Y. Nobukuni

发表

Characterization of genomic regions directing the cell-specific expression of the mouse aldose reductase gene.

H. Li, Y. Nobukuni, T. Gui, 1999, Biochemical and biophysical research communications.

Molecular diagnosis of maple syrup urine disease: Screening and identification of gene mutations in the branched-chain α-ketoacid dehydrogenase multienzyme complex

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1992, Journal of Inherited Metabolic Disease.

Characterization of the gene encoding human pituitary-specific transcription factor, Pit-1.

T. Ohta, Y. Nobukuni, F. Endo, 1992, Gene.

Complete Defect of the E1,f Subunit of the Branched Chain a-Ketoacid Dehydrogenase Complex Due to a Deletion of an 11-bp Repeat Sequence which Encodes a Mitochondrial Targeting Leader Peptide in a Family with the Disease

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1991 .

Maple syrup urine disease. Complete defect of the E1 beta subunit of the branched chain alpha-ketoacid dehydrogenase complex due to a deletion of an 11-bp repeat sequence which encodes a mitochondrial targeting leader peptide in a family with the disease.

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1991, The Journal of clinical investigation.

Antitumor agents 220. Antitumor-promoting effects of cimigenol and related compounds on Epstein-Barr virus activation and two-stage mouse skin carcinogenesis.

Y. Nobukuni, H. Nishino, M. Kozuka, 2003, Bioorganic & medicinal chemistry.

Enhancement of a Sense of Coherence and Natural Killer Cell Activity which Occurred in Subjects who Improved their Exercise Habits through Health Education in the Workplace

Shinichiro Sasahara, Y. Nobukuni, K. Ogino, 2003, Journal of occupational health.

Association of Single Nucleotide Polymorphisms in the Eosinophil Peroxidase Gene with Japanese Cedar Pollinosis

Shinichiro Sasahara, Y. Nobukuni, K. Ogino, 2004, International Archives of Allergy and Immunology.

Neonatal onset of medium-chain Acyl-CoA dehydrogenase deficiency in two siblings

Y. Nobukuni, F. Endo, Y. Tsuji, 1988, Brain and Development.

Genotypes and Haplotypes of CCR2 and CCR3 Genes in Japanese Cedar Pollinosis

Shinichiro Sasahara, Y. Nobukuni, K. Ogino, 2006, International Archives of Allergy and Immunology.

Maple syrup urine disease. Complete primary structure of the E1 beta subunit of human branched chain alpha-ketoacid dehydrogenase complex deduced from the nucleotide sequence and a gene analysis of patients with this disease.

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1990, The Journal of clinical investigation.

Complete primary structure of the transacylase (E2b) subunit of the human branched chain alpha-keto acid dehydrogenase complex.

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1989, Biochemical and biophysical research communications.

A late-appearing Philadelphia chromosome in acute lymphoblastic leukemia confirmed by expression of BCR-ABL mRNA.

Y. Kaneko, Y. Nobukuni, M. Migita, 1995, Leukemia.

Interiotherins C and D, two new lignans from Kadsura interior and antitumor-promoting effects of related neolignans on Epstein-Barr virus activation.

Y. Nobukuni, H. Nishino, M. Kozuka, 2002, Journal of natural products.

Alkaptonuria: such a long journey

S. Aaronson, Y. Nobukuni, K. Urabe, 1996, Nature Genetics.

Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance.

D. Fisher, Y. Nobukuni, I. Kobayashi, 2000, Human molecular genetics.

Analyses of loss-of-function mutations of the MITF gene suggest that haploinsufficiency is a cause of Waardenburg syndrome type 2A.

Y. Nobukuni, K. Takeda, H. Skarka, 1996, American journal of human genetics.

Gene analysis of mennonite maple syrup urine disease kindred using primer-specified restriction map modification

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1992, Journal of Inherited Metabolic Disease.

A T-to-A substitution in the E1α subunit gene of the branched-chain α-ketoacid dehydrogenase complex in two cell lines derived from menonite maple syrup urine disease patients

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1990 .

Characterization of the human glucocorticoid receptor promoter.

S. Detera-Wadleigh, G. Hager, Y. Nobukuni, 1995, Biochemistry.

[Hyperlipidemia: complex pathophysiology caused by multiple genetic and environmental factors--in considering the approaches to preventive medicine].

Y. Nobukuni, A. Eboshida, F. Higashikawa, 2005, Nihon eiseigaku zasshi. Japanese journal of hygiene.

Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency.

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1992, Biochemical and biophysical research communications.

Gene disruption of ribosomal protein L5 (RPL5) decreased the sensitivity of CHO-K1 cells to uncoupler carbonylcyanide-3-chlorophenylhydrazone.

Y. Nobukuni, K. Ohashi, M. Maeda, 2019, Drug discoveries & therapeutics.

Isolation and characterization of a complementary DNA clone coding for the E1 beta subunit of the bovine branched-chain alpha-ketoacid dehydrogenase complex: complete amino acid sequence of the precursor protein and its proteolytic processing.

K. Titani, Y. Nobukuni, F. Endo, 1990, Biochemistry.

Complete Primary Structure of the ElS Subunit of Human Branched Chain a-Ketoacid Dehydrogenase Complex Deduced from the Nucleotide Sequence and a Gene Analysis of Patients with This Disease

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1990 .

Maple syrup urine disease: Clinical and biochemical significance of gene analysis

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1991, Journal of Inherited Metabolic Disease.

Complete Primary Structure oftheElSSubunit ofHumanBranchedChaina-Ketoacid Dehydrogenase ComplexDeducedfromtheNucleotide SequenceandaGeneAnalysis ofPatients withThisDisease

Y. Nobukuni, H. Mitsubuchi, J. Asaka, 1990 .

Chemopreventive effects of emodin and cassiamin B in mouse skin carcinogenesis.

Y. Nobukuni, H. Nishino, J. Koyama, 2002, Cancer letters.

Experimental Exploration for Genes Related to Susceptibility and Resistance to Irinotecan

F. Fujita, Y. Akagi, Y. Nobukuni, 2022, AntiCancer Research.

Nonthermal effects of mobile-phone frequency microwaves on uteroplacental functions in pregnant rats.

Y. Nobukuni, K. Ogino, I. Matsuzaki, 2003, Reproductive toxicology.

Maple syrup urine disease: a possible biochemical basis for the clinical heterogeneity

Y. Nobukuni, F. Endo, I. Akaboshi, 1988, Human Genetics.

Structural organization and chromosomal localization of the gene for the E1 beta subunit of human branched chain alpha-keto acid dehydrogenase.

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1991, The Journal of biological chemistry.

Maple Syrup Urine Disease Caused by a Partial Deletion in the Inner E 2 Core Domain of the Branched Chain a-Keto Acid Dehydrogenase Complex due to Aberrant Splicing

Y. Nobukuni, F. Endo, I. Akaboshi, 2013 .

Structural Organization and Chromosomal Localization of the Gene for the El@ Subunit of Human Branched Chain a-Keto Acid Dehydrogenase*

Y. Nobukuni, F. Endo, H. Mitsubuchi, 1991 .

Interorgan metabolism of glutathione as the defence mechanism against oxidative stress.

Y. Nobukuni, Y. Morino, M. Hirota, 1986, Developments in toxicology and environmental science.

Unusual case of diffuse connective tissue disease with nodule formations in muscle, lung, kidney and brain

Y. Nobukuni, T. Miike, I. Matsuda, 1986, Brain and Development.

Gene Trap Mutagenesis-based Forward Genetic Approach Reveals That the Tumor Suppressor OVCA1 Is a Component of the Biosynthetic Pathway of Diphthamide on Elongation Factor 2*

K. Miyagawa, Y. Nobukuni, K. Kohno, 2005, Journal of Biological Chemistry.

Induction of myeloperoxidase and nitrotyrosine formation in a human eosinophilic leukemia cell line, EoL‐1

Y. Nobukuni, K. Ogino, Yasuhiro Kambayashi, 2004, Cell biochemistry and function.

[Hyperlipidemia: complex pathophysiology caused by multiple genetic and environmental factors--in considering the approaches to preventive medicine].

Y. Nobukuni, A. Eboshida, Kiyoshi Miyagawa, 2005, Nihon eiseigaku zasshi. Japanese journal of hygiene.

Maple syrup urine disease: Complete primary structure of the E1β subunit of human branched chain α-ketoacid dehydrogenase complex deduced from the nucleotide sequence and a gene analysis of patients with this disease

Y. Nobukuni, H. Mitsubuchi, I. Akaboshi, 1990 .