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Brendan Lee

Showing results (21-30 of 282) with videos related to

Pageof 29
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Human Molecular Genetics|September 22, 2023
Nitric oxide is required for lung alveolarization revealed by deficiency of argininosuccinate lyaseZixue Jin, Ming-Ming Jiang, Brendan Lee
Nature Reviews. Genetics|May 19, 2006
Inborn errors of metabolism: the flux from Mendelian to complex diseasesBrendan Lanpher, Nicola Brunetti-Pierri, Brendan Lee
Annual Review of Genomics and Human Genetics|August 10, 2010
Signaling pathways in human skeletal dysplasiasDustin Baldridge, Oleg Shchelochkov, Brian Kelley, et al.
Pediatric Research|October 1, 2015
Dissatisfaction with maintenance of certification in academic pediatricsKate G Ackerman, Brendan Lee, Jake A Kushner
Bone|February 25, 2017
Genetic causes and mechanisms of Osteogenesis ImperfectaJoohyun Lim, Ingo Grafe, Stefanie Alexander, et al.
Molecular Genetics and Metabolism|July 31, 2012
Optimizing therapy for argininosuccinic aciduriaSandesh C S Nagamani, Brendan Lee, Ayelet Erez
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 12, 2011
Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyondAyelet Erez, Sandesh C Sreenath Nagamani, Brendan Lee
The Journal of Nutrition|March 22, 2006
Reduced ornithine transcarbamylase activity does not impair ureagenesis in Otc(spf-ash) miceJuan C Marini, Brendan Lee, Peter J Garlick
American Journal of Human Genetics|March 3, 2023
Celebrating excellence, acknowledging past harms: Both are vital parts of ASHG's continuing journey to advance human geneticsBruce R Korf, Brendan Lee, Mona V Miller
The Journal of Nutrition|December 21, 2005
In vivo urea kinetic studies in conscious miceJuan C Marini, Brendan Lee, Peter J Garlick
Pageof 29

Showing results (21-30 of 282) with videos related to

Sort By:
Pageof 29
Human Molecular Genetics|September 22, 2023
Nitric oxide is required for lung alveolarization revealed by deficiency of argininosuccinate lyaseZixue Jin, Ming-Ming Jiang, Brendan Lee
Nature Reviews. Genetics|May 19, 2006
Inborn errors of metabolism: the flux from Mendelian to complex diseasesBrendan Lanpher, Nicola Brunetti-Pierri, Brendan Lee
Annual Review of Genomics and Human Genetics|August 10, 2010
Signaling pathways in human skeletal dysplasiasDustin Baldridge, Oleg Shchelochkov, Brian Kelley, et al.
Pediatric Research|October 1, 2015
Dissatisfaction with maintenance of certification in academic pediatricsKate G Ackerman, Brendan Lee, Jake A Kushner
Bone|February 25, 2017
Genetic causes and mechanisms of Osteogenesis ImperfectaJoohyun Lim, Ingo Grafe, Stefanie Alexander, et al.
Molecular Genetics and Metabolism|July 31, 2012
Optimizing therapy for argininosuccinic aciduriaSandesh C S Nagamani, Brendan Lee, Ayelet Erez
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 12, 2011
Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyondAyelet Erez, Sandesh C Sreenath Nagamani, Brendan Lee
The Journal of Nutrition|March 22, 2006
Reduced ornithine transcarbamylase activity does not impair ureagenesis in Otc(spf-ash) miceJuan C Marini, Brendan Lee, Peter J Garlick
American Journal of Human Genetics|March 3, 2023
Celebrating excellence, acknowledging past harms: Both are vital parts of ASHG's continuing journey to advance human geneticsBruce R Korf, Brendan Lee, Mona V Miller
The Journal of Nutrition|December 21, 2005
In vivo urea kinetic studies in conscious miceJuan C Marini, Brendan Lee, Peter J Garlick
Pageof 29