-
1
-
-
0028354531
-
Congenital oligonephropathy and the etiology of adult hypertension and progressive renal injury
-
Brenner B.M., and Chertow G.M. Congenital oligonephropathy and the etiology of adult hypertension and progressive renal injury. Am J Kidney Dis 23 (1994) 171-175
-
(1994)
Am J Kidney Dis
, vol.23
, pp. 171-175
-
-
Brenner, B.M.1
Chertow, G.M.2
-
2
-
-
32544455832
-
Nephron number, hypertension, renal disease, and renal failure
-
Hoy W.E., Hughson M.D., Bertram J.F., Douglas-Denton R., and Amann K. Nephron number, hypertension, renal disease, and renal failure. J Am Soc Nephrol 16 (2005) 2557-2564
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 2557-2564
-
-
Hoy, W.E.1
Hughson, M.D.2
Bertram, J.F.3
Douglas-Denton, R.4
Amann, K.5
-
3
-
-
0032965306
-
Nephron number: variability is the rule. Causes and consequences
-
Merlet-Bénichou C., Gilbert T., Vilar J., Moreau E., Freund N., and Lelièvre-Pégorier M. Nephron number: variability is the rule. Causes and consequences. Lab Invest 79 (1999) 515-527
-
(1999)
Lab Invest
, vol.79
, pp. 515-527
-
-
Merlet-Bénichou, C.1
Gilbert, T.2
Vilar, J.3
Moreau, E.4
Freund, N.5
Lelièvre-Pégorier, M.6
-
4
-
-
0022608327
-
Effects of aging on the renal glomerulus
-
Anderson S., and Brenner B.M. Effects of aging on the renal glomerulus. Am J Med 80 (1986) 435-442
-
(1986)
Am J Med
, vol.80
, pp. 435-442
-
-
Anderson, S.1
Brenner, B.M.2
-
5
-
-
0026502417
-
Glomerular number and size in relation to age, kidney weight, and body surface in normal man
-
Nyengaard J.R., and Bendtsen T.F. Glomerular number and size in relation to age, kidney weight, and body surface in normal man. Anat Rec 232 (1992) 194-201
-
(1992)
Anat Rec
, vol.232
, pp. 194-201
-
-
Nyengaard, J.R.1
Bendtsen, T.F.2
-
6
-
-
2342418469
-
Branching morphogenesis and kidney disease
-
Shah M.M., Sampogna R.V., Sakurai H., Bush K.T., and Nigam S.K. Branching morphogenesis and kidney disease. Development 131 (2004) 1449-1462
-
(2004)
Development
, vol.131
, pp. 1449-1462
-
-
Shah, M.M.1
Sampogna, R.V.2
Sakurai, H.3
Bush, K.T.4
Nigam, S.K.5
-
7
-
-
0024542325
-
Growth in utero, blood pressure in childhood and adult life, and mortality from cardiovascular disease
-
Barker D.J., Osmond C., Golding J., Kuh D., and Wadsworth M.E. Growth in utero, blood pressure in childhood and adult life, and mortality from cardiovascular disease. BMJ 298 (1989) 564-567
-
(1989)
BMJ
, vol.298
, pp. 564-567
-
-
Barker, D.J.1
Osmond, C.2
Golding, J.3
Kuh, D.4
Wadsworth, M.E.5
-
8
-
-
0028196706
-
Intrauterine growth retardation leads to a permanent nephron deficit in the rat
-
Merlet-Bénichou C., Gilbert T., Muffat-Joly M., Lelièvre-Pégorier M., and Leroy B. Intrauterine growth retardation leads to a permanent nephron deficit in the rat. Pediatr Nephrol 8 (1994) 175-180
-
(1994)
Pediatr Nephrol
, vol.8
, pp. 175-180
-
-
Merlet-Bénichou, C.1
Gilbert, T.2
Muffat-Joly, M.3
Lelièvre-Pégorier, M.4
Leroy, B.5
-
9
-
-
0026511196
-
The effect of intrauterine growth retardation on the development of renal nephrons
-
Hinchliffe S.A., Lynch M.R., Sargent P.H., Howard C.V., and Van Velzen D. The effect of intrauterine growth retardation on the development of renal nephrons. Br J Obstet Gynecol 99 (1992) 296-301
-
(1992)
Br J Obstet Gynecol
, vol.99
, pp. 296-301
-
-
Hinchliffe, S.A.1
Lynch, M.R.2
Sargent, P.H.3
Howard, C.V.4
Van Velzen, D.5
-
10
-
-
0033854478
-
Relationship between weight at birth and the number and size of renal glomeruli in humans: a histomorphometric study
-
Mañalich R., Reyes L., Herrera M., Melendi C., and Fundora I. Relationship between weight at birth and the number and size of renal glomeruli in humans: a histomorphometric study. Kidney Int 58 (2000) 770-773
-
(2000)
Kidney Int
, vol.58
, pp. 770-773
-
-
Mañalich, R.1
Reyes, L.2
Herrera, M.3
Melendi, C.4
Fundora, I.5
-
11
-
-
1942534671
-
Histomorphometric analysis of postnatal glomerulogenesis in extremely preterm infants
-
Rodríguez M.M., Gómez A.H., Abitbol C.L., Chandar J.J., Duara S., and Zilleruelo G.E. Histomorphometric analysis of postnatal glomerulogenesis in extremely preterm infants. Pediatr Dev Pathol 7 (2004) 17-25
-
(2004)
Pediatr Dev Pathol
, vol.7
, pp. 17-25
-
-
Rodríguez, M.M.1
Gómez, A.H.2
Abitbol, C.L.3
Chandar, J.J.4
Duara, S.5
Zilleruelo, G.E.6
-
12
-
-
0023739318
-
Glomeruli and blood pressure. Less of one, more the other?
-
Brenner B.M., Garcia D.L., and Anderson S. Glomeruli and blood pressure. Less of one, more the other?. Am J Hypertens 1 (1988) 335-347
-
(1988)
Am J Hypertens
, vol.1
, pp. 335-347
-
-
Brenner, B.M.1
Garcia, D.L.2
Anderson, S.3
-
13
-
-
0026902259
-
Large glomerular size in Pima Indians: lack of change with diabetic nephropathy
-
Schmidt K., Pesce C., Liu Q., Nelson R.G., Bennett P.H., Karnitschnig H., et al. Large glomerular size in Pima Indians: lack of change with diabetic nephropathy. J Am Soc Nephrol 3 (1992) 229-235
-
(1992)
J Am Soc Nephrol
, vol.3
, pp. 229-235
-
-
Schmidt, K.1
Pesce, C.2
Liu, Q.3
Nelson, R.G.4
Bennett, P.H.5
Karnitschnig, H.6
-
14
-
-
33745711909
-
Reduced nephron number and glomerulomegaly in Australian Aborigines: a group at high risk for renal disease and hypertension
-
Hoy W.E., Hughson M.D., Singh G.R., Douglas-Denton R., and Bertram J.F. Reduced nephron number and glomerulomegaly in Australian Aborigines: a group at high risk for renal disease and hypertension. Kidney Int 70 (2006) 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
-
15
-
-
33750992167
-
Racial and ethnic variations in albuminuria in the US Third National Health and Nutrition Examination Survey (NHANES III) population: associations with diabetes and level of CKD
-
Bryson C.L., Ross H.J., Boyko E.J., and Young B.A. Racial and ethnic variations in albuminuria in the US Third National Health and Nutrition Examination Survey (NHANES III) population: associations with diabetes and level of CKD. Am J Kidney Dis 48 (2006) 720-726
-
(2006)
Am J Kidney Dis
, vol.48
, pp. 720-726
-
-
Bryson, C.L.1
Ross, H.J.2
Boyko, E.J.3
Young, B.A.4
-
16
-
-
0034961701
-
Low birth weight contributes to the excess prevalence of end-stage renal disease in African Americans
-
Lackland D.T., Egan B.M., Fan Z.J., and Syddall H.E. Low birth weight contributes to the excess prevalence of end-stage renal disease in African Americans. J Clin Hypertens (Greenwich) 3 (2001) 29-31
-
(2001)
J Clin Hypertens (Greenwich)
, vol.3
, pp. 29-31
-
-
Lackland, D.T.1
Egan, B.M.2
Fan, Z.J.3
Syddall, H.E.4
-
17
-
-
0037426760
-
Nephron number in patients with primary hypertension
-
Keller G., Zimmer G., Mall G., Ritz E., and Amann K. Nephron number in patients with primary hypertension. N Engl J Med 348 (2003) 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
-
18
-
-
38149131097
-
Low birth weight increases risk for end-stage renal disease
-
Vikse B.E., Irgens L.M., Leivestad T., Hallan S., and Iversen B.M. Low birth weight increases risk for end-stage renal disease. J Am Soc Nephrol 19 (2008) 151-157
-
(2008)
J Am Soc Nephrol
, vol.19
, pp. 151-157
-
-
Vikse, B.E.1
Irgens, L.M.2
Leivestad, T.3
Hallan, S.4
Iversen, B.M.5
-
19
-
-
56049114651
-
Birth weight and stages of CKD: a case-control study in an Australian population
-
Al Salmi I., Hoy W.E., Kondalsamy-Chennakes S., Wang Z., Healy H., and Shaw J.E. Birth weight and stages of CKD: a case-control study in an Australian population. Am J Kidney Dis 52 (2008) 1070-1078
-
(2008)
Am J Kidney Dis
, vol.52
, pp. 1070-1078
-
-
Al Salmi, I.1
Hoy, W.E.2
Kondalsamy-Chennakes, S.3
Wang, Z.4
Healy, H.5
Shaw, J.E.6
-
20
-
-
42049091255
-
Birth weight relates to salt sensitivity of blood pressure in healthy adults
-
de Boer M.P., Ijzerman R.G., de Jongh R.T., Eringa E.C., Stehouwer C.D., Smulders Y.M., et al. Birth weight relates to salt sensitivity of blood pressure in healthy adults. Hypertension 51 (2008) 928-932
-
(2008)
Hypertension
, vol.51
, pp. 928-932
-
-
de Boer, M.P.1
Ijzerman, R.G.2
de Jongh, R.T.3
Eringa, E.C.4
Stehouwer, C.D.5
Smulders, Y.M.6
-
21
-
-
54749083916
-
Salt sensitivity of children with low birth weight
-
Simonetti G.D., Raio L., Surbek D., Nelle M., Frey F.J., and Mohaupt M.G. Salt sensitivity of children with low birth weight. Hypertension 52 (2008) 625-630
-
(2008)
Hypertension
, vol.52
, pp. 625-630
-
-
Simonetti, G.D.1
Raio, L.2
Surbek, D.3
Nelle, M.4
Frey, F.J.5
Mohaupt, M.G.6
-
22
-
-
33845238501
-
Mechanisms of disease: in utero programming in the pathogenesis of hypertension
-
Barker D.J., Bagby S.P., and Hanson M.A. Mechanisms of disease: in utero programming in the pathogenesis of hypertension. Nat Clin Pract Nephrol 2 (2006) 700-707
-
(2006)
Nat Clin Pract Nephrol
, vol.2
, pp. 700-707
-
-
Barker, D.J.1
Bagby, S.P.2
Hanson, M.A.3
-
23
-
-
0036755244
-
Nephron mass in kidney transplantation
-
Barbari A., Stephan A., Masri M.A., Kamel G., Karam A., Kilani H., et al. Nephron mass in kidney transplantation. Transplant Proc 34 (2002) 2401-2402
-
(2002)
Transplant Proc
, vol.34
, pp. 2401-2402
-
-
Barbari, A.1
Stephan, A.2
Masri, M.A.3
Kamel, G.4
Karam, A.5
Kilani, H.6
-
24
-
-
58149498813
-
Glomerular function, structure, and number in renal allografts from older deceased donors
-
Tan J.C., Workeneh B., Busque S., Blouch K., Derby G., and Myers B.D. Glomerular function, structure, and number in renal allografts from older deceased donors. J Am Soc Nephrol 20 (2009) 181-188
-
(2009)
J Am Soc Nephrol
, vol.20
, pp. 181-188
-
-
Tan, J.C.1
Workeneh, B.2
Busque, S.3
Blouch, K.4
Derby, G.5
Myers, B.D.6
-
25
-
-
0035071325
-
Obesity-related glomerulopathy: an emerging epidemic
-
Kambham N., Markowitz G.S., Valeri A.M., Lin J., and D'Agati V.D. Obesity-related glomerulopathy: an emerging epidemic. Kidney Int 59 (2001) 1498-1509
-
(2001)
Kidney Int
, vol.59
, pp. 1498-1509
-
-
Kambham, N.1
Markowitz, G.S.2
Valeri, A.M.3
Lin, J.4
D'Agati, V.D.5
-
26
-
-
0141961572
-
Secondary focal segmental glomerulosclerosis in non-obese patients with increased muscle mass
-
Schwimmer J.A., Markowitz G.S., Valeri A.M., Imbriano L.J., Alvis R., and D'Agati V.D. Secondary focal segmental glomerulosclerosis in non-obese patients with increased muscle mass. Clin Nephrol 60 (2003) 233-234
-
(2003)
Clin Nephrol
, vol.60
, pp. 233-234
-
-
Schwimmer, J.A.1
Markowitz, G.S.2
Valeri, A.M.3
Imbriano, L.J.4
Alvis, R.5
D'Agati, V.D.6
-
27
-
-
24944573143
-
Factors influencing the progression of renal damage in patients with unilateral renal agenesis and remnant kidney
-
González E., Gutiérrez E., Morales E., Hernandez E., Andres A., Bello I., et al. Factors influencing the progression of renal damage in patients with unilateral renal agenesis and remnant kidney. Kidney Int 168 (2005) 263-270
-
(2005)
Kidney Int
, vol.168
, pp. 263-270
-
-
González, E.1
Gutiérrez, E.2
Morales, E.3
Hernandez, E.4
Andres, A.5
Bello, I.6
-
28
-
-
30544442180
-
Long-term consequences of live kidney donation follow-up in 93% of living kidney donors in a single transplant center
-
Gossmann J., Wilhelm A., Kachel H.G., Jordan J., Sann U., Geiger H., et al. Long-term consequences of live kidney donation follow-up in 93% of living kidney donors in a single transplant center. Am J Transplant 5 (2005) 2417-2424
-
(2005)
Am J Transplant
, vol.5
, pp. 2417-2424
-
-
Gossmann, J.1
Wilhelm, A.2
Kachel, H.G.3
Jordan, J.4
Sann, U.5
Geiger, H.6
-
30
-
-
0030705219
-
Complications and risks of living donor nephrectomy
-
Johnson E.M., Remucal M.J., Gillingham K.J., Dahms R.A., Najarian J.S., and Matas A.J. Complications and risks of living donor nephrectomy. Transplantation 64 (1997) 1124-1128
-
(1997)
Transplantation
, vol.64
, pp. 1124-1128
-
-
Johnson, E.M.1
Remucal, M.J.2
Gillingham, K.J.3
Dahms, R.A.4
Najarian, J.S.5
Matas, A.J.6
-
31
-
-
0036871443
-
Long term (20-37 years) follow-up of living kidney donors
-
Ramcharan T., and Matas A. Long term (20-37 years) follow-up of living kidney donors. Am J Transplant 2 (2002) 959-964
-
(2002)
Am J Transplant
, vol.2
, pp. 959-964
-
-
Ramcharan, T.1
Matas, A.2
-
32
-
-
41549148572
-
Developmental biology of the human kidney
-
Rosenblum N.D. Developmental biology of the human kidney. Semin Fetal Neonatal Med 13 (2008) 125-132
-
(2008)
Semin Fetal Neonatal Med
, vol.13
, pp. 125-132
-
-
Rosenblum, N.D.1
-
34
-
-
0026630389
-
"Medullary ray glomerular counting" as a method of assessment of human nephrogenesis
-
Hinchliffe S.A., Sargent P.H., Chan Y.F., van Velzen D., Howard C.V., Hutton J.L., et al. "Medullary ray glomerular counting" as a method of assessment of human nephrogenesis. Pathol Res Pract 188 (1992) 775-782
-
(1992)
Pathol Res Pract
, vol.188
, pp. 775-782
-
-
Hinchliffe, S.A.1
Sargent, P.H.2
Chan, Y.F.3
van Velzen, D.4
Howard, C.V.5
Hutton, J.L.6
-
35
-
-
4043082810
-
The role of angiotensin II in kidney embryogenesis and kidney abnormalities
-
Sequeira Lopez M.L., and Gomez R.A. The role of angiotensin II in kidney embryogenesis and kidney abnormalities. Curr Opin Nephrol Hypertens 13 (2004) 117-122
-
(2004)
Curr Opin Nephrol Hypertens
, vol.13
, pp. 117-122
-
-
Sequeira Lopez, M.L.1
Gomez, R.A.2
-
36
-
-
34548787844
-
Renal abnormalities and their developmental origin
-
Schedl A. Renal abnormalities and their developmental origin. Nat Rev 8 (2007) 791-802
-
(2007)
Nat Rev
, vol.8
, pp. 791-802
-
-
Schedl, A.1
-
38
-
-
50649124537
-
Developmental plasticity and regenerative capacity in the renal ureteric bud/collecting duct system
-
Sweeney D., Lindström N., and Davies J.A. Developmental plasticity and regenerative capacity in the renal ureteric bud/collecting duct system. Development 135 (2008) 2505-2510
-
(2008)
Development
, vol.135
, pp. 2505-2510
-
-
Sweeney, D.1
Lindström, N.2
Davies, J.A.3
-
40
-
-
33845383892
-
Modulation of biological regulatory networks during nephrogenesis
-
Ramos K.S., Falahatpisheh M., Nanez A., and He Q. Modulation of biological regulatory networks during nephrogenesis. Drug Metab Rev 38 (2006) 677-683
-
(2006)
Drug Metab Rev
, vol.38
, pp. 677-683
-
-
Ramos, K.S.1
Falahatpisheh, M.2
Nanez, A.3
He, Q.4
-
41
-
-
0031046284
-
A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
-
Abdelhak S., Kalatzis V., Heilig R., Compain S., Samson D., Vincent C., et al. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family. Nat Genet 15 (1997) 157-164
-
(1997)
Nat Genet
, vol.15
, pp. 157-164
-
-
Abdelhak, S.1
Kalatzis, V.2
Heilig, R.3
Compain, S.4
Samson, D.5
Vincent, C.6
-
42
-
-
33747730205
-
The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development
-
Sakaki-Yumoto M., Kobayashi C., Sato A., Fujimura S., Matsumoto Y., Takasato M., et al. The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development. Development 133 (2006) 3005-3013
-
(2006)
Development
, vol.133
, pp. 3005-3013
-
-
Sakaki-Yumoto, M.1
Kobayashi, C.2
Sato, A.3
Fujimura, S.4
Matsumoto, Y.5
Takasato, M.6
-
43
-
-
0037872680
-
Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein
-
McGregor L., Makela V., Darling S.M., Vrontou S., Chalepakis G., Roberts C., et al. Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein. Nat Genet 34 (2003) 203-208
-
(2003)
Nat Genet
, vol.34
, pp. 203-208
-
-
McGregor, L.1
Makela, V.2
Darling, S.M.3
Vrontou, S.4
Chalepakis, G.5
Roberts, C.6
-
44
-
-
0025938481
-
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
-
Franco B., Guioli S., Pragliola A., Incerti B., Bardoni B., Tonlorenzi R., et al. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature 353 (1991) 529-536
-
(1991)
Nature
, vol.353
, pp. 529-536
-
-
Franco, B.1
Guioli, S.2
Pragliola, A.3
Incerti, B.4
Bardoni, B.5
Tonlorenzi, R.6
-
45
-
-
0000727177
-
Defective cholesterol biosynthesis associated with the Smith-Lemli-Opitz Syndrome
-
Tint G.S., Irons M., Elias E.R., Batta A.K., Frieden R., Chen T.S., et al. Defective cholesterol biosynthesis associated with the Smith-Lemli-Opitz Syndrome. N Engl J Med 330 (1994) 107-113
-
(1994)
N Engl J Med
, vol.330
, pp. 107-113
-
-
Tint, G.S.1
Irons, M.2
Elias, E.R.3
Batta, A.K.4
Frieden, R.5
Chen, T.S.6
-
46
-
-
40749161593
-
Renal aplasia in humans is associated with RET mutations
-
Skinner M.A., Safford S.D., Reeves J.G., Jackson M.E., and Freemerman A.J. Renal aplasia in humans is associated with RET mutations. Am J Hum Genet 82 (2008) 344-351
-
(2008)
Am J Hum Genet
, vol.82
, pp. 344-351
-
-
Skinner, M.A.1
Safford, S.D.2
Reeves, J.G.3
Jackson, M.E.4
Freemerman, A.J.5
-
47
-
-
0028966947
-
Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
-
Sanyanusin P., Schimmenti L.A., McNoe L.A., Ward T.A., Pierpont M.E., Sullivan M.J., et al. Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. Nat Genet 9 (1995) 358-364
-
(1995)
Nat Genet
, vol.9
, pp. 358-364
-
-
Sanyanusin, P.1
Schimmenti, L.A.2
McNoe, L.A.3
Ward, T.A.4
Pierpont, M.E.5
Sullivan, M.J.6
-
48
-
-
0041342009
-
Distinct molecular and morphogenetic properties of mutations in the human HNF1beta gene that lead to defective kidney development
-
Bohn S., Thomas H., Turan G., Ellard S., Bingham C., Hattersley A.T., et al. Distinct molecular and morphogenetic properties of mutations in the human HNF1beta gene that lead to defective kidney development. J Am Soc Nephrol 14 (2003) 2033-2041
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 2033-2041
-
-
Bohn, S.1
Thomas, H.2
Turan, G.3
Ellard, S.4
Bingham, C.5
Hattersley, A.T.6
-
49
-
-
0031963876
-
Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome
-
Kohlhase J., Wischermann A., Reichenbach H., Froster U., and Engel W. Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome. Nat Genet 18 (1998) 81-83
-
(1998)
Nat Genet
, vol.18
, pp. 81-83
-
-
Kohlhase, J.1
Wischermann, A.2
Reichenbach, H.3
Froster, U.4
Engel, W.5
-
50
-
-
0030914459
-
Mutations in the human Jagged1 gene are responsible for Alagille syndrome
-
Oda T., Elkahloun A.G., Pike B.L., Okajima K., Krantz I.D., Genin A., et al. Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat Genet 16 (1997) 235-242
-
(1997)
Nat Genet
, vol.16
, pp. 235-242
-
-
Oda, T.1
Elkahloun, A.G.2
Pike, B.L.3
Okajima, K.4
Krantz, I.D.5
Genin, A.6
-
51
-
-
16044364516
-
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
-
Hatada I., Ohashi H., Fukushima Y., Kaneko Y., Inoue M., Komoto Y., et al. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome. Nat Genet 14 (1996) 171-173
-
(1996)
Nat Genet
, vol.14
, pp. 171-173
-
-
Hatada, I.1
Ohashi, H.2
Fukushima, Y.3
Kaneko, Y.4
Inoue, M.5
Komoto, Y.6
-
52
-
-
6344263978
-
Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome
-
Niemitz E.L., DeBaun M.R., Fallon J., Murakami K., Kugoh H., Oshimura M., et al. Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome. Am J Hum Genet 75 (2004) 844-849
-
(2004)
Am J Hum Genet
, vol.75
, pp. 844-849
-
-
Niemitz, E.L.1
DeBaun, M.R.2
Fallon, J.3
Murakami, K.4
Kugoh, H.5
Oshimura, M.6
-
53
-
-
0037222510
-
Association of invitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19
-
DeBaun M.R., Niemitz E.L., and Feinberg A.P. Association of invitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. Am J Hum Genet 72 (2003) 156-160
-
(2003)
Am J Hum Genet
, vol.72
, pp. 156-160
-
-
DeBaun, M.R.1
Niemitz, E.L.2
Feinberg, A.P.3
-
54
-
-
0028589588
-
Autosomal sex reversal and compomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9
-
Wagner T., Wirth J., Meyer J., Zabel B., Held M., Zimmer J., et al. Autosomal sex reversal and compomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell 79 (1994) 1111-1120
-
(1994)
Cell
, vol.79
, pp. 1111-1120
-
-
Wagner, T.1
Wirth, J.2
Meyer, J.3
Zabel, B.4
Held, M.5
Zimmer, J.6
-
55
-
-
0020615253
-
The Campomelic syndrome: review, report of 17 cases and follow-up on the currently 17-year-old boy first reported by Maroteaux, et al. in 1971
-
Houston C.S., Opitz J.M., Spranger J.W., Macpherson R.I., Reed M.H., Gilbert E.F., et al. The Campomelic syndrome: review, report of 17 cases and follow-up on the currently 17-year-old boy first reported by Maroteaux, et al. in 1971. Am J Med Genet 15 (1998) 3-28
-
(1998)
Am J Med Genet
, vol.15
, pp. 3-28
-
-
Houston, C.S.1
Opitz, J.M.2
Spranger, J.W.3
Macpherson, R.I.4
Reed, M.H.5
Gilbert, E.F.6
-
56
-
-
0034721115
-
GATA3 haploinsufficiency causes human HDR syndrome
-
Van Esch H., Groenen P., Nesbit M.A., Schuffenhauer S., Lichtner P., Vanderlinden G., et al. GATA3 haploinsufficiency causes human HDR syndrome. Nature 406 (2000) 419-422
-
(2000)
Nature
, vol.406
, pp. 419-422
-
-
Van Esch, H.1
Groenen, P.2
Nesbit, M.A.3
Schuffenhauer, S.4
Lichtner, P.5
Vanderlinden, G.6
-
57
-
-
0030986873
-
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
-
Erratum in: Nat Genet. 1998;19:102
-
Bamshad M., Lin R.C., Law D.J., Watkins W.C., Krakowiak P.A., Moore M.E., et al. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome. Nat Genet 16 (1997) 311-315 Erratum in: Nat Genet. 1998;19:102
-
(1997)
Nat Genet
, vol.16
, pp. 311-315
-
-
Bamshad, M.1
Lin, R.C.2
Law, D.J.3
Watkins, W.C.4
Krakowiak, P.A.5
Moore, M.E.6
-
58
-
-
0031019090
-
GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome
-
Kang S., Graham Jr. J.M., Olney A.H., and Biesecker L.G. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome. Nat Genet 15 (1997) 266-268
-
(1997)
Nat Genet
, vol.15
, pp. 266-268
-
-
Kang, S.1
Graham Jr., J.M.2
Olney, A.H.3
Biesecker, L.G.4
-
59
-
-
33244463281
-
GLI3-dependent transcriptional repression of Gli1, Gli2 and kidney patterning genes disrupts renal morphogenesis
-
Hu M.C., Mo R., Bhella S., Wilson C.W., Chuang P.T., Hui C.C., et al. GLI3-dependent transcriptional repression of Gli1, Gli2 and kidney patterning genes disrupts renal morphogenesis. Development 133 (2006) 569-578
-
(2006)
Development
, vol.133
, pp. 569-578
-
-
Hu, M.C.1
Mo, R.2
Bhella, S.3
Wilson, C.W.4
Chuang, P.T.5
Hui, C.C.6
-
60
-
-
25144461158
-
Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis
-
Gribouval O., Gonzales M., Neuhaus T., Aziza J., Bieth E., Laurent N., et al. Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis. Nat Genet 37 (2005) 964-968
-
(2005)
Nat Genet
, vol.37
, pp. 964-968
-
-
Gribouval, O.1
Gonzales, M.2
Neuhaus, T.3
Aziza, J.4
Bieth, E.5
Laurent, N.6
-
61
-
-
13344261391
-
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
-
Pilia G., Hughes-Benzie R.M., MacKenzie A., Baybayan P., Chen E.Y., Huber R., et al. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Nat Genet 12 (1996) 241-247
-
(1996)
Nat Genet
, vol.12
, pp. 241-247
-
-
Pilia, G.1
Hughes-Benzie, R.M.2
MacKenzie, A.3
Baybayan, P.4
Chen, E.Y.5
Huber, R.6
-
62
-
-
0036103162
-
PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease
-
Preuss N., Brosius U., Biermanns M., Muntau A.C., Conzelmann E., and Garner J. PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease. Pediatr Res 51 (2002) 706-714
-
(2002)
Pediatr Res
, vol.51
, pp. 706-714
-
-
Preuss, N.1
Brosius, U.2
Biermanns, M.3
Muntau, A.C.4
Conzelmann, E.5
Garner, J.6
-
63
-
-
44349154833
-
ROBO2 gene variants are associated with familial vesicoureteral reflux
-
Bertoli-Avella A.M., Conte M.L., Punzo F., de Graaf B.M., Lama G., La Manna A., et al. ROBO2 gene variants are associated with familial vesicoureteral reflux. J Am Soc Nephrol 19 (2008) 825-831
-
(2008)
J Am Soc Nephrol
, vol.19
, pp. 825-831
-
-
Bertoli-Avella, A.M.1
Conte, M.L.2
Punzo, F.3
de Graaf, B.M.4
Lama, G.5
La Manna, A.6
-
64
-
-
42949137384
-
RET Gly691Ser mutation is associated with primary vesicoureteral reflux in the French-Canadian population from Quebec
-
Yang Y., Houle A.M., Letendre J., and Richter A. RET Gly691Ser mutation is associated with primary vesicoureteral reflux in the French-Canadian population from Quebec. Hum Mutat 29 (2008) 695-702
-
(2008)
Hum Mutat
, vol.29
, pp. 695-702
-
-
Yang, Y.1
Houle, A.M.2
Letendre, J.3
Richter, A.4
-
65
-
-
4744354539
-
Expression of Hairy/Enhancer of Split genes, Hes 1 and Hes 5, during murine nephron morphogenesis
-
Piscione T.D., Wu M.Y.J., and Quaggin S.E. Expression of Hairy/Enhancer of Split genes, Hes 1 and Hes 5, during murine nephron morphogenesis. Gene Express Patterns 4 (2004) 707-711
-
(2004)
Gene Express Patterns
, vol.4
, pp. 707-711
-
-
Piscione, T.D.1
Wu, M.Y.J.2
Quaggin, S.E.3
-
66
-
-
0037513368
-
Glomerular number and size in autopsy kidneys: the relationship to birth weight
-
Hughson M., Farris III A.B., Douglas-Denton R., Hoy W.E., and Bertram J.F. Glomerular number and size in autopsy kidneys: the relationship to birth weight. Kidney Int 63 (2003) 2113-2122
-
(2003)
Kidney Int
, vol.63
, pp. 2113-2122
-
-
Hughson, M.1
Farris III, A.B.2
Douglas-Denton, R.3
Hoy, W.E.4
Bertram, J.F.5
-
67
-
-
32544439900
-
Hypertension, glomerular number, and birth weight in African Americans and white subjects in the Southeastern United States
-
Hughson M.D., Douglas-Denton R., Bertram J.F., and Hoy W.E. Hypertension, glomerular number, and birth weight in African Americans and white subjects in the Southeastern United States. Kidney Int 96 (2006) 671-678
-
(2006)
Kidney Int
, vol.96
, pp. 671-678
-
-
Hughson, M.D.1
Douglas-Denton, R.2
Bertram, J.F.3
Hoy, W.E.4
-
68
-
-
0035069339
-
Maternal protein restriction suppresses the newborn renin-angiotensin system and programs adult hypertension in rats
-
Woods L.L., Ingelfinger J.R., Nyengaard J.R., and Rasch R. Maternal protein restriction suppresses the newborn renin-angiotensin system and programs adult hypertension in rats. Pediatr Res 49 (2001) 460-467
-
(2001)
Pediatr Res
, vol.49
, pp. 460-467
-
-
Woods, L.L.1
Ingelfinger, J.R.2
Nyengaard, J.R.3
Rasch, R.4
-
69
-
-
51549107892
-
Deficiency of angiotensin II type 2 receptor impairs homeo box-2 and N-myc expression during nephrogenesis
-
Chen W.Y., Tran S., Chenier I., Chan J.S., Ingelfinger J.R., Inagami T., et al. Deficiency of angiotensin II type 2 receptor impairs homeo box-2 and N-myc expression during nephrogenesis. Pediatr Nephrol 23 (2008) 1769-1777
-
(2008)
Pediatr Nephrol
, vol.23
, pp. 1769-1777
-
-
Chen, W.Y.1
Tran, S.2
Chenier, I.3
Chan, J.S.4
Ingelfinger, J.R.5
Inagami, T.6
-
70
-
-
33947285368
-
What genome-wide association studies can do for medicine
-
Christensen K., and Murray J.C. What genome-wide association studies can do for medicine. N Engl J Med 356 (2007) 1094-1097
-
(2007)
N Engl J Med
, vol.356
, pp. 1094-1097
-
-
Christensen, K.1
Murray, J.C.2
-
71
-
-
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 N.P., Cunliffe H., Chua L., McNoe L., et al. 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 (2000) 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
-
72
-
-
0035131829
-
PAX2 mutations in oligomeganephronia
-
Salomon R., Tellier A.L., Attie-Bitach T., Amiel J., Vekemans M., Lyonnet S., et al. PAX2 mutations in oligomeganephronia. Kidney Int 59 (2001) 457-462
-
(2001)
Kidney Int
, vol.59
, pp. 457-462
-
-
Salomon, R.1
Tellier, A.L.2
Attie-Bitach, T.3
Amiel, J.4
Vekemans, M.5
Lyonnet, S.6
-
73
-
-
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., et al. A common variant of the PAX2 gene is associated with reduced newborn kidney size. J Am Soc Nephrol 18 (2007) 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
-
74
-
-
54049124119
-
A common RET variant is associated with reduced newborn kidney size and function
-
Zhang Z., Quinlan J., Hoy W., Hughson M.D., Lemire M., Hudson T., et al. A common RET variant is associated with reduced newborn kidney size and function. J Am Soc Nephrol 19 (2008) 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
-
76
-
-
55749100670
-
Epigenetics, development and the kidney
-
Dressler G.R. Epigenetics, development and the kidney. J Am Soc Nephrol 19 (2008) 2060-2067
-
(2008)
J Am Soc Nephrol
, vol.19
, pp. 2060-2067
-
-
Dressler, G.R.1
-
77
-
-
58349113159
-
Epigenetics and the control of epithelial sodium channel expression in collecting duct
-
Zhang D., Yu Z.-Y., Cruz P., Kong Q., Li S., and Kone B.C. Epigenetics and the control of epithelial sodium channel expression in collecting duct. Kidney Int 75 (2009) 260-267
-
(2009)
Kidney Int
, vol.75
, pp. 260-267
-
-
Zhang, D.1
Yu, Z.-Y.2
Cruz, P.3
Kong, Q.4
Li, S.5
Kone, B.C.6
-
78
-
-
50949083520
-
Developmental potential for morphogenesis in vivo and in vitro
-
Kaneko K., Sato K., Michiue T., Okabayashi K., Ohnuma K., Danno H., et al. Developmental potential for morphogenesis in vivo and in vitro. J Exp Zoolog B Mol Dev Evol 310B (2008) 492-593
-
(2008)
J Exp Zoolog B Mol Dev Evol
, vol.310 B
, pp. 492-593
-
-
Kaneko, K.1
Sato, K.2
Michiue, T.3
Okabayashi, K.4
Ohnuma, K.5
Danno, H.6
-
79
-
-
0001102269
-
Genetic assimilation of an acquired character
-
Waddington C.H. Genetic assimilation of an acquired character. Evolution 7 (1953) 118-126
-
(1953)
Evolution
, vol.7
, pp. 118-126
-
-
Waddington, C.H.1
-
80
-
-
0142084634
-
Uteroplacental insufficiency increases apoptosis and alters p53 gene methylation in the full-term IUGR rat kidney
-
Pham T.D., MacLennan N.K., Chiu C.T., Laksana G.S., Hsu J.L., and Lane R.H. Uteroplacental insufficiency increases apoptosis and alters p53 gene methylation in the full-term IUGR rat kidney. Am J Physiol Regul Integr Comp Physiol 285 (2003) R962-R970
-
(2003)
Am J Physiol Regul Integr Comp Physiol
, vol.285
-
-
Pham, T.D.1
MacLennan, N.K.2
Chiu, C.T.3
Laksana, G.S.4
Hsu, J.L.5
Lane, R.H.6
-
81
-
-
33947517327
-
Epigenetic modification of the renin-angiotensin system in the fetal programming of hypertension
-
Bogdarina I., Welham S., King P.J., Burns S.P., and Clark A.J. Epigenetic modification of the renin-angiotensin system in the fetal programming of hypertension. Circ Res 100 (2007) 520-526
-
(2007)
Circ Res
, vol.100
, pp. 520-526
-
-
Bogdarina, I.1
Welham, S.2
King, P.J.3
Burns, S.P.4
Clark, A.J.5
-
82
-
-
43849095576
-
Epigenetics-a helpful tool to better understand processes in clinical nephrology?
-
Stenvinkel P., and Ekstrom T.J. Epigenetics-a helpful tool to better understand processes in clinical nephrology?. Nephrol Dial Transplant 23 (2008) 1493-1496
-
(2008)
Nephrol Dial Transplant
, vol.23
, pp. 1493-1496
-
-
Stenvinkel, P.1
Ekstrom, T.J.2
-
83
-
-
0043093697
-
Transposable elements: targets for early nutritional effects on epigenetic gene regulation
-
Waterland R.A., and Jirtle R.L. Transposable elements: targets for early nutritional effects on epigenetic gene regulation. Mol Cell Biol 23 (2003) 5293-5300
-
(2003)
Mol Cell Biol
, vol.23
, pp. 5293-5300
-
-
Waterland, R.A.1
Jirtle, R.L.2
-
86
-
-
33745832643
-
The association between birthweight and longevity in the rat is complex and modulated by maternal protein intake during fetal life
-
Langley-Evans S.C., and Sculley D.V. The association between birthweight and longevity in the rat is complex and modulated by maternal protein intake during fetal life. FEBS Lett 580 (2006) 4150-4153
-
(2006)
FEBS Lett
, vol.580
, pp. 4150-4153
-
-
Langley-Evans, S.C.1
Sculley, D.V.2
-
87
-
-
0036223411
-
Protein restriction in pregnancy is associated with increased apoptosis of mesenchymal cells at the start of rat metanephrogenesis
-
Welham S.J., Wade A., and Woolf A.S. Protein restriction in pregnancy is associated with increased apoptosis of mesenchymal cells at the start of rat metanephrogenesis. Kidney Int 61 (2002) 1231-1242
-
(2002)
Kidney Int
, vol.61
, pp. 1231-1242
-
-
Welham, S.J.1
Wade, A.2
Woolf, A.S.3
-
88
-
-
34447646867
-
Prenatal high-salt diet in the Sprague-Dawley rat programs blood pressure and heart rate hyperresponsiveness to stress in adult female offspring
-
Porter J.P., King S.H., and Honeycutt A.D. Prenatal high-salt diet in the Sprague-Dawley rat programs blood pressure and heart rate hyperresponsiveness to stress in adult female offspring. Am J Physiol Regul Integr Comp Physiol 293 (2007) R334-R342
-
(2007)
Am J Physiol Regul Integr Comp Physiol
, vol.293
-
-
Porter, J.P.1
King, S.H.2
Honeycutt, A.D.3
-
89
-
-
0036731781
-
Long-term programming of blood pressure by maternal dietary iron restriction in the rat
-
Lewis R.M., Forhead A.J., Petry C.J., Ozanne S.E., and Hales C.N. Long-term programming of blood pressure by maternal dietary iron restriction in the rat. Br J Nutr 88 (2002) 283-290
-
(2002)
Br J Nutr
, vol.88
, pp. 283-290
-
-
Lewis, R.M.1
Forhead, A.J.2
Petry, C.J.3
Ozanne, S.E.4
Hales, C.N.5
-
90
-
-
0031787741
-
Mild vitamin A deficiency leads to inborn nephron deficit in the rat
-
Lelièvre-Pégorier M., Vilar J., Ferrier M.L., Moreau E., Freund N., Gilbert T., et al. Mild vitamin A deficiency leads to inborn nephron deficit in the rat. Kidney Int 54 (1998) 1455-1462
-
(1998)
Kidney Int
, vol.54
, pp. 1455-1462
-
-
Lelièvre-Pégorier, M.1
Vilar, J.2
Ferrier, M.L.3
Moreau, E.4
Freund, N.5
Gilbert, T.6
-
91
-
-
0035051392
-
Effect of prenatal dexamethasone on rat renal development
-
Ortiz L.A., Quan A., Weinberg A., and Baum M. Effect of prenatal dexamethasone on rat renal development. Kidney Int 59 (2001) 1663-1669
-
(2001)
Kidney Int
, vol.59
, pp. 1663-1669
-
-
Ortiz, L.A.1
Quan, A.2
Weinberg, A.3
Baum, M.4
-
92
-
-
37349029461
-
Effect of intrauterine growth restriction on kidney function at young adult age: the Nord Trondelag Health (HUNT 2) study
-
Hallan S., Euser A.M., Irgens L.M., Finken M.J.J., Homen J., and Dekker F.W. Effect of intrauterine growth restriction on kidney function at young adult age: the Nord Trondelag Health (HUNT 2) study. Am J Kidney Dis 16 (2008) 10-20
-
(2008)
Am J Kidney Dis
, vol.16
, pp. 10-20
-
-
Hallan, S.1
Euser, A.M.2
Irgens, L.M.3
Finken, M.J.J.4
Homen, J.5
Dekker, F.W.6
-
93
-
-
21644460365
-
Microalbuminuria in adults after prenatal exposure to the Dutch famine
-
Painter R.C., Roseboom T.J., van Montfrans G.A., Bossuyt P.M., Krediet R.T., Osmond C., et al. Microalbuminuria in adults after prenatal exposure to the Dutch famine. J Am Soc Nephrol 16 (2005) 189-194
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 189-194
-
-
Painter, R.C.1
Roseboom, T.J.2
van Montfrans, G.A.3
Bossuyt, P.M.4
Krediet, R.T.5
Osmond, C.6
-
94
-
-
0030878266
-
Proteinuria and progressive renal disease: birth weight and microalbuminuria
-
Yudkin J.S., Phillips D.I., and Stanner S. Proteinuria and progressive renal disease: birth weight and microalbuminuria. Nephrol Dial Transplant 12 Suppl (1997) 10-13
-
(1997)
Nephrol Dial Transplant
, vol.12
, Issue.SUPPL
, pp. 10-13
-
-
Yudkin, J.S.1
Phillips, D.I.2
Stanner, S.3
-
95
-
-
17944369231
-
Fetal growth and urinary albumin excretion among middle-aged Danes
-
Johnsen S.P., Sørensen H.T., Thulstrup A.M., Nørgård B., Engberg M., and Lauritzen T. Fetal growth and urinary albumin excretion among middle-aged Danes. Scand J Urol Nephrol 35 (2001) 314-318
-
(2001)
Scand J Urol Nephrol
, vol.35
, pp. 314-318
-
-
Johnsen, S.P.1
Sørensen, H.T.2
Thulstrup, A.M.3
Nørgård, B.4
Engberg, M.5
Lauritzen, T.6
-
96
-
-
0021968449
-
Kidney size in childhood. Sonographical growth charts for kidney length and volume
-
Dinkel E., Ertel M., Dittrich M., Peters H., Berres M., and Schulte-Wissermann H. Kidney size in childhood. Sonographical growth charts for kidney length and volume. Pediatr Radiol 15 (1985) 38-43
-
(1985)
Pediatr Radiol
, vol.15
, pp. 38-43
-
-
Dinkel, E.1
Ertel, M.2
Dittrich, M.3
Peters, H.4
Berres, M.5
Schulte-Wissermann, H.6
-
97
-
-
0021339659
-
Sonographic assessment of renal length in normal children
-
Rosenbaum D.M., Korngold E., and Teele R.L. Sonographic assessment of renal length in normal children. AJR Am J Roentgenol 142 (1984) 467-469
-
(1984)
AJR Am J Roentgenol
, vol.142
, pp. 467-469
-
-
Rosenbaum, D.M.1
Korngold, E.2
Teele, R.L.3
-
98
-
-
45449091749
-
Associations of glomerular number and birth weight with clinicopathological features of African Americans and whites
-
Hughson M.D., Gobe G.C., Hoy W.E., Manning Jr. R.D., Douglas-Denton R., and Bertram J.F. Associations of glomerular number and birth weight with clinicopathological features of African Americans and whites. Am J Kidney Dis 52 (2008) 18-28
-
(2008)
Am J Kidney Dis
, vol.52
, pp. 18-28
-
-
Hughson, M.D.1
Gobe, G.C.2
Hoy, W.E.3
Manning Jr., R.D.4
Douglas-Denton, R.5
Bertram, J.F.6
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