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La ricerca find articoli where soggetti phrase all words 'SNP' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 203 riferimenti
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    1. Palmer, LJ; Cookson, WOCM
      Using single nucleotide polymorphisms as a means to understanding the pathophysiology of asthma

      RESPIRATORY RESEARCH
    2. Mizoguchi, M; Tamura, T; Yamaki, A; Higashihara, E; Shimizu, Y
      Mutations of the PKD1 gene among Japanese autosomal dominant polycystic kidney disease patients, including one heterozygous mutation identified in members of the same family

      JOURNAL OF HUMAN GENETICS
    3. 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
    4. 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
    5. Mabuchi, A; Ikeda, T; Fukuda, A; Koshizuka, Y; Hiraoka, H; Miyoshi, K; Haga, N; Kawaguchi, H; Kawakami, A; Yamamoto, S; Takatori, Y; Nakamura, K; Ikegawa, S
      Identification of sequence polymorphisms of the COMP (cartilage oligomericmatrix protein) gene and association study in osteoarthrosis of the knee and hip joints

      JOURNAL OF HUMAN GENETICS
    6. 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
    7. 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
    8. 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
    9. 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
    10. 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
    11. 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
    12. 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
    13. 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
    14. 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
    15. 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
    16. Kyo, K; Muto, T; Nagawa, H; Lathrop, GM; Nakamura, Y
      Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease

      JOURNAL OF HUMAN GENETICS
    17. 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
    18. Schneider, K; Weisshaar, B; Borchardt, DC; Salamini, F
      SNP frequency and allelic haplotype structure of Beta vulgaris expressed genes

      MOLECULAR BREEDING
    19. Kirov, G; Lowry, CA; Stephens, M; Oldfield, S; O'Donovan, MC; Lightman, SL; Owen, MJ
      Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder

      MOLECULAR PSYCHIATRY
    20. Saito, T; Guan, F; Papolos, DF; Lau, S; Klein, M; Fann, CSJ; Lachman, HM
      Mutation analysis of SYNJ1: a possible candidate gene for chromosome 21q22-linked bipolar disorder

      MOLECULAR PSYCHIATRY
    21. Saito, T; Guan, F; Papolos, DF; Rajouria, N; Fann, CSJ; Lachman, HM
      Polymorphism in SNAP29 gene promoter region associated with schizophrenia

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

      MOLECULAR PSYCHIATRY
    23. 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
    24. Vasques, LR; Pereira, LV
      Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs)

      DNA RESEARCH
    25. Tan, Z; Jiang, SS; Lin, ZX; Zhang, BF; Yu, J; Feng, GY; He, L
      Identification of SNPs in human gamma aminobutyric acid A receptor gamma 2gene

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    26. Cutler, DJ; Zwick, ME; Carrasquillo, MM; Yohn, CT; Tobin, KP; Kashuk, C; Mathews, DJ; Shah, NA; Eichler, EE; Warrington, JA; Chakravarti, A
      High-throughput variation detection and genotyping using microarrays

      GENOME RESEARCH
    27. Carter, DA; Taylor, JW; Dechairo, B; Burt, S; Koenig, GL; White, TJ
      Amplified single-nucleotide polymorphisms and a (GA)(n) microsatellite marker reveal genetic differentiation between populations of Histoplasma capsulatum from the Americas

      FUNGAL GENETICS AND BIOLOGY
    28. Rhodes, RB; Lewis, K; Shultz, J; Huber, S; Voelkerding, KV; Leonard, DGB; Tsongalis, GJ; Kephart, DD
      Analysis of the factor V Leiden mutation using the READIT Assay

      MOLECULAR DIAGNOSIS
    29. Zhang, G; Zhang, SZ; Chen, W; Qiu, WM; Wu, H; Wang, JM; Luo, JC; Gu, XC; Cotton, RGH
      Go!Poly: A gene-oriented polymorphism database

      HUMAN MUTATION
    30. Gelhaus, A; Scheding, A; Browne, E; Burchard, GD; Horstmann, RD
      Variability of the CD36 gene in West Africa

      HUMAN MUTATION
    31. Immervoll, T; Loesgen, S; Dutsch, G; Gohlke, H; Herbon, N; Klugbauer, S; Dempfle, A; Bickeboller, H; Becker-Follmann, J; Ruschendorf, F; Saar, K; Reis, A; Wichmann, HE; Wjst, M
      Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes

      HUMAN MUTATION
    32. Chen, H; Jawahar, S; Qian, YM; Duong, QY; Chan, GY; Parker, A; Meyer, JM; Moore, KJ; Chayen, S; Gross, DJ; Glaser, B; Permutt, MA; Fricker, LD
      Missense polymorphism in the human carboxypeptlidase E gene alters enzymatic activity

      HUMAN MUTATION
    33. Killian, JK; Oka, Y; Jang, HS; Fu, XL; Waterland, RA; Sohda, T; Sakaguchi, S; Jirtle, RL
      Mannose 6-phosphate/insulin-like growth factor 2 receptor (M6P/IGF2R) variants in American and Japanese populations

      HUMAN MUTATION
    34. Xiao, WZ; Oefner, PJ
      Denaturing high-performance liquid chromatography: A review

      HUMAN MUTATION
    35. Gut, IG
      Automation in genotyping of single nucleotide polymorphisms

      HUMAN MUTATION
    36. Lipkin, SM; Wang, V; Stoler, DL; Anderson, GR; Kirsch, I; Hadley, D; Lynch, HT; Collins, FS
      Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers

      HUMAN MUTATION
    37. Lehnert, V; Holzwarth, J; Ott, M; Thompson, A; Demmak, S; Foernzler, D
      A semi-automated system for analysis and storage of SNPs

      HUMAN MUTATION
    38. Collins, A; Ennis, S; Taillon-Miller, P; Kwok, PY; Morton, NE
      Allelic association with SNPs: Metrics, populations, and the linkage disequilibrium map

      HUMAN MUTATION
    39. Wang, Z; Moult, J
      SNPs, protein structure, and disease

      HUMAN MUTATION
    40. Underhill, PA; Passarino, G; Lin, AA; Marzuki, S; Oefner, PJ; Cavalli-Sforza, LL; Chambers, GK
      Maori origins, Y-chromosome haplotypes and implications for human history in the Pacific

      HUMAN MUTATION
    41. Ott, J; Hoh, J
      Statistical multilocus methods for disequilibrium analysis in complex traits

      HUMAN MUTATION
    42. Rohde, K; Fuerst, R
      Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information

      HUMAN MUTATION
    43. Bray, MS; Boerwinkle, E; Doris, PA
      High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry:Practice, problems and promise

      HUMAN MUTATION
    44. Ye, F; Li, MS; Taylor, JD; Nguyen, Q; Colton, HM; Casey, WM; Wagner, M; Weiner, MP; Chen, JW
      Fluorescent microsphere-based readout technology for multiplexed human single nucleotide polymorphism analysis and bacterial identification

      HUMAN MUTATION
    45. 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
    46. Cox, DG; Boillot, C; Canzian, F
      Data mining: Efficiency of using sequence databases for polymorphism discovery

      HUMAN MUTATION
    47. Ramana, GV; Su, B; Jin, L; Singh, L; Wang, N; Underhill, P; Chakraborty, R
      Y-chromosome SNP haplotypes suggest evidence of gene flow among caste, tribe, and the migrant Siddi populations of Andhra Pradesh, South India

      EUROPEAN JOURNAL OF HUMAN GENETICS
    48. Prince, JA; Feuk, L; Sawyer, SL; Gottfries, J; Ricksten, A; Nagga, K; Bogdanovic, N; Blennow, K; Brookes, AJ
      Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's disease

      EUROPEAN JOURNAL OF HUMAN GENETICS
    49. Abecasis, GR; Cherny, SS; Cardon, LR
      The impact of genotyping error on family-based analysis of quantitative traits

      EUROPEAN JOURNAL OF HUMAN GENETICS
    50. Miller, RD; Kwok, PY
      The birth and death of human single-nucleotide polymorphisms: new experimental evidence and implications for human history and medicine

      HUMAN MOLECULAR GENETICS
    51. Cardon, LR; Witte, J; Elston, R
      Testing drug response in the presence of genetic information - Reply

      PHARMACOGENETICS
    52. 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
    53. Lee, YJ; Lee, KH; Kim, HRC; Jessup, JM; Seol, DW; Kim, TH; Billiar, TR; Song, YK
      Sodium nitroprusside enhances TRAIL-induced apoptosis via a mitochondria-dependent pathway in human colorectal carcinoma CX-1 cells

      ONCOGENE
    54. Wright, AF
      Strategies for mapping susceptibility genes in age-related maculopathy

      EYE
    55. 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
    56. Gill, P
      An assessment of the utility of single nucleotide polymorphisms (SNPs) forforensic purposes

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    57. Beja-Pereira, A; Bento, P; Ferrand, N; Brenig, B
      Genetic polymorphism of the 17th exon at porcine RYR1 locus: a new variantin a local Portuguese pig breed demonstrated by SSCP analysis

      JOURNAL OF ANIMAL BREEDING AND GENETICS-ZEITSCHRIFT FUR TIERZUCHTUNG UND ZUCHTUNGSBIOLOGIE
    58. 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
    59. Ganesh, S; Shoda, K; Amano, K; Uchiyama, A; Kumada, S; Moriyama, N; Hirose, S; Yamakawa, K
      Mutation screening for Japanese Lafora's disease patients: identification of novel sequence variants in the coding and upstream regulatory regions ofEPM2A gene

      MOLECULAR AND CELLULAR PROBES
    60. 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
    61. Okajima, K; Paznekas, WA; Burstyn, T; Jabs, EW
      Polymorphisms in the human SNAIL (SNAI1) gene

      MOLECULAR AND CELLULAR PROBES
    62. Agabio, R; Carai, MAM; Lobina, C; Pani, M; Reali, R; Vacca, G; Gessa, GL; Colombo, G
      Alcohol stimulates motor activity in selectively bred Sardinian alcohol-preferring (sP), but not in Sardinian alcohol-nonpreferring (sNP), rats

      ALCOHOL
    63. Barton, A; Chapman, P; Myerscough, A; Pinel, T; Davies, N; Worthington, J; John, S
      The single-nucleotide polymorphism lottery: How useful are a few common SNPs in identifying disease-associated alleles?

      GENETIC EPIDEMIOLOGY
    64. Genin, E
      Selection of single nucleotide polymorphisms for association studies in candidate genes

      GENETIC EPIDEMIOLOGY
    65. Huang, QQ; Morrison, AC; Boerwinkle, E
      Linkage disequilibrium structure and its impact on the localization of a candidate functional mutation

      GENETIC EPIDEMIOLOGY
    66. Kooperberg, C; Ruczinski, I; LeBlanc, ML; Hsu, L
      Sequence analysis using logic regression

      GENETIC EPIDEMIOLOGY
    67. Norris, JM; Selinger-Leneman, H; Genin, E
      Investigation of a candidate gene, environment, and GxE interaction using case-control and case-parent study designs

      GENETIC EPIDEMIOLOGY
    68. Martins-Lopes, P; Zhang, H; Koebner, R
      Detection of single nucleotide mutations in wheat using single strand conformation polymorphism gels

      PLANT MOLECULAR BIOLOGY REPORTER
    69. Jobling, MA
      Y-chromosomal SNP haplotype diversity in forensic analysis

      FORENSIC SCIENCE INTERNATIONAL
    70. McLeod, HL; Evans, WE
      Pharmacogenomics: Unlocking the human genome for better drug therapy

      ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY
    71. Gant, TM; Riba, P; Lee, NM
      Morphine tolerance in mice is independent of polymorphisms in opioid receptor sequences

      BRAIN RESEARCH BULLETIN
    72. Grosch, S; Niederberger, E; Lotsch, J; Skarke, C; Geisslinger, G
      A rapid screening method for a single nucleotide polymorphism (SNP) in thehuman MOR gene

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

      ANIMAL GENETICS
    74. Tang, JM; Freedman, DO; Allen, S; Karita, E; Musonda, R; Braga, C; Margolick, J; Kaslow, RA
      TAP1 polymorphisms in several human ethnic groups: Characteristics, evolution, and genotyping strategies

      HUMAN IMMUNOLOGY
    75. Hajeer, AH; Hutchinson, IV
      Influence of TNF alpha gene polymorphisms on TNF alpha production and disease

      HUMAN IMMUNOLOGY
    76. Lee, VHL; Sporty, JL; Fandy, TE
      Pharmacogenomics of drug transporters: the next drug delivery challenge

      ADVANCED DRUG DELIVERY REVIEWS
    77. Ueda, H; Ikegami, H; Kawaguchi, Y; Fujisawa, T; Nojima, K; Babaya, N; Yamada, K; Shibata, M; Yamato, E; Ogihara, T
      Mapping and promoter sequencing of HNF-1 beta gene in diabetes-prone and -resistant mice

      DIABETES RESEARCH AND CLINICAL PRACTICE
    78. Ribas, G; Neville, MJ; Campbell, RD
      Single-nucleotide polymorphism detection by denaturing high-performance liquid chromatography and direct sequencing in genes in the MHC class III region encoding novel cell surface molecules

      IMMUNOGENETICS
    79. 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
    80. Georges, M
      Recent progress in livestock genomics and potential impact on breeding programs

      THERIOGENOLOGY
    81. Quinn, GA; Langford, G
      The porcine endogenous retrovirus long terminal repeat contains a single nucleotide polymorphism that confers distinct differences in estrogen receptor binding affinity between PERV A and PERV B/C subtypes

      VIROLOGY
    82. Fedetz, M; Matesanz, F; Pascual, M; Martin, J; Fernandez, O; Guerrero, M; Alcina, A
      The-174/-597 promoter polymorphisms in the interleukin-6 gene are not associated with susceptibility to multiple sclerosis

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    83. Iorga, B; Savignac, P
      Controlled monohalogenation of phosphonates Part IV. Selective synthesis of monohalogenomethylenediphosphonates

      JOURNAL OF ORGANOMETALLIC CHEMISTRY
    84. Chasman, D; Adams, RM
      Predicting the functional consequences of non-synonymous single nucleotidepolymorphisms: Structure-based assessment of amino acid variation

      JOURNAL OF MOLECULAR BIOLOGY
    85. Gozukara, EM; Khan, SG; Metin, A; Emmert, S; Busch, DB; Shahlavi, T; Coleman, DM; Miller, M; Chinsomboon, N; Stefanini, M; Kraemer, KH
      A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: Molecular genetic evidence for a common ancestor

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    86. Tsunoda, K; Sanke, T; Nakagawa, T; Furuta, H; Nanjo, K
      Single nucleotide polymorphism (D68D, T to C) in the syntaxin 1A gene correlates to age at onset and insulin requirement in Type II diabetic patients

      DIABETOLOGIA
    87. Gupta, PK; Roy, JK; Prasad, M
      Single nucleotide polymorphisms: A new paradigm for molecular marker technology and DNA polymorphism detection with emphasis on their use in plants

      CURRENT SCIENCE
    88. Wedemeyer, N; Potter, T
      Flow cytometry: an 'old' tool for novel applications in medical genetics

      CLINICAL GENETICS
    89. Chang, HG; Fujita, T
      PicSNP: A browsable catalog of nonsynonymous single nucleotide polymorphisms in the human genome

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    90. 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
    91. 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
    92. Huber, M; Losert, D; Hiller, R; Harwanegg, C; Mueller, MW; Schmidt, WM
      Detection of single base alterations in genomic DNA by solid phase polymerase chain reaction on oligonucleotide microarrays

      ANALYTICAL BIOCHEMISTRY
    93. Abecasis, GR; Cookson, WOC; Cardon, LR
      The power to detect linkage disequilibrium with quantitative traits in selected samples

      AMERICAN JOURNAL OF HUMAN GENETICS
    94. Sano, K; Yabuki, K; Imagawa, Y; Shiina, T; Mizuki, N; Ohno, S; Kulski, JK; Inoko, H
      The absence of disease-specific polymorphisms within the HLA-B51 gene thatis the susceptible locus for Behcet's disease

      TISSUE ANTIGENS
    95. Milicic, A; Brown, MA; Wordsworth, BP
      Polymorphism in codon 17 of the CTLA-4 gene (+49 A/G) is not associated with susceptibility to rheumatoid arthritis in British Caucasians

      TISSUE ANTIGENS
    96. Bijlsma, FJ; Bruggink, AH; Hartman, M; Gmelig-Meyling, FHJ; Tilanus, MGJ; de Jonge, N; de Weger, RA
      No association between IL-10 promoter gene polymorphism and heart failure or rejection following cardiac transplantation

      TISSUE ANTIGENS
    97. Barton, A; Myerscough, A; John, S; Gonzalez-Gay, M; Ollier, W; Worthington, J
      A single nucleotide polymorphism in exon 1 of cytotoxic T-lymphocyte-associated-4 (CTLA-4) is not associated with rheumatoid arthritis

      RHEUMATOLOGY
    98. Tonisson, N; Kurg, A; Kaasik, K; Lohmussaar, E; Metspalu, A
      Unravelling genetic data by arrayed primer extension

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    99. Seki, T; Tanaka, T; Nakamura, Y
      Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene

      JOURNAL OF HUMAN GENETICS
    100. Orimo, H; Nakajima, E; Yamamoto, M; Ikejima, M; Emi, M; Shimada, T
      Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability

      JOURNAL OF HUMAN GENETICS


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Documento generato il 16/02/20 alle ore 20:35:08