-
1
-
-
0036837356
-
Forging the link between structure and function of electrogenic cotransporters: The renal type IIa Na+/Pi cotransporter as a case study
-
Forster IC, Kohler K, Biber J, Murer H: Forging the link between structure and function of electrogenic cotransporters: The renal type IIa Na+/Pi cotransporter as a case study. Prog Biophys Mol Biol 80: 69-108, 2002
-
(2002)
Prog Biophys Mol Biol
, vol.80
, pp. 69-108
-
-
Forster, I.C.1
Kohler, K.2
Biber, J.3
Murer, H.4
-
2
-
-
1242317643
-
The sodium phosphate cotransporter family SLC34
-
Murer H, Forster I, Biber J: The sodium phosphate cotransporter family SLC34. Pflugers Arch 447: 763-767, 2004
-
(2004)
Pflugers Arch
, vol.447
, pp. 763-767
-
-
Murer, H.1
Forster, I.2
Biber, J.3
-
3
-
-
33750203846
-
Proximal tubular handling of phosphate: A molecular perspective
-
Forster IC, Hernando N, Biber J, Murer H: Proximal tubular handling of phosphate: A molecular perspective. Kidney Int 70: 1548-1559, 2006
-
(2006)
Kidney Int
, vol.70
, pp. 1548-1559
-
-
Forster, I.C.1
Hernando, N.2
Biber, J.3
Murer, H.4
-
4
-
-
33947111420
-
Phosphate transport: Molecular basis, regulation and pathophysiology
-
Tenenhouse HS: Phosphate transport: Molecular basis, regulation and pathophysiology. J Steroid Biochem Mol Biol 103: 572-577, 2007
-
(2007)
J Steroid Biochem Mol Biol
, vol.103
, pp. 572-577
-
-
Tenenhouse, H.S.1
-
5
-
-
2142746439
-
FGF-23 is a potent regulator of vitamin D metabolism and phosphate homeostasis
-
Shimada T, Hasegawa H, Yamazaki Y, Muto T, Hino R, Takeuchi Y, Fujita T, Nakahara K, Fukumoto S, Yamashita T: FGF-23 is a potent regulator of vitamin D metabolism and phosphate homeostasis. J Bone Miner Res 19: 429-435, 2004
-
(2004)
J Bone Miner Res
, vol.19
, pp. 429-435
-
-
Shimada, T.1
Hasegawa, H.2
Yamazaki, Y.3
Muto, T.4
Hino, R.5
Takeuchi, Y.6
Fujita, T.7
Nakahara, K.8
Fukumoto, S.9
Yamashita, T.10
-
6
-
-
0038587687
-
Na+-dependent phosphate transporters in the murine osteoclast: Cellular distribution and protein interactions
-
Khadeer MA, Tang Z, Tenenhouse HS, Eiden MV, Murer H, Hernando N, Weinman EJ, Chellaiah MA, Gupta A: Na+-dependent phosphate transporters in the murine osteoclast: Cellular distribution and protein interactions. Am J Physiol Cell Physiol 284: C1633-C1644, 2003
-
(2003)
Am J Physiol Cell Physiol
, vol.284
-
-
Khadeer, M.A.1
Tang, Z.2
Tenenhouse, H.S.3
Eiden, M.V.4
Murer, H.5
Hernando, N.6
Weinman, E.J.7
Chellaiah, M.A.8
Gupta, A.9
-
7
-
-
36048958880
-
Parathyroid hormone inhibits renal phosphate transport by phosphorylation of serine 77 of sodium-hydrogen exchanger regulatory factor-1
-
Weinman EJ, Biswas RS, Peng Q, Shen L, Turner CL, Steplock D, Shenolikar S, Cunningham R: Parathyroid hormone inhibits renal phosphate transport by phosphorylation of serine 77 of sodium-hydrogen exchanger regulatory factor-1. J Clin Invest 117: 3412-3420, 2007
-
(2007)
J Clin Invest
, vol.117
, pp. 3412-3420
-
-
Weinman, E.J.1
Biswas, R.S.2
Peng, Q.3
Shen, L.4
Turner, C.L.5
Steplock, D.6
Shenolikar, S.7
Cunningham, R.8
-
8
-
-
0032574725
-
Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities
-
Beck L, Karaplis AC, Amizuka N, Hewson AS, Ozawa H, Tenenhouse HS: Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities. Proc Natl Acad Sci U S A 95: 5372-5377, 1998
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 5372-5377
-
-
Beck, L.1
Karaplis, A.C.2
Amizuka, N.3
Hewson, A.S.4
Ozawa, H.5
Tenenhouse, H.S.6
-
9
-
-
0242497210
-
Differential effects of Npt2a gene ablation and X-linked Hyp mutation on renal expression of Npt2c
-
Tenenhouse HS, Martel J, Gauthier C, Segawa H, Miyamoto K: Differential effects of Npt2a gene ablation and X-linked Hyp mutation on renal expression of Npt2c. Am J Physiol Renal Physiol 285: F1281-F1278, 2003
-
(2003)
Am J Physiol Renal Physiol
, vol.285
-
-
Tenenhouse, H.S.1
Martel, J.2
Gauthier, C.3
Segawa, H.4
Miyamoto, K.5
-
10
-
-
0012311140
-
Renal calcification in mice homozygous for the disrupted type IIa Na/Pi cotransporter gene Npt2
-
Chau H, El-Maadawy S, McKee MD, Tenenhouse HS: Renal calcification in mice homozygous for the disrupted type IIa Na/Pi cotransporter gene Npt2. J Bone Miner Res 18: 6446-6457, 2003
-
(2003)
J Bone Miner Res
, vol.18
, pp. 6446-6457
-
-
Chau, H.1
El-Maadawy, S.2
McKee, M.D.3
Tenenhouse, H.S.4
-
11
-
-
0036448310
-
Novel phosphate-regulating genes in the pathogenesis of renal phosphate wasting disorders
-
Tenenhouse HS, Sabbagh Y: Novel phosphate-regulating genes in the pathogenesis of renal phosphate wasting disorders. Pflugers Arch 444: 317-326, 2002
-
(2002)
Pflugers Arch
, vol.444
, pp. 317-326
-
-
Tenenhouse, H.S.1
Sabbagh, Y.2
-
12
-
-
0022002364
-
Hereditary hypophosphatemic rickets with hypercalciuria
-
Tieder M, Modai D, Samuel R, Arie R, Halabe A, Bab I, Gabizon D, Liberman UA: Hereditary hypophosphatemic rickets with hypercalciuria. N Engl J Med 312: 611-617, 1985
-
(1985)
N Engl J Med
, vol.312
, pp. 611-617
-
-
Tieder, M.1
Modai, D.2
Samuel, R.3
Arie, R.4
Halabe, A.5
Bab, I.6
Gabizon, D.7
Liberman, U.A.8
-
13
-
-
0023127407
-
Idiopathic hypercalciuria and hereditary hypophosphatemic rickets: Two phenotypical expressions of a common genetic defect
-
Tieder M, Modai D, Shaked U, Samuel R, Arie R, Halabe A, Maor J, Weissgarten J, Averbukh Z, Cohen N: "Idiopathic" hypercalciuria and hereditary hypophosphatemic rickets: Two phenotypical expressions of a common genetic defect. N Engl J Med 316: 125-129, 1987
-
(1987)
N Engl J Med
, vol.316
, pp. 125-129
-
-
Tieder, M.1
Modai, D.2
Shaked, U.3
Samuel, R.4
Arie, R.5
Halabe, A.6
Maor, J.7
Weissgarten, J.8
Averbukh, Z.9
Cohen, N.10
-
14
-
-
0035126513
-
Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene
-
Jones A, Tzenova J, Frappier D, Crumley M, Roslin N, Kos C, Tieder M, Langman C, Proesmans W, Carpenter T, Rice A, Anderson D, Morgan K, Fujiwara T, Tenenhouse H: Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene. J Am Soc Nephrol 12: 507-514, 2001
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 507-514
-
-
Jones, A.1
Tzenova, J.2
Frappier, D.3
Crumley, M.4
Roslin, N.5
Kos, C.6
Tieder, M.7
Langman, C.8
Proesmans, W.9
Carpenter, T.10
Rice, A.11
Anderson, D.12
Morgan, K.13
Fujiwara, T.14
Tenenhouse, H.15
-
15
-
-
31544481921
-
SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis
-
Bergwitz C, Roslin NM, Tieder M, Loredo-Osti JC, Bastepe M, Abu-Zahra H, Frappier D, Burkett K, Carpenter TO, Anderson D, Garabedian M, Sermet I, Fujiwara TM, Morgan K, Tenenhouse HS, Juppner H: SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis. Am J Hum Genet 78: 179-192, 2006
-
(2006)
Am J Hum Genet
, vol.78
, pp. 179-192
-
-
Bergwitz, C.1
Roslin, N.M.2
Tieder, M.3
Loredo-Osti, J.C.4
Bastepe, M.5
Abu-Zahra, H.6
Frappier, D.7
Burkett, K.8
Carpenter, T.O.9
Anderson, D.10
Garabedian, M.11
Sermet, I.12
Fujiwara, T.M.13
Morgan, K.14
Tenenhouse, H.S.15
Juppner, H.16
-
16
-
-
31544460435
-
Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodiumphosphate cotransporter gene SLC34A3
-
Lorenz-Depiereux B, Benet-Pages A, Eckstein G, Tenenbaum-Rakover Y, Wagenstaller J, Tiosano D, Gershoni-Baruch R, Albers N, Lichtner P, Schnabel D, Hochberg Z, Strom TM: Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodiumphosphate cotransporter gene SLC34A3. Am J Hum Genet 78: 193-201, 2006
-
(2006)
Am J Hum Genet
, vol.78
, pp. 193-201
-
-
Lorenz-Depiereux, B.1
Benet-Pages, A.2
Eckstein, G.3
Tenenbaum-Rakover, Y.4
Wagenstaller, J.5
Tiosano, D.6
Gershoni-Baruch, R.7
Albers, N.8
Lichtner, P.9
Schnabel, D.10
Hochberg, Z.11
Strom, T.M.12
-
17
-
-
0042336008
-
Factor XII deficiency is strongly associated with primary recurrent abortions
-
Pauer HU, Burfeind P, Kostering H, Emons G, Hinney B: Factor XII deficiency is strongly associated with primary recurrent abortions. Fertil Steril 80: 590-594, 2003
-
(2003)
Fertil Steril
, vol.80
, pp. 590-594
-
-
Pauer, H.U.1
Burfeind, P.2
Kostering, H.3
Emons, G.4
Hinney, B.5
-
18
-
-
33745320535
-
Plasma levels of bradykinin are suppressed in factor XII-deficient mice
-
Iwaki T, Castellino FJ: Plasma levels of bradykinin are suppressed in factor XII-deficient mice. Thromb Haemost 95: 1003-1010, 2006
-
(2006)
Thromb Haemost
, vol.95
, pp. 1003-1010
-
-
Iwaki, T.1
Castellino, F.J.2
-
19
-
-
0037179681
-
Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter
-
Prie D, Huart V, Bakouh N, Planelles G, Dellis O, Gerard B, Hulin P, Benque-Blanchet F, Silve C, Grandchamp B, Friedlander G: Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter. N Engl J Med 347: 983-991, 2002
-
(2002)
N Engl J Med
, vol.347
, pp. 983-991
-
-
Prie, D.1
Huart, V.2
Bakouh, N.3
Planelles, G.4
Dellis, O.5
Gerard, B.6
Hulin, P.7
Benque-Blanchet, F.8
Silve, C.9
Grandchamp, B.10
Friedlander, G.11
-
20
-
-
0344442745
-
Functional characterization of two naturally occurring mutations in the human sodium-phosphate cotransporter type IIa
-
Virkki LV, Forster IC, Hernando N, Biber J, Murer H: Functional characterization of two naturally occurring mutations in the human sodium-phosphate cotransporter type IIa. J Bone Miner Res 18: 2135-2141, 2003
-
(2003)
J Bone Miner Res
, vol.18
, pp. 2135-2141
-
-
Virkki, L.V.1
Forster, I.C.2
Hernando, N.3
Biber, J.4
Murer, H.5
-
21
-
-
0025345577
-
Expression of renal transport systems for inorganic phosphate and sulfate in Xenopus laevis oocytes
-
Werner A, Biber J, Forgo J, Palacin M, Murer H: Expression of renal transport systems for inorganic phosphate and sulfate in Xenopus laevis oocytes. J Biol Chem 265: 12331-12336, 1990
-
(1990)
J Biol Chem
, vol.265
, pp. 12331-12336
-
-
Werner, A.1
Biber, J.2
Forgo, J.3
Palacin, M.4
Murer, H.5
-
22
-
-
0028181761
-
Cloning of a Na/Pi cotransporter from opossum kidney cells
-
Sorribas V, Markovich D, Hayes G, Stange G, Forgo J, Biber J, Murer H: Cloning of a Na/Pi cotransporter from opossum kidney cells. J Biol Chem 269: 6615-6621, 1994
-
(1994)
J Biol Chem
, vol.269
, pp. 6615-6621
-
-
Sorribas, V.1
Markovich, D.2
Hayes, G.3
Stange, G.4
Forgo, J.5
Biber, J.6
Murer, H.7
-
23
-
-
0034073493
-
Asymmetrical targeting of type II Na-P(i) cotransporters in renal and intestinal epithelial cell lines
-
Hernando N, Sheikh S, Karim-Jimenez Z, Galliker H, Forgo J, Biber J, Murer H: Asymmetrical targeting of type II Na-P(i) cotransporters in renal and intestinal epithelial cell lines. Am J Physiol Renal Physiol 278: F361-F368, 2000
-
(2000)
Am J Physiol Renal Physiol
, vol.278
-
-
Hernando, N.1
Sheikh, S.2
Karim-Jimenez, Z.3
Galliker, H.4
Forgo, J.5
Biber, J.6
Murer, H.7
-
24
-
-
0026658476
-
Altered protein folding may be the molecular basis of most cases of cystic fibrosis
-
Thomas PJ, Ko YH, Pedersen PL: Altered protein folding may be the molecular basis of most cases of cystic fibrosis. FEBS Lett 312: 7-9, 1992
-
(1992)
FEBS Lett
, vol.312
, pp. 7-9
-
-
Thomas, P.J.1
Ko, Y.H.2
Pedersen, P.L.3
-
25
-
-
0032867811
-
Processing of CFTR bearing the P574H mutation differs from wild-type and deltaF508-CFTR
-
Ostedgaard LS, Zeiher B, Welsh MJ: Processing of CFTR bearing the P574H mutation differs from wild-type and deltaF508-CFTR. J Cell Sci 112: 2091-2098, 1999
-
(1999)
J Cell Sci
, vol.112
, pp. 2091-2098
-
-
Ostedgaard, L.S.1
Zeiher, B.2
Welsh, M.J.3
-
26
-
-
0242577536
-
Unusually common cystic fibrosis mutation in Portugal encodes a misprocessed protein
-
Mendes F, Roxo-Rosa M, Dragomir A, Farinha CM, Roomans GM, Amaral MD, Penque D: Unusually common cystic fibrosis mutation in Portugal encodes a misprocessed protein. Biochem Biophys Res Commun 311: 665-671, 2003
-
(2003)
Biochem Biophys Res Commun
, vol.311
, pp. 665-671
-
-
Mendes, F.1
Roxo-Rosa, M.2
Dragomir, A.3
Farinha, C.M.4
Roomans, G.M.5
Amaral, M.D.6
Penque, D.7
-
27
-
-
0037160530
-
Genomic organization of profilin-III and evidence for a transcript expressed exclusively in testis
-
Braun A, Aszodi A, Hellebrand H, Berna A, Fassler R, Brandau O: Genomic organization of profilin-III and evidence for a transcript expressed exclusively in testis. Gene 283: 219-225, 2002
-
(2002)
Gene
, vol.283
, pp. 219-225
-
-
Braun, A.1
Aszodi, A.2
Hellebrand, H.3
Berna, A.4
Fassler, R.5
Brandau, O.6
-
28
-
-
0028938413
-
An improved PCR method for walking in uncloned genomic DNA
-
Siebert PD, Chenchik A, Kellogg DE, Lukyanov KA, Lukyanov SA: An improved PCR method for walking in uncloned genomic DNA. Nucleic Acids Res 23: 1087-1088, 1995
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 1087-1088
-
-
Siebert, P.D.1
Chenchik, A.2
Kellogg, D.E.3
Lukyanov, K.A.4
Lukyanov, S.A.5
-
29
-
-
0030775316
-
Mice lacking Factor VII develop normally but suffer fatal perinatal bleeding
-
Rosen E, Chan JC, Idusogie E, Clotman F, Vlasuk G, Luther T, Jalbert L, Albrecht S, Zhong L, Lissens A, Schoonjans L, Moons L, Collen D, Castellino FJ, Carmeliet P: Mice lacking Factor VII develop normally but suffer fatal perinatal bleeding. Nature 390: 290-294, 1997
-
(1997)
Nature
, vol.390
, pp. 290-294
-
-
Rosen, E.1
Chan, J.C.2
Idusogie, E.3
Clotman, F.4
Vlasuk, G.5
Luther, T.6
Jalbert, L.7
Albrecht, S.8
Zhong, L.9
Lissens, A.10
Schoonjans, L.11
Moons, L.12
Collen, D.13
Castellino, F.J.14
Carmeliet, P.15
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