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Neil Billington

Showing results (41-50 of 49) with videos related to

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The Journal of Cell Biology|August 5, 2022
Pericentrin interacts with Kinesin-1 to drive centriole motilityMatthew R Hannaford, Rong Liu, Neil Billington, et al.
Communications Biology|September 14, 2024
TUBB4B is essential for the cytoskeletal architecture of cochlear supporting cells and motile cilia developmentUrikhan Sanzhaeva, Helen Boyd-Pratt, Philip T R Bender, et al.
Plos Pathogens|February 23, 2026
Src-dependent tyrosine-phosphorylation of NM2A has a protective role against bacterial pore-forming toxinsCláudia Brito, Francisco S Mesquita, Joana M Pereira, et al.
Biorxiv : the Preprint Server for Biology|July 28, 2023
Myosin-5 varies its steps along the irregular F-actin trackAdam Fineberg, Yasuharu Takagi, Kavitha Thirumurugan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 20, 2024
Myosin-5 varies its step length to carry cargo straight along the irregular F-actin trackAdam Fineberg, Yasuharu Takagi, Kavitha Thirumurugan, et al.
Current Biology : CB|March 11, 2015
Myosin 18A coassembles with nonmuscle myosin 2 to form mixed bipolar filamentsNeil Billington, Jordan R Beach, Sarah M Heissler, et al.
Science (New York, N.Y.)|April 28, 2018
Quantitative mass imaging of single biological macromoleculesGavin Young, Nikolas Hundt, Daniel Cole, et al.
American Journal of Human Genetics|January 7, 2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86Atteeq U Rehman, Regie Lyn P Santos-Cortez, Robert J Morell, et al.
American Journal of Human Genetics|April 2, 2013
Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered proteaseEmma M Jenkinson, Atteeq U Rehman, Tom Walsh, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
The Journal of Cell Biology|August 5, 2022
Pericentrin interacts with Kinesin-1 to drive centriole motilityMatthew R Hannaford, Rong Liu, Neil Billington, et al.
Communications Biology|September 14, 2024
TUBB4B is essential for the cytoskeletal architecture of cochlear supporting cells and motile cilia developmentUrikhan Sanzhaeva, Helen Boyd-Pratt, Philip T R Bender, et al.
Plos Pathogens|February 23, 2026
Src-dependent tyrosine-phosphorylation of NM2A has a protective role against bacterial pore-forming toxinsCláudia Brito, Francisco S Mesquita, Joana M Pereira, et al.
Biorxiv : the Preprint Server for Biology|July 28, 2023
Myosin-5 varies its steps along the irregular F-actin trackAdam Fineberg, Yasuharu Takagi, Kavitha Thirumurugan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 20, 2024
Myosin-5 varies its step length to carry cargo straight along the irregular F-actin trackAdam Fineberg, Yasuharu Takagi, Kavitha Thirumurugan, et al.
Current Biology : CB|March 11, 2015
Myosin 18A coassembles with nonmuscle myosin 2 to form mixed bipolar filamentsNeil Billington, Jordan R Beach, Sarah M Heissler, et al.
Science (New York, N.Y.)|April 28, 2018
Quantitative mass imaging of single biological macromoleculesGavin Young, Nikolas Hundt, Daniel Cole, et al.
American Journal of Human Genetics|January 7, 2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86Atteeq U Rehman, Regie Lyn P Santos-Cortez, Robert J Morell, et al.
American Journal of Human Genetics|April 2, 2013
Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered proteaseEmma M Jenkinson, Atteeq U Rehman, Tom Walsh, et al.
Pageof 5