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    1. Rivero, MT; Vazquez-Gundin, F; Goyanes, V; Campos, A; Blasco, M; Gosalvez, J; Fernandez, JL
      High frequency of constitutive alkali-labile sites in mouse major satellite DNA, detected by DNA breakage detection-fluorescence in situ hybridization

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    2. Olesen, C; Hansen, C; Bendsen, E; Byskov, AG; Schwinger, E; Lopez-Pajares, I; Jensen, PKA; Kristoffersson, U; Schubert, R; Van Assche, E; Wahlstroem, J; Lespinasse, J; Tommerup, N
      Identification of human candidate genes for male infertility by digital differential display

      MOLECULAR HUMAN REPRODUCTION
    3. Shaikh, TH; Kurahashi, H; Emanuel, BS
      Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: An update and literature review

      GENETICS IN MEDICINE
    4. Inoue, K; Dewar, K; Katsanis, N; Reiter, LT; Lander, ES; Devon, KL; Wyman, DW; Lupski, JR; Birren, B
      The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes

      GENOME RESEARCH
    5. Kurahashi, H; Emanuel, BS
      Unexpected high rate of de novo constitutional t(11;22) translocations in sperm from normal males

      NATURE GENETICS
    6. State, MW; Pauls, DL; Leckman, JF
      Tourette's syndrome and related disorders

      CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
    7. Fioretos, T; Panagopoulos, I; Lassen, C; Swedin, A; Billstrom, R; Isaksson, M; Strombeck, B; Olofsson, T; Mitelman, F; Johansson, B
      Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: The first fusion gene involving BCR but not ABL

      GENES CHROMOSOMES & CANCER
    8. Van Roy, N; Van Limbergen, H; Vandesompele, J; Van Gele, M; Poppe, B; Salwen, H; Laureys, G; Manoel, N; De Paepe, A; Speleman, F
      Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines

      GENES CHROMOSOMES & CANCER
    9. Jeffs, AR; Wells, E; Morris, CM
      Nonrandom distribution of interspersed repeat elements in the BCR and ABLIgenes and its relation to breakpoint cluster regions

      GENES CHROMOSOMES & CANCER
    10. Nucci, MR; Weremowicz, S; Neskey, DM; Sornberger, K; Tallini, G; Morton, CC; Quade, BJ
      Chromosomal translocation t(8;12) induces aberrant HMGIC expression in aggressive angiomyxoma of the vulva

      GENES CHROMOSOMES & CANCER
    11. Mathew, S; Shurtleff, SA; Raimondi, SC
      Novel cryptic, complex rearrangements involving ETV6-CBFA2 (TEL-AMLI) genes identified by fluorescence in situ hybridization in pediatric patients with acute lymphoblastic leukemia

      GENES CHROMOSOMES & CANCER
    12. Karamysheva, TB; Matveeva, VG; Shorina, AP; Rubtsov, NB
      Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial trisomy 3p and partial trisomy 10q in humans

      RUSSIAN JOURNAL OF GENETICS
    13. Rubtsov, NB; Karamysheva, TV; Matveeva, VG; Sablina, OV; Sosnitskaya, SV; Andreenkova, OV; Gainer, TA; Degtyareva, MM
      Reverse in situ hybridization of DNA probes of abnormal chromosomes in diagnostics of chromosomal pathologies

      RUSSIAN JOURNAL OF GENETICS
    14. Weimer, J; Koehler, MR; Wiedemann, U; Attermeyer, P; Jacobsen, A; Karow, D; Kiechle, M; Jonat, W; Arnold, N
      Highly comprehensive karyotype analysis by a combination of spectral karyotyping (SKY), microdissection, and reverse painting (SKY-MD)

      CHROMOSOME RESEARCH
    15. Bandyopadhyay, R; Berend, SA; Page, SL; Choo, KHA; Shaffer, LG
      Satellite III sequences on 14p and their relevance to Robertsonian translocation formation

      CHROMOSOME RESEARCH
    16. Martinez-Lopez, W; Folle, GA; Obe, G; Jeppesen, P
      Chromosome regions enriched in hyperacetylated histone H4 are preferred sites for endonuclease- and radiation-induced breakpoints

      CHROMOSOME RESEARCH
    17. Panagopoulos, I; Fioretos, T; Isaksson, M; Samuelsson, U; Billstrom, R; Strombeck, B; Mitelman, F; Johansson, B
      Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)

      HUMAN MOLECULAR GENETICS
    18. Kurahashi, H; Emanuel, BS
      Long AT-rich palindromes and the constitutional t(11;22) breakpoint

      HUMAN MOLECULAR GENETICS
    19. Craig, WA
      Re-evaluating current antibiotic therapy

      RESPIRATORY MEDICINE
    20. Ladanyi, M
      Fusions of the SYT and SSX genes in synovial sarcoma

      ONCOGENE
    21. Harrer, J; Hammon, G; Wagner, T; Bolkenius, M
      Lipoblastoma and lipoblastomatosis: A report of two cases and review of the literature

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    22. Yang, LV; Nicholson, RH; Kaplan, J; Galy, A; Li, L
      Hemogen is a novel nuclear factor specifically expressed in mouse hematopoietic development and its human homologue EDAG maps to chromosome 9q22, a region containing breakpoints of hematological neoplasms

      MECHANISMS OF DEVELOPMENT
    23. Sakuma, T; Li, QL; Jin, YH; Choi, LW; Kim, EG; Ito, K; Ito, Y; Nomura, S; Bae, SC
      Cloning and expression pattern of a novel PEBP2 beta-binding protein (charged amino acid rich leucine zipper-1 [Crl-1]) in the mouse

      MECHANISMS OF DEVELOPMENT
    24. Perea, E
      Clinical relevance of laboratory susceptibility data

      INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS
    25. Hanamura, I; Iida, S; Akano, Y; Hayami, Y; Kato, M; Miura, K; Harada, S; Banno, S; Wakita, A; Kiyoi, H; Naoe, T; Shimizu, S; Sonta, S; Nitta, M; Taniwaki, M; Ueda, R
      Ectopic expression of MAFB gene in human myeloma cells carrying (14;20)(q32;q11) chromosomal translocations

      JAPANESE JOURNAL OF CANCER RESEARCH
    26. Broberg, K; Tallini, G; Hoglund, M; Lindstrand, A; Toksvig-Larsen, S; Mertens, F
      The tumor-associated gene HMGIC is expressed in normal and osteoarthritis-affected synovia

      MODERN PATHOLOGY
    27. Kaplan, SL; Mason, EO; Barson, WJ; Tan, TQ; Schutze, GE; Bradley, JS; Givner, LB; Kim, KS; Yogev, R; Wald, ER
      Outcome of invasive infections outside the central nervous system caused by Streptococcus pneumoniae isolates nonsusceptible to ceftriaxone in children treated with beta-lactam antibiotics

      PEDIATRIC INFECTIOUS DISEASE JOURNAL
    28. Bagheri-Fam, S; Ferraz, C; Demaille, J; Scherer, G; Pfeifer, D
      Comparative genomics of the SOX9 region in human and Fugu rubripes: Conservation of short regulatory sequence elements within large intergenic regions

      GENOMICS
    29. Mumm, S; Herrera, L; Waeltz, PW; Scardovi, A; Nagaraja, R; Esposito, T; Schlessinger, D; Rocchi, M; Forabosco, A
      X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes

      GENOMICS
    30. Gutierrez, NC; Hernandez, JM; Garcia, JL; Canizo, MC; Gonzalez, M; Hernandez, J; Gonzalez, MB; Garcia-Marcos, MA; San Miguel, JF
      Differences in genetic changes between multiple myeloma and plasma cell leukemia demonstrated by comparative genomic hybridization

      LEUKEMIA
    31. Shteper, PJ; Siegfried, Z; Asimakopoulos, FA; Palumbo, GA; Rachmilewitz, EA; Ben-Neriah, Y; Ben-Yehuda, D
      ABL1 methylation in Ph-positive ALL is exclusively associated with the P210 form of BCR-ABL

      LEUKEMIA
    32. Zinner, SH; Vostrov, SN; Lubenko, IY; Portnoy, YA; Cornaglia, G; Firsov, AA
      Comparative anti-staphylococcal effects of gemifloxacin and trovafloxacin in an in vitro dynamic model in terms of AUC/MIC and dose relationships

      DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE
    33. Kim, SK; Kim, HJ; Yang, YH; Kim, IK; Bai, SW; Kim, JY; Park, KH; Cho, DJ; Song, CH
      A case with balanced chromosome rearrangement involving chromosomes 9, 14,and 13 in a woman with recurrent abortion

      YONSEI MEDICAL JOURNAL
    34. Wieser, R; Schreiner, U; Wollenberg, B; Neubauer, A; Fonatsch, C; Rieder, H
      Masked inv(3)(q21q26) in a patient with minimally differentiated acute myeloid leukemia

      HAEMATOLOGICA
    35. Levanon, D; Glusman, C; Bangsow, T; Ben-Asher, E; Male, DA; Avidan, N; Bangsow, C; Hattori, M; Taylor, TD; Taudien, S; Blechschmidt, K; Shimizu, N; Rosenthal, A; Sakaki, Y; Lancet, D; Groner, Y
      Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1

      GENE
    36. Zenmyo, M; Komiya, S; Hamada, T; Hiraoka, K; Nagata, K; Tsuji, S; Hashimoto, H; Inoue, A
      Intraneural monophasic synovial sarcoma - A case report

      SPINE
    37. Waters, JJ; Campbell, PL; Crocker, AJM; Campbell, CM
      Phenotypic effects of balanced X-autosome translocations in females: a retrospective survey of 104 cases reported from UK laboratories

      HUMAN GENETICS
    38. Chennathukuzhi, VM; Kurihara, Y; Bray, JD; Yang, JX; Hecht, NB
      Altering the GTP binding site of the DNA/RNA-binding protein, Translin/TB-RBP, decreases RNA binding and may create a dominant negative phenotype

      NUCLEIC ACIDS RESEARCH
    39. Kozicki, S; Tinsley, PA
      Shifting endpoints in the term structure of interest rates

      JOURNAL OF MONETARY ECONOMICS
    40. Lanesberg, R; Yee, H; Datikashvili, M; Ahmed, ANZ
      Unilateral mandibular lip anesthesia as the sole presenting symptom of Burkitt's lymphoma: Case report and review of literature

      JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY
    41. White, DG; Acar, J; Anthony, F; Franklin, A; Gupta, B; Nicholls, T; Tamura, Y; Thompson, S; Threlfall, EJ; Vose, D; van Vuuren, M; Wegener, HC; Costarrica, ML
      Antimicrobial resistance: standardisation and harmonisation of laboratory methodologies for the detection and quantification of antimicrobial resistance

      REVUE SCIENTIFIQUE ET TECHNIQUE DE L OFFICE INTERNATIONAL DES EPIZOOTIES
    42. Chen, CP; Chern, SR; Tzen, CY; Lee, MS; Pan, CW; Chang, TY; Wang, W
      Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts

      PRENATAL DIAGNOSIS
    43. Ueda, C; Yamada, H; Akasaka, T; Ohmori, K; Sasada, M; Uchiyama, T; Ohno, H
      Establishment and characterization of a new human myeloma cell line, KY delta-1, producing the delta/kappa type immunoglobulin

      CANCER GENETICS AND CYTOGENETICS
    44. Cheng, LR; Ramesh, KH; Radel, E; Ratech, H; Wei, DM; Cannizzaro, LA
      Characterization of t(11;19)(q23;p13.3) by fluorescence in situ hybridization analysis in a pediatric patient with therapy-related acute myelogenous leukemia

      CANCER GENETICS AND CYTOGENETICS
    45. Kahl, C; Gesk, S; Harder, L; Harbott, J; French, L; Deloukas, P; Grote, W; Schlegelberger, B; Siebert, R
      Detection of translocations involving the HOX11/TCL3-locus in 10q24 by interphase fluorescence in situ hybridization

      CANCER GENETICS AND CYTOGENETICS
    46. Cockwell, AE; Davalos, IP; Rivera, HR; Crolla, JA
      FISH characterization of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    47. Brinkschmidt, C; Christiansen, H; Terpe, HJ; Simon, R; Lampert, F; Boecker, W; Dockhorn-Dworniczak, B
      Distal chromosome 17 gains in neuroblastomas detected by comparative genomic hybridization (CGH) are associated with a poor clinical outcome

      MEDICAL AND PEDIATRIC ONCOLOGY
    48. Lastowska, M; Van Roy, N; Bown, N; Speleman, F; Roberts, P; Lunec, J; Strachan, T; Pearson, ADJ; Jackson, MS
      Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma

      MEDICAL AND PEDIATRIC ONCOLOGY
    49. Kronvall, G; Karlsson, I
      Fluconazole and voriconazole multidisk testing of Candida species for disktest calibration and MIC estimation

      JOURNAL OF CLINICAL MICROBIOLOGY
    50. Smith, P
      Accuracy, precision and meaning of antimicrobial agent susceptibility testing of bacteria associated with fish diseases

      AQUACULTURE
    51. O'Reilly, A; Smith, P
      Use of indirect conductimetry to establish predictive no effect concentrations of oxytetracycline and oxolinic acid in aquatic sediments

      AQUACULTURE
    52. Syrrou, M; Fryns, JP
      Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay

      JOURNAL OF MEDICAL GENETICS
    53. Borck, G; Wirth, J; Hardt, T; Tonnies, H; Brondum-Nielsen, K; Bugge, M; Tommerup, N; Nothwang, HG; Ropers, HH; Haaf, T
      Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome

      JOURNAL OF MEDICAL GENETICS
    54. Valdes-Flores, M; Kofman-Alfaro, SH; Vaca, ALJ; Cuevas-Covarrubias, SA
      Deletion of exons 1-5 of the STS gene causing X-linked ichthyosis

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    55. Wilstermann, AM; Osheroff, N
      Positioning the 3 '-DNA terminus for topoisomerase II-mediated religation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    56. Chu, C; Khotz, DS
      Identification of the E2A gene products as regulatory targets of the G(1) cyclin-dependent kinases

      JOURNAL OF BIOLOGICAL CHEMISTRY
    57. Hrdlicka, I; Zadina, J; Krejci, R; Srbova, A; Kucerova, M
      Patterns of deletions and the distribution of breakpoints in the dystrophin gene in Czech patients with Duchenne and Becker muscular dystrophy (statistical comparison with results from several other countries)

      FOLIA BIOLOGICA
    58. McGhee, EM; Qu, Y; Wohlferd, MM; Goldberg, JD; Norton, ME; Cotter, PD
      Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p

      CLINICAL GENETICS
    59. Bayani, J; Squire, JA
      Advances in the detection of chromosomal aberrations using spectral karyotyping

      CLINICAL GENETICS
    60. Betti, CJ; Villalobos, MJ; Diaz, MO; Vaughan, ATM
      Apoptotic triggers initiate translocations within the MLL gene involving the nonhomologous end joining repair system

      CANCER RESEARCH
    61. Andersen, MK; Christiansen, DH; Jensen, BA; Ernst, P; Hauge, G; Pedersen-Bjergaard, J
      Therapy-related acute lymphoblastic leukaemia with MLL rearrangements following DNA topoisomerase II inhibitors, an increasing problem: report on twonew cases and review of the literature since 1992

      BRITISH JOURNAL OF HAEMATOLOGY
    62. Yata, K; Sadahira, Y; Otsuki, T; Sakaguchi, H; Isozaki, Y; Uno, M; Kurebayashi, J; Fujii, T; Eda, S; Ueki, A; Yawata, Y; Yamada, O; Sugihara, T
      Cell cycle analysis and expression of cell cycle regulator genes in myeloma cells overexpressing cyclin D1

      BRITISH JOURNAL OF HAEMATOLOGY
    63. Todd, R; Bia, B; Johnson, E; Jones, C; Cotter, F
      Molecular characterization of a myelodysplasia-associated chromosome 7 inversion

      BRITISH JOURNAL OF HAEMATOLOGY
    64. Sawyer, JR; Lukacs, JL; Thomas, EL; Swanson, CM; Goosen, LS; Sammartino, G; Gilliland, JC; Munshi, NC; Tricot, G; Shaughnessy, JD; Barlogie, B
      Multicolour spectral karyotyping identifies new translocations and a recurring pathway for chromosome loss in multiple myeloma

      BRITISH JOURNAL OF HAEMATOLOGY
    65. Maia, AT; Ford, AM; Jalali, GR; Harrison, CJ; Taylor, GM; Eden, OB; Greaves, MF
      Molecular tracking of leukemogenesis in a triplet pregnancy

      BLOOD
    66. Hou, CD; Chiang, JT; Tai, JJ
      Identifying chromosomal fragile sites from a hierarchical-clustering pointof view

      BIOMETRICS
    67. Lovett, BD; Strumberg, D; Blair, IA; Pang, SK; Burden, DA; Megonigal, MD; Rappaport, EF; Rebbeck, TR; Osheroff, N; Pommier, YG; Felix, CA
      Etoposide metabolites enhance DNA topoisomerase II cleavage near leukemia-associated MLL translocation breakpoints

      BIOCHEMISTRY
    68. Morishita, M; Kishino, T; Furukawa, K; Yonekura, A; Miyazaki, Y; Kanematsu, T; Yamashita, S; Tsukazaki, T
      A 30-base-pair element in them first intron of SOX9 acts as an enhancer inATDC5

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    69. Kotzot, D; Holland, H; Kohler, M; Froster, UG
      A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotyping

      ANNALES DE GENETIQUE
    70. Aarskog, NK; Vedeler, CA
      Recombination breakpoints in the Charcot-Marie-Tooth 1A repeat sequence inNorwegian families

      ACTA NEUROLOGICA SCANDINAVICA
    71. Martinez-Lopez, W; Porro, V; Folle, GA; Mendez-Acuna, L; Savage, JRK; Obe, G
      Interchromosomal distribution of gamma ray-induced chromatid aberrations in Chinese hamster ovary cells

      GENETICS AND MOLECULAR BIOLOGY
    72. Puerto, S; Marcos, R; Ramirez, MJ; Creus, A; Boei, JJWA; Meijers, M; Natarajan, AT; Surralles, J
      Induction, processing and persistence of radiation-induced chromosomal aberrations involving hamster euchromatin and heterochromatin

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    73. Kronvall, G
      MIC determination of fusidic acid and of ciprofloxacin using multidisk diffusion tests

      CLINICAL MICROBIOLOGY AND INFECTION
    74. Kronvall, G; Holst, E
      Calibration of the disk diffusion test for trovafloxacin susceptibility testing of four anaerobic species

      CLINICAL MICROBIOLOGY AND INFECTION
    75. Nordgren, A; Sorensen, AG; Tinggaard-Pedersen, N; Blennow, E; Larsson, C; Lagercrantz, S
      New chromosomal breakpoints in non-Hodgkin's lymphomas revealed by spectral karyotyping and G-banding

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    76. Ottolenghi, C; McElreavey, K
      Deletions of 9p and the quest for a conserved mechanism of sex determination

      MOLECULAR GENETICS AND METABOLISM
    77. Fan, YS; Siu, VM; Jung, JH; Xu, J
      Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements

      GENETIC TESTING
    78. Ji, YG; Rebert, NA; Joslin, JM; Higgins, MJ; Schultz, RA; Nicholls, RD
      Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human

      GENOME RESEARCH
    79. Potocki, L; Chen, KS; Park, SS; Osterholm, DE; Withers, MA; Kimonis, V; Summers, AM; Meschino, WS; Anyane-Yeboa, K; Kashork, CD; Shaffer, LG; Lupski, JR
      Molecular mechanism for duplication 17p11.2 - the homologous recombinationreciprocal of the Smith-Magenis microdeletion

      NATURE GENETICS
    80. Takeda, Y; Baba, A; Nakamura, F; Ito, M; Honma, H; Koyama, T
      Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15

      SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    81. Antonescu, CR; Kawai, A; Leung, DH; Lonardo, F; Woodruff, JM; Healey, JH; Ladanyi, M
      Strong association of SYT-SSX fusion type and morphologic epithelial differentiation in synovial sarcoma

      DIAGNOSTIC MOLECULAR PATHOLOGY
    82. Payne, SR; Newman, B; King, MC
      Complex germline rearrangement of BRCAI associated with breast and ovariancancer

      GENES CHROMOSOMES & CANCER
    83. Ligon, AH; Morton, CC
      Genetics of uterine leiomyomata

      GENES CHROMOSOMES & CANCER
    84. Janoueix-Lerosey, I; Penther, D; Thioux, M; de Cremoux, P; Derre, J; Ambros, P; Vielh, P; Benard, J; Aurias, A; Delattre, O
      Molecular analysis of chromosome arm 17q gain neuroblastoma

      GENES CHROMOSOMES & CANCER
    85. 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
    86. Castorina, P; Rodeschini, O; Nocera, G; Larizza, L
      Reproductive follow-up of carriers of familial reciprocal balanced translocations Involving chromosome 9 and comparison with predicted outcome

      GENETIC COUNSELING
    87. Kiuru, A; Lindholm, C; Auvinen, A; Salomaa, S
      Localization of radiation-induced chromosomal breakpoints along human chromosome 1 using a combination of G-banding and FISH

      INTERNATIONAL JOURNAL OF RADIATION BIOLOGY
    88. 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
    89. Williams, ME; Swerdlow, SH
      Correspondence re: Chibbar R, Leung K, McCormick S, Ritzkalla K, Strickler J, Staggs R, et al. Bcl-1 gene rearrangements in amntle cell lymphoma: A comprehensive analysis of 118 cases, including B-5-fixed tissue, by polymerase chain reaction and southern transfer analysis. Mod Pathol 1998;11 : 1089-97

      MODERN PATHOLOGY
    90. Pajor, L; Vass, JA; Kereskai, L; Kajtar, P; Szomor, A; Egyed, M; Ivanyi, J; Jakso, P
      The existence of lymphoid lineage restricted Philadelphia chromosome-positive acute lymphoblastic leukemia with heterogeneous bcr-abl rearrangement

      LEUKEMIA
    91. De Angeli, C; Gandini, D; Cuneo, A; Moretti, S; Bigoni, R; Roberti, MG; Bardi, A; Castoldi, GL; Del Senno, L
      BCL-1 rearrangements and p53 mutations in atypical chronic lymphocytic leukemia with t(11;14)(q13;q32)

      HAEMATOLOGICA
    92. Xu, XM; Li, ZQ; Liu, ZY; Zhong, XL; Zhao, YZ; Mo, QH
      Molecular characterization and PCR detection of a deletional HPFH: Application to rapid prenatal diagnosis for compound heterozygotes of this defect with beta-thalassemia in a Chinese family

      AMERICAN JOURNAL OF HEMATOLOGY
    93. Wan, TSK; Ma, SK; Chan, LC
      Acquired pericentric inversion of chromosome 9 in essential thrombocythemia

      HUMAN GENETICS
    94. Toledo, F; Coquelle, A; Svetlova, E; Debatisse, M
      Enhanced flexibility and aphidicolin-induced DNA breaks near mammalian replication origins: implications for replicon mapping and chromosome fragility

      NUCLEIC ACIDS RESEARCH
    95. Guo, ZY; Johansson, SL; Rhim, JS; Vishwanatha, JK
      Fragile histidine triad gene expression in primary prostate cancer and in an in vitro model

      PROSTATE
    96. Dow, CR; Lin, CM
      Adaptive distributed breakpoint detection and checkpoint space reduction in message passing programs

      COMPUTERS AND ARTIFICIAL INTELLIGENCE
    97. Astier, P; Cardini, A; Cousins, RD; Letessier-Selvon, A; Popov, BA; Vinogradova, T
      Kalman filter track fits and track breakpoint analysis

      NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT
    98. Tunca, B; Egeli, U; Zorluoglu, A; Yilmazlar, T; Yerci, O; Kizil, A
      The expression frequency of common fragile sites and genetic predisposition to colon cancer

      CANCER GENETICS AND CYTOGENETICS
    99. Bruckner, R; Jentsch-Ullrich, K; Franke, A; Wieacker, P; Stumm, M
      A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemia

      CANCER GENETICS AND CYTOGENETICS
    100. Sinclair, EJ; Jalihal, S; Watmore, AE
      Acute monocytic leukemia with a novel 10;11 rearrangement resolved by fluorescence in situ hybridization

      CANCER GENETICS AND CYTOGENETICS


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Documento generato il 21/10/20 alle ore 19:26:30