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Journal of Virology|May 1, 2009
Human immunodeficiency virus type 1 Nef protein targets CD4 to the multivesicular body pathwayLuis L P daSilva, Rachid Sougrat, Patricia V Burgos, et al.
Molecular Biology of the Cell|June 29, 2007
The trans-Golgi network accessory protein p56 promotes long-range movement of GGA/clathrin-containing transport carriers and lysosomal enzyme sortingGonzalo A Mardones, Patricia V Burgos, Doug A Brooks, et al.
Molecular Biology of the Cell|June 1, 2007
Canonical interaction of cyclin G associated kinase with adaptor protein 1 regulates lysosomal enzyme sortingSatoshi Kametaka, Kengo Moriyama, Patricia V Burgos, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 11, 2005
Structural mechanism for ubiquitinated-cargo recognition by the Golgi-localized, gamma-ear-containing, ADP-ribosylation-factor-binding proteinsGali Prag, Sangho Lee, Rafael Mattera, et al.
Developmental Cell|April 21, 2012
The clathrin adaptor AP-1A mediates basolateral polarityDiego Gravotta, Jose Maria Carvajal-Gonzalez, Rafael Mattera, et al.
Nature Structural & Molecular Biology|February 8, 2006
Structural basis for ubiquitin recognition and autoubiquitination by Rabex-5Sangho Lee, Yien Che Tsai, Rafael Mattera, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2012
Basolateral sorting of the coxsackie and adenovirus receptor through interaction of a canonical YXXPhi motif with the clathrin adaptors AP-1A and AP-1BJose Maria Carvajal-Gonzalez, Diego Gravotta, Rafael Mattera, et al.
Journal of Molecular Medicine (Berlin, Germany)|September 13, 2024
Revising pathogenesis of AP1S1-related MEDNIK syndrome: a missense variant in the AP1S1 gene as a causal genetic lesionMarketa Rackova, Rafael Mattera, Michael Svaton, et al.
The Journal of Clinical Investigation|March 23, 2023
Intrathecal AAV9/AP4M1 gene therapy for hereditary spastic paraplegia 50 shows safety and efficacy in preclinical studiesXin Chen, Thomas Dong, Yuhui Hu, et al.
Plos Genetics|April 27, 2018
Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndromeRaffaella De Pace, Miguel Skirzewski, Markus Damme, et al.
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