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Brendan H Lee

Showing results (11-20 of 81) with videos related to

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Molecular Genetics and Metabolism|March 13, 2010
Early orthotopic liver transplantation in urea cycle defects: follow up of a developmental outcome studyPhilippe M Campeau, Penelope J Pivalizza, Geoffrey Miller, et al.
Molecular Genetics and Metabolism|May 4, 2012
Decreased bone mineralization in children with Noonan syndrome: another consequence of dysregulated RAS MAPKinase pathway?Kiran S Choudhry, Monica Grover, Alyssa A Tran, et al.
Arthroscopy, Sports Medicine, and Rehabilitation|May 2, 2022
Double-Spin Leukocyte-Rich Platelet-Rich Plasma Is Predominantly Lymphocyte Rich With Notable Concentrations of Other White Blood Cell SubtypesAnuj Marathe, Shiv J Patel, Bo Song, et al.
The Journal of Biological Chemistry|February 4, 2015
Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutationsDavid M Hudson, Kyu Sang Joeng, Rachel Werther, et al.
The American Journal of Sports Medicine|March 20, 2019
Effects of Aspirin on Growth Factor Release From Freshly Isolated Leukocyte-Rich Platelet-Rich Plasma in Healthy Men: A Prospective Fixed-Sequence Controlled Laboratory StudyPrathap Jayaram, Peter Yeh, Shiv J Patel, et al.
American Journal of Obstetrics & Gynecology MFM|March 30, 2021
Pregnancy in women with osteogenesis imperfecta: pregnancy characteristics, maternal, and neonatal outcomesRashmi Rao, David Cuthbertson, Sandesh C S Nagamani, et al.
The Journal of Clinical Investigation|June 20, 2017
Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasisKyu Sang Joeng, Yi-Chien Lee, Joohyun Lim, et al.
JBMR Plus|May 5, 2022
<i>miRNA-34c</i> Suppresses Osteosarcoma Progression In Vivo by Targeting Notch and E2FYangjin Bae, Huan-Chang Zeng, Yi-Ting Chen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 16, 2013
Osteogenesis imperfecta without features of type V caused by a mutation in the IFITM5 geneMonica Grover, Philippe M Campeau, Caressa Dee Lietman, et al.
The Journal of Biological Chemistry|January 25, 2017
P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIADavid M Hudson, MaryAnn Weis, Jyoti Rai, et al.
Pageof 9

Showing results (11-20 of 81) with videos related to

Sort By:
Pageof 9
Molecular Genetics and Metabolism|March 13, 2010
Early orthotopic liver transplantation in urea cycle defects: follow up of a developmental outcome studyPhilippe M Campeau, Penelope J Pivalizza, Geoffrey Miller, et al.
Molecular Genetics and Metabolism|May 4, 2012
Decreased bone mineralization in children with Noonan syndrome: another consequence of dysregulated RAS MAPKinase pathway?Kiran S Choudhry, Monica Grover, Alyssa A Tran, et al.
Arthroscopy, Sports Medicine, and Rehabilitation|May 2, 2022
Double-Spin Leukocyte-Rich Platelet-Rich Plasma Is Predominantly Lymphocyte Rich With Notable Concentrations of Other White Blood Cell SubtypesAnuj Marathe, Shiv J Patel, Bo Song, et al.
The Journal of Biological Chemistry|February 4, 2015
Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutationsDavid M Hudson, Kyu Sang Joeng, Rachel Werther, et al.
The American Journal of Sports Medicine|March 20, 2019
Effects of Aspirin on Growth Factor Release From Freshly Isolated Leukocyte-Rich Platelet-Rich Plasma in Healthy Men: A Prospective Fixed-Sequence Controlled Laboratory StudyPrathap Jayaram, Peter Yeh, Shiv J Patel, et al.
American Journal of Obstetrics & Gynecology MFM|March 30, 2021
Pregnancy in women with osteogenesis imperfecta: pregnancy characteristics, maternal, and neonatal outcomesRashmi Rao, David Cuthbertson, Sandesh C S Nagamani, et al.
The Journal of Clinical Investigation|June 20, 2017
Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasisKyu Sang Joeng, Yi-Chien Lee, Joohyun Lim, et al.
JBMR Plus|May 5, 2022
<i>miRNA-34c</i> Suppresses Osteosarcoma Progression In Vivo by Targeting Notch and E2FYangjin Bae, Huan-Chang Zeng, Yi-Ting Chen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 16, 2013
Osteogenesis imperfecta without features of type V caused by a mutation in the IFITM5 geneMonica Grover, Philippe M Campeau, Caressa Dee Lietman, et al.
The Journal of Biological Chemistry|January 25, 2017
P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIADavid M Hudson, MaryAnn Weis, Jyoti Rai, et al.
Pageof 9