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    1. Wang, Z; Taramino, G; Yang, D; Liu, G; Tingey, SV; Miao, GH; Wang, GL
      Rice ESTs with disease-resistance gene- or defense-response gene-like sequences mapped to regions containing major resistance genes or QTLs

      MOLECULAR GENETICS AND GENOMICS
    2. Pociot, F; Larsen, ZM; Zavattari, P; Deidda, E; Nerup, J; Cattaneo, M; Chiaramonte, R; Comi, P; Sabbadini, M; Zollo, M; Biunno, I; Cucca, F
      No evidence for SEL1L as a candidate gene for IDDM11-conferred susceptibility

      DIABETES-METABOLISM RESEARCH AND REVIEWS
    3. Mercer, JFB
      The molecular basis of copper-transport diseases

      TRENDS IN MOLECULAR MEDICINE
    4. Massat, I; Souery, D; Del-Favero, J; Oruc, L; Jakovljevic, M; Folnegovic, V; Adolfsson, R; Kaneva, R; Papadimitriou, G; Dikeos, D; Jazin, E; Milanova, V; Van Broeckhoven, C; Mendlewicz, J
      Lack of association between GABRA3 and unipolar affective disorder: a multicentre study

      INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY
    5. Sun, GF; Tomita, H; Shakkottai, VG; Gargus, JJ
      Genomic organization and promoter analysis of human KCNN3 gene

      JOURNAL OF HUMAN GENETICS
    6. Bissig, KD; La Fontaine, S; Mercer, JFB; Solioz, M
      Expression of the human menkes ATPase in Xenopus laevis oocytes

      BIOLOGICAL CHEMISTRY
    7. Pflieger, S; Lefebvre, V; Causse, M
      The candidate gene approach in plant genetics: a review

      MOLECULAR BREEDING
    8. Yano, M
      Genetic and molecular dissection of naturally occurring variation

      CURRENT OPINION IN PLANT BIOLOGY
    9. 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
    10. Bowen, T; Williams, N; Norton, N; Spurlock, G; Wittekindt, OH; Morris-Rosendahl, DJ; Williams, H; Brzustowicz, L; Hoogendoorn, B; Zammit, S; Jones, G; Sanders, RD; Jones, LA; McCarthy, G; Jones, S; Bassett, A; Cardno, AG; Owen, MJ; O'Donovan, MC
      Mutation screening of the KCNN3 gene reveals a rare frameshift mutation

      MOLECULAR PSYCHIATRY
    11. 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
    12. 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
    13. Wang, T; Franke, P; Neidt, H; Cichon, S; Knapp, M; Lichtermann, D; Maier, W; Propping, P; Nothen, MM
      Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach

      MOLECULAR PSYCHIATRY
    14. Haider, MZ; Devarajan, LV; Al-Essa, M; Srivastva, BS; Kumar, H; Azad, R; Rashwan, N
      Retinopathy of prematurity: Mutations in the Norrie disease gene and the risk of progression to advanced stages

      PEDIATRICS INTERNATIONAL
    15. Hahn, S; Cho, K; Ryu, K; Kim, J; Pai, K; Kim, M; Park, H; Yoo, O
      Identification of four novel mutations in classical menkes disease and successful prenatal DNA diagnosis

      MOLECULAR GENETICS AND METABOLISM
    16. 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
    17. Weyer, C; Wolford, JK; Hanson, RL; Foley, JE; Tataranni, PA; Bogardus, C; Pratley, RE
      Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21-q23 and is associated with a common polymorphism in LMNA in Pima Indians

      MOLECULAR GENETICS AND METABOLISM
    18. Lewis, MT
      Hedgehog signaling in mouse mammary gland development and neoplasia

      JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
    19. Lucotte, G
      Frequency analysis and allele map in favor of the Celtic origin of the C282Y mutation of hemochromatosis

      BLOOD CELLS MOLECULES AND DISEASES
    20. Jerome, LA; Papaioannou, VE
      DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

      NATURE GENETICS
    21. Bayes, M; Prieto, I; Noguchi, J; Barbero, JL; Jurado, LAP
      Evaluation of the Stag3 gene and the synaptonemal complex in a rat model (as/as) for male infertility

      MOLECULAR REPRODUCTION AND DEVELOPMENT
    22. Safronova, LD; Kudryavtsev, IV
      Transmission ratio distortion, sterility, and control of the t-complex function in sperm

      RUSSIAN JOURNAL OF GENETICS
    23. Blaveri, E; Kalsi, G; Lawrence, J; Quested, D; Moorey, H; Lamb, G; Kohen, D; Shiwach, R; Chowdhury, U; Curtis, D; McQuillin, A; Gramoustianou, ES; Gurling, HMD
      Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1)

      EUROPEAN JOURNAL OF HUMAN GENETICS
    24. Chai, JH; Locke, DP; Ohta, T; Greally, JM; Nicholls, RD
      Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site

      MAMMALIAN GENOME
    25. Tang, ZH; Tracy, RP
      Candidate genes and confirmed genetic polymorphisms associated with cardiovascular diseases: A tabular assessment

      JOURNAL OF THROMBOSIS AND THROMBOLYSIS
    26. Brewer, GJ
      Commentary: Landmark articles on copper in the field of human health

      JOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE
    27. Hedera, P
      Ethical principles and pitfalls of genetic testing for dementia

      JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
    28. Nurmi, EL; Bradford, Y; Chen, YH; Hall, J; Arnone, B; Gardiner, MB; Hutcheson, HB; Gilbert, JR; Pericak-Vance, MA; Copeland-Yates, SA; Michaelis, RC; Wassink, TH; Santangelo, SL; Sheffield, VC; Piven, J; Folstein, SE; Haines, JL; Sutcliffe, JS
      Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

      GENOMICS
    29. Cunliffe, P; Reed, V; Boyd, Y
      Intragenic deletions at Atp7a in mouse models for Menkes disease

      GENOMICS
    30. Shimizu, M; Higuchi, K; Kasai, S; Tsuboyama, T; Matsushita, M; Mori, M; Shimizu, Y; Nakamura, T; Hosokawa, M
      Chromosome 13 locus, Pbd2, regulates bone density in mice

      JOURNAL OF BONE AND MINERAL RESEARCH
    31. Palmer, CA; Percy, AK
      Neuropathology of occipital horn syndrome

      JOURNAL OF CHILD NEUROLOGY
    32. Rommelspacher, H; Smolka, M; Schmidt, LG; Samochowiec, J; Hoehe, MR
      Genetic analysis of the mu-opioid receptor in alcohol-dependent individuals

      ALCOHOL
    33. Kraft, P
      A robust score test for linkage disequilibrium in general pedigrees

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

      GENETIC EPIDEMIOLOGY
    35. 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
    36. Willett-Brozick, JE; Savul, SA; Richey, LE; Baysal, BE
      Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation

      HUMAN GENETICS
    37. John, S; Eyre, S; Myerscough, A; Barrett, J; Silman, A; Ollier, W; Worthington, J
      Linkage and association analysis of candidate genes in rheumatoid arthritis

      JOURNAL OF RHEUMATOLOGY
    38. 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
    39. Rossi, L; De Martino, A; Marchese, E; Piccirilli, S; Rotilio, G; Ciriolo, MR
      Neurodegeneration in the animal model of Menkes' disease involves Bcl-2-linked apoptosis

      NEUROSCIENCE
    40. Fox, MS; Pera, RAR
      Male infertility, genetic analysis of the DAZ genes on the human Y chromosome and genetic analysis of DNA repair

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    41. Waters, PD; Duffy, B; Frost, CJ; Delbridge, ML; Graves, JAM
      The human Y chromosome derives largely from a single autosomal region added to the sex chromosomes 80-130 million years ago

      CYTOGENETICS AND CELL GENETICS
    42. Pigullo, S; Di Maria, E; Marchese, R; Assini, A; Bellone, E; Scaglione, C; Vitale, C; Bonuccelli, U; Barone, P; Ajmar, F; Martinelli, P; Abbruzzese, G; Mandich, P
      No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients

      JOURNAL OF NEURAL TRANSMISSION
    43. Schonfeld-Warden, NA; Warden, CH
      Physiological effects of variants in human uncoupling proteins: UCP2 influences body-mass index

      BIOCHEMICAL SOCIETY TRANSACTIONS
    44. Quinton, R; Duke, VM; Robertson, A; Kirk, JMW; Matfin, G; de Zoysa, PA; Azcona, C; MacColl, GS; Jacobs, HS; Conway, GS; Besser, M; Stanhope, RG; Bouloux, PMG
      Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization

      CLINICAL ENDOCRINOLOGY
    45. van Mil, SWC; Klomp, LWJ; Bull, LN; Houwen, RHJ
      FIC1 disease: A spectrum of intrahepatic cholestatic disorders

      SEMINARS IN LIVER DISEASE
    46. Hansel, DE; May, V; Eipper, BA; Ronnett, GV
      Pituitary adenylyl cyclase-activating peptides and alpha-amidation in olfactory neurogenesis and neuronal survival in vitro

      JOURNAL OF NEUROSCIENCE
    47. De Lucia, F; Lorain, S; Scamps, C; Galisson, F; Machold, J; Lipinski, M
      Subnuclear localization and mitotic phosphorylation of HIRA, the human homologue of Saccharomyces cerevisiae transcriptional regulators Hir1p/Hir2p

      BIOCHEMICAL JOURNAL
    48. Robertson, A; MacColl, GS; Nash, JAB; Boehm, MK; Perkins, SJ; Bouloux, PMG
      Molecular modelling and experimental studies of mutation and cell-adhesionsites in the fibronectin type III and whey acidic protein domains of humananosmin-1

      BIOCHEMICAL JOURNAL
    49. Staessen, JA; Wang, JG; Brand, E; Barlassina, C; Birkenhager, WH; Herrmann, SM; Fagard, R; Tizzoni, L; Bianchi, G
      Effects of three candidate genes on prevalence and incidence of hypertension in a Caucasian population

      JOURNAL OF HYPERTENSION
    50. Meddeb-Garnaoui, A; Gritli, S; Garbouj, S; Ben Fadhel, M; El Kares, R; Mansour, L; Kaabi, B; Chouchane, L; Ben Salah, A; Dellagi, K
      Association analysis of HLA-class II and class III gene polymorphisms in the susceptibility to mediterranean visceral leishmaniasis

      HUMAN IMMUNOLOGY
    51. Riordan, SM; Williams, R
      The Wilson's disease gene and phenotypic diversity

      JOURNAL OF HEPATOLOGY
    52. 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
    53. Lorain, S; Lecluse, Y; Scamps, C; Mattei, MG; Lipinski, M
      Identification of human and mouse HIRA-interacting protein-5 (HIRIP5), twomammalian representatives in a family of phylogenetically conserved proteins with a role in the biogenesis of Fe/S proteins

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    54. Moczulski, DK; Grzeszczak, W; Gawlik, B
      Role of hemochromatosis C282Y and H63D mutations in HFE gene in development of type 2 diabetes and diabetic nephropathy

      DIABETES CARE
    55. Wassink, TH; Piven, J; Vieland, VJ; Huang, J; Swiderski, RE; Pietila, J; Braun, T; Beck, G; Folstein, SE; Haines, JL; Sheffield, VC
      Evidence supporting WNT2 as an autism susceptibility gene

      AMERICAN JOURNAL OF MEDICAL GENETICS
    56. Yamada, K; Limprasert, P; Ratanasukon, M; Tengtrisorn, S; Yingchareonpukdee, J; Vasiknsenonte, P; Kitaoka, T; Ghadami, M; Niikawa, N; Kishino, T
      Two Thai families with Norrie disease (ND): Association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier

      AMERICAN JOURNAL OF MEDICAL GENETICS
    57. Pflieger, S; Palloix, A; Caranta, C; Blattes, A; Lefebvre, V
      Defense response genes co-localize with quantitative disease resistance loci in pepper

      THEORETICAL AND APPLIED GENETICS
    58. Huh, JH; Kang, BC; Nahm, SH; Kim, S; Ha, KS; Lee, MH; Kim, BD
      A candidate gene approach identified phytoene synthase as the locus for mature fruit color in red pepper (Capsicum spp.)

      THEORETICAL AND APPLIED GENETICS
    59. Zhou, H; Liu, W; Lamont, SJ
      Genetic variation among chicken lines and mammalian species in specific genes

      POULTRY SCIENCE
    60. Wang, XL; Woo, YM; Kim, CS; Larkins, BA
      Quantitative trait locus mapping of loci influencing elongation factor 1 alpha content in maize endosperm

      PLANT PHYSIOLOGY
    61. Andrews, NC
      Mining copper transport genes

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    62. Kuo, YM; Zhou, B; Cosco, D; Gitschier, J
      The copper transporter CTR1 provides an essential function in mammalian embryonic development

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    63. van Tilburg, J; van Haeften, TW; Pearson, P; Wijmenga, C
      Defining the genetic contribution of type 2 diabetes mellitus

      JOURNAL OF MEDICAL GENETICS
    64. Dundar, M; Gordon, TM; Ozyazgan, I; Oguzkaya, F; Ozkul, Y; Cooke, A; Wilkinson, AG; Holloway, S; Goodman, FR; Tolmie, JL
      A novel acropectoral syndrome maps to chromosome 7q36

      JOURNAL OF MEDICAL GENETICS
    65. Goldberg, AFX; Fales, LM; Hurley, JB; Khattree, N
      Folding and subunit assembly of photoreceptor peripherin/rds is mediated by determinants within the extracellular/intradiskal EC2 domain - Implications for heterogeneous molecular pathologies

      JOURNAL OF BIOLOGICAL CHEMISTRY
    66. Hou, ZJ; Narindrasorasak, S; Bhushan, B; Sarkar, B; Mitra, B
      Functional analysis of chimeric proteins of the Wilson Cu(I)-ATPase (ATP7B) and ZntA, a Pb(II)/Zn(II)/Cd(II)-ATPase from Escherichia coli

      JOURNAL OF BIOLOGICAL CHEMISTRY
    67. Arnesano, F; Banci, L; Bertini, I; Cantini, F; Ciofi-Baffoni, S; Huffman, DL; O'Halloran, TV
      Characterization of the binding interface between the copper chaperone Atx1 and the first cytosolic domain of Ccc2 ATPase

      JOURNAL OF BIOLOGICAL CHEMISTRY
    68. Kotenko, SV; Izotova, LS; Mirochnitchenko, OV; Esterova, E; Dickensheets, H; Donnelly, RP; Pestka, S
      Identification of the functional interleukin-22 (IL-22) receptor complex -The IL-10R2 chain (IL-10R beta) is a common chain of both the IL-10 and IL-22 (IL-10-related T cell-derived inducible factor, IL-TIF) receptor complexes

      JOURNAL OF BIOLOGICAL CHEMISTRY
    69. Wang, DX; Quillan, JM; Winans, K; Lucas, JL; Sadee, W
      Single nucleotide polymorphisms in the human mu opioid receptor gene alterbasal G protein coupling and calmodulin binding

      JOURNAL OF BIOLOGICAL CHEMISTRY
    70. Voskoboinik, I; Mar, J; Strausak, D; Camakaris, J
      The regulation of catalytic activity of the menkes copper-translocating P-type ATPase - Role of high affinity copper-binding sites

      JOURNAL OF BIOLOGICAL CHEMISTRY
    71. Tsivkovskii, R; MacArthurs, BC; Lutsenko, S
      The Lys(1010)-Lys(1325) fragment of the Wilson's disease protein binds nucleotides and interacts with the N-terminal domain of this protein in a copper-dependent manner

      JOURNAL OF BIOLOGICAL CHEMISTRY
    72. Campbell, WA; Thompson, NL
      Overexpression of LAT1/CD98 light chain is sufficient to increase system L-amino acid transport activity in mouse hepatocytes but not fibroblasts

      JOURNAL OF BIOLOGICAL CHEMISTRY
    73. Banci, L; Bertini, I; Ciofi-Baffoni, S; Huffman, DL; O'Halloran, TV
      Solution structure of the yeast copper transporter domain Ccc2a in the apoand Cu(I)-loaded states

      JOURNAL OF BIOLOGICAL CHEMISTRY
    74. Rasmussen, ML; Folsom, AR; Catellier, DJ; Tsai, MY; Garg, U; Eckfeldt, JH
      A prospective study of coronary heart disease and the hemochromatosis gene(HFE) C282Y mutation: the Atherosclerosis Risk in Communities (ARIC) study

      ATHEROSCLEROSIS
    75. Clark, RM; Marker, PC; Roessler, E; Dutra, A; Schimenti, JC; Muenke, M; Kingsley, DM
      Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1

      GENETICS
    76. Luo, TH; Zhao, Y; Li, G; Yuan, WT; Zhao, JJ; Chen, JL; Huang, W; Luo, M
      A genome-wide search for Type II diabetes susceptibility genes in Chinese Hans

      DIABETOLOGIA
    77. Le Gac, G; Mura, C; Ferec, C
      Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC

      CLINICAL CHEMISTRY
    78. Lyon, E; Frank, EL
      Hereditary hemochromatosis since discovery of the HFE gene

      CLINICAL CHEMISTRY
    79. Dereure, O; Aguilar-Martinez, P; Bessis, D; Perney, P; Vallat, C; Guillot, B; Blanc, F; Guilhou, JJ
      HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France

      BRITISH JOURNAL OF DERMATOLOGY
    80. Hatanaka, T; Huang, W; Ling, R; Prasad, PD; Sugawara, M; Leibach, FH; Ganapathy, V
      Evidence for the transport of neutral as well as cationic amino acids by ATA3, a novel and liver-specific subtype of amino acid transport system A

      BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
    81. Wu, ZY; Wang, N; Lin, MT; Fang, L; Murong, SX; Yu, L
      Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in Chinese patients with Wilson disease

      ARCHIVES OF NEUROLOGY
    82. Steinbart, EJ; Smith, CO; Poorkaj, P; Bird, TD
      Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia

      ARCHIVES OF NEUROLOGY
    83. Xu, PY; Liang, XL; Jankovic, J; Le, W
      Identification of a high frequency of mutation at exon 8 of the ATP7B genein a Chinese population with Wilson disease by fluorescent PCR

      ARCHIVES OF NEUROLOGY
    84. Dagenais, SL; Adam, AN; Innis, JW; Glover, TW
      A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipitalhorn syndrome and not in Menkes disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    85. Herzing, LBK; Kim, SJ; Cook, EH; Ledbetter, DH
      The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression

      AMERICAN JOURNAL OF HUMAN GENETICS
    86. Slager, SL; Schaid, DJ
      Case-control studies of genetic markers: Power and sample size approximations for Armitage's test for trend

      HUMAN HEREDITY
    87. Scimeca, JC; Franchi, A; Trojani, C; Parrinello, H; Grosgeorge, J; Robert, C; Jaillon, O; Poirier, C; Gaudray, P; Carle, GF
      The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants

      BONE
    88. Rankinen, T; Perusse, L; Gagnon, J; Chagnon, YC; Leon, AS; Skinner, JS; Wilmore, JH; Rao, DC; Bouchard, C
      Angiotensin-converting enzyme ID polymorphism and fitness phenotype in theHERITAGE Family Study

      JOURNAL OF APPLIED PHYSIOLOGY
    89. Pang, CP; Baum, L; Lam, DSC
      Hunting for disease genes in multi-functional diseases

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    90. Lee, CC; Wu, JY; Tsai, FJ; Kodama, H; Abe, T; Yang, CF; Tsai, CH
      Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association

      JOURNAL OF HUMAN GENETICS
    91. Ogawa, A; Yamamoto, S; Kanazawa, M; Ogawa, E; Takayanagi, M; Hasegawa, S; Kohno, Y
      Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population

      JOURNAL OF HUMAN GENETICS
    92. Gion, JM; Rech, P; Grima-Pettenati, J; Verhaegen, D; Plomion, C
      Mapping candidate genes in Eucalyptus with emphasis on lignification genes

      MOLECULAR BREEDING
    93. Himelblau, E; Amasino, RM
      Delivering copper within plant cells

      CURRENT OPINION IN PLANT BIOLOGY
    94. Wassink, TH; Crowe, RR; Andreasen, NC
      Tumor necrosis factor receptor-II: heritability and effect on brain morphology in schizophrenia

      MOLECULAR PSYCHIATRY
    95. Tahir, E; Yazgan, Y; Cirakoglu, B; Ozbay, F; Waldman, I; Asherson, PJ
      Association and linkage of DRD4 and DRD5 with attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children

      MOLECULAR PSYCHIATRY
    96. Chowdari, KV; Wood, J; Ganguli, R; Gottesman, II; Nimgaonkar, VL
      Lack of association between schizophrenia and a CAG repeat polymorphism ofthe hSKCa3 gene in a North Eastern US sample

      MOLECULAR PSYCHIATRY
    97. Grunhage, F; Schulze, TG; Muller, DJ; Lanczik, M; Franzek, E; Albus, M; Borrmann-Hassenbach, M; Knapp, M; Cichon, S; Maier, W; Rietschel, M; Propping, P; Nothen, MM
      Systematic screening for DNA sequence Variation in the coding region of the human dopamine transporter gene (DAT1)

      MOLECULAR PSYCHIATRY
    98. Franke, P; Nothen, MM; Wang, T; Knapp, M; Lichtermann, D; Neidt, H; Sander, T; Propping, P; Maier, W
      DRD4 exon IIIVNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach

      MOLECULAR PSYCHIATRY
    99. Sfaello, I; Castelnau, P; Blanc, N; Ogier, H; Evrard, P; Arzimanoglou, A
      Infantile spasms and Menkes disease

      EPILEPTIC DISORDERS
    100. Dubois-Laforgue, D; Larger, E; Timsit, J
      Is diabetes mellitus a sufficient condition to suspect hemochromatosis?

      DIABETES & METABOLISM


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/06/20 alle ore 17:07:29