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C Beaulieu

Showing results (151-160 of 157) with videos related to

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Journal of Experimental Botany|November 19, 2008
An early Ca2+ influx is a prerequisite to thaxtomin A-induced cell death in Arabidopsis thaliana cellsR Errakhi, A Dauphin, P Meimoun, et al.
Pediatric Diabetes|February 9, 2022
Youth with type 2 diabetes have a high rate of treatment failure after discontinuation of insulin: A Pediatric Diabetes Consortium studyRisa M Wolf, Peiyao Cheng, Robin L Gal, et al.
Clinical Genetics|July 13, 2010
A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disordersA M Innes, K M Boycott, E G Puffenberger, et al.
Journal of Food Science|March 31, 2015
Flavor of fresh blueberry juice and the comparison to amount of sugars, acids, anthocyanidins, and physicochemical measurementsKaren L Bett-Garber, Jeanne M Lea, Michael A Watson, et al.
Bioorganic & Medicinal Chemistry Letters|October 13, 2001
Design and synthesis of a novel class of histone deacetylase inhibitorsR Lavoie, G Bouchain, S Frechette, et al.
Clinical Genetics|June 1, 2018
A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneysY A Ito, A C Smith, K D Kernohan, et al.
Clinical Genetics|January 16, 2015
LIMS2 mutations are associated with a novel muscular dystrophy, severe cardiomyopathy and triangular tonguesJodi Warman Chardon, A C Smith, J Woulfe, et al.
Pageof 16

Showing results (151-160 of 157) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 157 results.
Journal of Experimental Botany|November 19, 2008
An early Ca2+ influx is a prerequisite to thaxtomin A-induced cell death in Arabidopsis thaliana cellsR Errakhi, A Dauphin, P Meimoun, et al.
Pediatric Diabetes|February 9, 2022
Youth with type 2 diabetes have a high rate of treatment failure after discontinuation of insulin: A Pediatric Diabetes Consortium studyRisa M Wolf, Peiyao Cheng, Robin L Gal, et al.
Clinical Genetics|July 13, 2010
A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disordersA M Innes, K M Boycott, E G Puffenberger, et al.
Journal of Food Science|March 31, 2015
Flavor of fresh blueberry juice and the comparison to amount of sugars, acids, anthocyanidins, and physicochemical measurementsKaren L Bett-Garber, Jeanne M Lea, Michael A Watson, et al.
Bioorganic & Medicinal Chemistry Letters|October 13, 2001
Design and synthesis of a novel class of histone deacetylase inhibitorsR Lavoie, G Bouchain, S Frechette, et al.
Clinical Genetics|June 1, 2018
A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneysY A Ito, A C Smith, K D Kernohan, et al.
Clinical Genetics|January 16, 2015
LIMS2 mutations are associated with a novel muscular dystrophy, severe cardiomyopathy and triangular tonguesJodi Warman Chardon, A C Smith, J Woulfe, et al.
Pageof 16