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M Pittman

Showing results (161-170 of 218) with videos related to

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Orphanet Journal of Rare Diseases|November 4, 2017
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegiaConceição Bettencourt, Vincenzo Salpietro, Stephanie Efthymiou, et al.
Physical Review Letters|August 23, 2002
Deuterium-deuterium fusion dynamics in low-density molecular-cluster jets irradiated by intense ultrafast laser pulsesG Grillon, Ph Balcou, J- P Chambaret, et al.
Human Molecular Genetics|July 8, 2005
The H1c haplotype at the MAPT locus is associated with Alzheimer's diseaseA J Myers, M Kaleem, L Marlowe, et al.
Magnetic Resonance in Medicine|July 21, 2022
Directional and inter-acquisition variability in diffusion-weighted imaging and editing for restricted diffusionBatuhan Gundogdu, Jay M Pittman, Aritrick Chatterjee, et al.
Journal of Clinical Medicine|July 11, 2019
Utility of Whole Blood Thiamine Pyrophosphate Evaluation in <i>TPK1</i>-Related DiseasesEnrico Bugiardini, Simon Pope, René G Feichtinger, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|September 26, 2012
Energy transport in short-pulse-laser-heated targets measured using extreme ultraviolet laser backlightingL A Wilson, G J Tallents, J Pasley, et al.
Neurobiology of Aging|May 19, 2012
The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological featuresEleanna Kara, Helen Ling, Alan M Pittman, et al.
Human Molecular Genetics|February 4, 2010
Fine-scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locusDalemari Crowther-Swanepoel, Peter Broderick, Yussanne Ma, et al.
Allergy and Asthma Proceedings|September 19, 2024
Immunodeficiency: Complement disordersJeremy C McMurray, Brandon J Schornack, Andrew L Weskamp, et al.
Optics Letters|June 16, 2018
Hartmann wavefront sensor characterization of a high charge vortex beam in the extreme ultraviolet spectral rangeF Sanson, A K Pandey, F Harms, et al.
Pageof 22

Showing results (161-170 of 218) with videos related to

Sort By:
Pageof 22
Orphanet Journal of Rare Diseases|November 4, 2017
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegiaConceição Bettencourt, Vincenzo Salpietro, Stephanie Efthymiou, et al.
Physical Review Letters|August 23, 2002
Deuterium-deuterium fusion dynamics in low-density molecular-cluster jets irradiated by intense ultrafast laser pulsesG Grillon, Ph Balcou, J- P Chambaret, et al.
Human Molecular Genetics|July 8, 2005
The H1c haplotype at the MAPT locus is associated with Alzheimer's diseaseA J Myers, M Kaleem, L Marlowe, et al.
Magnetic Resonance in Medicine|July 21, 2022
Directional and inter-acquisition variability in diffusion-weighted imaging and editing for restricted diffusionBatuhan Gundogdu, Jay M Pittman, Aritrick Chatterjee, et al.
Journal of Clinical Medicine|July 11, 2019
Utility of Whole Blood Thiamine Pyrophosphate Evaluation in <i>TPK1</i>-Related DiseasesEnrico Bugiardini, Simon Pope, René G Feichtinger, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|September 26, 2012
Energy transport in short-pulse-laser-heated targets measured using extreme ultraviolet laser backlightingL A Wilson, G J Tallents, J Pasley, et al.
Neurobiology of Aging|May 19, 2012
The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological featuresEleanna Kara, Helen Ling, Alan M Pittman, et al.
Human Molecular Genetics|February 4, 2010
Fine-scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locusDalemari Crowther-Swanepoel, Peter Broderick, Yussanne Ma, et al.
Allergy and Asthma Proceedings|September 19, 2024
Immunodeficiency: Complement disordersJeremy C McMurray, Brandon J Schornack, Andrew L Weskamp, et al.
Optics Letters|June 16, 2018
Hartmann wavefront sensor characterization of a high charge vortex beam in the extreme ultraviolet spectral rangeF Sanson, A K Pandey, F Harms, et al.
Pageof 22