Ngā hua rapu - Bertrand Boisson

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  1. 1
    Unexpected Protein Families Including Cell Defense Components Feature in the N-Myristoylome of a Higher Eukaryote

    Unexpected Protein Families Including Cell Defense Components Feature in the N-Myristoylome of a Higher Eukaryote mā Bertrand Boisson, Carmela Giglione, Thierry Meinnel

    I whakaputaina 2003
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    Immunological loss-of-function due to genetic gain-of-function in humans: autosomal dominance of the third kind

    Immunological loss-of-function due to genetic gain-of-function in humans: autosomal dominance of the third kind mā Bertrand Boisson, Pierre Quartier, Jean‐Laurent Casanova

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Revisão
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  3. 3
    Genetics and clinical phenotypes in common variable immunodeficiency

    Genetics and clinical phenotypes in common variable immunodeficiency mā Charlotte Cunningham‐Rundles, Jean‐Laurent Casanova, Bertrand Boisson

    I whakaputaina 2024
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency

    Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency mā Bertrand Boisson, Anne Puel, Capucine Pïcard, Jean‐Laurent Casanova

    I whakaputaina 2017
    Whiwhi kuputuhi katoa
    Revisão
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  5. 5
    Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms

    Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms mā Carmela Giglione, Alexandre Serero, M. Pierre, Bertrand Boisson, Thierry Meinnel

    I whakaputaina 2000
    Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    Human hyper-IgE syndrome: singular or plural?

    Human hyper-IgE syndrome: singular or plural? mā Qian Zhang, Bertrand Boisson, Vivien Béziat, Anne Puel, Jean‐Laurent Casanova

    I whakaputaina 2018
    Whiwhi kuputuhi katoa
    Revisão
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  7. 7
    Genetic Diagnosis Using Whole Exome Sequencing in Common Variable Immunodeficiency

    Genetic Diagnosis Using Whole Exome Sequencing in Common Variable Immunodeficiency mā Patrick Maffucci, Charles A. Filion, Bertrand Boisson, Yuval Itan, Lei Shang, Jean‐Laurent Casanova, Charlotte Cunningham‐Rundles

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    Carboxypeptidases B of <i>Anopheles gambiae</i> as Targets for a <i>Plasmodium falciparum</i> Transmission-Blocking Vaccine

    Carboxypeptidases B of <i>Anopheles gambiae</i> as Targets for a <i>Plasmodium falciparum</i> Transmission-Blocking Vaccine mā Catherine Lavazec, Christian Boudin, Renaud Lacroix, Sarah Bonnet, Abdoulaye Diop, Sabine Thiberge, Bertrand Boisson, Rachida Tahar, Catherine Bourgouin

    I whakaputaina 2007
    Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations

    PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations mā Peng Zhang, Benedetta Bigio, Franck Rapaport, Shen‐Ying Zhang, Jean‐Laurent Casanova, Laurent Abel, Bertrand Boisson, Yuval Itan

    I whakaputaina 2018
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  10. 10
    TNF and IL-1 exhibit distinct ubiquitin requirements for inducing NEMO–IKK supramolecular structures

    TNF and IL-1 exhibit distinct ubiquitin requirements for inducing NEMO–IKK supramolecular structures mā Nadine Tarantino, Jean-Yves Tinévez, Elizabeth Faris Crowell, Bertrand Boisson, Ricardo Henriques, Musa M. Mhlanga, Fabrice Agou, Alain Israël, Emmanuel Laplantine

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    A recurrent dominant negative E47 mutation causes agammaglobulinemia and BCR– B cells

    A recurrent dominant negative E47 mutation causes agammaglobulinemia and BCR– B cells mā Bertrand Boisson, Yong‐Dong Wang, Amma Bosompem, S. Cindy, Apiradee Lim, Tatiana Kochetkov, Stuart G. Tangye, Jean‐Laurent Casanova, Mary Ellen Conley

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants

    Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants mā Aziz Belkadi, Alexandre Bolze, Yuval Itan, Aurélie Cobat, Quentin B. Vincent, Alexander Antipenko, Lei Shang, Bertrand Boisson, Jean‐Laurent Casanova, Laurent Abel

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    Host Cell Traversal Is Important for Progression of the Malaria Parasite through the Dermis to the Liver

    Host Cell Traversal Is Important for Progression of the Malaria Parasite through the Dermis to the Liver mā Rogério Amino, Donatella Giovannini, Sabine Thiberge, Pascale Gueirard, Bertrand Boisson, Jean‐François Dubremetz, Marie‐Christine Prévost, Tomoko Ishino, Masao Yuda, Robert Ménard

    I whakaputaina 2008
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    Clonal Conditional Mutagenesis in Malaria Parasites

    Clonal Conditional Mutagenesis in Malaria Parasites mā Audrey Combe, Donatella Giovannini, Teresa G. Carvalho, Stephan S. Späth, Bertrand Boisson, Céline Loussert-Fonta, Sabine Thiberge, Céline Lacroix, Pascale Gueirard, Robert Ménard

    I whakaputaina 2009
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  15. 15
    LISP1 is important for the egress of<i>Plasmodium berghei</i>parasites from liver cells

    LISP1 is important for the egress of<i>Plasmodium berghei</i>parasites from liver cells mā Tomoko Ishino, Bertrand Boisson, Yuki Orito, Céline Lacroix, Emmanuel Bischoff, Céline Loussert-Fonta, Chris J. Janse, Robert Ménard, Masao Yuda, Patricia Baldacci

    I whakaputaina 2009
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  16. 16
    HGCS: an online tool for prioritizing disease-causing gene variants by biological distance

    HGCS: an online tool for prioritizing disease-causing gene variants by biological distance mā Yuval Itan, Mark Mazel, Benjamin Mazel, Avinash Abhyankar, Patrick Nitschké, Lluı́s Quintana-Murci, Stéphanie Boisson‐Dupuis, Bertrand Boisson, Laurent Abel, Shen‐Ying Zhang, Jean‐Laurent Casanova

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  17. 17
    An ACT1 Mutation Selectively Abolishes Interleukin-17 Responses in Humans with Chronic Mucocutaneous Candidiasis

    An ACT1 Mutation Selectively Abolishes Interleukin-17 Responses in Humans with Chronic Mucocutaneous Candidiasis mā Bertrand Boisson, Chenhui Wang, Vincent Pedergnana, Ling Wu, Sophie Cypowyj, M. Rybojad, Aziz Belkadi, Capucine Pïcard, Laurent Abel, Claire Fieschi, Anne Puel, Xiaoxia Li, Jean‐Laurent Casanova

    I whakaputaina 2013
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  18. 18
    Exome and genome sequencing for inborn errors of immunity

    Exome and genome sequencing for inborn errors of immunity mā Isabelle Meyts, Barbara Bosch, Alexandre Bolze, Bertrand Boisson, Yuval Itan, Aziz Belkadi, Vincent Pedergnana, Leen Moens, Capucine Pïcard, Aurélie Cobat, Xavier Bossuyt, Laurent Abel, Jean‐Laurent Casanova

    I whakaputaina 2016
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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  19. 19
    Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma

    Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma mā Minji Byun, Avinash Abhyankar, Virginie Lelarge, Sabine Plancoulaine, Ayşe Palandüz, Leyla Telhan, Bertrand Boisson, Capucine Pïcard, Scott Dewell, Connie Zhao, Emmanuelle Jouanguy, Stefan Feske, Laurent Abel, Jean‐Laurent Casanova

    I whakaputaina 2010
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  20. 20
    Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

    Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery mā Eric Scott, Anason Halees, Yuval Itan, Emily Spencer, Yupeng He, Mostafa Abdellateef Azab, Stacey Gabriel, Aziz Belkadi, Bertrand Boisson, Laurent Abel, Andrew G. Clark, Fowzan S. Alkuraya, Jean‐Laurent Casanova, Joseph G. Gleeson

    I whakaputaina 2016
    Whiwhi kuputuhi katoa
    Artigo
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