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    1. Schafer, AI
      Genetic polymorphisms in arterial thrombosis and vascular disease - Commentary

      JOURNAL OF ENDOVASCULAR THERAPY
    2. Iida, A; Saito, S; Sekine, A; Kitamura, Y; Kondo, K; Mishima, C; Osawa, S; Harigae, S; Nakamura, Y
      High-density single-nucleotide polymorphism (SNP) map of the 150-kb regioncorresponding to the human ATP-binding cassette transporter A1 (ABCA1) gene

      JOURNAL OF HUMAN GENETICS
    3. Iwasaki, H; Shinohara, Y; Ezura, Y; Ishida, R; Kodaira, M; Kajita, M; Nakajima, T; Shiba, T; Emi, M
      Thirteen single-nucleotide polymorphisms in the human osteopontin gene identified by sequencing of the entire gene in Japanese individuals

      JOURNAL OF HUMAN GENETICS
    4. Iwasa, H; Kurabayashi, M; Nagai, R; Nakamura, Y; Tanaka, T
      Genetic variations in five genes involved in the excitement of cardiomyocytes

      JOURNAL OF HUMAN GENETICS
    5. Shinohara, Y; Ezura, Y; Iwasaki, H; Nakazawa, I; Ishida, R; Kodaira, M; Kajita, M; Shiba, T; Emi, M
      Linkage disequilibrium and haplotype analysis among ten single-nucleotide polymorphisms of interleukin 11 identified by sequencing of the gene

      JOURNAL OF HUMAN GENETICS
    6. Iida, A; Saito, S; Sekine, A; Kitamoto, T; Kitamura, Y; Mishima, C; Osawa, S; Kondo, K; Harigae, S; Nakamura, Y
      Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families

      JOURNAL OF HUMAN GENETICS
    7. Iwasa, H; Kurabayashi, M; Nagai, R; Nakamura, Y; Tanaka, T
      Multiple single-nucleotide polymorphisms (SNPs) in the Japanese populationin six candidate genes for long QT syndrome

      JOURNAL OF HUMAN GENETICS
    8. Takeoka, S; Unoki, M; Onouchi, Y; Doi, S; Fujiwara, H; Miyatake, A; Fujita, K; Inoue, I; Nakamura, Y; Tamari, M
      Amino-acid substitutions in the IKAP gene product significantly increase risk for bronchial asthma in children

      JOURNAL OF HUMAN GENETICS
    9. Nishio, Y; Noguchi, E; Ito, S; Ichikawa, E; Umebayashi, Y; Otsuka, F; Arinami, T
      Mutation and association analysis of the interferon regulatory factor 2 gene (IRF2) with atopic dermatitis

      JOURNAL OF HUMAN GENETICS
    10. Iida, A; Saito, S; Sekine, A; Mishima, C; Kondo, K; Kitamura, Y; Harigae, S; Osawa, S; Nakamura, Y
      Catalog of 258 single-nucleotide polymorphisms (SNPs) in genes encoding three organic anion transporters, three organic anion-transporting polypeptides, and three NADH : ubiquinone oxidoreductase flavoproteins

      JOURNAL OF HUMAN GENETICS
    11. Ishida, R; Ezura, Y; Iwasaki, H; Nakazawa, I; Kajita, M; Kodaira, M; Ito, H; Emi, M
      Linkage disequilibrium and haplotype analysis among four novel single-nucleotide polymorphisms in the human leukemia inhibitory factor (LIF) gene

      JOURNAL OF HUMAN GENETICS
    12. Iida, A; Saito, S; Sekine, A; Harigae, S; Osawa, S; Mishima, C; Kondo, K; Kitamura, Y; Nakamura, Y
      Catalog of 46 single-nucleotide polymorphisms (SNPs) in the microsomal glutathione S-transferase 1 (MGST1) gene

      JOURNAL OF HUMAN GENETICS
    13. Iida, A; Ohnishi, Y; Ozaki, K; Ariji, Y; Nakamura, Y; Tanaka, T
      High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2

      JOURNAL OF HUMAN GENETICS
    14. Iwasaki, H; Ota, N; Nakajima, T; Shinohara, Y; Kodaira, M; Kajita, M; Emi, M
      Five novel single-nucleotide polymorphisms of human interferon gamma identified by sequencing the entire gene

      JOURNAL OF HUMAN GENETICS
    15. Kajita, M; Iwasaki, H; Ota, N; Shinohara, Y; Kodaira, M; Nakajima, T; Emi, M
      Novel single nucleotide polymorphisms of the human colony-stimulating factor 2 (CSF2) gene identified by sequencing the entire gene

      JOURNAL OF HUMAN GENETICS
    16. Shinohara, Y; Iwasaki, H; Ota, N; Nakajima, T; Kodaira, M; Kajita, M; Shiba, T; Emi, M
      Novel single nucleotide polymorphisms of the human nuclear factor kappa-B 2 gene identified by sequencing the entire gene

      JOURNAL OF HUMAN GENETICS
    17. Sreelekha, TT; Ramadas, K; Pandey, M; Thomas, G; Nalinakumari, KR; Pillai, MR
      Genetic polymorphism of CYP1A1, GSTM1 and GSTT1 genes in Indian oral cancer

      ORAL ONCOLOGY
    18. Doi, Y; Minowa, M; Uchiyama, M; Okawa, M
      Subjective sleep quality and sleep problems in the general Japanese adult population

      PSYCHIATRY AND CLINICAL NEUROSCIENCES
    19. Furuno, T; Kawanishi, C; Iseki, E; Onishi, H; Sugiyama, N; Suzuki, K; Kosaka, K
      No evidence of an association between CYP2D6 polymorphisms among Japanese and dementia with Lewy bodies

      PSYCHIATRY AND CLINICAL NEUROSCIENCES
    20. He, X; Zhu, DL; Chu, SL; Jin, L; Xiong, MM; Wang, GL; Zhang, WZ; Zhou, HF; Mao, SY; Zhan, YM; Zhuang, QN; Liu, XM; Zhao, Y; Huang, W
      alpha-adducin gene and essential hypertension in China

      CLINICAL AND EXPERIMENTAL HYPERTENSION
    21. Pan, HC; Lin, HM; Ku, WY; Li, TC; Li, SY; Lin, CC; Hsiao, KM
      Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan:implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1

      EUROPEAN JOURNAL OF HUMAN GENETICS
    22. Ramamoorthy, Y; Tyndale, RF; Sellers, EM
      Cytochrome P450 2D6.1 and cytochrome P450 2D6.10 differ in catalytic activity for multiple substrates

      PHARMACOGENETICS
    23. Nowotny, P; Kwon, JM; Goate, AM
      SNP analysis to dissect human traits

      CURRENT OPINION IN NEUROBIOLOGY
    24. Leung, TF; Tang, NLS; Chan, IHS; Li, AM; Ha, G; Lam, CWK
      A polymorphism in the coding region of interleukin-13 gene is associated with atopy but not asthma in Chinese children

      CLINICAL AND EXPERIMENTAL ALLERGY
    25. Tanaka, K; Sugiura, H; Uehara, M; Hashimoto, Y; Donnelly, C; Montgomery, DS
      Lack of association between atopic eczema and the genetic variants of interleukin-4 and the interleukin-4 receptor alpha chain gene: heterogeneity ofgenetic backgrounds on immunoglobulin E production in atopic eczema patients

      CLINICAL AND EXPERIMENTAL ALLERGY
    26. Yamada, S; Onda, M; Kato, S; Matsuda, N; Matsuhisa, T; Yamada, N; Miki, M; Matsukura, N
      Genetic differences in CYP2C19 single nucleotide polymorphisms among four Asian populations

      JOURNAL OF GASTROENTEROLOGY
    27. Davis, MP; Homsi, J
      The importance of cytochrome P450 monooxygenase CYP2D6 in palliative medicine

      SUPPORTIVE CARE IN CANCER
    28. Li, T; Underhill, J; Liu, XH; Sham, PC; Donaldson, P; Murray, RM; Wright, P; Collier, DA
      Transmission disequilibrium analysis of HLA class II DRB1, DQA1, DQB1 and DPB1 polymorphisms in schizophrenia using family trios from a Han Chinese population

      SCHIZOPHRENIA RESEARCH
    29. Hong, SH; Song, J; Kim, JQ
      Genetic variation of the methylenetetrahydrofolate reductase and cystathionine beta-synthase genes in Korean patients with coronary artery disease and a new polymorphism in intron 7

      MOLECULAR AND CELLULAR PROBES
    30. Sharma, D; Gupta, M; Thelma, BK
      Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population

      GENETIC EPIDEMIOLOGY
    31. Tan, QH; Yashin, AI; Bladbjerg, EM; de Maat, MPM; Andersen-Ranberg, K; Jeune, B; Christensen, K; Vaupel, JW
      Variations of cardiovascular disease associated genes exhibit sex-dependent influence on human longevity

      EXPERIMENTAL GERONTOLOGY
    32. Ota, M; Katsuyama, Y; Liu, CY; Takayanagi, K; Asamura, H; Fukushima, H
      Allelic structure and distribution of two STR loci, D8S58O and D22S442, inthe Japanese population

      FORENSIC SCIENCE INTERNATIONAL
    33. Douabin-Gicquel, V; Soriano, N; Ferran, H; Wojcik, F; Palierne, E; Tamim, S; Jovelin, T; McKie, AT; Le Gall, JY; David, V; Mosser, J
      Identification of 96 single nucleotide polymorphisms in eight genes involved in iron metabolism: efficiency of bioinformatic extraction compared witha systematic sequencing approach

      HUMAN GENETICS
    34. Dermaut, B; Roks, G; Theuns, J; Rademakers, R; Houwing-Duistermaat, JJ; Serneels, S; Hofman, A; Breteler, MMB; Cruts, M; Van Broeckhoven, C; van Duijn, CM
      Variable expression of presenilin 1 is not a major determinant of risk forlate-onset Alzheimer's Disease

      JOURNAL OF NEUROLOGY
    35. Takahashi, H; Echizen, H
      Pharmacogenetics of warfarin elimination and its clinical implications

      CLINICAL PHARMACOKINETICS
    36. Scordo, MG; Aklillu, E; Yasar, U; Dahl, ML; Spina, E; Ingelman-Sundberg, M
      Genetic polymorphism of cytochrome P4502C9 in a Caucasian and a black African population

      BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
    37. Yoon, YR; Shon, JH; Kim, MK; Lim, YC; Lee, HR; Park, JY; Cha, IJ; Shin, JG
      Frequency of cytochrome P4502C9 mutant alleles in a Korean population

      BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
    38. Izumi, Y; Morino, H; Oda, M; Maruyama, H; Udaka, F; Kameyama, M; Nakamura, S; Kawakami, H
      Genetic studies in Parkinson's disease with an alpha-synuclein/NACP gene polymorphism in Japan

      NEUROSCIENCE LETTERS
    39. Buzza, M; Fripp, Y; Mitchell, RJ
      Apolipoprotein AI and CIII gene polymorphisms and their association with lipid levels in Italian, Greek and Anglo-Irish populations of Australia

      ANNALS OF HUMAN BIOLOGY
    40. Luiselli, D; Maiolini, E; Pelotti, S; Bini, C; Ferri, G; Pappalardo, G
      The HUMFIBRA (FGA) polymorphism in an Italian population and a world-wide frequency distribution analysis

      ANNALS OF HUMAN BIOLOGY
    41. Asano-Kato, N; Fukagawa, K; Tsubota, K; Urayama, K; Takahashi, S; Fujishima, H
      Quantitative evaluation of atopic blepharitis by scoring of eyelid conditions and measuring the water content of the skin and evaporation from the eyelid surface

      CORNEA
    42. Redman, AR
      Implications of cytochrome P4502C9 polymorphism on Warfarin metabolism anddosing

      PHARMACOTHERAPY
    43. Teh, LK; Ismail, R; Yusoff, R; Hussein, A; Isa, MN; Rahman, ARA
      Heterogeneity of the CYP2D6 gene among Malays in Malaysia

      JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS
    44. Nagahara, A; Miwa, H; Yamada, T; Kurosawa, A; Ohkura, R; Sato, N
      Five-day proton pump inhibitor-based quadruple therapy regimen is more effective than 7-day triple therapy regimen for Helicobacter pylori infection

      ALIMENTARY PHARMACOLOGY & THERAPEUTICS
    45. Gisbert, JP; Pajares, JM
      Helicobacter pylori therapy: First-line options and rescue regimen

      DIGESTIVE DISEASES
    46. Miwa, H; Misawa, H; Yamada, T; Nagahara, A; Ohtaka, K; Sato, N
      Clarithromycin resistance, but not CYP2C-19 polymorphism, has a major impact on treatment success in 7-day treatment regimen for cure of H-pylori infection - A multiple logistic regression analysis

      DIGESTIVE DISEASES AND SCIENCES
    47. Limprasert, P; Saechan, V; Ruangdaraganon, N; Sura, T; Vasiknanote, P; Jaruratanasirikul, S; Brown, WT
      Haplotype analysis at the FRAXA locus in Thai subjects

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Eriksson, CJP; Fukunaga, T; Sarkola, T; Chen, WJ; Chen, CC; Ju, JM; Cheng, ATA; Yamamoto, H; Kohlenberg-Muller, K; Kimura, M; Murayama, M; Matsushita, S; Kashima, H; Higuchi, S; Carr, L; Viljoen, D; Brooke, L; Stewart, T; Foroud, T; Su, J; Li, TK; Whitfield, JB
      Functional relevance of human ADH polymorphism

      ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
    49. Song, N; Tan, W; Xing, DY; Lin, DX
      CYP 1A1 polymorphism and risk of lung cancer in relation to tobacco smoking: a case-control study in China

      CARCINOGENESIS
    50. Hiraoka, M; Taniguchi, T; Nakai, H; Kino, M; Okada, Y; Tanizawa, A; Tsukahara, H; Ohshima, Y; Muramatsu, I; Mayumi, M
      No evidence for AT2R gene derangement in human urinary tract anomalies

      KIDNEY INTERNATIONAL
    51. Morrison, AC; Doris, PA; Folsom, AR; Nieto, FJ; Boerwinkle, E
      G-protein beta 3 subunit and alpha-adducin polymorphisms and risk of subclinical and clinical stroke

      STROKE
    52. Sy, SKB; Tang, BK; Pastrakuljic, A; Roberts, EA; Kalow, W
      Detailed characterization of experimentally derived human hepatic CYP1A1 activity and expression using differential inhibition of ethoxyresorufin O-deethylation by fluvoxamine

      EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY
    53. Kabesch, M
      Asthma and allergic diseases. Genetic disposition and environmental factors

      MONATSSCHRIFT KINDERHEILKUNDE
    54. Yoshimoto, T; Yamamoto, T; Uchihi, R; Tamaki, K; Huang, XL; Mizutani, M; Tanaka, M; Armour, JAL; Katsumata, Y
      A new tripler STR system without irregular alleles by silver staining and its potential application to forensic analysis

      JOURNAL OF FORENSIC SCIENCES
    55. Yamamoto, T; Tamaki, K; Huang, XL; Yoshimoto, T; Mizutani, M; Uchihi, R; Katsumata, Y; Jeffreys, AJ
      The application of minisatellite variant repeat mapping by PCR (MVR-PCR) in a paternity case showing false exclusion due to STR mutation

      JOURNAL OF FORENSIC SCIENCES
    56. Russo, GT; Meigs, JB; Cupples, LA; Demissie, S; Otvos, JD; Wilson, PWF; Lahoz, C; Cucinotta, D; Couture, P; Mallory, T; Schaefer, EJ; Ordovas, JM
      Association of the Sst-I polymorphism at the APOC3 gene locus with variations in lipid levels, lipoprotein subclass profiles and coronary heart disease risk: the Framingham offspring study

      ATHEROSCLEROSIS
    57. Gaedigk, A; Casley, WL; Tyndale, RF; Sellers, EM; Jurima-Romet, M; Leeder, JS
      Cytochrome P4502C9 (CYP2C9) allele frequencies in canadian native indian and inuit populations

      CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
    58. Faradz, SMH; Leggo, J; Murray, A; Lam-Po-Tang, PRL; Buckley, MF; Holden, JJA
      Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asian populations

      ANNALS OF HUMAN GENETICS
    59. Kimura, H; Sekiguchi, K; Kitamori, T; Sawada, T; Mukaida, M
      Assay of spherical cell surface molecules by thermal lens microscopy and its application to blood cell substances

      ANALYTICAL CHEMISTRY
    60. Hebert, LE; Scherr, PA; McCann, JJ; Beckett, LA; Evans, DA
      Is the risk of developing Alzheimer's disease greater for women than for men?

      AMERICAN JOURNAL OF EPIDEMIOLOGY
    61. Shea, SH; Wall, TL; Carr, LG; Li, TK
      ADH2 and alcohol-related phenotypes in Ashkenazic Jewish American college students

      BEHAVIOR GENETICS
    62. Gauderman, WJ; Siegmund, KD
      Gene-environment interaction and affected sib pair linkage analysis

      HUMAN HEREDITY
    63. Matsuzaka, Y; Makino, S; Nakajima, K; Tomizawa, M; Oka, A; Bahram, S; Kulski, JK; Tamiya, G; Inoko, H
      New polymorphic microsatellite markers in the human MHC class III region

      TISSUE ANTIGENS
    64. Wattanapitayakul, SK; Mihm, MJ; Young, AP; Bauer, JA
      Therapeutic implications of human endothelial nitric oxide synthase gene polymorphism

      TRENDS IN PHARMACOLOGICAL SCIENCES
    65. Iwasa, H; Itoh, T; Nagai, R; Nakamura, Y; Tanaka, T
      Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

      JOURNAL OF HUMAN GENETICS
    66. Grzybowska, E; Butkiewicz, D; Motykiewicz, G; Chorazy, M
      The effect of the genetic polymorphisms of CYP1A1,CYP2D6, GSTM1 and CSTP1 on aromatic DNA adduct levels in the population of healthy women

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    67. Zusterzeel, PLM; Nelen, WLDM; Roelofs, HMJ; Peters, WHM; Blom, HJ; Steegers, EAP
      Polymorphisms in biotransformation enzymes and the risk for recurrent early pregnancy loss

      MOLECULAR HUMAN REPRODUCTION
    68. Jorm, AF; Prior, M; Sanson, A; Smart, D; Zhang, Y; Easteal, S
      Association of a functional polymorphism of the serotonin transporter genewith anxiety-related temperament and behavior problems in children: a longitudinal study from infancy to the mid-teens

      MOLECULAR PSYCHIATRY
    69. Chistyakov, DA; Savost'anov, KV; Turakulov, RI; Nosikov, VV
      Genetic determinants of Graves disease

      MOLECULAR GENETICS AND METABOLISM
    70. Wang, XL; Wang, J
      Endothelial nitric oxide synthase gene sequence variations and vascular disease

      MOLECULAR GENETICS AND METABOLISM
    71. Chistyakov, DA; Savost'anov, KV; Turakulov, RI; Petunina, NA; Trukhina, LV; Kudinova, AV; Balabolkin, MI; Nosikov, VV
      Complex association analysis of Graves disease using a set of polymorphic markers

      MOLECULAR GENETICS AND METABOLISM
    72. Nagahara, A; Miwa, H; Ogawa, K; Kurosawa, A; Ohkura, R; Iida, N; Sato, N
      Addition of metronidazole to rabeprazole-amoxicillin-clarithromycin regimen for Helicobacter pylori infection provides an excellent cure rate with five-day therapy

      HELICOBACTER
    73. Postma, DS; Koppelman, GH; Meyers, DA
      The genetics of atopy and airway hyperresponsiveness

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    74. London, SJ; Yuan, JM; Coetzee, GA; Gao, YT; Ross, RK; Yu, MC
      CYP1A1 I462V genetic polymorphism and lung cancer risk in a cohort of men in Shanghai, China

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    75. Rao, CR; Gutierrez, MI; Bhatia, K; Fend, F; Franklin, J; Appaji, L; Gallo, G; O'Conor, G; Lalitha, N; Magrath, I
      Association of Burkitt's lymphoma with the Epstein-Barr virus in two developing countries

      LEUKEMIA & LYMPHOMA
    76. Tanaka, H; Shimada, Y; Harada, H; Shinoda, M; Hatooka, S; Imamura, M; Ishizaki, K
      Polymorphic variation of the ARP gene on 3p21 in Japanese esophageal cancer patients

      ONCOLOGY REPORTS
    77. Crawford, DC; Zhang, FP; Wilson, B; Warren, ST; Sherman, SL
      Fragile X CGG repeat structures among African-Americans: identification ofa novel factor responsible for repeat instability

      HUMAN MOLECULAR GENETICS
    78. Sarmanova, J; Tynkova, L; Susova, S; Gut, I; Soucek, P
      Genetic polymorphisms of biotransformation enzymes: allele frequencies in the population of the Czech Republic

      PHARMACOGENETICS
    79. Bhasker, CR; McKinnon, W; Stone, A; Lo, ACT; Kubota, T; Ishizaki, T; Miners, JO
      Genetic polymorphism of UDP-glucuronosyltransferase 2B7 (UGT2B7) at amino acid 268: ethnic diversity of alleles and potential clinical significance

      PHARMACOGENETICS
    80. Stucker, I; Jacquet, M; de Waziers, I; Cenee, S; Beaune, P; Kremers, P; Hemon, D
      Relation between inducibility of CYP1A1, GSTM1 and lung cancer in a Frenchpopulation

      PHARMACOGENETICS
    81. Houlston, RS
      CYP1A1 polymorphisms and lung cancer risk: a meta-analysis

      PHARMACOGENETICS
    82. Smart, J; Daly, AK
      Variation in induced CYP1A1 levels: relationship to CYP1A1, Ah receptor and GSTM1 polymorphisms

      PHARMACOGENETICS
    83. Alam, S; Liyou, N; Davis, D; Tresillian, M; Johnson, AG
      The 460Trp polymorphism of the human alpha-adducin gene is not associated with isolated systolic hypertension in elderly Australian Caucasians

      JOURNAL OF HUMAN HYPERTENSION
    84. Psaty, BM; Doggen, C; Vos, HL; Vandenbroucke, JP; Rosendaal, FR
      Association of the alpha-adducin polymorphism with blood pressure and riskof myocardial infarction

      JOURNAL OF HUMAN HYPERTENSION
    85. Melander, O; Bengtsson, K; Orho-Melander, M; Lindblad, U; Forsblom, C; Rastam, L; Groop, L; Hulthen, UL
      Role of the Gly460Trp polymorphism of the alpha-adducin gene in primary hypertension in Scandinavians

      JOURNAL OF HUMAN HYPERTENSION
    86. Adachi, K; Iwasawa, T; Ono, T
      Screening for abdominal aortic aneurysms during a basic medical checkup inresidents of a Japanese rural community

      SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY
    87. Ferrari, P; Bianchi, G
      Genetic mapping and tailored antihypertensive therapy

      CARDIOVASCULAR DRUGS AND THERAPY
    88. Ferrari, P; Ferrandi, M; Torielli, L; Tripodi, G; Bianchi, G
      PST 2238: A new antihypertensive compound that modulates the Na-K pump 'invivo' and 'in vitro'

      Hypertension research
    89. Bray, MS; Li, L; Turner, ST; Kardia, SLR; Boerwinkle, E
      Association and linkage analysis of the alpha-adducin gene and blood pressure

      AMERICAN JOURNAL OF HYPERTENSION
    90. Ranade, K; Hsuing, AC; Wu, KD; Chang, MS; Chen, YT; Hebert, J; Chen, YDI; Olshen, R; Curb, D; Dzau, V; Botstein, D; Cox, D; Risch, N
      Lack of evidence for an association between alpha-adducin and blood pressure regulation in Asian populations

      AMERICAN JOURNAL OF HYPERTENSION
    91. Barlassina, C; Norton, GR; Samani, NJ; Woodwiss, AJ; Candy, GC; Radevski, I; Citterio, L; Bianchi, G; Cusi, D
      alpha-adducin polymorphism in hypertensives of South African ancestry

      AMERICAN JOURNAL OF HYPERTENSION
    92. Bianchi, G; Cusi, D
      Association and linkage analysis of alpha-adducin polymorphism: Is the glass half full or half empty?

      AMERICAN JOURNAL OF HYPERTENSION
    93. Jeng, JR
      Carotid thickening, cardiac hypertrophy, and angiotensin converting enzymegene polymorphism in patients with hypertension

      AMERICAN JOURNAL OF HYPERTENSION
    94. Bhattacharyya, S; Leaves, NI; Wiltshire, S; Cox, R; Cookson, WOCM
      A high-density genetic map of the chromosome 13q14 atopy locus

      GENOMICS
    95. Miwa, H; Sato, N
      Functional dyspepsia and Helicobacter pylori infection: A recent consensusup to 1999

      JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
    96. Thompson, MD; Gonzalez, N; Nguyen, T; Comings, DE; George, SR; O'Dowd, BF
      Serotonin transporter gene polymorphisms in alcohol dependence

      ALCOHOL
    97. Hara, M; Takada, A; Ro, A; Saito, K; Kido, A
      Association between LDLR polymorphism and diseases in the Japanese population: aging and distribution of the polymorphism

      FORENSIC SCIENCE INTERNATIONAL
    98. Indulski, JA; Lutz, W
      Metabolic genotype in relation to individual susceptibility to environmental carcinogens

      INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH
    99. Wang, XL
      Cigarette smoking, DNA variants in endothelial nitric oxide synthase gene and vascular disease

      CIGARETTE SMOKING AND THE KIDNEY
    100. Kim, KW; Jhoo, HJ; Lee, KU; Lee, DY; Lee, JH; Youn, JY; Lee, BJ; Woo, JI
      No association between presenilin 1 (PS1) intronic polymorphism and sporadic Alzheimer's disease in Koreans

      JOURNAL OF NEURAL TRANSMISSION


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Documento generato il 21/01/20 alle ore 01:04:57