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1
المؤلفون: Masahiko Takahashi, Kazuyoshi Hosomichi, Hirofumi Nakaoka, Haruhito Sakata, Naoya Uesato, Kentaro Murakami, Masayuki Kano, Takeshi Toyozumi, Yasunori Matsumoto, Tetsuro Isozaki, Nobufumi Sekino, Ryota Otsuka, Itsuro Inoue, Hisahiro Matsubara
المصدر: Esophagus. 19:294-302
مصطلحات موضوعية: Esophageal Neoplasms, Tumor Suppressor Proteins, Mutation, Gastroenterology, Humans, Esophageal Squamous Cell Carcinoma, Tumor Suppressor Protein p53, Alleles, Transcription Factors
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2
المؤلفون: Nobufumi Sekino, Fumitaka Ishige, Kentaro Murakami, Hiroshi Suito, Takayoshi Suzuki, Yasunori Matsumoto, Masahiko Takahashi, Keiko Iida, Isamu Hoshino, Yasunori Akutsu, Aki Komatsu, Hisahiro Matsubara, Yosuke Iwatate, Itsuro Inoue
المصدر: Oncology Letters
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, lysine-specific histone demethylase 1, Biology, medicine.disease_cause, Transcriptome, 03 medical and health sciences, 0302 clinical medicine, Gene expression, medicine, lysine-specific histone demethylase 1 inhibitor, Articles, Cell cycle, esophageal squamous cell carcinoma, 030104 developmental biology, Histone, Oncology, Acetylation, histone demethylase inhibitor, 030220 oncology & carcinogenesis, biology.protein, Cancer research, chromatin immunoprecipitation-seq, Demethylase, Carcinogenesis, Chromatin immunoprecipitation
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3
المؤلفون: Masaya Yokoyama, Masayuki Kano, Kentaro Murakami, Hisahiro Matsubara, Naoyuki Hanari, Ryota Otsuka, Yasunori Akutsu, Yasunori Matsumoto, Itsuro Inoue, Hirofumi Nakaoka, Nobufumi Sekino, Masahiko Takahashi
المصدر: Molecular Cancer Therapeutics. 16:B07-B07
مصطلحات موضوعية: Genetics, Cancer Research, Mutation, Somatic cell, Cancer, Synthetic lethality, Biology, medicine.disease_cause, medicine.disease, Germline mutation, MRNA Sequencing, Oncology, medicine, Gene, Exome sequencing
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8c83ce475cfb7f0a902124a7ea6204cf
https://doi.org/10.1158/1538-8514.synthleth-b07 -
4
المؤلفون: Itsuro, INOUE
المصدر: 総研大ジャーナル = Sokendai journal. 15:14-17
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=jairo_______::75d546844177fc85583fe86a003b929f
http://id.nii.ac.jp/1013/00002004/ -
5
المؤلفون: Shuji Izumo, Yasushi Isashiki, Itsuro Inoue, Taiji Sakamoto, Shozo Sonoda, Hiroshi Tachikui
المصدر: Ophthalmic Research. 35:224-231
مصطلحات موضوعية: Mitochondrial DNA, DNA Mutational Analysis, Molecular Sequence Data, Population, Optic Atrophy, Hereditary, Leber, Biology, medicine.disease_cause, DNA, Mitochondrial, Nucleotide diversity, Cellular and Molecular Neuroscience, Japan, medicine, Humans, Point Mutation, education, Phylogeny, mtDNA control region, Genetics, Mutation, education.field_of_study, Polymorphism, Genetic, Base Sequence, Haplotype, Leber's hereditary optic neuropathy, Nucleic acid sequence, General Medicine, medicine.disease, Molecular biology, eye diseases, Sensory Systems, Mitochondria, Ophthalmology, Haplotypes
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6
المؤلفون: Makoto Takahashi, Yoshitaka Matsusue, Yoshiharu Kawaguchi, Morio Matsumoto, Shiro Ikegawa, Itsuro Inoue, Tomoatsu Kimura, Hisatoshi Baba, Kanji Mori, Taizo Horikoshi, Kozo Nakamura, Shigeru Hirabayashi, Koichi Maeda, Hisashi Inoue, Hiroshi Kawaguchi, Kazuhiro Chiba, Kazuhito Sugimori, Yu Koshizuka
المصدر: Human genetics. 119(6)
مصطلحات موضوعية: Adult, Male, Candidate gene, Adolescent, Single-nucleotide polymorphism, Biology, Ossification of Posterior Longitudinal Ligament, Bioinformatics, Polymorphism, Single Nucleotide, Polymorphism (computer science), Genetics, medicine, Posterior longitudinal ligament, Humans, Genetic Predisposition to Disease, Allele, Child, Genetics (clinical), Genetic association, Aged, Aged, 80 and over, Ossification, Case-control study, Middle Aged, Case-Control Studies, Child, Preschool, Female, medicine.symptom
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7
المؤلفون: Masayoshi Nagao, Takeyori Saheki, Tooru Nakao, Kazuhiko Oyanagi, Naoki Takayanagi, Akira Tsuchiyama, Yoshihiro Itakura, Itsuro Inoue, Keiji Tsubakihara
المصدر: The Tohoku journal of experimental medicine. 152(1)
مصطلحات موضوعية: Male, Mutant, Ornithine transcarbamylase, Deficient mutant, Enzyme-Linked Immunosorbent Assay, General Biochemistry, Genetics and Molecular Biology, Mice, Antigen, medicine, Animals, Humans, Elisa method, Ornithine Carbamoyltransferase, chemistry.chemical_classification, Radial immunodiffusion, Chemistry, Hyperammonemia, General Medicine, Hydrogen-Ion Concentration, medicine.disease, Molecular biology, Ornithine Carbamoyltransferase Deficiency Disease, Kinetics, Enzyme, Liver, Female
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7341987766401fafaf24848c7332a88f
https://pubmed.ncbi.nlm.nih.gov/3617058 -
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المؤلفون: M. Uono, Kenzo Takeshita, Masako Nakajima, Tatsuhiko Yuasa, Ryoko Koike, Itsuro Inoue, K. Sakoda, M. Koura, Takeyori Saheki, Tadashi Miyatake, K. Kayanuma
المصدر: Journal of inherited metabolic disease. 10(3)
مصطلحات موضوعية: Ornithine, Chemistry, Mitochondria, Liver, Mitochondrion, Kinetics, Citrulline synthesis, Biochemistry, Ammonia, Genetics, Homocitrullinuria, Citrulline, Humans, Abnormality, Amino Acid Metabolism, Inborn Errors, Genetics (clinical)
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9
المؤلفون: Takashi Mito, Keiichi Ichihara, Kenzo Takeshita, Itsuro Inoue, Shougo Ishii, Masako Nakajima, Sachio Takashima, Hiroki Takakura, Takeyori Saheki, Hideo Akiyoshi
المصدر: Braindevelopment. 10(3)
مصطلحات موضوعية: Male, Ornithine, Pathology, medicine.medical_specialty, Central nervous system, Mitochondria, Liver, Arginine, Endoplasmic Reticulum, Lethargy, Developmental Neuroscience, Ammonia, Internal medicine, medicine, Humans, Child, Amino Acid Metabolism, Inborn Errors, Hyperornithinemia, Ornithinemia, business.industry, Brain, Hyperammonemia, General Medicine, medicine.disease, Liver Glycogen, medicine.anatomical_structure, Endocrinology, Cerebellar vermis atrophy, Pediatrics, Perinatology and Child Health, Ornithine transport, Citrulline, Neurology (clinical), business, Tomography, X-Ray Computed, Truncal ataxia
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10
المؤلفون: Itsuro Inoue, Ryoko Koike, Takeyori Saheki, K. Fujimori, Tadashi Miyatake, Tatsuhiko Yuasa
المصدر: Neurology. 37(11)
مصطلحات موضوعية: Adult, Male, Ornithine, medicine.medical_specialty, Adolescent, Ornithine aminotransferase, chemistry.chemical_compound, Ammonia, Reference Values, Internal medicine, medicine, Citrulline, Humans, Amino Acids, Amino Acid Metabolism, Inborn Errors, Hyperornithinemia, Skin, Cerebellar ataxia, business.industry, Hyperammonemia, Fibroblasts, medicine.disease, Endocrinology, chemistry, Liver, Ornithine transport, Neurology (clinical), medicine.symptom, business, Myoclonus
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b42118e4a3482b3058156598a0eec707
https://pubmed.ncbi.nlm.nih.gov/3670619