture.

J. Furuyama, Y. Kuroda, 1963, Cancer research.

High sensitivity of Xeroderma pigmentosum cells to the carcinogen 4-nitroguinoline-1-oxide.

H. Takebe, J. Furuyama, S. Kondo, 1972, Mutation research.

Matrix metalloproteinases and tissue inhibitors of metalloproteinases in human gliomas.

J. Furuyama, K. Miyazaki, A. Nakano, 1995, Journal of neurosurgery.

A testis-specific antigen of the C57BL/6 mouse.

O. Mikami, J. Furuyama, Y. Yamamoto, 1989, Journal of reproductive immunology.

Mucolipidosis with β‐Galactosidase Deficiency: a Type of Sialidosis

J. Furuyama, K. Inui, K. Yamashita, 1981 .

Polymorphisms of the TNF gene and the TNF receptor superfamily member 1B gene are associated with susceptibility to ulcerative colitis and Crohn's disease, respectively

K. Tamura, Yoshihiro Yamamoto, J. Furuyama, 2002, Immunogenetics.

Mechanism of carcinogenesis in familial tumors

T. Iwama, K. Tamura, J. Utsunomiya, 2004, International Journal of Clinical Oncology.

Inactivation of the cholinesterase gene by Alu insertion: possible mechanism for human gene transposition.

T. Kaneko, Y. Yamamoto, T. Hada, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Expression and role of p27kip1 in neuronal differentiation of embryonal carcinoma cells

T. Sakai, H. Tachibana, T. Tamaoki, 2000 .

A new alternative splice variant of the mouse Fas antigen with a deletion in the N-terminal portion of the extracellular domain.

T. Tamaoki, J. Furuyama, T. Hashimoto, 1996, Life sciences.

Localization of Fas antigen mRNA induced in postischemic murine forebrain by in situ hybridization.

R. Hata, M. Tagaya, A. Wanaka, 1995, Brain research. Molecular brain research.

A new type of human calcitonin receptor isoform generated by alternative splicing.

J. Furuyama, Misa Nakamura, K. Kakudo, 1995, Biochemical and biophysical research communications.

Inactivation of both APC alleles in an early stage of colon adenomas in a patient with familial adenomatous polyposis (FAP).

Y. Nakamura, J. Utsunomiya, A. Horii, 1992, Human molecular genetics.

Establishment of cell lines derived from ataxia telangiectasia and xeroderma pigmentosum patients with high radiation sensitivity.

J. Furuyama, Y. Nakano, T. Kakunaga, 1986, Mutation research.

Detailed analysis of genetic alterations in colorectal tumors from patients with and without familial adenomatous polyposis (FAP).

M. Emi, Y. Miyoshi, J. Utsunomiya, 1993, Oncogene.

Spontaneous and cAMP‐dependent induction of a resting phase and neurite formation in cell hybrids between human neuroblastoma cells and thymidine auxotrophs of rat nerve‐like cells

J. Furuyama, M. Hatanaka, Y. Adachi, 1990, Journal of cellular physiology.

Apoptosis of human glioma cells in response to calphostin C, a specific protein kinase C inhibitor.

J. Furuyama, A. Nakano, H. Ikemoto, 1995, Journal of neurosurgery.

Stabilization of c-myc protein in human glioma cells

J. Furuyama, E. Tani, H. Shindo, 2004, Acta Neuropathologica.

IL18 polymorphism is associated with an increased risk of Crohn’s disease

H. Okamura, K. Tamura, Yoshihiro Yamamoto, 2002, Journal of Gastroenterology.

Amplification and expression of a multidrug resistance gene in human glioma cell lines.

J. Furuyama, E. Tani, H. Shindo, 1990, Journal of neurosurgery.

Early detection of relapse and evaluation of treatment for mixed chimerism using fluorescence in situ hybridization following allogeneic hematopoietic cell transplant for hematological malignancies

J. Furuyama, Y. Fujimori, Y. Takemoto, 2000, Annals of Hematology.

Hematopoietic recovery from host progenitors with normal karyotype devoid of Philadelphia chromosome in a patient with CML after allogeneic BMT.

J. Furuyama, K. Nagai, A. Kanamaru, 1993, Bone marrow transplantation.

[Familial spontaneous pneumothorax in three siblings including identical twins].

A. Moriguchi, J. Furuyama, K. Fujiwara, 1989, Nihon Kyobu Shikkan Gakkai zasshi.

Germline p53 mutation at codon 133 in a cancer-prone family

K. Tamura, Y. Saeki, J. Utsunomiya, 1997, Journal of Molecular Medicine.

Increased expression of human DNA repair genes, XRCC1, XRCC3 and RAD51, in radioresistant human KB carcinoma cell line N10.

J. Furuyama, T. Yanagisawa, M. Urade, 1998, Oral oncology.

Deoxyribonucleic acid analyses of five families with familial inherited thyroid stimulating hormone deficiency.

Y. Hayashizaki, T. Hashimoto, A. Labbé, 1990, The Journal of clinical endocrinology and metabolism.

High frequency of tetraploidy detected in malignant melanoma of Japanese patients by fluorescence in situ hybridization.

Y. Kitano, K. Mihara, M. Namba, 2000, International journal of oncology.

Possible complex translocation t(9; 14; 13)(q12;pl?;q31) in mother of a child with 9p-trisomy syndrome

J. Furuyama, T. Abe, H. Fujita, 2004, Humangenetik.

Reciprocal translocation t(5;6)(p13;q27) through three generations: Case report of cri du chat syndrome

J. Furuyama, T. Hashimoto, H. Chiyo, 1980, Human Genetics.

Intragenic suppression in the uvrD gene of Escherichia coli. I. Temperature-sensitive uvrD mutations.

Y. Yamamoto, J. Furuyama, M. Yabuki, 1988, Mutation research.

The nucleotide sequence for a proline-activating domain of gramicidin S synthetase 2 gene from Bacillus brevis.

Y. Yamamoto, K. Tokita, K. Okamura, 1991, Journal of biochemistry.

Expression of Interleukin‐18 and its Receptor in Mouse Ovary

H. Okamura, J. Furuyama, A. Hasegawa, 2001, American journal of reproductive immunology.

Genetic variation of mitochondrial cytochrome b genes among the subspecies of koala, Phascolarctos cinereus.

Y. Yamamoto, M. Harada, J. Furuyama, 1998, The Journal of veterinary medical science.

Different properties in lymphoblastoid cell lines from patients with Bloom syndrome.

J. Furuyama, T. Hashimoto, P. Lopetegui, 1984, Basic life sciences.

Frequencies of polymorphisms in the rhodopsin gene of Japanese retinitis pigmentosa and normal individuals

H. Kawano, K. Fujiki, A. Kanai, 1995, Japanese Journal of Human Genetics.

[Recent trends in studies on carcinogenesis in familial adenomatous polyposis].

Y. Miki, J. Utsunomiya, J. Furuyama, 1988, Gan to kagaku ryoho. Cancer & chemotherapy.

Molecular cloning and nucleotide sequence of the gramicidin S synthetase 1 gene.

Y. Yamamoto, K. Okamura, T. Minetoki, 1989, Journal of biochemistry.

Expression and role of p27(kip1) in neuronal differentiation of embryonal carcinoma cells.

T. Sakai, H. Tachibana, T. Tamaoki, 2000, Brain research. Molecular brain research.

Molecular characterization of galactosemia (Type 1)mutations in Japanese

J. Reichardt, G. Isshiki, J. Furuyama, 1995, Human mutation.