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    1. Millon, R; Muller, D; Schultz, I; Salvi, R; Ghnassia, JP; Frebourg, T; Wasylyk, B; Abecassis, J
      Loss of MDM2 expression in human head and neck squamous cell carcinomas and clinical significance

      ORAL ONCOLOGY
    2. Auroy, S; Avril, MF; Chompret, A; Pham, D; Goldstein, AM; Bianchi-Scarra, G; Frebourg, T; Joly, P; Spatz, A; Rubino, C; Demenais, F; Bressac-de Paillerets, B
      Sporadic multiple primary melanoma cases: CDKN2A germline mutations with afounder effect

      GENES CHROMOSOMES & CANCER
    3. Amiel, J; Bougeard, G; Francannet, C; Raclin, V; Munnich, A; Lyonnet, S; Frebourg, T
      TP63 gene mutation in ADULT syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Maurici, D; Monti, P; Campomenosi, P; North, S; Frebourg, T; Fronza, G; Hainaut, P
      Amifostine (WR2721) restores transcriptional activity of specific p53 mutant proteins in a yeast functional assay

      ONCOGENE
    5. Campomenosi, P; Monti, P; Aprile, A; Abbondandolo, A; Frebourg, T; Gold, B; Crook, T; Inga, A; Resnick, MA; Iggo, R; Fronza, G
      p53 mutants can often transactivate promoters containing a p21 but not Baxor PIG3 responsive elements

      ONCOGENE
    6. Saugier-Veber, P; Drouot, N; Wolf, LM; Kuhn, JM; Frebourg, T; Lefebvre, H
      Identification of a novel mutation in the autoimmune regulator (AIRE-1) gene in a French family with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    7. Drouin-Garraud, V; Belgrand, M; Grunewald, S; Seta, N; Dacher, JN; Henocq, A; Matthijs, G; Cormier-Daire, V; Frebourg, T; Saugier-Veber, P
      Neurological presentation of a congenital disorder of glycosylation CDG-Ia: Implications for diagnosis and genetic counseling

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Saugier-Veber, P; Drouot, N; Lefebvre, S; Charbonnier, F; Vial, E; Munnich, A; Frebourg, T
      Detection of heterozygous SMN1 deletions in SMA families using a simple fluorescent multiplex PCR method

      JOURNAL OF MEDICAL GENETICS
    9. Bougeard, G; Limacher, JM; Martin, C; Charbonnier, F; Killian, A; Delattre, O; Longy, M; Jonveaux, P; Fricker, JP; Stoppa-Lyonnet, D; Flaman, JM; Frebourg, T
      Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome

      JOURNAL OF MEDICAL GENETICS
    10. Limacher, JM; Frebourg, T; Natarajan-Ame, S; Bergerat, JP
      Two metachronous tumors in the radiotherapy fields of a patient with Li-Fraumeni syndrome

      INTERNATIONAL JOURNAL OF CANCER
    11. Frebourg, T; Ebel, A; Bonaiti-Pellie, C; Brugieres, L; Berthet, P; Bressac-De Paillerets, B; Chevrier, A; Chompret, A; Cohen-Haguenauer, O; Delattre, O; Feingold, J; Feunteun, J; Frappaz, D; Fricker, JP; Gesta, P; Jonveaux, P; Kalifa, C; Lasset, C; Leheup, B; Limacher, JM; Longy, M; Nogues, C; Oppenheim, D; Sommelet, D; Soubrier, F; Stoll, C; Stoppa-Lyonnet, D; Tristant, H
      Li-Fraumeni syndrome: update, new data and guidelines for clinical management

      BULLETIN DU CANCER
    12. Lamy, A; Metayer, J; Thiberville, L; Frebourg, T; Sesboue, R
      Re: Promoter methylation and silencing of the retinoic acid receptor-beta gene in lung carcinomas

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    13. Zurutuza, L; Verpillat, P; Raux, G; Hannequin, D; Puel, M; Belliard, S; Michon, A; Pothin, Y; Camuzat, A; Penet, C; Martin, C; Brice, A; Campion, D; Clerget-Darpoux, F; Frebourg, T
      APOE promoter polymorphisms do not confer independent risk for Alzheimer'sdisease in a French population

      EUROPEAN JOURNAL OF HUMAN GENETICS
    14. Camuzat, A; Verpillat, P; Dubois, B; Penet, C; Agid, CPY; Brice, A; Clerget-Darpoux, F; Moreaud, O; Puel, M; Kinter, J; Kozlov, S; Berger, P; Sonderegger, P; Raux, G; Campion, D; Hannequin, D; Frebourg, T
      Mutations in the neuroserpin gene are rare in familial dementia

      ANNALS OF NEUROLOGY
    15. Gantier, R; Gilbert, D; Dumanchin, C; Campion, D; Davoust, D; Toma, F; Frebourg, T
      The pathogenic L392V mutation of presenilin 1 decreases the affinity to glycogen synthase kinase-3 beta

      NEUROSCIENCE LETTERS
    16. Robert, V; Michel, P; Flaman, JM; Chiron, A; Martin, C; Charbonnier, F; Paillot, B; Frebourg, T
      High frequency in esophageal cancers of p53 alterations inactivating the regulation of genes involved in cell cycle and apoptosis

      CARCINOGENESIS
    17. Raux, G; Gantier, R; Thomas-Anterion, C; Boulliat, J; Verpillat, P; Hannequin, D; Brice, A; Frebourg, T; Campion, D
      Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation

      NEUROLOGY
    18. Charbonnier, F; Raux, G; Wang, Q; Drouot, N; Cordier, F; Limacber, JM; Saurin, JC; Puisieux, A; Olschwang, S; Frebourg, T
      Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments

      CANCER RESEARCH
    19. Chompret, A; Brugieres, L; Ronsin, M; Gardes, M; Dessarps-Freichey, F; Abel, A; Hua, D; Ligot, L; Dondon, MG; Bressac-de Paillerets, B; Frebourg, T; Lemerle, J; Bonaiti-Pellie, C; Feunteun, J
      p53 germline mutations in childhood cancers and cancer risk for carrier individuals

      BRITISH JOURNAL OF CANCER
    20. Lopez-Perez, E; Dumanchin, C; Czech, C; Campion, D; Goud, B; Pradier, L; Frebourg, T; Checler, F
      Overexpression of Rab11 or constitutively active Rab11 does not affect sAPP alpha and A beta secretions by wild-type and Swedish mutated beta APP-expressing HEK293 cells

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    21. Bonnet-Brilhault, F; Laurent, C; Campion, D; Thibaut, F; Lafargue, C; Charbonnier, F; Deleuze, JF; Menard, JF; Jay, M; Petit, M; Frebourg, T; Mallet, J
      No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    22. Dumanchin, C; Czech, C; Campion, D; Cuif, MH; Poyot, T; Martin, C; Charbonnier, F; Goud, B; Pradier, L; Frebourg, T
      Presenilins interact with Rab11, a small GTPase involved in the regulationof vesicular transport

      HUMAN MOLECULAR GENETICS
    23. Gantier, R; Dumanchin, C; Campion, D; Loutelier, C; Lange, C; Gagnon, J; Davoust, D; Frebourg, T; Toma, F
      The L392V mutation of presenilin 1 associated with autosomal dominant early-onset Alzheimer's disease alters the secondary structure of the hydrophilic loop

      NEUROREPORT
    24. Ancolio, K; Dumanchin, C; Barelli, H; Warter, JM; Brice, A; Campion, D; Frebourg, T; Checler, F
      Unusual phenotypic alteration of beta amyloid precursor protein (beta APP)maturation by a new Val-715 -> Met beta APP-770 mutation responsible for probable early-onset Alzheimer's disease

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    25. Pfister, C; Flaman, JM; Dunet, F; Grise, P; Frebourg, T
      p53 mutations in bladder tumors inactivate the transactivation of the p21 and Bax genes, and have a predictive value for the clinical outcome after bacillus Calmette-Guerin therapy

      JOURNAL OF UROLOGY
    26. Pfister, C; Flaman, JM; Martin, C; Grise, P; Frebourg, T
      Selective detection of inactivating mutations of the tumor suppressor genep53 in bladder tumors

      JOURNAL OF UROLOGY
    27. Campion, D; Dumanchin, C; Hannequin, D; Dubois, B; Belliard, S; Puel, M; Thomas-Anterion, C; Michon, A; Martin, C; Charbonnier, F; Raux, G; Camuzat, A; Penet, C; Mesnage, V; Martinez, M; Clerget-Darpoux, F; Brice, A; Frebourg, T
      Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum

      AMERICAN JOURNAL OF HUMAN GENETICS
    28. SAUGIERVEBER P; MARTIN C; LEMEUR N; LYONNET S; MUNNICH A; DAVID A; HENOCQ A; HERON D; JONVEAUX P; ODENT S; MANOUVRIER S; MONCLA A; MORICHON N; PHILIP N; SATGE D; TOSI M; FREBOURG T
      IDENTIFICATION OF NOVEL L1CAM MUTATIONS USING FLUORESCENCE-ASSISTED MISMATCH ANALYSIS

      Human mutation
    29. DUMANCHIN C; CAMUZAT A; CAMPION D; VERPILLAT P; HANNEQUIN D; DUBOIS B; SAUGIERVEBER P; MARTIN C; PENET C; CHARBONNIER F; AGID Y; FREBOURG T; BRICE A
      SEGREGATION OF A MISSENSE MUTATION IN THE MICROTUBULE-ASSOCIATED PROTEIN-TAU GENE WITH FAMILIAL FRONTOTEMPORAL DEMENTIA AND PARKINSONISM

      Human molecular genetics (Print)
    30. FLAMAN JM; ROBERT V; LENGLET S; MOREAU V; IGGO R; FREBOURG T
      IDENTIFICATION OF HUMAN P53 MUTATIONS WITH DIFFERENTIAL-EFFECTS ON THE BAX AND P21 PROMOTERS USING FUNCTIONAL ASSAYS IN YEAST

      Oncogene
    31. THIBAUT F; CORON B; HANNEQUIN D; SEGARD L; MARTIN C; DOLLFUS S; CAMPION D; FREBOURG T; PETIT M
      NO ASSOCIATION OF APOLIPOPROTEIN EPSILON-4 ALLELE WITH SCHIZOPHRENIA EVEN IN COGNITIVELY IMPAIRED PATIENTS

      Schizophrenia research
    32. BANINE F; GANGNEUX C; LEBRETON JP; FREBOURG T; SALIER JP
      STRUCTURAL AND FUNCTIONAL-ANALYSIS OF THE 5'-TRANSCRIPTION CONTROL REGION FOR THE HUMAN ALPHA-2-HS GLYCOPROTEIN GENE

      Biochimica et biophysica acta, N. Gene structure and expression
    33. HANNEQUIN D; CAMPION D; DUMANCHIN C; MARTINEZ M; AGID Y; CLERGETDARPOUX F; FREBOURG T; BRICE A
      GENETICS OF ALZHEIMERS-DISEASE

      Revue neurologique
    34. PFISTER C; FLAMAN JM; DUNET F; GRISE P; FREBOURG T
      PRELIMINARY-RESULTS IN DETECTION OF P53 MUTATIONS IN BLADDER-TUMORS WITH A FUNCTIONAL ASSAY

      The Journal of urology
    35. DUMANCHIN C; BRICE A; CAMPION D; HANNEQUIN D; MARTIN C; MOREAU V; AGID Y; MARTINEZ M; CLERGETDARPOUX F; FREBOURG T
      DE-NOVO PRESENILIN-1 MUTATIONS ARE RARE IN CLINICALLY SPORADIC, EARLY-ONSET ALZHEIMERS-DISEASE CASES

      Journal of Medical Genetics
    36. CERALINE J; DEPLANQUE G; DUCLOS B; LIMACHER JM; HAJRI A; NOEL F; ORVAIN C; FREBOURG T; KLEINSOYER C; BERGERAT JP
      INACTIVATION OF P53 IN NORMAL HUMAN-CELLS INCREASES G(2) M ARREST ANDSENSITIVITY TO DNA-DAMAGING AGENTS/

      International journal of cancer
    37. Soussi, T; Frebourg, T; Bressac-de Paillerets, B
      hMSH2 (human homolog of MutS)

      BULLETIN DU CANCER
    38. MARTIN A; FLAMAN JM; FREBOURG T; DAVI F; ELMANSOURI S; AMOUROUX J; RAPHAEL M
      FUNCTIONAL-ANALYSIS OF THE P53 PROTEIN IN AIDS-RELATED NON-HODGKINS-LYMPHOMAS AND POLYMORPHIC LYMPHOPROLIFERATIONS

      British Journal of Haematology
    39. MARTINEZ M; CAMPION D; BRICE A; HANNEQUIN D; DUBOIS B; DIDIERJEAN O; MICHON A; THOMASANTERION C; PUEL M; FREBOURG T; AGID Y; CLERGETDARPOUX F
      APOLIPOPROTEIN-E EPSILON-4 ALLELE AND FAMILIAL AGGREGATION OF ALZHEIMER-DISEASE

      Archives of neurology
    40. MARTIN A; FLAMAN JM; DAVI F; ELMANSOURI S; FREBOURG T; RAPHAEL M
      FUNCTIONAL-ANALYSIS OF THE TUMOR-SUPPRESSOR GENE P53 IN NON-HODGKINS-LYMPHOMAS AND ATYPICAL LYMPHOPROLIFERATIVE DISORDERS RELATED TO AIDS

      Journal of acquired immune deficiency syndromes and human retrovirology
    41. WARIDEL F; ESTREICHER A; BRON L; FLAMAN JM; FONTOLLIET C; MONNIER P; FREBOURG T; IGGO R
      FIELD CANCERIZATION AND POLYCLONAL P53 MUTATION IN THE UPPER AERODIGESTIVE TRACT

      Oncogene
    42. FREBOURG T
      GERMLINE MUTATIONS OF THE P53 GENE

      Pathologie et biologie
    43. BORG JY; YASTREMSKY F; DESHAYES A; TOULLEC J; CHRETIEN MH; VASSE M; SALADINTHIRON C; FREBOURG T
      RELIABLE IDENTIFICATION OF FACTOR-V-LEIDEN INDIVIDUALS BY MODIFIED APC RESISTANCE TESTS

      Thrombosis and haemostasis
    44. DIDIERJEAN O; MARTINEZ M; CAMPION D; HANNEQUIN D; DUBOIS B; MARTIN C; PUEL M; ANTERION CT; PASQUIER F; MOREAU O; BABRON MC; PENET C; AGID Y; CLERGETDARPOUX F; FREBOURG T; BRICE A
      NO EFFECT OF THE ALPHA-1-ANTICHYMOTRYPSIN-A ALLELE IN ALZHEIMERS-DISEASE

      Journal of Neurology, Neurosurgery and Psychiatry
    45. CHIRON A; FLAMAN JM; MITCHEL P; MARTIN C; MOREAU V; PAILLOT B; FREBOURG T
      DETECTION OF SOMATIC MUTATIONS OF P53 WITH A FUNCTIONAL TEST IN ESOPHAGEAL CANCER

      Gastroenterology
    46. MAUILLON J; MICHEL P; LIMACHER JM; LATOUCHE JB; CHARBONNIER F; MARTIN C; MOREAU V; PAILLOT B; FREBOURG T
      IDENTIFICATION OF NOVEL GERMLINE HMLH1 MUTATIONS INCLUDING A 22-KB ALU-MEDIATED DELETION IN PATIENTS WITH FAMILIAL COLORECTAL-CANCER

      Gastroenterology
    47. FREBOURG T
      THE LI-FRAUMENI-SYNDROME

      Bulletin du cancer
    48. ALHENCGELAS M; LECAMDUCHEZ V; EMMERICH J; FREBOURG T; FIESSINGER JN; BORG JY; AIACH M
      THE A20210-ALLELE OF THE PROTHROMBIN GENE IS NOT FREQUENTLY ASSOCIATED WITH THE FACTOR-V-ARG-506-TO-GLN-MUTATION IN THROMBOPHILIC FAMILIES

      Blood
    49. FREBOURG T; LENGLET S; IGGO R; FLAMAN JM
      DEVELOPMENT OF NEW FUNCTIONAL ASSAYS IN YEAST FOR THE TRANSCRIPTIONALANALYSIS OF THE P53 TUMOR-SUPPRESSOR GENE

      American journal of human genetics
    50. SEROVASINILNIKOVA OM; BOUTRAND L; STOPPALYONNET D; BRESSACDEPAILLERETS B; DUBOIS V; LASSET C; JANIN N; BIGNON YJ; LONGY M; MAUGARD C; LIDEREAU R; LEROUX D; FREBOURG T; MAZOYER S; LENOIR GM
      BRCA2 MUTATIONS IN HEREDITARY BREAST AND OVARIAN-CANCER IN FRANCE

      American journal of human genetics
    51. BICKEBOLLER H; CAMPION D; BRICE A; AMOUYEL P; HANNEQUIN D; DIDIERJEAN O; PENET C; MARTIN C; PEREZTUR J; MICHON A; DUBOIS B; LEDOZE F; THOMASANTERION C; PASQUIER F; PUEL M; DEMONET JF; MOREAUD O; BABRON MC; MEULIEN D; GUEZ D; CHARTIERHARLIN MC; FREBOURG T; AGID Y; MARTINEZ M; CLERGETDARPOUX F
      APOLIPOPROTEIN-E AND ALZHEIMER-DISEASE - GENOTYPE-SPECIFIC RISKS BY AGE AND SEX

      American journal of human genetics
    52. SHERRINGTON R; FROELICH S; SORBI S; CAMPION D; CHI H; ROGAEVA EA; LEVESQUE G; ROGAEV EI; LIN C; LIANG Y; IKEDA M; MAR L; BRICE A; AGID Y; PERCY ME; CLERGETDARPOUX F; PIACENTINI S; MARCON G; NACMIAS B; AMADUCCI L; FREBOURG T; LANNFELT L; ROMMENS JM; STGEORGEHYSLOP PH
      ALZHEIMERS-DISEASE ASSOCIATED WITH MUTATIONS IN PRESENILIN-2 IS RARE AND VARIABLY PENETRANT

      Human molecular genetics
    53. CAMPION D; BRICE A; DUMANCHIN C; PUEL M; BAULAC M; DELASAYETTE V; HANNEQUIN D; DUYCKAERTS C; MICHON A; MARTIN C; MOREAU V; PENET C; MARTINEZ M; CLERGETDARPOUX F; AGID Y; FREBOURG T
      A NOVEL PRESENILIN-1 MUTATION RESULTING IN FAMILIAL ALZHEIMERS-DISEASE WITH AN ONSET AGE OF 29 YEARS

      NeuroReport
    54. FLAMAN JM; WARIDEL F; ESTREICHER A; VANNIER A; LIMACHER JM; GILBERT D; IGGO R; FREBOURG T
      THE HUMAN TUMOR-SUPPRESSOR GENE P53 IS ALTERNATIVELY SPLICED IN NORMAL-CELLS

      Oncogene
    55. CAMPION D; BRICE A; HANNEQUIN D; FREBOURG T; MARTINEZ M; AGID Y; CLERGETDARPOUX F
      GENETIC DETERMINISM OF ALZHEIMERS-DISEASE

      MS. Medecine sciences
    56. HANNEQUIN D; CAMPION D; BRICE A; FREBOURG T; MARTINEZ M; CLERGETDARPOUX F; AGID Y
      GENETICS OF ALZHEIMERS-DISEASE

      La Revue de medecine interne
    57. CORON B; CAMPION D; THIBAUT F; DOLLFUS S; PRETERRE P; LANGLOIS S; VASSE T; MOREAU V; MARTIN C; CHARBONNIER F; LAURENT C; MALLET J; PETIT M; FREBOURG T
      ASSOCIATION STUDY BETWEEN SCHIZOPHRENIA AND MONOAMINE-OXIDASE-A AND MONOAMINE-OXIDASE-B DNA POLYMORPHISMS

      Psychiatry research
    58. BRICE A; DUBOIS B; AGID Y; CAMPION D; MARTINEZ M; CLERGETDARPOUX F; BELLIS M; MALLET J; FREBOURG T; HANNEQUIN D; PUEL M; LEDOZE F; PASQUIER F; ZIMMERMAN MA; THOMASANTERION C; MOREAU O; GOAS JY
      DOMINANT AUTOSOMAL FORMS OF ALZHEIMERS-DI SEASE - 3 GENES AND ONE PHENOTYPE

      Revue neurologique
    59. CAMPION D; BRICE A; HANNEQUIN D; CHARBONNIER F; DUBOIS B; MARTIN C; MICHON A; PENET C; BELLIS M; CALENDA A; MARTINEZ M; AGID Y; CLERGETDARPOUX F; FREBOURG T
      NO FOUNDER EFFECT IN 3 NOVEL ALZHEIMERS-DISEASE FAMILIES WITH APP-717VAL-]ILE MUTATION

      Journal of Medical Genetics
    60. BRICE A; TARDIEU S; DIDIERJEAN O; LEGUERN E; MICHON A; PILLON B; HAHN V; DUBOIS B; PENET C; AGID Y; CAMPION D; MARTINEZ M; BABRON MC; CLERGETDARPOUX F; BELLIS M; CALANDA A; HEILIG R; WEISSENBACH J; MALLET J; FREBOURG T; HANNEQUIN D; PUEL M; LEDOZE F; PASQUIER F; ZIMMERMANN MA; THOMASANTERION C; MOREAU O
      APOLIPOPROTEIN-E GENOTYPE DOES NOT AFFECT AGE AT ONSET IN PATIENTS WITH CHROMOSOME-14 ENCODED ALZHEIMERS-DISEASE

      Journal of Medical Genetics
    61. MAUILLON JL; MICHEL P; LIMACHER JM; LATOUCHE JB; DECHELOTTE P; CHARBONNIER F; MARTIN C; MOREAU V; METAYER J; PAILLOT B; FREBOURG T
      IDENTIFICATION OF NOVEL GERMLINE HMLH1 MUTATIONS INCLUDING A 22 KB ALU-MEDIATED DELETION IN PATIENTS WITH FAMILIAL COLORECTAL-CANCER

      Cancer research
    62. CAMPION D; FLAMAN JM; BRICE A; HANNEQUIN D; DUBOIS B; MARTIN C; MOREAU V; CHARBONNIER F; DIDIERJEAN O; TARDIEU S; PENET C; PUEL M; PASQUIER F; LEDOZE F; BELLIS G; CALENDA A; HEILIG R; MARTINEZ M; MALLET J; BELLIS M; CLERGETDARPOUX F; AGID Y; FREBOURG T
      MUTATIONS OF THE PRESENILIN-I GENE IN FAMILIES WITH EARLY-ONSET ALZHEIMERS-DISEASE

      Human molecular genetics
    63. CAMPION D; MARTIN C; HEILIG R; CHARBONNIER F; MOREAU V; FLAMAN JM; PETIT JL; HANNEQUIN D; BRICE A; FREBOURG T
      THE NACP SYNUCLEIN GENE - CHROMOSOMAL ASSIGNMENT AND SCREENING FOR ALTERATIONS IN ALZHEIMER-DISEASE/

      Genomics
    64. JOVELIN F; GILBERT D; BRARD F; BERNARDI T; MARCHE P; FREBOURG T; TRON F
      SIMPLE PROTOCOL FOR RAPID, DIRECT SEQUENCING OF IMMUNOGLOBULIN VARIABLE REGION GENES

      BioTechniques
    65. GUNTHER M; FREBOURG T; LAITHIER M; FOSSAR N; BOUZIANEOUARTINI M; LAVIALLE C; BRISON O
      AN SP1 BINDING-SITE AND THE MINIMAL PROMOTER CONTRIBUTE TO OVEREXPRESSION OF THE CYTOKERATIN-18 GENE IN TUMORIGENIC CLONES RELATIVE TO THATIN NONTUMORIGENIC CLONES OF A HUMAN CARCINOMA CELL-LINE

      Molecular and cellular biology
    66. FLAMAN JM; FREBOURG T; MOREAU V; CHARBONNIER F; MARTIN C; CHAPPUIS P; SAPPINO AP; LIMACHER JM; BRON L; BENHATTAR J; TADA M; VANMEIR EG; ESTREICHER A; IGGO RD
      A SIMPLE P53 FUNCTIONAL ASSAY FOR SCREENING CELL-LINES, BLOOD, AND TUMORS

      Proceedings of the National Academy of Sciences of the United Statesof America
    67. CHARBONNIER F; MARTIN C; SCOTTE M; SIBERT L; MOREAU V; FREBOURG T
      ALTERNATIVE SPLICING OF MLH1 MESSENGER-RNA IN HUMAN NORMAL-CELLS

      Cancer research
    68. BEUFE S; BORG JY; VASSE M; CHARBONNIER F; MOREAU V; MONCONDUIT M; FREBOURG T
      CO-SEGREGATION OF THROMBOSIS WITH THE FACTOR-V Q506 MUTATION IN AN EXTENDED FAMILY WITH RESISTANCE TO ACTIVATED PROTEIN-C

      British Journal of Haematology
    69. FREBOURG T; BARBIER N; YAN YX; GARBER JE; DREYFUS M; FRAUMENI J; LI FP; FRIEND SH
      GERM-LINE P53 MUTATIONS IN 15 FAMILIES WITH LI-FRAUMENI SYNDROME

      American journal of human genetics
    70. FLAMAN JM; FREBOURG T; MOREAU V; CHARBONNIER F; MARTIN C; ISHIOKA C; FRIEND SH; IGGO R
      A RAPID PCR FIDELITY ASSAY

      Nucleic acids research
    71. FRIEND SH; IGGO R; ISHIOKA C; FITZGERALD M; HOOVER I; ONEILL E; FREBOURG T
      OVERCOMING COMPLEXITIES IN GENETIC SCREENING FOR CANCER SUSCEPTIBILITY

      Cold Spring Harbor Symposia on Quantitative Biology
    72. PONCHEL F; PUISIEUX A; TABONE E; MICHOT JP; FROSCHL G; MOREL AP; FREBOURG T; FONTANIERE B; OBERHAMMER F; OZTURK M
      HEPATOCARCINOMA-SPECIFIC MUTANT P53-249SER INDUCES MITOTIC-ACTIVITY BUT HAS NO EFFECT ON TRANSFORMING GROWTH-FACTOR BETA-1-MEDIATED APOPTOSIS

      Cancer research
    73. FREBOURG T; SADELAIN M; NG YS; KASSEL J; FRIEND SH
      EQUAL TRANSCRIPTION OF WILD-TYPE AND MUTANT P53 USING BICISTRONIC VECTORS RESULTS IN THE WILD-TYPE PHENOTYPE

      Cancer research
    74. ISHIOKA C; FREBOURG T; YAN YX; VIDAL M; FRIEND SH; SCHMIDT S; IGGO R
      SCREENING PATIENTS FOR HETEROZYGOUS-P53 MUTATIONS USING A FUNCTIONAL ASSAY IN YEAST

      Nature genetics
    75. FREBOURG T; FRIEND SH
      THE IMPORTANCE OF P53 GENE ALTERATIONS IN HUMAN CANCER - IS THERE MORE THAN CIRCUMSTANTIAL EVIDENCE

      Journal of the National Cancer Institute


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/21 alle ore 14:27:00