-
1
-
-
0000786264
-
Gonadoblastoma associated with pure gonadal dysgenesis in monozygotic twins
-
Frasier S, Bashore R, Mosllur H: Gonadoblastoma associated with pure gonadal dysgenesis in monozygotic twins. J Pediatr 64: 740-745, 1964
-
(1964)
J Pediatr
, vol.64
, pp. 740-745
-
-
Frasier, S.1
Bashore, R.2
Mosllur, H.3
-
2
-
-
16944365351
-
Donor splice-site mutations in WT1 are responsible for Frasier syndrome
-
Barbaux S, Niaudet P, Gubler M-C, Grunfeld J-P, Jaubert F, Kuttenn F, Fekete CN, Souleyreau-Therville N, Thibauld E, Fellous M, McElreavey K: Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Nat Genet 17: 467-470, 1997
-
(1997)
Nat Genet
, vol.17
, pp. 467-470
-
-
Barbaux, S.1
Niaudet, P.2
Gubler, M.-C.3
Grunfeld, J.-P.4
Jaubert, F.5
Kuttenn, F.6
Fekete, C.N.7
Souleyreau-Therville, N.8
Thibauld, E.9
Fellous, M.10
McElreavey, K.11
-
3
-
-
0029941043
-
The WT1 Wilms' tumor suppressor gene: How much do we really know?
-
Reddy J, Licht J: The WT1 Wilms' tumor suppressor gene: How much do we really know? Biochem Biophys Acta 1287: 1-28, 1996
-
(1996)
Biochem Biophys Acta
, vol.1287
, pp. 1-28
-
-
Reddy, J.1
Licht, J.2
-
4
-
-
0031922880
-
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms
-
Klamt B, Koziell A, Poulat F, Wieacker P, Scambler P, Berta P, Gessler M: Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms. Hum Mol Genet 7: 709-714, 1998
-
(1998)
Hum Mol Genet
, vol.7
, pp. 709-714
-
-
Klamt, B.1
Koziell, A.2
Poulat, F.3
Wieacker, P.4
Scambler, P.5
Berta, P.6
Gessler, M.7
-
5
-
-
0032921040
-
WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis
-
Yang Y, Jeanpierre C, Dressler G, Lacoste M, Niaudet P, Gubler M-C: WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis. Am J Pathol 154: 181-192, 1999
-
(1999)
Am J Pathol
, vol.154
, pp. 181-192
-
-
Yang, Y.1
Jeanpierre, C.2
Dressler, G.3
Lacoste, M.4
Niaudet, P.5
Gubler, M.-C.6
-
6
-
-
0014775569
-
A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease
-
Drash A, Sherman F, Hartmann W, Blizzard R: A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease. J Pediatr 76: 585-593, 1970
-
(1970)
J Pediatr
, vol.76
, pp. 585-593
-
-
Drash, A.1
Sherman, F.2
Hartmann, W.3
Blizzard, R.4
-
7
-
-
0026094584
-
Germ-line mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
-
Pelletier J, Bruening W, Kashtan C, Mauer S, Manivel J, Striegel J, Houghton D, Junien C, Habib R, Fouser L, Fine R, Silverman B, Haber D, Housman D: Germ-line mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 67: 437-447, 1991
-
(1991)
Cell
, vol.67
, pp. 437-447
-
-
Pelletier, J.1
Bruening, W.2
Kashtan, C.3
Mauer, S.4
Manivel, J.5
Striegel, J.6
Houghton, D.7
Junien, C.8
Habib, R.9
Fouser, L.10
Fine, R.11
Silverman, B.12
Haber, D.13
Housman, D.14
-
8
-
-
0026906620
-
Dominant negative mutations in the Wilms' tumour (WT1) gene cause Denys-Drash syndrome - Proof that a tumour-suppressor gene plays a crucial role in normal genitourinary development
-
Hastie N: Dominant negative mutations in the Wilms' tumour (WT1) gene cause Denys-Drash syndrome - proof that a tumour-suppressor gene plays a crucial role in normal genitourinary development. Hum Mol Genet 1: 293-295, 1992
-
(1992)
Hum Mol Genet
, vol.1
, pp. 293-295
-
-
Hastie, N.1
-
9
-
-
0018668497
-
Aniridia-Wilms' tumor association: Evidence for specific deletion of 11p13
-
Francke U, Holmes L, Atkins L, Riccardi V: Aniridia-Wilms' tumor association: Evidence for specific deletion of 11p13. Cytogenet Cell Genet 24: 185-192, 1978
-
(1978)
Cytogenet Cell Genet
, vol.24
, pp. 185-192
-
-
Francke, U.1
Holmes, L.2
Atkins, L.3
Riccardi, V.4
-
10
-
-
0032913826
-
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor
-
Barbosa A, Hadjiathanasiou C, Theodoridis C, Papathanasiou A, Tar A, Merksz M, Gyorvari B, Sultan C, Dumas R, Jaubert F, Niaudet P, Moreira-Filho C, Cotinot C, Fellous M: The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor. Hum Mutat 13: 146-153, 1999
-
(1999)
Hum Mutat
, vol.13
, pp. 146-153
-
-
Barbosa, A.1
Hadjiathanasiou, C.2
Theodoridis, C.3
Papathanasiou, A.4
Tar, A.5
Merksz, M.6
Gyorvari, B.7
Sultan, C.8
Dumas, R.9
Jaubert, F.10
Niaudet, P.11
Moreira-Filho, C.12
Cotinot, C.13
Fellous, M.14
-
11
-
-
0027182741
-
WT-1 is required for early kidney development
-
Kriedberg J, Sariola H, Loring J, Maeda M, Pelletier J, Housman D, Jaenisch R: WT-1 is required for early kidney development. Cell 74: 679-691, 1993
-
(1993)
Cell
, vol.74
, pp. 679-691
-
-
Kriedberg, J.1
Sariola, H.2
Loring, J.3
Maeda, M.4
Pelletier, J.5
Housman, D.6
Jaenisch, R.7
-
12
-
-
0032076964
-
Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression
-
Nachtigal M, Hirokawa Y, Enyeart-VanHouten D, Flanagan J, Hammer G, Ingraham H: Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression. Cell 93: 445-454, 1998
-
(1998)
Cell
, vol.93
, pp. 445-454
-
-
Nachtigal, M.1
Hirokawa, Y.2
Enyeart-VanHouten, D.3
Flanagan, J.4
Hammer, G.5
Ingraham, H.6
-
13
-
-
0032990419
-
A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans
-
Achermann J, Ito M, Ito M, Hindmarsh P, Jameson J: A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans. Nat Genet 22: 125-126, 1999
-
(1999)
Nat Genet
, vol.22
, pp. 125-126
-
-
Achermann, J.1
Ito, M.2
Ito, M.3
Hindmarsh, P.4
Jameson, J.5
-
14
-
-
0031796372
-
Role of Ahch in gonadal development and gametogenesis
-
Yu R, Saunders T, Camper S, Jameson J: Role of Ahch in gonadal development and gametogenesis. Nat Genet 20: 353-357, 1998
-
(1998)
Nat Genet
, vol.20
, pp. 353-357
-
-
Yu, R.1
Saunders, T.2
Camper, S.3
Jameson, J.4
-
15
-
-
0029654207
-
Xp duplications and sex reversal
-
Zanaria E, Bardoni B, Dabovic B, Calvari V, Fraccaro M, Zuffardi O, Camerino G: Xp duplications and sex reversal, Philosophical Transactions of the Royal Society of London - Series B, Biological Sciences 350: 291-296, 1995
-
(1995)
Philosophical Transactions of the Royal Society of London - Series B, Biological Sciences
, vol.350
, pp. 291-296
-
-
Zanaria, E.1
Bardoni, B.2
Dabovic, B.3
Calvari, V.4
Fraccaro, M.5
Zuffardi, O.6
Camerino, G.7
-
16
-
-
0029583243
-
The genetic basis of murine and human sex determination: A review
-
McElreavey K, Barbaux S, Ion A, Fellous M: The genetic basis of murine and human sex determination: A review. Heredity 75: 599-611, 1995
-
(1995)
Heredity
, vol.75
, pp. 599-611
-
-
McElreavey, K.1
Barbaux, S.2
Ion, A.3
Fellous, M.4
-
17
-
-
0032981181
-
The Wilms' tumor suppressor gene (wt1) product regulates Dax-1 gene expression during gonadal differentiation
-
Kim J, Prawitt D, Bardeesy N, Torban E, Vicaner C, Goodyer P, Zabel B, Pelletier J: The Wilms' tumor suppressor gene (wt1) product regulates Dax-1 gene expression during gonadal differentiation. Mol Cell Biol 19: 2289-2299, 1999
-
(1999)
Mol Cell Biol
, vol.19
, pp. 2289-2299
-
-
Kim, J.1
Prawitt, D.2
Bardeesy, N.3
Torban, E.4
Vicaner, C.5
Goodyer, P.6
Zabel, B.7
Pelletier, J.8
|