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Showing results (141-150 of 150) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|February 29, 2012
Opposing effects of fructokinase C and A isoforms on fructose-induced metabolic syndrome in miceTakuji Ishimoto, Miguel A Lanaspa, Myphuong T Le, et al.
Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.
Nature Communications|September 12, 2013
Endogenous fructose production and metabolism in the liver contributes to the development of metabolic syndromeMiguel A Lanaspa, Takuji Ishimoto, Nanxing Li, et al.
Hepatology (Baltimore, Md.)|July 2, 2013
High-fat and high-sucrose (western) diet induces steatohepatitis that is dependent on fructokinaseTakuji Ishimoto, Miguel A Lanaspa, Christopher J Rivard, et al.
Nature Genetics|November 22, 2011
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Clare V Logan, Barbara Lucke, Caroline Pottinger, et al.
Plos Genetics|September 19, 2014
HEATR2 plays a conserved role in assembly of the ciliary motile apparatusChristine P Diggle, Daniel J Moore, Girish Mali, et al.
Journal of the American Society of Nephrology : JASN|May 31, 2014
Endogenous fructose production and fructokinase activation mediate renal injury in diabetic nephropathyMiguel A Lanaspa, Takuji Ishimoto, Christina Cicerchi, et al.
Human Mutation|May 4, 2012
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosisChristine P Diggle, David A Parry, Clare V Logan, et al.
American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.
American Journal of Human Genetics|April 9, 2016
Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in InfancyChristine P Diggle, Stacey J Sukoff Rizzo, Michael Popiolek, et al.
Pageof 15

Showing results (141-150 of 150) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 150 results.
Proceedings of the National Academy of Sciences of the United States of America|February 29, 2012
Opposing effects of fructokinase C and A isoforms on fructose-induced metabolic syndrome in miceTakuji Ishimoto, Miguel A Lanaspa, Myphuong T Le, et al.
Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.
Nature Communications|September 12, 2013
Endogenous fructose production and metabolism in the liver contributes to the development of metabolic syndromeMiguel A Lanaspa, Takuji Ishimoto, Nanxing Li, et al.
Hepatology (Baltimore, Md.)|July 2, 2013
High-fat and high-sucrose (western) diet induces steatohepatitis that is dependent on fructokinaseTakuji Ishimoto, Miguel A Lanaspa, Christopher J Rivard, et al.
Nature Genetics|November 22, 2011
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Clare V Logan, Barbara Lucke, Caroline Pottinger, et al.
Plos Genetics|September 19, 2014
HEATR2 plays a conserved role in assembly of the ciliary motile apparatusChristine P Diggle, Daniel J Moore, Girish Mali, et al.
Journal of the American Society of Nephrology : JASN|May 31, 2014
Endogenous fructose production and fructokinase activation mediate renal injury in diabetic nephropathyMiguel A Lanaspa, Takuji Ishimoto, Christina Cicerchi, et al.
Human Mutation|May 4, 2012
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosisChristine P Diggle, David A Parry, Clare V Logan, et al.
American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.
American Journal of Human Genetics|April 9, 2016
Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in InfancyChristine P Diggle, Stacey J Sukoff Rizzo, Michael Popiolek, et al.
Pageof 15