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R L Margolis

Showing results (131-140 of 153) with videos related to

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The EMBO Journal|November 15, 1996
Distinct specificity in the recognition of phosphoinositides by the pleckstrin homology domains of dynamin and Bruton's tyrosine kinaseK Salim, M J Bottomley, E Querfurth, et al.
AJNR. American Journal of Neuroradiology|December 19, 2015
Quantitative Susceptibility Mapping Suggests Altered Brain Iron in Premanifest Huntington DiseaseJ M G van Bergen, J Hua, P G Unschuld, et al.
Annals of Neurology|February 24, 2001
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian familyH Fujigasaki, I C Verma, A Camuzat, et al.
American Journal of Medical Genetics|July 13, 2001
Familial influence on age of onset among siblings with Huntington diseaseA Rosenblatt, R R Brinkman, K Y Liang, et al.
Nature Genetics|November 6, 2001
A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2S E Holmes, E O'Hearn, A Rosenblatt, et al.
Molecular Psychiatry|July 8, 1999
Family-based association analysis of the hSKCa3 potassium channel gene in bipolar disorderM G McInnis, T S Breschel, R L Margolis, et al.
Neurology|July 14, 2004
Onset and rate of striatal atrophy in preclinical Huntington diseaseE H Aylward, B F Sparks, K M Field, et al.
Molecular Psychiatry|January 6, 2010
Differential effects of prenatal and postnatal expressions of mutant human DISC1 on neurobehavioral phenotypes in transgenic mice: evidence for neurodevelopmental origin of major psychiatric disordersY Ayhan, B Abazyan, J Nomura, et al.
American Journal of Medical Genetics|April 9, 1996
Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorderS Jain, J Leggo, L E DeLisi, et al.
Neurology|March 17, 2012
A comparison of nine scales to detect depression in Parkinson disease: which scale to use?J R Williams, E S Hirsch, K Anderson, et al.
Pageof 16

Showing results (131-140 of 153) with videos related to

Sort By:
Pageof 16
The EMBO Journal|November 15, 1996
Distinct specificity in the recognition of phosphoinositides by the pleckstrin homology domains of dynamin and Bruton's tyrosine kinaseK Salim, M J Bottomley, E Querfurth, et al.
AJNR. American Journal of Neuroradiology|December 19, 2015
Quantitative Susceptibility Mapping Suggests Altered Brain Iron in Premanifest Huntington DiseaseJ M G van Bergen, J Hua, P G Unschuld, et al.
Annals of Neurology|February 24, 2001
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian familyH Fujigasaki, I C Verma, A Camuzat, et al.
American Journal of Medical Genetics|July 13, 2001
Familial influence on age of onset among siblings with Huntington diseaseA Rosenblatt, R R Brinkman, K Y Liang, et al.
Nature Genetics|November 6, 2001
A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2S E Holmes, E O'Hearn, A Rosenblatt, et al.
Molecular Psychiatry|July 8, 1999
Family-based association analysis of the hSKCa3 potassium channel gene in bipolar disorderM G McInnis, T S Breschel, R L Margolis, et al.
Neurology|July 14, 2004
Onset and rate of striatal atrophy in preclinical Huntington diseaseE H Aylward, B F Sparks, K M Field, et al.
Molecular Psychiatry|January 6, 2010
Differential effects of prenatal and postnatal expressions of mutant human DISC1 on neurobehavioral phenotypes in transgenic mice: evidence for neurodevelopmental origin of major psychiatric disordersY Ayhan, B Abazyan, J Nomura, et al.
American Journal of Medical Genetics|April 9, 1996
Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorderS Jain, J Leggo, L E DeLisi, et al.
Neurology|March 17, 2012
A comparison of nine scales to detect depression in Parkinson disease: which scale to use?J R Williams, E S Hirsch, K Anderson, et al.
Pageof 16