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    1. Gillespie, JW; Ahram, M; Best, CJM; Swalwell, JI; Krizman, DB; Petricoin, EF; Liotta, LA; Emmert-Buck, MR
      The role of tissue microdissection in cancer research

      CANCER JOURNAL
    2. Kazuki, Y; Shinohara, T; Tomizuka, K; Katoh, M; Ohguma, A; Ishida, I; Oshimura, M
      Germline transmission of a transferred human chromosome 21 fragment in transchromosomal mice

      JOURNAL OF HUMAN GENETICS
    3. 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
    4. Barlow, GM; Chen, XN; Shi, ZY; Lyons, GE; Kurnit, DM; Celle, L; Spinner, NB; Zackai, E; Pettenati, MJ; Van Riper, AJ; Vekemans, MJ; Mjaatvedt, CH; Korenberg, JR
      Down syndrome congenital heart disease: A narrowed region and a candidate gene

      GENETICS IN MEDICINE
    5. Frazer, KA; Sheehan, JB; Stokowski, RP; Chen, XY; Hosseini, R; Cheng, JF; Fodor, SPA; Cox, DR; Patil, N
      Evolutionarily conserved sequences on human chromosome 21

      GENOME RESEARCH
    6. Taub, JW
      Relationship of chromosome 21 and acute leukemia in children with Down syndrome

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    7. Moller, JC; Hamer, HM; Oertel, WH; Rosenow, F
      Late-onset myoclonic epilepsy in Down's syndrome (LOMEDS)

      SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    8. Dal Cin, P; Atkins, L; Ford, C; Ariyanayagam, S; Armstrong, SA; George, R; Cleary, A; Morton, CC
      Amplification of AML1 in childhood acute lymphoblastic leukemias

      GENES CHROMOSOMES & CANCER
    9. Shi, QH; Ko, E; Barclay, L; Hoang, T; Rademaker, A; Martin, R
      Cigarette smoking and aneuploidy in human sperm

      MOLECULAR REPRODUCTION AND DEVELOPMENT
    10. Lizcano-Gil, LA; Burgos, K; Guarin, DF
      Prenatal diagnosis and false negative result for a case of Down syndrome with normal karyotype

      GENETIC COUNSELING
    11. Saccone, S; Pavlicek, A; Federico, C; Paces, J; Bernardi, G
      Genes, isochores and bands in human chromosomes 21 and 22

      CHROMOSOME RESEARCH
    12. Altafaj, X; Dierssen, M; Baamonde, C; Marti, E; Visa, J; Guimera, J; Oset, M; Gonzalez, JR; Florez, J; Fillat, C; Estivill, X
      Neurodevelopmental delay, motor abnormalities and cognitive deficits in transgenic mice overexpressing Dyrk1A (minibrain), a murine model of Down's syndrome

      HUMAN MOLECULAR GENETICS
    13. Shinohara, T; Tomizuka, K; Miyabara, S; Takehara, S; Kazuki, Y; Inoue, J; Katoh, M; Nakane, H; Iino, A; Ohguma, A; Ikegami, S; Inokuchi, K; Ishida, I; Reeves, RH; Oshimura, M
      Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome

      HUMAN MOLECULAR GENETICS
    14. Tuggle, CK; Genet, C; Shi, XW; Chardon, P; Sanchez-Serrano, I; Cravens, G; Milan, D; Yerle, M
      Cytogenetic and radiation hybrid mapping reveals conserved synteny and gene order between human Chromosome 21 and pig Chromosome 13

      MAMMALIAN GENOME
    15. Casas, C; Martinez, S; Pritchard, MA; Fuentes, JJ; Nadal, M; Guimera, J; Arbones, M; Florez, J; Soriano, E; Estivill, X; Alcantara, S
      Dscr1, a novel endogenous inhibitor of calcineurin signaling, is expressedin the primitive ventricle of the heart and during neurogenesis

      MECHANISMS OF DEVELOPMENT
    16. Toyota, T; Shimizu, H; Yamada, K; Yoshitsugu, K; Meerabux, J; Hattori, E; Ichimiya, T; Yoshikawa, T
      Karyotype analysis of 161 unrelated schizophrenics: no increased rates of X chromosome mosaicism or inv(9), using ethnically matched and age-stratified controls

      SCHIZOPHRENIA RESEARCH
    17. Chen, YW; Yu, P; Lu, D; Tagle, DA; Cai, T
      A novel isoform of beta-spectrin II localizes to cerebellar Purkinje-cell bodies and interacts with neurofibromatosis type 2 gene product schwannomin

      JOURNAL OF MOLECULAR NEUROSCIENCE
    18. Reymond, A; Friedli, M; Henrichsen, CN; Chapot, F; Deutsch, S; Ucla, C; Rossier, C; Lyle, R; Guipponi, M; Antonarakis, SE
      From PREDs and open reading frames to cDNA isolation: Revisiting the humanchromosome 21 transcription map

      GENOMICS
    19. Olivier, M; Bustos, VI; Levy, MR; Smick, GA; Moreno, I; Bushard, JM; Almendras, AA; Sheppard, K; Zierten, DL; Aggarwal, A; Carlson, CS; Foster, BD; Vo, N; Kelly, L; Liu, X; Cox, DR
      Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21

      GENOMICS
    20. Davisson, MT; Bechtel, LJ; Akeson, EC; Fortna, A; Slavov, D; Gardiner, K
      Evolutionary breakpoints on human chromosome 21

      GENOMICS
    21. Pletcher, MT; Wiltshire, T; Cabin, DE; Villanueva, M; Reeves, RH
      Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21

      GENOMICS
    22. Clay, O; Bernardi, G
      Compositional heterogeneity within and among isochores in mammalian genomes - II. Some general comments

      GENE
    23. Oliver, JL; Bernaola-Galvan, P; Carpena, P; Roman-Roldan, R
      Isochore chromosome maps of eukaryotic genomes

      GENE
    24. Tam, W
      Identification and characterization of human BIC, a gene on chromosome 21 that encodes a noncoding RNA

      GENE
    25. Kurdyukov, SG; Lebedev, YB; Artamonova, II; Gorodentseva, TN; Batrak, AV; Mamedov, IZ; Azhikina, TL; Legchilina, SP; Efimenko, IG; Gardiner, K; Sverdlov, ED
      Full-sized HERV-K (HML-2) human endogenous retroviral LTR sequences on human chromosome 21: map locations and evolutionary history

      GENE
    26. Nizetic, D
      Functional genomics of the Down syndrome

      CROATIAN MEDICAL JOURNAL
    27. Verlinsky, Y; Cieslak, J; Ivakhnenko, V; Evsikov, S; Wolf, G; White, M; Lifchez, A; Kaplan, B; Moise, J; Valle, J; Ginsberg, N; Strom, C; Kuliev, A
      Chromosomal abnormalities in the first and second polar body

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    28. Akeson, EC; Lambert, JP; Narayanswami, S; Gardiner, K; Bechtel, LJ; Davisson, MT
      Ts65Dn - localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome

      CYTOGENETICS AND CELL GENETICS
    29. Caria, H; Chaveca, T; Rueff, J
      Aneuploidy induced in lymphocytes of parents of trisomic 21 children

      TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS
    30. Scriven, PN; Flinter, FA; Braude, PR; Ogilvie, CM
      Robertsonian translocations - reproductive risks and indications for preimplantation genetic diagnosis

      HUMAN REPRODUCTION
    31. Ge, YB; Konrad, MA; Matherly, LH; Taub, JW
      Transcriptional regulation of the human cystathionine beta-synthase-1b basal promoter: synergistic transactivation by transcription factors NF-Y and Sp1/Sp3

      BIOCHEMICAL JOURNAL
    32. Capone, GT
      Down syndrome: Advances in molecular biology and the neurosciences

      JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS
    33. Fortna, A; Gardiner, K
      Genomic sequence analysis tools: a user's guide

      TRENDS IN GENETICS
    34. Reeves, RH; Baxter, LL; Richtsmeier, JT
      Too much of a good thing: mechanisms of gene action in Down syndrome

      TRENDS IN GENETICS
    35. Hyde, LA; Frisone, DF; Crnic, LS
      Ts65Dn mice, a model for Down syndrome, have deficits in context discrimination learning suggesting impaired hippocampal function

      BEHAVIOURAL BRAIN RESEARCH
    36. Odagaki, T; Sugimoto, T; Matsuo, M; Tatsumi, E; Saigo, K
      Tetrasomy 21 as the sole acquired karyotypic abnormality in acute myeloblastic leukemia

      CANCER GENETICS AND CYTOGENETICS
    37. Antonarakis, SE; Lyle, R; Chrast, R; Scott, HS
      Differential gene expression studies to explore the molecular pathophysiology of Down syndrome

      BRAIN RESEARCH REVIEWS
    38. Lee, C; Fowler, DJ; Lemyre, E; Sandstrom, MM; Holmes, LB; Morton, CC
      Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy14 and monosomy 21

      AMERICAN JOURNAL OF MEDICAL GENETICS
    39. Sykhanov, AV; Korolenko, TP; Vinogradova, TE; Voevoda, MI; Feigin, VL
      Molecular genetic risk factors of Alzheimer's disease

      ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA
    40. Lassus, H; Laitinen, MPE; Anttonen, M; Heikinheimo, M; Aaltonen, LA; Ritvos, O; Butzow, R
      Comparison of serous and mucinous ovarian carcinomas: Distinct pattern of allelic loss at distal 8p and expression of transcription factor GATA-4

      LABORATORY INVESTIGATION
    41. Ornstein, DK; Cinquanta, M; Weiler, S; Duray, PH; Emmert-Buck, MR; Vocke, CD; Linehan, WM; Ferretti, JA
      Expression studies and mutational analysis of the androgen regulated homeobox gene NKX3.1 in benign and malignant prostate epithelium

      JOURNAL OF UROLOGY
    42. Nadal, M; Vigo, CG; Melaragno, MI; Andrade, JAD; Alonso, LG; Brunini, D; Pritchard, M; Estivill, X
      Clinical and cytogenetic characterisation of a patient with Down syndrome resulting from a 21q22.1 -> qter duplication

      JOURNAL OF MEDICAL GENETICS
    43. Rogers, MA; Langbein, L; Winter, H; Ehmann, C; Praetzel, S; Korn, B; Schweizer, J
      Characterization of a cluster of human high/ultrahigh sulfur keratin-associated protein genes embedded in the type I keratin gene domain on chromosome 17q12-21

      JOURNAL OF BIOLOGICAL CHEMISTRY
    44. Boker, LK; Blumstein, T; Sadetzki, S; Luxenburg, O; Litvak, I; Akstein, E; Modan, B
      Incidence of leukemia and other cancers in Down syndrome subjects in Israel

      INTERNATIONAL JOURNAL OF CANCER
    45. Layman, LC; McDonough, PG; Cohen, DP; Maddox, M; Tho, SPT; Reindollar, RH
      Familial gonadotropin-releasing hormone resistance and hypogonadotropic hypogonadism in a family with multiple affected individuals

      FERTILITY AND STERILITY
    46. Hyde, LA; Crnic, LS; Pollock, A; Bickford, PC
      Motor learning in Ts65Dn mice, a model for Down syndrome

      DEVELOPMENTAL PSYCHOBIOLOGY
    47. Forster-Gibson, CJ; Davies, J; MacKenzie, JJ; Harrison, K
      Cryptic duplication of 21q in an individual with a clinical diagnosis of Down syndrome

      CLINICAL GENETICS
    48. Lazzaro, SJ; Speevak, MD; Farrell, SA
      Recombinant Down syndrome: a case report and literature review

      CLINICAL GENETICS
    49. Yamamoto, N; Uzawa, K; Yakushiji, T; Shibahara, T; Noma, H; Tanzawa, H
      Analysis of the ANA gene as a candidate for the chromosome 21q oval cancersusceptibility locus

      BRITISH JOURNAL OF CANCER
    50. Ding, BC; Witt, TL; Hukku, B; Heng, H; Zhang, L; Matherly, LH
      Association of deletions and translocation of the reduced folate carrier gene with profound loss of gene expression in methotrexate-resistant K562 human erythroleukemia cells

      BIOCHEMICAL PHARMACOLOGY
    51. Alers, JC; Krijtenburg, PJ; Vis, AN; Hoedemaeker, RF; Wildhagen, MF; Hop, WCJ; van der Kwast, TH; Schroder, FH; Tanke, HJ; van Dekken, H
      Molecular cytogenetic analysis of prostatic adenocarcinomas from screeningstudies - Early cancers may contain aggressive genetic features

      AMERICAN JOURNAL OF PATHOLOGY
    52. Li, JM; Sherman, SL; Lamb, N; Zhao, HY
      Multipoint genetic mapping with trisomy data

      AMERICAN JOURNAL OF HUMAN GENETICS
    53. Pogribna, M; Melnyk, S; Pogribny, I; Chango, A; Yi, P; James, SJ
      Homocysteine metabolism in children with Down syndrome: In vitro modulation

      AMERICAN JOURNAL OF HUMAN GENETICS
    54. Chabert, C; Cherfouh, A; Delabar, JM; Duquenne, V
      Assessing implications between genotypic and phenotypic variables through lattice analysis

      BEHAVIOR GENETICS
    55. Shi, QH; Chen, JF; Adler, ID; Zhang, JX; Martin, R; Pan, SJ; Zhang, XR; Shan, XN
      Increased nondisjunction of chromosome 21 with age in human peripheral lymphocytes

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    56. Maroun, LE; Heffernan, TN; Hallam, DM
      Partial IFN-alpha/beta and IFN-gamma receptor knockout trisomy 16 mouse fetuses show improved growth and cultured neuron viability

      JOURNAL OF INTERFERON AND CYTOKINE RESEARCH
    57. Groet, J; Ives, JH; Jones, TA; Danton, M; Flomen, RH; Sheer, D; Hrascan, R; Pavelic, K; Nizetic, D
      Narrowing of the region of allelic loss in 21q11-21 in squamous non-small cell lung carcinoma and cloning of a novel ubiquitin-specific protease genefrom the deleted segment

      GENES CHROMOSOMES & CANCER
    58. Prejean, C; Colamonici, OR
      Role of the cytoplasmic domains of the type I interferon receptor subunitsin signalling

      SEMINARS IN CANCER BIOLOGY
    59. Lee, SG; Cho, KA; Choi, YH; Montgomery, K; Lee, E; Miller, A; Kucherlapati, R; Song, K
      A sequence-ready map for human chromosome 12q15-21

      DNA SEQUENCE
    60. Kotzot, D; Schinzel, A
      Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46,XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    61. Chrast, R; Scott, HS; Madani, R; Huber, L; Wolfer, DP; Prinz, M; Aguzzi, A; Lipp, HP; Antonarakis, SE
      Mice trisomic for a bacterial artificial chromosome with the single-minded2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome

      HUMAN MOLECULAR GENETICS
    62. Thiery, E; Gosset, P; Damotte, D; Delezoide, AL; de Saint-Sauveur, N; Vayssettes, C; Creau, N
      Developmentally regulated expression of the murine ortholog of the potassium channel KIR4.2 (KCNJ15)

      MECHANISMS OF DEVELOPMENT
    63. Rachidi, M; Lopes, C; Gassanova, S; Sinet, PM; Vekemans, M; Attie, T; Delezoide, AL; Delabar, JM
      Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic development

      MECHANISMS OF DEVELOPMENT
    64. Egeo, A; Di Lisi, R; Mazzocco, M; Lapide, M; Schiaffino, S; Scartezzini, P
      Developmental expression of the SH3BGR gene, mapping to the Down syndrome heart critical region

      MECHANISMS OF DEVELOPMENT
    65. Wynn, SL; Fisher, RA; Pagel, C; Price, M; Liu, QY; Khan, IM; Zammit, P; Dadrah, K; Mazrani, W; Kessling, A; Lee, JS; Buluwela, L
      Organization and conservation of the GART/SON/DONSON locus in mouse and human genomes

      GENOMICS
    66. Strippoli, P; Lenzi, L; Petrini, M; Carinci, P; Zannotti, M
      A new gene family including DSCR1 (Down syndrome candidate region 1) and ZAKI-4: Characterization from yeast to human and identification of DSCR1-like 2, a novel human member (DSCR1L2)

      GENOMICS
    67. Niini, T; Kanerva, J; Vettenranta, K; Saarinen-Pihkala, UM; Knuutila, S
      AML1 gene amplification: a novel finding in childhood acute lymphoblastic leukemia

      HAEMATOLOGICA
    68. Abe, E; Kuwahara, K; Yoshida, M; Suzuki, M; Terasaki, H; Matsuo, Y; Takahashi, E; Sakaguchi, N
      Structure, expression, and chromosomal localization of the human gene encoding a germinal center-associated nuclear protein (GANP) that associates with MCM3 involved in the initiation of DNA replication

      GENE
    69. Slavov, D; Hattori, M; Sakaki, Y; Rosenthal, A; Shimizu, N; Minoshima, S; Kudoh, J; Yaspo, ML; Ramser, J; Reinhardt, R; Reimer, C; Clancy, K; Rynditch, A; Gardiner, K
      Criteria for gene identification and features of genome organization: analysis of 6.5 Mb of DNA sequence from human chromosome 21

      GENE
    70. Sugimoto, T; Das, H; Imoto, S; Murayama, T; Gomyo, H; Chakraborty, S; Taniguchi, R; Isobe, T; Nakagawa, T; Nishimura, R; Koizumi, T
      Quantitation of minimal residual disease in t(8;21)-positive acute myelogenous leukemia patients using real-time quantitative RT-PCR

      AMERICAN JOURNAL OF HEMATOLOGY
    71. Baptista, MJ; Fairbrother, UL; Howard, CM; Farrer, MJ; Davies, GE; Trikka, D; Maratou, K; Redington, A; Greve, G; Njolstad, PR; Kessling, AM
      Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

      HUMAN GENETICS
    72. Tazi-Ahnini, R; di Giovine, FS; McDonagh, AJG; Messenger, AG; Amadou, C; Cox, A; Duff, GW; Cork, MJ
      Structure and polymorphism of the human gene for the interferon-induced p78 protein (MX1): evidence of association with alopecia areata in the Down syndrome region

      HUMAN GENETICS
    73. Maratou, K; Siddique, Y; Kessling, AM; Davies, GE
      Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

      HUMAN GENETICS
    74. Solans, A; Estivill, X; de la Luna, S
      Cloning and characterization of human FTCD on 21q22.3, a candidate gene for glutamate formiminotransferase deficiency

      CYTOGENETICS AND CELL GENETICS
    75. Kentrup, H; Joost, HG; Heimann, G; Becker, W
      Minibrain/DYRK1A-gene: Candidate gene for mental retardation in Down syndrome?

      KLINISCHE PADIATRIE
    76. Roncalli, M; Bianchi, P; Grimaldi, GC; Ricci, D; Laghi, L; Maggioni, M; Opocher, E; Borzio, M; Coggi, G
      Fractional allelic loss in non-end-stage cirrhosis: Correlations with hepatocellular carcinoma development during follow-up

      HEPATOLOGY
    77. Vialard, F; Toyama, K; Vernoux, S; Carlson, EJ; Epstein, CJ; Sinet, PM; Rahmani, Z
      Overexpression of mSim2 gene in the zona limitans of the diencephalon of segmental trisomy 16 Ts1Cje fetuses, a mouse model for trisomy 21: a novel whole-mount based RNA hybridization study

      DEVELOPMENTAL BRAIN RESEARCH
    78. Braddock, SR; Henley, KM; Potter, KL; Nguyen, HG; Huang, THM
      Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21in a four-generation family

      AMERICAN JOURNAL OF MEDICAL GENETICS
    79. Tsezou, A; Kitsiou, S; Galla, A; Petersen, MB; Karadima, G; Syrrou, M; Sahlen, S; Blennow, E
      Molecular cytogenetic characterization and origin of two de novo duplication 9p cases

      AMERICAN JOURNAL OF MEDICAL GENETICS
    80. Kondo, M; Kudo, K; Kimura, H; Inaba, J; Kato, K; Kojima, S; Matsuyama, T; Horibe, K
      Real-time quantitative reverse transcription-polymerase chain reaction forthe detection of AML1-MTG8 fusion transcripts in t(8;21)-positive acute myelogenous leukemia

      LEUKEMIA RESEARCH
    81. Hattori, M; Fujiyama, A; Taylor, TD; Watanabe, H; Yada, T; Park, HS; Toyoda, A; Ishii, K; Totoki, Y; Choi, DK; Soeda, E; Ohki, M; Takagi, T; Sakaki, Y; Taudien, S; Blechschmidt, K; Polley, A; Menzel, U; Delabar, J; Kumpf, K; Lehmann, R; Patterson, D; Reichwald, K; Rump, A; Schillhabel, M; Schudy, A; Zimmermann, W; Rosenthal, A; Kudoh, J; Shibuya, K; Kawasaki, K; Asakawa, S; Shintani, A; Sasaki, T; Nagamine, K; Mitsuyama, S; Antonarakis, SE; Minoshima, S; Shimizu, N; Nordsiek, G; Hornischer, K; Brandt, P; Scharfe, M; Schon, O; Desario, A; Reichelt, J; Kauer, G; Blocker, H; Ramser, J; Beck, A; Klages, S; Hennig, S; Riesselmann, L; Dagand, E; Haaf, T; Wehrmeyer, S; Borzym, K; Gardiner, K; Nizetic, D; Francis, F; Lehrach, H; Reinhardt, R; Yaspo, ML
      The DNA sequence of human chromosome 21

      NATURE
    82. Alers, JC; Rochat, J; Krijtenburg, PJ; Hop, WCJ; Kranse, R; Rosenberg, C; Tanke, HJ; Schroder, FH; van Dekken, H
      Identification of genetic markers for prostatic cancer progression

      LABORATORY INVESTIGATION
    83. Acquati, F; Accarino, M; Nucci, C; Fumagalli, P; Jovine, L; Ottolenghi, S; Taramelli, R
      The gene encoding DRAP (BACE2), a glycosylated transmembrane protein of the aspartic protease family, maps to the Down critical region

      FEBS LETTERS
    84. Wolstenholme, J; Angell, RR
      Maternal age and trisomy - a unifying mechanism of formation

      CHROMOSOMA
    85. Bowen, C; Bubendorf, L; Voeller, HJ; Slack, R; Willi, N; Sauter, G; Gasser, TC; Koivisto, P; Lack, EE; Kononen, J; Kallioniemi, OP; Gelmann, EP
      Loss of NKX3.1 expression in human prostate cancers correlates with tumor progression

      CANCER RESEARCH
    86. Cuneo, A; Roberti, MG; Bigoni, R; Minotto, C; Bardi, A; Milani, R; Tieghi, A; Campioni, D; Cavazzini, F; De Angeli, C; Negrini, M; Castoldi, G
      Four novel non-random chromosome rearrangements in B-cell chronic lymphocytic leukaemia: 6p24-25 and 12p12-13 translocations, 4q21 anomalies and monosomy 21

      BRITISH JOURNAL OF HAEMATOLOGY
    87. Kim, SH; Yoo, BC; Broers, JLV; Cairns, N; Lubec, G
      Neuroendocrine-specific protein C, a marker of neuronal differentiation, is reduced in brain of patients with Down syndrome and Alzheimer's disease

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    88. Inoue, T; Shinohara, T; Takahara, S; Inoue, J; Kamino, H; Kugoh, H; Oshimura, M
      Specific impairment of cardiogenesis in mouse ES cells containing a human chromosome 21

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    89. Vidal-Taboada, JM; Lu, A; Pique, M; Pons, G; Gil, J; Oliva, R
      Down syndrome critical region gene 2: Expression during mouse development and in human cell lines indicates a function related to cell proliferation

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    90. Shibuya, K; Kudoh, J; Minoshima, S; Kawasaki, K; Asakawa, S; Shimizu, N
      Isolation of two novel genes, DSCR5 and DSCR6, from Down syndrome criticalregion on human chromosome 21q22.2

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    91. Paulien, S; Busson-Le Coniat, M; Berger, R
      Acute megakaryocytic leukaemia with acquired polysomy 21 and translocationt(1;21)

      ANNALES DE GENETIQUE
    92. Gomez, D; Solsona, E; Guitart, M; Baena, N; Gabau, E; Egozcue, J; Caballin, MR
      Origin of trisomy 21 in Down syndrome cases from a Spanish population registry

      ANNALES DE GENETIQUE
    93. Kline, J; Kinney, A; Levin, B; Warburton, D
      Trisomic pregnancy and earlier age at menopause

      AMERICAN JOURNAL OF HUMAN GENETICS
    94. Broman, KW; Weber, JL
      Characterization of human crossover interference

      AMERICAN JOURNAL OF HUMAN GENETICS
    95. Feingold, E; Brown, AS; Sherman, SL
      Multipoint estimation of genetic maps for human trisomies with one parent or other partial data

      AMERICAN JOURNAL OF HUMAN GENETICS
    96. Erbersdobler, A; Graefen, M; Wullbrand, A; Hammerer, P; Henke, RP
      Allelic losses at 8p, 10q, 11p, 13q, 16q, 17p, and 18q in prostatic carcinomas: The impact of zonal location, Gleason grade, and tumour multifocality

      PROSTATE CANCER AND PROSTATIC DISEASES
    97. Yang, QH; Sherman, SL; Hassold, TJ; Allran, K; Taft, L; Pettay, D; Khoury, MJ; Erickson, JD; Freeman, SB
      Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a population based case control study

      GENETICS IN MEDICINE
    98. Hildmann, T; Kong, XG; O'Brien, J; Riesselman, L; Christensen, HM; Dagand, E; Lehrach, H; Yaspo, ML
      A contiguous 3-Mb sequence-ready map in the S3-MX region on 21q22.2 based on high-throughput nonisotopic library screenings

      GENOME RESEARCH
    99. Wang, SY; Cruts, M; Del-Favero, J; Zhang, Y; Tissir, F; Potier, MC; Patterson, D; Nizetic, D; Bosch, A; Chen, HM; Bennett, L; Estivill, X; Kessling, A; Antonarakis, SE; van Broeckhoven, C
      A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes

      GENOME RESEARCH
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 01/11/20 alle ore 00:18:47