-
1
-
-
0001379637
-
The inheritance of nephronophthisis
-
Spitzer A, Avner E, eds. Kluwer Academic Publishers. Boston
-
Kleinknecht C. The inheritance of nephronophthisis. In: Spitzer A, Avner E, eds. Inheritance of Kidney and Urinary Tract Diseases. Kluwer Academic Publishers. Boston: 1989: 277-294
-
(1989)
Inheritance of Kidney and Urinary Tract Diseases
, pp. 277-294
-
-
Kleinknecht, C.1
-
2
-
-
77049339267
-
Die familiäre juvenile Nephronophthise
-
Fanconi G, Hanhart E, Albertini A, Uhlinger E, Dolivo G, Prader A. Die familiäre juvenile Nephronophthise. Helv Paediatr Acta 1951; 6: 1-49
-
(1951)
Helv Paediatr Acta
, vol.6
, pp. 1-49
-
-
Fanconi, G.1
Hanhart, E.2
Albertini, A.3
Uhlinger, E.4
Dolivo, G.5
Prader, A.6
-
3
-
-
0031055335
-
Molecular genetic identification of families with juvenile nephronophthisis type 1: Rate of progression to renal failure
-
Hildebrandt F, Strahm B, Nothwang HG et al. Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. Kidney Int 1997; 51: 261-269
-
(1997)
Kidney int
, vol.51
, pp. 261-269
-
-
Hildebrandt, F.1
Strahm, B.2
Nothwang, H.G.3
-
4
-
-
0020062324
-
The nephronophthisis complex. A clinicopathologic study in children
-
Pathol Anat
-
Waldherr R, Lennert T, Weber HP, Fodisch HJ, Schärer K. The nephronophthisis complex. A clinicopathologic study in children. Virchows Arch [Pathol Anat] 1982; 394: 235-254
-
(1982)
Virchows Arch
, vol.394
, pp. 235-254
-
-
Waldherr, R.1
Lennert, T.2
Weber, H.P.3
Fodisch, H.J.4
Schärer, K.5
-
5
-
-
0027402309
-
A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p
-
Antignac C, Arduy CH, Beckmann JS et al. A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p. Nature Genet 1993; 3: 342-345
-
(1993)
Nature Genet
, vol.3
, pp. 342-345
-
-
Antignac, C.1
Arduy, C.H.2
Beckmann, J.S.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. Nature Genet 1997; 17: 149-153
-
(1997)
Nature Genet
, vol.17
, pp. 149-153
-
-
Hildebrandt, F.1
Otto, E.2
Rensing, C.3
-
7
-
-
9044227270
-
Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis
-
Konrad M, Saunier S, Heidet L et al. Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis. Hum Mol Genet 1996; 5: 367-371
-
(1996)
Hum Mol Genet
, vol.5
, pp. 367-371
-
-
Konrad, M.1
Saunier, S.2
Heidet, L.3
-
8
-
-
0029925360
-
Mice lacking angiotensin-converting enzyme have low blood pressure, renal pathology, and reduced male fertility
-
Esther CRJ, Howard TE, Marino EM, Goddard JM, Capecchi MR, Bernstein KE. Mice lacking angiotensin-converting enzyme have low blood pressure, renal pathology, and reduced male fertility. Lab Invest 1996; 74: 953-965
-
(1996)
Lab Invest
, vol.74
, pp. 953-965
-
-
Esther, C.R.J.1
Howard, T.E.2
Marino, E.M.3
Goddard, J.M.4
Capecchi, M.R.5
Bernstein, K.E.6
-
10
-
-
0029060861
-
Male-female differences in fertility and blood pressure in ACE-deficient mice
-
Krege JH, John SW, Langenbach LL et al. Male-female differences in fertility and blood pressure in ACE-deficient mice. Nature 1995; 375: 146-148
-
(1995)
Nature
, vol.375
, pp. 146-148
-
-
Krege, J.H.1
John, S.W.2
Langenbach, L.L.3
-
11
-
-
0027427492
-
Bcl-2 deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair
-
Veis DJ, Sorenson CM, Shutter JR, Korsmeyer SJ. Bcl-2 deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair. Cell 1993; 75: 229-240
-
(1993)
Cell
, vol.75
, pp. 229-240
-
-
Veis, D.J.1
Sorenson, C.M.2
Shutter, J.R.3
Korsmeyer, S.J.4
-
13
-
-
0017571342
-
Possibility of EB virus preferentially transforming a subpopulation of human B lymphocytes
-
Steel CM, Philipson J, Arthur E, Gardiner SE, Newton MS, McIntosh RV. Possibility of EB virus preferentially transforming a subpopulation of human B lymphocytes. Nature 1977; 270: 729-731
-
(1977)
Nature
, vol.270
, pp. 729-731
-
-
Steel, C.M.1
Philipson, J.2
Arthur, E.3
Gardiner, S.E.4
Newton, M.S.5
McIntosh, R.V.6
-
14
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites [see comments]. Nature 1996; 380: 152-154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
-
15
-
-
0026849428
-
Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension
-
Jeunemaitre X, Lifton RP, Hunt SC, Williams RR, Lalouel JM. Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension. Nature Genet 1992; 1: 72-75
-
(1992)
Nature Genet
, vol.1
, pp. 72-75
-
-
Jeunemaitre, X.1
Lifton, R.P.2
Hunt, S.C.3
Williams, R.R.4
Lalouel, J.M.5
-
17
-
-
0027143906
-
LODVIEW: A computer program for the graphical evaluation of lod score results in exclusion mapping of human disease genes
-
Hildebrandt F, Pohlmann A, Omran H. LODVIEW: a computer program for the graphical evaluation of lod score results in exclusion mapping of human disease genes. Comput Biomed Res 1993; 26: 592-599
-
(1993)
Comput Biomed Res
, vol.26
, pp. 592-599
-
-
Hildebrandt, F.1
Pohlmann, A.2
Omran, H.3
-
18
-
-
0015367003
-
Red and blonde hair in renal medullary cystic disease
-
Rayfield EJ, McDonald FD. Red and blonde hair in renal medullary cystic disease. Arch Intern Med 1972; 130: 72-75
-
(1972)
Arch Intern Med
, vol.130
, pp. 72-75
-
-
Rayfield, E.J.1
McDonald, F.D.2
-
19
-
-
0031800503
-
Identification of a gene for nephronophthisis
-
Hildebrandt F. Identification of a gene for nephronophthisis. Nephrol Dial Transplant 1998; 13: 1334-1336
-
(1998)
Nephrol Dial Transplant
, vol.13
, pp. 1334-1336
-
-
Hildebrandt, F.1
|