Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Colin Smith

Showing results (211-220 of 274) with videos related to

Pageof 28
Sort By:
Science Advances|April 21, 2023
Cell-autonomous immune dysfunction driven by disrupted autophagy in <i>C9orf72</i>-ALS iPSC-derived microglia contributes to neurodegenerationPoulomi Banerjee, Arpan R Mehta, Raja S Nirujogi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Frequency and signature of somatic variants in 1461 human brain exomesWei Wei, Michael J Keogh, Juvid Aryaman, et al.
Journal of Neurogenetics|January 10, 2025
The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.
Brain Communications|May 27, 2021
Epigenetic predictors of lifestyle traits applied to the blood and brainDanni A Gadd, Anna J Stevenson, Robert F Hillary, et al.
Glia|November 1, 2023
Inhibiting CSF1R alleviates cerebrovascular white matter disease and cognitive impairmentKatharine E Askew, Joshua Beverley, Emma Sigfridsson, et al.
Nature Communications|February 27, 2020
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant informationSebastian Guelfi, Karishma D'Sa, Juan A Botía, et al.
Acta Neuropathologica|February 27, 2020
Biallelic mutations in NRROS cause an early onset lethal microgliopathyColin Smith, Barry W McColl, Anirudh Patir, et al.
Acta Neuropathologica Communications|December 15, 2015
Erratum to: Post-mortem brain analyses of the Lothian Birth Cohort 1936: extending lifetime cognitive and brain phenotyping to the level of the synapseChristopher M Henstridge, Rosemary J Jackson, JeeSoo M Kim, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 8, 2016
Arterial ischemic stroke in HIV: Defining and classifying etiology for research studiesLaura A Benjamin, Alan Bryer, Sebastian Lucas, et al.
Journal of Neurology|March 29, 2025
PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker featuresThomas Coysh, Zane Jaunmuktane, Laszlo L P Hosszu, et al.
Pageof 28

Showing results (211-220 of 274) with videos related to

Sort By:
Pageof 28
Science Advances|April 21, 2023
Cell-autonomous immune dysfunction driven by disrupted autophagy in <i>C9orf72</i>-ALS iPSC-derived microglia contributes to neurodegenerationPoulomi Banerjee, Arpan R Mehta, Raja S Nirujogi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2018
Frequency and signature of somatic variants in 1461 human brain exomesWei Wei, Michael J Keogh, Juvid Aryaman, et al.
Journal of Neurogenetics|January 10, 2025
The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's diseaseLeah Holm-Mercer, Thomas Coysh, Tze How Mok, et al.
Brain Communications|May 27, 2021
Epigenetic predictors of lifestyle traits applied to the blood and brainDanni A Gadd, Anna J Stevenson, Robert F Hillary, et al.
Glia|November 1, 2023
Inhibiting CSF1R alleviates cerebrovascular white matter disease and cognitive impairmentKatharine E Askew, Joshua Beverley, Emma Sigfridsson, et al.
Nature Communications|February 27, 2020
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant informationSebastian Guelfi, Karishma D'Sa, Juan A Botía, et al.
Acta Neuropathologica|February 27, 2020
Biallelic mutations in NRROS cause an early onset lethal microgliopathyColin Smith, Barry W McColl, Anirudh Patir, et al.
Acta Neuropathologica Communications|December 15, 2015
Erratum to: Post-mortem brain analyses of the Lothian Birth Cohort 1936: extending lifetime cognitive and brain phenotyping to the level of the synapseChristopher M Henstridge, Rosemary J Jackson, JeeSoo M Kim, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|July 8, 2016
Arterial ischemic stroke in HIV: Defining and classifying etiology for research studiesLaura A Benjamin, Alan Bryer, Sebastian Lucas, et al.
Journal of Neurology|March 29, 2025
PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker featuresThomas Coysh, Zane Jaunmuktane, Laszlo L P Hosszu, et al.
Pageof 28