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1. Full Text Functional Delineation and Differentiation Dynamics of Human CD4+ T Cells Expressing the FoxP3 Transcription Factor
by Miyara, Makoto and Yoshioka, Yumiko and Kitoh, Akihiko and Shima, Tomoko and Wing, Kajsa and Niwa, Akira and Parizot, Christophe and Taflin, Cécile and Heike, Toshio and Valeyre, Dominique and Mathian, Alexis and Nakahata, Tatsutoshi and Yamaguchi, Tomoyuki and Nomura, Takashi and Ono, Masahiro and Amoura, Zahir and Gorochov, Guy and Sakaguchi, Shimon
Immunity (Cambridge, Mass.), ISSN 1074-7613, 06/2009, Volume 30, Issue 6, pp. 899 - 911
MOLIMMUNO | CELLIMMUNO | Life Sciences & Biomedicine | Immunology | Science & Technology | Forkhead Transcription Factors - biosynthesis | T-Lymphocytes, Regulatory - metabolism | Leukocyte Common Antigens - metabolism | T-Lymphocytes, Helper-Inducer - metabolism | Humans | CD4-Positive T-Lymphocytes - metabolism | T-Lymphocytes, Regulatory - immunology | CD4-Positive T-Lymphocytes - immunology | Leukocyte Common Antigens - immunology | Young Adult | Cell Differentiation - immunology | Interleukin-2 Receptor alpha Subunit - metabolism | T-Lymphocytes, Helper-Inducer - immunology | Adolescent | Aged, 80 and over | Adult | Aged | Interleukin-2 Receptor alpha Subunit - immunology | Proteins | Automation | Disease | Cytokines | Cloning | DNA methylation | Autoimmune diseases | Gene expression | Deoxyribonucleic acid--DNA | Index Medicus
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2. Full Text Early prophylaxis of central venous catheter-related thrombosis using 1% chlorhexidine gluconate and chlorhexidine-gel-impregnated dressings: a retrospective cohort study
by Yamashita, Tomoko and Takamori, Ayako and Nakagawachi, Akira and Tanigawa, Yoshinori and Hamada, Yohei and Aoki, Yosuke and Sakaguchi, Yoshiro
Scientific reports, ISSN 2045-2322, 12/2020, Volume 10, Issue 1, pp. 15952 - 15952
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Index Medicus
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3. Full Text Truncating mutation in CSNK2B and myoclonic epilepsy
by Sakaguchi, Yuri and Uehara, Tomoko and Suzuki, Hisato and Kosaki, Kenjiro and Takenouchi, Toshiki
Human mutation, ISSN 1059-7794, 11/2017, Volume 38, Issue 11, pp. 1611 - 1612
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Epilepsy | Genetic aspects | Index Medicus
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4. Full Text D85N, a KCNE1 Polymorphism, Is a Disease-Causing Gene Variant in Long QT Syndrome
by Nishio, Yukiko, MD and Makiyama, Takeru, MD, PhD and Itoh, Hideki, MD, PhD and Sakaguchi, Tomoko, MD, PhD and Ohno, Seiko, MD, PhD and Gong, Yin-Zhi, MD, PhD and Yamamoto, Satoshi, MD and Ozawa, Tomoya, MD, PhD and Ding, Wei-Guang, MD, PhD and Toyoda, Futoshi, PhD and Kawamura, Mihoko, MD and Akao, Masaharu, MD, PhD and Matsuura, Hiroshi, MD, PhD and Kimura, Takeshi, MD, PhD and Kita, Toru, MD, PhD and Horie, Minoru, MD, PhD
Journal of the American College of Cardiology, ISSN 0735-1097, 2009, Volume 54, Issue 9, pp. 812 - 819
Cardiovascular | Internal Medicine | long QT syndrome | single nucleotide polymorphism | disease-causing variant | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Cricetinae | Humans | Middle Aged | Male | Case-Control Studies | Polymorphism, Genetic | Animals | Adolescent | Long QT Syndrome - genetics | Adult | Female | Aged | Mutation | Child | Potassium Channels, Voltage-Gated - genetics | Long QT syndrome | Respiratory agents | Genetic aspects | Universities and colleges | Hamsters | Medical colleges | Genes | Genetic polymorphisms | Cardiovascular agents | Electrocardiography | Cardiac arrhythmia | Index Medicus | Abridged Index Medicus
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5. Full Text Usefulness of serum biopterin as a predictive biomarker for childhood asthma control: A prospective cohort study
by Kasuga, Saki and Kabata, Daijiro and Sakaguchi, Tomoko and Kudoh, Satoshi and Nishigaki, Satsuki and Higa, Yusuke and Fujikawa, Shiori and Fujitani, Hiroko and Shintani, Ayumi and Hamazaki, Takashi and Shintaku, Haruo and bDepartment of Medical Statistics and Osaka City University Graduate School of Medicine and aDepartment of Pediatrics
Allergology international, ISSN 1323-8930, 2019, Volume 68, Issue 1, pp. 96 - 100
Biomarker | Biopterin | Neopterin | Child | Asthma | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Spirometry | Prospective Studies | Asthma - physiopathology | Humans | Breath Tests | Male | Biopterin - blood | Biomarkers - blood | Asthma - blood | Adolescent | Female | Respiratory Sounds | Nitric Oxide - metabolism | Index Medicus
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6. Full Text Relationships between the antral follicle count, steroidogenesis, and secretion of follicle-stimulating hormone and anti-Mullerian hormone during follicular growth in cattle
by Sakaguchi, Kenichiro and Yanagawa, Yojiro and Yoshioka, Koji and Suda, Tomoko and Katagiri, Seiji and Nagano, Masashi
Reproductive biology and endocrinology, ISSN 1477-7827, 11/2019, Volume 17, Issue 1, pp. 88 - 88
Endocrinology & Metabolism | Life Sciences & Biomedicine | Reproductive Biology | Science & Technology | Estradiol - metabolism | Follicle Stimulating Hormone - metabolism | Gonadal Steroid Hormones - metabolism | Oocytes - metabolism | Ovarian Follicle - growth & development | Cell Count | Cells, Cultured | Ovary - cytology | Granulosa Cells - metabolism | Oocytes - cytology | Testosterone - metabolism | Animals | Cattle | Progesterone - metabolism | Female | Anti-Mullerian Hormone - metabolism | Ovarian Follicle - cytology | Ovarian Follicle - metabolism | Granulosa Cells - cytology | Ovary - metabolism | Index Medicus | Anti-Müllerian hormone | Antral follicle count | In vitro growth | Steroidogenesis | Follicle stimulating hormone
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7. Full Text Existence of SARS-CoV-2 Entry Molecules in the Oral Cavity
by Sakaguchi, Wakako and Kubota, Nobuhisa and Shimizu, Tomoko and Saruta, Juri and Fuchida, Shinya and Kawata, Akira and Yamamoto, Yuko and Sugimoto, Masahiro and Yakeishi, Mayumi and Tsukinoki, Keiichi
International journal of molecular sciences, ISSN 1422-0067, 09/2020, Volume 21, Issue 17, p. 6000
Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Multidisciplinary | Science & Technology | Pandemics | Spike Glycoprotein, Coronavirus - metabolism | Humans | Betacoronavirus - metabolism | Virus Internalization | COVID-19 | Pneumonia, Viral - metabolism | Angiotensin-Converting Enzyme 2 | Mouth Mucosa - metabolism | Gingiva - metabolism | SARS-CoV-2 | Coronavirus Infections - metabolism | Saliva - metabolism | Peptidyl-Dipeptidase A - metabolism | Serine Endopeptidases - metabolism | Tongue - metabolism | Furin - metabolism | Tongue | Serine | Viral diseases | Viruses | Coatings | Angiotensin-converting enzyme 2--ACE2 | Proteins | Peptidyl-dipeptidase A | Protease | Furin | Localization | Severe acute respiratory syndrome | Proteinase inhibitors | Coronaviruses | Gene expression | Epithelium | Severe acute respiratory syndrome coronavirus 2 | Oral cavity | Protease inhibitors | Respiratory diseases | Angiotensin | Coating | Gingiva | Immunofluorescence | Saliva | Surface layers | Cytoplasm | Viral infections | Index Medicus | saliva | oral cavity | taste cell | ACE2 | tongue coating
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8. Full Text CNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome
by Uehara, Tomoko and Takenouchi, Toshiki and Yamaguchi, Yu and Daimon, Yumi and Suzuki, Hisato and Sakaguchi, Yuri and Kosaki, Kenjiro
American journal of medical genetics. Part A, ISSN 1552-4825, 04/2019, Volume 179, Issue 4, pp. 659 - 662
developmental delay | nasal voice | chromosome 12q15 | CNOT2 | intellectual disability | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Abnormalities, Multiple - pathology | Chromosome Deletion | Prognosis | Humans | Intellectual Disability - pathology | Repressor Proteins - genetics | Developmental Disabilities - genetics | Syndrome | Intellectual Disability - genetics | Developmental Disabilities - pathology | Female | Child | Chromosomes, Human, Pair 12 - genetics | Abnormalities, Multiple - genetics | Medical research | Phenotype | DNA microarrays | Analysis | Genes | Genetic research | Medicine, Experimental | Genetic aspects | Gene expression | Phenotypes | Enzymatic activity | Intellectual disabilities | Syndactyly | Chromosome 12 | Cleft lip/palate | Haploinsufficiency | Index Medicus
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9. Full Text 1097-P: Disposition Index Is a Predictor of Urinary Glucose Excretion in Subjects Treated with SGLT2 Inhibitors
by SAKAGUCHI, KAZUHIKO and SO, ANNA and ITO, JUN and KANEKO, AKIHIRO and MORITA, YASUKO and YAMADA, TOMOKO and MIURA, HIROSHI and OTOWA-SUEMATSU, NATSU and NAKAMURA, TOMOAKI and KOMADA, HISAKO and OKADA, YUKO and HIROTA, YUSHI and TAMORI, YOSHIKAZU and OGAWA, WATARU
Diabetes (New York, N.Y.), ISSN 0012-1797, 06/2020, Volume 69, Issue Supplement 1, p. 1097
Glucose tolerance | Excretion | Epidermal growth factor receptors | Secretion | Physiology | Glucose | Multivariate analysis | Diabetes mellitus (non-insulin dependent) | Insulin | Glomerular filtration rate
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10. Full Text 1020-P: Effects of Insulin Degludec and Insulin Glargine U300 on Interday Glycemic Variability in Individuals with Type 1 Diabetes: A Multicenter, Randomized, Crossover Study
by MIURA, HIROSHI and SAKAGUCHI, KAZUHIKO and KANEKO, AKIHIRO and ITO, JUN and MORITA, YASUKO and YAMADA, TOMOKO and OTOWA-SUEMATSU, NATSU and SO, ANNA and NAKAMURA, TOMOAKI and KOMADA, HISAKO and OKADA, YUKO and HIROTA, YUSHI and TAMORI, YOSHIKAZU and OGAWA, WATARU
Diabetes (New York, N.Y.), ISSN 0012-1797, 06/2020, Volume 69, Issue Supplement 1, p. 1020
Diabetes mellitus (insulin dependent) | Glucose | Diabetes | Hypoglycemia | Insulin
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11. Full Text Structural stability of flagellin subunit affects the rate of flagellin export in the absence of FliS chaperone
by Furukawa, Yukio and Inoue, Yumi and Sakaguchi, Aya and Mori, Yoko and Fukumura, Takuma and Miyata, Tomoko and Namba, Keiichi and Minamino, Tohru
Molecular microbiology, ISSN 0950-382X, 11/2016, Volume 102, Issue 3, pp. 405 - 416
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Microbiology | Science & Technology | Sigma Factor - metabolism | Flagella - metabolism | Molecular Chaperones - metabolism | Flagellin - biosynthesis | Flagellin - metabolism | Protein Binding | Bacterial Proteins - metabolism | Structure-Activity Relationship | Protein Transport | Salmonella typhimurium - metabolism | Proteolysis | Exports | Protein expression | Mutation | Protein folding | Index Medicus
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12. Full Text Haploinsufficiency of NCOR1 associated with autism spectrum disorder, scoliosis, and abnormal palatogenesis
by Sakaguchi, Yuri and Uehara, Tomoko and Suzuki, Hisato and Sakamoto, Yoshiaki and Fujiwara, Mineko and Kosaki, Kenjiro and Takenouchi, Toshiki
American journal of medical genetics. Part A, ISSN 1552-4825, 11/2018, Volume 176, Issue 11, pp. 2466 - 2469
NCOR1 | autism spectrum disorder | bifid uvula | intellectual disability | Smith‐Magenis syndrome | scoliosis | Smith-Magenis syndrome | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Medicine, Experimental | Medical research | Autism | Scoliosis | Analysis | Polymerase chain reaction | Splicing | Deacetylation | mRNA turnover | Reverse transcription | Mutation | Acetylation | Cleft lip/palate | Haploinsufficiency | Index Medicus
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