-
1
-
-
0000275805
-
The influence of the metabolism of human erythrocytes on their potassium content
-
Harris JE: The influence of the metabolism of human erythrocytes on their potassium content. J Biol Chem 1941;141:579-595.
-
(1941)
J Biol Chem
, vol.141
, pp. 579-595
-
-
Harris, J.E.1
-
2
-
-
0029794875
-
+ channel, ROMK
-
+ channel, ROMK. Nat Genet 1996;14:152-156.
-
(1996)
Nat Genet
, vol.14
, pp. 152-156
-
-
Simon, D.B.1
Karet, F.E.2
Rodriguez-Soriano, J.3
Hamdan, J.H.4
DiPietro, A.5
Trachtman, H.6
Sanjad, S.A.7
Lifton, R.P.8
-
3
-
-
13144262840
-
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis
-
Karet FE, Gainza FJ, Gyory AZ, Unwin RJ, Wrong O, Tanner MJ, Nayir A, Alpay H, Santos F, Hulton SA, Bakkaloglu A, Ozen S, Cunningham MJ, di Pietro A, Walker WG, Lifton RP: Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis. Proc Natl Acad Sci USA 1998;95:6337-6342.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 6337-6342
-
-
Karet, F.E.1
Gainza, F.J.2
Gyory, A.Z.3
Unwin, R.J.4
Wrong, O.5
Tanner, M.J.6
Nayir, A.7
Alpay, H.8
Santos, F.9
Hulton, S.A.10
Bakkaloglu, A.11
Ozen, S.12
Cunningham, M.J.13
Di Pietro, A.14
Walker, W.G.15
Lifton, R.P.16
-
4
-
-
0033512935
-
The hereditary stomatocytoses and allied disorders: Congenital disorders of erythrocyte membrane permeability to Na and K
-
Stewart GW, Turner EJ: The hereditary stomatocytoses and allied disorders: congenital disorders of erythrocyte membrane permeability to Na and K. Baillière's Best Pract Res Clinical Haematol 1999;12:707-728.
-
(1999)
Baillière's Best Pract Res Clinical Haematol
, vol.12
, pp. 707-728
-
-
Stewart, G.W.1
Turner, E.J.2
-
5
-
-
85088671385
-
Xerocytosis with concomitant intrauterine ascites: First description and therapeutic approach
-
Entazami M, Becker R, Mensen H, Marcinkowki M, Versmold H: Xerocytosis with concomitant intrauterine ascites: First description and therapeutic approach. Blood 1996;90:5392-5393.
-
(1996)
Blood
, vol.90
, pp. 5392-5393
-
-
Entazami, M.1
Becker, R.2
Mensen, H.3
Marcinkowki, M.4
Versmold, H.5
-
6
-
-
0345272099
-
ATP-dependent vesiculation in red cell membranes from different hereditary stomatocytosis variants
-
in press
-
Turner EJ, Jarvis HJ, Chetty MC, Landau G, Ho MM, Stewart GW: ATP-dependent vesiculation in red cell membranes from different hereditary stomatocytosis variants. Br J Haematol 2002; in press.
-
(2002)
Br J Haematol
-
-
Turner, E.J.1
Jarvis, H.J.2
Chetty, M.C.3
Landau, G.4
Ho, M.M.5
Stewart, G.W.6
-
7
-
-
0020465211
-
Missing band 7 membrane protein in two patients with high Na, low K erythrocytes
-
Lande WM, Thiemann PW, Mentzer WM: Missing band 7 membrane protein in two patients with high Na, low K erythrocytes. J Clin Invest 1982;70:1273-1280.
-
(1982)
J Clin Invest
, vol.70
, pp. 1273-1280
-
-
Lande, W.M.1
Thiemann, P.W.2
Mentzer, W.M.3
-
8
-
-
0345703625
-
The 'stomatin' gene and protein in overhydrated hereditary stomatocytosis
-
submitted
-
Fricke B, Argent A, Pizzey A, Chetty M, Ho M, Iolascon A, Düring M von, Stewart G: The 'stomatin' gene and protein in overhydrated hereditary stomatocytosis. Blood 2002; submitted.
-
(2002)
Blood
-
-
Fricke, B.1
Argent, A.2
Pizzey, A.3
Chetty, M.4
Ho, M.5
Iolascon, A.6
Von Düring, M.7
Stewart, G.8
-
9
-
-
0032231446
-
Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): Mapping of locus to chromosome 16 (q23-qter)
-
Carella M, Stewart GW, Ajetunmobi JF, Perrotta S, Grootenboer S, Tchernia G, Delaunay J, Totaro A, Zelante L, Gasparini P, Iolascon A: Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): Mapping of locus to chromosome 16 (q23-qter). Am J Hum Genet 1998;63:810-816.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 810-816
-
-
Carella, M.1
Stewart, G.W.2
Ajetunmobi, J.F.3
Perrotta, S.4
Grootenboer, S.5
Tchernia, G.6
Delaunay, J.7
Totaro, A.8
Zelante, L.9
Gasparini, P.10
Iolascon, A.11
-
10
-
-
0033121167
-
Stomatocytosis is absent in 'stomatin'-deficient murine red blood cells
-
Zhu Y, Paszty C, Turetsky T, Tsai S, Kuypers FA, Lee G, Cooper P, Gallagher PG, Stevens ME, Rubin E, Mohandas N, Mentzer WC: Stomatocytosis is absent in 'stomatin'-deficient murine red blood cells. Blood 1999;93:2404-2410.
-
(1999)
Blood
, vol.93
, pp. 2404-2410
-
-
Zhu, Y.1
Paszty, C.2
Turetsky, T.3
Tsai, S.4
Kuypers, F.A.5
Lee, G.6
Cooper, P.7
Gallagher, P.G.8
Stevens, M.E.9
Rubin, E.10
Mohandas, N.11
Mentzer, W.C.12
-
11
-
-
0028839194
-
A stomatin-like protein necessary for mechanosensation in C. elegans
-
Huang M, Gu G, Ferguson E, Chalfie M: A stomatin-like protein necessary for mechanosensation in C. elegans. Nature 1995;378:292-295.
-
(1995)
Nature
, vol.378
, pp. 292-295
-
-
Huang, M.1
Gu, G.2
Ferguson, E.3
Chalfie, M.4
-
12
-
-
0037186523
-
MEC-2 regulates C. elegans DEG/ENaC channels needed for mechanosensation
-
Goodman MB, Ernstrom GG, Chelur DS, O'Hagan R, Yao CA, Chalfie M: MEC-2 regulates C. elegans DEG/ENaC channels needed for mechanosensation. Nature 2002;415:1039-1042.
-
(2002)
Nature
, vol.415
, pp. 1039-1042
-
-
Goodman, M.B.1
Ernstrom, G.G.2
Chelur, D.S.3
O'Hagan, R.4
Yao, C.A.5
Chalfie, M.6
-
13
-
-
0032708149
-
Association of stomatin with lipid-protein complexes in the plasma membrane and the endocytic compartment
-
Snyers L, Umlauf E, Prohaska R: Association of stomatin with lipid-protein complexes in the plasma membrane and the endocytic compartment. Eur J Cell Biol 1999;78:802-812.
-
(1999)
Eur J Cell Biol
, vol.78
, pp. 802-812
-
-
Snyers, L.1
Umlauf, E.2
Prohaska, R.3
-
14
-
-
0037072733
-
Endogenously expressed epithelial sodium channel is present in lipid rafts in A6 cells
-
Hill WG, An B, Johnson JP: Endogenously expressed epithelial sodium channel is present in lipid rafts in A6 cells. J Biol Chem 2002;277:33541-33544.
-
(2002)
J Biol Chem
, vol.277
, pp. 33541-33544
-
-
Hill, W.G.1
An, B.2
Johnson, J.P.3
-
16
-
-
0034034757
-
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
-
Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C: NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet 2000;24:349-354.
-
(2000)
Nat Genet
, vol.24
, pp. 349-354
-
-
Boute, N.1
Gribouval, O.2
Roselli, S.3
Benessy, F.4
Lee, H.5
Fuchshuber, A.6
Dahan, K.7
Gubler, M.C.8
Niaudet, P.9
Antignac, C.10
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