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Nieh

Showing results (461-470 of 471) with videos related to

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Nature|November 9, 2018
Dopamine enhances signal-to-noise ratio in cortical-brainstem encoding of aversive stimuliCaitlin M Vander Weele, Cody A Siciliano, Gillian A Matthews, et al.
Plos Genetics|October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyriaSamin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
Human Genetics|November 23, 2006
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene lociHossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, et al.
Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.
Cell|May 8, 2018
Corticoamygdala Transfer of Socially Derived Information Gates Observational LearningStephen A Allsop, Romy Wichmann, Fergil Mills, et al.
Journal of the American Chemical Society|June 25, 2020
Bicelles Rich in both Sphingolipids and Cholesterol and Their Use in Studies of Membrane ProteinsJames M Hutchison, Kuo-Chih Shih, Holger A Scheidt, et al.
Journal of Medical Genetics|October 28, 2010
A clinical and molecular genetic study of 112 Iranian families with primary microcephalyH Darvish, S Esmaeeli-Nieh, G B Monajemi, et al.
Chemical Society Reviews|April 17, 2018
Current characterization methods for cellulose nanomaterialsE Johan Foster, Robert J Moon, Umesh P Agarwal, et al.
Nature|September 23, 2011
Deep sequencing reveals 50 novel genes for recessive cognitive disordersHossein Najmabadi, Hao Hu, Masoud Garshasbi, et al.
Nature|August 13, 2013
De novo mutations in epileptic encephalopathies, , Andrew S Allen, et al.
Pageof 48

Showing results (461-470 of 471) with videos related to

Sort By:
Pageof 48
Nature|November 9, 2018
Dopamine enhances signal-to-noise ratio in cortical-brainstem encoding of aversive stimuliCaitlin M Vander Weele, Cody A Siciliano, Gillian A Matthews, et al.
Plos Genetics|October 8, 2013
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyriaSamin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, et al.
Human Genetics|November 23, 2006
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene lociHossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, et al.
Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.
Cell|May 8, 2018
Corticoamygdala Transfer of Socially Derived Information Gates Observational LearningStephen A Allsop, Romy Wichmann, Fergil Mills, et al.
Journal of the American Chemical Society|June 25, 2020
Bicelles Rich in both Sphingolipids and Cholesterol and Their Use in Studies of Membrane ProteinsJames M Hutchison, Kuo-Chih Shih, Holger A Scheidt, et al.
Journal of Medical Genetics|October 28, 2010
A clinical and molecular genetic study of 112 Iranian families with primary microcephalyH Darvish, S Esmaeeli-Nieh, G B Monajemi, et al.
Chemical Society Reviews|April 17, 2018
Current characterization methods for cellulose nanomaterialsE Johan Foster, Robert J Moon, Umesh P Agarwal, et al.
Nature|September 23, 2011
Deep sequencing reveals 50 novel genes for recessive cognitive disordersHossein Najmabadi, Hao Hu, Masoud Garshasbi, et al.
Nature|August 13, 2013
De novo mutations in epileptic encephalopathies, , Andrew S Allen, et al.
Pageof 48