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La ricerca find articoli where soggetti phrase all words 'COMPLEMENTATION GROUPS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 52 riferimenti
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    1. Matsumoto, N; Tamura, S; Moser, A; Moser, HW; Braverman, N; Suzuki, Y; Shimozawa, N; Kondo, N; Fujiki, Y
      The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6

      JOURNAL OF HUMAN GENETICS
    2. Mondovits, B; Vermylen, C; Brichard, B; Cornu, G
      Molecular biology's contribution to the understanding and treatment of Fanconi anemia

      ARCHIVES DE PEDIATRIE
    3. Gaillard, PHL; Wood, RD
      Activity of individual ERCC1 and XPF subunits in DNA nucleotide excision repair

      NUCLEIC ACIDS RESEARCH
    4. Yamada, T; Tachibana, A; Shimizu, T; Mugishima, H; Okubo, M; Sasaki, MS
      Novel mutations of the FANCG gene causing alternative splicing in JapaneseFanconi anemia

      JOURNAL OF HUMAN GENETICS
    5. van de Vrugt, HJ; Cheng, NC; de Vries, Y; Rooimans, MA; de Groot, J; Scheper, RJ; Zhi, Y; Hoatlin, ME; Joenje, H; Arwert, F
      Cloning and characterization of murine Fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary

      MAMMALIAN GENOME
    6. Macieira-Coelho, A
      Ups and downs of aging studies in vitro: The crooked path of science

      GERONTOLOGY
    7. Islam, MQ; Islam, K
      Evidence for suppression of cellular growth in vitro and selection againstthe indigenous mouse X chromosome in A9 cell hybrids after microcell-mediated transfer of an X from other mammalian species

      CYTOGENETICS AND CELL GENETICS
    8. Wijker, M; Morgan, NV; Herterich, S; van Berkel, CGM; Tipping, AJ; Gross, HJ; Gille, JJP; Pals, G; Savino, M; Altay, C; Mohan, S; Dokal, I; Cavenagh, J; Marsh, J; Van Weel, M; Ortega, JJ; Schuler, D; Samochatova, E; Karwacki, M; Bekassy, AN; Abecasis, M; Ebell, W; Kwee, ML; de Ravel, T; Gibson, RA; Gluckman, E; Arwert, F; Joenje, H; Savoia, A; Hoehn, H; Pronk, JC; Mathew, CG
      Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene

      EUROPEAN JOURNAL OF HUMAN GENETICS
    9. Amrani, L; Cecchetto, G; Scazzocchio, C; Glatigny, A
      The hxB gene, necessary for the post-translational activation of purine hydroxylases in Aspergillus nidulans, is independently controlled by the purine utilization and the nicotinate utilization transcriptional activating systems

      MOLECULAR MICROBIOLOGY
    10. Sanford, KK; Parshad, R
      The contribution of deficient DNA repair to chromosomal radiosensitivity of CHO cells after G(2) irradiation

      CANCER GENETICS AND CYTOGENETICS
    11. Sanchez, MDE; Cantoni, AC; Alvarez, BM; Cruz-Alcivar, R; Sandoval, SS; Laguna, LG; Vazquez, SF
      Clinical and cytogenetic variability on twelve Fanconi anemia families andits relationship with complementation group assignment

      REVISTA DE INVESTIGACION CLINICA
    12. Ghaedi, K; Itagaki, A; Toyama, R; Tamura, S; Matsumura, T; Kawai, A; Shimozawa, N; Suzuki, Y; Kondo, N; Fujiki, Y
      Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesisdisorders and one novel group in mammals

      EXPERIMENTAL CELL RESEARCH
    13. Ghaedi, K; Kawai, A; Okumoto, K; Tamura, S; Shimozawa, N; Suzuki, Y; Kondo, N; Fujiki, Y
      Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein

      EXPERIMENTAL CELL RESEARCH
    14. Battaile, KP; Bateman, RL; Mortimer, D; Mulcahy, J; Rathbun, RK; Bagby, G; Fleming, WH; Grompe, M
      In vivo selection of wild-type hematopoietic stem cells in a murine model of Fanconi anemia

      BLOOD
    15. PULSIPHER M; KUPFER GM; NAF D; SULIMAN A; LEE JS; JAKOBS P; GROMPE M; JOENJE H; SIEFF C; GUINAN E; MULLIGAN R; DANDREA AD
      SUBTYPING ANALYSIS OF FANCONI-ANEMIA BY IMMUNOBLOTTING AND RETROVIRALGENE-TRANSFER

      Molecular medicine (Cambridge, Mass.)
    16. Imamura, A; Tamura, S; Shimozawa, N; Suzuki, Y; Zhang, ZY; Tsukamoto, T; Orii, T; Kondo, N; Osumi, T; Fujiki, Y
      Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders

      HUMAN MOLECULAR GENETICS
    17. VREESWIJK MPG; OVERKAMP MWJI; WESTLAND BE; VANHEESSTUIVENBERG S; VRIELING H; ZDZIENICKA MZ; VANZEELAND AA; MULLENDERS LHF
      ENHANCED UV-INDUCED MUTAGENESIS IN THE UV61 CELL-LINE, THE CHINESE-HAMSTER HOMOLOG OF COCKAYNES-SYNDROME-B, IS ASSOCIATED WITH DEFECTIVE TRANSCRIPTION COUPLED REPAIR OF CYCLOBUTANE PYRIMIDINE DIMERS

      Mutation research. DNA repair
    18. DAPOLITO M; ZELANTE L; SAVOIA A
      MOLECULAR-BASIS OF FANCONI-ANEMIA

      Haematologica
    19. MIYAUCHIHASHIMOTO H; AKAEDA T; MAIHARA T; IKENAGA M; HORIO T
      COCKAYNE-SYNDROME WITHOUT TYPICAL CLINICAL MANIFESTATIONS INCLUDING NEUROLOGIC ABNORMALITIES

      Journal of the American Academy of Dermatology
    20. ESCARCELLER M; BUCHWALD M; SINGLETON BK; JEGGO PA; JACKSON SP; MOUSTACCHI E; PAPADOPOULO D
      FANCONI-ANEMIA C-GENE-PRODUCT PLAYS A ROLE IN THE FIDELITY OF BLUNT DNA END-JOINING

      Journal of Molecular Biology
    21. ABE I; OKUMOTO K; TAMURA S; FUJIKI Y
      CLOFIBRATE-INDUCIBLE, 2X-KDA PEROXISOMAL INTEGRAL MEMBRANE-PROTEIN ISENCODED BY PEX11

      FEBS letters
    22. ABE I; FUJIKI Y
      CDNA CLONING AND CHARACTERIZATION OF A CONSTITUTIVELY EXPRESSED ISOFORM OF THE HUMAN PEROXIN PEX11P

      Biochemical and biophysical research communications (Print)
    23. RODRIGUEZPOMBO P; HOENICKA J; MURO S; PEREZ B; PEREZCERDA C; RICHARD E; DESVIAT LR; UGARTE M
      HUMAN PROPIONYL-COA CARBOXYLASE BETA-SUBUNIT GENE - EXON-INTRON DEFINITION AND MUTATION SPECTRUM IN SPANISH AND LATIN-AMERICAN PROPIONIC ACIDEMIA PATIENTS

      American journal of human genetics
    24. BLANCO P; SIEIRO C; REBOREDO NM; VILLA TG
      GENETIC DETERMINATION OF POLYGALACTURONASE PRODUCTION IN WILD-TYPE AND LABORATORY STRAINS OF SACCHAROMYCES-CEREVISIAE

      Archives of microbiology
    25. TATEISHI K; OKUMOTO K; SHIMOZAWA N; TSUKAMOTO T; OSUMI T; SUZUKI Y; KONDO N; OKANO I; FUJIKI Y
      NEWLY IDENTIFIED CHINESE-HAMSTER OVARY CELL MUTANTS DEFECTIVE IN PEROXISOME BIOGENESIS REPRESENT 2 NOVEL COMPLEMENTATION GROUPS IN MAMMALS

      European journal of cell biology
    26. KRUYT FAE; WAISFISZ Q; DIJKMANS LM; HERMSEN MAJA; YOUSSOUFIAN H; ARWERT F; JOENJE H
      CYTOPLASMIC LOCALIZATION OF A FUNCTIONALLY ACTIVE FANCONI-ANEMIA GROUP-A GREEN FLUORESCENT PROTEIN CHIMERA IN HUMAN 293-CELLS

      Blood
    27. KUPFER GM; YAMASHITA T; NAF D; SULIMAN A; ASANO S; DANDREA AD
      THE FANCONI-ANEMIA POLYPEPTIDE, FAC, BINDS TO THE CYCLIN-DEPENDENT KINASE, CDC2

      Blood
    28. TSUKAMOTO T; BOGAKI A; OKUMOTO K; TATEISHI K; FUJIKI Y; SHIMOZAWA N; SUZUKI Y; KONDO N; OSUMI T
      ISOLATION OF A NEW PEROXISOME-DEFICIENT CHO CELL MUTANT DEFECTIVE IN PEROXISOME TARGETING SIGNAL-1 RECEPTOR

      Biochemical and biophysical research communications
    29. BERGER R; JONVEAUX P
      CLONAL CHROMOSOME-ABNORMALITIES IN FANCONI-ANEMIA

      HEMATOLOGY AND CELL THERAPY
    30. TENFOE JRL; ROOIMANS MA; BOSNOYANCOLLINS L; ALON N; WIJKER M; PARKER L; LIGHTFOOT J; CARREAU M; CALLEN DF; SAVOIA A; CHENG NC; VANBERKEL CGM; STRUNK MHP; GILLE JJP; PALS G; KRUYT FAE; PRONK JC; ARWERT F; BUCHWALD M; JOENJE H
      EXPRESSION CLONING OF A CDNA FOR THE MAJOR FANCONI-ANEMIA GENE, FAA

      Nature genetics
    31. MIRZAYANS R; ENNS L; DIETRICH K; BARLEY RDC; PATERSON MC
      FAULTY DNA-POLYMERASE DELTA EPSILON-MEDIATED EXCISION-REPAIR IN RESPONSE TO GAMMA-RADIATION OR ULTRAVIOLET-LIGHT IN P53-DEFICIENT FIBROBLAST STRAINS FROM AFFECTED MEMBERS OF A CANCER-PRONE FAMILY WITH LI-FRAUMENI SYNDROME/

      Carcinogenesis
    32. FRIAS S; GOMEZ L; MOLINA B; ROJAS E; OSTROSKYWEGMAN P; CARNEVALE A
      EFFECT OF HYDROXYUREA AND NORMAL PLASMA ON DNA-SYNTHESIS IN LYMPHOCYTES FROM FANCONI-ANEMIA PATIENTS

      Mutation research
    33. YOUSSOUFIAN H
      CYTOPLASMIC LOCALIZATION OF FAC IS ESSENTIAL FOR THE CORRECTION OF A PREREPAIR DEFECT IN FANCONI-ANEMIA GROUP-C CELLS

      The Journal of clinical investigation
    34. KUPFER GM; DANDREA AD
      THE EFFECT OF THE FANCONI-ANEMIA POLYPEPTIDE, FAC, UPON P53 INDUCTIONAND G2 CHECKPOINT REGULATION

      Blood
    35. VANVUUREN AJ; APPELDOORN E; ODIJK H; HUMBERT S; MONCOLLIN V; EKER APM; JASPERS NGJ; EGLY JM; HOEIJMAKERS JHJ
      PARTIAL CHARACTERIZATION OF THE DNA-REPAIR PROTEIN COMPLEX, CONTAINING THE ERCC1, ERCC4, ERCC11 AND XPF CORRECTING ACTIVITIES

      Mutation research. DNA repair
    36. SANFORD KK; PARSHAD R; PRICE FM; TARONE RE; LEHMANN AR
      G(2) PHASE REPAIR OF X-RAY-INDUCED CHROMOSOMAL DNA-DAMAGE IN TRICHOTHIODYSTROPHY CELLS

      Mutation research. Mutation research letters
    37. ABOUSSEKHRA A; WOOD RD
      DETECTION OF NUCLEOTIDE EXCISION-REPAIR INCISIONS IN HUMAN FIBROBLASTS BY IMMUNOSTAINING FOR PCNA

      Experimental cell research
    38. DOSSANTOS CC; GAVISH H; BUCHWALD M
      FANCONI-ANEMIA REVISITED - OLD IDEAS AND NEW ADVANCES

      Stem cells
    39. CHAO CCK
      ENHANCED EXCISION-REPAIR OF DNA-DAMAGE DUE TO CIS-DIAMMINEDICHLOROPLATINUM(II) IN RESISTANT CERVIX CARCINOMA HELA-CELLS

      European journal of pharmacology. Molecular pharmacology section
    40. JONES NJ
      GENETIC-ANALYSIS OF MITOMYCIN C-HYPERSENSITIVE CHINESE-HAMSTER CELL MUTANTS

      Mutagenesis
    41. ROSSELLI F; DUCHAUD E; AVERBECK D; MOUSTACCHI E
      COMPARISON OF THE EFFECTS OF DNA TOPOISOMERASE INHIBITORS ON LYMPHOBLASTS FROM NORMAL AND FANCONI-ANEMIA DONORS

      Mutation research. Mutation research letters
    42. YOUSSOUFIAN H
      LOCALIZATION OF FANCONI-ANEMIA C-PROTEIN TO THE CYTOPLASM OF MAMMALIAN-CELLS

      Proceedings of the National Academy of Sciences of the United Statesof America
    43. STUDZIAN K; TELLEMAN P; VANDERSCHANS GP; ZDZIENICKA MZ
      MUTAGENIC RESPONSE AND REPAIR OF CIS-DDP-INDUCED DNA CROSS-LINKS IN THE CHINESE-HAMSTER V79 CELL MUTANT V-H4 WHICH IS HOMOLOGOUS TO FANCONI-ANEMIA (GROUP-A)

      MUTATION RESEARCH
    44. HAMAINABA H; SHIMAZU Y; TAKUSAGAWA M; SATO K; MORIMYO M
      CHO-CENTER-DOT-K1 CELL MUTANTS SENSITIVE TO ACTIVE OXYGEN-GENERATING AGENTS .1. ISOLATION AND GENETIC-STUDIES

      Mutation research
    45. CHAO CCK
      DECREASED ACCUMULATION AS A MECHANISM OF RESISTANCE TO CIS-DIAMINEDICHLOROPLATINUM(II) IN CERVIX CARCINOMA HELA-CELLS - RELATION TO DNA-REPAIR

      Molecular pharmacology
    46. KRAEMER KH; LEVY DD; PARRIS CN; GOZUKARA EM; MORIWAKI S; ADELBERG S; SEIDMAN MM
      XERODERMA-PIGMENTOSUM AND RELATED DISORDERS - EXAMINING THE LINKAGE BETWEEN DEFECTIVE-DNA REPAIR AND CANCER

      Journal of investigative dermatology
    47. RIGAUD G; PAIOLA F; ACCOLLA RS
      IN-VIVO MODIFICATION OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II DRAPROMOTER OCCUPANCY MEDIATED BY THE AIR-1 TRANSACTIVATOR

      European Journal of Immunology
    48. MIRZAYANS R; DIETRICH K; PATERSON MC
      APHIDICOLIN AND 1-BETA-D-ARABINOFURANOSYLCYTOSINE STRONGLY INHIBIT TRANSCRIPTIONALLY ACTIVE DNA-REPAIR IN NORMAL HUMAN FIBROBLASTS

      Carcinogenesis
    49. LEADON SA; COOPER PK
      PREFERENTIAL REPAIR OF IONIZING RADIATION-INDUCED DAMAGE IN THE TRANSCRIBED STRAND OF AN ACTIVE HUMAN GENE IS DEFECTIVE IN COCKAYNE-SYNDROME

      Proceedings of the National Academy of Sciences of the United Statesof America
    50. PARSHAD R; TARONE RE; PRICE FM; SANFORD KK
      CYTOGENETIC EVIDENCE FOR DIFFERENCES IN DNA INCISION ACTIVITY IN XERODERMA-PIGMENTOSUM GROUP A-CELLS, C-CELLS AND D-CELLS AFTER X-IRRADIATION DURING G(2)-PHASE

      MUTATION RESEARCH
    51. REY JP; SCOTT R; MULLER H
      INDUCTION AND REMOVAL OF INTERSTRAND CROSS-LINKS IN THE RIBOSOMAL-RNAGENES OF LYMPHOBLASTOID CELL-LINES FROM PATIENTS WITH FANCONI-ANEMIA

      MUTATION RESEARCH
    52. PRESLEY JF; MAYOR S; DUNN KW; JOHNSON LS; MCGRAW TE; MAXFIELD FR
      THE END2 MUTATION IN CHO CELLS SLOWS THE EXIT OF TRANSFERRIN RECEPTORS FROM THE RECYCLING COMPARTMENT BUT BULK MEMBRANE RECYCLING IS UNAFFECTED

      The Journal of cell biology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 01/06/20 alle ore 22:58:48