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    1. Arlt, MF; Miller, DE; Beer, DG; Glover, TW
      Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

      GENES CHROMOSOMES & CANCER
    2. Emanuel, BS; Shaikh, TH
      Segmental duplications: An 'expanding' role in genomic instability and disease

      NATURE REVIEWS GENETICS
    3. Kayahara, H; Yamagata, H; Tanioka, H; Miki, T; Hamakawa, H
      Frequent loss of heterozygosity at 3p25-p26 is associated with invasive oral squamous cell carcinoma

      JOURNAL OF HUMAN GENETICS
    4. Caruso, JA; Reiners, JJ; Emond, J; Shultz, T; Tainsky, MA; Alaoui-Jamali, M; Batist, G
      Genetic alteration of chromosome 8 is a common feature of human mammary epithelial cell lines transformed in vitro with benzo[a]pyrene

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    5. Martinez, A; Walker, RA; Shaw, JA; Dearing, SJ; Maher, ER; Latif, F
      Chromosome 3p allele loss in early invasive breast cancer: detailed mapping and association with clinicopathological features

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    6. Kurimoto, F; Gemma, A; Hosoya, Y; Seike, M; Takenaka, K; Uematsu, K; Yoshimura, A; Shibuya, M; Kudoh, S
      Unchanged frequency of loss of heterozygosity and size of the deleted region at 8p21-23 during metastasis of lung cancer

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    7. 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
    8. Tuck-Muller, CM; Goodman, BK; Li, SB; Martinez, JE; Chen, XN; Wertelecki, W; Korenberg, JR; Stetten, G
      Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel

      GENETICS IN MEDICINE
    9. Pavelic, K; Krizanac, S; Cacev, T; Hadzija, MP; Radosevic, S; Crnic, I; Levanat, S; Kapitanovic, S
      Aberration of FHIT gene is associated with increased tumor proliferation and decreased apoptosis - Clinical evidence in lung and head and neck carcinomas

      MOLECULAR MEDICINE
    10. Cohen, N; Betts, DR; Trakhtenbrot, L; Niggli, FK; Amariglio, N; Brok-Simoni, F; Rechavi, G; Meitar, D
      Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY)

      GENES CHROMOSOMES & CANCER
    11. Odero, MD; Carlson, K; Calasanz, MJ; Lahortiga, I; Chinwalla, V; Rowley, JD
      Identification of new translocations involving ETV6 in hematologic malignancies by fluorescence in situ hybridization and spectral karyotyping

      GENES CHROMOSOMES & CANCER
    12. Spieker, N; Beitsma, M; Van Sluis, P; Chan, A; Caron, H; Versteeg, R
      Three chromosomal rearrangements in neuroblastoma cluster within a 300-kb region on 1p36.1

      GENES CHROMOSOMES & CANCER
    13. Phillips, JL; Ghadimi, BM; Wangsa, D; Padilla-Nash, H; Worrell, R; Hewitt, S; Walther, M; Linehan, WM; Klausner, RD; Ried, T
      Molecular cytogenetic characterization of early and late renal cell carcinomas in Von Hippel-Lindau disease

      GENES CHROMOSOMES & CANCER
    14. Caron, H; Spieker, N; Godfried, N; Veenstra, M; van Sluis, P; de Kraker, J; Voute, P; Versteeg, R
      Chromosome bands Ip35-36 contain two distinct neuroblastoma tumor suppressor loci, one of which is imprinted

      GENES CHROMOSOMES & CANCER
    15. Chernykh, VB; Kurilo, LF
      Genetically controlled hormonal regulation of human sexual differentiationand reproductive system development

      RUSSIAN JOURNAL OF GENETICS
    16. Lui, WO; Tanenbaum, DM; Larsson, C
      High level amplification of 1p32-33 and 2p22-24 in small cell lung carcinomas

      INTERNATIONAL JOURNAL OF ONCOLOGY
    17. Sasiadek, M; Stembalska-Kozlowska, A; Smigiel, R; Krecicki, T; Blin, N; Mirghomizadeh, F
      Microsatellite and chromosome instability in squamous cell laryngeal carcinoma

      INTERNATIONAL JOURNAL OF ONCOLOGY
    18. Dufke, A; Walczak, C; Liehr, T; Starke, H; Trifonov, V; Rubtsov, N; Schoning, M; Enders, H; Eggermann, T
      Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker

      EUROPEAN JOURNAL OF HUMAN GENETICS
    19. Eisenberg, I; Hochner, H; Shemesh, M; Levi, T; Potikha, T; Sadeh, M; Argov, Z; Jackson, CL; Mitrani-Rosenbaum, S
      Physical and transcriptional map of the hereditary inclusion body myopathylocus on chromosome 9p12-p13

      EUROPEAN JOURNAL OF HUMAN GENETICS
    20. Giannakudis, J; Ropke, A; Kujat, A; Krajewska-Walasek, M; Hughes, H; Fryns, JP; Bankier, A; Amor, D; Schlicker, M; Hansmann, I
      Parental mosaicism of JAG1 mutations in families with Alagille syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    21. Barajas-Barjas, LO; Velarde-Felix, S; Elizarraras-Rivas, J; Hernandez-Zaragoza, G; Vazquez-Herrera, JA
      De novo ring chromosome 3 in a girl with hypoplastic thumb and coloboma ofiris

      GENETIC COUNSELING
    22. 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
    23. Astuti, D; Agathanggelou, A; Honorio, S; Dallol, A; Martinsson, T; Kogner, P; Cummins, C; Neumann, HPH; Voutilainen, R; Dahia, P; Eng, C; Maher, ER; Latif, F
      RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours

      ONCOGENE
    24. Fukuhara, H; Maruyama, T; Nomura, S; Oshimura, M; Kitamura, T; Sekiya, T; Murakami, Y
      Functional evidence for the presence of tumor suppressor gene on chromosome 10p15 in human prostate cancers

      ONCOGENE
    25. Agathanggelou, A; Honorio, S; Macartney, DP; Martinez, A; Dallol, A; Radar, J; Fullwood, P; Chauhan, A; Walker, R; Shaw, JA; Hosoe, S; Lerman, MI; Minna, JD; Maher, ER; Latif, F
      Methylation associated inactivation of RASSF1A from region 3p21.3 in lung,breast and ovarian tumours

      ONCOGENE
    26. Malou, E; Gekas, J; Troucelier-Lucas, V; Mornet, E; Razafimanantsoa, L; Cuvelier, B; Mathieu, M; Thepot, F
      X-linked recessive chondrodysplasia punctata: cytogenetic and molecular biology study.

      ARCHIVES DE PEDIATRIE
    27. Clement, Y; Lepicard, E; Chapouthier, G
      An animal model for the study of the genetic bases of behaviour in men: the multiple marker strains (MMS)

      EUROPEAN PSYCHIATRY
    28. Russo, J; Hu, YF; Tahin, Q; Mihaila, D; Slater, C; Lareef, MH; Russo, IH
      Carcinogenicity of estrogens in human breast epithelial cells

      APMIS
    29. Russo, J; Hu, YF; Tahin, Q; Mihaila, D; Slater, C; Lareef, MH; Russo, IH
      Carcinogenicity of estrogens in human breast epithelial cells

      APMIS
    30. Dufner-Beattie, J; Lemons, RS; Thorburn, A
      Retinoic acid-induced expression of autotaxin in N-myc-amplified neuroblastoma cells

      MOLECULAR CARCINOGENESIS
    31. Guo, ZM; Wu, F; Asplund, A; Hu, XR; Mazurenko, N; Kisseljov, F; Ponten, J; Wilander, E
      Analysis of intratumoral heterogeneity of chromosome 3p deletions and genetic evidence of polyclonal origin of cervical squamous carcinoma

      MODERN PATHOLOGY
    32. Bernasconi, S; Mariani, S; Falcinelli, C; Milioli, S; Iughetti, L; Forabosco, A
      SHOX gene in Leri-Weill syndrome and in idiopathic short stature

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    33. Pascual-Castroviejo, I; Pascual-Pascual, SI; Viano, J; Martinez, V; Palencia, R
      Unilateral polymicrogyria: a common cause of hemiplegia of prenatal origin

      BRAIN & DEVELOPMENT
    34. Joyce, CA; Dennis, NR; Cooper, S; Browne, CE
      Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH

      HUMAN GENETICS
    35. Imanishi, Y; Tahara, H
      Putative parathyroid tumor suppressor on 1p: Independent molecular mechanisms of tumorigenesis from 11q allelic loss

      AMERICAN JOURNAL OF KIDNEY DISEASES
    36. Benzacken, B; Monier-Gavelle, F; Siffroi, JP; Agbo, P; Chalvon, A; Wolf, JP
      Acrocentric chromosome polymorphisms: beware of cryptic translocations

      PRENATAL DIAGNOSIS
    37. Qin, LX; Tang, ZY; Ye, SL; Liu, YK; Ma, ZC; Zhou, XD; Wu, ZQ; Lin, ZY; Sun, FX; Tian, J; Guan, XY; Pack, SD; Zhuang, ZP
      Chromosome 8p deletion is associated with metastasis of human hepatocellular carcinoma when high and low metastatic models are compared

      JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
    38. Jin, YS; Jin, C; Wennerberg, J; Hoglund, M; Mertens, F
      Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas

      CANCER GENETICS AND CYTOGENETICS
    39. Finelli, P; Francchiolla, NS; Giardino, D; Gottardi, G; Deliliers, DL; Cortelezzi, A; Larizza, L; Deliliers, GL
      FISH characterization of t(8;12)(q12;p13) observed as the sole karyotypic anomaly in a myelodysplastic syndrome patient

      CANCER GENETICS AND CYTOGENETICS
    40. Gursky, S; Olopade, OI; Rowley, JD
      Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types

      CANCER GENETICS AND CYTOGENETICS
    41. Park, SY; Choi, HC; Chun, YH; Kim, H; Park, SH
      Characterization of chromosomal aberrations in lung cancer cell lines by cross-species color banding

      CANCER GENETICS AND CYTOGENETICS
    42. Vassal, H; Medeira, A; Cordeiro, I; Santos, HG; Castedo, S; Saraiva, C; da Silva, PM; Monteiro, C
      Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Leri-Weill dyschondrosteosis, developmental delay, and ichthyosis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    43. Wolpert, CM; Donnelly, SL; Cuccaro, ML; Hedges, DJ; Poole, CP; Wright, HH; Gilbert, JR; Pericak-Vance, MA
      De novo partial duplication of chromosome 7p in a male with autistic disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Stankiewicz, P; Thiele, H; Baldermann, C; Kruger, A; Giannakudis, I; Dorr, S; Werner, N; Kunz, J; Rappold, GA; Hansmann, I
      Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. Sutcliffe, MJ; Mueller, OT; Kousseff, BG; Dumont, DP; McFarland, JA; Mawani, F; Conforto, D; Ranells, JD
      Three cell line mosaicism involving structural and numerical abnormalitiesof chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX

      AMERICAN JOURNAL OF MEDICAL GENETICS
    46. Stankiewicz, P; Brozek, I; Helias-Rodzewicz, Z; Wierzba, J; Pilch, J; Bocian, E; Balcerska, A; Wozniak, A; Kardas, I; Wirth, J; Mazurczak, T; Limon, J
      Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18

      AMERICAN JOURNAL OF MEDICAL GENETICS
    47. Kanerva, J; Niini, T; Vettenranta, K; Riikonen, P; Makipernaa, A; Karhu, R; Knuutila, S; Saarinen-Pihkala, UM
      Loss at 12p detected by comparative genomic hybridization (CGH): Association with TEL-AML1 fusion and favorable prognostic features in childhood acute lymphoblastic leukemia (ALL). A multi-institutional study

      MEDICAL AND PEDIATRIC ONCOLOGY
    48. Maris, JM; Guo, C; Blake, D; White, PS; Hogarty, MD; Thompson, PM; Rajalingam, V; Gerbing, R; Stram, DO; Matthay, KK; Seeger, RC; Brodeur, GM
      Comprehensive analysis of chromosome 1p deletions in neuroblastoma

      MEDICAL AND PEDIATRIC ONCOLOGY
    49. Ejeskar, K; Sjoberg, RM; Abel, F; Kogner, P; Ambros, PF; Martinsson, T
      Fine mapping of a tumour suppressor candidate gene region in 1p36.2-3, commonly deleted in neuroblastomas and germ cell tumours

      MEDICAL AND PEDIATRIC ONCOLOGY
    50. Liu, FS; Hsieh, YT; Chen, JT; Ho, ESC; Hung, MJ; Lin, AJ
      FHIT (fragile histidine triad) gene analysis in cervical intraepithelial neoplasia

      GYNECOLOGIC ONCOLOGY
    51. Chuaqui, R; Silva, M; Emmert-Buck, M
      Allelic deletion mapping on chromosome 6q and X chromosome inactivation clonality patterns in cervical intraepithelial neoplasia and invasive carcinoma

      GYNECOLOGIC ONCOLOGY
    52. Yang, Y; Kost-Alimova, M; Ingvarsson, S; Qiu, QH; Kiss, H; Szeles, A; Kholodnyuk, I; Cuthbert, A; Klein, G; Imreh, S
      Similar regions of human chromosome 3 are eliminated from or retained in human/human and human/mouse microcell hybrids during tumor growth in severe combined immunodeficient (SCID) mice

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    53. Dreijerink, K; Braga, E; Kuzmin, I; Geil, L; Duh, FM; Angeloni, D; Zbar, B; Lerman, MI; Stanbridge, EJ; Minna, JD; Protopopov, A; Li, JF; Kashuba, V; Klein, G; Zabarovsky, ER
      The candidate tumor suppressor gene, RASSF1A, from human chromosome 3p21.3is involved in kidney tumorigenesis

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    54. Bazov, IV; Kazubskaya, TP; Ermilova, VD; Gar'kavtseva, RF; Loginov, VI; Zabarovsky, ER; Braga, EA
      Allele deletion mapping of the short arm of human chromosome 3 in renal carcinoma

      MOLECULAR BIOLOGY
    55. Seitz, S; Poppe, K; Fischer, J; Nothnagel, A; Estevez-Schwarz, L; Haensch, W; Schlag, PM; Scherneck, S
      Detailed deletion mapping in sporadic breast cancer at chromosomal region 17p13 distal to the TP53 gene: association with clinicopathological parameters

      JOURNAL OF PATHOLOGY
    56. Wolter, M; Reifenberger, J; Blaschke, B; Ichimura, K; Schmidt, EE; Collins, VP; Reifenberger, G
      Oligodendroglial tumors frequently demonstrate hypermethylation of the CDKN2A (MTS1, p16(INK4a)), p14(ARF), and CDKN2B (MTS2, p15(INK4b)) tumor suppressor genes

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    57. Boucher, CA; Sargent, CA; Ogata, T; Affara, NA
      Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location

      JOURNAL OF MEDICAL GENETICS
    58. Tobias, ES; Bryce, G; Farmer, G; Barton, J; Colgan, J; Morrison, N; Cooke, A; Tolmie, JL
      Absence of learning difficulties in a hyperactive boy with a terminal Xp deletion encompassing the MRX49 locus

      JOURNAL OF MEDICAL GENETICS
    59. Liu, HX; Oei, PTSP; Mitchell, EA; McGaughran, JM
      Interstitial deletion of 3p22.2-p24.2: the first reported case

      JOURNAL OF MEDICAL GENETICS
    60. Mainardi, PC; Perfumo, C; Cali, A; Coucourde, G; Pastore, G; Cavani, S; Zara, F; Overhauser, J; Pierluigi, M; Bricarelli, FD
      Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation

      JOURNAL OF MEDICAL GENETICS
    61. Megarbane, A; Le Lorch, M; Elghezal, H; Joly, G; Gosset, P; Souraty, N; Samaras, L; Prieur, M; Vekemans, M; Turleau, C; Romana, SP
      Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes

      JOURNAL OF MEDICAL GENETICS
    62. Stratakis, CA; Taymans, SE; Schteingart, D; Haddad, BR
      Segmental uniparental isodisomy (UPD) for 2p16 without clinical symptoms: implications for UPD and other genetic studies of chromosome 2

      JOURNAL OF MEDICAL GENETICS
    63. Aguiar, RCT; Cox, G; Pomeroy, SL; Dahia, PLM
      Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    64. Nielsen, PK; Yamada, Y
      Identification of cell-binding sites on the laminin alpha(5) N-terminal domain by site-directed mutagenesis

      JOURNAL OF BIOLOGICAL CHEMISTRY
    65. Van Gele, M; Leonard, JH; Van Roy, N; Cook, AL; De Paepe, A; Speleman, F
      Frequent allelic loss at 10q23 but low incidence of PTEN mutations in Merkel cell carcinoma

      INTERNATIONAL JOURNAL OF CANCER
    66. Stankiewicz, P; Park, SS; Holder, SE; Waters, CS; Palmer, RW; Berend, SA; Shaffer, LG; Potocki, L; Lupski, JR
      Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derivedfrom chromosome 17: molecular analysis and delineation of the phenotype

      CLINICAL GENETICS
    67. Seidel, J; Schiller, S; Kelbova, C; Beensen, V; Orth, U; Vogt, S; Claussen, U; Zintl, F; Rappold, GA
      Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation

      CLINICAL GENETICS
    68. Morrissey, C; Martinez, A; Zatyka, M; Agathanggelou, A; Honorio, S; Astuti, D; Morgan, NV; Moch, H; Richards, FM; Kishida, T; Yao, M; Schraml, P; Latif, F; Maher, ER
      Epigenetic inactivation of the RASSF1A 3p21.3 tumor suppressor gene in both clear cell and papillary renal cell carcinoma

      CANCER RESEARCH
    69. Roman, J; Castillejo, JA; Jimenez, A; Bornstein, R; Gonzalez, MG; Rodriguez, MD; Barrios, M; Maldonado, J; Torres, A
      Hypermethylation of the calcitonin gene in acute lymphoblastic leukaemia is associated with unfavourable clinical outcome

      BRITISH JOURNAL OF HAEMATOLOGY
    70. Luttikhuis, MEMO; Powell, JE; Rees, SA; Genus, T; Chughtai, S; Ramani, P; Mann, JR; McConville, CM
      Neuroblastomas with chromosome 11q loss and single copy MYCN comprise a biologically distinct group of tumours with adverse prognosis

      BRITISH JOURNAL OF CANCER
    71. Bostrom, J; Meyer-Puttlitz, B; Wolter, M; Blaschke, B; Weber, RG; Lichter, P; Ichimura, K; Collins, VP; Reifenberger, G
      Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas

      AMERICAN JOURNAL OF PATHOLOGY
    72. Gurling, HMD; Kalsi, G; Brynjolfson, J; Sigmundsson, T; Sherrington, R; Mankoo, BS; Read, T; Murphy, P; Blaveri, E; McQuillin, A; Petursson, H; Curtis, D
      Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

      AMERICAN JOURNAL OF HUMAN GENETICS
    73. Gardiner, RM
      The molecular genetic basis of the neuronal ceroid lipofuscinoses

      NEUROLOGICAL SCIENCES
    74. Sankaranarayanan, K; Chakraborty, R
      Ionizing radiation and genetic risks XII. The concept of "potential recoverability correction factor" (PRCF) and its use for predicting the risk of radiation-inducible genetic disease in human live births

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    75. Zhong, N
      Neuronal ceroid lipofuscinoses and possible pathogenic mechanism

      MOLECULAR GENETICS AND METABOLISM
    76. Arbieva, ZH; Banerjee, K; Kim, SY; Edassery, SL; Maniatis, VS; Horrigan, SK; Westbrook, CA
      High-resolution physical map and transcript identification of a prostate cancer deletion interval on 8p22

      GENOME RESEARCH
    77. Baffa, R; Santoro, R; Bullrich, F; Mandes, B; Ishii, H; Croce, CM
      Definition and refinement of chromosome 8p regions of loss of heterozygosity in gastric cancer

      CLINICAL CANCER RESEARCH
    78. Shen, T; Zhuang, ZP; Gersell, DJ; Tavassoli, FA
      Allelic deletion of VHL gene detected in papillary tumors of the broad ligament, epididymis, and retroperitoneum in von Hippel-Lindau disease patients

      INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY
    79. Wilson, PJ; McGlinn, E; Marsh, A; Evans, T; Arnold, J; Wright, K; Biden, K; Young, J; Wainwright, B; Wicking, C; Chenevix-Trench, G
      Sequence variants of DLC1 in colorectal and ovarian tumours

      HUMAN MUTATION
    80. Rafi, SK; El Gebaly, H; Qumsiyeh, MB
      ETV6/CBFA2 fusions in childhood B-cell precursor acute lymphoblastic leukemia with myeloid markers

      DIAGNOSTIC MOLECULAR PATHOLOGY
    81. Miracca, EC; Yamamoto, L; Contado, D; Takimoto, MDS; Kowalski, LP; Nagai, MA
      Distinct chromosomal deleted regions defining different subsets of head and neck tumors

      DIAGNOSTIC MOLECULAR PATHOLOGY
    82. Lu, X; Nikaido, T; Toki, T; Zhai, YL; Kita, N; Konishi, I; Fujii, S
      Loss of heterozygosity among tumor suppressor genes in invasive and in situ carcinoma of the uterine cervix

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER
    83. Tosi, S; Harbott, J; Teigler-Schlegel, A; Haas, OA; Pirc-Danoewinata, H; Harrison, CJ; Biondi, A; Cazzaniga, G; Kempski, H; Scherer, SW; Kearney, L
      t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia

      GENES CHROMOSOMES & CANCER
    84. Angeloni, D; Danilkovitch-Miagkova, A; Ivanov, SV; Breathnach, R; Johnson, BE; Leonard, EJ; Lerman, MI
      Gene structure of the human receptor tyrosine kinase RON and mutation analysis in lung cancer samples

      GENES CHROMOSOMES & CANCER
    85. Oyama, T; Miyoshi, Y; Koyama, K; Nakagawa, H; Yamori, T; Ito, T; Matsuda, H; Arakawa, H; Nakamura, Y
      Isolation of a novel gene on 8p21.3-22 whose expression is reduced significantly in human colorectal cancers with liver metastasis

      GENES CHROMOSOMES & CANCER
    86. Fang, W; Piao, Z; Simon, D; Sheu, JC; Huang, S
      Mapping of a minimal deleted region in human hepatocellular carcinoma to 1p36.13-p36.23 and mutational analysis of the RIZ (PRDM2) gene localized to the region

      GENES CHROMOSOMES & CANCER
    87. Nomoto, S; Haruki, N; Tatematsu, Y; Konishi, H; Mitsudomi, T; Takahashi, T; Takahashi, T
      Frequent allelic imbalance suggests involvement of a tumor suppressor geneat 1p36 in the pathogenesis of human lung cancers

      GENES CHROMOSOMES & CANCER
    88. Chaffanet, M; Gressin, L; Preudhomme, C; Soenen-Cornu, V; Birnbaum, D; Pebusque, MJ
      MOZ is fused to p300 in an acute monocytic leukemia with t(8;22)

      GENES CHROMOSOMES & CANCER
    89. Spieker, N; Beitsma, M; van Sluis, P; Roobeek, I; den Dunnen, JT; Speleman, F; Caron, H; Versteeg, R
      An integrated 5-Mb physical, genetic, and radiation hybrid map of a 1p36.1region implicated in neuroblastoma pathogenesis

      GENES CHROMOSOMES & CANCER
    90. Kempski, HM; Sturt, NT
      The TEL-AML1 fusion accompanied by loss of the untranslocated TEL allele in B-precursor acute lymphoblastic leukaemia of childhood

      LEUKEMIA & LYMPHOMA
    91. Ichikawa, T; Hosoki, S; Suzuki, H; Akakura, K; Igarashi, T; Furuya, Y; Oshimura, M; Rinker-Schaeffer, CW; Nihei, N; Barrett, JC; Isaacs, JT; Ito, H
      Mapping of metastasis suppressor genes for prostate cancer by microcell-mediated chromosome transfer

      ASIAN JOURNAL OF ANDROLOGY
    92. He, ZW; Xie, L; Xu, LG; Lan, K; Liu, WD; Zhang, L; Ren, CP; Shi, JL; Zhou, W; Yao, KT
      Cloning of a novel gene associated with human nasopharyngeal carcinoma

      CHINESE SCIENCE BULLETIN
    93. Lahn, BT; Page, DC
      A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins

      HUMAN MOLECULAR GENETICS
    94. Incerti, B; Cortese, K; Pizzigoni, A; Surace, EM; Varani, S; Coppola, M; Jeffery, G; Seeliger, M; Jaissle, G; Bennett, DC; Marigo, V; Schiaffino, MV; Tacchetti, C; Ballabio, A
      Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1

      HUMAN MOLECULAR GENETICS
    95. Takita, J; Hayashi, Y; Takei, K; Yamaguchi, N; Hanada, R; Yamamoto, K; Yokota, J
      Allelic imbalance on chromosome 18 in neuroblastoma

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    96. Seitz, S; Werner, S; Fischer, J; Nothnagel, A; Schlag, PM; Scherneck, S
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      Genetics of the neuronal ceroid lipofuscinoses

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    98. Jenkin, A; Renner, D; Hahn, F; Larsen, J
      A case of primary amenorrhea, diabetes and anosmia

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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/01/21 alle ore 18:51:21