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    1. Johanneson, B; Alarcon-Riquelme, ME
      An update on the genetics of systemic lupus erythematosus

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    2. Weetman, AP
      Determinants of autoimmune thyroid disease

      NATURE IMMUNOLOGY
    3. Gloyn, AL; McCarthy, MI
      The genetics of type 2 diabetes

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    4. Barakat, K; Hitman, GA
      Genetic susceptibility to macrovascular complications of type 2 diabetes mellitus

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    5. Ahmad, YA; Bruce, IN
      Genetic epidemiology - Systemic lupus erythematosus

      ARTHRITIS RESEARCH
    6. Brandi, ML; Gennari, L; Cerinic, MM; Becherini, L; Falchetti, A; Masi, L; Gennari, C; Reginster, JY
      Genetic markers of osteoarticular disorders: facts and hopes

      ARTHRITIS RESEARCH
    7. 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
    8. 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
    9. 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
    10. 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
    11. 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
    12. 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
    13. 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
    14. Carlson, CS; Newman, TL; Nickerson, DA
      SNPing in the human genome

      CURRENT OPINION IN CHEMICAL BIOLOGY
    15. Kamp, C; Huellen, K; Fernandes, S; Sousa, M; Schlegel, PN; Mielnik, A; Kleiman, S; Yavetz, H; Krause, W; Kupker, W; Johannisson, R; Schulze, W; Weidner, W; Barros, A; Vogt, PH
      High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome

      MOLECULAR HUMAN REPRODUCTION
    16. Baron, M
      The search for complex disease genes: fault by linkage or fault by association?

      MOLECULAR PSYCHIATRY
    17. Franks, S; Gharani, N; McCarthy, M
      Genetics and infertility II - Candidate genes in polycystic ovary syndrome

      HUMAN REPRODUCTION UPDATE
    18. Tonini, GP; McConville, C; Cusano, R; Rees, SA; Dagnino, M; Longo, L; De Bernardi, B; Conte, M; Garaventa, A; Romeo, G; Devoto, M; Seri, M
      Exclusion of candidate genes and chromosomal regions in familial neuroblastoma

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    19. Ten Asbroek, ALMA; Olsen, J; Housman, D; Baas, F; Stanton, V
      Genetic variation in mRNA coding sequences of highly conserved genes

      PHYSIOLOGICAL GENOMICS
    20. Milner, CM; Campbell, RD
      Genetic organization of the human MHC class III region

      FRONTIERS IN BIOSCIENCE
    21. Garcia, CK; Mues, G; Liao, YL; Hyatt, T; Patil, N; Cohen, JC; Hobbs, HH
      Sequence diversity in genes of lipid metabolism

      GENOME RESEARCH
    22. Deutsch, S; Iseli, C; Bucher, P; Antonarakis, SE; Scott, HS
      A cSNP map and database for human chromosome 21

      GENOME RESEARCH
    23. Dawson, E; Chen, Y; Hunt, S; Smink, LJ; Hunt, A; Rice, K; Livingston, S; Bumpstead, S; Bruskiewich, R; Sham, P; Ganske, R; Adams, M; Kawasaki, K; Shimizu, N; Minoshima, S; Roe, B; Bentley, D; Dunham, I
      A SNP resource for human chromosome 22: Extracting dense clusters of SNPs from the genomic sequence

      GENOME RESEARCH
    24. Goto, Y; Yue, LJ; Yokoi, A; Nishimura, R; Uehara, T; Koizumi, S; Saikawa, Y
      A novel single-nucleotide polymorphism in the 3 '-untranslated region of the human dihydrofolate reductase gene with enhanced expression

      CLINICAL CANCER RESEARCH
    25. 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
    26. 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
    27. Ban, Y; Taniyama, M; Tozaki, T; Yanagawa, T; Tomita, M; Ban, Y
      SEL1L microsatellite polymorphism in Japanese patients with autoimmune thyroid diseases

      THYROID
    28. Tomer, Y
      Unraveling the genetic susceptibility to autoimmune thyroid diseases: CTLA-4 takes the stage

      THYROID
    29. 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
    30. Uthoff, SMS; Eichenberger, MR; Lewis, RK; Fox, MP; Hamilton, CJ; McAuliffe, TL; Grimes, HL; Galandiuk, S
      Identification of candidate genes in ulcerative colitis and Crohn's disease using cDNA array technology

      INTERNATIONAL JOURNAL OF ONCOLOGY
    31. Castro, J; Telleria, JJ; Blanco-Quiros, A
      Susceptibility genes for asthma and allergy: Hits and questions

      JOURNAL OF INVESTIGATIONAL ALLERGOLOGY & CLINICAL IMMUNOLOGY
    32. Sunyaev, S; Ramensky, V; Koch, I; Lathe, W; Kondrashov, AS; Bork, P
      Prediction of deleterious human alleles

      HUMAN MOLECULAR GENETICS
    33. Sakai, K; Shirasawa, S; Ishikawa, N; Ito, K; Tamai, H; Kuma, K; Akamizu, T; Tanimura, M; Furugaki, K; Yamamoto, K; Sasazuki, T
      Identification of susceptibility loci for autoimmune thyroid disease to 5q31-q133 and Hashimoto's thyroiditis to 8q23-q24 by multipoint affected sib-pair linkage analysis in Japanese

      HUMAN MOLECULAR GENETICS
    34. Nowotny, P; Kwon, JM; Goate, AM
      SNP analysis to dissect human traits

      CURRENT OPINION IN NEUROBIOLOGY
    35. Bennet, AM; Naslund, TI; Morgenstern, R; de Faire, U
      Bioinformatic and experimental tools for identification of single-nucleotide polymorphisms in genes with a potential role for the development of the insulin resistance syndrome

      JOURNAL OF INTERNAL MEDICINE
    36. Frossard, PM; Malloy, MJ; Lestringant, GG; Kane, JP
      Haplotypes of the human renin gene associated with essential hypertension and stroke

      JOURNAL OF HUMAN HYPERTENSION
    37. Roesen, P; Ferber, P; Tschoepe, D
      Macrovascular disease in diabetes: current status

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    38. Comuzzie, AG; Williams, JT; Martin, LJ; Blangero, J
      Searching for genes underlying normal variation in human adiposity

      JOURNAL OF MOLECULAR MEDICINE-JMM
    39. Lesch, KP
      Variation of serotonergic gene expression: neurodevelopment and the complexity of response to psychopharmacologic drugs

      EUROPEAN NEUROPSYCHOPHARMACOLOGY
    40. Mann, JJ; Brent, DA; Arango, V
      The neurobiology and genetics of suicide and attempted suicide: A focus onthe serotonergic system

      NEUROPSYCHOPHARMACOLOGY
    41. Freeman, K; Nakao, K; Leinwand, LA
      Low sequence variation in the gene encoding the human beta-myosin heavy chain

      GENOMICS
    42. Fossum, E; Berge, KE; Hoieggen, A; Moan, A; Rostrup, M; Kjeldsen, SE; Eide, I; Berg, K
      Polymorphisms in candidate genes for blood pressure regulation in young men with normal or elevated screening blood pressure

      BLOOD PRESSURE
    43. Sheehan, D; Bennett, T; Cashman, KD
      An assessment of genetic markers as predictors of bone turnover in healthyadults

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    44. 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
    45. Muthane, U; Jain, S; Gururaj, G
      Hunting genes in Parkinson's disease from the roots

      MEDICAL HYPOTHESES
    46. Tan, EK; Nagamitsu, S; Matsuura, T; Khajavi, M; Jankovic, J; Ondo, W; Ashizawa, T
      Alcohol dehydrogenase polymorphism and Parkinson's disease

      NEUROSCIENCE LETTERS
    47. Paiss, T; Bochum, S; Herkommer, K; Maier, C; Roesch, K; Taweemonkonsap, T; Haeussler, J; Hautmann, RE; Vogel, W
      Hereditary prostate cancer in Germany

      EUROPEAN UROLOGY
    48. Schonfeld-Warden, NA; Warden, CH
      Physiological effects of variants in human uncoupling proteins: UCP2 influences body-mass index

      BIOCHEMICAL SOCIETY TRANSACTIONS
    49. Miller, EA; Stanford, JL; Hsu, L; Noonan, E; Ostrander, EA
      Polymorphic repeats in the androgen receptor gene in high-risk sibships

      PROSTATE
    50. Foresta, C; Moro, E; Ferlin, A
      Prognostic value of Y deletion analysis - The role of current methods

      HUMAN REPRODUCTION
    51. Danziger, RS
      Hypertension in an anthropological and evolutionary paradigm

      HYPERTENSION
    52. Galluzzi, JR; Cupples, LA; Meigs, JB; Wilson, PWF; Schaefer, EJ; Ordovas, JM
      Association of the ala54-thr polymorphism in the intestinal fatty acid-binding protein with 2-h postchallenge insulin levels in the Framingham Offspring Study

      DIABETES CARE
    53. Smoller, JW; Rosenbaum, JF; Biederman, J; Susswein, LS; Kennedy, J; Kagan, J; Snidman, N; Laird, N; Tsuang, MT; Faraone, SV; Schwarz, A; Slaugenhaupt, SA
      Genetic association analysis of behavioral inhibition using candidate locifrom mouse models

      AMERICAN JOURNAL OF MEDICAL GENETICS
    54. Houdayer, C; Bonaiti-Pellie, C; Erguy, C; Soupre, V; Dondon, MG; Burglen, L; Cougoureux, E; Couderc, R; Vazquez, MP; Bahuau, M
      Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    55. Kamnasaran, D; O'Brien, PCM; Schuffenhauer, S; Quarrell, O; Lupski, JR; Grammatico, P; Ferguson-Smith, MA; Cox, DW
      Defining the breakpoints of proximal chromosome 14q rearrangements in ninepatients using flow-sorted chromosomes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    56. 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
    57. Gebhardt, C; Valkonen, JPT
      Organization of genes controlling disease resistance in the potato genome

      ANNUAL REVIEW OF PHYTOPATHOLOGY
    58. Vicente, JG; King, GJ
      Characterisation of disease resistance gene-like sequences in Brassica oleracea L.

      THEORETICAL AND APPLIED GENETICS
    59. Chen, X; Salamini, F; Gebhardt, C
      A potato molecular-function map for carbohydrate metabolism and transport

      THEORETICAL AND APPLIED GENETICS
    60. Yoon, PW; Rasmussen, SA; Lynberg, MC; Moore, CA; Anderka, M; Carmichael, SL; Costa, P; Druschel, C; Hobbs, CA; Romitti, PA; Langlois, PH; Edmonds, LD
      The National Birth Defects Prevention Study

      PUBLIC HEALTH REPORTS
    61. Koo, SH; Cunningham, MC; Arabshahi, B; Gruss, JS; Grant, JH
      The transforming growth factor-beta 3 knock-out mouse: An animal model forcleft palate

      PLASTIC AND RECONSTRUCTIVE SURGERY
    62. Prentice, A
      The relative contribution of diet and genotype to bone development

      PROCEEDINGS OF THE NUTRITION SOCIETY
    63. Sachidanandam, R; Weissman, D; Schmidt, SC; Kakol, JM; Stein, LD; Mullikin, JC; Mortimore, BJ; Willey, DL; Hunt, SE; Cole, CG; Coggill, PC; Rice, CM; Ning, ZM; Rogers, J; Bentley, DR; Kwok, PY; Mardis, ER; Yeh, RT; Schultz, B; Cook, L; Davenport, R; Dante, M; Fulton, L; Hillier, L; Waterston, RH; McPherson, JD; Gilman, B; Schaffner, S; Van Etten, WJ; Reich, D; Higgins, J; Daly, MJ; Blumenstiel, B; Baldwin, J; Stange-Thomann, NS; Zody, MC; Linton, L; Lander, ES; Altshuler, D
      A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

      NATURE
    64. de Cid, R; Volpini, V; Almasy, L; Otero, D; Estivill, X; Lazaro, C
      Analysis of the susceptibility regions to psoriasis in Spanish population:evidence of a major gene involved in psoriasis in 6p21

      MEDICINA CLINICA
    65. Bertin, P; Gallais, A
      Genetic variation for nitrogen use efficiency in a set of recombinant inbred lines II - QTL detection and coincidences

      MAYDICA
    66. Karpov, RS; Puzyrev, KV; Pavlyukova, EN; Stepanov, VA
      Molecular-genetic analysis of the left ventricular hypertrophy

      KARDIOLOGIYA
    67. Pirinen, S; Kentala, A; Nieminen, P; Varilo, T; Thesleff, I; Arte, S
      Recessively inherited lower incisor hypodontia

      JOURNAL OF MEDICAL GENETICS
    68. Pallaud, C; Gueguen, R; Sass, C; Grow, M; Cheng, S; Siest, G; Visvikis, S
      Genetic influences on lipid metabolism trait variability within the Stanislas Cohort

      JOURNAL OF LIPID RESEARCH
    69. Arte, S; Nieminen, P; Apajalahti, S; Haavikko, K; Thesleff, I; Pirinen, S
      Characteristics of incisor-premolar hypodontia in families

      JOURNAL OF DENTAL RESEARCH
    70. Foresta, C; Bettella, A; Moro, E; Roverato, A; Merico, M; Ferlin, A
      Sertoli cell function in infertile patients with and without microdeletions of the azoospermia factors on the Y chromosome long arm

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    71. Imrie, H; Vaidya, B; Perros, P; Kelly, WF; Toft, AD; Young, ET; Kendall-Taylor, P; Pearce, SHS
      Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    72. Linville, RC; Pomp, D; Johnson, RK; Rothschild, MF
      Candidate gene analysis for loci affecting litter size and ovulation rate in swine

      JOURNAL OF ANIMAL SCIENCE
    73. Krause, MM; Homuth, V; Schmider, A; Luft, FC
      Genetic associations of preeclampsia

      GYNAKOLOGE
    74. Chiu, KC; Chuang, LM; Chu, A; Yoon, C
      Fatty acid binding protein 2 and insulin resistance

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    75. Pallaud, C; Sass, C; Zannad, F; Siest, G; Visvikis, S
      APOC3, CETP, fibrinogen, and MTHFR are genetic determinants of carotid intima-media thickness in healthy men (the Stanislas Cohort)

      CLINICAL GENETICS
    76. Hoppe, C; Cheng, S; Grow, M; Silbergleit, A; Klitz, W; Trachtenberg, E; Erlich, H; Vichinsky, E; Styles, L
      A novel multilocus genotyping assay to identify genetic predictors of stroke in sickle cell anaemia

      BRITISH JOURNAL OF HAEMATOLOGY
    77. Kloting, I; van den Brandt, J; Kuttler, B
      Genes of SHR rats protect spontaneously diabetic BB/OK rats from diabetes:Lessons from congenic BB.SHR rat strains

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    78. Lin, CT; Sargan, DR
      Generation and analysis of canine retinal ESTs: Isolation and expression of retina-specific gene transcripts

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    79. Nanavaty, U; Goldstein, AD; Levine, SJ
      Polymorphisms in candidate asthma genes

      AMERICAN JOURNAL OF THE MEDICAL SCIENCES
    80. DeAngelis, MM; McGee, TL; Keats, BJB; Slim, R; Berson, EL; Dryja, TP
      Two families from New England with Usher syndrome type IC with distinct haplotypes

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    81. Atkinson, TP; Schaffer, AA; Grimbacher, B; Schroeder, HW; Woellner, C; Zerbe, CS; Puck, JM
      An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family

      AMERICAN JOURNAL OF HUMAN GENETICS
    82. Mitchell, LE; Murray, JC; O'Brien, S; Christensen, K
      Evaluation of two putative susceptibility loci for oral clefts in the Danish population

      AMERICAN JOURNAL OF EPIDEMIOLOGY
    83. Bouchard, C; Rankinen, T; Chagnon, YC; Rice, T; Perusse, L; Gagnon, J; Borecki, I; An, P; Leon, AS; Skinner, JS; Wilmore, JH; Province, M; Rao, DC
      Genomic scan for maximal oxygen uptake and its response to training in theHERITAGE Family Study

      JOURNAL OF APPLIED PHYSIOLOGY
    84. Maalej, A; Kacem, HH; Bellassoued, M; Abid, M; Makni, H; Ayadi, H
      Polymorphisms of HLA DQB1 CAR1/CAR2 and TNF alpha IR2/IR4 microsatellite markers in patients affected with Graves disease

      CLINICAL IMMUNOLOGY
    85. Visvikis, S; Sass, C; Pallaud, C; Grow, MA; Zannad, F; Siest, G; Erlich, HA; Cheng, S
      Familial studies on the genetics of cardiovascular diseases: The Stanislascohort

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    86. Rojas, K; Liang, L; Johnson, E; Berrettini, WH; Overhauser, J
      Identification of candidate genes for psychiatric disorders on 18P11

      MOLECULAR PSYCHIATRY
    87. Marre, M; Hadjadj, S; Bouhanick, B
      Hereditary factors in the development of diabetic renal disease

      DIABETES & METABOLISM
    88. Rotig, A; Valnot, I; Mugnier, C; Rustin, P; Munnich, A
      Screening human EST database for identification of candidate genes in respiratory chain deficiency

      MOLECULAR GENETICS AND METABOLISM
    89. Beuzen, ND; Stear, MJ; Chang, KC
      Molecular markers and their use in animal breeding

      VETERINARY JOURNAL
    90. Fan, JB; Chen, XQ; Halushka, MK; Berno, A; Huang, XH; Ryder, T; Lipshutz, RJ; Lockhart, DJ; Chakravarti, A
      Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays

      GENOME RESEARCH
    91. Ohuchi, T; Yanagisawa, M; Gariepy, CE
      Renal tubular effects of endothelin-B receptor signaling: its role in cardiovascular homeostasis and extracellular volume regulation

      CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
    92. Weiss, KM; Terwilliger, JD
      How many diseases does it take to map a gene with SNPs?

      NATURE GENETICS
    93. Wirth, B
      An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)

      HUMAN MUTATION
    94. Carinci, F; Pezzetti, F; Scapoli, L; Martinelli, M; Carinci, P; Tognon, M
      Genetics of nonsyndromic cleft lip and palate: A review of international studies and data regarding the Italian population

      CLEFT PALATE-CRANIOFACIAL JOURNAL
    95. Park, YJ; Chung, HK; Park, DJ; Kim, WB; Kim, SW; Koh, JJ; Cho, BY
      Polymorphism in the promoter and exon 1 of the cytotoxic T lymphocyte antigen-4 gene associated with autoimmune thyroid disease in Koreans

      THYROID
    96. Shin, S; Park, SS; Hwang, YS; Lee, KW; Chung, SG; Lee, YJ; Park, MH
      Deletion of SMN and NAIP genes in Korean patients with spinal muscular atrophy

      JOURNAL OF KOREAN MEDICAL SCIENCE
    97. Gray, IC; Campbell, DA; Spurr, NK
      Single nucleotide polymorphisms as tools in human genetics

      HUMAN MOLECULAR GENETICS
    98. Munroe, PB; Caulfield, MJ
      Genetics of hypertension

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    99. Johnson, GCL; Todd, JA
      Strategies in complex disease mapping

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    100. Lee, WK; Padmanabhan, S; Dominiczak, AF
      Genetics of hypertension: from experimental models to clinical applications

      JOURNAL OF HUMAN HYPERTENSION


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Documento generato il 18/02/20 alle ore 14:36:57