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M Payne

Showing results (861-870 of 910) with videos related to

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Genetics|December 5, 2000
Extragenic suppressors of the nimX2(cdc2) mutation of Aspergillus nidulans affect nuclear division, septation and conidiationS L McGuire, D L Roe, B W Carter, et al.
British Journal of Cancer|March 6, 2008
A phase I trial of ispinesib, a kinesin spindle protein inhibitor, with docetaxel in patients with advanced solid tumoursS P Blagden, L R Molife, A Seebaran, et al.
Pain Medicine (Malden, Mass.)|August 26, 2010
Neurosteroids and self-reported pain in veterans who served in the U.S. Military after September 11, 2001Jason D Kilts, Larry A Tupler, Francis J Keefe, et al.
Nanotechnology|October 6, 2009
The stabilization and targeting of surfactant-synthesized gold nanorodsBetty C Rostro-Kohanloo, Lissett R Bickford, Courtney M Payne, et al.
Neurology|August 17, 2016
Neurocognitive outcomes in neurofibromatosis clinical trials: Recommendations for the domain of attentionKarin S Walsh, Jennifer Janusz, Pamela L Wolters, et al.
ACS Applied Materials & Interfaces|February 15, 2014
Systematic reliability study of top-gate p- and n-channel organic field-effect transistorsDo Kyung Hwang, Canek Fuentes-Hernandez, Mathieu Fenoll, et al.
Nature Genetics|December 30, 1999
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosisM M Sohocki, S J Bowne, L S Sullivan, et al.
Neuropsychology|February 13, 2025
Agreement, reliability, feasibility, and acceptability of home-based telehealth versus face-to-face pediatric neuropsychological testing: A within-person crossover studyKristina M Haebich, Hayley Darke, Francesca Lami, et al.
Molecular Autism|January 5, 2022
Delineating the autistic phenotype in children with neurofibromatosis type 1Anita K Chisholm, Kristina M Haebich, Natalie A Pride, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 5, 2013
Structural characterization of a unique marine animal family 7 cellobiohydrolase suggests a mechanism of cellulase salt toleranceMarcelo Kern, John E McGeehan, Simon D Streeter, et al.
Pageof 91

Showing results (861-870 of 910) with videos related to

Sort By:
Pageof 91
Genetics|December 5, 2000
Extragenic suppressors of the nimX2(cdc2) mutation of Aspergillus nidulans affect nuclear division, septation and conidiationS L McGuire, D L Roe, B W Carter, et al.
British Journal of Cancer|March 6, 2008
A phase I trial of ispinesib, a kinesin spindle protein inhibitor, with docetaxel in patients with advanced solid tumoursS P Blagden, L R Molife, A Seebaran, et al.
Pain Medicine (Malden, Mass.)|August 26, 2010
Neurosteroids and self-reported pain in veterans who served in the U.S. Military after September 11, 2001Jason D Kilts, Larry A Tupler, Francis J Keefe, et al.
Nanotechnology|October 6, 2009
The stabilization and targeting of surfactant-synthesized gold nanorodsBetty C Rostro-Kohanloo, Lissett R Bickford, Courtney M Payne, et al.
Neurology|August 17, 2016
Neurocognitive outcomes in neurofibromatosis clinical trials: Recommendations for the domain of attentionKarin S Walsh, Jennifer Janusz, Pamela L Wolters, et al.
ACS Applied Materials & Interfaces|February 15, 2014
Systematic reliability study of top-gate p- and n-channel organic field-effect transistorsDo Kyung Hwang, Canek Fuentes-Hernandez, Mathieu Fenoll, et al.
Nature Genetics|December 30, 1999
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosisM M Sohocki, S J Bowne, L S Sullivan, et al.
Neuropsychology|February 13, 2025
Agreement, reliability, feasibility, and acceptability of home-based telehealth versus face-to-face pediatric neuropsychological testing: A within-person crossover studyKristina M Haebich, Hayley Darke, Francesca Lami, et al.
Molecular Autism|January 5, 2022
Delineating the autistic phenotype in children with neurofibromatosis type 1Anita K Chisholm, Kristina M Haebich, Natalie A Pride, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 5, 2013
Structural characterization of a unique marine animal family 7 cellobiohydrolase suggests a mechanism of cellulase salt toleranceMarcelo Kern, John E McGeehan, Simon D Streeter, et al.
Pageof 91