खोज परिणाम - Line Lapointe

  • प्रदर्शित 1 - 5 परिणाम 5
परिणाम को परिष्कृत करें
  1. 1
    Diethylstilbestrol regulates trophoblast stem cell differentiation as a ligand of orphan nuclear receptor ERRβ

    Diethylstilbestrol regulates trophoblast stem cell differentiation as a ligand of orphan nuclear receptor ERRβ द्वारा Gilles B. Tremblay, Tilo Kunath, D Bergeron, Line Lapointe, Céline Champigny, Jo-Ann Bader, Janet Rossant, Vincent Giguère

    प्रकाशित 2001
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  2. 2
    Tyrosine phosphorylation of DEP-1/CD148 as a mechanism controlling Src kinase activation, endothelial cell permeability, invasion, and capillary formation

    Tyrosine phosphorylation of DEP-1/CD148 as a mechanism controlling Src kinase activation, endothelial cell permeability, invasion, and capillary formation द्वारा Kathleen Spring, Catherine Chabot, Simon Langlois, Line Lapointe, Nguyen Thu Ngan Trinh, Christine Caron, Jagoda K. Hebda, Julie Gavard, Mounib Elchebly, Isabelle Royal

    प्रकाशित 2012
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  3. 3
    Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord

    Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord द्वारा Alexandre Montpetit, Stéphanie Côté, Edna Brustein, Christian A. Drouin, Line Lapointe, Michèle Boudreau, Caroline Meloche, Régen Drouin, Thomas J. Hudson, Pierre Drapeau, Patrick Cossette

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  4. 4
    SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth

    SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth द्वारा Anna Corradi, Manuela Fadda, Amélie Piton, Lysanne Patry, Antonella Marte, Pia Rossi, Maxime Cadieux‐Dion, Julie Gauthier, Line Lapointe, Laurent Mottron, Flavia Valtorta, Guy A. Rouleau, Anna Fassio, Fabio Benfenati, Patrick Cossette

    प्रकाशित 2013
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  5. 5
    SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

    SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function द्वारा Anna Fassio, Lysanne Patry, Sonia Congia, Franco Onofri, Amélie Piton, Julie Gauthier, Davide Pozzi, Mirko Messa, Enrico Defranchi, Manuela Fadda, Anna Corradi, Pietro Baldelli, Line Lapointe, Judith St‐Onge, Caroline Meloche, Laurent Mottron, Flavia Valtorta, Dang Khoa Nguyen, Guy A. Rouleau, Fabio Benfenati, Patrick Cossette

    प्रकाशित 2011
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:

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