-
1
-
-
33745777086
-
Clinical impact and biological basis of kidney malformations
-
Woolf AS. Clinical impact and biological basis of kidney malformations. Semin Nephrol 1995; 15: 561-72
-
(1995)
Semin Nephrol
, vol.15
, pp. 561-572
-
-
Woolf, A.S.1
-
4
-
-
0014132760
-
Mechanisms of organotypic tissue interactions
-
Grobstein C. Mechanisms of organotypic tissue interactions. Nat Cancer Inst Monog 1967: 26: 279-99
-
(1967)
Nat Cancer Inst Monog
, vol.26
, pp. 279-299
-
-
Grobstein, C.1
-
7
-
-
0028073019
-
Lohnes D. Decimo D et al. Function of the retinoic acid receptors (RAR) during development
-
Mendelsohn C. Lohnes D. Decimo D et al. Function of the retinoic acid receptors (RAR) during development. Development 1994: 120: 2749-71
-
(1994)
Development
, vol.120
, pp. 2749-2771
-
-
Mendelsohn, C.1
-
10
-
-
0029071508
-
Charlieu J-P. Miyagawa K et al. Subnuclear localisation of WT1 in splicing of transcription factor domains is regulated by alternative splicing
-
Larsson SH. Charlieu J-P. Miyagawa K et al. Subnuclear localisation of WT1 in splicing of transcription factor domains is regulated by alternative splicing. Cell 1995: 81: 391-401
-
(1995)
Cell
, vol.81
, pp. 391-401
-
-
Larsson, S.H.1
-
11
-
-
0027182741
-
Loring JM et al. WT-1 is required for early kidney development
-
Kreidberg JA, Sariola H. Loring JM et al. WT-1 is required for early kidney development. Cell 1991: 74: 679-91
-
(1991)
Cell
, vol.74
, pp. 679-691
-
-
Kreidberg, J.A.1
Sariola, H.2
-
14
-
-
0027477275
-
Wilkinson JE. Rothenpieler UW. Patterson LT. Williams-Simons L, Westphal H. Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities
-
Dressler GR. Wilkinson JE. Rothenpieler UW. Patterson LT. Williams-Simons L, Westphal H. Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities. Nature 1993; 362: 65-7
-
(1993)
Nature
, vol.362
, pp. 65-67
-
-
Dressler, G.R.1
-
15
-
-
0029901727
-
Renal agenesis and the absence of enteric neurones in mice lacking GDNF
-
Sanchez MP, Silos-Santiago I, Frisen J, He B, Lira SA, Barbacid M. Renal agenesis and the absence of enteric neurones in mice lacking GDNF. Nature 1996; 382: 70-3
-
(1996)
Nature
, vol.382
, pp. 70-73
-
-
Sanchez, M.P.1
Silos-Santiago, I.2
Frisen, J.3
He, B.4
Lira, S.A.5
Barbacid, M.6
-
16
-
-
0028174023
-
Defects in kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
-
Schuchardt A, D'Agati V, Larsson-Blomberg L, Costantini F, Pachnis V. Defects in kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 1994; 367: 381-5
-
(1994)
Nature
, vol.367
, pp. 381-385
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson-Blomberg, L.3
Costantini, F.4
Pachnis, V.5
-
17
-
-
0028798286
-
Roles of hepatocyte growth factor/scatter factor (HGF/SF) and the met receptor in early development of the metanephros
-
Woolf AS, Kolatsi-Joannou M, Hardman P et al. Roles of hepatocyte growth factor/scatter factor (HGF/SF) and the met receptor in early development of the metanephros. J Cell Biol 1995: 128: 171-84
-
(1995)
J Cell Biol
, vol.128
, pp. 171-184
-
-
Woolf, A.S.1
Kolatsi-Joannou, M.2
Hardman, P.3
-
19
-
-
0029075612
-
Basic flbroblast growth factor can mediate the early inductive events in renal development
-
Perantoni AO, Dove LF, Karavanova I. Basic flbroblast growth factor can mediate the early inductive events in renal development. Proc Natl Acad Sei USA 1995: 92: 4696-700
-
(1995)
Proc Natl Acad Sei USA
, vol.92
, pp. 4696-4700
-
-
Perantoni, A.O.1
Dove, L.F.2
Karavanova, I.3
-
20
-
-
0028588919
-
Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4
-
Stark K, Vainio S, Vassileva G, McMahon AP. Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4. Nature 1994; 372: 679-83
-
(1994)
Nature
, vol.372
, pp. 679-683
-
-
Stark, K.1
Vainio, S.2
Vassileva, G.3
McMahon, A.P.4
-
21
-
-
0028832707
-
A requirement for bone morphogenetic protein-7 during development of the mammalian eye and kidney
-
Dudley AT, Lyons KM, Robertson EJ. A requirement for bone morphogenetic protein-7 during development of the mammalian eye and kidney. Genes Devel 1995: 9: 2795807
-
(1995)
Genes Devel
, vol.9
, pp. 2795807
-
-
Dudley, A.T.1
Lyons, K.M.2
Robertson, E.J.3
-
24
-
-
0028963661
-
Activin disrupts epithelial branching morphogenesis in developing glandular organs of the mouse
-
Rivtos 0, Tuuri T, Eramaa M et al. Activin disrupts epithelial branching morphogenesis in developing glandular organs of the mouse. Mech Dev 1995: 50: 229-45
-
(1995)
Mech Dev
, vol.50
, pp. 229-245
-
-
Rivtos1
Tuuri, T.2
Eramaa, M.3
-
25
-
-
0025778897
-
The ES-cell inhibition factor reversibly blocks nephrogenesis in cultured mouse kidney rudiments
-
Bard JBH, Ross ASA. The ES-cell inhibition factor reversibly blocks nephrogenesis in cultured mouse kidney rudiments. Development 1991: 113: 193-9
-
(1991)
Development
, vol.113
, pp. 193-199
-
-
Bard, J.B.H.1
Ross, A.S.A.2
-
27
-
-
0028979955
-
Larsson E, Ibraghimov-Beskrovnaya 0, Roberds SL, Campbell KP, Ekblom P
-
Durbeej M, Larsson E, Ibraghimov-Beskrovnaya 0, Roberds SL, Campbell KP, Ekblom P. Non-muscle a-dystroglycan is involved in epithelial development. / Cell Biol 1995; 130: 79-91
-
(1995)
Non-muscle A-dystroglycan Is Involved in Epithelial Development. / Cell Biol
, vol.130
, pp. 79-91
-
-
Durbeej, M.1
-
29
-
-
0029127384
-
The renal glomerulus of mice lacking s-laminin/ laminin 2: Nephrosis despite molecular compensation by laminin l
-
Noakes PG, Miner JH, Gautam M, Cunningham JM, Sanes J, Merlie JP. The renal glomerulus of mice lacking s-laminin/ laminin 2: nephrosis despite molecular compensation by laminin l. Nature Genet 1995; 10: 400-6
-
(1995)
Nature Genet
, vol.10
, pp. 400-406
-
-
Noakes, P.G.1
Miner, J.H.2
Gautam, M.3
Cunningham, J.M.4
Sanes, J.5
Merlie, J.P.6
-
32
-
-
0030034551
-
Deregulation of cell survival in cystic and dysplastic renal development
-
Winyard PJD, Nauta J, Lirenman DS et al. Deregulation of cell survival in cystic and dysplastic renal development. Kidney Int 1996: 49: 135-46
-
(1996)
Kidney Int
, vol.49
, pp. 135-146
-
-
Winyard, P.J.D.1
Nauta, J.2
Lirenman, D.S.3
-
35
-
-
0028966947
-
Mutations of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
-
Sanyanusin P, Schimmenti LA, McNoe LA et al. Mutations of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. Nature Genet 1995; 9: 358-64
-
(1995)
Nature Genet
, vol.9
, pp. 358-364
-
-
Sanyanusin, P.1
Schimmenti, L.A.2
McNoe, L.A.3
-
37
-
-
0027359015
-
Huff V. Pelletier J. Denys-Drash syndrome: Relating a clinical disorder to alterations in the tumor suppressor gene WT1
-
Coppes MJ. Huff V. Pelletier J. Denys-Drash syndrome: relating a clinical disorder to alterations in the tumor suppressor gene WT1. / Paed 1993; 123: 673-8
-
(1993)
/ Paed
, vol.123
, pp. 673-678
-
-
Coppes, M.J.1
-
40
-
-
0025858403
-
Insulin-like growth factors I and II are produced in the metanephros and are required for growth and development in vitro
-
Rogers SA, Ryan G, Hammerman MR. Insulin-like growth factors I and II are produced in the metanephros and are required for growth and development in vitro. J Cell Bio/ 1991; 113: 1447-53
-
(1991)
J Cell Bio
, vol.113
, pp. 1447-1453
-
-
Rogers, S.A.1
Ryan, G.2
Hammerman, M.R.3
-
41
-
-
0026353251
-
Dependence of kidney morphogenesis on the expression of nerve growth factor receptor
-
Sariola H, Saarma M, Sainio K et al. Dependence of kidney morphogenesis on the expression of nerve growth factor receptor. Science 1991; 254: 571-3
-
(1991)
Science
, vol.254
, pp. 571-573
-
-
Sariola, H.1
Saarma, M.2
Sainio, K.3
-
42
-
-
0028875438
-
Sainio K. Palgi J, Saarma M, Saxen L, Sariola H. Neurotrophin-3 rescues neuronal precursors from apoptosis and promotes neuronal differentiation in the embryonic metanephric kidney
-
Karavanov A. Sainio K. Palgi J, Saarma M, Saxen L, Sariola H. Neurotrophin-3 rescues neuronal precursors from apoptosis and promotes neuronal differentiation in the embryonic metanephric kidney. Proc Natl Acad Sei USA 1995; 92: 11279-83
-
(1995)
Proc Natl Acad Sei USA
, vol.92
, pp. 11279-11283
-
-
Karavanov, A.1
-
43
-
-
0028858380
-
Carone FA. Cloning of mouse c-ros renal cDNA. its role in development and relationship to extracellular matrix glycoproteins
-
Kanwar YS, Liu ZZ, Kumar A, Wada J. Carone FA. Cloning of mouse c-ros renal cDNA. its role in development and relationship to extracellular matrix glycoproteins. Kidney Int 1995: 48: 1646-59
-
(1995)
Kidney Int
, vol.48
, pp. 1646-1659
-
-
Kanwar, Y.S.1
Liu, Z.Z.2
Kumar, A.3
Wada, J.4
-
45
-
-
0029741093
-
Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2
-
Hatini V, Huh SO, Herzlinger D, Soares VC, Lai E. Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2. Genes Devel 1996; 10: 1467-78
-
(1996)
Genes Devel
, vol.10
, pp. 1467-1478
-
-
Hatini, V.1
Huh, S.O.2
Herzlinger, D.3
Soares, V.C.4
Lai, E.5
-
47
-
-
0028059309
-
Abnormal kidney development and hematological disorders in platelet derived growth factor -receptor mutant mice
-
Soriano P. Abnormal kidney development and hematological disorders in platelet derived growth factor -receptor mutant mice. Genes Devel 1994; 8: 1888-96
-
(1994)
Genes Devel
, vol.8
, pp. 1888-1896
-
-
Soriano, P.1
-
48
-
-
0027936261
-
Pekny M
-
Leveen P. Pekny M. Gebre Mehdin S, Swolin B, Larsson E. Betsholtz C. Mice deficient for PDGF show renal, cardiovascular, and hematological abnormalities. Genes Devel 1994; 8: 1875-87
-
(1994)
Gebre Mehdin S, Swolin B, Larsson E. Betsholtz C. Mice Deficient for PDGF show Renal, Cardiovascular, and Hematological Abnormalities. Genes Devel
, vol.8
, pp. 1875-1887
-
-
Leveen, P.1
-
49
-
-
0028194994
-
Elfering S. Glaser T, Jepeal L. Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (Id) mutation
-
Maas R. Elfering S. Glaser T, Jepeal L. Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (Id) mutation. Devel Dijnam 1994: 199: 214-8
-
(1994)
Devel Dijnam
, vol.199
, pp. 214-218
-
-
Maas, R.1
-
50
-
-
0028117114
-
Pfaff e et al the glomerulosclerosis gene Mp\'17 encodes a peroxisomal protein producing reactive oxygen species
-
Zwacka RM, Reuter A. Pfaff E et al The glomerulosclerosis gene Mp\'17 encodes a peroxisomal protein producing reactive oxygen species. EMBO / 1994: 13: 5129-34
-
(1994)
EMBO
, vol.13
, pp. 5129-5134
-
-
Zwacka, R.M.1
Reuter, A.2
-
52
-
-
0026523576
-
A human gene responsible for Zellweger syndrome that affects peroxisome assembly
-
Shimozawa N, Tsukamoto T, Suzuki Y et al A human gene responsible for Zellweger syndrome that affects peroxisome assembly. Science 1992: 255: 1132-4
-
(1992)
Science
, vol.255
, pp. 1132-1134
-
-
Shimozawa, N.1
Tsukamoto, T.2
Suzuki, Y.3
-
54
-
-
0027940062
-
Kalatzis V. Compain S et al. a proposed new contiguous gene syndrome on 8q consists of Branchio-oto-renal (BOR) syndrome. Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia: Implication for the mapping of the BOR gene
-
Vincent C. Kalatzis V. Compain S et al. A proposed new contiguous gene syndrome on 8q consists of Branchio-oto-renal (BOR) syndrome. Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia: implication for the mapping of the BOR gene. Hum Mol Genet 1994: 3: 1859-66
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1859-1866
-
-
Vincent, C.1
-
55
-
-
0028998317
-
Collins J. Gong W et al. Cloning a balanced translocation associated with di George syndrome and identification of a disrupted candidate gene
-
Budarf M. Collins J. Gong W et al. Cloning a balanced translocation associated with Di George syndrome and identification of a disrupted candidate gene. Nature Genet 1995: 10: 269-71
-
(1995)
Nature Genet
, vol.10
, pp. 269-271
-
-
Budarf, M.1
-
56
-
-
0028980029
-
Salonen R. Weissenbach J. Peltonen L. the locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24
-
Paavola P. Salonen R. Weissenbach J. Peltonen L. The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24. Nature Genet 1995: 11: 21 3-5
-
(1995)
Nature Genet
, vol.11
, pp. 213-215
-
-
Paavola, P.1
-
57
-
-
0023222453
-
Dominantly inherited renal adysplasia
-
McPherson E. Carey f. Kramer A et al. Dominantly inherited renal adysplasia. Am / Med Genet 1987: 26: 863-72
-
(1987)
Am / Med Genet
, vol.26
, pp. 863-872
-
-
McPherson, E.1
Carey2
Kramer, A.3
|