I. Ueno

发表

A novel non-pathogenetic polymorphism of the APC gene in a patient with familial adenomatous polyposis coli.

Y. Fukushima, Y. Ogiso, T. Katsuyama, 2000, Japanese journal of clinical oncology.

Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients.

T. Aoyama, K. Tanaka, T. Hashimoto, 1995, American journal of human genetics.

Specificity of PCR-SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency

I. Matsuda, I. Ueno, S. Komaki, 1993, Journal of Inherited Metabolic Disease.

Quantitative RT-PCR analysis demonstrates that synthesis of the recombinant fibrinogen is dependent on the transcription and synthesis of γ-chain

F. Terasawa, H. Shigematsu, M. Sugano, 2002 .

Restriction Fragment Length Polymorphism (RFLP) of Genomic DNA of Moraxella (Branhamella) catarrhalis Isolates in a Hospital

H. Matsumoto, Y. Kawakami, T. Katsuyama, 1994, Microbiology and immunology.

Novel BCR–ABL transcript containing an intronic sequence insert in a patient with Philadelphia‐positive acute lymphoblastic leukaemia

F. Ishida, T. Katsuyama, E. Hidaka, 2000, British journal of haematology.

Retinal changes in human cytomegalovirus infection. An electron microscopic study.

H. Kawanishi, I. Ueno, I. Tsukahara, 1966, American journal of ophthalmology.

Sandhoff disease in Cyprus: population screening by biochemical and DNA analysis indicates a high frequency of carriers in the Maronite community

A. Drousiotou, P. Ioannou, G. Christopoulos, 2000, Human Genetics.

‘Severe’ Prader–Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation

J. Sutcliffe, Y. Fukushima, E. Nurmi, 2002, Clinical genetics.

Internalization of beta-amyloid causes downregulation of apolipoprotein E mRNA expression in neuroblastoma cells.

K. Matsuda, T. Katsuyama, E. Hidaka, 2003, Annals of clinical and laboratory science.

Effect of retinoic acid and 12-O-tetradecanoyl phorbol-13-acetate on the binding of epidermal growth factor to its cellular receptors.

K. Egawa, I. Ueno, M. Saito, 1982, Biochimica et biophysica acta.

Nucleotide sequence of the human 70 kDa peroxisomal membrane protein: a member of ATP-binding cassette transporters.

K. Kamijo, T. Osumi, I. Ueno, 1992, Biochimica et biophysica acta.

The 70-kDa Peroxisomal Membrane Protein

T. Hashimoto, K. Kamijo, T. Osumi, 1992 .

Fibrinogen Matsumoto I: A γ364 Asp → His (GAT→CAT) Substitution Associated with Defective Fibrin Polymerization

F. Terasawa, T. Katsuyama, K. Furihata, 1996, Thrombosis and Haemostasis.

Fibrinogen Matsumoto II: γ308Asn → Lys (AAT → AAG) mutation associated with bleeding tendency

F. Terasawa, T. Katsuyama, K. Furihata, 1996 .

Characterization of factor XII Tenri, a rare CRM-negative factor XII deficiency.

T. Katsuyama, H. Hidaka, K. Yamauchi, 2004, Annals of clinical and laboratory science.

Specific Autoantibodies to Platelet Glycoproteins in Epstein-Barr Virus—Associated Immune Thrombocytopenia

T. Kamijo, K. Koike, Y. Nakazawa, 2003, International journal of hematology.

Evaluation of immunoglobulin G preparations for anti-cytomegalovirus antibodies with reference to neutralizing antibody in the presence of complement

I. Ueno, Y. Eizuru, Y. Minamishima, 1988, Journal of clinical microbiology.

Rat very-long-chain acyl-CoA dehydrogenase, a novel mitochondrial acyl-CoA dehydrogenase gene product, is a rate-limiting enzyme in long-chain fatty acid beta-oxidation system. cDNA and deduced amino acid sequence and distinct specificities of the cDNA-expressed protein.

T. Hashimoto, T. Aoyama, I. Ueno, 1994, The Journal of biological chemistry.

Virological, Serological and Molecular Analysis of a Case with Congenital Cytomegalovirus Infection

Y. Eizuru, Y. Minamishima, I. Ueno, 1988, Acta paediatrica Japonica : Overseas edition.

Radioimmunoassay detection of aflatoxin B1 in monkey and human urine.

A. D. Campbell, A. Pohland, I. Ueno, 1980 .

Novel deletional mutation of the MEN1 gene in a kindred with multiple endocrine neoplasia type 1

T. Kakizawa, K. Hashizume, I. Ueno, 2000, Clinical Genetics.

Familial amyloid polyneuropathy in Taiwan: Identification of transthyretin variant (Leu55 → Pro)

N. Yanagisawa, Kunihiro Yoshida, S. Ikeda, 1994, Muscle & nerve.

Genetic analyses in homozygous and heterozygous variants of lactate dehydrogenase-B (H) subunit--LD-B Matsumoto I and II (LD-B W323R).

F. Terasawa, T. Katsuyama, H. Hidaka, 1999, Clinica chimica acta; international journal of clinical chemistry.

Transthyretin Met 30 familial amyloid polyneuropathy in China. Usefulness of mass spectrometry for screening a variant TTR in serum

A. Nakamura, T. Tokuda, N. Yanagisawa, 1997 .

Sensitive identification of mycobacterial species using PCR-RFLP on bronchial washings.

T. Honda, K. Kubo, T. Katsuyama, 2000, American Journal of Respiratory and Critical Care Medicine.

Detection of aflatoxin B1 in imported food products into Japan by enzyme-linked immunosorbent assay and high performance liquid chromatography.

Y. Adachi, I. Ueno, N. Kumazawa, 1991, The Journal of veterinary medical science.

A comprehensive system to explore p53 mutations.

Y. Ogiso, T. Katsuyama, K. Furihata, 1998, American journal of clinical pathology.

Novel β‐thalassemia trait (IVS I‐1 G→C) in a Japanese family

T. Katsuyama, Eizaburo Ishii, K. Yamauchi, 2003 .