-
1
-
-
0015030432
-
An inherited kidney disease of mice resembling human nephronophthisis
-
LYON MF, HULSE EV: An inherited kidney disease of mice resembling human nephronophthisis. J Med Genet 8:41-48, 1971
-
(1971)
J Med Genet
, vol.8
, pp. 41-48
-
-
Lyon, M.F.1
Hulse, E.V.2
-
2
-
-
0021684196
-
Spontaneous interstitial nephritis in kdkd mice. I. An experimental model of autoimmune renal disease
-
NEILSON EG, MCCAFFERTY E, FELDMAN A, et al: Spontaneous interstitial nephritis in kdkd mice. I. An experimental model of autoimmune renal disease. J Immunol 133:2560-2565, 1984
-
(1984)
J Immunol
, vol.133
, pp. 2560-2565
-
-
Neilson, E.G.1
McCafferty, E.2
Feldman, A.3
-
3
-
-
0030766553
-
Characterization of cellular infiltration and adhesion molecule expression in CBA/CaH-kdkd mice with tubulointerstitial renal disease
-
SIBALIC V, FAN X, WUTHRICH RP: Characterization of cellular infiltration and adhesion molecule expression in CBA/CaH-kdkd mice with tubulointerstitial renal disease. Histochem Cell Biol 108:235-242, 1997
-
(1997)
Histochem Cell Biol
, vol.108
, pp. 235-242
-
-
Sibalic, V.1
Fan, X.2
Wuthrich, R.P.3
-
4
-
-
0022645362
-
+ effector T cell that mediates destructive tubulointerstitial injury
-
+ effector T cell that mediates destructive tubulointerstitial injury. J Immunol 136:526-531, 1986
-
(1986)
J Immunol
, vol.136
, pp. 526-531
-
-
Kelly, C.J.1
Korngold, R.2
Mann, R.3
-
5
-
-
0033773184
-
Localization of the mouse kidney disease (kd) gene to a YAC/BAC contig on Chromosome 10
-
DELL KM, LI Y-X, PENG M, et al: Localization of the mouse kidney disease (kd) gene to a YAC/BAC contig on Chromosome 10. Mammalian Genome 11:967-971, 2000
-
(2000)
Mammalian Genome
, vol.11
, pp. 967-971
-
-
Dell, K.M.1
Li, Y.-X.2
Peng, M.3
-
6
-
-
0030868540
-
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1
-
HILDEBRANDT F, OTTO E, RENSING C, et al: A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1. Nat Genet 17:149-153, 1997
-
(1997)
Nat Genet
, vol.17
, pp. 149-153
-
-
Hildebrandt, F.1
Otto, E.2
Rensing, C.3
-
7
-
-
0032231645
-
A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping
-
HAIDER NB, CARMI R, SHALEV H, et al: A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping. Am J Hum Genet 63:1404-1410, 1998
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1404-1410
-
-
Haider, N.B.1
Carmi, R.2
Shalev, H.3
-
8
-
-
0033941201
-
Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree
-
OMRAN H, FERNANDEZ C, JUNG M, et al: Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree. Am J Hum Genet 66:118-127, 2000
-
(2000)
Am J Hum Genet
, vol.66
, pp. 118-127
-
-
Omran, H.1
Fernandez, C.2
Jung, M.3
-
9
-
-
0036842902
-
A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution
-
OTTO E, HOEFELE J, RUF R, et al: A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution. Am J Hum Genet 71:1161-1167, 2002
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1161-1167
-
-
Otto, E.1
Hoefele, J.2
Ruf, R.3
-
10
-
-
0041832375
-
Cutting edge: Multiple autoimmune pathways in kdkd mice
-
HANCOCK WW, TSAI T-L, MADAIO M, GASSER DL: Cutting edge: Multiple autoimmune pathways in kdkd mice. J Immunol 171:2778-2781, 2003
-
(2003)
J Immunol
, vol.171
, pp. 2778-2781
-
-
Hancock, W.W.1
Tsai, T.-L.2
Madaio, M.3
Gasser, D.L.4
-
11
-
-
0000424512
-
Electron microscopic immunocytochemical approaches to the localization of ligands, receptors, transducers, and transporters
-
edited by de Pablo F, Scanes CG, Weintraub BD, London, Academic Press
-
SMITH RM, JARETT L: Electron microscopic immunocytochemical approaches to the localization of ligands, receptors, transducers, and transporters, in Handbook of Endocrine Research Techniques, edited by de Pablo F, Scanes CG, Weintraub BD, London, Academic Press, 1993, pp 227-264
-
(1993)
Handbook of Endocrine Research Techniques
, pp. 227-264
-
-
Smith, R.M.1
Jarett, L.2
-
12
-
-
0025364138
-
Elucidation of the deficiency in two yeast coenzyme Q mutants
-
ASHBY MN, EDWARDS PA: Elucidation of the deficiency in two yeast coenzyme Q mutants. J Biol Chem 265: 13157-13164, 1990
-
(1990)
J Biol Chem
, vol.265
, pp. 13157-13164
-
-
Ashby, M.N.1
Edwards, P.A.2
-
13
-
-
0028216631
-
Branch-point reactions in the biosynthesis of cholesterol, dolichol, ubiquinone and prenylated proteins
-
GRUNLER J, ERICSSON J, DALLNER G: Branch-point reactions in the biosynthesis of cholesterol, dolichol, ubiquinone and prenylated proteins. Biochim Biophys Acta 1212: 259-277, 1994
-
(1994)
Biochim Biophys Acta
, vol.1212
, pp. 259-277
-
-
Grunler, J.1
Ericsson, J.2
Dallner, G.3
-
14
-
-
0028288510
-
Autoantigens targeted in systemic lupus erythematosus are clustered in two populations of surface structures on apoptotic keratinocytes
-
CASCIOLA-ROSEN LA, ANHALT G, ROSEN A: Autoantigens targeted in systemic lupus erythematosus are clustered in two populations of surface structures on apoptotic keratinocytes. J Exp Med 179:1317-1330, 1994
-
(1994)
J Exp Med
, vol.179
, pp. 1317-1330
-
-
Casciola-Rosen, L.A.1
Anhalt, G.2
Rosen, A.3
-
15
-
-
0019571083
-
Stoichiometry and coupling of active transport to oxidative metabolism in epithelial tissues
-
MANDEL LJ, BALABAN RS: Stoichiometry and coupling of active transport to oxidative metabolism in epithelial tissues. Am J Physiol 240:F357-F371, 1981
-
(1981)
Am J Physiol
, vol.240
-
-
Mandel, L.J.1
Balaban, R.S.2
-
16
-
-
0023612929
-
Oxygen and substrate dependence of hepatic cellular respiration: Sinusoidal oxygen gradient and effects of ethanol in isolated perfused liver and hepatocytes
-
KEKONEN EM, JAUHONEN VP, HASSINEN IE: Oxygen and substrate dependence of hepatic cellular respiration: Sinusoidal oxygen gradient and effects of ethanol in isolated perfused liver and hepatocytes. J Cell Physiol 133:119-126, 1987
-
(1987)
J Cell Physiol
, vol.133
, pp. 119-126
-
-
Kekonen, E.M.1
Jauhonen, V.P.2
Hassinen, I.E.3
-
17
-
-
0031849291
-
The role of phosphatidylserine in recognition of apoptotic cells by phagocytosis
-
FADOK VA, BRATTON DL, FRASCH SC, et al: The role of phosphatidylserine in recognition of apoptotic cells by phagocytosis. Cell Death Differ 5:551-562, 1998
-
(1998)
Cell Death Differ
, vol.5
, pp. 551-562
-
-
Fadok, V.A.1
Bratton, D.L.2
Frasch, S.C.3
-
18
-
-
0038823610
-
Regional loss of the mitochondrial membrane potential in the hepatocyte is rapidly followed by externalization of phosphatidylserines at that specific site during apoptosis
-
BLOM WM, DE BONT HJGM, NAGELKERKE JF: Regional loss of the mitochondrial membrane potential in the hepatocyte is rapidly followed by externalization of phosphatidylserines at that specific site during apoptosis. J Biol Chem 278:12467-12474, 2003
-
(2003)
J Biol Chem
, vol.278
, pp. 12467-12474
-
-
Blom, W.M.1
De Bont, H.J.G.M.2
Nagelkerke, J.F.3
-
19
-
-
0028258316
-
Mitochondrial DNA deletion: A cause of chronic tubulointerstitial nephropathy
-
SZABOLCS MJ, SEIGLE R, SHANSKE S, et al: Mitochondrial DNA deletion: A cause of chronic tubulointerstitial nephropathy. Kidney Int 45:1388-1396, 1994
-
(1994)
Kidney Int
, vol.45
, pp. 1388-1396
-
-
Szabolcs, M.J.1
Seigle, R.2
Shanske, S.3
-
20
-
-
0031000805
-
Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis
-
ZSURKA G, ORMOS J, IVANYI B, et al: Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis. Hum Genet 99:484-487, 1997
-
(1997)
Hum Genet
, vol.99
, pp. 484-487
-
-
Zsurka, G.1
Ormos, J.2
Ivanyi, B.3
|