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Biochemical and Biophysical Research Communications
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July 1, 2008
NBCe2 exhibits a 3 HCO3(-):1 Na+ stoichiometry in mouse choroid plexus epithelial cells
Ian D Millar, Peter D Brown
Cerebrospinal Fluid Research
|
September 22, 2007
Ion channel diversity, channel expression and function in the choroid plexuses
Ian 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 cells
Ian 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 bestrophinopathy
Alice 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 humans
Rosemary 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 pigmentosa
Alice E Davidson, Ian D Millar, Jill E Urquhart, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Biochemical and Biophysical Research Communications
|
July 1, 2008
NBCe2 exhibits a 3 HCO3(-):1 Na+ stoichiometry in mouse choroid plexus epithelial cells
Ian D Millar, Peter D Brown
Cerebrospinal Fluid Research
|
September 22, 2007
Ion channel diversity, channel expression and function in the choroid plexuses
Ian 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 cells
Ian 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 bestrophinopathy
Alice 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 humans
Rosemary 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 pigmentosa
Alice E Davidson, Ian D Millar, Jill E Urquhart, et al.
Page
of 1