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L Beaulieu

Showing results (171-180 of 187) with videos related to

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The Journal of Head Trauma Rehabilitation|January 3, 2024
Characterization and Treatment of Chronic Pain After Traumatic Brain Injury-Comparison of Characteristics Between Individuals With Current Pain, Past Pain, and No Pain: A NIDILRR and VA TBI Model Systems Collaborative ProjectCynthia Harrison-Felix, Mitch Sevigny, Cynthia L Beaulieu, et al.
Organic Letters|August 9, 2014
A highly concise and convergent synthesis of HCV polymerase inhibitor Deleobuvir (BI 207127): application of a one-pot borylation-Suzuki coupling reactionYongda Zhang, Bruce Z Lu, Guisheng Li, et al.
American Journal of Human Genetics|July 2, 2013
Mutations in PIK3R1 cause SHORT syndromeDavid A Dyment, Amanda C Smith, Diana Alcantara, et al.
Journal of Medicinal Chemistry|May 29, 1999
Ligands for the tyrosine kinase p56lck SH2 domain: discovery of potent dipeptide derivatives with monocharged, nonhydrolyzable phosphate replacementsP L Beaulieu, D R Cameron, J M Ferland, et al.
Physical Review Letters|March 5, 2004
Isospin diffusion and the nuclear symmetry energy in heavy ion reactionsM B Tsang, T X Liu, L Shi, et al.
American Journal of Human Genetics|December 7, 2015
SLC39A8 Deficiency: A Disorder of Manganese Transport and GlycosylationJulien H Park, Max Hogrebe, Marianne Grüneberg, et al.
American Journal of Human Genetics|June 7, 2014
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery projectChandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, et al.
Journal of Medicinal Chemistry|July 13, 2001
Nonpeptidic, monocharged, cell permeable ligands for the p56lck SH2 domainJ R Proudfoot, R Betageri, M Cardozo, et al.
Physical Review Letters|September 16, 2000
Signals for a transition from surface to bulk emission in thermal multifragmentationL Beaulieu, T Lefort, K Kwiatkowski, et al.
American Journal of Human Genetics|December 7, 2015
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8Kym M Boycott, Chandree L Beaulieu, Kristin D Kernohan, et al.
Pageof 19

Showing results (171-180 of 187) with videos related to

Sort By:
Pageof 19
The Journal of Head Trauma Rehabilitation|January 3, 2024
Characterization and Treatment of Chronic Pain After Traumatic Brain Injury-Comparison of Characteristics Between Individuals With Current Pain, Past Pain, and No Pain: A NIDILRR and VA TBI Model Systems Collaborative ProjectCynthia Harrison-Felix, Mitch Sevigny, Cynthia L Beaulieu, et al.
Organic Letters|August 9, 2014
A highly concise and convergent synthesis of HCV polymerase inhibitor Deleobuvir (BI 207127): application of a one-pot borylation-Suzuki coupling reactionYongda Zhang, Bruce Z Lu, Guisheng Li, et al.
American Journal of Human Genetics|July 2, 2013
Mutations in PIK3R1 cause SHORT syndromeDavid A Dyment, Amanda C Smith, Diana Alcantara, et al.
Journal of Medicinal Chemistry|May 29, 1999
Ligands for the tyrosine kinase p56lck SH2 domain: discovery of potent dipeptide derivatives with monocharged, nonhydrolyzable phosphate replacementsP L Beaulieu, D R Cameron, J M Ferland, et al.
Physical Review Letters|March 5, 2004
Isospin diffusion and the nuclear symmetry energy in heavy ion reactionsM B Tsang, T X Liu, L Shi, et al.
American Journal of Human Genetics|December 7, 2015
SLC39A8 Deficiency: A Disorder of Manganese Transport and GlycosylationJulien H Park, Max Hogrebe, Marianne Grüneberg, et al.
American Journal of Human Genetics|June 7, 2014
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery projectChandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, et al.
Journal of Medicinal Chemistry|July 13, 2001
Nonpeptidic, monocharged, cell permeable ligands for the p56lck SH2 domainJ R Proudfoot, R Betageri, M Cardozo, et al.
Physical Review Letters|September 16, 2000
Signals for a transition from surface to bulk emission in thermal multifragmentationL Beaulieu, T Lefort, K Kwiatkowski, et al.
American Journal of Human Genetics|December 7, 2015
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8Kym M Boycott, Chandree L Beaulieu, Kristin D Kernohan, et al.
Pageof 19