खोज परिणाम - Dominique Stoppa‐Lyonnet

परिणाम को परिष्कृत करें
  1. 1
    The biological effects and clinical implications of BRCA mutations: where do we go from here?

    The biological effects and clinical implications of BRCA mutations: where do we go from here? द्वारा Dominique Stoppa‐Lyonnet

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  2. 2
    Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements.

    Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements. द्वारा Dominique Stoppa‐Lyonnet, P E Carter, T Meo, Mario Tosi

    प्रकाशित 1990
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  3. 3
    Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays

    Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays द्वारा Tatiana Popova, Élodie Manié, Dominique Stoppa‐Lyonnet, Guillem Rigaill, Emmanuel Barillot, Marc‐Henri Stern

    प्रकाशित 2009
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  4. 4
    Inactivation of the ATM Gene in T-Cell Prolymphocytic Leukemias

    Inactivation of the ATM Gene in T-Cell Prolymphocytic Leukemias द्वारा Dominique Stoppa‐Lyonnet, Jean Soulier, Anthony Laugé, Hélène Dastot, Richard Garand, François Sigaux, Marc‐Henri Stern

    प्रकाशित 1998
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  5. 5
    Sensitivity and predictive value of criteria for p53germline mutation screening

    Sensitivity and predictive value of criteria for p53germline mutation screening द्वारा Agnès Chompret, Anne S. Abel, Dominique Stoppa‐Lyonnet, Laurence Brugières, Sabine Pagès, Jean Feunteun, Catherine Bonaïti‐Pellié

    प्रकाशित 2001
    पूर्ण पाठ प्राप्त करें
    Carta
    सूची में सहेजें
    में बचाया:
  6. 6
    Risk of Serous Endometrial Carcinoma in Women With Pathogenic BRCA1/2 Variant After Risk-Reducing Salpingo-Oophorectomy

    Risk of Serous Endometrial Carcinoma in Women With Pathogenic BRCA1/2 Variant After Risk-Reducing Salpingo-Oophorectomy द्वारा Claire Saule, Emmanuelle Mouret‐Fourme, Adrien Briaux, Véronique Becette, Roman Rouzier, Claude Houdayer, Dominique Stoppa‐Lyonnet

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  7. 7
    Inactivation of the ATM Gene in T-Cell Prolymphocytic Leukemias

    Inactivation of the ATM Gene in T-Cell Prolymphocytic Leukemias द्वारा Dominique Stoppa‐Lyonnet, Jean Soulier, Anthony Laugé, Hélène Dastot, Richard Garand, François Sigaux, Marc‐Henri Stern

    प्रकाशित 1998
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  8. 8
    Rapid detection of novelBRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments

    Rapid detection of novelBRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments द्वारा Federica Casilli, Zorika Christiana Di Rocco, Sophie Gad, Isabelle Tournier, Dominique Stoppa‐Lyonnet, Thierry Frébourg, Mario Tosi

    प्रकाशित 2002
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  9. 9
    Distinct BRCA1 Rearrangements Involving the BRCA1 Pseudogene Suggest the Existence of a Recombination Hot Spot

    Distinct BRCA1 Rearrangements Involving the BRCA1 Pseudogene Suggest the Existence of a Recombination Hot Spot द्वारा Nadine Puget, Sophie Gad, Laure Perrin-Vidoz, Olga M. Sinilnikova, Dominique Stoppa‐Lyonnet, Gilbert Lenoir, Sylvie Mazoyer

    प्रकाशित 2002
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  10. 10
    Does the nonsense-mediated mRNA decay mechanism prevent the synthesis of truncated BRCA1, CHK2, and p53 proteins?

    Does the nonsense-mediated mRNA decay mechanism prevent the synthesis of truncated BRCA1, CHK2, and p53 proteins? द्वारा Olga Anczuków, Mark D. Ware, Monique Buisson, Almoutassem Billah Zetoune, Dominique Stoppa‐Lyonnet, Olga M. Sinilnikova, Sylvie Mazoyer

    प्रकाशित 2007
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  11. 11
    Non-Coding Variants in BRCA1 and BRCA2 Genes: Potential Impact on Breast and Ovarian Cancer Predisposition

    Non-Coding Variants in BRCA1 and BRCA2 Genes: Potential Impact on Breast and Ovarian Cancer Predisposition द्वारा Elizabeth Santana Dos Santos, François Lallemand, Leslie Burke, Dominique Stoppa‐Lyonnet, Melissa A. Brown, Sandrine M. Caputo, Étienne Rouleau

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  12. 12
    An Alu-Mediated 6-kb Duplication in the BRCA1 Gene: A New Founder Mutation?

    An Alu-Mediated 6-kb Duplication in the BRCA1 Gene: A New Founder Mutation? द्वारा Nadine Puget, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet, Carole Audoynaud, Sabine Pagès, Henry T. Lynch, David E. Goldgar, Gilbert Lenoir, Sylvie Mazoyer

    प्रकाशित 1999
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Carta
    सूची में सहेजें
    में बचाया:
  13. 13
    Is the breast-conserving treatment with radiotherapy appropriate in BRCA1/2 mutation carriers? Long-term results and review of the literature

    Is the breast-conserving treatment with radiotherapy appropriate in BRCA1/2 mutation carriers? Long-term results and review of the literature द्वारा Youlia Kirova, Alexia Savignoni, Brigitte Sigal‐Zafrani, Anne de la Rochefordière, Rémy Salmon, Pascale This, Bernard Asselain, Dominique Stoppa‐Lyonnet, Alain Fourquet

    प्रकाशित 2009
    पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  14. 14
    Genotype–phenotype correlations in hereditary familial retinoblastoma

    Genotype–phenotype correlations in hereditary familial retinoblastoma द्वारा Mélissa Taylor, Catherine Dehainault, Laurence Desjardins, François Doz, Christine Lévy, Xavier Sastre, Jérôme Couturier, Dominique Stoppa‐Lyonnet, Claude Houdayer, Marion Gauthier‐Villars

    प्रकाशित 2006
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  15. 15
    Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia

    Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia द्वारा Massimo Bogliolo, Dominique Bluteau, James Lespinasse, Roser Pujol, Nadia Vasquez, Catherine Dubois d’Enghien, Dominique Stoppa‐Lyonnet, Thierry Leblanc, Jean Soulier, Jordi Surrallés

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  16. 16
    Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families

    Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families द्वारा Nicolas Janin, Nadine Andrieu, Katia Ossian, Anthony Laugé, M. F. Croquette, C Griscelli, Marianne Debré, Brigitte Bressac–de Paillerets, Alain Aurias, Dominique Stoppa‐Lyonnet

    प्रकाशित 1999
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  17. 17
    Denaturing High-Performance Liquid Chromatography Detects Reliably BRCA1 and BRCA2 Mutations

    Denaturing High-Performance Liquid Chromatography Detects Reliably BRCA1 and BRCA2 Mutations द्वारा Teresa Wagner, Dominique Stoppa‐Lyonnet, E. Fleischmann, Daniela Muhr, Sabine Pagès, Therese Sandberg, Virginie Caux, Regina Moeslinger, Gudrun Langbauer, Åke Borg, Peter J. Oefner

    प्रकाशित 1999
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  18. 18
    Incidence, Presentation, and Prognosis of Malignancies in Ataxia-Telangiectasia: A Report From the French National Registry of Primary Immune Deficiencies

    Incidence, Presentation, and Prognosis of Malignancies in Ataxia-Telangiectasia: A Report From the French National Registry of Primary Immune Deficiencies द्वारा Felipe Suárez, Nizar Mahlaoui, Danielle Canioni, Chantal Andriamanga, Catherine Dubois d’Enghien, Nicole Brousse, Jean‐Philippe Jaïs, Alain Fischer, Olivier Hermine, Dominique Stoppa‐Lyonnet

    प्रकाशित 2014
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  19. 19
    Deep learning identifies morphological patterns of homologous recombination deficiency in luminal breast cancers from whole slide images

    Deep learning identifies morphological patterns of homologous recombination deficiency in luminal breast cancers from whole slide images द्वारा Tristan Lazard, Guillaume Bataillon, Peter Naylor, Tatiana Popova, François‐Clément Bidard, Dominique Stoppa‐Lyonnet, Marc‐Henri Stern, Étienne Decencière, Thomas Walter, Anne Vincent‐Salomon

    प्रकाशित 2022
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  20. 20
    A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation

    A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation द्वारा Catherine Dehainault, Dorothée Michaux, Sabine Pagès-Berhouet, Virginie Caux‐Moncoutier, François Doz, Laurence Desjardins, Jérôme Couturier, Philippe Parent, Dominique Stoppa‐Lyonnet, Marion Gauthier‐Villars, Claude Houdayer

    प्रकाशित 2007
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:

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