Resultats de la cerca - Amanda G. Kautzman

  • Mostrar 1 - 5 resultats de 5
Refinar resultats
  1. 1
    Sox2 Regulates Cholinergic Amacrine Cell Positioning and Dendritic Stratification in the Retina

    Sox2 Regulates Cholinergic Amacrine Cell Positioning and Dendritic Stratification in the Retina per Irene E. Whitney, Patrick W. Keeley, Ace J. St. John, Amanda G. Kautzman, Jeremy N. Kay, Benjamin E. Reese

    Publicat 2014
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  2. 2
    Complement Targets Newborn Retinal Ganglion Cells for Phagocytic Elimination by Microglia

    Complement Targets Newborn Retinal Ganglion Cells for Phagocytic Elimination by Microglia per Sarah Anderson, Jianmin Zhang, Michael R. Steele, Cesar O. Romero, Amanda G. Kautzman, Dorothy P. Schafer, Monica L. Vetter

    Publicat 2019
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  3. 3
    A Developmental Analysis of Juxtavascular Microglia Dynamics and Interactions with the Vasculature

    A Developmental Analysis of Juxtavascular Microglia Dynamics and Interactions with the Vasculature per Erica Mondo, Shannon C. Becker, Amanda G. Kautzman, Martina Schifferer, Christina E. Baer, Jiapei Chen, Eric J. Huang, Mikael Simons, Dorothy P. Schafer

    Publicat 2020
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  4. 4
    Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner

    Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner per Dorothy P. Schafer, Emily K. Lehrman, Amanda G. Kautzman, Ryuta Koyama, Alan R. Mardinly, Ryo Yamasaki, Richard M. Ransohoff, Michael E. Greenberg, Ben A. Barres, Beth Stevens

    Publicat 2012
    Obtenir text complet Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:
  5. 5
    Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations

    Medulloblastoma exome sequencing uncovers subtype-specific somatic mutations per Trevor J. Pugh, Shyamal Dilhan Weeraratne, Tenley C. Archer, Daniel A. Pomeranz Krummel, Daniel Auclair, James Bochicchio, Mauricio O. Carneiro, Scott L. Carter, Kristian Cibulskis, Rachel Erlich, Heidi Greulich, Michael S. Lawrence, Niall J. Lennon, Aaron McKenna, James C. Meldrim, Alex H. Ramos, Michael Ross, Carsten Russ, Erica Shefler, Andrey Sivachenko, Brian Sogoloff, Petar Stojanov, Pablo Tamayo, Jill P. Mesirov, Vladimir Amani, Natalia Teider, Soma Sengupta, Jessica Pierre Francois, Paul A. Northcott, Michael D. Taylor, Furong Yu, Robert H. Crabtree, Amanda G. Kautzman, Stacey Gabriel, Gad Getz, Natalie Jäger, David Jones, Peter Lichter, Stefan M. Pfister, Thomas M. Roberts, Matthew Meyerson, Scott L. Pomeroy, Yoon‐Jae Cho

    Publicat 2012
    Obtenir text complet
    Artigo
    Afegir a favorits
    Guardat en:

Eines de cerca: