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S Lincoln

Showing results (51-60 of 60) with videos related to

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Nature Medicine|April 18, 1998
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1R Crook, A Verkkoniemi, J Perez-Tur, et al.
The Journal of Biological Chemistry|September 25, 1999
A loss of function mutation of presenilin-2 interferes with amyloid beta-peptide production and notch signalingH Steiner, K Duff, A Capell, et al.
Neuroscience Letters|August 24, 1999
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, et al.
Neurology|May 29, 2003
Parkin-proven disease: common founders but divergent phenotypesS Lincoln, J Wiley, T Lynch, et al.
Annals of Neurology|December 10, 1997
Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22M Baker, J B Kwok, S Kucera, et al.
Neuroreport|July 8, 1996
Structure and alternative splicing of the presenilin-2 geneG Prihar, R A Fuldner, J Perez-Tur, et al.
Brain : a Journal of Neurology|February 9, 2002
Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic studyD J Nicholl, J R Vaughan, N L Khan, et al.
Science (New York, N.Y.)|November 1, 2003
alpha-Synuclein locus triplication causes Parkinson's diseaseA B Singleton, M Farrer, J Johnson, et al.
Neurology|April 23, 2003
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonismN Rawal, M Periquet, E Lohmann, et al.
Nature|June 26, 1998
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17M Hutton, C L Lendon, P Rizzu, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Nature Medicine|April 18, 1998
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1R Crook, A Verkkoniemi, J Perez-Tur, et al.
The Journal of Biological Chemistry|September 25, 1999
A loss of function mutation of presenilin-2 interferes with amyloid beta-peptide production and notch signalingH Steiner, K Duff, A Capell, et al.
Neuroscience Letters|August 24, 1999
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, et al.
Neurology|May 29, 2003
Parkin-proven disease: common founders but divergent phenotypesS Lincoln, J Wiley, T Lynch, et al.
Annals of Neurology|December 10, 1997
Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22M Baker, J B Kwok, S Kucera, et al.
Neuroreport|July 8, 1996
Structure and alternative splicing of the presenilin-2 geneG Prihar, R A Fuldner, J Perez-Tur, et al.
Brain : a Journal of Neurology|February 9, 2002
Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic studyD J Nicholl, J R Vaughan, N L Khan, et al.
Science (New York, N.Y.)|November 1, 2003
alpha-Synuclein locus triplication causes Parkinson's diseaseA B Singleton, M Farrer, J Johnson, et al.
Neurology|April 23, 2003
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonismN Rawal, M Periquet, E Lohmann, et al.
Nature|June 26, 1998
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17M Hutton, C L Lendon, P Rizzu, et al.
Pageof 6