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    1. ARTIOLI G; DUGNANI M
      Geochronology of metamorphic rocks

      Periodico di Mineralogia
    2. VILLA I M
      Geochronology of metamorphic rocks

      Periodico di Mineralogia
    3. Cortes, J
      On the construction of upwind schemes for non-equilibrium transient two-phase flows

      COMPUTERS & FLUIDS
    4. Liu, JJ; Juo, SH; Holopainen, P; Terwilliger, J; Tong, XM; Grunn, A; Brito, M; Green, P; Mustalahti, K; Maki, M; Gilliam, TC; Partanen, J
      Genomewide linkage analysis of celiac disease in Finnish families

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Nakajima, T; Jorde, LB; Ishigami, T; Umemura, S; Emi, M; Lalouel, JM; Inoue, I
      Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Cordell, HJ; Clayton, DG
      A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: Application to HLA in type 1 diabetes

      AMERICAN JOURNAL OF HUMAN GENETICS
    7. Currat, M; Trabuchet, G; Rees, D; Perrin, P; Harding, RM; Clegg, JB; Langaney, A; Excoffier, L
      Molecular analysis of the beta-globin gene cluster in the niokholo mandenka population reveals a recent origin of the beta(S) senegal mutation

      AMERICAN JOURNAL OF HUMAN GENETICS
    8. Sheel, AW; Edwards, MR; Hunte, GS; McKenzie, DC
      Influence of inhaled nitric oxide on gas exchange during normoxic and hypoxic exercise in highly trained cyclists

      JOURNAL OF APPLIED PHYSIOLOGY
    9. Turcotte, DL; Paul, D; White, WM
      Thorium-uranium systematics require layered mantle convection

      JOURNAL OF GEOPHYSICAL RESEARCH-SOLID EARTH
    10. Wandstrat, A; Wakeland, E
      The genetics of complex autoimmune diseases: non-MHC susceptibility genes

      NATURE IMMUNOLOGY
    11. Scriver, CR
      Human genetics: Lessons from Quebec populations

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    12. Kere, J
      Human population genetics: Lessons from Finland

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    13. Beilman, DW; Vitt, DH; Halsey, LA
      Localized permafrost Peatlands in Western Canada: Definition, distributions, and degradation

      ARCTIC ANTARCTIC AND ALPINE RESEARCH
    14. Gilmour, KM; Perry, SF; Bernier, NJ; Henry, RP; Wood, CM
      Extracellular carbonic anhydrase in the dogfish, Squalus acanthias: A rolein CO2 excretion

      PHYSIOLOGICAL AND BIOCHEMICAL ZOOLOGY
    15. Thomson, G
      An overview of the genetic analysis of complex diseases, with reference totype I diabetes

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    16. Kelly, MA; Mijovic, CH; Barnett, AH
      Genetics of type I diabetes

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    17. Boutin, P; Froguel, P
      Genetics of human obesity

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    18. Park, Y; Eisenbarth, GS
      Genetic susceptibility factors of Type 1 diabetes in Asians

      DIABETES-METABOLISM RESEARCH AND REVIEWS
    19. Taylor, JG; Choi, EH; Foster, CB; Chanock, SJ
      Using genetic variation to study human disease

      TRENDS IN MOLECULAR MEDICINE
    20. Brookes, AJ
      Rethinking genetic strategies to study complex diseases

      TRENDS IN MOLECULAR MEDICINE
    21. Cardon, LR; Bell, JI
      Association study designs for complex diseases

      NATURE REVIEWS GENETICS
    22. Folstein, SE; Rosen-Sheidley, B
      Genetics of autism: Complex aetiology for a heterogeneous disorder

      NATURE REVIEWS GENETICS
    23. Ostrer, H
      A genetic profile of contemporary Jewish populations

      NATURE REVIEWS GENETICS
    24. Mackay, TFC
      Quantitative trait loci in Drosophila

      NATURE REVIEWS GENETICS
    25. Palmer, LJ; Cookson, WOCM
      Using single nucleotide polymorphisms as a means to understanding the pathophysiology of asthma

      RESPIRATORY RESEARCH
    26. Graham, RR; Langefeld, CD; Gaffney, PM; Ortmann, WA; Selby, SA; Baechler, EC; Shark, KB; Ockenden, TC; Rohlf, KE; Moser, KL; Brown, WM; Gabriel, SE; Messner, RP; King, RA; Horak, P; Elder, JT; Stuart, PE; Rich, SS; Behrens, TW
      Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosus

      ARTHRITIS RESEARCH
    27. Villaseca, C; Romera, CM; Barbero, L
      Melts and residua geochemistry in a low-to-mid crustal section (Central Spain)

      PHYSICS AND CHEMISTRY OF THE EARTH PART A-SOLID EARTH AND GEODESY
    28. Ohashi, J; Tokunaga, K
      The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers

      JOURNAL OF HUMAN GENETICS
    29. 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
    30. Nakazawa, I; Nakajima, T; Ishigami, T; Umemura, S; Emi, M
      Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA)gene

      JOURNAL OF HUMAN GENETICS
    31. Takashima, M; Ishikawa, K; Nagaoka, U; Shoji, S; Mizusawa, H
      A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan

      JOURNAL OF HUMAN GENETICS
    32. Richter, B; Stegmann, K; Roper, B; Boddeker, I; Ngo, ETKM; Koch, MC
      Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population

      JOURNAL OF HUMAN GENETICS
    33. 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
    34. 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
    35. Camill, P; Lynch, JA; Clark, JS; Adams, JB; Jordan, B
      Changes in biomass, aboveground net primary production, and peat accumulation following permafrost thaw in the boreal peatlands of Manitoba, Canada

      ECOSYSTEMS
    36. Angerer, WP
      A note on the evaluation of fluctuation experiments

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    37. Carlson, CS; Newman, TL; Nickerson, DA
      SNPing in the human genome

      CURRENT OPINION IN CHEMICAL BIOLOGY
    38. Jannink, JL; Bink, MCAM; Jansen, RC
      Using complex plant pedigrees to map valuable genes

      TRENDS IN PLANT SCIENCE
    39. Zak, NB; Shifman, S; Shalom, A; Darvasi, A
      Population-based gene discovery in the post-genomic era

      DRUG DISCOVERY TODAY
    40. 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
    41. Curran, S; Mill, J; Tahir, E; Kent, L; Richards, S; Gould, A; Huckett, L; Sharp, J; Batten, C; Fernando, S; Ozbay, F; Yazgan, Y; Simonoff, E; Thompson, M; Taylor, E; Asherson, P
      Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples

      MOLECULAR PSYCHIATRY
    42. Tordjman, S; Gutknecht, L; Carlier, M; Spitz, E; Antoine, C; Slama, F; Carsalade, V; Cohen, DJ; Ferrari, P; Roubertoux, PL; Anderson, GM
      Role of the serotonin transporter gene in the behavioral expression of autism

      MOLECULAR PSYCHIATRY
    43. Hattori, E; Ebihara, M; Yamada, K; Ohba, H; Shibuya, H; Yoshikawa, T
      Identification of a compound short tandem repeat stretch in the 5 '-upstream region of the cholecystokinin gene, and its association with panic disorder but not with schizophrenia

      MOLECULAR PSYCHIATRY
    44. Baron, M
      The search for complex disease genes: fault by linkage or fault by association?

      MOLECULAR PSYCHIATRY
    45. Persico, AM; D'Agruma, L; Maiorano, N; Totaro, A; Militerni, R; Bravaccio, C; Wassink, TH; Schneider, C; Melmed, R; Trillo, S; Montecchi, F; Palermo, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, KL; Conciatori, M; Marino, R; Quattrocchi, CC; Baldi, A; Zelante, L; Gasparini, P; Keller, F
      Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

      MOLECULAR PSYCHIATRY
    46. Veenstra-VanderWeele, J; Kim, SJ; Gonen, D; Hanna, GL; Leventhal, BL; Cook, EH
      Genomic organization of the SLC1A1/EAAC1 gene and mutation screening in early-onset obsessive-compulsive disorder

      MOLECULAR PSYCHIATRY
    47. Yoshikawa, T; Kikuchi, M; Saito, K; Watanabe, A; Yamada, K; Shibuya, H; Nankai, M; Kurumaji, A; Hattori, E; Ishiguro, H; Shimizu, H; Okubo, Y; Toru, M; Detera-Wadleigh, SD
      Evidence for association of the myo-inositol monophosphatase 2 (IMPA2) gene with schizophrenia in Japanese samples

      MOLECULAR PSYCHIATRY
    48. Ohtsuki, T; Sakurai, K; Dou, H; Toru, M; Yamakawa-Kobayashi, K; Arinami, T
      Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia

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

      MOLECULAR PSYCHIATRY
    50. Semwal, P; Prasad, S; Bhatia, T; Deshpande, SN; Wood, J; Nimgaonkar, VL; Thelma, BK
      Family-based association studies of monoaminergic gene polymorphisms amongNorth Indians with schizophrenia

      MOLECULAR PSYCHIATRY
    51. Frisch, A; Laufer, N; Danziger, Y; Michaelovsky, E; Leor, S; Carel, C; Stein, D; Fenig, S; Mimouni, M; Apter, A; Weizman, A
      Association of anorexia nervosa with the high activity allele of the COMT gene: a family-based study in Israeli patients

      MOLECULAR PSYCHIATRY
    52. Hamilton, SP; Slager, SL; Helleby, L; Heiman, GA; Klein, DF; Hodge, SE; Weissman, MM; Fyer, AJ; Knowles, JA
      No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder

      MOLECULAR PSYCHIATRY
    53. 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
    54. Bykhovskaya, Y; Yang, HY; Taylor, K; Hang, T; Tun, RYM; Estivill, X; Casano, RAMS; Majamaa, K; Shohat, M; Fischel-Ghodsian, N
      Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness

      GENETICS IN MEDICINE
    55. Mathews, DJ; Kashuk, C; Brightwell, G; Eichler, EE; Chakravarti, A
      Sequence variation within the fragile x locus

      GENOME RESEARCH
    56. Lai, E
      Application of SNP technologies in medicine: Lessons learned and future challenges

      GENOME RESEARCH
    57. Fallin, D; Cohen, A; Essioux, L; Chumakov, I; Blumenfeld, M; Cohen, D; Schork, NJ
      Genetic analysis of case/control data using estimated haplotype frequencies: Application to APOE locus variation and Alzheimer's disease

      GENOME RESEARCH
    58. Sachot, S; Moirand, R; Jouanolle, AM; Mosser, J; Fergelot, P; Deugnier, Y; Brissot, P; le Gall, JY; David, V
      Low penetrant hemochromatosis phenotype in eight families: No evidence of modifiers in the MHC region

      BLOOD CELLS MOLECULES AND DISEASES
    59. Depner, TA
      Daily hemodialysis efficiency: An analysis of solute kinetics

      ADVANCES IN RENAL REPLACEMENT THERAPY
    60. Sklar, P
      The genomic approach to candidate genes

      HARVARD REVIEW OF PSYCHIATRY
    61. Da Silveira, LA; Ribeiro, WL; Kirchgatter, K; Wunderlich, G; Matsuoka, H; Tanabe, K; Ferreira, MU
      Sequence diversity and linkage disequilibrium within the merozoite surfaceprotein-1 (Msp-1) locus of Plasmodium falciparum: A longitudinal study in Brazil

      JOURNAL OF EUKARYOTIC MICROBIOLOGY
    62. Matsubara, M; Omori, F; Fujita, S; Metoki, E; Kikuya, M; Fujiwara, T; Araki, T; Imai, Y
      Haplotypes of aldosterone synthase (CYP11132) gene in the general population of Japan: The Ohasama study

      CLINICAL AND EXPERIMENTAL HYPERTENSION
    63. Jeffreys, AJ; Kauppi, L; Neumann, R
      Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

      NATURE GENETICS
    64. Daly, MJ; Rioux, JD; Schaffner, SE; Hudson, TJ; Lander, ES
      High-resolution haplotype structure in the human genome

      NATURE GENETICS
    65. Johnson, GCL; Esposito, L; Barratt, BJ; Smith, AN; Heward, J; Di Genova, G; Ueda, H; Cordell, HJ; Eaves, IA; Dudbridge, F; Twells, RCJ; Payne, F; Hughes, W; Nutland, S; Stevens, H; Carr, P; Tuomilehto-Wolf, E; Tuomilehto, J; Gough, SCL; Clayton, DG; Todd, JA
      Haplotype tagging for the identification of common disease genes

      NATURE GENETICS
    66. Shifman, S; Darvasi, A
      The value of isolated populations

      NATURE GENETICS
    67. Laitinen, T; Daly, MJ; Rioux, JD; Kauppi, P; Laprise, C; Petays, T; Green, T; Cargill, M; Haahtela, T; Lander, ES; Laitinen, LA; Hudson, TJ; Kere, J
      A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population

      NATURE GENETICS
    68. Kruglyak, L; Nickerson, DA
      Variation is the spice of life

      NATURE GENETICS
    69. Watanabe, Y; Murray, JC; Bjork, BC; Bird, CP; Chiang, PW; Gregory, SG; Kurnit, DM; Schutte, BC
      Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41

      HUMAN MUTATION
    70. 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
    71. Rannala, B; Bertorelle, G
      Using linked markers to infer the age of a mutation

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

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

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

      HUMAN MUTATION
    75. Cook, EH
      Genetics of autism

      CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
    76. Yoshida, K; Hamajima, N; Kozaki, K; Saito, H; Maeno, K; Sugiura, T; Ookuma, K; Takahashi, T
      Association between the dopamine D2 receptor A2/A2 genotype and smoking behavior in the Japanese

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    77. Beaty, TH; Wang, H; Hetmanski, JB; Fan, YT; Zeiger, JS; Liang, KY; Chiu, YF; Vanderkolk, CA; Seifert, KC; Wulfsberg, EA; Raymond, G; Panny, SR; McIntosh, I
      A case-control study of nonsyndromic oral clefts in Maryland

      ANNALS OF EPIDEMIOLOGY
    78. Djouadi, K; Nedelec, B; Tamouza, R; Genin, E; Ramasawmy, R; Charron, D; Delpech, M; Laoussadi, S
      Interleukin 1 gene cluster polymorphisms in multiplex families with spondylarthropathies

      CYTOKINE
    79. Hohler, T; Marker-Hermann, E
      Psoriatic arthritis: clinical aspects, genetics, and the role of T cells

      CURRENT OPINION IN RHEUMATOLOGY
    80. Tetushkin, EY
      Genetics and the origin of human "races"

      RUSSIAN JOURNAL OF GENETICS
    81. Vorechovsky, I; Kralovicova, J; Laycock, MD; Webster, ADB; Marsh, SGE; Madrigal, A; Hammarstrom, L
      Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region

      EUROPEAN JOURNAL OF HUMAN GENETICS
    82. 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
    83. Verpillat, P; Bouley, S; Campion, D; Hannequin, D; Dubois, B; Belliard, S; Puel, M; Thomas-Anterion, C; Agid, Y; Brice, A; Clerget-Darpoux, F
      Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population

      EUROPEAN JOURNAL OF HUMAN GENETICS
    84. Paavola, P; Helio, T; Kiuru, M; Halme, L; Turunen, U; Terwilliger, J; Karvonen, AL; Julkunen, R; Niemela, S; Nurmi, H; Farkkila, M; Kontula, K
      Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21

      EUROPEAN JOURNAL OF HUMAN GENETICS
    85. Lee, MH; Gordon, D; Ott, J; Lu, KM; Ose, L; Miettinen, T; Gylling, H; Stalenhoef, AF; Pandya, A; Hidaka, H; Brewer, B; Kojima, H; Sakuma, N; Pegoraro, R; Salen, G; Patel, SB
      Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities

      EUROPEAN JOURNAL OF HUMAN GENETICS
    86. Akey, J; Jin, L; Xiong, MM
      Haplotypes vs single marker linkage disequilibrium tests: what do we gain?

      EUROPEAN JOURNAL OF HUMAN GENETICS
    87. Horvath, S; Xu, X; Laird, NM
      The family based association test method: strategies for studying general genotype-phenotype associations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    88. Zouali, H; Chamaillard, M; Lesage, S; Cezard, JP; Colombel, JF; Belaiche, J; Almer, S; Tysk, C; Montague, S; Gassull, M; Christensen, S; Finkel, Y; Gower-Rousseau, C; Modigliani, R; Macry, J; Selinger-Leneman, H; Thomas, G; Hugot, JP
      Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease

      EUROPEAN JOURNAL OF HUMAN GENETICS
    89. Bergman, A; Einbeigi, Z; Olofsson, U; Taib, Z; Wallgren, A; Karlsson, P; Wahlstrom, J; Martinsson, T; Nordling, M
      The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation

      EUROPEAN JOURNAL OF HUMAN GENETICS
    90. Tao, SH; Liu, XM; Chu, JH; Zhang, RM; Du, LP; Luo, ZW
      Rate of decay in admixture linkage disequilibrium and its implication in gene mapping

      CHINESE SCIENCE BULLETIN
    91. Tao, SH; Zhang, RM; Chu, JH; Liu, XM; Du, LP; Qi, QY; Luo, ZW
      A population genetics model of linkage disequilibrium in admired populations

      CHINESE SCIENCE BULLETIN
    92. Li, SG; Sun, WD; Zhang, ZQ; Li, QL
      Nd isotopic disequilibrium between minerals and Rb-Sr age of the secondaryphengite in eclogite from the Yangkou area, Qingdao, eastern China

      CHINESE SCIENCE BULLETIN
    93. Dawood, YH
      Uranium-series disequilibrium dating of secondary uranium ore from the south Eastern Desert of Egypt

      APPLIED RADIATION AND ISOTOPES
    94. Abdul-Hadi, A; Alhassanieh, O; Ghafar, M
      Disequilibrium of uranium isotopes in some Syrian groundwater

      APPLIED RADIATION AND ISOTOPES
    95. Bonotto, DM; Andrews, JN; Darbyshire, DPF
      A laboratory study of the transfer of U-234 and U-238 during water-rock interactions in the Carnmenellis granite (Cornwall, England) and implicationsfor the interpretation of field data

      APPLIED RADIATION AND ISOTOPES
    96. Asfahani, J; Abdul-Hadi, A
      Geophysical natural gamma-ray well logging and spectrometric signatures ofsouth AL-Abter phosphatic deposits in Syria

      APPLIED RADIATION AND ISOTOPES
    97. Palferman, S; Matthews, N; Turner, H; Moore, J; Hervas, A; Aubin, A; Wallace, S; Michelotti, J; Wainhouse, C; Paul, A; Thompson, E; Murin, M; Gupta, R; Garner, C; Pickles, A; Rutter, M; Bailey, A; Lamb, JA; Marlow, A; Scudder, P; Barnby, G; Monaco, AP; Baird, G; Cox, A; Docherty, Z; Warburton, P; Green, EP; Abbs, SJ; Le Couteur, A; McConachie, HR; Berney, T; Kelly, TP; De Vries, PJ; Bolton, P; Green, J; Gilchrist, A; Whittacker, J; Bolton, B; Packer, R; Maestrini, E; Van Engeland, H; De Jonge, MV; Kemner, C; Klauck, SM; Beyer, KS; Epp, S; Poustka, A; Benner, A; Poustka, F; Ruhl, D; Schmotzer, G; Bolte, S; Feineis-Matthews, S; Fombonne, E; Roge, B; Fremolle-Kruck, J; Pienkowski, C; Tauber, MT; Pedersen, L; Brondum-Nielsen, K; Eriksen, G; Haracopos, D; Cotterill, RMJ; Tsiantis, J; Papanikolaou, K; Lord, C; Corsello, C; Guter, S; Leventhal, B; Cook, E; Smalley, S; Bailey, J; Liu, A; Dedricks, M; Chrzanowski, L; Levitt, J; Pauls, D; Volkmar, F; Weeks, DE
      Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q

      HUMAN MOLECULAR GENETICS
    98. Ogorelkova, M; Kraft, HG; Ehnholm, C; Utermann, G
      Single nucleotide polymorphisms in exons of the apo(a) kringles IV types 6to 10 domain affect Lp(a) plasma concentrations and have different patterns in Africans and Caucasians

      HUMAN MOLECULAR GENETICS
    99. Zavattari, P; Lampis, R; Motzo, C; Loddo, M; Mulargia, A; Whalen, M; Maioli, M; Angius, E; Todd, JA; Cucca, F
      Conditional linkage disequilibrium analysis of a complex disease superlocus, IDDM1 in the HLA region, reveals the presence of independent modifying gene effects influencing the type 1 diabetes risk encoded by the major HLA-DQB1,-DRB1 disease loci

      HUMAN MOLECULAR GENETICS
    100. 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


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Documento generato il 28/10/20 alle ore 04:06:52