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M Pittman

Showing results (181-190 of 218) with videos related to

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International Journal of Cardiology|October 20, 2019
Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotypeCharlotte L Hall, Mohammed M Akhtar, Maria Sabater-Molina, et al.
Journal of Medical Genetics|March 29, 2005
Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degenerationA M Pittman, A J Myers, P Abou-Sleiman, et al.
Human Molecular Genetics|June 23, 2012
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathiesDaniah Trabzuni, Selina Wray, Jana Vandrovcova, et al.
Environmental Science & Technology|July 17, 2025
Occurrence and Maternal Transfer of Per- and Polyfluoroalkyl Substances (PFAS) in Pregnant Sharks from Florida Coastal WatersQaim Mehdi, Thomas D Sinkway, Lauren E Blackman, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 4, 2024
The Intellectual Disability Risk Gene <i>Kdm5b</i> Regulates Long-Term Memory Consolidation in the HippocampusLeticia Pérez-Sisqués, Shail U Bhatt, Rugile Matuleviciute, et al.
JAMA Neurology|July 9, 2014
A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlationsEleanna Kara, Aoife P Kiely, Christos Proukakis, et al.
Neurobiology of Disease|December 19, 2006
The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcriptsAmanda J Myers, Alan M Pittman, Alice S Zhao, et al.
Plos Genetics|September 24, 2010
Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3HAlan M Pittman, Silvia Naranjo, Sanni E Jalava, et al.
Neurology. Genetics|May 24, 2019
Autosomal dominant optic atrophy and cataract "plus" phenotype including axonal neuropathyAlejandro Horga, Enrico Bugiardini, Andreea Manole, et al.
Journal of Breast Imaging|May 31, 2021
Impact of the COVID-19 Pandemic on Breast Imaging EducationJames S Chalfant, Sarah M Pittman, Pranay D Kothari, et al.
Pageof 22

Showing results (181-190 of 218) with videos related to

Sort By:
Pageof 22
International Journal of Cardiology|October 20, 2019
Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotypeCharlotte L Hall, Mohammed M Akhtar, Maria Sabater-Molina, et al.
Journal of Medical Genetics|March 29, 2005
Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degenerationA M Pittman, A J Myers, P Abou-Sleiman, et al.
Human Molecular Genetics|June 23, 2012
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathiesDaniah Trabzuni, Selina Wray, Jana Vandrovcova, et al.
Environmental Science & Technology|July 17, 2025
Occurrence and Maternal Transfer of Per- and Polyfluoroalkyl Substances (PFAS) in Pregnant Sharks from Florida Coastal WatersQaim Mehdi, Thomas D Sinkway, Lauren E Blackman, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 4, 2024
The Intellectual Disability Risk Gene <i>Kdm5b</i> Regulates Long-Term Memory Consolidation in the HippocampusLeticia Pérez-Sisqués, Shail U Bhatt, Rugile Matuleviciute, et al.
JAMA Neurology|July 9, 2014
A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlationsEleanna Kara, Aoife P Kiely, Christos Proukakis, et al.
Neurobiology of Disease|December 19, 2006
The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcriptsAmanda J Myers, Alan M Pittman, Alice S Zhao, et al.
Plos Genetics|September 24, 2010
Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3HAlan M Pittman, Silvia Naranjo, Sanni E Jalava, et al.
Neurology. Genetics|May 24, 2019
Autosomal dominant optic atrophy and cataract "plus" phenotype including axonal neuropathyAlejandro Horga, Enrico Bugiardini, Andreea Manole, et al.
Journal of Breast Imaging|May 31, 2021
Impact of the COVID-19 Pandemic on Breast Imaging EducationJames S Chalfant, Sarah M Pittman, Pranay D Kothari, et al.
Pageof 22