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Nano Letters
|
August 29, 2012
An electrically-driven GaAs nanowire surface plasmon source
Pengyu Fan, Carlo Colombo, Kevin C Y Huang, et al.
Diabetes Care
|
October 9, 2008
Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodies
Riccardo Bonfanti, Carlo Colombo, Valentina Nocerino, et al.
The Journal of Biological Chemistry
|
November 29, 2002
Opposite effects of background genotype on muscle and liver insulin sensitivity of lipoatrophic mice. Role of triglyceride clearance
Carlo Colombo, Martin Haluzik, Jaime J Cutson, et al.
Endocrinology
|
April 3, 2004
Genetic background (C57BL/6J versus FVB/N) strongly influences the severity of diabetes and insulin resistance in ob/ob mice
Martin Haluzik, Carlo Colombo, Oksana Gavrilova, et al.
Pediatric Diabetes
|
June 15, 2012
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation
Domenica Battaglia, Yu-Wen Lin, Claudia Brogna, et al.
Diabetes
|
October 29, 2010
Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management
Karen J Loechner, Alejandro Akrouh, Harley T Kurata, et al.
Diabetes Care
|
July 26, 2014
No sign of proliferative retinopathy in 15 patients with permanent neonatal diabetes with a median diabetes duration of 24 years
Dario Iafusco, Silvana Salardi, Giovanni Chiari, et al.
The Journal of Clinical Investigation
|
May 3, 2008
Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus
Carlo Colombo, Ottavia Porzio, Ming Liu, et al.
Molecular Endocrinology (Baltimore, Md.)
|
November 4, 2009
Opposite clinical phenotypes of glucokinase disease: Description of a novel activating mutation and contiguous inactivating mutations in human glucokinase (GCK) gene
Fabrizio Barbetti, Nadia Cobo-Vuilleumier, Carlo Dionisi-Vici, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 29 results.
Nano Letters
|
August 29, 2012
An electrically-driven GaAs nanowire surface plasmon source
Pengyu Fan, Carlo Colombo, Kevin C Y Huang, et al.
Diabetes Care
|
October 9, 2008
Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodies
Riccardo Bonfanti, Carlo Colombo, Valentina Nocerino, et al.
The Journal of Biological Chemistry
|
November 29, 2002
Opposite effects of background genotype on muscle and liver insulin sensitivity of lipoatrophic mice. Role of triglyceride clearance
Carlo Colombo, Martin Haluzik, Jaime J Cutson, et al.
Endocrinology
|
April 3, 2004
Genetic background (C57BL/6J versus FVB/N) strongly influences the severity of diabetes and insulin resistance in ob/ob mice
Martin Haluzik, Carlo Colombo, Oksana Gavrilova, et al.
Pediatric Diabetes
|
June 15, 2012
Glyburide ameliorates motor coordination and glucose homeostasis in a child with diabetes associated with the KCNJ11/S225T, del226-232 mutation
Domenica Battaglia, Yu-Wen Lin, Claudia Brogna, et al.
Diabetes
|
October 29, 2010
Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management
Karen J Loechner, Alejandro Akrouh, Harley T Kurata, et al.
Diabetes Care
|
July 26, 2014
No sign of proliferative retinopathy in 15 patients with permanent neonatal diabetes with a median diabetes duration of 24 years
Dario Iafusco, Silvana Salardi, Giovanni Chiari, et al.
The Journal of Clinical Investigation
|
May 3, 2008
Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus
Carlo Colombo, Ottavia Porzio, Ming Liu, et al.
Molecular Endocrinology (Baltimore, Md.)
|
November 4, 2009
Opposite clinical phenotypes of glucokinase disease: Description of a novel activating mutation and contiguous inactivating mutations in human glucokinase (GCK) gene
Fabrizio Barbetti, Nadia Cobo-Vuilleumier, Carlo Dionisi-Vici, et al.
Page
of 3