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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 1, 2001
Biochemical characterization of bona fide polycystin-1 in vitro and in vivo
A Boletta, F Qian, L F Onuchic, et al.
Journal of the American Society of Nephrology : JASN
|
February 1, 1997
New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels
S M Mulders, N V Knoers, A F Van Lieburg, et al.
American Journal of Human Genetics
|
October 1, 1994
Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene
A F van Lieburg, M A Verdijk, V V Knoers, et al.
The Journal of Clinical Investigation
|
July 3, 1998
An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex
S M Mulders, D G Bichet, J P Rijss, et al.
Genomics
|
June 21, 2001
A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice
D J Sidjanin, D M Parker-Wilson, A Neuhäuser-Klaus, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 55) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 55 results.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 1, 2001
Biochemical characterization of bona fide polycystin-1 in vitro and in vivo
A Boletta, F Qian, L F Onuchic, et al.
Journal of the American Society of Nephrology : JASN
|
February 1, 1997
New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels
S M Mulders, N V Knoers, A F Van Lieburg, et al.
American Journal of Human Genetics
|
October 1, 1994
Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene
A F van Lieburg, M A Verdijk, V V Knoers, et al.
The Journal of Clinical Investigation
|
July 3, 1998
An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex
S M Mulders, D G Bichet, J P Rijss, et al.
Genomics
|
June 21, 2001
A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice
D J Sidjanin, D M Parker-Wilson, A Neuhäuser-Klaus, et al.
Page
of 6