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    1. Pras, E; Pras, E; Bakhan, T; Levy-Nissenbaum, E; Lahat, H; Assia, EI; Garzozi, HJ; Kastner, DL; Goldman, B; Frydman, M
      A gene causing autosomal recessive cataract maps to the short arm of chromosome 3

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    2. Marziali, A; Akeson, M
      New DNA sequencing methods

      ANNUAL REVIEW OF BIOMEDICAL ENGINEERING
    3. Andrews, RP; Burrell, L; Rosa-Rosa, L; Cunningham, CM; Brzezinski, JL; Bernstein, JA; Hershey, GKK
      Analysis of the Ser786Pro interleukin-4 receptor alpha allelic variant in allergic and nonallergic asthma and its functional consequences

      CLINICAL IMMUNOLOGY
    4. Crawley, E; Kon, S; Woo, P
      Hereditary predisposition to low interleukin-10 production in children with extended oligoarticular juvenile idiopathic arthritis

      RHEUMATOLOGY
    5. 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
    6. Saito, S; Iida, A; Sekine, A; Miura, Y; Sakamoto, T; Ogawa, C; Kawauchi, S; Higuchi, S; Nakamura, Y
      Identification of 197 genetic variations in six human methyltransferase genes in the Japanese population

      JOURNAL OF HUMAN GENETICS
    7. 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
    8. 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
    9. Ohnishi, Y; Tanaka, T; Ozaki, K; Yamada, R; Suzuki, H; Nakamura, Y
      A high-throughput SNP typing system for genome-wide association studies

      JOURNAL OF HUMAN GENETICS
    10. 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
    11. 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
    12. Sekine, A; Saito, S; Iida, A; Mitsunobu, Y; Higuchi, S; Harigae, S; Nakamura, Y
      Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1, and L1CAM in the Japanese population

      JOURNAL OF HUMAN GENETICS
    13. Saito, S; Iida, A; Sekine, A; Eguchi, C; Miura, Y; Nakamura, Y
      Seventy genetic variations in human microsomal and soluble epoxide hydrolase genes (EPHX1 and EPHX2) in the Japanese population

      JOURNAL OF HUMAN GENETICS
    14. Ota, N; Nakajima, T; Nakazawa, I; Suzuki, T; Hosoi, T; Orimo, H; Inoue, S; Shirai, Y; Emi, M
      A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density

      JOURNAL OF HUMAN GENETICS
    15. Inazu, A; Nishimura, Y; Terada, Y; Mabuchi, H
      Effects of hepatic lipase gene promoter nucleotide variations on serum HDLcholesterol concentration in the general Japanese population

      JOURNAL OF HUMAN GENETICS
    16. Yoshida, S; Fukino, K; Harada, H; Nagai, H; Imoto, I; Inazawa, J; Takahashi, H; Teramoto, A; Emi, M
      The c-Jun NH2-terminal kinase3 (JNK3) gene: genomic structure, chromosomalassignment, and loss of expression in brain tumors

      JOURNAL OF HUMAN GENETICS
    17. Iida, A; Sekine, A; Saito, S; Kitamura, Y; Kitamoto, T; Osawa, S; Mishima, C; Nakamura, Y
      Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes

      JOURNAL OF HUMAN GENETICS
    18. Suzuki, C; Unoki, M; Nakamura, Y
      Identification and allelic frequencies of novel single-nucleotide polymorphisms in the DUSP1 and BTG1 genes

      JOURNAL OF HUMAN GENETICS
    19. 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
    20. Finnila, S; Majamaa, K
      Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish population

      JOURNAL OF HUMAN GENETICS
    21. 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
    22. 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
    23. Hirano, A; Nagai, H; Harada, H; Terada, Y; Haga, S; Kajiwara, T; Emi, M
      Nine novel single-nucleotide polymorphisms in the integrin beta 4 (ITGB4) gene in the Japanese population

      JOURNAL OF HUMAN GENETICS
    24. 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
    25. 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
    26. Kusser, B; Braun, A; Praun, M; Illi, S; von Mutius, E; Roscher, AA
      Polymorphisms in the bradykinin B2 receptor gene and childhood asthma

      BIOLOGICAL CHEMISTRY
    27. Meksem, K; Ruben, E; Hyten, DL; Schmidt, ME; Lightfoot, DA
      High-throughput genotyping for a polymorphism linked to soybean cyst nematode resistance gene Rhg4 by using Taqman (TM) probes

      MOLECULAR BREEDING
    28. Rice, SR; Niu, N; Berman, DB; Heston, LL; Sobell, JL
      Identification of single nucleotide polymorphisms (SNPs) and other sequence changes and estimation of nucleotide diversity in coding and flanking regions of the NMDAR1 receptor gene in schizophrenic patients

      MOLECULAR PSYCHIATRY
    29. Iwata, N; Ozaki, N; Inada, T; Goldman, D
      Association of a 5-MT5A receptor polymorphism, Pro15Ser, to schizophrenia

      MOLECULAR PSYCHIATRY
    30. Ronai, Z; Szekely, A; Nemoda, Z; Lakatos, K; Gervai, J; Staub, M; Sasvari-Szekely, M
      Association between Novelty Seeking and the-521 C/T polymorphism in the promoter region of the DRD4 gene

      MOLECULAR PSYCHIATRY
    31. Wolford, JK; Hanson, RL; Kobes, S; Bogardus, C; Prochazka, M
      Analysis of linkage disequilibrium between polymorphisms in the KCNJ9 genewith type 2 diabetes mellitus in Pima Indians

      MOLECULAR GENETICS AND METABOLISM
    32. Thameem, F; Wolford, JK; Bogardus, C; Prochazka, M
      Analysis of SLC19A2, on 1q23.3 encoding a thiamine transporter as a candidate gene for type 2 diabetes mellitus in Pima Indians

      MOLECULAR GENETICS AND METABOLISM
    33. Nakatani, K; Sando, S; Saito, I
      Scanning of guanine-guanine mismatches in DNA by synthetic ligands using surface plasmon resonance

      NATURE BIOTECHNOLOGY
    34. Ghilardi, G; Biondi, ML; Mangoni, J; Leviti, S; DeMonti, M; Guagnellini, E; Scorza, R
      Matrix metalloproteinase-1 promoter polymorphism 1G/2G is correlated with colorectal cancer invasiveness

      CLINICAL CANCER RESEARCH
    35. Milchevsky, JV; Ramensky, VE; Esipova, NG; Tumanyan, VG; Zorov, BS
      Molecular modelling of disease-causing single-nucleotide polymorphisms in collagen

      SAR AND QSAR IN ENVIRONMENTAL RESEARCH
    36. Nickerson, ML; Warren, MB; Zbar, B; Schmidt, LS
      Random mutagenesis-PCR to introduce alterations into defined DNA sequencesfor validation of SNP and mutation detection methods

      HUMAN MUTATION
    37. Kubota, T; Horie, M; Takano, M; Yoshida, H; Takenaka, K; Watanabe, E; Tsuchiya, T; Otani, H; Sasayama, S
      Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias

      JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
    38. Takakura, S; Kohno, T; Manda, R; Okamoto, A; Tanaka, T; Yokota, J
      Genetic alterations and expression of the protein phosphatase 1 genes in human cancers

      INTERNATIONAL JOURNAL OF ONCOLOGY
    39. Livneh, A; Aksentijevich, I; Langevitz, P; Torosyna, Y; G-Shoham, N; Shinar, Y; Pras, E; Zaks, N; Padeh, S; Kastner, DL; Pras, M
      A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behcet's disease (FMF-BD)

      EUROPEAN JOURNAL OF HUMAN GENETICS
    40. Zhao, XB; Feng, JD; Li, N; Wang, AH; Wu, CX
      Genetic typing of mitochondrial DNA in sheep (Ovis aries)

      PROGRESS IN NATURAL SCIENCE
    41. Richards, RI
      Dynamic mutations: a decade of unstable expanded repeats in human genetic disease

      HUMAN MOLECULAR GENETICS
    42. Saetre, GP; Borge, T; Lindell, J; Moum, T; Primmer, CR; Sheldon, BC; Haavie, J; Johnsen, A; Ellegren, H
      Speciation, introgressive hybridization and nonlinear rate of molecular evolution in flycatchers

      MOLECULAR ECOLOGY
    43. Wennerholm, A; Johansson, I; Hidestrand, M; Bertilsson, L; Gustafsson, LL; Ingelman-Sundberg, M
      Characterization of the CYP2D6*29 allele commonly present in a blade Tanzanian population causing reduced catalytic activity

      PHARMACOGENETICS
    44. Ameyaw, MM; Regateiro, F; Li, T; Liu, XH; Tariq, M; Mobarek, A; Thornton, N; Folayan, GO; Githang'a, J; Indalo, A; Ofori-Adjei, D; Price-Evans, DA; McLeod, HL
      MDR1 pharmacogenetics: frequency of the C3435T mutation in exon 26 is significantly influenced by ethnicity

      PHARMACOGENETICS
    45. Andolfatto, P
      Adaptive hitchhiking effects on genome variability

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    46. Fu, Y; Katsuya, T; Higaki, J; Asai, T; Fukuda, M; Takiuchi, S; Hatanaka, Y; Rakugi, H; Ogihara, T
      A common mutation of low-density lipoprotein receptor gene is associated with essential hypertension among Japanese

      JOURNAL OF HUMAN HYPERTENSION
    47. Barbaux, S; Poirier, O; Cambien, F
      Use of degenerate oligonucleotide primed PCR (DOP-PCR) for the genotyping of low-concentration DNA samples

      JOURNAL OF MOLECULAR MEDICINE-JMM
    48. Naito, E; Umetsu, K; Yuasa, I; Dewa, K; Sumi, H; Yamanouchi, H
      A novel dimorphism in the human SRY gene: usefulness in human migration studies

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    49. Adan, RAH; Vink, T
      Drug target discovery by pharmacogenetics: mutations in the melanocortin system and eating disorders

      EUROPEAN NEUROPSYCHOPHARMACOLOGY
    50. Sugawara, F; Yamada, Y; Kuroe, A; Someya, Y; Kubota, A; Ihara, Y; Takahashi, K; Seino, Y
      Human TSC-22 gene: No association with type 2 diabetes

      INTERNAL MEDICINE
    51. Sugiyama, T; Kato, N; Ishinaga, Y; Yamori, Y; Yazaki, Y
      Evaluation of selected polymorphisms of the Mendelian hypertensive diseasegenes in the Japanese population

      Hypertension research
    52. Tanaka, K; Nishioka, J; Kato, K; Nakamura, A; Mouri, T; Miki, C; Kusunoki, M; Nobori, T
      Mitotic checkpoint protein hsMAD2 as a marker predicting liver metastasis of human gastric cancers

      JAPANESE JOURNAL OF CANCER RESEARCH
    53. Matsushita, M; Miyakawa, H; Tanaka, A; Hijikata, M; Kikuchi, K; Fujikawa, H; Arai, J; Sainokami, S; Hino, K; Terai, I; Mishiro, S; Gershwin, ME
      Single nucleotide polymorphisms of the mannose-binding lectin are associated with susceptibility to primary biliary cirrhosis

      JOURNAL OF AUTOIMMUNITY
    54. Angeloni, D; Duh, FM; Wei, MH; Johnson, BE; Lerman, MI
      A C-to-A single nucleotide polymorphism in intron 2 of the human CACNA2D2 gene that maps at 3p21.3

      MOLECULAR AND CELLULAR PROBES
    55. Okajima, K; Paznekas, WA; Burstyn, T; Jabs, EW
      Polymorphisms in the human SNAIL (SNAI1) gene

      MOLECULAR AND CELLULAR PROBES
    56. Olivier, M; Bustos, VI; Levy, MR; Smick, GA; Moreno, I; Bushard, JM; Almendras, AA; Sheppard, K; Zierten, DL; Aggarwal, A; Carlson, CS; Foster, BD; Vo, N; Kelly, L; Liu, X; Cox, DR
      Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21

      GENOMICS
    57. McGrath, SB; Bounpheng, M; Torres, L; Calavetta, M; Scott, CB; Suh, Y; Rines, D; van Orsouw, N; Vijg, J
      High-speed, multicolor fluorescent two-dimensional gene scanning

      GENOMICS
    58. Hsieh, YY; Tsai, FJ; Chang, CC; Chen, WC; Tsai, CH; Tsai, HD; Lin, CC
      p21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis

      JOURNAL OF CLINICAL LABORATORY ANALYSIS
    59. Kallioniemi, OP
      Biochip technologies in cancer research

      ANNALS OF MEDICINE
    60. Saunders, CL; Crockford, GP; Bishop, DT; Barrett, JH
      Using single nucleotide, polymorphisms to investigate association between a candidate gene and disease

      GENETIC EPIDEMIOLOGY
    61. Fijal, BA; Kim, LL; Buxbaum, SG; Witte, JS
      Predicting quantitative trait levels by modeling SNP interaction

      GENETIC EPIDEMIOLOGY
    62. Suchard, MA; Bailey, JN; Elashoff, DA; Sinsheimer, JS
      SNPing away at candidate genes

      GENETIC EPIDEMIOLOGY
    63. Saito, H; Tada, S; Ebinuma, H; Wakabayashi, K; Takagi, T; Saito, Y; Nakamoto, N; Kurita, S; Ishii, H
      Interferon regulatory factor 1 promoter polymorphism and response to type 1 interferon

      JOURNAL OF CELLULAR BIOCHEMISTRY
    64. Helmberg, A
      DNA-microarrays: novel techniques to study aging and guide gerontologic medicine

      EXPERIMENTAL GERONTOLOGY
    65. Liu, Z; Kim, S; Kucuktas, H; Karsi, A
      Multiple isoforms and an unusual cathodic isoform of creatine kinase from channel catfish (Ictalurus punctatus)

      GENE
    66. Anello, G; Gueant, JL; Romano, C; Barone, C; Pettinato, R; Pillot, T; Rodriguez, RM; Romano, A; Bosco, P
      Allele epsilon 4 of apolipoprotein E gene is less frequent in Down syndrome patient of the Sicilian population and has no influence on the grade of mental retardation

      NEUROSCIENCE LETTERS
    67. Shinmura, K; Yamaguchi, S; Saitoh, T; Kohno, T; Yokota, J
      Somatic mutations and single nucleotide polymorphisms of base excision repair genes involved in the repair of 8-hydroxyguanine in damaged DNA

      CANCER LETTERS
    68. Freeze, HH; Westphal, V
      Balancing N-linked glycosylation to avoid disease

      BIOCHIMIE
    69. Blakely, RD
      Physiological genomics of antidepressant targets: Keeping the periphery inmind

      JOURNAL OF NEUROSCIENCE
    70. Shubitowski, DM; Venta, PJ; Douglass, CL; Zhou, RX; Ewart, SL
      Polymorphism identification within 50 equine gene-specific sequence taggedsites

      ANIMAL GENETICS
    71. Snapir, A; Heinonen, P; Tuomainen, TP; Lakka, TA; Kauhanen, J; Salonen, JT; Scheinin, M
      G-protein beta(3) subunit C825T polymorphism: no association with risk forhypertension and obesity

      JOURNAL OF HYPERTENSION
    72. Wang, W; Bittles, AH
      Imperfect units of an extended microsatellite structure involving single nucleotide changes

      ELECTROPHORESIS
    73. Ronai, Z; Barta, C; Guttman, A; Lakatos, K; Gervai, J; Staub, M; Sasvari-Szekely, M
      Genotyping the-521C/T functional polymorphism in the promoter region of dopamine D4 receptor (DRD4) gene

      ELECTROPHORESIS
    74. Andersson, H; van der Wijngaart, W; Stemme, G
      Micromachined filter-chamber array with passive valves for biochemical assays on beads

      ELECTROPHORESIS
    75. Zhou, GH; Kamahori, M; Okano, K; Harada, K; Kambara, H
      Miniaturized pyrosequencer for DNA analysis with capillaries to deliver deoxynucleotides

      ELECTROPHORESIS
    76. Kaczanowski, R; Trzeciak, L; Kucharczyk, K
      Multitemperature single-strand conformation polymorphism

      ELECTROPHORESIS
    77. Biros, E; Kalina, I; Kohut, A; Stubna, J; Salagovic, J
      Germ line polymorphisms of the tumor suppressor gene p53 and lung cancer

      LUNG CANCER
    78. Thameem, F; Wolford, JK; Bogardus, C; Prochazka, M
      Analysis of PBX1 as a candidate gene for type 2 diabetes mellitus in Pima Indians

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    79. Cigler, T; LaForge, KS; McHugh, PF; Kapadia, SU; Leal, SM; Kreek, MJ
      Novel and previously reported single-nucleotide polymorphisms in the human5-HT(1B)receptor gene: No association with cocaine or alcohol abuse or dependence

      AMERICAN JOURNAL OF MEDICAL GENETICS
    80. Sobetzko, D; Sander, T; Becker, CM
      Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    81. Greenwood, TA; Alexander, M; Keck, PE; McElroy, S; Sadovnick, AD; Remick, RA; Kelsoe, JR
      Evidence for linkage disequilibrium between the dopamine transporter and bipolar disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    82. Kurumaji, A; Nomoto, H; Yamada, K; Yoshikawa, T; Toru, M
      No association of two missense variations of the benzodiazepine receptor (peripheral) gene and mood disorders in a Japanese sample

      AMERICAN JOURNAL OF MEDICAL GENETICS
    83. Kurumaji, A; Nomoto, H; Okano, T; Toru, M
      An association study between polymorphisms of L1CAM gene and schizophreniain a Japanese sample

      AMERICAN JOURNAL OF MEDICAL GENETICS
    84. Furuya, T; Salstrom, JL; Joe, B; Hashiramoto, A; Dobbins, DE; Wilder, RL; Remmers, EF
      Polymorphisms of the tumor necrosis factor receptor type 1 locus among autoimmune susceptible and resistant inbred rat strains

      IMMUNOGENETICS
    85. Amexis, G; Fineschi, N; Chumakov, K
      Correlation of genetic variability with safety of mumps vaccine Urabe AM9 strain

      VIROLOGY
    86. Melotto, M; Kelly, JD
      Fine mapping of the Co-4 locus of common bean reveals a resistance gene candidate, COK-4, that encodes for a protein kinase

      THEORETICAL AND APPLIED GENETICS
    87. Cato, SA; Gardner, RC; Kent, J; Richardson, TE
      A rapid PCR-based method for genetically mapping ESTs

      THEORETICAL AND APPLIED GENETICS
    88. Zhang, BP; Dhillon, S; Geary, I; Howell, WM; Iannotti, F; Day, INM; Ye, S
      Polymorphisms in matrix metalloproteinase-1,-3,-9, and-12 genes in relation to subarachnoid hemorrhage

      STROKE
    89. Bar-Ziv, R; Libchaber, A
      Effects of DNA sequence and structure on binding of RecA to single-stranded DNA

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    90. Chasman, D; Adams, RM
      Predicting the functional consequences of non-synonymous single nucleotidepolymorphisms: Structure-based assessment of amino acid variation

      JOURNAL OF MOLECULAR BIOLOGY
    91. Kriegesmann, B; Dierkes, B; Leeb, T; Jansen, S; Brenig, B
      Two breed-specific bovine MC1-R alleles in Brown Swiss and Saler breeds

      JOURNAL OF DAIRY SCIENCE
    92. Matsubara, A; Wasson, JC; Donelan, SS; Welling, CM; Glaser, B; Permutt, MA
      Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes

      DIABETOLOGIA
    93. Wolford, JK; Hanson, RL; Bogardus, C; Prochazka, M
      Analysis of the Lamin A/C gene as a candidate for Type II diabetes susceptibility in Pima Indians

      DIABETOLOGIA
    94. Colomb, E; Nguyen, TD; Bechetoille, A; Dascotte, JC; Valtot, F; Brezin, AP; Berkani, M; Copin, B; Gomez, L; Polansky, JR; Garchon, HJ
      Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open-angle glaucoma

      CLINICAL GENETICS
    95. Wedemeyer, N; Potter, T
      Flow cytometry: an 'old' tool for novel applications in medical genetics

      CLINICAL GENETICS
    96. Schmitz, G; Aslanidis, C; Lackner, KJ
      Pharmacogenomics: implications for laboratory medicine

      CLINICA CHIMICA ACTA
    97. Ye, S; Dhillon, S; Turner, SJ; Bateman, AC; Theaker, JM; Pickering, RM; Day, I; Howell, WM
      Invasiveness of cutaneous malignant melanoma is influenced by Matrix Metalloproteinase 1 gene polymorphism

      CANCER RESEARCH
    98. Osawa, H; Onuma, H; Murakami, A; Ochi, M; Nishimiya, T; Kato, K; Shimizu, I; Fujii, Y; Ohashi, J; Makino, H
      Systematic search for single nucleotide polymorphisms in the insulin gene:Evidence for a high frequency of-23T -> A in Japanese subjects

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    99. Ueda, T; Ugawa, S; Ishida, Y; Shibata, Y; Murakami, S; Shimada, S
      Identification of coding single-nucleotide polymorphisms in human taste receptor genes involving bitter tasting

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    100. Kozaki, T; Shono, T; Tomita, T; Kono, Y
      Polymorphism in the acetylcholinesterase gene of the housefly, Musca domestica L. (Diptera : Muscidae)

      APPLIED ENTOMOLOGY AND ZOOLOGY


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Documento generato il 28/10/20 alle ore 19:18:31