-
1
-
-
0001994983
-
Diseases of the kidney
-
Schrier, R. W & Gottschalk, C. W. (eds), (Little, Brown; Boston
-
(1997)
, pp. 521-560
-
-
Gabow, P.A.1
Grantham, J.J.2
-
2
-
-
0028278058
-
The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosme 16
-
The European Polycystic Kidney Disease Consortium
-
(1994)
Cell
, vol.77
, pp. 881-894
-
-
-
3
-
-
15844385078
-
PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein
-
(1996)
Science
, vol.272
, pp. 1339-1342
-
-
Mochizuki, T.1
-
5
-
-
0032540226
-
Somatic inactivation of Pkd2 results in polycystic kidney disease
-
(1998)
Cell
, vol.93
, pp. 177-188
-
-
Wu, G.1
-
6
-
-
0031252295
-
Perinatal lethality with kidney and pancreas defects in mice with a targeted Pkd1 mutation
-
(1997)
Nature Genet.
, vol.17
, pp. 179-181
-
-
Lu, W.1
-
7
-
-
0033989173
-
Cardiac defects and renal failure in mice with targeted mutations in Pkd2
-
(2000)
Nature Genet.
, vol.24
, pp. 75-78
-
-
Wu, G.1
-
8
-
-
0030909957
-
PKD1 interacts with PKD2 through a probable coiled-coil domain
-
(1997)
Nature Genet.
, vol.16
, pp. 179-183
-
-
Qian, F.1
-
9
-
-
0034700483
-
Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents
-
(2000)
Nature
, vol.408
, pp. 990-994
-
-
Hanaoka, K.1
-
10
-
-
0035806961
-
The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway
-
(2001)
Curr. Biol.
, vol.11
, pp. 1341-1346
-
-
Barr, M.M.1
-
12
-
-
0033214702
-
Identification and characterization of polycystin-2, the PKD2 gene product
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 28557-28565
-
-
Cai, Y.1
-
14
-
-
0033021438
-
Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissue
-
(1999)
Am. J. Pathol.
, vol.154
, pp. 1721-1729
-
-
Ong, A.C.1
-
15
-
-
0033399409
-
The rat Pkd2 protein assumes distinct subcellular distributions in different organs
-
(1999)
Am. J. Physiol.
, vol.277
, pp. F914-F925
-
-
Obermuller, N.1
-
16
-
-
0035970112
-
From the Cover: Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel
-
(2001)
Proc. Natl Acad. Sci. USA
, vol.98
, pp. 1182-1187
-
-
Gonzalez-Perrett, S.1
-
19
-
-
0034693131
-
In vivo interaction of the adapter protein CD2-associated protein with the type 2 polycystic kidney disease protein, polycystin-2
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 32888-32893
-
-
Lehtonen, S.1
-
23
-
-
0024259980
-
Inositol 1, 4, 5-trisphosphate activates a channel from smooth muscle sarcoplasmic reticulum
-
(1988)
Nature
, vol.336
, pp. 583-586
-
-
Ehrlich, B.E.1
Watras, J.2
-
31
-
-
0033598347
-
Polycystin-L is a calcium-regulated cation channel permeable to calcium ions
-
(1999)
Nature
, vol.401
, pp. 383-386
-
-
Chen, X.Z.1
-
32
-
-
0034617192
-
Characterization of a phosphoinositide-mediated odor transduction pathway reveals plasma membrane localization of an inositol 1, 4, 5-trisphosphate receptor in lobster olfactory receptor neurons
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 20450-20457
-
-
Munger, S.D.1
-
33
-
-
0033816585
-
Basic properties of an inositol 1, 4, 5-trisphosphate-gated channel in carp olfactory cilia
-
(2000)
Eur. J. Neurosci.
, vol.12
, pp. 2805-2811
-
-
Cadiou, H.1
-
36
-
-
0032480821
-
3 receptors and store-operated Htrp3 channels
-
(1998)
Nature
, vol.396
, pp. 478-482
-
-
Kiselyov, K.1
-
39
-
-
0029977293
-
The sea urchin sperm receptor for egg jelly is a modular protein with extensive homology to the human polycystic kidney disease protein, PKD1
-
(1996)
J. Cell Biol.
, vol.133
, pp. 809-817
-
-
Moy, G.W.1
-
41
-
-
0033598394
-
A polycystic kidney disease gene homolog required for male mating behavior in Caenorhabiditis elegans
-
(1999)
Nature
, vol.401
, pp. 386-389
-
-
Barr, M.M.1
Sternberg, P.W.2
-
42
-
-
0033760264
-
Cloning of the gene encoding a novel integral membrane protein, mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IV
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1110-1120
-
-
Bassi, M.T.1
-
43
-
-
0034641869
-
Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2471-2478
-
-
Sun, M.1
-
45
-
-
0024201809
-
Computer programs for calculating total from specified free or free from specified total ionic concentrations in aqueous solutions containing multiple metals and ligands
-
(1988)
Methods Enzymol.
, vol.157
, pp. 378-417
-
-
Fabiato, A.1
|