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Wyświetlanie 1-15 z 15
Tytuł:
Effect of DNMT3A polymorphisms on CpG island hypermethylation in gastric mucosa.
Autorzy:
Takano H; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Shibata T; Department of Gastroenterology, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, 470-1192, Japan.
Nakamura M; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Sakurai N; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Hayashi T; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Ota M; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Nomura-Horita T; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Hayashi R; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Shimasaki T; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Otsuka T; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Tahara T; Department of Gastroenterology and Hepatology, Kansai Medical University, 2-5-1 Shin-machi, Hirakata, Osaka, 573-1010, Japan.
Arisawa T; Department of Gastroenterology, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan. .
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Źródło:
BMC medical genetics [BMC Med Genet] 2020 Oct 16; Vol. 21 (1), pp. 205. Date of Electronic Publication: 2020 Oct 16.
Typ publikacji:
Journal Article
MeSH Terms:
DNA Methylation*
Polymorphism, Single Nucleotide*
CpG Islands/*genetics
DNA (Cytosine-5-)-Methyltransferases/*genetics
Gastric Mucosa/*metabolism
Aged ; Alleles ; Antigens, CD/genetics ; Cadherins/genetics ; Cyclin-Dependent Kinase Inhibitor p16/genetics ; DNA Methyltransferase 3A ; Death-Associated Protein Kinases/genetics ; Female ; Gastric Mucosa/microbiology ; Gene Frequency ; Genotype ; Helicobacter Infections/diagnosis ; Helicobacter Infections/microbiology ; Helicobacter pylori/physiology ; Humans ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Influence of MIF polymorphisms on CpG island hyper-methylation of CDKN2A in the patients with ulcerative colitis.
Autorzy:
Sakurai N; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Shibata T; Department of Gastroenterology, Fujita Health University, 1-98, Dengakugakubo, Kutsukake-cho, Toyoake, 470-1192, Japan.
Nakamura M; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Takano H; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Hayashi T; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Ota M; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Nomura-Horita T; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Hayashi R; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Shimasaki T; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Ostuka T; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan.
Tahara T; Department of Gastroenterology and Hepatology, Kansai Medical University, 2-5-1 Shin-machi, Hirakata, Osaka, 573-1010, Japan.
Arisawa T; Department of Gastroenterology, Kanazawa Medical University, 1-1, Daigaku, Uchinada-machi, Ishikawa, 920-0293, Japan. .
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Źródło:
BMC medical genetics [BMC Med Genet] 2020 Oct 12; Vol. 21 (1), pp. 201. Date of Electronic Publication: 2020 Oct 12.
Typ publikacji:
Journal Article
MeSH Terms:
DNA Methylation*
Polymorphism, Single Nucleotide*
Colitis, Ulcerative/*genetics
CpG Islands/*genetics
Cyclin-Dependent Kinase Inhibitor p16/*genetics
Intramolecular Oxidoreductases/*genetics
Macrophage Migration-Inhibitory Factors/*genetics
Adult ; Alleles ; Colitis, Ulcerative/diagnosis ; Female ; Gene Frequency ; Genotype ; Humans ; Male ; Middle Aged ; Risk Factors
Czasopismo naukowe
Tytuł:
Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population.
Autorzy:
Sakono T; Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
Meguro A; Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
Takeuchi M; Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
Yamane T; Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
Teshigawara T; Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.; Yokosuka Chuoh Eye Clinic, Kanagawa, Japan.; Tsurumi Chuoh Eye Clinic, Kanagawa, Japan.
Kitaichi N; Department of Ophthalmology, Health Sciences University of Hokkaido, Hokkaido, Japan.
Horie Y; Department of Ophthalmology, Health Sciences University of Hokkaido, Hokkaido, Japan.
Namba K; Department of Ophthalmology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Hokkaido, Japan.
Ohno S; Department of Ophthalmology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Hokkaido, Japan.
Nakao K; Department of Ophthalmology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Sakamoto T; Department of Ophthalmology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Sakai T; Department of Ophthalmology, Jikei University School of Medicine, Tokyo, Japan.
Nakano T; Department of Ophthalmology, Jikei University School of Medicine, Tokyo, Japan.
Keino H; Department of Ophthalmology, Kyorin University School of Medicine, Tokyo, Japan.
Okada AA; Department of Ophthalmology, Kyorin University School of Medicine, Tokyo, Japan.
Takeda A; Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Ito T; Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Mashimo H; Department of Ophthalmology, Japan Community Health care Organization Osaka Hospital, Osaka, Japan.
Ohguro N; Department of Ophthalmology, Japan Community Health care Organization Osaka Hospital, Osaka, Japan.
Oono S; Department of Ophthalmology, Saga University Faculty of Medicine, Saga, Japan.; Hoshiai Eye Clinic, Saitama, Japan.
Enaida H; Department of Ophthalmology, Saga University Faculty of Medicine, Saga, Japan.
Okinami S; Department of Ophthalmology, Saga University Faculty of Medicine, Saga, Japan.; Department of Ophthalmology, Kurashiki Central Hospital, Okayama, Japan.
Horita N; Department of Pulmonology, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
Ota M; Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.; Division of Hepatology and Gastroenterology, Department of Medicine, Shinshu University School of Medicine, Nagano, Japan.
Mizuki N; Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
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Źródło:
PloS one [PLoS One] 2020 May 21; Vol. 15 (5), pp. e0233464. Date of Electronic Publication: 2020 May 21 (Print Publication: 2020).
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Polymorphism, Single Nucleotide*
DNA-Binding Proteins/*genetics
Early Growth Response Protein 2/*genetics
Oxygenases/*genetics
Receptors, Interleukin/*genetics
Transcription Factors/*genetics
Uveomeningoencephalitic Syndrome/*genetics
Adult ; Alleles ; Asian People/genetics ; Carotenoids ; Case-Control Studies ; Female ; Gene Frequency ; Genome-Wide Association Study ; HLA-DR4 Antigen/genetics ; Humans ; Japan ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
A cis-eQTL of HLA-DPB1 Affects Susceptibility to Type 1 Autoimmune Hepatitis.
Autorzy:
Yamazaki T; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.
Umemura T; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan. .; Research Center for Next Generation Medicine, Shinshu University, Matsumoto, Japan. .
Joshita S; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.; Research Center for Next Generation Medicine, Shinshu University, Matsumoto, Japan.
Yoshizawa K; Department of Gastroenterology, NHO Ueda Medical Center, Ueda, Japan.
Tanaka E; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.
Ota M; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.
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Źródło:
Scientific reports [Sci Rep] 2018 Aug 09; Vol. 8 (1), pp. 11924. Date of Electronic Publication: 2018 Aug 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Quantitative Trait Loci*
Genetic Predisposition to Disease/*genetics
HLA-DP beta-Chains/*genetics
Hepatitis, Autoimmune/*genetics
3' Untranslated Regions/genetics ; Aged ; Alleles ; Asian People/genetics ; Female ; Gene Frequency ; Genetic Predisposition to Disease/ethnology ; Genotype ; Hepatitis, Autoimmune/classification ; Hepatitis, Autoimmune/ethnology ; Humans ; Japan ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Genetic Association of PTPN22 Polymorphisms with Autoimmune Hepatitis and Primary Biliary Cholangitis in Japan.
Autorzy:
Umemura T; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.
Joshita S; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.
Yamazaki T; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.
Komatsu M; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.
Katsuyama Y; Department of Pharmacy, Shinshu University Hospital, Matsumoto, Japan.
Yoshizawa K; Department of Gastroenterology, NHO Shinshu Ueda Medical Center, Ueda, Japan.
Tanaka E; Department of Medicine, Division of Hepatology and Gastroenterology, Shinshu University School of Medicine, Matsumoto, Japan.
Ota M; Department of Legal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
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Źródło:
Scientific reports [Sci Rep] 2016 Jul 11; Vol. 6, pp. 29770. Date of Electronic Publication: 2016 Jul 11.
Typ publikacji:
Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Haplotypes*
Mutation, Missense*
Polymorphism, Single Nucleotide*
Cholangitis/*genetics
Hepatitis, Autoimmune/*genetics
Protein Tyrosine Phosphatase, Non-Receptor Type 22/*genetics
Adult ; Aged ; Aged, 80 and over ; Cholangitis/enzymology ; Cholangitis/epidemiology ; Female ; Hepatitis, Autoimmune/enzymology ; Hepatitis, Autoimmune/epidemiology ; Humans ; Japan/epidemiology ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study.
Autorzy:
Nishisako M; a Department of Ophthalmology , Yokohama City University School of Medicine , Yokohama , Kanagawa , Japan .
Meguro A; a Department of Ophthalmology , Yokohama City University School of Medicine , Yokohama , Kanagawa , Japan .
Nomura E; a Department of Ophthalmology , Yokohama City University School of Medicine , Yokohama , Kanagawa , Japan .
Yamane T; a Department of Ophthalmology , Yokohama City University School of Medicine , Yokohama , Kanagawa , Japan .
Takeuchi M; a Department of Ophthalmology , Yokohama City University School of Medicine , Yokohama , Kanagawa , Japan .; b Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health , Bethesda , Maryland , USA .
Ota M; c Department of Legal Medicine , Shinshu University School of Medicine , Nagano , Japan .
Kashiwagi K; d Department of Ophthalmology , University of Yamanashi, Faculty of Medicine , Yamanashi , Japan .
Mabuchi F; d Department of Ophthalmology , University of Yamanashi, Faculty of Medicine , Yamanashi , Japan .
Iijima H; d Department of Ophthalmology , University of Yamanashi, Faculty of Medicine , Yamanashi , Japan .
Kawase K; e Department of Ophthalmology , Gifu University Graduate School of Medicine , Gifu , Japan .
Yamamoto T; e Department of Ophthalmology , Gifu University Graduate School of Medicine , Gifu , Japan .
Nakamura M; f Department of Surgery, Division of Ophthalmology , Kobe University Graduate School of Medicine , Kobe , Hyogo , Japan .
Negi A; f Department of Surgery, Division of Ophthalmology , Kobe University Graduate School of Medicine , Kobe , Hyogo , Japan .
Sagara T; g Department of Ophthalmology , Yamaguchi University School of Medicine , Ube , Yamaguchi , Japan .
Nishida T; g Department of Ophthalmology , Yamaguchi University School of Medicine , Ube , Yamaguchi , Japan .
Inatani M; h Department of Ophthalmology and Visual Science , Graduate School of Medical Sciences, Kumamoto University , Kumamoto , Japan .; i Department of Ophthalmology, Faculty of Medical Science , University of Fukui , Fukui , Japan .
Tanihara H; h Department of Ophthalmology and Visual Science , Graduate School of Medical Sciences, Kumamoto University , Kumamoto , Japan .
Aihara M; j Department of Ophthalmology , University of Tokyo School of Medicine , Tokyo , Japan .
Araie M; j Department of Ophthalmology , University of Tokyo School of Medicine , Tokyo , Japan .
Fukuchi T; k Division of Ophthalmology and Visual Science , Graduate School of Medical and Dental Sciences, Niigata University , Niigata , Japan .
Abe H; k Division of Ophthalmology and Visual Science , Graduate School of Medical and Dental Sciences, Niigata University , Niigata , Japan .
Higashide T; l Department of Ophthalmology and Visual Science , Kanazawa University Graduate School of Medical Science , Kanazawa , Ishikawa , Japan .
Sugiyama K; l Department of Ophthalmology and Visual Science , Kanazawa University Graduate School of Medical Science , Kanazawa , Ishikawa , Japan .
Kanamoto T; m Department of Ophthalmology and Visual Science , Graduate School of Biomedical Sciences, Hiroshima University , Hiroshima , Japan .
Kiuchi Y; m Department of Ophthalmology and Visual Science , Graduate School of Biomedical Sciences, Hiroshima University , Hiroshima , Japan .
Iwase A; n Department of Ophthalmology , Tajimi Municipal Hospital , Gifu , Japan .
Chin S; o Department of Ophthalmology , Hokkaido University Graduate School of Medicine , Sapporo , Hokkaido , Japan , and.
Ohno S; o Department of Ophthalmology , Hokkaido University Graduate School of Medicine , Sapporo , Hokkaido , Japan , and.
Inoko H; p Department of Genetic Information, Division of Molecular Life Science , Tokai University School of Medicine , Sagamihara , Kanagawa , Japan.
Mizuki N; a Department of Ophthalmology , Yokohama City University School of Medicine , Yokohama , Kanagawa , Japan .
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Źródło:
Ophthalmic genetics [Ophthalmic Genet] 2016 Jun; Vol. 37 (2), pp. 194-200. Date of Electronic Publication: 2016 Jan 15.
Typ publikacji:
Journal Article
MeSH Terms:
Polymorphism, Single Nucleotide*
Excitatory Amino Acid Transporter 3/*genetics
Low Tension Glaucoma/*genetics
Adult ; Asian People/genetics ; Female ; Gene Frequency ; Genetic Association Studies ; Genotype ; Genotyping Techniques ; Humans ; Japan/epidemiology ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Lymphocyte Antigen 75 Polymorphisms Are Associated with Disease Susceptibility and Phenotype in Japanese Patients with Inflammatory Bowel Disease.
Autorzy:
Hirayama A; Department of Medicine, Division of Gastroenterology and Hepatology, Shinshu University School of Medicine, Matsumoto, Japan.
Joshita S; Department of Medicine, Division of Gastroenterology and Hepatology, Shinshu University School of Medicine, Matsumoto, Japan.
Kitahara K; Department of Medicine, Division of Gastroenterology and Hepatology, Shinshu University School of Medicine, Matsumoto, Japan.
Mukawa K; Department of Gastroenterology, Japanese Red Cross Society Suwa Hospital, Suwa, Japan.
Suga T; Department of Medicine, Division of Gastroenterology and Hepatology, Shinshu University School of Medicine, Matsumoto, Japan.
Umemura T; Department of Medicine, Division of Gastroenterology and Hepatology, Shinshu University School of Medicine, Matsumoto, Japan.
Tanaka E; Department of Medicine, Division of Gastroenterology and Hepatology, Shinshu University School of Medicine, Matsumoto, Japan.
Ota M; Department of Legal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
Pokaż więcej
Źródło:
Disease markers [Dis Markers] 2016; Vol. 2016, pp. 6485343. Date of Electronic Publication: 2016 Nov 14.
Typ publikacji:
Comparative Study; Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Antigens, CD/*genetics
Biomarkers/*analysis
Haplotypes/*genetics
Inflammatory Bowel Diseases/*genetics
Lectins, C-Type/*genetics
Minor Histocompatibility Antigens/*genetics
Polymorphism, Single Nucleotide/*genetics
Receptors, Cell Surface/*genetics
Adult ; Case-Control Studies ; Female ; Follow-Up Studies ; Genome-Wide Association Study ; Genotype ; Humans ; Inflammatory Bowel Diseases/epidemiology ; Japan/epidemiology ; Male ; Middle Aged ; Phenotype ; Prognosis
Czasopismo naukowe
Tytuł:
Polymorphisms of the tissue inhibitor of metalloproteinase 3 gene are associated with resistance to high-altitude pulmonary edema (HAPE) in a Japanese population: a case control study using polymorphic microsatellite markers.
Autorzy:
Kobayashi N; First Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Nagano, Japan ; Department of Legal Medicine, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.
Hanaoka M
Droma Y
Ito M
Katsuyama Y
Kubo K
Ota M
Pokaż więcej
Źródło:
PloS one [PLoS One] 2013 Aug 22; Vol. 8 (8), pp. e71993. Date of Electronic Publication: 2013 Aug 22 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Altitude Sickness/*genetics
Genetic Predisposition to Disease/*genetics
Hypertension, Pulmonary/*genetics
Tissue Inhibitor of Metalloproteinase-3/*genetics
Adolescent ; Adult ; Aged ; Alleles ; Altitude Sickness/ethnology ; Asian People/genetics ; Case-Control Studies ; Female ; Gene Frequency ; Genetic Predisposition to Disease/ethnology ; Genome-Wide Association Study ; Genotype ; Haplotypes ; Humans ; Hypertension, Pulmonary/ethnology ; Japan ; Linkage Disequilibrium ; Male ; Microsatellite Repeats/genetics ; Middle Aged ; Young Adult
SCR Disease Name:
Pulmonary edema of mountaineers
Czasopismo naukowe
Tytuł:
Identification of single nucleotide polymorphisms regulating peripheral blood mRNA expression with genome-wide significance: an eQTL study in the Japanese population.
Autorzy:
Sasayama D; Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Ogawahigashi, Kodaira, Tokyo, Japan.
Hori H
Nakamura S
Miyata R
Teraishi T
Hattori K
Ota M
Yamamoto N
Higuchi T
Amano N
Kunugi H
Pokaż więcej
Źródło:
PloS one [PLoS One] 2013; Vol. 8 (1), pp. e54967. Date of Electronic Publication: 2013 Jan 24.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Quantitative Trait Loci*
RNA, Messenger/*blood
Adult ; Female ; Genome-Wide Association Study ; Humans ; Japan ; Likelihood Functions ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
The association of Toll-like receptor 4 gene polymorphisms with the development of emphysema in Japanese subjects: a case control study.
Autorzy:
Ito M; First Department of Medicine, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Japan.
Hanaoka M
Droma Y
Kobayashi N
Yasuo M
Kitaguchi Y
Horiuchi T
Ikegawa K
Katsuyama Y
Kubo K
Ota M
Pokaż więcej
Źródło:
BMC research notes [BMC Res Notes] 2012 Jan 18; Vol. 5, pp. 36. Date of Electronic Publication: 2012 Jan 18.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Asian People/*genetics
Emphysema/*genetics
Pulmonary Disease, Chronic Obstructive/*genetics
Toll-Like Receptor 4/*genetics
Aged ; Alleles ; Case-Control Studies ; Emphysema/complications ; Emphysema/pathology ; Female ; Forced Expiratory Volume ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Haplotypes ; Humans ; Linkage Disequilibrium ; Male ; Middle Aged ; Odds Ratio ; Phenotype ; Pulmonary Disease, Chronic Obstructive/complications ; Pulmonary Disease, Chronic Obstructive/pathology ; Up-Regulation
Czasopismo naukowe
Tytuł:
Possible association between interleukin-1β gene and schizophrenia in a Japanese population.
Autorzy:
Sasayama D; Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, 187-8502, Japan. />Hori H
Teraishi T
Hattori K
Ota M
Iijima Y
Tatsumi M
Higuchi T
Amano N
Kunugi H
Pokaż więcej
Źródło:
Behavioral and brain functions : BBF [Behav Brain Funct] 2011 Aug 16; Vol. 7, pp. 35. Date of Electronic Publication: 2011 Aug 16.
Typ publikacji:
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Asian People/*genetics
Interleukin-1beta/*genetics
Polymorphism, Single Nucleotide/*genetics
Schizophrenia/*genetics
Adult ; Female ; Genetic Association Studies/methods ; Haplotypes/genetics ; Humans ; Male ; Middle Aged ; Schizophrenia/diagnosis
Czasopismo naukowe
Tytuł:
Association of interleukin-1β genetic polymorphisms with cognitive performance in elderly females without dementia.
Autorzy:
Sasayama D; Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan. />Hori H
Teraishi T
Hattori K
Ota M
Matsuo J
Kawamoto Y
Kinoshita Y
Higuchi T
Amano N
Kunugi H
Pokaż więcej
Źródło:
Journal of human genetics [J Hum Genet] 2011 Aug; Vol. 56 (8), pp. 613-6. Date of Electronic Publication: 2011 May 26.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Cognition/*physiology
Interleukin-1beta/*genetics
Psychomotor Performance/*physiology
Aged ; Analysis of Variance ; Dementia/genetics ; Female ; Gene Frequency ; Genotype ; Genotyping Techniques ; Humans ; Intelligence/genetics ; Intelligence/physiology ; Male ; Middle Aged ; Wechsler Scales
Czasopismo naukowe
Tytuł:
Modulation of cortisol responses to the DEX/CRH test by polymorphisms of the interleukin-1beta gene in healthy adults.
Autorzy:
Sasayama D; Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan. />Hori H
Iijima Y
Teraishi T
Hattori K
Ota M
Fujii T
Higuchi T
Amano N
Kunugi H
Pokaż więcej
Źródło:
Behavioral and brain functions : BBF [Behav Brain Funct] 2011 Jul 05; Vol. 7, pp. 23. Date of Electronic Publication: 2011 Jul 05.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Corticotropin-Releasing Hormone*
Dexamethasone*
Hydrocortisone/*metabolism
Interleukin-1beta/*genetics
Pituitary-Adrenal Function Tests/*methods
Polymorphism, Single Nucleotide/*genetics
Adult ; Alleles ; Female ; Genotype ; Humans ; Hypothalamo-Hypophyseal System/physiology ; Interleukin-1beta/physiology ; Male ; Middle Aged ; Pituitary-Adrenal System/physiology ; Sex Characteristics
Czasopismo naukowe
Tytuł:
Investigation of association between TLR9 gene polymorphisms and VKH in Japanese patients.
Autorzy:
Ito R; Department of Ophthalmology and Visual Science, Yokohama City University Graduate School of Medicine, Yokohama, Kanagawa, Japan.
Ota M
Meguro A
Katsuyama Y
Uemoto R
Nomura E
Nishide T
Kitaichi N
Horie Y
Namba K
Ohno S
Inoko H
Mizuki N
Pokaż więcej
Źródło:
Ocular immunology and inflammation [Ocul Immunol Inflamm] 2011 Jun; Vol. 19 (3), pp. 202-5.
Typ publikacji:
Journal Article
MeSH Terms:
Polymorphism, Single Nucleotide*
Asian People/*genetics
Toll-Like Receptor 9/*genetics
Uveomeningoencephalitic Syndrome/*genetics
Gene Frequency ; Genotype ; Haplotypes ; Humans ; Linkage Disequilibrium
Czasopismo naukowe
Tytuł:
Lack of association of Toll-like receptor 9 gene polymorphism with Behçet's disease in Japanese patients.
Autorzy:
Ito A; Department of Ophthalmology, Yokohama City University School of Medicine, Yokohama, Kanagawa, Japan.
Ota M
Katsuyama Y
Inoko H
Ohno S
Mizuki N
Pokaż więcej
Źródło:
Tissue antigens [Tissue Antigens] 2007 Nov; Vol. 70 (5), pp. 423-6. Date of Electronic Publication: 2007 Sep 14.
Typ publikacji:
Journal Article; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
MeSH Terms:
Polymorphism, Single Nucleotide*
Behcet Syndrome/*genetics
Toll-Like Receptor 9/*genetics
Asian People ; Female ; Genetic Predisposition to Disease ; Humans ; Japan ; Male
Czasopismo naukowe
    Wyświetlanie 1-15 z 15

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