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    1. Santos, CB; Lima, MAC; Pimentel, MMG
      A new PCR assay useful for screening of FRAXE/FMR2 mental impairment amongmales

      HUMAN MUTATION
    2. State, MW; Pauls, DL; Leckman, JF
      Tourette's syndrome and related disorders

      CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
    3. Andersen, MK; Christiansen, DH; Kirchhoff, M; Pedersen-Bjergaard, J
      Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents

      GENES CHROMOSOMES & CANCER
    4. Padilla-Nash, HM; Heselmeyer-Haddad, K; Wangsa, N; Zhang, HG; Ghadimi, BM; Macville, M; Augustus, M; Schrock, E; Hilgenfeld, E; Ried, T
      Jumping translocations are common in solid tumor cell lines and result in recurrent fusions of whole chromosome arms

      GENES CHROMOSOMES & CANCER
    5. Fang, JM; Arlt, MF; Burgess, AC; Dagenais, SL; Beer, DG; Glover, TW
      Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome3 in an esophageal adenocarcinoma

      GENES CHROMOSOMES & CANCER
    6. Weinstein, SJ; Ziegler, RG; Selhub, J; Fears, TR; Strickler, HD; Brinton, LA; Hamman, RF; Levine, RS; Mallin, K; Stolley, PD
      Elevated serum homocysteine levels and increased risk of invasive cervicalcancer in US women

      CANCER CAUSES & CONTROL
    7. Michael, D; Rajewsky, MF
      Induction of the common fragile site FRA3B does not affect FHIT expression

      ONCOGENE
    8. Perl, A
      Endogenous retroviruses in pathogenesis of autoimmunity

      JOURNAL OF RHEUMATOLOGY
    9. Savelyeva, L; Schwab, M
      Amplification of oncogenes revisited: from expression profiling to clinical application

      CANCER LETTERS
    10. Bolivar, J; Garcia-Cozar, FJ; Astola, A; Iglesias, C; Pendon, C; Valdivia, MM
      Genomic structure and chromosome location of the human gene encoding the zinc finger autoantigen ZNF330

      CYTOGENETICS AND CELL GENETICS
    11. Ray, GN; Shahid, M; Husain, SA
      Status of chromosome breaks and gaps in breast cancer: a follow-up study

      CANCER GENETICS AND CYTOGENETICS
    12. Latham, C; Zhang, AJ; Nalbanti, A; Maner, S; Zickert, P; Blegen, H; Zetterberg, A
      Frequent co-amplification of two different regions on 17q in aneuploid breast carcinomas

      CANCER GENETICS AND CYTOGENETICS
    13. Maluf, SW; Erdtmann, B
      Genomic instability in Down syndrome and Fanconi anemia assessed by micronucleus analysis and single-cell gel electrophoresis

      CANCER GENETICS AND CYTOGENETICS
    14. Megarbane, A; Waked, N; Chouery, E; Moglabey, YB; Saliba, N; Mornet, E; Serre, JL; Slim, R
      Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. Plaja, A; Miro, R; Fuster, C; Perez, C; Sarret, E; Esteve, P; Egozcue, J
      Bends in human mitotic metaphase chromosomes revisited: 15q11-13 is the most frequent non-random autosomal bend in blood cultures

      AMERICAN JOURNAL OF MEDICAL GENETICS
    16. Odierna, G; Aprea, G; Arribas, O; Carriglione, T
      A chromosomal study of the Pyrenean endemic brown frog species, Rana pyrenaica, and various Italian populations of R-dalmatina and R-italica

      FOLIA ZOOLOGICA
    17. Smith, L; Plug, A; Thayer, M
      Delayed replication timing leads to delayed mitotic chromosome condensation and chromosomal instability of chromosome translocations

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    18. Kolomietz, E; Al-Maghrabi, J; Brennan, S; Karaskova, J; Minkin, S; Lipton, J; Squire, JA
      Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis

      BLOOD
    19. Kannan, K; Munirajan, AK; Bhuvarahamurthy, V; Mohanprasad, BKC; Shankar, P; Tsuchida, N; Shanmugam, G
      FHIT Gene mutations and single nucleotide polymorphism in Indian oral and cervical squamous cell carcinomas

      ORAL ONCOLOGY
    20. Yamauchi, M; Tsuji, S; Mita, K; Saito, T; Morimyo, M
      A novel minisatellite repeat expansion identified at FRA16B in a Japanese carrier.

      GENES & GENETIC SYSTEMS
    21. Karkera, JD; Ayache, S; Ransome, RJ; Jackson, MA; Elsayem, AF; Sridhar, R; Detera-Wadleigh, SD; Wadleigh, RG
      Refinement of regions with allelic loss on chromosome 18p11.2 and 18q12.2 in esophageal squamous cell carcinoma

      CLINICAL CANCER RESEARCH
    22. Szuhai, K; Bezrookove, V; Wiegant, J; Vrolijk, J; Dirks, RW; Rosenberg, C; Raap, AK; Tanke, HJ
      Simultaneous molecular karyotyping and mapping of viral DNA integration sites by 25-color COBRA-FISH

      GENES CHROMOSOMES & CANCER
    23. Egeli, U; Ozkan, L; Tunca, B; Kahraman, S; Cecener, G; Ergul, E; Engin, K
      The relationship between genetic susceptibility to head and neck cancer with the expression of common fragile sites

      HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
    24. Fundia, A; Gorostiaga, M; Mudry, M
      Expression of common fragile sites in two Ceboidea species: Saimiri boliviensis and Alouatta caraya (Primates : Platyrrhini)

      GENETICS SELECTION EVOLUTION
    25. Adra, CN; Donato, JL; Badovinac, R; Syed, F; Kheraj, R; Cai, HB; Moran, C; Kolker, MT; Turner, H; Weremowicz, S; Shirakawa, T; Morton, CC; Schnipper, LE; Drews, R
      SMARCAD1, a novel human helicase family-defining member associated with genetic instability: Cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases

      GENOMICS
    26. Courtay-Cahen, C; Morris, JS; Edwards, PAW
      Chromosome translocations in breast cancer with breakpoints at 8p12

      GENOMICS
    27. Lindquist, R; Forsblom, AM; Ost, A; Gahrton, G
      Mutagen exposures and chromosome 3 aberrations in acute myelocytic leukemia

      LEUKEMIA
    28. Bode, J; Benham, C; Ernst, E; Knopp, A; Marschalek, R; Strick, R; Strissel, P
      Fatal connections: When DNA ends meet on the nuclear matrix

      JOURNAL OF CELLULAR BIOCHEMISTRY
    29. Tukun, A; Renda, Y; Topcu, M; Tuncali, T; Bokesoy, I
      Mental retardation with rare fragile site expressed at 2q11

      BRAIN & DEVELOPMENT
    30. Morelli, C; Magnanini, C; Mungall, AJ; Negrini, M; Barbanti-Brodano, G
      Cloning and characterization of two overlapping genes in a subregion at 6q21 involved in replicative senescence and schizophrenia

      GENE
    31. Tunca, B; Egeli, U; Zorluoglu, A; Yilmazlar, T; Yerci, O; Kizil, A
      The expression of fragile sites in lymphocytes of patients with rectum cancer and their first-degree relatives

      CANCER LETTERS
    32. Roy, SK; Trivedi, AH; Bakshi, SR; Patel, RK; Shukla, PH; Patel, SJ; Bhatavdekar, JM; Patel, DD; Shah, PM
      Spontaneous chromosomal instability in breast cancer families

      CANCER GENETICS AND CYTOGENETICS
    33. Thomson, SW; Heimburger, DC; Cornwell, PE; Turner, ME; Sauberlich, HE; Fox, LM; Butterworth, CE
      Effect of total plasma homocysteine on cervical dysplasia risk

      NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL
    34. Kerbeshian, J; Severud, R; Burd, L; Larson, L
      Peek-a-boo fragile site at 16D associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    35. Luceri, C; Guglielmi, F; De Filippo, C; Caderni, G; Mini, E; Biggeri, A; Napoli, C; Tonelli, F; Cianchi, F; Dolara, P
      Clinicopathologic features and FHIT gene expression in sporadic colorectaladenocarcinomas

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    36. Sastre-Garau, X; Favre, M; Couturier, J; Orth, G
      Distinct patterns of alteration of myc genes associated with integration of human papillomavirus type 16 or type 45 DNA in two genital tumours

      JOURNAL OF GENERAL VIROLOGY
    37. Helland, A; Kraggerud, SM; Kristensen, GB; Holm, R; Abeler, VM; Huebner, K; Borresen-Dale, AL; Lothe, RA
      Primary cervical carcinomas show 2 common regions of deletion at 3P, 1 within the FHIT gene: Evaluation of allelic imbalance at FHIT, RB1 and TP53 inrelation to survival

      INTERNATIONAL JOURNAL OF CANCER
    38. Bednarek, AK; Laflin, KJ; Daniel, RL; Liao, QY; Hawkins, KA; Aldaz, CM
      WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer

      CANCER RESEARCH
    39. Yuan, BZ; Keck-Waggoner, C; Zimonjic, DB; Thorgeirsson, SS; Popescu, NC
      Alterations of the FHIT gene in human hepatocellular carcinoma

      CANCER RESEARCH
    40. Weisberg, E; Griffin, JD
      Mechanism of resistance to the ABL tyrosine kinase inhibitor STI571 in BCR/ABL-transformed hematopoietic cell lines

      BLOOD
    41. Carme, F; Rosa, M; Josep, E
      Chromosome aberrations induced by aphidicolin

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    42. Adinolfi, S; Bagni, C; Musco, G; Gibson, T; Mazzarella, L; Pastore, A
      Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains

      RNA-A PUBLICATION OF THE RNA SOCIETY
    43. Russo, C; Rocco, L; Stingo, V; Aprea, G; Odierna, G
      A cytogenetic analysis of Gambusia holbrooki (Cyprinodontiformes, Poecilidae) from the River Sarno

      ITALIAN JOURNAL OF ZOOLOGY
    44. Rithidech, KN; Cronkite, EP; Bond, VP
      Advantages of the CBA mouse in leukemogenesis research

      BLOOD CELLS MOLECULES AND DISEASES
    45. Hallas, C; Albitar, M; Letofsky, J; Keating, MJ; Huebner, K; Croce, CM
      Loss of FHIT expression in acute lymphoblastic leukemia

      CLINICAL CANCER RESEARCH
    46. Schwab, M
      Oncogene amplification in solid tumors

      SEMINARS IN CANCER BIOLOGY
    47. Autiero, M; Culerrier, R; Bouchier, C; Basmaciogullari, S; Gaubin, M; El Marhomy, S; Blanchet, P; Paradis, V; Jardin, A; Guardiola, J; Piatier-Tonneau, D
      Abnormal restriction pattern of PIP gene associated with human primary prostate cancers

      DNA AND CELL BIOLOGY
    48. Hocking, T; Feichtinger, W; Schmid, M; Haan, EA; Baker, E; Sutherland, GR
      Homozygotes for FRA16B are normal

      CHROMOSOME RESEARCH
    49. Ashley-Koch, A; Wolpert, CM; Menold, MM; Zaeem, L; Basu, S; Donnelly, SL; Ravan, SA; Powell, CM; Qumsiyeh, MB; Aylsworth, AS; Vance, JM; Gilbert, JR; Wright, HH; Abramson, RK; DeLong, GR; Cuccaro, ML; Pericak-Vance, MA
      Genetic studies of autistic disorder and chromosome 7

      GENOMICS
    50. Croce, CM; Sozzi, G; Huebner, K
      Role of FHIT in human cancer

      JOURNAL OF CLINICAL ONCOLOGY
    51. Makinen, A; Andersson, M; Hakkinen, A; Kuosmanen, S
      A reciprocal translocation between autosomes 8 and 10 in a boar used for artificial insemination service and its effects on litter size

      ANIMAL REPRODUCTION SCIENCE
    52. Hou, CD; Chiang, JT; Tai, JJ
      Testing the nonrandomness of chromosomal breakpoints using highest observed breakages

      HUMAN GENETICS
    53. Melnyk, S; Pogribna, M; Miller, BJ; Basnakian, AG; Pogribny, IP; James, SJ
      Uracil misincorporation, DNA strand breaks, and gene amplification are associated with tumorigenic cell transformation in folate deficient/repleted Chinese hamster ovary cells

      CANCER LETTERS
    54. Park, JS; Dong, SM; Kim, HS; Lee, JY; Um, SJ; Park, IS; Kim, SJ; Namkoong, SE
      Detection of p16 gene alteration in cervical cancer using tissue microdissection and LOH study

      CANCER LETTERS
    55. Luft, F; Gebert, J; Schneider, A; Melsheimer, P; Doeberitz, MV
      Frequent allelic imbalance of tumor suppressor gene loci in cervical dysplasia

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
    56. Peschka, B; Leygraaf, J; van der Ven, K; Montag, M; Schartmann, B; Schubert, R; van der Ven, H; Schwanitz, G
      Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection

      HUMAN REPRODUCTION
    57. Ilyinskikh, NN; Ilyinskikh, IN; Ilyinskikh, EN
      Chromosome breakage at sites of oncogenes in a population accidentally exposed to radioactive chemical pollution

      MUTAGENESIS
    58. Nesina, IP; Polishchuk, LZ
      Human chromosomal fragile sites and malignant tumours

      EXPERIMENTAL ONCOLOGY
    59. Schwab, M
      From fish to FISH: the comparative pathology of neuroblastomas in humans, mice and fish

      JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
    60. Karkera, JD; Balan, KV; Yoshikawa, T; Lipman, TO; Korman, L; Sharma, A; Patterson, RH; Sani, N; Detera-Wadleigh, SD; Wadleigh, RG
      Systematic screening of chromosome 18 for loss of heterozygosity in esophageal squamous cell carcinoma

      CANCER GENETICS AND CYTOGENETICS
    61. Vernole, P; Tullio, A; Caporossi, D; Didona, B; Melino, G; Tedeschi, B
      Bleomycin-induced chromosome aberrations in lymphocytes derived from patients with lamellar ichthyosis

      CANCER GENETICS AND CYTOGENETICS
    62. Maitra, A; Wistuba, II; Gibbons, D; Gazdar, AF; Albores-Saavedra, J
      Allelic losses at chromosome 3p are seen in human papilloma virus 16 associated transitional cell carcinoma of the cervix

      GYNECOLOGIC ONCOLOGY
    63. Balci, A; Ekmekc, A; Cetin, R
      The expression of common fragile sites in peripheral blood lymphocytes of breast and colorectal cancer patients with aphidicolin

      TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE
    64. Mitra, AB
      Genetic deletion and human papillomavirus infection in cervical cancer: Loss of heterozygosity sites at 3p and 5p are important genetic events

      INTERNATIONAL JOURNAL OF CANCER
    65. Guven, GS; Hacihanefioglu, S; Cenani, A
      Expression of aphidicolin, FUdR and caffeine-induced fragile sites in lymphocytes of healthy Turkish individuals

      GENETICA
    66. Velickovic, M; Delahunt, B; Grebe, SKG
      Loss of heterozygosity at 3p14.2 in clear cell renal cell carcinoma is an early event and is highly localized to the FHIT gene locus

      CANCER RESEARCH
    67. Koopman, LA; Szuhai, K; van Eendenburg, JDH; Bezrookove, V; Kenter, GG; Schuuring, E; Tanke, H; Fleuren, GJ
      Recurrent integration of human papillomaviruses 16, 45, and 67 near translocation breakpoints in new cervical cancer cell lines

      CANCER RESEARCH
    68. Monni, O; Zhu, Y; Franssila, K; Oinonen, R; Hoglund, P; Elonen, E; Joensuu, H; Knuutila, S
      Molecular characterization of deletion at 11q22.1-23.3 in mantle cell lymphoma

      BRITISH JOURNAL OF HAEMATOLOGY
    69. BOUFFLER SD
      INVOLVEMENT OF TELOMERIC SEQUENCES IN CHROMOSOMAL-ABERRATIONS

      Mutation research. Fundamental and molecular mechanisms of mutagenesis
    70. SIMI S; ATTOLINI C; GIULOTTO E
      INTRACHROMOSOMAL TELOMERIC REPEATS AND STABILIZATION OF TRUNCATED CHROMOSOMES IN V79 CHINESE-HAMSTER CELLS

      Mutation research. Fundamental and molecular mechanisms of mutagenesis
    71. SIMI S; SIMILI M; BONATTI S; CAMPAGNA M; ABBONDANDOLO A
      FRAGILE SITES AT THE CENTROMERE OF CHINESE-HAMSTER CHROMOSOMES - A POSSIBLE MECHANISM OF CHROMOSOME LOSS

      Mutation research. Fundamental and molecular mechanisms of mutagenesis
    72. CHOW M; KOO J; NG P; RUBIN H
      RANDOM POPULATION-WIDE GENETIC-DAMAGE INDUCED IN REPLICATING CELLS TREATED WITH METHOTREXATE

      Mutation research. Genetic toxicology and environmental mutagenesis
    73. Colls, P; Martinez-Pasarell, O; Perez, MM; Egozcue, J; Templado, C
      Cytogenetic analysis of spermatozoa in the father of a child with a de-novo reciprocal translocation t(7;9) (q22;p23)

      MOLECULAR HUMAN REPRODUCTION
    74. BIECHE I; LATIL A; BECETTE V; LIDEREAU R
      STUDY OF FHIT TRANSCRIPTS IN NORMAL AND MALIGNANT BREAST-TISSUE

      Genes chromosomes & cancer (Print)
    75. LEBEAU MM; DRABKIN H; GLOVER TW; GEMMILL R; RASSOOL FV; MCKEITHAN TW; SMITH DI
      AN FHIT TUMOR-SUPPRESSOR GENE

      Genes, chromosomes & cancer
    76. CASTRO PD; FAIRMAN J; NAGARAJAN L
      THE UNEXPLORED 5Q13 LOCUS - A ROLE IN HEMATOPOIETIC MALIGNANCIES

      Leukemia & lymphoma
    77. RIVADENEIRA ED; POPESCU NC; ZIMONJIC DB; CHENG GS; NELSON PJ; ROSS MD; DIPAOLO JA; KLOTMAN ME
      SITES OF RECOMBINANT ADENOASSOCIATED VIRUS INTEGRATION

      International journal of oncology
    78. SMITH DI; HUANG HJ; WANG L
      COMMON FRAGILE SITES AND CANCER (REVIEW)

      International journal of oncology
    79. Ott, G; Haaf, T; Schmid, M
      Inhibition of condensation in human chromosomes induced by the thymidine analogue 5-iododeoxyuridine

      CHROMOSOME RESEARCH
    80. BERGTHORSSON JT; JOHANNSDOTTIR J; JONASDOTTIR A; EIRIKSDOTTIR G; EGILSSON V; INGVARSSON S; BARKARDOTTIR RB; ARASON A
      CHROMOSOME IMBALANCE AT THE 3P14 REGION IN HUMAN BREAST-TUMORS - HIGH-FREQUENCY IN PATIENTS WITH INHERITED PREDISPOSITION DUE TO BRCA2

      European journal of cancer
    81. MANGANO R; PIDDINI E; CARRAMUSA L; DUHIG T; FEO S; FRIED M
      CHIMERIC AMPLICONS CONTAINING THE C-MYC GENE IN HL60 CELLS

      Oncogene
    82. MATTHIAS C; BOCKMUHL U; JAHNKE V; PETERSEN I; DIETEL M; FRYER A; STRANGE RC
      INFLUENCE OF POLYMORPHISMS AT GLUTATHIONE -S-TRANSFERASE GENE LOCI ONALLELIC LOSSES IN HEAD AND NECK SQUAMOUS-CELL CARCINOMAS

      Laryngo-, Rhino-, Otologie
    83. RUFFIN MT; LANCASTER WD
      CLINICAL-MODELS OF CHEMOPREVENTION FOR CERVICAL-CANCER

      Hematology/oncology clinics of North America
    84. NICKERSON E; NELSON DL
      MOLECULAR DEFINITION OF PERICENTRIC-INVERSION BREAKPOINTS OCCURRING DURING THE EVOLUTION OF HUMANS AND CHIMPANZEES

      Genomics (San Diego, Calif.)
    85. SLENTZKESLER KA; HALE LP; KAUFMAN RE
      IDENTIFICATION AND CHARACTERIZATION OF K12 (SECTM1), A NOVEL HUMAN GENE THAT ENCODES A GOLGI-ASSOCIATED PROTEIN WITH TRANSMEMBRANE AND SECRETED ISOFORMS

      Genomics
    86. Di Berardino, D; Burguete, I
      High resolution RBA-banding comparison between early prometaphase chromosomes of cattle (Bos taurus L.) and goat (Capra hircus L.) at 700 band level

      CYTOGENETICS AND CELL GENETICS
    87. EGELI U
      INDUCTION OF SISTER-CHROMATID EXCHANGES BY PYRIMETHAMINE IN HUMAN LYMPHOCYTE-CULTURES

      Teratogenesis, carcinogenesis, and mutagenesis
    88. Cecener, G; Egeli, U; Tasdelen, I; Tunca, B; Duman, H; Kizil, A
      Common fragile site expression and genetic predisposition to breast cancer

      TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS
    89. COLLS P; MARTINEZPASARELL O; PEREZ MM; EGOZCUE J; TEMPLADO C
      SPERM CHROMOSOME ANALYSIS IN THE FATHER OF A CHILD WITH A DE-NOVO RECIPROCAL TRANSLOCATION T(11-15)(Q12-Q22) BY G-BANDING AND FLUORESCENCE IN-SITU HYBRIDIZATION

      Human reproduction
    90. RADHA S; NATARAJAN AT
      SODIUM ARSENITE-INDUCED CHROMOSOMAL-ABERRATIONS IN THE XQ ARM OF CHINESE-HAMSTER CELL-LINES

      Mutagenesis
    91. PIPIRAS E; COQUELLE A; BIETH A; DEBATISSE M
      INTERSTITIAL DELETIONS AND INTRACHROMOSOMAL AMPLIFICATION INITIATED FROM A DOUBLE-STRAND BREAK TARGETED TO A MAMMALIAN CHROMOSOME

      EMBO journal
    92. KOLIALEXI A; MAVROU A; TSENGHI C; TSANGARIS GT; DAFERMOU E; TZORTZATOU F; POLYCHRONOPOULOU S; HAIDAS S; METAXOTOU C
      CHROMOSOME FRAGILITY AND PREDISPOSITION TO CHILDHOOD MALIGNANCIES

      Anticancer research
    93. TRIVEDI AH; ROY SK; BHACHECH SH; PATEL RK; DALAL AA; BHATAVDEKAR JM; PATEL DD
      CYTOGENETIC EVALUATION OF 20 SPORADIC BREAST-CANCER PATIENTS AND THEIR FIRST-DEGREE RELATIVES

      Breast cancer research and treatment
    94. RAO NM; PAI SA; SHINDE SR; GHOSH SN
      REDUCED DNA-REPAIR CAPACITY IN BREAST-CANCER PATIENTS AND UNAFFECTED INDIVIDUALS FROM BREAST-CANCER FAMILIES

      Cancer genetics and cytogenetics
    95. SISLEY K; BRAND C; PARSONS MA; MALTBY E; REES RC; RENNIE IG
      CYTOGENETICS OF IRIS MELANOMAS - DISPARITY WITH OTHER UVEAL TRACT MELANOMAS

      Cancer genetics and cytogenetics
    96. MICHAELIS RC; VELAGALETI GVN; JONES C; PIVNICK EK; PHELAN MC; BOYD E; TARLETON J; WILROY RS; TUNNACLIFFE A; THARAPEL AT
      MOST JACOBSEN-SYNDROME DELETION BREAKPOINTS OCCUR DISTAL TO FRA11B

      American journal of medical genetics
    97. Huebner, K; Garrison, PN; Barnes, LD; Croce, CM
      The role of the FHIT/FRA3B locus in cancer

      ANNUAL REVIEW OF GENETICS
    98. SMITH MDA; BORSATTO B
      DOWNS-SYNDROME, AGING AND FRAGILE SITES

      Mechanism of ageing and development
    99. PINEAU P; MARCHIO A; MATTEI MG; KIM WH; YOUN JK; TIOLLAIS P; DEJEAN A
      EXTENSIVE ANALYSIS OF DUPLICATED-INVERTED HEPATITIS-B VIRUS INTEGRATIONS IN HUMAN HEPATOCELLULAR-CARCINOMA

      Journal of General Virology
    100. MANGEL L; TERNES T; SCHMITZ B; DOERFLER W
      NEW 5'-(CGG)(N)-3' REPEATS IN THE HUMAN GENOME

      The Journal of biological chemistry


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 19/01/21 alle ore 00:49:52