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    1. Mullerad, M; Falik, T; Madeb, R; Nativ, O
      Hereditary prostate cancer - the search for the gene

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    2. Zicha, J; Negrin, CD; Dobesova, Z; Carr, F; Vokurkova, M; McBride, MW; Kunes, J; Dominiczak, AF
      Altered Na+-K+ pump activity and plasma lipids in salt-hypertensive Dahl rats: relationship to Atp1a1 gene

      PHYSIOLOGICAL GENOMICS
    3. Dutil, J; Deng, AY
      Further chromosomal mapping of a blood pressure QTL in Dahl rats on chromosome 2 using congenic strains

      PHYSIOLOGICAL GENOMICS
    4. Ventura, M; Archidiacono, N; Rocchi, M
      Centromere emergence in evolution

      GENOME RESEARCH
    5. Goode, EL; Stanford, JL; Peters, MA; Janer, M; Gibbs, M; Kolb, S; Badzioch, MD; Hood, L; Ostrander, EA; Jarvik, GP
      Clinical characteristics of prostate cancer in an analysis of linkage to four putative susceptibility loci

      CLINICAL CANCER RESEARCH
    6. Frich, L; Glattre, E; Akslen, LA
      Familial occurrence of nonmedullary thyroid cancer: A population-based study of 5673 first-degree relatives of thyroid cancer patients from Norway

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    7. Harach, HR
      Familial nonmedullary thyroid neoplasia

      ENDOCRINE PATHOLOGY
    8. Alsanea, O; Clark, OH
      Familial thyroid cancer

      CURRENT OPINION IN ONCOLOGY
    9. Grunder, S; Geisler, HS; Rainier, S; Fink, JK
      Acid-sensing ion channel (ASCI) 4 gene: physical mapping, genomic organisation, and evaluation as a candidate for paroxysmal dystonia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    10. Cancel-Tassin, G; Latil, A; Valeri, A; Mangin, P; Fournier, G; Berthon, P; Cussenot, O
      PCAP is the major known prostate cancer predisposing locus in families from south and west Europe

      EUROPEAN JOURNAL OF HUMAN GENETICS
    11. Fan, XP; Dion, P; Laganiere, J; Brais, B; Rouleau, GA
      Oligomerization of polyalanine expanded PABPN1 facilitates nuclear proteinaggregation that is associated with cell death

      HUMAN MOLECULAR GENETICS
    12. Cox, NJ
      Challenges in identifying genetic variation affecting susceptibility to type 2 diabetes: Examples from studies of the calpain-10 gene

      HUMAN MOLECULAR GENETICS
    13. Nwosu, V; Carpten, J; Trent, JM; Sheridan, R
      Heterogeneity of genetic alterations in prostate cancer: evidence of the complex nature of the disease

      HUMAN MOLECULAR GENETICS
    14. Marshall, JC; Sites, JW
      A comparison of nuclear and mitochondrial dine shapes in a hybrid zone in the Sceloporus grammicus complex (Squamata : Phrynosomatidae)

      MOLECULAR ECOLOGY
    15. Sambuughin, N; Nelson, TE; Jankovic, J; Xin, CL; Meissner, G; Mullakandov, M; Ji, J; Rosenberg, H; Sivakumar, K; Goldfarb, LG
      Identification and functional characterization of a novel ryanodine receptor mutation causing malignant hyperthermia in North American and South American families

      NEUROMUSCULAR DISORDERS
    16. Meuleman, J; Pou-Serradell, A; Lofgren, A; Ceuterick, C; Martin, JJ; Timmerman, V; Van Broeckhoven, C; De Jonghe, P
      A novel 3 '-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies

      NEUROMUSCULAR DISORDERS
    17. Nomiyama, H; Hieshima, K; Nakayama, T; Sakaguchi, T; Fujisawa, R; Tanase, S; Nishiura, H; Matsuno, K; Takamori, H; Tabira, Y; Yamamoto, T; Miura, R; Yoshie, O
      Human CC chemokine liver-expressed chemokine/CCL16 is a functional ligand for CCR1, CCR2 and CCR5, and constitutively expressed by hepatocytes

      INTERNATIONAL IMMUNOLOGY
    18. Choi, DK; Suzuki, Y; Yoshimura, S; Togashi, T; Hida, M; Taylor, TD; Wang, YP; Sugano, S; Hattori, M; Sakaki, Y
      Molecular cloning and characterization of a gene expressed in mouse developing tongue, mDscr5 gene, a homolog of human DSCR5 (Down syndrome critical region gene 5)

      MAMMALIAN GENOME
    19. Dutil, J; Deng, AY
      Mapping a blood pressure quantitative trait locus to a 5.7-cM region in Dahl salt-sensitive rats

      MAMMALIAN GENOME
    20. Sood, R; Bonner, TI; Makalowska, I; Stephan, DA; Robbins, CM; Connors, TD; Morgenbesser, SD; Su, K; Faruque, MU; Pinkett, H; Graham, C; Baxevanis, AD; Klinger, KW; Landes, GM; Trent, JM; Carpten, JD
      Cloning and characterization of 13 novel transcripts and the human RC58 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus

      GENOMICS
    21. Rigat, BA; Lorimore, SA; Plumb, MA; Wright, EG
      A PCR-based clonal analysis of radiation-induced loss of heterozygosity inhaemopoietic stem cells

      LEUKEMIA
    22. Forssmann, U; Magert, HJ; Adermann, K; Escher, SE; Forssmann, WG
      Hemofiltrate CC chemokines with unique biochemical properties: HCC-1/CCL14a and HCC-2/CCL15

      JOURNAL OF LEUKOCYTE BIOLOGY
    23. Liang, KY; Chiu, YF; Beaty, TH; Wjst, M
      Multipoint analysis using affected sib pairs: Incorporating linkage evidence from unlinked regions

      GENETIC EPIDEMIOLOGY
    24. Herrmann, T; Buchkremer, F; Gosch, I; Hall, AM; Bernlohr, DA; Stremmel, W
      Mouse fatty acid transport protein 4 (FATP4): Characterization of the geneand functional assessment as a very long chain acyl-CoA synthetase

      GENE
    25. Seranski, P; Hoff, C; Radelof, U; Hennig, S; Reinhardt, R; Schwartz, CE; Heiss, NS; Poustka, A
      RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients

      GENE
    26. Modarressi, MH; Cameron, J; Taylor, KE; Wolfe, J
      Identification and characterisation of a novel gene, TSGA10, expressed in testis

      GENE
    27. 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
    28. Pravenec, M; Zidek, V; Musilova, A; Vorlicek, J; Kren, V; St Lezin, E; Kurtz, TW
      Genetic isolation of a blood pressure quantitative trait locus on chromosome 2 in the spontaneously hypertensive rat

      JOURNAL OF HYPERTENSION
    29. Barnard, R; Kelly, G; Manzetti, SO; Harris, EL
      Neither the New Zealand genetically hypertensive strain nor Dahl salt-sensitive strain has an A1079T transversion in the alpha 1 isoform of the Na+,K+-ATPase gene

      HYPERTENSION
    30. Stanford, JL; Ostrander, EA
      Familial prostate cancer

      EPIDEMIOLOGIC REVIEWS
    31. Hayes, RB
      Gene-environment interrelations in prostate cancer

      EPIDEMIOLOGIC REVIEWS
    32. Malakooti, J; Dahdal, RY; Dudeja, PK; Layden, TJ; Ramaswamy, K
      The human Na+/H+ exchanger NHE2 gene: genomic organization and promoter characterization

      AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
    33. Zhu, G; Gillessen-Kaesbach, G; Wirth, J; Passarge, E; Bartsch, O
      Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    34. Sullivan, PF; O'Neill, FA; Walsh, D; Ma, YL; Kendler, KS; Straub, RE
      Analysis of epistasis in linked regions in the Irish Study of High-DensitySchizophrenia Families

      AMERICAN JOURNAL OF MEDICAL GENETICS
    35. Riegel, M; Morava, E; Czako, M; Kosztolanyi, G; Schinzel, A
      Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    36. Roggenbuck, JA; Fink, JM; Mendelsohn, NJ
      Unique case of trisomy 2p24.3-pter with no associated monosomy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    37. Infante, J; Garcia, A; Combarros, O; Mateo, JI; Berciano, J; Sedano, MJ; Gutierrez-Rivas, EJ; Palau, F
      Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion

      MUSCLE & NERVE
    38. Dematteis, M; Pepin, JL; Jeanmart, M; Deschaux, C; Labarre-Vila, A; Levy, P
      Charcot-Marie-Tooth disease and sleep apnoea syndrome: a family study

      LANCET
    39. Heinonen, S; Eloranta, ML; Heiskanen, J; Punnonen, K; Helisalmi, S; Mannermaa, A; Hiltunen, M
      Maternal susceptibility locus for obstetric cholestasis maps to chromosomeregion 2p13 in Finnish patients

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    40. Aarskog, NK; Aadland, S; Gjerde, IO; Vedeler, CA
      Molecular genetic analysis of Charcot-Marie-Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    41. Albrecht, B; Mergenthaler, S; Eggermann, K; Zerres, K; Passarge, E; Eggermann, T
      Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)

      JOURNAL OF MEDICAL GENETICS
    42. Bashirova, AA; Geijtenbeek, TBH; van Duijnhoven, GCF; van Vliet, SJ; Eilering, JBG; Martin, MP; Wu, L; Martin, TD; Viebig, N; Knolle, PA; KewalRamani, VN; van Kooyk, Y; Carrington, M
      A dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (DC-SIGN)-related protein is highly expressed on human liver sinusoidal endothelial cells and promotes HIV-1 infection

      JOURNAL OF EXPERIMENTAL MEDICINE
    43. Cordell, HJ; Todd, JA; Hill, NJ; Lord, CJ; Lyons, PA; Peterson, LB; Wicker, LS; Clayton, DG
      Statistical modeling of interlocus interactions in a complex disease: Rejection of the multiplicative model of epistasis in type 1 diabetes

      GENETICS
    44. Rueffert, H; Olthoff, D; Deutrich, C; Froster, UG
      Determination of a positive malignant hyperthermia (MH) disposition without the in vitro contracture test in families carrying the RYR1 Arg614Cys mutation

      CLINICAL GENETICS
    45. Wang, L; McDonnell, SK; Elkins, DA; Slager, SL; Christensen, E; Marks, AF; Cunningham, JM; Peterson, BJ; Jacobsen, SJ; Cerhan, JR; Blute, ML; Schaid, DJ; Thibodeau, SN
      Role of HPC2/ELAC2 in hereditary prostate cancer

      CANCER RESEARCH
    46. Thomas, F; Jais, P; Cohen-Akenine, A
      Genetics of prostate cancer

      BULLETIN DU CANCER
    47. Rueffert, H; Olthoff, D; Deutrich, C; Thamm, B; Froster, UG
      Homozygous and heterozygous Arg614Cys mutations (1840C -> T) in the ryanodine receptor gene co-segregate with malignant hyperthermia susceptibility in a German family

      BRITISH JOURNAL OF ANAESTHESIA
    48. Wiktor, A; Feldman, GL; Bawle, EV; Czarnecki, P; Conard, JV; Van Dyke, DL
      Deletion of 2q37 and duplication of 10q24: Two cases in the same family and review of the literature

      ANNALES DE GENETIQUE
    49. Hsieh, CL; Oakley-Girvan, I; Balise, RR; Halpern, J; Gallagher, RP; Wu, AH; Kolonel, LN; O'Brien, LE; Lin, IPG; Van den Berg, DJ; Teh, CZ; West, DW; Whittemore, AS
      A genome screen of families with multiple cases of prostate cancer: Evidence of genetic heterogeneity

      AMERICAN JOURNAL OF HUMAN GENETICS
    50. Xu, JF; Zheng, SQL; Carpten, JD; Nupponen, NN; Robbins, CM; Mestre, J; Moses, TY; Faith, DA; Kelly, BD; Isaacs, SD; Wiley, KE; Ewing, DM; Bujnowszky, P; Chang, BI; Bailey-Wilson, J; Bleecker, ER; Walsh, PC; Trent, JM; Meyers, DA; Isaacs, WB
      Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer

      AMERICAN JOURNAL OF HUMAN GENETICS
    51. Ogunkolade, WB; Ramachandran, A; McDermott, MF; Kumarajeewa, TR; Curtis, D; Snehalatha, C; Mohan, V; Cassell, PG; Eskdale, J; Gallagher, G; Hitman, GA
      Family association studies of markers on chromosome 2q and Type 1 diabetesin subjects from South India

      DIABETES-METABOLISM RESEARCH AND REVIEWS
    52. Singh, R; Eeles, RA; Durocher, F; Simard, J; Edwards, S; Badzioch, M; Kote-Jarai, Z; Teare, D; Ford, D; Dearnaley, D; Ardern-Jones, A; Murkin, A; Dowe, A; Shearer, R; Kelly, J; Labrie, F; Easton, D; Narod, SA; Tonin, PN; Foulkes, WD
      High risk genes predisposing to prostate cancer development - do they exist?

      PROSTATE CANCER AND PROSTATIC DISEASES
    53. Barr, CL; Feng, Y; Wigg, K; Bloom, S; Roberts, W; Malone, M; Schachar, R; Tannock, R; Kennedy, JL
      Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder

      MOLECULAR PSYCHIATRY
    54. Kurotobi, S; Kado, Y; Miki, K; Hara, T; Nakanishi, K; Taniguchi, M; Shin, K; Honda, A; Matsuoka, T; Nagai, T
      Deletion of the long arm of chromosome 2 (2q22-q24.2): Case report and review of the literature

      PEDIATRICS INTERNATIONAL
    55. Akiba, T; Odake, A; Shirahata, E; Matsunaga, A; Sakamoto, M; Yazaki, N
      Three patients with different phenotypes in a family with chromosome 22q11.2 deletions

      PEDIATRICS INTERNATIONAL
    56. Cowley, AW; Stoll, M; Greene, AS; Kaldunski, ML; Roman, RJ; Tonellato, PJ; Schork, NJ; Dumas, P; Jacob, HJ
      Genetically defined risk of salt sensitivity in an intercross of Brown Norway and Dahl S rats

      PHYSIOLOGICAL GENOMICS
    57. Reifsnyder, PC; Churchill, G; Leiter, EH
      Maternal environment and genotype interact to establish diabesity in mice

      GENOME RESEARCH
    58. Saito, S; Nishimura, H; Phelps, RG; Wolf, I; Suzuki, M; Honjo, T; Bona, C
      Induction of skin fibrosis in mice expressing a mutated fibrillin-1 gene

      MOLECULAR MEDICINE
    59. Altshuler, D; Daly, M; Kruglyak, L
      Guilt by association

      NATURE GENETICS
    60. Horikawa, Y; Oda, N; Cox, NJ; Li, XQ; Orho-Melander, M; Hara, M; Hinokio, Y; Lindner, TH; Mashima, H; Schwarz, PEH; del Bosque-Plata, L; Horikawa, Y; Oda, Y; Yoshiuchi, I; Colilla, S; Polonsky, KS; Wei, S; Concannon, P; Iwasaki, N; Schulze, T; Baier, LJ; Bogardus, C; Groop, L; Boerwinkle, E; Hanis, CL; Bell, GI
      Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

      NATURE GENETICS
    61. Pennisi, D; Gardner, J; Chambers, D; Hosking, B; Peters, J; Muscat, G; Abbott, C; Koopman, P
      Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice

      NATURE GENETICS
    62. McCarthy, TV; Quane, KA; Lynch, PJ
      Ryanodine receptor mutations in malignant hyperthermia and central core disease

      HUMAN MUTATION
    63. Aman, AK; Jonsson, BA; Damber, JE; Bergh, A; Emanuelsson, M; Gronberg, H
      Low frequency of allelic imbalance at the prostate cancer susceptibility loci HPC1 and 1p36 in Swedish men with hereditary prostate cancer

      GENES CHROMOSOMES & CANCER
    64. Achuthan, R; Bell, SM; Leek, JP; Roberts, P; Horgan, K; Markham, AF; Selby, PJ; MacLennan, KA
      Novel translocation of the BCL10 gene in a case of mucosa associated lymphoid tissue lymphoma

      GENES CHROMOSOMES & CANCER
    65. Debeer, P; Schoenmakers, EFPM; Thoelen, R; Holvoet, M; Kuittinen, T; Fabry, G; Fryns, JP; Goodman, FR; Van de Ven, WJM
      Physical map of a 1.5 Mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint

      EUROPEAN JOURNAL OF HUMAN GENETICS
    66. Friedrich, U; Houman, M; Sandgaard, J; Rosgaard, A; Sunde, L
      Microdissection of chromosome 2 - between-arm intrachromosomal insertion

      EUROPEAN JOURNAL OF HUMAN GENETICS
    67. Bal, M; Schrander-Stumpel, CTRM; Meers, LEC; Theunissen, PMVM; Hamers, AJH; Wennekes, MJ; Engelen, JJM
      De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphism

      GENETIC COUNSELING
    68. Kasai, F; Takahashi, E; Koyama, K; Terao, K; Suto, Y; Tokunaga, K; Nakamura, Y; Hirai, M
      Comparative FISH mapping of the ancestral fusion point of human chromosome2

      CHROMOSOME RESEARCH
    69. Cattanach, BM; Peters, J; Ball, S; Rasberry, C
      Two imprinted gene mutations: three phenotypes

      HUMAN MOLECULAR GENETICS
    70. Brown, RL; Pollock, AN; Couchman, KG; Hodges, M; Hutchinson, DO; Waaka, R; Lynch, P; McCarthy, TV; Stowell, KM
      A novel ryanodine receptor mutation and genotype-phenotype correlation in a large malignant hyperthermia New Zealand Maori pedigree

      HUMAN MOLECULAR GENETICS
    71. Dubourg, O; Mouton, P; Brice, A; LeGuern, E; Bouche, P
      Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies

      NEUROMUSCULAR DISORDERS
    72. Maximo, V; Sobrinho-Simoes, M
      Hurthle cell tumours of the thyroid. A review with emphasis on mitochondrial abnormalities with clinical relevance

      VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    73. Pennisi, DJ; James, KM; Hosking, B; Muscat, GEO; Koopman, P
      Structure, mapping, and expression of human SOX18

      MAMMALIAN GENOME
    74. Lesca, G; Meunier, S; Zine, A; Jeannoel, P; Latour, P; Vandenberghe, A
      Hereditary neuropathy with liability to pressure palsies (HNPP) in a child: clinical and biological features

      ARCHIVES DE PEDIATRIE
    75. Pazzaglia, S; Pariset, L; Rebessi, S; Saran, A; Coppola, M; Covelli, V; Moody, J; Bouffler, S; Cox, R; Silver, A
      Somatic cell hybrids for high-density mapping of chromosome 2 breakpoints in radiation-induced myeloid leukemia cell lines from inbred mice

      MOLECULAR CARCINOGENESIS
    76. Sakao, Y; Kawai, T; Takeuchi, O; Copeland, NG; Gilbert, DJ; Jenkins, NA; Takeda, K; Akira, S
      Mouse proteasomal ATPases Psmc3 and Psmc4: Genomic organization and gene targeting

      GENOMICS
    77. Hayashi, S; Wakabayashi, K; Ishikawa, A; Nagai, H; Saito, M; Maruyama, M; Takahashi, T; Ozawa, T; Tsuji, S; Takahashi, H
      An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene

      MOVEMENT DISORDERS
    78. Kumar, S; Mitnik, C; Valente, G; Floyd-Smith, G
      Expansion and molecular evolution of the interferon-induced 2 '-5 ' oligoadenylate synthetase gene family

      MOLECULAR BIOLOGY AND EVOLUTION
    79. Tukun, A; Renda, Y; Topcu, M; Tuncali, T; Bokesoy, I
      Mental retardation with rare fragile site expressed at 2q11

      BRAIN & DEVELOPMENT
    80. Saito, M; Maruyama, M; Ikeuchi, K; Kondo, H; Ishikawa, A; Yuasa, T; Tsuji, S
      Autosomal recessive juvenile parkinsonism

      BRAIN & DEVELOPMENT
    81. Cicirata, F; Parenti, R; Spinella, F; Giglio, S; Tuorto, F; Zuffardi, O; Gulisano, M
      Genomic organization and chromosomal localization of the mouse Connexin36 (mCx36) gene

      GENE
    82. Boucher, CA; Winchester, CL; Hamilton, GM; Winter, AD; Johnson, KJ; Bailey, MES
      Structure, mapping and expression of the human gene encoding the homeodomain protein, SIX2

      GENE
    83. Vaidyanathan, VV; Roche, PA
      Structure and chromosomal localization of the mouse SNAP-23 gene

      GENE
    84. Singh, DP; Kimura, A; Chylack, LT; Shinohara, T
      Lens epithelium-derived growth factor (LEDGF/p75) and p52 are derived froma single gene by alternative splicing

      GENE
    85. Maruyama, M; Ikeuchi, T; Saito, M; Ishikawa, A; Yuasa, T; Tanaka, H; Hayashi, S; Wakabayashi, K; Takahashi, H; Tsuji, S
      Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

      ANNALS OF NEUROLOGY
    86. Numakura, C; Lin, CQ; Oka, N; Akiguchi, I; Hayasaka, K
      Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1

      ANNALS OF NEUROLOGY
    87. Aarskog, NK; Vedeler, CA
      Real-time quantitative polymerase chain reaction - A new method that detects both the peripheral myelin protein 22 duplication in Charcot-Marie-Toothtype 1A disease and the peripheral myelin protein 22 deletion in hereditary neuropathy with liability to pressure palsies

      HUMAN GENETICS
    88. Maraj, BH; Leek, JP; Carr, IM; Markham, AF
      Identification of a novel microsatellite marker tightly linked to the KAI-1 gene for predicting prostate cancer progression

      EUROPEAN UROLOGY
    89. Liu, Q; Yu, L; Gao, J; Fu, Q; Zhang, JX; Zhang, PZ; Chen, J; Zhao, SY
      Cloning, tissue expression pattern and genomic organization of latexin, a human homologue of rat carboxypeptidase A inhibitor

      MOLECULAR BIOLOGY REPORTS
    90. Zhang, Q; Topol, LZ; Athanasiou, M; Copeland, NG; Gilbert, DJ; Jenkins, NA; Blair, DG
      Cloning of the murine Drm gene (Cktsf1b1)and characterization of its oncogene suppressible promoter

      CYTOGENETICS AND CELL GENETICS
    91. Suarez, BK; Lin, J; Witte, JS; Conti, DV; Resnick, MI; Klein, EA; Burmester, JK; Vaske, DA; Banerjee, TK; Catalona, WJ
      Replication linkage study for prostate cancer susceptibility genes

      PROSTATE
    92. Beaty, TH; Khoury, MJ
      Interface of genetics and epidemiology

      EPIDEMIOLOGIC REVIEWS
    93. Wambutt, R; Murphy, G; Volckaert, G; Pohl, T; Dusterhoft, A; Stiekema, W; Entian, KD; Terryn, N; Harris, B; Ansorge, W; Brandt, P; Grivell, L; Rieger, M; Weichselgartner, M; de Simone, V; Obermaier, B; Mache, R; Muller, M; Kreis, M; Delseny, M; Puigdomenech, P; Watson, M; Schmidtheini, T; Reichert, B; Portatelle, D; Perez-Alonso, M; Boutry, M; Bancroft, I; Vos, P; Hoheisel, J; Zimmermann, W; Wedler, H; Ridley, P; Langham, SA; McCullagh, B; Bilham, L; Robben, J; Van der Schueren, J; Grymonprez, B; Chuang, YJ; Vandenbussche, F; Braeken, M; Weltjens, I; Voet, M; Bastiaens, I; Aert, R; Defoor, E; Weitzenegger, T; Bothe, G; Ramsperger, U; Hilbert, H; Braun, M; Holzer, E; Brandt, A; Peters, S; van Staveren, M; Dirkse, W; Mooijman, P; Lankhorst, RK; Rose, M; Hauf, J; Kotter, P; Berneiser, S; Hempel, S; Feldpausch, M; Lamberth, S; Van den Daele, H; De Keyser, A; Buysshaert, C; Gielen, J; Villarroel, R; De Clercq, R; Van Montagu, M; Rogers, J; Cronin, A; Quail, M; Bray-Allen, S; Clark, L; Doggett, J; Hall, S; Kay, M; Lennard, N; McLay, K; Mayes, R; Pettett, A; Rajandream, MA; Lyne, M; Benes, V; Rechmann, S; Borkova, D; Blocker, H; Scharfe, M; Grimm, M; Lohnert, TH; Dose, S; de Haan, M; Maarse, A; Schafer, M; Muller-Auer, S; Gabel, C; Fuchs, M; Fartmann, B; Granderath, K; Dauner, D; Herzl, A; Neumann, S; Argiriou, A; Vitale, D; Liguori, R; Piravandi, E; Massenet, O; Quigley, F; Clabauld, G; Mundlein, A; Felber, R; Schnabl, S; Hiller, R; Schmidt, W; Lecharny, A; Aubourg, S; Gy, I; Cooke, R; Berger, C; Monfort, A; Casacuberta, E; Gibbons, T; Weber, N; Vandenbol, M; Bargues, M; Terol, J; Torres, A; Perez-Perez, A; Purnelle, B; Bent, E; Johnson, S; Tacon, D; Jesse, T; Heijnen, L; Schwarz, S; Scholler, P; Heber, S; Bielke, C; Frishmann, D; Haase, D; Lemcke, K; Mewes, HW; Stocker, S; Zaccaria, P; Mayer, K; Schuller, C; Bevan, M
      Progress in Arabidopsis genome sequencing and functional genomics

      JOURNAL OF BIOTECHNOLOGY
    94. Wang, L; Menting, JGT; Stowers, A; Charoenvit, Y; Sacci, JB; Coppel, RL
      Antigens cross reactive with Plasmodium falciparum merozoite surface protein 4 are found in pre-erythrocytic and sexual stages

      MOLECULAR AND BIOCHEMICAL PARASITOLOGY
    95. Kedzierski, L; Black, CG; Coppel, RL
      Characterisation of the merozoite surface protein 4/5 gene of Plasmodium berghei and Plasmodium yoelii

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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/08/20 alle ore 04:05:53