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La ricerca find articoli where soggetti phrase all words '11P15.5' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 45 riferimenti
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    1. Cleary, MA; van Raamsdonk, CD; Levorse, J; Zheng, BH; Bradley, A; Tilghman, SM
      Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice

      NATURE GENETICS
    2. Perotti, D; Testi, MA; Mondini, P; Pilotti, S; Green, ED; Pession, A; Sozzi, G; Pierotti, MA; Fossati-Bellani, F; Radice, P
      Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours

      GENES CHROMOSOMES & CANCER
    3. Zhao, BH; Bepler, G
      Transcript map and complete genomic sequence for the 310 kb region of minimal allele loss on chromosome segment 11p15.5 in non-small-cell lung cancer

      ONCOGENE
    4. Lam, DH; Aplan, PD
      NUP98 gene fusions in hematologic malignancies

      LEUKEMIA
    5. Kaffer, CR; Grinberg, A; Pfeifer, K
      Regulatory mechanisms at the mouse Igf2/H19 locus

      MOLECULAR AND CELLULAR BIOLOGY
    6. Benzacken, B; Monier-Gavelle, F; Siffroi, JP; Agbo, P; Chalvon, A; Wolf, JP
      Acrocentric chromosome polymorphisms: beware of cryptic translocations

      PRENATAL DIAGNOSIS
    7. Kotsinas, A; Gorgoulis, VG; Zacharatos, P; Mariatos, G; Kokotas, S; Liloglou, T; Ikonomopoulos, J; Zoumpourlis, V; Kyroudi, A; Field, JK; Asimacopoulos, PJ; Kittas, C
      Additional characterization of a hexanucleotide polymorphic site in the first intron of human H-ras gene: comparative study of its alterations in non-small cell lung carcinomas and sporadic invasive breast carcinomas

      CANCER GENETICS AND CYTOGENETICS
    8. Krskova-Honzatkova, L; Cermak, J; Sajdova, J; Stary, J; Sedlacek, P; Sieglova, Z
      Loss of heterozygosity and heterogeneity of its appearance and persisting in the course of acute myeloid leukemia and myelodysplastic syndromes

      LEUKEMIA RESEARCH
    9. Sakatani, T; Wei, M; Katoh, M; Okita, C; Wada, D; Mitsuya, K; Meguro, M; Ikeguchi, M; Ito, H; Tycko, B; Oshimura, M
      Epigenetic heterogeneity at imprinted loci in normal populations

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    10. Higashimoto, K; Soejima, H; Yatsuki, H; Katsuki, T; Mukai, T
      An NsiI RFLP in the human long QT intronic transcript 1 (LIT1)

      JOURNAL OF HUMAN GENETICS
    11. Higashimoto, K; Soejima, H; Katsuki, T; Mukai, T
      Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene

      JOURNAL OF HUMAN GENETICS
    12. Muller, S; van den Boom, D; Zirkel, D; Koster, H; Berthold, F; Schwab, M; Westphal, M; Zumkeller, W
      Retention of imprinting of the human apoptosis-related gene TSSC3 in humanbrain tumors

      HUMAN MOLECULAR GENETICS
    13. Paulsen, M; El-Maarri, O; Engemann, S; Strodicke, M; Franck, O; Davies, K; Reinhardt, R; Reik, W; Walter, J
      Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

      HUMAN MOLECULAR GENETICS
    14. Enklaar, T; Esswein, M; Oswald, M; Hilbert, K; Winterpacht, A; Higgins, M; Zabel, B; Prawitt, D
      Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene family

      GENOMICS
    15. Fert-Ferrer, S; Guichet, A; Tantau, J; Delezoide, AL; Ozilou, C; Romana, SP; Gosset, P; Viot, G; Loison, S; Moraine, C; Morichon-Delvallez, N; Turleau, C; Vekemans, M; Prieur, M
      Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features

      PRENATAL DIAGNOSIS
    16. Manji, SSM; Parker, NJ; Williams, RT; van Stekelenburg, L; Pearson, RB; Dziadek, M; Smith, PJ
      STIM1: a novel phosphoprotein located at the cell surface

      BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY
    17. Moore, ES; Ward, RE; Escobar, LF; Carlin, ME
      Heterogeneity in Wiedemann-Beckwith syndrome: Anthropometric evidence

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. Catchpoole, D; Smallwood, AV; Joyce, JA; Murrell, A; Lam, W; Tang, T; Munroe, D; Reik, W; Schofield, PN; Maher, ER
      Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

      JOURNAL OF MEDICAL GENETICS
    19. Schwienbacher, C; Angioni, A; Scelfo, R; Veronese, A; Calin, GA; Massazza, G; Hatada, I; Barbanti-Brodano, G; Negrini, M
      Abnormal RNA expression of 11p15 imprinted genes and kidney developmental genes in Wilms' tumor

      CANCER RESEARCH
    20. Oya, M; Schulz, WA
      Decreased expression of p57(KIP2) mRNA in human bladder cancer

      BRITISH JOURNAL OF CANCER
    21. Blaker, H; Hofmann, WJ; Rieker, RJ; Penzel, R; Graf, M; Otto, HF
      beta-catenin accumulation and mutation of the CTNNBI gene in hepatoblastoma

      GENES CHROMOSOMES & CANCER
    22. Lee, MP; Brandenburg, S; Landes, GM; Adams, M; Miller, G; Feinberg, AP
      Two novel genes in the center of the 11p15 imprinted domain escape genomicimprinting

      HUMAN MOLECULAR GENETICS
    23. John, RM; Hedges, M; Little, P; Barton, SC; Surani, MA
      A human p57(KIP2) transgene is not activated by passage through the maternal mouse germline

      HUMAN MOLECULAR GENETICS
    24. Day, CD; Smilinich, NJ; Fitzpatrick, GV; deJong, PJ; Shows, TB; Higgins, MJ
      The imprinted domain in mouse distal chromosome 7: reagents for mutagenesis and sequencing

      MAMMALIAN GENOME
    25. Desseyn, JL; Rousseau, K; Laine, A
      Fifty-nine bp repeat polymorphism in the uncommon intron 36 of the human mucin gene MUC5B

      ELECTROPHORESIS
    26. Samuel, DP; Tsokos, M; DeBaun, MR
      Hemihypertrophy and a poorly differentiated embryonal rhabdomyosarcoma of the pelvis

      MEDICAL AND PEDIATRIC ONCOLOGY
    27. Lee, MP; DeBaun, MR; Mitsuya, K; Galonek, HL; Brandenburg, S; Oshimura, M; Feinberg, AP
      Loss of imprinting of a paternally expressed transcript, with antisense orientation to K(V)LQT1, occurs frequently in Beckwith-Wiedemann syndrome andis independent of insulin-like growth factor II imprinting

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    28. Lam, WWK; Hatada, I; Ohishi, S; Mukai, T; Joyce, JA; Cole, TRP; Donnai, D; Reik, W; Schofield, PN; Maher, ER
      Analysis of germline CDKN1C (p57(KIP2)) mutations in familial and sporadicBeckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

      JOURNAL OF MEDICAL GENETICS
    29. MIYAMOTO T; JINNO Y; MIURA K; SENGOKU K; SOEJIMA H; YUN K; YAGINUMA Y; NIIKAWA N; ISHIKAWA M
      A SACII POLYMORPHISM IN THE HUMAN ASCL2 (HASH2) GENE REGION

      JOURNAL OF HUMAN GENETICS
    30. Miura, K; Masuzaki, H; Ishimaru, T; Niikawa, N; Jinno, Y
      A HhaI/BstUI polymorphism in a novel gene at human chromosome 11p15.5

      JOURNAL OF HUMAN GENETICS
    31. KLAMT B; SCHULZE M; THATE C; MARES J; GOETZ P; KODET R; SCHEURLEN W; WEIRICH A; GRAF N; GESSLER M
      ALLELE LOSS IN WILMS-TUMORS OF CHROMOSOME ARMS 11Q, 16Q, AND 22Q CORRELATES WITH CLINICOPATHOLOGICAL PARAMETERS

      Genes, chromosomes & cancer
    32. DAO D; FRANK D; QIAN NF; OKEEFE D; VOSATKA RJ; WALSH CP; TYCKO B
      IMPT1, AN IMPRINTED GENE SIMILAR TO POLYSPECIFIC TRANSPORTER AND MULTIDRUG-RESISTANCE GENES

      Human molecular genetics
    33. OVERALL ML; PARKER NJ; SCARCELLA DL; SMITH PJ; DZIADEK M
      MURINE STIM1 MAPS TO DISTAL CHROMOSOME-7 AND IS NOT IMPRINTED

      Mammalian genome
    34. DESSEYN JL; BUISINE MP; PORCHET N; AUBERT JP; DEGAND P; LAINE A
      EVOLUTIONARY HISTORY OF THE 11P15 HUMAN MUCIN GENE FAMILY

      Journal of molecular evolution
    35. REECE M; PRAWITT D; LANDERS J; KAST C; GROS P; HOUSMAN D; ZABEL BU; PELLETIER J
      FUNCTIONAL-CHARACTERIZATION OF ORCTL2 - AN ORGANIC CATION TRANSPORTEREXPRESSED IN THE RENAL PROXIMAL TUBULES

      FEBS letters
    36. HU RJ; LEE MP; CONNORS TD; JOHNSON LA; BURN TC; SU K; LANDES GM; FEINBERG AP
      A 2.5-MB TRANSCRIPT MAP OF A TUMOR-SUPPRESSING SUBCHROMOSOMAL TRANSFERABLE FRAGMENT FROM 11P15.5, AND ISOLATION AND SEQUENCE-ANALYSIS OF 3 NOVEL GENES

      Genomics
    37. OKEEFE D; DAO D; ZHAO L; SANDERSON R; WARBURTON D; WEISS L; ANYANEYEBOA K; TYCKO B
      CODING MUTATIONS IN P57(KIP2) ARE PRESENT IN SOME CASES OF BECKWITH-WIEDEMANN-SYNDROME BUT ARE RARE OR ABSENT IN WILMS-TUMORS

      American journal of human genetics
    38. TYCKO B
      DNA METHYLATION IN GENOMIC IMPRINTING

      Mutation research-reviews in mutation research
    39. WEKSBERG R; SQUIRE JA
      MOLECULAR-BIOLOGY OF BECKWITH-WIEDEMANN SYNDROME

      Medical and pediatric oncology
    40. NORDENSKJOLD A; FRIEDMAN E; SANDSTEDT B; SODERHALL S; ANVRET M
      CONSTITUTIONAL AND SOMATIC MUTATIONS IN THE WT1 GENE IN WILMS-TUMOR PATIENTS

      International journal of cancer
    41. STRATTON RF; LAZARUS KH; RITCHIE EJL; BELL AM
      DELETION (11)(Q14.1Q21)

      American journal of medical genetics
    42. GRUNDY P; WILSON B; TELZEROW P; ZHOU W; PATERSON MC
      UNIPARENTAL DISOMY OCCURS INFREQUENTLY IN WILMS-TUMOR PATIENTS

      American journal of human genetics
    43. BONAITIPELLIE C; CHOMPRET A; TOURNADE MF; LEMERLE J; VOUTE PA; DELEMARRE JFM
      EXCESS OF MULTIFOCAL TUMORS IN NEPHROBLASTOMA - IMPLICATIONS FOR MECHANISMS OF TUMOR-DEVELOPMENT AND GENETIC-COUNSELING

      Human genetics
    44. ROBERTS P; LOCKWOOD LR; LEWIS IJ; BAILEY CC; BATCUP G; WILLIAMS J
      CYTOGENETIC ABNORMALITIES IN MESOBLASTIC NEPHROMA - A LINK TO WILMS-TUMOR

      Medical and pediatric oncology
    45. AUSTRUY E; COHENSALMON M; ANTIGNAC C; BEROUD C; HENRY I; CONG NV; BRUGIERES L; JUNIEN C; JEANPIERRE C
      ISOLATION OF KIDNEY COMPLEMENTARY DNAS DOWN-EXPRESSED IN WILMS-TUMOR BY A SUBTRACTIVE HYBRIDIZATION APPROACH

      Cancer research


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 08/08/20 alle ore 17:30:13