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Lisa Astuto

Showing results (1-10 of 4) with videos related to

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Journal of Cell Science|May 21, 2009
Syntaxin 3 and SNAP-25 pairing, regulated by omega-3 docosahexaenoic acid, controls the delivery of rhodopsin for the biogenesis of cilia-derived sensory organelles, the rod outer segmentsJana Mazelova, Nancy Ransom, Lisa Astuto-Gribble, et al.
Scientific Reports|July 15, 2022
Evaluating changes in growth and pigmentation of Cladosporium cladosporioides and Paecilomyces variotii in response to gamma and ultraviolet irradiationJesse Bland, Lisa Astuto Gribble, Michael C Hamel, et al.
The EMBO Journal|January 21, 2009
Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4Jana Mazelova, Lisa Astuto-Gribble, Hiroki Inoue, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 9, 2004
Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12)Ronald J E Pennings, Vedat Topsakal, Lisa Astuto, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Journal of Cell Science|May 21, 2009
Syntaxin 3 and SNAP-25 pairing, regulated by omega-3 docosahexaenoic acid, controls the delivery of rhodopsin for the biogenesis of cilia-derived sensory organelles, the rod outer segmentsJana Mazelova, Nancy Ransom, Lisa Astuto-Gribble, et al.
Scientific Reports|July 15, 2022
Evaluating changes in growth and pigmentation of Cladosporium cladosporioides and Paecilomyces variotii in response to gamma and ultraviolet irradiationJesse Bland, Lisa Astuto Gribble, Michael C Hamel, et al.
The EMBO Journal|January 21, 2009
Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4Jana Mazelova, Lisa Astuto-Gribble, Hiroki Inoue, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 9, 2004
Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12)Ronald J E Pennings, Vedat Topsakal, Lisa Astuto, et al.
Pageof 1