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Human Molecular Genetics
|
September 22, 2023
Nitric oxide is required for lung alveolarization revealed by deficiency of argininosuccinate lyase
Zixue Jin, Ming-Ming Jiang, Brendan Lee
Nature Reviews. Genetics
|
May 19, 2006
Inborn errors of metabolism: the flux from Mendelian to complex diseases
Brendan Lanpher, Nicola Brunetti-Pierri, Brendan Lee
Annual Review of Genomics and Human Genetics
|
August 10, 2010
Signaling pathways in human skeletal dysplasias
Dustin Baldridge, Oleg Shchelochkov, Brian Kelley, et al.
Pediatric Research
|
October 1, 2015
Dissatisfaction with maintenance of certification in academic pediatrics
Kate G Ackerman, Brendan Lee, Jake A Kushner
Bone
|
February 25, 2017
Genetic causes and mechanisms of Osteogenesis Imperfecta
Joohyun Lim, Ingo Grafe, Stefanie Alexander, et al.
Molecular Genetics and Metabolism
|
July 31, 2012
Optimizing therapy for argininosuccinic aciduria
Sandesh 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 beyond
Ayelet 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) mice
Juan 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 genetics
Bruce R Korf, Brendan Lee, Mona V Miller
The Journal of Nutrition
|
December 21, 2005
In vivo urea kinetic studies in conscious mice
Juan C Marini, Brendan Lee, Peter J Garlick
Page
of 29
Search research articles
Search
Showing results (21-30 of 282) with videos related to
Sort By:
Page
of 29
Human Molecular Genetics
|
September 22, 2023
Nitric oxide is required for lung alveolarization revealed by deficiency of argininosuccinate lyase
Zixue Jin, Ming-Ming Jiang, Brendan Lee
Nature Reviews. Genetics
|
May 19, 2006
Inborn errors of metabolism: the flux from Mendelian to complex diseases
Brendan Lanpher, Nicola Brunetti-Pierri, Brendan Lee
Annual Review of Genomics and Human Genetics
|
August 10, 2010
Signaling pathways in human skeletal dysplasias
Dustin Baldridge, Oleg Shchelochkov, Brian Kelley, et al.
Pediatric Research
|
October 1, 2015
Dissatisfaction with maintenance of certification in academic pediatrics
Kate G Ackerman, Brendan Lee, Jake A Kushner
Bone
|
February 25, 2017
Genetic causes and mechanisms of Osteogenesis Imperfecta
Joohyun Lim, Ingo Grafe, Stefanie Alexander, et al.
Molecular Genetics and Metabolism
|
July 31, 2012
Optimizing therapy for argininosuccinic aciduria
Sandesh 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 beyond
Ayelet 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) mice
Juan 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 genetics
Bruce R Korf, Brendan Lee, Mona V Miller
The Journal of Nutrition
|
December 21, 2005
In vivo urea kinetic studies in conscious mice
Juan C Marini, Brendan Lee, Peter J Garlick
Page
of 29