-
1
-
-
0036233703
-
Renal aplasia is the predominant cause of congenital solitary kidneys
-
Hiraoka M, Tsukahara H, Ohshima Y, Kasuga K, Ishihara Y, Mayumi M 2002 Renal aplasia is the predominant cause of congenital solitary kidneys. Kidney Int. 61:1840-1844
-
(2002)
Kidney Int.
, vol.61
, pp. 1840-1844
-
-
Hiraoka, M.1
Tsukahara, H.2
Ohshima, Y.3
Kasuga, K.4
Ishihara, Y.5
Mayumi, M.6
-
2
-
-
0028354531
-
Congenital oligonephropathy and the etiology of adult hypertension and progressive renal injury
-
Brenner BM, Chertow GM 1994 Congenital oligonephropathy and the etiology of adult hypertension and progressive renal injury. Am J Kidney Dis 23:171-175
-
(1994)
Am J Kidney Dis
, vol.23
, pp. 171-175
-
-
Brenner, B.M.1
Chertow, G.M.2
-
3
-
-
0023739318
-
Glomeruli and blood pressure. Less of one, more the other?
-
Brenner BM, Garcia DL, Anderson S 1988 Glomeruli and blood pressure. Less of one, more the other? Am J Hypertens 1:335-347
-
(1988)
Am J Hypertens
, vol.1
, pp. 335-347
-
-
Brenner, B.M.1
Garcia, D.L.2
Anderson, S.3
-
4
-
-
33745711909
-
Reduced nephron number and glomerulomegaly in Australian Aborigines: A group at high risk for renal disease and hypertension
-
Hoy WE, Hughson MD, Singh GR, Douglas-Denton R, Bertram JF 2006 Reduced nephron number and glomerulomegaly in Australian Aborigines: a group at high risk for renal disease and hypertension. Kidney Int. 70:104-110
-
(2006)
Kidney Int.
, vol.70
, pp. 104-110
-
-
Hoy, W.E.1
Hughson, M.D.2
Singh, G.R.3
Douglas-Denton, R.4
Bertram, J.F.5
-
5
-
-
32544439900
-
Hypertension, glomerular number, and birth weight in African Americans and white subjects in the southeastern United States
-
Hughson MD, Douglas-Denton R, Bertram JF, Hoy WE 2006 Hypertension, glomerular number, and birth weight in African Americans and white subjects in the southeastern United States. Kidney Int. 69:671-678
-
(2006)
Kidney Int.
, vol.69
, pp. 671-678
-
-
Hughson, M.D.1
Douglas-Denton, R.2
Bertram, J.F.3
Hoy, W.E.4
-
6
-
-
0037426760
-
Nephron number in patients with primary hypertension
-
Keller G, Zimmer G, Mall G, Ritz E, Amann K 2003 Nephron number in patients with primary hypertension. N Engl J Med 348:101-108
-
(2003)
N Engl J Med
, vol.348
, pp. 101-108
-
-
Keller, G.1
Zimmer, G.2
Mall, G.3
Ritz, E.4
Amann, K.5
-
7
-
-
34548300072
-
Genetic approaches to human renal agenesis/hypoplasia and dysplasia
-
Sanna-Cherchi S, Caridi G, Weng PL, Scolari F, Perfumo F, Gharavi AG, Ghiggeri GM 2007 Genetic approaches to human renal agenesis/hypoplasia and dysplasia. Pediatr Nephrol 22:1675-1684
-
(2007)
Pediatr Nephrol
, vol.22
, pp. 1675-1684
-
-
Sanna-Cherchi, S.1
Caridi, G.2
Weng, P.L.3
Scolari, F.4
Perfumo, F.5
Gharavi, A.G.6
Ghiggeri, G.M.7
-
8
-
-
34548787844
-
Renal abnormalities and their developmental origin
-
Schedl A 2007 Renal abnormalities and their developmental origin. Nat Rev Genet 8:791-802
-
(2007)
Nat Rev Genet
, vol.8
, pp. 791-802
-
-
Schedl, A.1
-
10
-
-
0037248617
-
A stereological study of glomerular number and volume: Preliminary findings in a multiracial study of kidneys at autopsy
-
Hoy WE, Douglas-Denton RN, Hughson MD, Cass A, Johnson K, Bertram JF 2003 A stereological study of glomerular number and volume: preliminary findings in a multiracial study of kidneys at autopsy. Kidney Int. Suppl 63:S31-S37
-
(2003)
Kidney Int. Suppl
, vol.63
-
-
Hoy, W.E.1
Douglas-Denton, R.N.2
Hughson, M.D.3
Cass, A.4
Johnson, K.5
Bertram, J.F.6
-
11
-
-
0028174023
-
Defects in the 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 1994 Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367:380-383
-
(1994)
Nature
, vol.367
, pp. 380-383
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson-Blomberg, L.3
Costantini, F.4
Pachnis, V.5
-
12
-
-
4444324911
-
A targeting mutation of tyrosine 1062 in Ret causes a marked decrease of enteric neurons and renal hypoplasia
-
Jijiwa M, Fukuda T, Kawai K, Nakamura A, Kurokawa K, Murakumo Y, Ichihara M, Takahashi M 2004 A targeting mutation of tyrosine 1062 in Ret causes a marked decrease of enteric neurons and renal hypoplasia. Mol Cell Biol 24:8026-8036
-
(2004)
Mol Cell Biol
, vol.24
, pp. 8026-8036
-
-
Jijiwa, M.1
Fukuda, T.2
Kawai, K.3
Nakamura, A.4
Kurokawa, K.5
Murakumo, Y.6
Ichihara, M.7
Takahashi, M.8
-
13
-
-
0020444106
-
Genetics, pathoanatomy and prenatal diagnosis of Potter i syndrome and other urogenital tract diseases
-
Schmidt W, Schroeder TM, Buchinger G, Kubli F 1982 Genetics, pathoanatomy and prenatal diagnosis of Potter I syndrome and other urogenital tract diseases. Clin Genet 22:105-127
-
(1982)
Clin Genet
, vol.22
, pp. 105-127
-
-
Schmidt, W.1
Schroeder, T.M.2
Buchinger, G.3
Kubli, F.4
-
14
-
-
54049124119
-
A common RET variant is associated with reduced newborn kidney size and function
-
Zhang Z, Quinlan J, Hoy W, Hughson MD, Lemire M, Hudson T, Hueber PA, Benjamin A, Roy A, Pascuet E, Goodyer M, Raju C, Houghton F, Bertram J, Goodyer P 2008 A common RET variant is associated with reduced newborn kidney size and function. J Am Soc Nephrol 19:2027-2034
-
(2008)
J Am Soc Nephrol
, vol.19
, pp. 2027-2034
-
-
Zhang, Z.1
Quinlan, J.2
Hoy, W.3
Hughson, M.D.4
Lemire, M.5
Hudson, T.6
Hueber, P.A.7
Benjamin, A.8
Roy, A.9
Pascuet, E.10
Goodyer, M.11
Raju, C.12
Houghton, F.13
Bertram, J.14
Goodyer, P.15
-
15
-
-
0043172526
-
Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development
-
Majumdar A, Vainio S, Kispert A, McMahon J, McMahon AP 2003 Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development. Development 130:3175-3185
-
(2003)
Development
, vol.130
, pp. 3175-3185
-
-
Majumdar, A.1
Vainio, S.2
Kispert, A.3
McMahon, J.4
McMahon, A.P.5
-
16
-
-
70350712283
-
Deletion of Frs2alpha from the ureteric epithelium causes renal hypoplasia
-
Sims-Lucas S, Cullen-McEwen L, Eswarakumar VP, Hains D, Kish K, Becknell B, Zhang J, Bertram JF, Wang F, Bates CM 2009 Deletion of Frs2alpha from the ureteric epithelium causes renal hypoplasia. Am J Physiol Renal Physiol 297:F1208-F1219
-
(2009)
Am J Physiol Renal Physiol
, vol.297
-
-
Sims-Lucas, S.1
Cullen-Mcewen, L.2
Eswarakumar, V.P.3
Hains, D.4
Kish, K.5
Becknell, B.6
Zhang, J.7
Bertram, J.F.8
Wang, F.9
Bates, C.M.10
-
17
-
-
9944233235
-
Role of fibroblast growth factor receptors 1 and 2 in the ureteric bud
-
Zhao H, Kegg H, Grady S, Truong HT, Robinson ML, Baum M, Bates CM 2004 Role of fibroblast growth factor receptors 1 and 2 in the ureteric bud. Dev Biol 276:403-415
-
(2004)
Dev Biol
, vol.276
, pp. 403-415
-
-
Zhao, H.1
Kegg, H.2
Grady, S.3
Truong, H.T.4
Robinson, M.L.5
Baum, M.6
Bates, C.M.7
-
18
-
-
70649095116
-
Etv4 and Etv5 are required downstream of GDNF and Ret for kidney branching morphogenesis
-
Lu BC, Cebrian C, Chi X, Kuure S, Kuo R, Bates CM, Arber S, Hassell J, MacNeil L, Hoshi M, Jain S, Asai N, Takahashi M, Schmidt-Ott KM, Barasch J, D'Agati V, Costantini F 2009 Etv4 and Etv5 are required downstream of GDNF and Ret for kidney branching morphogenesis. Nat Genet 41:1295-1302
-
(2009)
Nat Genet
, vol.41
, pp. 1295-1302
-
-
Lu, B.C.1
Cebrian, C.2
Chi, X.3
Kuure, S.4
Kuo, R.5
Bates, C.M.6
Arber, S.7
Hassell, J.8
MacNeil, L.9
Hoshi, M.10
Jain, S.11
Asai, N.12
Takahashi, M.13
Schmidt-Ott, K.M.14
Barasch, J.15
D'Agati, V.16
Costantini, F.17
-
19
-
-
59849127924
-
Met and the epidermal growth factor receptor act cooperatively to regulate final nephron number and maInt.ain collecting duct morphology
-
Ishibe S, Karihaloo A, Ma H, Zhang J, Marlier A, Mitobe M, Togawa A, Schmitt R, Czyczk J, Kashgarian M, Geller DS, Thorgeirsson SS, Cantley LG 2009 Met and the epidermal growth factor receptor act cooperatively to regulate final nephron number and maInt.ain collecting duct morphology. Development 136:337-345
-
(2009)
Development
, vol.136
, pp. 337-345
-
-
Ishibe, S.1
Karihaloo, A.2
Ma, H.3
Zhang, J.4
Marlier, A.5
Mitobe, M.6
Togawa, A.7
Schmitt, R.8
Czyczk, J.9
Kashgarian, M.10
Geller, D.S.11
Thorgeirsson, S.S.12
Cantley, L.G.13
-
20
-
-
77950615161
-
Goodyer P 2010 Targeted Inactivation of EGF Receptor Inhibits Renal Collecting Duct Development and Function
-
Zhang Z, Pascuet E, Hueber PA, Chu L, Bichet DG, Lee TC, Threadgill DW, Goodyer P 2010 Targeted Inactivation of EGF Receptor Inhibits Renal Collecting Duct Development and Function. J Am Soc Nephrol 21:573-578
-
J Am Soc Nephrol
, vol.21
, pp. 573-578
-
-
Zhang, Z.1
Pascuet, E.2
Hueber, P.A.3
Chu, L.4
Bichet, D.G.5
Lee, T.C.6
Threadgill, D.W.7
-
21
-
-
21644437758
-
Distinct and sequential tissue-specific activities of the LIM-class ho-meobox gene Lim1 for tubular morphogenesis during kidney development
-
Kobayashi A, Kwan KM, Carroll TJ, McMahon AP, Mendelsohn CL, Behringer RR 2005 Distinct and sequential tissue-specific activities of the LIM-class ho-meobox gene Lim1 for tubular morphogenesis during kidney development. Development 132:2809-2823
-
(2005)
Development
, vol.132
, pp. 2809-2823
-
-
Kobayashi, A.1
Kwan, K.M.2
Carroll, T.J.3
McMahon, A.P.4
Mendelsohn, C.L.5
Behringer, R.R.6
-
22
-
-
0035205768
-
Renal-coloboma syndrome: Report of a novel PAX2 gene mutation
-
Chung GW, Edwards AO, Schimmenti LA, Manligas GS, Zhang YH, Ritter R III 2001 Renal-coloboma syndrome: report of a novel PAX2 gene mutation. Am J Ophthalmol 132:910-914
-
(2001)
Am J Ophthalmol
, vol.132
, pp. 910-914
-
-
Chung, G.W.1
Edwards, A.O.2
Schimmenti, L.A.3
Manligas, G.S.4
Zhang, Y.H.5
-
23
-
-
0035281926
-
Renal-coloboma syndrome: Prenatal detection and clinical spectrum in a large family
-
Ford B, Rupps R, Lirenman D, Van Allen MI, Farquharson D, Lyons C, Friedman JM 2001 Renal-coloboma syndrome: prenatal detection and clinical spectrum in a large family. Am J Med Genet 99:137-141
-
(2001)
Am J Med Genet
, vol.99
, pp. 137-141
-
-
Ford, B.1
Rupps, R.2
Lirenman, D.3
Van Allen, M.I.4
Farquharson, D.5
Lyons, C.6
Friedman, J.M.7
-
24
-
-
0035084677
-
Redefining papillorenal syndrome: An underdiagnosed cause of ocular and renal morbidity
-
Parsa CF, Silva ED, Sundin OH, Goldberg MF, De Jong MR, Sunness JS, Zeimer R, Hunter DG 2001 Redefining papillorenal syndrome: an underdiagnosed cause of ocular and renal morbidity. Ophthalmology 108:738-749
-
(2001)
Ophthalmology
, vol.108
, pp. 738-749
-
-
Parsa, C.F.1
Silva, E.D.2
Sundin, O.H.3
Goldberg, M.F.4
De Jong, M.R.5
Sunness, J.S.6
Zeimer, R.7
Hunter, D.G.8
-
25
-
-
0034916168
-
PAX2 gene mutation in a family with isolated renal hypoplasia
-
Nishimoto K, Iijima K, Shirakawa T, Kitagawa K, Satomura K, Nakamura H, Yoshikawa N 2001 PAX2 gene mutation in a family with isolated renal hypoplasia. J Am Soc Nephrol 12:1769-1772
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 1769-1772
-
-
Nishimoto, K.1
Iijima, K.2
Shirakawa, T.3
Kitagawa, K.4
Satomura, K.5
Nakamura, H.6
Yoshikawa, N.7
-
26
-
-
34249874880
-
A common variant of the PAX2 gene is associated with reduced newborn kidney size
-
Quinlan J, Lemire M, Hudson T, Qu H, Benjamin A, Roy A, Pascuet E, Goodyer M, Raju C, Zhang Z, Houghton F, Goodyer P 2007 A common variant of the PAX2 gene is associated with reduced newborn kidney size. J Am Soc Nephrol 18:1915-1921
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 1915-1921
-
-
Quinlan, J.1
Lemire, M.2
Hudson, T.3
Qu, H.4
Benjamin, A.5
Roy, A.6
Pascuet, E.7
Goodyer, M.8
Raju, C.9
Zhang, Z.10
Houghton, F.11
Goodyer, P.12
-
27
-
-
0034013279
-
Primary renal hypoplasia in humans and mice with PAX2 mutations: Evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/\mutant mice
-
Porteous S, Torban E, Cho NP, Cunliffe H, Chua L, McNoe L, Ward T, Souza C, Gus P, Giugliani R, Sato T, Yun K, Favor J, Sicotte M, Goodyer P, Eccles M 2000 Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/\mutant mice. Hum Mol Genet 9:1-11
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1-11
-
-
Porteous, S.1
Torban, E.2
Cho, N.P.3
Cunliffe, H.4
Chua, L.5
McNoe, L.6
Ward, T.7
Souza, C.8
Gus, P.9
Giugliani, R.10
Sato, T.11
Yun, K.12
Favor, J.13
Sicotte, M.14
Goodyer, P.15
Eccles, M.16
-
28
-
-
33646920859
-
Suppression of ureteric bud apoptosis rescues nephron endowment and adult renal function in Pax2 mutant mice
-
Dziarmaga A, Eccles M, Goodyer P 2006 Suppression of ureteric bud apoptosis rescues nephron endowment and adult renal function in Pax2 mutant mice. J Am Soc Nephrol 17:1568-1575
-
(2006)
J Am Soc Nephrol
, vol.17
, pp. 1568-1575
-
-
Dziarmaga, A.1
Eccles, M.2
Goodyer, P.3
-
29
-
-
0142213920
-
Ureteric bud apoptosis and renal hypoplasia in transgenic PAX2-Bax fetal mice mimics the renal-coloboma syndrome
-
Dziarmaga A, Clark P, Stayner C, Julien JP, Torban E, Goodyer P, Eccles M 2003 Ureteric bud apoptosis and renal hypoplasia in transgenic PAX2-Bax fetal mice mimics the renal-coloboma syndrome. J Am Soc Nephrol 14:2767-2774
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 2767-2774
-
-
Dziarmaga, A.1
Clark, P.2
Stayner, C.3
Julien, J.P.4
Torban, E.5
Goodyer, P.6
Eccles, M.7
-
30
-
-
33751356546
-
Regulation of c-Ret in the developing kidney is responsive to Pax2 gene dosage
-
Clarke JC, Patel SR, Raymond RM Jr, Andrew S, Robinson BG, Dressler GR, Brophy PD 2006 Regulation of c-Ret in the developing kidney is responsive to Pax2 gene dosage. Hum Mol Genet 15:3420-3428
-
(2006)
Hum Mol Genet
, vol.15
, pp. 3420-3428
-
-
Clarke, J.C.1
Patel, S.R.2
Raymond Jr., R.M.3
Andrew, S.4
Robinson, B.G.5
Dressler, G.R.6
Brophy, P.D.7
-
31
-
-
73649124593
-
Cereghini S 2010 vHNF1 functions in distinct regulatory circuits to control ureteric bud branching and early nephrogenesis
-
Lokmane L, Heliot C, Garcia-Villalba P, Fabre M, Cereghini S 2010 vHNF1 functions in distinct regulatory circuits to control ureteric bud branching and early nephrogenesis. Development 137:347-357
-
Development
, vol.137
, pp. 347-357
-
-
Lokmane, L.1
Heliot, C.2
Garcia-Villalba, P.3
Fabre, M.4
-
32
-
-
0037408284
-
Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation
-
Bingham C, Ellard S, van't Hoff WG, Simmonds HA, Marinaki AM, Badman MK, Winocour PH, Stride A, Lockwood CR, Nicholls AJ, Owen KR, Spyer G, Pearson ER, Hattersley AT 2003 Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation. Kidney Int. 63:1645-1651
-
(2003)
Kidney Int.
, vol.63
, pp. 1645-1651
-
-
Bingham, C.1
Ellard, S.2
Van'T Hoff, W.G.3
Simmonds, H.A.4
Marinaki, A.M.5
Badman, M.K.6
Winocour, P.H.7
Stride, A.8
Lockwood, C.R.9
Nicholls, A.J.10
Owen, K.R.11
Spyer, G.12
Pearson, E.R.13
Hattersley, A.T.14
-
33
-
-
0029925957
-
Wild-type p53 transgenic mice exhibit altered differentiation of the ureteric bud and possess small kidneys
-
Godley LA, Kopp JB, Eckhaus M, Paglino JJ, Owens J, Varmus HE 1996 Wild-type p53 transgenic mice exhibit altered differentiation of the ureteric bud and possess small kidneys. Genes Dev 10:836-850
-
(1996)
Genes Dev
, vol.10
, pp. 836-850
-
-
Godley, L.A.1
Kopp, J.B.2
Eckhaus, M.3
Paglino, J.J.4
Owens, J.5
Varmus, H.E.6
-
34
-
-
70350217255
-
GLI3 repressor controls nephron number via regulation of Wnt11 and Ret in ureteric tip cells
-
Cain JE, Islam E, Haxho F, Chen L, Bridgewater D, Nieuwenhuis E, Hui CC, Rosenblum ND 2009 GLI3 repressor controls nephron number via regulation of Wnt11 and Ret in ureteric tip cells. PLoS One 4:e7313
-
(2009)
PLoS One
, vol.4
-
-
Cain, J.E.1
Islam, E.2
Haxho, F.3
Chen, L.4
Bridgewater, D.5
Nieuwenhuis, E.6
Hui, C.C.7
Rosenblum, N.D.8
-
35
-
-
0027993962
-
The Pallister-Hall syndrome
-
Sama A, Mason JD, Gibbin KP, Young ID, Hewitt M 1994 The Pallister-Hall syndrome. J Med Genet 31:740
-
(1994)
J Med Genet
, vol.31
, pp. 740
-
-
Sama, A.1
Mason, J.D.2
Gibbin, K.P.3
Young, I.D.4
Hewitt, M.5
-
36
-
-
20144387269
-
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: Robust phenotype prediction from the type and position of GLI3 mutations
-
Johnston JJ, Olivos-Glander I, Killoran C, Elson E, Turner JT, Peters KF, Abbott MH, Aughton DJ, Aylsworth AS, Bamshad MJ, Booth C, Curry CJ, David A, Dinulos MB, Flannery DB, Fox MA, Graham JM, Grange DK, Guttmacher AE, Hannibal MC, Henn W, Hennekam RC, Holmes LB, Hoyme HE, Leppig KA, Lin AE, Macleod P, Manchester DK, Marcelis C, Mazzanti L, McCann E, McDonald MT, Mendelsohn NJ, Moeschler JB, Moghaddam B, Neri G, Newbury-Ecob R, Pagon RA, Phillips JA, Sadler LS, Stoler JM, Tilstra D, Walsh Vockley CM, Zackai EH, Zadeh TM, Brueton L, Black GC, Biesecker LG 2005 Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations. Am J Hum Genet 76:609-622
-
(2005)
Am J Hum Genet
, vol.76
, pp. 609-622
-
-
Johnston, J.J.1
Olivos-Glander, I.2
Killoran, C.3
Elson, E.4
Turner, J.T.5
Peters, K.F.6
Abbott, M.H.7
Aughton, D.J.8
Aylsworth, A.S.9
Bamshad, M.J.10
Booth, C.11
Curry, C.J.12
David, A.13
Dinulos, M.B.14
Flannery, D.B.15
Fox, M.A.16
Graham, J.M.17
Grange, D.K.18
Guttmacher, A.E.19
Hannibal, M.C.20
Henn, W.21
Hennekam, R.C.22
Holmes, L.B.23
Hoyme, H.E.24
Leppig, K.A.25
Lin, A.E.26
MacLeod, P.27
Manchester, D.K.28
Marcelis, C.29
Mazzanti, L.30
McCann, E.31
McDonald, M.T.32
Mendelsohn, N.J.33
Moeschler, J.B.34
Moghaddam, B.35
Neri, G.36
Newbury-Ecob, R.37
Pagon, R.A.38
Phillips, J.A.39
Sadler, L.S.40
Stoler, J.M.41
Tilstra, D.42
Walsh Vockley, C.M.43
Zackai, E.H.44
Zadeh, T.M.45
Brueton, L.46
Black, G.C.47
Biesecker, L.G.48
more..
-
37
-
-
0022587985
-
The lethal multiple congenital anomaly syndrome of polydactyly, sex reversal, renal hypopla-sia, and unilobular lungs
-
Donnai D, Young ID, Owen WG, Clark SA, Miller PF, Knox WF 1986 The lethal multiple congenital anomaly syndrome of polydactyly, sex reversal, renal hypopla-sia, and unilobular lungs. J Med Genet 23:64-71
-
(1986)
J Med Genet
, vol.23
, pp. 64-71
-
-
Donnai, D.1
Young, I.D.2
Owen, W.G.3
Clark, S.A.4
Miller, P.F.5
Knox, W.F.6
-
38
-
-
15844384629
-
Renal and neuronal abnormalities in mice lacking GDNF
-
Moore MW, Klein RD, Farinas I, Sauer H, Armanini M, Phillips H, Reichardt LF, Ryan AM, Carver-Moore K, Rosenthal A 1996 Renal and neuronal abnormalities in mice lacking GDNF. Nature 382:76-79
-
(1996)
Nature
, vol.382
, pp. 76-79
-
-
Moore, M.W.1
Klein, R.D.2
Farinas, I.3
Sauer, H.4
Armanini, M.5
Phillips, H.6
Reichardt, L.F.7
Ryan, A.M.8
Carver-Moore, K.9
Rosenthal, A.10
-
39
-
-
15844426332
-
Defects in enteric inner-vation and kidney development in mice lacking GDNF
-
Pichel JG, Shen L, Sheng HZ, Granholm AC, Drago J, Grinberg A, Lee EJ, Huang SP, Saarma M, Hoffer BJ, Sariola H, Westphal H 1996 Defects in enteric inner-vation and kidney development in mice lacking GDNF. Nature 382:73-76
-
(1996)
Nature
, vol.382
, pp. 73-76
-
-
Pichel, J.G.1
Shen, L.2
Sheng, H.Z.3
Granholm, A.C.4
Drago, J.5
Grinberg, A.6
Lee, E.J.7
Huang, S.P.8
Saarma, M.9
Hoffer, B.J.10
Sariola, H.11
Westphal, H.12
-
40
-
-
0029901727
-
Renal agenesis and the absence of enteric neurons in mice lacking GDNF
-
Sanchez MP, Silos-Santiago I, Frisen J, He B, Lira SA, Barbacid M 1996 Renal agenesis and the absence of enteric neurons in mice lacking GDNF. Nature 382:70-73
-
(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
-
41
-
-
0034951079
-
Nephron endowment in glial cell line-derived neurotrophic factor (GDNF) heterozygous mice
-
Cullen-McEwen LA, Drago J, Bertram JF 2001 Nephron endowment in glial cell line-derived neurotrophic factor (GDNF) heterozygous mice. Kidney Int. 60:31-36
-
(2001)
Kidney Int.
, vol.60
, pp. 31-36
-
-
Cullen-Mcewen, L.A.1
Drago, J.2
Bertram, J.F.3
-
42
-
-
0037313494
-
Nephron number, renal function, and arterial pressure in aged GDNF heterozygous mice
-
Cullen-McEwen LA, Kett MM, Dowling J, Anderson WP, Bertram JF 2003 Nephron number, renal function, and arterial pressure in aged GDNF heterozygous mice. Hypertension 41:335-340
-
(2003)
Hypertension
, vol.41
, pp. 335-340
-
-
Cullen-Mcewen, L.A.1
Kett, M.M.2
Dowling, J.3
Anderson, W.P.4
Bertram, J.F.5
-
43
-
-
67650283803
-
Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn
-
Zhang Z, Quinlan J, Grote D, Lemire M, Hudson T, Benjamin A, Roy A, Pascuet E, Goodyer M, Raju C, Houghton F, Bouchard M, Goodyer P 2009 Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn. Pediatr Nephrol 24:1151-1157
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 1151-1157
-
-
Zhang, Z.1
Quinlan, J.2
Grote, D.3
Lemire, M.4
Hudson, T.5
Benjamin, A.6
Roy, A.7
Pascuet, E.8
Goodyer, M.9
Raju, C.10
Houghton, F.11
Bouchard, M.12
Goodyer, P.13
-
44
-
-
0029026767
-
Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11
-
Davis AP, Witte DP, Hsieh-Li HM, Potter SS, Capecchi MR 1995 Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11. Nature 375:791-795
-
(1995)
Nature
, vol.375
, pp. 791-795
-
-
Davis, A.P.1
Witte, D.P.2
Hsieh-Li, H.M.3
Potter, S.S.4
Capecchi, M.R.5
-
45
-
-
0037447954
-
Regulation of metanephric kidney development by growth/differentiation factor 11
-
Esquela AF, Lee SJ 2003 Regulation of metanephric kidney development by growth/differentiation factor 11. Dev Biol 257:356-370
-
(2003)
Dev Biol
, vol.257
, pp. 356-370
-
-
Esquela, A.F.1
Lee, S.J.2
-
46
-
-
0034948886
-
Hoxa11 and Hoxd11 regulate branching morphogenesis of the ureteric bud in the developing kidney
-
Patterson LT, Pembaur M, Potter SS 2001 Hoxa11 and Hoxd11 regulate branching morphogenesis of the ureteric bud in the developing kidney. Development 128:2153-2161
-
(2001)
Development
, vol.128
, pp. 2153-2161
-
-
Patterson, L.T.1
Pembaur, M.2
Potter, S.S.3
-
47
-
-
0032842838
-
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
-
Xu PX, Adams J, Peters H, Brown MC, Heaney S, Maas R 1999 Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia. Nat Genet 23:113-117
-
(1999)
Nat Genet
, vol.23
, pp. 113-117
-
-
Xu, P.X.1
Adams, J.2
Peters, H.3
Brown, M.C.4
Heaney, S.5
Maas, R.6
-
48
-
-
34147143953
-
Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome
-
Hoskins BE, Cramer CH, Silvius D, Zou D, Raymond RM, Orten DJ, Kimberling WJ, Smith RJ, Weil D, Petit C, Otto EA, Xu PX, Hildebrandt F 2007 Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. Am J Hum Genet 80:800-804
-
(2007)
Am J Hum Genet
, vol.80
, pp. 800-804
-
-
Hoskins, B.E.1
Cramer, C.H.2
Silvius, D.3
Zou, D.4
Raymond, R.M.5
Orten, D.J.6
Kimberling, W.J.7
Smith, R.J.8
Weil, D.9
Petit, C.10
Otto, E.A.11
Xu, P.X.12
Hildebrandt, F.13
-
49
-
-
2542620650
-
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes
-
Ruf RG, Xu PX, Silvius D, Otto EA, Beekmann F, Muerb UT, Kumar S, Neuhaus TJ, Kemper MJ, Raymond RM Jr, Brophy PD, Berkman J, Gattas M, Hyland V, Ruf EM, Schwartz C, Chang EH, Smith RJ, Stratakis CA, Weil D, Petit C, Hildebrandt F 2004 SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes. Proc Natl Acad Sci USA 101:8090-8095
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 8090-8095
-
-
Ruf, R.G.1
Xu, P.X.2
Silvius, D.3
Otto, E.A.4
Beekmann, F.5
Muerb, U.T.6
Kumar, S.7
Neuhaus, T.J.8
Kemper, M.J.9
Raymond Jr., R.M.10
Brophy, P.D.11
Berkman, J.12
Gattas, M.13
Hyland, V.14
Ruf, E.M.15
Schwartz, C.16
Chang, E.H.17
Smith, R.J.18
Stratakis, C.A.19
Weil, D.20
Petit, C.21
Hildebrandt, F.22
more..
-
50
-
-
44049097197
-
SIX2 and BMP4 mutations associate with anomalous kidney development
-
Weber S, Taylor JC, Winyard P, Baker KF, Sullivan-Brown J, Schild R, Knuppel T, Zurowska AM, Caldas-Alfonso A, Litwin M, Emre S, Ghiggeri GM, Bakkaloglu A, Mehls O, Antignac C, Network E, Schaefer F, Burdine RD 2008 SIX2 and BMP4 mutations associate with anomalous kidney development. J Am Soc Nephrol 19:891-903
-
(2008)
J Am Soc Nephrol
, vol.19
, pp. 891-903
-
-
Weber, S.1
Taylor, J.C.2
Winyard, P.3
Baker, K.F.4
Sullivan-Brown, J.5
Schild, R.6
Knuppel, T.7
Zurowska, A.M.8
Caldas-Alfonso, A.9
Litwin, M.10
Emre, S.11
Ghiggeri, G.M.12
Bakkaloglu, A.13
Mehls, O.14
Antignac, C.15
Network, E.16
Schaefer, F.17
Burdine, R.D.18
-
51
-
-
0034840126
-
Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development
-
Nishinakamura R, Matsumoto Y, Nakao K, Nakamura K, Sato A, Copeland NG, Gilbert DJ, Jenkins NA, Scully S, Lacey DL, Katsuki M, Asashima M, Yokota T 2001 Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development. Development 128:3105-3115
-
(2001)
Development
, vol.128
, pp. 3105-3115
-
-
Nishinakamura, R.1
Matsumoto, Y.2
Nakao, K.3
Nakamura, K.4
Sato, A.5
Copeland, N.G.6
Gilbert, D.J.7
Jenkins, N.A.8
Scully, S.9
Lacey, D.L.10
Katsuki, M.11
Asashima, M.12
Yokota, T.13
-
52
-
-
33846809132
-
A Sall4 mutant mouse model useful for studying the role of Sall4 in early embryonic development and organogenesis
-
Warren M, Wang W, Spiden S, Chen-Murchie D, Tannahill D, Steel KP, Bradley A 2007 A Sall4 mutant mouse model useful for studying the role of Sall4 in early embryonic development and organogenesis. Genesis 45:51-58
-
(2007)
Genesis
, vol.45
, pp. 51-58
-
-
Warren, M.1
Wang, W.2
Spiden, S.3
Chen-Murchie, D.4
Tannahill, D.5
Steel, K.P.6
Bradley, A.7
-
53
-
-
0036155512
-
Okihiro syndrome and acro-renal-ocular syndrome: Clinical overlap, expansion of the phenotype, and absence of PAX2 mutations in two new families
-
Becker K, Beales PL, Calver DM, Matthijs G, Mohammed SN 2002 Okihiro syndrome and acro-renal-ocular syndrome: clinical overlap, expansion of the phenotype, and absence of PAX2 mutations in two new families. J Med Genet 39:68-71
-
(2002)
J Med Genet
, vol.39
, pp. 68-71
-
-
Becker, K.1
Beales, P.L.2
Calver, D.M.3
Matthijs, G.4
Mohammed, S.N.5
-
54
-
-
0031034967
-
Townes-Brocks syndrome presenting as end stage renal failure
-
Newman WG, Brunet MD, Donnai D 1997 Townes-Brocks syndrome presenting as end stage renal failure. Clin Dysmorphol 6:57-60
-
(1997)
Clin Dysmorphol
, vol.6
, pp. 57-60
-
-
Newman, W.G.1
Brunet, M.D.2
Donnai, D.3
-
55
-
-
0028073019
-
Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants
-
Mendelsohn C, Lohnes D, Decimo D, Lufkin T, LeMeur M, Chambon P, Mark M 1994 Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants. Development 120:2749-2771
-
(1994)
Development
, vol.120
, pp. 2749-2771
-
-
Mendelsohn, C.1
Lohnes, D.2
Decimo, D.3
Lufkin, T.4
Lemeur, M.5
Chambon, P.6
Mark, M.7
-
56
-
-
73649142406
-
Mendelsohn C 2010 Non-cell-autonomous retinoid signaling is crucial for renal development
-
Rosselot C, Spraggon L, Chia I, Batourina E, Riccio P, Lu B, Niederreither K, Dolle P, Duester G, Chambon P, Costantini F, Gilbert T, Molotkov A, Mendelsohn C 2010 Non-cell-autonomous retinoid signaling is crucial for renal development. Development 137:283-292
-
Development
, vol.137
, pp. 283-292
-
-
Rosselot, C.1
Spraggon, L.2
Chia, I.3
Batourina, E.4
Riccio, P.5
Lu, B.6
Niederreither, K.7
Dolle, P.8
Duester, G.9
Chambon, P.10
Costantini, F.11
Gilbert, T.12
Molotkov, A.13
-
57
-
-
0035158921
-
Vitamin A controls epithelial/mesenchymal Int.eractions through Ret expression
-
Batourina E, Gim S, Bello N, Shy M, Clagett-Dame M, Srinivas S, Costantini F, Mendelsohn C 2001 Vitamin A controls epithelial/mesenchymal Int.eractions through Ret expression. Nat Genet 27:74-78
-
(2001)
Nat Genet
, vol.27
, pp. 74-78
-
-
Batourina, E.1
Gim, S.2
Bello, N.3
Shy, M.4
Clagett-Dame, M.5
Srinivas, S.6
Costantini, F.7
Mendelsohn, C.8
-
58
-
-
0031787741
-
Mild vitamin A deficiency leads to inborn nephron deficit in the rat
-
Lelievre-Pegorier M, Vilar J, Ferrier ML, Moreau E, Freund N, Gilbert T, Merlet-Benichou C 1998 Mild vitamin A deficiency leads to inborn nephron deficit in the rat. Kidney Int. 54:1455-1462
-
(1998)
Kidney Int.
, vol.54
, pp. 1455-1462
-
-
Lelievre-Pegorier, M.1
Vilar, J.2
Ferrier, M.L.3
Moreau, E.4
Freund, N.5
Gilbert, T.6
Merlet-Benichou, C.7
-
59
-
-
84958699162
-
An analysis of the syndrome of malformations induced by maternal vitamin A deficiency. Effects of restoration of vitamin A at various times during gestation
-
Wilson JG, Roth CB, Warkany J 1953 An analysis of the syndrome of malformations induced by maternal vitamin A deficiency. Effects of restoration of vitamin A at various times during gestation. Am J Anat 92:189-217
-
(1953)
Am J Anat
, vol.92
, pp. 189-217
-
-
Wilson, J.G.1
Roth, C.B.2
Warkany, J.3
-
60
-
-
0033002113
-
FGF-7 modulates ureteric bud growth and nephron number in the developing kidney
-
Qiao J, Uzzo R, Obara-Ishihara T, Degenstein L, Fuchs E, Herzlinger D 1999 FGF-7 modulates ureteric bud growth and nephron number in the developing kidney. Development 126:547-554
-
(1999)
Development
, vol.126
, pp. 547-554
-
-
Qiao, J.1
Uzzo, R.2
Obara-Ishihara, T.3
Degenstein, L.4
Fuchs, E.5
Herzlinger, D.6
-
61
-
-
76749138524
-
Costantini F 2010 Kidney development in the absence of Gdnf and Spry1 requires Fgf10
-
Michos O, Cebrian C, Hyink D, Grieshammer U, Williams L, D'Agati V, Licht JD, Martin GR, Costantini F 2010 Kidney development in the absence of Gdnf and Spry1 requires Fgf10. PLoS Genet 6:e1000809
-
PLoS Genet
, vol.6
-
-
Michos, O.1
Cebrian, C.2
Hyink, D.3
Grieshammer, U.4
Williams, L.5
D'Agati, V.6
Licht, J.D.7
Martin, G.R.8
-
62
-
-
0034597752
-
FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development
-
Ohuchi H, Hori Y, Yamasaki M, Harada H, Sekine K, Kato S, Itoh N 2000 FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development. Biochem Biophys Res Commun 277:643-649
-
(2000)
Biochem Biophys Res Commun
, vol.277
, pp. 643-649
-
-
Ohuchi, H.1
Hori, Y.2
Yamasaki, M.3
Harada, H.4
Sekine, K.5
Kato, S.6
Itoh, N.7
-
63
-
-
0034660561
-
Role of N-myc in the developing mouse kidney
-
Bates CM, Kharzai S, Erwin T, Rossant J, Parada LF 2000 Role of N-myc in the developing mouse kidney. Dev Biol 222:317-325
-
(2000)
Dev Biol
, vol.222
, pp. 317-325
-
-
Bates, C.M.1
Kharzai, S.2
Erwin, T.3
Rossant, J.4
Parada, L.F.5
-
64
-
-
59649102542
-
C-myc as a modulator of renal stem/progenitor cell population
-
Couillard M, Trudel M 2009 C-myc as a modulator of renal stem/progenitor cell population. Dev Dyn 238:405-414
-
(2009)
Dev Dyn
, vol.238
, pp. 405-414
-
-
Couillard, M.1
Trudel, M.2
-
65
-
-
0028229760
-
Bcl-2 protein expression during murine development
-
Novack DV, Korsmeyer SJ 1994 Bcl-2 protein expression during murine development. Am J Pathol 145:61-73
-
(1994)
Am J Pathol
, vol.145
, pp. 61-73
-
-
Novack, D.V.1
Korsmeyer, S.J.2
-
66
-
-
0029928192
-
Apoptosis during an early stage of nephrogenesis induces renal hypoplasia in bcl-2-deficient mice
-
Nagata M, Nakauchi H, Nakayama K, Nakayama K, Loh D, Watanabe T 1996 Apoptosis during an early stage of nephrogenesis induces renal hypoplasia in bcl-2-deficient mice. Am J Pathol 148:1601-1611
-
(1996)
Am J Pathol
, vol.148
, pp. 1601-1611
-
-
Nagata, M.1
Nakauchi, H.2
Nakayama, K.3
Nakayama, K.4
Loh, D.5
Watanabe, T.6
-
67
-
-
0028887385
-
Fulminant metanephric apoptosis and abnormal kidney development in bcl-2-deficient mice
-
Sorenson CM, Rogers SA, Korsmeyer SJ, Hammerman MR 1995 Fulminant metanephric apoptosis and abnormal kidney development in bcl-2-deficient mice. Am J Physiol 268:F73-F81
-
(1995)
Am J Physiol
, vol.268
-
-
Sorenson, C.M.1
Rogers, S.A.2
Korsmeyer, S.J.3
Hammerman, M.R.4
-
68
-
-
48149095359
-
Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development
-
Kobayashi A, Valerius MT, Mugford JW, Carroll TJ, Self M, Oliver G, McMahon AP 2008 Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development. Cell Stem Cell 3:169-181
-
(2008)
Cell Stem Cell
, vol.3
, pp. 169-181
-
-
Kobayashi, A.1
Valerius, M.T.2
Mugford, J.W.3
Carroll, T.J.4
Self, M.5
Oliver, G.6
McMahon, A.P.7
-
69
-
-
33750455113
-
Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidney
-
Self M, Lagutin OV, Bowling B, Hendrix J, Cai Y, Dressler GR, Oliver G 2006 Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidney. EMBO J 25:5214-5228
-
(2006)
EMBO J
, vol.25
, pp. 5214-5228
-
-
Self, M.1
Lagutin, O.V.2
Bowling, B.3
Hendrix, J.4
Cai, Y.5
Dressler, G.R.6
Oliver, G.7
-
70
-
-
66049099828
-
Deficiency in Six2 during prenatal development is associated with reduced nephron number, chronic renal failure, and hypertension in Br/+ adult mice
-
Fogelgren B, Yang S, Sharp IC, Huckstep OJ, Ma W, Somponpun SJ, Carlson EC, Uyehara CF, Lozanoff S 2009 Deficiency in Six2 during prenatal development is associated with reduced nephron number, chronic renal failure, and hypertension in Br/+ adult mice. Am J Physiol Renal Physiol 296:F1166-F1178
-
(2009)
Am J Physiol Renal Physiol
, vol.296
-
-
Fogelgren, B.1
Yang, S.2
Sharp, I.C.3
Huckstep, O.J.4
Ma, W.5
Somponpun, S.J.6
Carlson, E.C.7
Uyehara, C.F.8
Lozanoff, S.9
-
71
-
-
33745475323
-
Can adult cardiovascular disease be programmed in utero?
-
Denton KM 2006 Can adult cardiovascular disease be programmed in utero? J Hypertens 24:1245-1247
-
(2006)
J Hypertens
, vol.24
, pp. 1245-1247
-
-
Denton, K.M.1
-
72
-
-
0037338396
-
Kidney development and the fetal programming of adult disease
-
Moritz KM, Dodic M, WInt.our EM 2003 Kidney development and the fetal programming of adult disease. Bioessays 25:212-220
-
(2003)
Bioessays
, vol.25
, pp. 212-220
-
-
Moritz, K.M.1
Dodic, M.2
Wintour, E.M.3
-
73
-
-
34249876219
-
Normal lactational environment restores nephron endowment and prevents hypertension after placental restriction in the rat
-
Wlodek ME, Mibus A, Tan A, Siebel AL, Owens JA, Moritz KM 2007 Normal lactational environment restores nephron endowment and prevents hypertension after placental restriction in the rat. J Am Soc Nephrol 18:1688-1696
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 1688-1696
-
-
Wlodek, M.E.1
Mibus, A.2
Tan, A.3
Siebel, A.L.4
Owens, J.A.5
Moritz, K.M.6
-
74
-
-
34548445397
-
Nephrogenesis and the renal renin-angiotensin system in fetal sheep: Effects of Int.rauterine growth restriction during late gestation
-
Zohdi V, Moritz KM, Bubb KJ, Cock ML, Wreford N, Harding R, Black MJ 2007 Nephrogenesis and the renal renin-angiotensin system in fetal sheep: effects of Int.rauterine growth restriction during late gestation. Am J Physiol Regul Int.egr Comp Physiol 293:R1267-R1273
-
(2007)
Am J Physiol Regul Int.egr Comp Physiol
, vol.293
-
-
Zohdi, V.1
Moritz, K.M.2
Bubb, K.J.3
Cock, M.L.4
Wreford, N.5
Harding, R.6
Black, M.J.7
-
75
-
-
50649099986
-
Differential effects of maternal nutrient restriction through pregnancy on kidney development and later blood pressure control in the resulting offspring
-
Brennan KA, Kaufman S, Reynolds SW, McCook BT, Kan G, Christiaens I, Symonds ME, Olson DM 2008 Differential effects of maternal nutrient restriction through pregnancy on kidney development and later blood pressure control in the resulting offspring. Am J Physiol Regul Int.egr Comp Physiol 295:R197-R205
-
(2008)
Am J Physiol Regul Int.egr Comp Physiol
, vol.295
-
-
Brennan, K.A.1
Kaufman, S.2
Reynolds, S.W.3
McCook, B.T.4
Kan, G.5
Christiaens, I.6
Symonds, M.E.7
Olson, D.M.8
-
76
-
-
19444381092
-
Maternal nutrient restriction in sheep: Hypertension and decreased nephron number in offspring at 9 months of age
-
Gilbert JS, Lang AL, Grant AR, Nijland MJ 2005 Maternal nutrient restriction in sheep: hypertension and decreased nephron number in offspring at 9 months of age. J Physiol 565:137-147
-
(2005)
J Physiol
, vol.565
, pp. 137-147
-
-
Gilbert, J.S.1
Lang, A.L.2
Grant, A.R.3
Nijland, M.J.4
-
78
-
-
34848860761
-
Retinoic acid enhances nephron endowment in rats exposed to maternal protein restriction
-
Makrakis J, Zimanyi MA, Black MJ 2007 Retinoic acid enhances nephron endowment in rats exposed to maternal protein restriction. Pediatr Nephrol 22:1861-1867
-
(2007)
Pediatr Nephrol
, vol.22
, pp. 1861-1867
-
-
Makrakis, J.1
Zimanyi, M.A.2
Black, M.J.3
-
79
-
-
33749990306
-
Early renal structure alteration in rat offspring from dams fed low protein diet
-
Pires KM, Aguila MB, Mandarim-de-Lacerda CA 2006 Early renal structure alteration in rat offspring from dams fed low protein diet. Life Sci 79:2128-2134
-
(2006)
Life Sci
, vol.79
, pp. 2128-2134
-
-
Pires, K.M.1
Aguila, M.B.2
Mandarim-De-Lacerda, C.A.3
-
80
-
-
70349286258
-
Hypertension and kidney alterations in rat offspring from low protein pregnancies
-
Villar-Martini VC, Carvalho JJ, Neves MF, Aguila MB, Mandarim-de-Lacerda CA 2009 Hypertension and kidney alterations in rat offspring from low protein pregnancies. J Hypertens 27:S47-S51
-
(2009)
J Hypertens
, vol.27
-
-
Villar-Martini, V.C.1
Carvalho, J.J.2
Neves, M.F.3
Aguila, M.B.4
Mandarim-De-Lacerda, C.A.5
-
81
-
-
50349100544
-
Mechanisms of impaired nephrogenesis with fetal growth restriction: Altered renal transcription and growth factor expression
-
Abdel-Hakeem AK, Henry TQ, Magee TR, Desai M, Ross MG, Mansano RZ, Torday JS, Nast CC 2008 Mechanisms of impaired nephrogenesis with fetal growth restriction: altered renal transcription and growth factor expression. Am J Obstet Gynecol 199:252.e1-252.e7
-
(2008)
Am J Obstet Gynecol
, vol.199
-
-
Abdel-Hakeem, A.K.1
Henry, T.Q.2
Magee, T.R.3
Desai, M.4
Ross, M.G.5
Mansano, R.Z.6
Torday, J.S.7
Nast, C.C.8
-
82
-
-
25144453720
-
Maternal diet programs embryonic kidney gene expression
-
Welham SJ, Riley PR, Wade A, Hubank M, Woolf AS 2005 Maternal diet programs embryonic kidney gene expression. Physiol Genomics 22:48-56
-
(2005)
Physiol Genomics
, vol.22
, pp. 48-56
-
-
Welham, S.J.1
Riley, P.R.2
Wade, A.3
Hubank, M.4
Woolf, A.S.5
-
83
-
-
0032759830
-
Adverse effects of hyperglycemia on kidney development in rats: In vivo and in vitro studies
-
Amri K, Freund N, Vilar J, Merlet-Benichou C, Lelievre-Pegorier M 1999 Adverse effects of hyperglycemia on kidney development in rats: in vivo and in vitro studies. Diabetes 48:2240-2245
-
(1999)
Diabetes
, vol.48
, pp. 2240-2245
-
-
Amri, K.1
Freund, N.2
Vilar, J.3
Merlet-Benichou, C.4
Lelievre-Pegorier, M.5
-
84
-
-
0028866504
-
Congenital genitourinary tract abnormalities following cocaine exposure in utero
-
Battin M, Albersheim S, Newman D 1995 Congenital genitourinary tract abnormalities following cocaine exposure in utero. Am J Perinatol 12:425-428
-
(1995)
Am J Perinatol
, vol.12
, pp. 425-428
-
-
Battin, M.1
Albersheim, S.2
Newman, D.3
-
85
-
-
0023925141
-
Maternal cocaine use and genitourinary tract malformations
-
Chasnoff IJ, Chisum GM, Kaplan WE 1988 Maternal cocaine use and genitourinary tract malformations. Teratology 37:201-204
-
(1988)
Teratology
, vol.37
, pp. 201-204
-
-
Chasnoff, I.J.1
Chisum, G.M.2
Kaplan, W.E.3
-
86
-
-
0025346366
-
Congenital renal abnormalities in infants with in utero cocaine exposure
-
Rosenstein BJ, Wheeler JS, Heid PL 1990 Congenital renal abnormalities in infants with in utero cocaine exposure. J Urol 144:110-112
-
(1990)
J Urol
, vol.144
, pp. 110-112
-
-
Rosenstein, B.J.1
Wheeler, J.S.2
Heid, P.L.3
-
87
-
-
0018934868
-
Anomalies of the kidneys and genitourinary tract in alcoholic embryopathy
-
Havers W, Majewski F, Olbing H, Eickenberg HU 1980 Anomalies of the kidneys and genitourinary tract in alcoholic embryopathy. J Urol 124:108-110
-
(1980)
J Urol
, vol.124
, pp. 108-110
-
-
Havers, W.1
Majewski, F.2
Olbing, H.3
Eickenberg, H.U.4
-
88
-
-
0018358811
-
Renal anomalies in fetal alcohol syndrome
-
Qazi Q, Masakawa A, Milman D, McGann B, Chua A, Haller J 1979 Renal anomalies in fetal alcohol syndrome. Pediatrics 63:886-889
-
(1979)
Pediatrics
, vol.63
, pp. 886-889
-
-
Qazi, Q.1
Masakawa, A.2
Milman, D.3
McGann, B.4
Chua, A.5
Haller, J.6
-
89
-
-
0028030817
-
Incidence of renal anomalies in children prenatally exposed to ethanol
-
Taylor CL, Jones KL, Jones MC, Kaplan GW 1994 Incidence of renal anomalies in children prenatally exposed to ethanol. Pediatrics 94:209-212
-
(1994)
Pediatrics
, vol.94
, pp. 209-212
-
-
Taylor, C.L.1
Jones, K.L.2
Jones, M.C.3
Kaplan, G.W.4
-
90
-
-
51149107617
-
Repeated ethanol exposure during late gestation decreases nephron endowment in fetal sheep
-
Gray SP, Kenna K, Bertram JF, Hoy WE, Yan EB, Bocking AD, Brien JF, Walker DW, Harding R, Moritz KM 2008 Repeated ethanol exposure during late gestation decreases nephron endowment in fetal sheep. Am J Physiol Regul Int.egr Comp Physiol 295:R568-R574
-
(2008)
Am J Physiol Regul Int.egr Comp Physiol
, vol.295
-
-
Gray, S.P.1
Kenna, K.2
Bertram, J.F.3
Hoy, W.E.4
Yan, E.B.5
Bocking, A.D.6
Brien, J.F.7
Walker, D.W.8
Harding, R.9
Moritz, K.M.10
-
91
-
-
33846259288
-
Maternal dexamethasone treatment at midgestation reduces nephron number and alters renal gene expression in the fetal spiny mouse
-
Dickinson H, Walker DW, WInt.our EM, Moritz K 2007 Maternal dexamethasone treatment at midgestation reduces nephron number and alters renal gene expression in the fetal spiny mouse. Am J Physiol Regul Int.egr Comp Physiol 292:R453-R461
-
(2007)
Am J Physiol Regul Int.egr Comp Physiol
, vol.292
-
-
Dickinson, H.1
Walker, D.W.2
Wintour, E.M.3
Moritz, K.4
-
92
-
-
0036841532
-
Programming effects of short prenatal exposure to dexamethasone in sheep
-
Dodic M, Abouantoun T, O'Connor A, WInt.our EM, Moritz KM 2002 Programming effects of short prenatal exposure to dexamethasone in sheep. Hypertension 40:729-734
-
(2002)
Hypertension
, vol.40
, pp. 729-734
-
-
Dodic, M.1
Abouantoun, T.2
O'Connor, A.3
Wintour, E.M.4
Moritz, K.M.5
-
93
-
-
33847679962
-
Prenatal corticosterone exposure results in altered AT1/AT2, nephron deficit and hypertension in the rat offspring
-
Singh RR, Cullen-McEwen LA, Kett MM, Boon WM, Dowling J, Bertram JF, Moritz KM 2007 Prenatal corticosterone exposure results in altered AT1/AT2, nephron deficit and hypertension in the rat offspring. J Physiol 579:503-513
-
(2007)
J Physiol
, vol.579
, pp. 503-513
-
-
Singh, R.R.1
Cullen-Mcewen, L.A.2
Kett, M.M.3
Boon, W.M.4
Dowling, J.5
Bertram, J.F.6
Moritz, K.M.7
-
95
-
-
0037821215
-
Reduced nephron number in adult sheep, hypertensive as a result of prenatal glucocorticoid treatment
-
WInt.our EM, Moritz KM, Johnson K, Ricardo S, Samuel CS, Dodic M 2003 Reduced nephron number in adult sheep, hypertensive as a result of prenatal glucocorticoid treatment. J Physiol 549:929-935
-
(2003)
J Physiol
, vol.549
, pp. 929-935
-
-
Wintour, E.M.1
Moritz, K.M.2
Johnson, K.3
Ricardo, S.4
Samuel, C.S.5
Dodic, M.6
-
96
-
-
0017414973
-
Thalidomide embryopathy
-
McBride WG 1977 Thalidomide embryopathy. Teratology 16:79-82
-
(1977)
Teratology
, vol.16
, pp. 79-82
-
-
McBride, W.G.1
-
97
-
-
0026761072
-
Recognition of thalidomide defects
-
Smithells RW, Newman CG 1992 Recognition of thalidomide defects. J Med Genet 29:716-723
-
(1992)
J Med Genet
, vol.29
, pp. 716-723
-
-
Smithells, R.W.1
Newman, C.G.2
-
98
-
-
0026794788
-
New dysmorphic features in Rubinstein-Taybi syndrome
-
Kanjilal D, Basir MA, Verma RS, Rajegowda BK, Lala R, Nagaraj A 1992 New dysmorphic features in Rubinstein-Taybi syndrome. J Med Genet 29:669-670
-
(1992)
J Med Genet
, vol.29
, pp. 669-670
-
-
Kanjilal, D.1
Basir, M.A.2
Verma, R.S.3
Rajegowda, B.K.4
Lala, R.5
Nagaraj, A.6
-
99
-
-
0026764814
-
Branchio-oto-renal syndrome: Further delineation of an underdiagnosed syndrome
-
Chitayat D, Hodgkinson KA, Chen MF, Haber GD, Nakishima S, Sando I 1992 Branchio-oto-renal syndrome: further delineation of an underdiagnosed syndrome. Am J Med Genet 43:970-975
-
(1992)
Am J Med Genet
, vol.43
, pp. 970-975
-
-
Chitayat, D.1
Hodgkinson, K.A.2
Chen, M.F.3
Haber, G.D.4
Nakishima, S.5
Sando, I.6
-
100
-
-
0036712853
-
Fraser syndrome and cryptophthalmos: Review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes
-
Slavotinek AM, Tifft CJ 2002 Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes. J Med Genet 39:623-633
-
(2002)
J Med Genet
, vol.39
, pp. 623-633
-
-
Slavotinek, A.M.1
Tifft, C.J.2
-
101
-
-
0032545468
-
Familial Williams-Beuren syndrome
-
Ounap K, Laidre P, Bartsch O, Rein R, Lipping-Sitska M 1998 Familial Williams-Beuren syndrome. Am J Med Genet 80:491-493
-
(1998)
Am J Med Genet
, vol.80
, pp. 491-493
-
-
Ounap, K.1
Laidre, P.2
Bartsch, O.3
Rein, R.4
Lipping-Sitska, M.5
|