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H Sherr

Showing results (241-250 of 290) with videos related to

Pageof 29
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Genomics|September 15, 1996
Mapping of unconventional myosins in mouse and humanT Hasson, J F Skowron, D J Gilbert, et al.
Human Brain Mapping|May 25, 2016
Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplicationsYi Shin Chang, Julia P Owen, Nicholas J Pojman, et al.
Blood|July 19, 2003
The shared tumor-associated antigen cytochrome P450 1B1 is recognized by specific cytotoxic T cellsBritta Maecker, David H Sherr, Robert H Vonderheide, 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.
Neurology|January 26, 2011
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous familiesR M Hanna, S E Marsh, D Swistun, et al.
Science Translational Medicine|November 24, 2017
Targeting STUB1-tissue factor axis normalizes hyperthrombotic uremic phenotype without increasing bleeding riskMoshe Shashar, Mostafa E Belghasem, Shinobu Matsuura, et al.
Human Mutation|September 9, 2020
Overcoming presynaptic effects of VAMP2 mutations with 4-aminopyridine treatmentRoxanne L Simmons, Haiyan Li, Baris Alten, 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.
American Journal of Human Genetics|March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasiaNaiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
Blood|June 1, 2013
The aryl hydrocarbon receptor directs hematopoietic progenitor cell expansion and differentiationBrenden W Smith, Sarah S Rozelle, Amy Leung, et al.
Pageof 29

Showing results (241-250 of 290) with videos related to

Sort By:
Pageof 29
Genomics|September 15, 1996
Mapping of unconventional myosins in mouse and humanT Hasson, J F Skowron, D J Gilbert, et al.
Human Brain Mapping|May 25, 2016
Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplicationsYi Shin Chang, Julia P Owen, Nicholas J Pojman, et al.
Blood|July 19, 2003
The shared tumor-associated antigen cytochrome P450 1B1 is recognized by specific cytotoxic T cellsBritta Maecker, David H Sherr, Robert H Vonderheide, 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.
Neurology|January 26, 2011
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous familiesR M Hanna, S E Marsh, D Swistun, et al.
Science Translational Medicine|November 24, 2017
Targeting STUB1-tissue factor axis normalizes hyperthrombotic uremic phenotype without increasing bleeding riskMoshe Shashar, Mostafa E Belghasem, Shinobu Matsuura, et al.
Human Mutation|September 9, 2020
Overcoming presynaptic effects of VAMP2 mutations with 4-aminopyridine treatmentRoxanne L Simmons, Haiyan Li, Baris Alten, 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.
American Journal of Human Genetics|March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasiaNaiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
Blood|June 1, 2013
The aryl hydrocarbon receptor directs hematopoietic progenitor cell expansion and differentiationBrenden W Smith, Sarah S Rozelle, Amy Leung, et al.
Pageof 29