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

M Nicholson

Showing results (781-790 of 801) with videos related to

Pageof 81
Sort By:
Brain Pathology (Zurich, Switzerland)|March 12, 2021
Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficitsRosa Rademakers, Alexandra M Nicholson, Yingxue Ren, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
Acta Neuropathologica|May 7, 2015
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron diseaseCyril Pottier, Kevin F Bieniek, NiCole Finch, et al.
Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Neuron|September 28, 2011
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSMariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, et al.
Australian and New Zealand Journal of Public Health|April 18, 2022
A review of Australian Government funding of parenting intervention researchSophie S Havighurst, Carys Chainey, Frances L Doyle, et al.
Neurology. Genetics|June 30, 2017
Abnormal expression of homeobox genes and transthyretin in <i>C9ORF72</i> expansion carriersNiCole A Finch, Xue Wang, Matthew C Baker, et al.
Nature Communications|June 20, 2020
Bone marrow adipose tissue is a unique adipose subtype with distinct roles in glucose homeostasisKarla J Suchacki, Adriana A S Tavares, Domenico Mattiucci, et al.
Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.
Journal of Biotechnology|July 12, 2005
Development of a large-scale chemogenomics database to improve drug candidate selection and to understand mechanisms of chemical toxicity and actionBrigitte Ganter, Stuart Tugendreich, Cecelia I Pearson, et al.
Pageof 81

Showing results (781-790 of 801) with videos related to

Sort By:
Pageof 81
Brain Pathology (Zurich, Switzerland)|March 12, 2021
Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficitsRosa Rademakers, Alexandra M Nicholson, Yingxue Ren, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
Acta Neuropathologica|May 7, 2015
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron diseaseCyril Pottier, Kevin F Bieniek, NiCole Finch, et al.
Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Neuron|September 28, 2011
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSMariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, et al.
Australian and New Zealand Journal of Public Health|April 18, 2022
A review of Australian Government funding of parenting intervention researchSophie S Havighurst, Carys Chainey, Frances L Doyle, et al.
Neurology. Genetics|June 30, 2017
Abnormal expression of homeobox genes and transthyretin in <i>C9ORF72</i> expansion carriersNiCole A Finch, Xue Wang, Matthew C Baker, et al.
Nature Communications|June 20, 2020
Bone marrow adipose tissue is a unique adipose subtype with distinct roles in glucose homeostasisKarla J Suchacki, Adriana A S Tavares, Domenico Mattiucci, et al.
Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.
Journal of Biotechnology|July 12, 2005
Development of a large-scale chemogenomics database to improve drug candidate selection and to understand mechanisms of chemical toxicity and actionBrigitte Ganter, Stuart Tugendreich, Cecelia I Pearson, et al.
Pageof 81