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Ian D Millar

Showing results (1-10 of 6) with videos related to

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Biochemical and Biophysical Research Communications|July 1, 2008
NBCe2 exhibits a 3 HCO3(-):1 Na+ stoichiometry in mouse choroid plexus epithelial cellsIan D Millar, Peter D Brown
Cerebrospinal Fluid Research|September 22, 2007
Ion channel diversity, channel expression and function in the choroid plexusesIan D Millar, Jason Ie Bruce, Peter D Brown
Pflugers Archiv : European Journal of Physiology|November 21, 2007
Kv1 and Kir2 potassium channels are expressed in rat brain endothelial cellsIan D Millar, Shanshan Wang, Peter D Brown, et al.
Investigative Ophthalmology & Visual Science|February 19, 2011
Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathyAlice E Davidson, Ian D Millar, Rosemary Burgess-Mullan, et al.
American Journal of Human Genetics|January 9, 2008
Biallelic mutation of BEST1 causes a distinct retinopathy in humansRosemary Burgess, Ian D Millar, Bart P Leroy, et al.
American Journal of Human Genetics|October 27, 2009
Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosaAlice E Davidson, Ian D Millar, Jill E Urquhart, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Biochemical and Biophysical Research Communications|July 1, 2008
NBCe2 exhibits a 3 HCO3(-):1 Na+ stoichiometry in mouse choroid plexus epithelial cellsIan D Millar, Peter D Brown
Cerebrospinal Fluid Research|September 22, 2007
Ion channel diversity, channel expression and function in the choroid plexusesIan D Millar, Jason Ie Bruce, Peter D Brown
Pflugers Archiv : European Journal of Physiology|November 21, 2007
Kv1 and Kir2 potassium channels are expressed in rat brain endothelial cellsIan D Millar, Shanshan Wang, Peter D Brown, et al.
Investigative Ophthalmology & Visual Science|February 19, 2011
Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathyAlice E Davidson, Ian D Millar, Rosemary Burgess-Mullan, et al.
American Journal of Human Genetics|January 9, 2008
Biallelic mutation of BEST1 causes a distinct retinopathy in humansRosemary Burgess, Ian D Millar, Bart P Leroy, et al.
American Journal of Human Genetics|October 27, 2009
Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosaAlice E Davidson, Ian D Millar, Jill E Urquhart, et al.
Pageof 1