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Jacquelyn Bond

Showing results (21-30 of 26) with videos related to

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Stem Cell Reports|July 4, 2024
Retinal cells derived from patients with DRAM2-dependent CORD21 dystrophy exhibit key lysosomal enzyme deficiency and lysosomal content accumulationRozaliya Tsikandelova, Eldo Galo, Edvinas Cerniauskas, et al.
Cell Reports|September 30, 2023
Affimer-mediated locking of p21-activated kinase 5 in an intermediate activation state results in kinase inhibitionHeather L Martin, Amy L Turner, Julie Higgins, et al.
Nature Genetics|March 29, 2005
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain sizeJacquelyn Bond, Emma Roberts, Kelly Springell, et al.
American Journal of Human Genetics|May 5, 2009
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in miceDavid A Parry, Carmel Toomes, Lina Bida, et al.
Nature Genetics|June 16, 2009
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune responseGillian I Rice, Jacquelyn Bond, Aruna Asipu, et al.
Nature Cell Biology|July 14, 2015
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genesGabrielle Wheway, Miriam Schmidts, Dorus A Mans, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Stem Cell Reports|July 4, 2024
Retinal cells derived from patients with DRAM2-dependent CORD21 dystrophy exhibit key lysosomal enzyme deficiency and lysosomal content accumulationRozaliya Tsikandelova, Eldo Galo, Edvinas Cerniauskas, et al.
Cell Reports|September 30, 2023
Affimer-mediated locking of p21-activated kinase 5 in an intermediate activation state results in kinase inhibitionHeather L Martin, Amy L Turner, Julie Higgins, et al.
Nature Genetics|March 29, 2005
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain sizeJacquelyn Bond, Emma Roberts, Kelly Springell, et al.
American Journal of Human Genetics|May 5, 2009
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in miceDavid A Parry, Carmel Toomes, Lina Bida, et al.
Nature Genetics|June 16, 2009
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune responseGillian I Rice, Jacquelyn Bond, Aruna Asipu, et al.
Nature Cell Biology|July 14, 2015
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genesGabrielle Wheway, Miriam Schmidts, Dorus A Mans, et al.
Pageof 3