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Mia Horowitz

Showing results (31-40 of 46) with videos related to

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Orphanet Journal of Rare Diseases|September 12, 2013
Unfolded protein response in Gaucher disease: from human to DrosophilaGali Maor, Sigal Rencus-Lazar, Mirella Filocamo, et al.
Human Molecular Genetics|May 11, 2016
The contribution of mutant GBA to the development of Parkinson disease in DrosophilaGali Maor, Or Cabasso, Olga Krivoruk, et al.
Cells|April 3, 2021
The Uncovered Function of the <i>Drosophila GBA1a</i>-Encoded ProteinOr Cabasso, Sumit Paul, Gali Maor, et al.
Brain Research. Molecular Brain Research|October 8, 2004
Conservation of expression and alternative splicing in the prosaposin geneTsadok Cohen, Liat Ravid, Netta Altman, et al.
International Journal of Molecular Sciences|November 25, 2023
Animal Models for the Study of Gaucher DiseaseOr Cabasso, Aparna Kuppuramalingam, Lindsey Lelieveld, et al.
Molecular and Cellular Biology|March 4, 2005
The exon 8-containing prosaposin gene splice variant is dispensable for mouse development, lysosomal function, and secretionTsadok Cohen, Wojtek Auerbach, Liat Ravid, et al.
Journal of Cell Science|January 29, 2009
Drosophila Past1 is involved in endocytosis and is required for germline development and survival of the adult flyYael Olswang-Kutz, Yaron Gertel, Sigi Benjamin, et al.
The Journal of Investigative Dermatology|January 10, 2016
Establishment of Two Mouse Models for CEDNIK Syndrome Reveals the Pivotal Role of SNAP29 in Epidermal DifferentiationStina A Schiller, Christina Seebode, Georg L Wieser, et al.
The Biochemical Journal|July 16, 2011
EHD2 mediates trafficking from the plasma membrane by modulating Rac1 activitySigi Benjamin, Hilla Weidberg, Debora Rapaport, et al.
Traffic (Copenhagen, Denmark)|February 1, 2006
Recycling to the plasma membrane is delayed in EHD1 knockout miceDebora Rapaport, Wojtek Auerbach, Naava Naslavsky, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Orphanet Journal of Rare Diseases|September 12, 2013
Unfolded protein response in Gaucher disease: from human to DrosophilaGali Maor, Sigal Rencus-Lazar, Mirella Filocamo, et al.
Human Molecular Genetics|May 11, 2016
The contribution of mutant GBA to the development of Parkinson disease in DrosophilaGali Maor, Or Cabasso, Olga Krivoruk, et al.
Cells|April 3, 2021
The Uncovered Function of the <i>Drosophila GBA1a</i>-Encoded ProteinOr Cabasso, Sumit Paul, Gali Maor, et al.
Brain Research. Molecular Brain Research|October 8, 2004
Conservation of expression and alternative splicing in the prosaposin geneTsadok Cohen, Liat Ravid, Netta Altman, et al.
International Journal of Molecular Sciences|November 25, 2023
Animal Models for the Study of Gaucher DiseaseOr Cabasso, Aparna Kuppuramalingam, Lindsey Lelieveld, et al.
Molecular and Cellular Biology|March 4, 2005
The exon 8-containing prosaposin gene splice variant is dispensable for mouse development, lysosomal function, and secretionTsadok Cohen, Wojtek Auerbach, Liat Ravid, et al.
Journal of Cell Science|January 29, 2009
Drosophila Past1 is involved in endocytosis and is required for germline development and survival of the adult flyYael Olswang-Kutz, Yaron Gertel, Sigi Benjamin, et al.
The Journal of Investigative Dermatology|January 10, 2016
Establishment of Two Mouse Models for CEDNIK Syndrome Reveals the Pivotal Role of SNAP29 in Epidermal DifferentiationStina A Schiller, Christina Seebode, Georg L Wieser, et al.
The Biochemical Journal|July 16, 2011
EHD2 mediates trafficking from the plasma membrane by modulating Rac1 activitySigi Benjamin, Hilla Weidberg, Debora Rapaport, et al.
Traffic (Copenhagen, Denmark)|February 1, 2006
Recycling to the plasma membrane is delayed in EHD1 knockout miceDebora Rapaport, Wojtek Auerbach, Naava Naslavsky, et al.
Pageof 5