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La ricerca find articoli where authors phrase all words ' Wiegant, J' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 45 riferimenti
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    1. Fodde, R; Kuipers, J; Rosenberg, C; Smits, R; Kielman, M; Gaspar, C; van Es, JH; Bruekel, C; Wiegant, J; Giles, RH; Clevers, H
      Mutations in the APC tumour suppressor gene cause chromosomal instability

      NATURE CELL BIOLOGY
    2. Eriksson, L; Mertens, F; Akerman, M; Wiegant, J
      Calcium pyrophosphate dihydrate crystal deposition disease in the temporomandibular joint: Diagnostic difficulties and clonal chromosome aberrations in a case followed up for 5 years

      JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY
    3. Gilhuis, HJ; Bernsen, HJJA; Jeuken, JWM; Wesseling, P; Sprenger, SHE; Kerstens, HMJ; Wiegant, J; Boerman, RH
      The relationship between genetic aberrations as detected by comparative genomic hybridization and vascularization in glioblastoma xenografts (vol 51,pg 121, 2001)

      JOURNAL OF NEURO-ONCOLOGY
    4. Wiegant, J; Bezrookove, V; Rosenberg, C; Tanke, HJ; Raap, AK; Zhang, HG; Bittner, M; Trent, JM; Meltzer, P
      Differentially painting human chromosome arms with combined binary ratio-labeling fluorescence in situ hybridization

      GENOME RESEARCH
    5. 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
    6. van Gijlswijk, RPM; van de Corput, MPC; Bezrookove, V; Wiegant, J; Tanke, HJ; Raap, AK
      Synthesis and purification of horseradish peroxidase-labeled oligonucleotides for tyramide-based fluorescence in situ hybridization

      HISTOCHEMISTRY AND CELL BIOLOGY
    7. Bezrookove, V; Hansson, K; van der Burg, M; van der Smagt, JJ; Hilhorst-Hofstee, Y; Wiegant, J; Beverstock, GC; Raap, AK; Tanke, H; Breuning, MH; Rosenberg, C
      Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH

      HUMAN GENETICS
    8. Gisselsson, D; Pettersson, L; Hoglund, M; Heidenblad, M; Gorunova, L; Wiegant, J; Mertens, F; Dal Cin, P; Mitelman, F; Mandahl, N
      Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    9. Tanke, HJ; Wiegant, J; van Gijlswijk, RPM; Bezrookove, V; Pattenier, H; Heetebrij, RJ; Talman, EG; Raap, AK; Vrolijk, J
      New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling

      EUROPEAN JOURNAL OF HUMAN GENETICS
    10. ROSENBERG C; VANGILSWIJK RPM; VOS CBJ; WIEGANT J; CORNELISSE CJ; TANKE HJ; RAAP AK
      COMPARATIVE GENOMIC HYBRIDIZATION WITH LISSAMINE-LABELED AND FLUORESCEIN-LABELED NUCLEOTIDES

      Cytometry
    11. MIOZZO M; CASTORINA P; RIVA P; DALPRA L; CONTI AMF; VOLPI L; HOE TS; KHOO A; WIEGANT J; ROSENBERG C; LARIZZA L
      CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM 2 SIBS WITH ROTHMUND-THOMSON-SYNDROME

      International journal of cancer
    12. VANDECORPUT MPC; DIRKS RW; WIEGANT WW; WIEGANT J; MUHLEGGER K; RAAP AK
      ESTRADIOL, A NEW HAPTEN FOR DETECTING NUCLEIC-ACID SEQUENCES BY FISH

      HISTOCHEMISTRY AND CELL BIOLOGY
    13. LASAN R; LETICA L; HITREC V; MUZINIC D; BEGOVIC D; WIEGANT J
      IDENTIFICATION OF 3 CASES OF CHROMOSOME REARRANGEMENTS BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Cytogenetics and cell genetics
    14. CASTORINA P; MIOZZO M; RIVA P; CONTI AMF; WIEGANT J; ROSENBERG C; DALPRA L; VOLPI L; MAK JW; LARIZZA L
      HIGH CHROMOSOMAL INSTABILITY IN FIBROBLASTS AND MESENCHYMAL TUMORS FROM A SIBSHIP OF AN INBRED PEDIGREE WITH ROTHMUND-THOMSON SYNDROME (RTS)

      Cytogenetics and cell genetics
    15. GARCIAISIDORO M; TABERNERO MD; GARCIA JL; NAJERA ML; HERNANDEZ JM; WIEGANT J; RAAP A; SANMIGUEL J; ORFAO A
      DETECTION OF THE MBCR ABL TRANSLOCATION IN CHRONIC MYELOID-LEUKEMIA BY FLUORESCENCE IN-SITU HYBRIDIZATION - COMPARISON WITH CONVENTIONAL CYTOGENETICS AND IMPLICATIONS FOR MINIMAL RESIDUAL DISEASE DETECTION/

      Human pathology
    16. VANGIJLSWIJK RPM; ZIJLMANS HJMAA; WIEGANT J; BOBROW MN; ERICKSON TJ; ADLER KE; TANKE HJ; RAAP AK
      FLUOROCHROME-LABELED TYRAMIDES - USE IN IMMUNOCYTOCHEMISTRY AND FLUORESCENCE IN-SITU HYBRIDIZATION

      The Journal of histochemistry and cytochemistry
    17. FRANSZ PF; STAM M; MONTIJN B; TENHOOPEN R; WIEGANT J; KOOTER JM; OUD O; NANNINGA N
      DETECTION OF SINGLE-COPY GENES AND CHROMOSOME REARRANGEMENTS IN PETUNIA-HYBRIDA BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Plant journal
    18. VANGIJLSWIJK RPM; WIEGANT J; VERVENNE R; LASAN R; TANKE HJ; RAAP AK
      HORSERADISH PEROXIDASE-LABELED OLIGONUCLEOTIDES AND FLUORESCENT TYRAMIDES FOR RAPID DETECTION OF CHROMOSOME-SPECIFIC REPEAT SEQUENCES

      Cytogenetics and cell genetics
    19. WIEGANT J; VERWOERD N; MASCHERETTI S; BOLK M; TANKE HJ; RAAP AK
      AN EVALUATION OF A NEW SERIES OF FLUORESCENT DUTPS FOR FLUORESCENCE IN-SITU HYBRIDIZATION

      The Journal of histochemistry and cytochemistry
    20. VANGIJLSWIJK RPM; WIEGANT J; RAAP AK; TANKE HJ
      IMPROVED LOCALIZATION OF FLUORESCENT TYRAMIDES FOR FLUORESCENCE IN-SITU HYBRIDIZATION USING DEXTRAN SULFATE AND POLYVINYL-ALCOHOL

      The Journal of histochemistry and cytochemistry
    21. VANEIJSDEN R; JELSMA T; HEETEBRIJ R; BOELENS Y; WIEGANT J
      DEVELOPMENT OF A RAPID AND HIGHLY SENSITIVE LABELING METHOD OF DNA AND RNA PROBES FOR (FLUORESCENT) IN-SITU HYBRIDIZATION

      Clinical chemistry
    22. COIGNET LJA; SCHUURING E; KIBBELAAR RE; RAAP TK; KLEIVERDA KK; BERTHEAS MF; WIEGANT J; BEVERSTOCK G; KLUIN PM
      DETECTION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC NEOPLASIAS BY DOUBLE-COLOR FLUORESCENCE IN-SITU HYBRIDIZATION

      Blood
    23. TABERNERO D; SANMIGUEL JF; GARCIASANZ R; NAJERA L; GARCIAISIDORO M; PEREZSIMON JA; GONZALEZ M; WIEGANT J; RAAP AK; ORFAO A
      INCIDENCE OF CHROMOSOME NUMERICAL CHANGES IN MULTIPLE-MYELOMA - FLUORESCENCE IN-SITU HYBRIDIZATION ANALYSIS USING 15 CHROMOSOME-SPECIFIC PROBES

      The American journal of pathology
    24. FLORIJN RJ; BONDEN LAJ; VROLIJK H; WIEGANT J; VAANDRAGER JW; BAAS F; DENDUNNEN JT; TANKE HJ; VANOMMEN GJB; RAAP AK
      HIGH-RESOLUTION DNA FIBER-FISH FOR GENOMIC DNA MAPPING AND COLOR BAR-CODING OF LARGE GENES

      Human molecular genetics
    25. RAAP AK; VANDECORPUT MPC; VERVENNE RAW; VANGIJLSWIJK RPM; TANKE HJ; WIEGANT J
      ULTRA-SENSITIVE FISH USING PEROXIDASE-MEDIATED DEPOSITION OF BIOTIN-TYRAMIDE OR FLUOROCHROME-TYRAMIDE

      Human molecular genetics
    26. TABERNERO MD; SANMIGUEL JF; GARCIA JL; GARCIAISIDORO M; WIEGANT J; CIUDAD J; GONZALEZ M; RIOS A; RAAP A; ORFAO A
      CLINICAL, BIOLOGICAL, AND IMMUNOPHENOTYPICAL CHARACTERISTICS OF B-CELL CHRONIC LYMPHOCYTIC-LEUKEMIA WITH TRISOMY-12 BY FLUORESCENCE IN-SITUHYBRIDIZATION

      Cytometry
    27. HOOVERS JMN; KALIKIN LM; JOHNSON LA; ALDERS M; REDEKER B; LAW DJ; BLIEK J; STEENMAN M; BENEDICT M; WIEGANT J; LENGAUER C; TAILLONMILLER P; SCHLESSINGER D; EDWARDS MC; ELLEDGE SJ; IVENS A; WESTERVELD A; LITTLE P; MANNENS M; FEINBERG AP
      MULTIPLE GENETIC-LOCI WITHIN 11P15 DEFINED BY BECKWITH-WIEDEMANN SYNDROME REARRANGEMENT BREAKPOINTS AND SUBCHROMOSOMAL TRANSFERABLE FRAGMENTS

      Proceedings of the National Academy of Sciences of the United Statesof America
    28. TANKE HJ; FLORIJN RJ; WIEGANT J; RAAP AK; VROLIJK J
      CCD MICROSCOPY AND IMAGE-ANALYSIS OF CELLS AND CHROMOSOMES STAINED BYFLUORESCENCE IN-SITU HYBRIDIZATION

      Histochemical Journal
    29. TABERNERO MD; ORFAO A; GARCIASANZ R; NAJERA ML; GARCIAISIDORO M; PEREZSIMON JA; GONZALEZ M; WIEGANT J; RAAP AK; SANMIGUEL JF
      CHROMOSOME NUMERICAL ABNORMALITIES IN MULTIPLE-MYELOMA ANALYZED BY FLUORESCENCE IN-SITU HYBRIDIZATION - A STUDY WITH 15 CHROMOSOME-SPECIFICPROBES

      Blood
    30. COIGNET LJA; SCHUURING E; KIBBELAAR RE; RAAP AK; KLEIVERDA JK; BERTHEAS MF; WIEGANT J; BEVERSTOCK GC; KLUIN PM
      DELETION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC MALIGNANCIES BY DOUBLE COLOR FLUORESCENCE IN-SITU HYBRIDIZATION

      Blood
    31. DONEDA L; WIEGANT J; LARIZZA L
      3-WAY AND 2-WAY REARRANGEMENTS INVOLVING CHROMOSOMES 10, 2, 5 AND 5, 2 IN 2 MARKER CHROMOSOMES OF A HUMAN-MELANOMA CELL-LINE

      Melanoma research
    32. TAGARRO I; WIEGANT J; RAAP AK; GONZALEZAGUILERA JJ; FERNANDEZPERALTA AM
      ASSIGNMENT OF HUMAN SATELLITE-1 DNA AS REVEALED BY FLUORESCENT IN-SITU HYBRIDIZATION WITH OLIGONUCLEOTIDES

      Human genetics
    33. HAGENAARS CE; KAWILARANGDEHAAS EWM; HAZEKAMP J; WIEGANT J; NIJWEIDE PJ
      OSTEOCLAST DEVELOPMENT IN THE COCULTURE SYSTEM OF PERIOSTLESS METATARSAL BONES AND HEMATOPOIETIC-CELLS STUDIED BY IN-SITU HYBRIDIZATION WITH A PROBE FOR Y-CHROMOSOMES

      Calcified tissue international
    34. TABERNERO MD; GARCIA JL; GARCIAISIDORO M; WIEGANT J; RAAP A; GARCIAMARCOS MA; RIOS A; SANMIGUEL JF; ORFAO A
      CLINICAL, BIOLOGICAL AND IMMUNOPHENOTYPICAL CHARACTERISTICS OF B-CELLCHRONIC LYMPHOCYTIC-LEUKEMIA WITH TRISOMY-12 BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Blood
    35. ROELOFS H; SCHUURING E; WIEGANT J; MICHALIDES R; GIPHARTGASSLER M
      AMPLIFICATION OF THE 11Q13 REGION IN HUMAN CARCINOMA CELL-LINES - A MECHANISTIC VIEW

      Genes, chromosomes & cancer
    36. DAUWERSE JG; WESSELS JW; GILES RH; WIEGANT J; VANDERREIJDEN BA; FUGAZZA G; JUMELET EA; SMIT E; BAAS F; RAAP AK; HAGEMEIJER A; BEVERSTOCK GC; VANOMMEN GJB; BREUNING MH
      CLONING THE BREAKPOINT CLUSTER REGION OF THE INV(16) IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO

      Human molecular genetics
    37. ALKEMA MJ; WIEGANT J; RAAP AK; BERNS A; VANLOHUIZEN M
      CHARACTERIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN PROTOONCOGENE BMI-1

      Human molecular genetics
    38. GIBBS S; FIJNEMAN R; WIEGANT J; VANKESSEL AG; VANDEPUTTE P; BACKENDORF C
      MOLECULAR CHARACTERIZATION AND EVOLUTION OF THE SPRR FAMILY OF KERATINOCYTE DIFFERENTIATION MARKERS ENCODING SMALL PROLINE-RICH PROTEINS

      Genomics
    39. JONGMANS W; WIEGANT J; OSHIMURA M; JAMES MR; LOHMAN PHM; ZDZIENICKA MZ
      HUMAN CHROMOSOME-11 COMPLEMENTS ATAXIA-TELANGIECTASIA CELLS BUT DOES NOT COMPLEMENT THE DEFECT IN AT-LIKE CHINESE-HAMSTER CELL MUTANTS

      Human genetics
    40. LEBO RV; CHANCE PF; DYCK PJ; REDILAFLORES MT; LYNCH ED; GOLBUS MS; BIRD TD; KING MC; ANDERSON LA; HALL J; WIEGANT J; JIANG ZR; DAZIN PF; PUNNETT HH; SCHONBERG SA; MOORE K; SHULL MM; GENDLER S; HURKO O; LOVELACE RE; LATOV N; TROFATTER J; CONNEALLY PM
      CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION (VOL 88, PG 1, 1991)

      Human genetics
    41. SCHURINGBLOM GH; KEIJZER M; JAKOBS ME; VANDENBRANDE DM; VISSER HM; WIEGANT J; HOOVERS JMN; LESCHOT NJ
      MOLECULAR CYTOGENETIC ANALYSIS OF TERM PLACENTAE SUSPECTED OF MOSAICISM USING FLUORESCENCE IN-SITU HYBRIDIZATION

      Prenatal diagnosis
    42. PUTMAN CAJ; DEGROOTH BG; WIEGANT J; RAAP AK; VANDERWERF KO; VANHULST NF; GREVE J
      DETECTION OF INSITU HYBRIDIZATION TO HUMAN-CHROMOSOMES WITH THE ATOMIC FORCE MICROSCOPE

      Cytometry
    43. MICHALOVA K; BARTSCH O; STARY J; JELINEK J; WIEGANT J; BUBANSKA E
      PARTIAL TRISOMY OF 3Q DETECTED BY CHROMOSOME PAINTING IN A CASE OF JUVENILE CHRONIC MYELOMONOCYTIC LEUKEMIA

      Cancer genetics and cytogenetics
    44. SACCONE S; DESARIO A; WIEGANT J; RAAP AK; DELLAVALLE G; BERNARDI G
      CORRELATIONS BETWEEN ISOCHORES AND CHROMOSOMAL BANDS IN THE HUMAN GENOME

      Proceedings of the National Academy of Sciences of the United Statesof America
    45. DAUWERSE JG; WESSELS JW; WIEGANT J; GILES RHG; HAGEMEIJER A; BAAS F; BEVERSTOCK G; VANOMMEN GJB; BREUNING MH
      CLONING THE REGION SPANNING THE INV(16) BREAKPOINT IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/10/20 alle ore 14:26:12