-
1
-
-
84965236793
-
Hereditary familial congenital hemoragic nephritis
-
Alport AC (1927) Hereditary familial congenital hemoragic nephritis. BMJ 1:504-506
-
(1927)
BMJ
, vol.1
, pp. 504-506
-
-
Alport, A.C.1
-
3
-
-
0017207102
-
Experimenteller Beweis einer gemeinsamen Antigenizität zwischen Innenohr und Niere
-
Arnold W, Weidauer H, Seelig HP (1976) Experimenteller Beweis einer gemeinsamen Antigenizität zwischen Innenohr und Niere. Arch Otorhinolaryngol 212:99-117
-
(1976)
Arch Otorhinolaryngol
, vol.212
, pp. 99-117
-
-
Arnold, W.1
Weidauer, H.2
Seelig, H.P.3
-
4
-
-
0002204298
-
Alport syndrome
-
Schrier RW, Gotschalk CW (eds) Little Brown, Boston
-
Atkin CL, Gregory MC, Border WA (1988) Alport syndrome. In: Schrier RW, Gotschalk CW (eds) Diseases of the kidney. Little Brown, Boston, pp 617-641
-
(1988)
Diseases of the Kidney
, pp. 617-641
-
-
Atkin, C.L.1
Gregory, M.C.2
Border, W.A.3
-
6
-
-
0030047197
-
A gene resposible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23
-
Chaib H, Place C, Salem N, Chardenoux S, Vincent C, Weissenbach J, El-Zir E, Loiselt J, Petit CH (1996) A gene resposible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23. Hum Mol Genet 5:155-158
-
(1996)
Hum Mol Genet
, vol.5
, pp. 155-158
-
-
Chaib, H.1
Place, C.2
Salem, N.3
Chardenoux, S.4
Vincent, C.5
Weissenbach, J.6
El-Zir, E.7
Loiselt, J.8
Petit, C.H.9
-
7
-
-
0015132411
-
Isolation of collagen from basement membranes containing three identical a chains
-
Kafalides NA (1971) Isolation of collagen from basement membranes containing three identical a chains. Biochem Biophys Res Commun 45:226-234
-
(1971)
Biochem Biophys Res Commun
, vol.45
, pp. 226-234
-
-
Kafalides, N.A.1
-
8
-
-
0027431434
-
The human homolog of the glomerulosclerosis gene MPV17: Structure and genomic organization
-
Karasawa M, Zwacka RM, Reuter A, Fink T, Hsieh CL, Lichter O, Francke U, Weiher H (1993) The human homolog of the glomerulosclerosis gene MPV17: structure and genomic organization. Hum Mol Genet 11:1829-1834
-
(1993)
Hum Mol Genet
, vol.11
, pp. 1829-1834
-
-
Karasawa, M.1
Zwacka, R.M.2
Reuter, A.3
Fink, T.4
Hsieh, C.L.5
Lichter, O.6
Francke, U.7
Weiher, H.8
-
9
-
-
0028168648
-
Identification of mutations in the 3(IV) and 4(IV) collagen genes in autosomal recessive Alport syndrome
-
Mochizuki T, Lemmink HH, Mariyama M, Antignac C, Gubler MC, Pirson Y, Verellen-Dumoulin C, Chan B, Schröder CH, Smeets HJ, Reeders ST (1994) Identification of mutations in the (3(IV) and (4(IV) collagen genes in autosomal recessive Alport syndrome. Nat Genet 8:77-82
-
(1994)
Nat Genet
, vol.8
, pp. 77-82
-
-
Mochizuki, T.1
Lemmink, H.H.2
Mariyama, M.3
Antignac, C.4
Gubler, M.C.5
Pirson, Y.6
Verellen-Dumoulin, C.7
Chan, B.8
Schröder, C.H.9
Smeets, H.J.10
Reeders, S.T.11
-
10
-
-
0015898757
-
The relationship between cochlea and kidney
-
Quick CA, Fish A, Brown C (1973) The relationship between cochlea and kidney. Laryngoscope 83:1469-1482
-
(1973)
Laryngoscope
, vol.83
, pp. 1469-1482
-
-
Quick, C.A.1
Fish, A.2
Brown, C.3
-
11
-
-
0029006543
-
Functional rescue of the glomerulosclerosis phenotype in Mpv17 mice by transgenesis with the human Mpv17 homologue
-
Schenkel J, Zwacka RM, Rutenberg CH, Reuter A, Waldherr R, Weiher H (1995) Functional rescue of the glomerulosclerosis phenotype in Mpv17 mice by transgenesis with the human Mpv17 homologue. Kidney Int 48:80-84
-
(1995)
Kidney Int
, vol.48
, pp. 80-84
-
-
Schenkel, J.1
Zwacka, R.M.2
Rutenberg, C.H.3
Reuter, A.4
Waldherr, R.5
Weiher, H.6
-
12
-
-
0023196349
-
Pigment anomaly associated inner ear deafness
-
Stockh
-
Schrott A, Spoendlin H (1987) Pigment anomaly associated inner ear deafness. Acta Otolaryngol (Stockh) 103:451-457
-
(1987)
Acta Otolaryngol
, vol.103
, pp. 451-457
-
-
Schrott, A.1
Spoendlin, H.2
-
14
-
-
0024314157
-
Another role for melanocytes: Their importance for normal stria vascularis development in the mammalian inner ear
-
Steel KP, Barkway C (1989) Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear. Development 107:453-463
-
(1989)
Development
, vol.107
, pp. 453-463
-
-
Steel, K.P.1
Barkway, C.2
-
16
-
-
0023186403
-
Striai dysfunction in mice with cochleo-saccular abnormalities
-
Steel KP, Barkway C, Bock GR (1987) Striai dysfunction in mice with cochleo-saccular abnormalities. Hear Res 27:11-26
-
(1987)
Hear Res
, vol.27
, pp. 11-26
-
-
Steel, K.P.1
Barkway, C.2
Bock, G.R.3
-
17
-
-
0026700424
-
Localization of type IV collagen and laminin in the guinea pig inner ear
-
Tokahashi M, Hokunan K (1992) Localization of type IV collagen and laminin in the guinea pig inner ear. Ann Otol Rhinol Laryngol 191:58-62
-
(1992)
Ann Otol Rhinol Laryngol
, vol.191
, pp. 58-62
-
-
Tokahashi, M.1
Hokunan, K.2
-
19
-
-
0021858397
-
The spiral ganglion and cochlear nuclei of deafness mice
-
Webster DB (1985) The spiral ganglion and cochlear nuclei of deafness mice. Hear Res 18:19-27
-
(1985)
Hear Res
, vol.18
, pp. 19-27
-
-
Webster, D.B.1
-
20
-
-
0017227724
-
Strukturelle Veränderungen am Hörorgan beim Alport Syndrom
-
Weidauer H, Arnold W (1976) Strukturelle Veränderungen am Hörorgan beim Alport Syndrom. Z Laryngol Rhinol Otol 55: 6-16
-
(1976)
Z Laryngol Rhinol Otol
, vol.55
, pp. 6-16
-
-
Weidauer, H.1
Arnold, W.2
-
21
-
-
0027349159
-
The glomerulosclerosis in transgenic mice: The gene and its human homoloque
-
Grünfeld JP, Bach JF, Kreis H, Maxwell MH (eds) Mosby Year Book, St. Louis
-
Weiher H (1993) The glomerulosclerosis in transgenic mice: the gene and its human homoloque. In: Grünfeld JP, Bach JF, Kreis H, Maxwell MH (eds) Advances in nephrology, vol 22. Mosby Year Book, St. Louis, pp 37-42
-
(1993)
Advances in Nephrology
, vol.22
, pp. 37-42
-
-
Weiher, H.1
-
22
-
-
0025091459
-
Transgenic mouse model of kidney disease: Insertional inactivation of ubiquitously expressed gene leads to nephrotic syndrome
-
Weiher H, Noda T, Gray DA, Sharpe AH, Jeanisch R (1990) Transgenic mouse model of kidney disease: insertional inactivation of ubiquitously expressed gene leads to nephrotic syndrome. Cell 62:425-434
-
(1990)
Cell
, vol.62
, pp. 425-434
-
-
Weiher, H.1
Noda, T.2
Gray, D.A.3
Sharpe, A.H.4
Jeanisch, R.5
-
23
-
-
0028117114
-
The glomerulosclerosis gene Mpv17 encodes a peroxisomal protein producing reactive oxygen species
-
Zwacka R, Reuter A, Pfaff E, Moll J, Gorgas K, Karasawa M, Weiher H (1994) The glomerulosclerosis gene Mpv17 encodes a peroxisomal protein producing reactive oxygen species. EMBO J 13:5129-5134
-
(1994)
EMBO J
, vol.13
, pp. 5129-5134
-
-
Zwacka, R.1
Reuter, A.2
Pfaff, E.3
Moll, J.4
Gorgas, K.5
Karasawa, M.6
Weiher, H.7
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