-
1
-
-
77956392383
-
Molecular genetics of Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity
-
New York: Nova Science Publishers Inc Catlin RB
-
Molecular genetics of Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity. BS Shastry, In retinal degeneration: causes, diagnosis and treatment New York: Nova Science Publishers Inc, Catlin RB, 2009 89 106
-
(2009)
Retinal Degeneration: Causes, Diagnosis and Treatment
, pp. 89-106
-
-
Shastry, B.S.1
-
2
-
-
33644627458
-
The incidence and course of retinopathy of prematurity: Finding from the early treatment for retinopathy of prematurity study
-
10.1542/peds.2004-1413. 15995025
-
The incidence and course of retinopathy of prematurity: finding from the early treatment for retinopathy of prematurity study. WV Good RJ Hardy V Dobson EA Plamer DL Phelps M Quintos B Tung, Pediatrics 2005 116 15 23 10.1542/peds.2004-1413 15995025
-
(2005)
Pediatrics
, vol.116
, pp. 15-23
-
-
Good, W.V.1
Hardy, R.J.2
Dobson, V.3
Plamer, E.A.4
Phelps, D.L.5
Quintos, M.6
Tung, B.7
-
3
-
-
0041335139
-
Late - Onset retinal detachment associated with regressed retinopathy of prematurity
-
10.1016/S0021-5155(03)00088-1. 12967866
-
Late - onset retinal detachment associated with regressed retinopathy of prematurity. H Terasaki T Hirose, Jpn J Ophthalmol 2003 47 492 497 10.1016/S0021-5155(03)00088-1 12967866
-
(2003)
Jpn J Ophthalmol
, vol.47
, pp. 492-497
-
-
Terasaki, H.1
Hirose, T.2
-
5
-
-
0042192111
-
Retinopathy of prematurity
-
10.2165/00129785-200303040-00004. 12930159
-
Retinopathy of prematurity. H Mechoulam EA Pierce, Am J Pharmacogenomics 2003 3 261 277 10.2165/00129785-200303040-00004 12930159
-
(2003)
Am J Pharmacogenomics
, vol.3
, pp. 261-277
-
-
Mechoulam, H.1
Pierce, E.A.2
-
7
-
-
73449130903
-
SNPs: Impact on gene function and phenotype
-
full-text. 19768584
-
SNPs: impact on gene function and phenotype. BS Shastry, Methods Mol Biol 2009 578 3 22 full-text 19768584
-
(2009)
Methods Mol Biol
, vol.578
, pp. 3-22
-
-
Shastry, B.S.1
-
8
-
-
76049123494
-
Next generation sequencing of a 40 Mb linkage interval reveals TSPAN 12 mutations in patients with familial exudative vitreoretinopathy
-
10.1016/j.ajhg.2009.12.016. 20159111
-
Next generation sequencing of a 40 Mb linkage interval reveals TSPAN 12 mutations in patients with familial exudative vitreoretinopathy. K Nikopoulos C Gilissen A Hoischen CE van Nouhuys FN Boonstra EA Blokland P Arts N Wieskamp TM Strom C Ayuso MA Tilanus S Bouwhuis A Mukhopadhyay H Scheffer LH Hoefsloot JA Veltman FP Cremers RW Collin, Am J Hum Genet 2010 86 240 247 10.1016/j.ajhg.2009.12.016 20159111
-
(2010)
Am J Hum Genet
, vol.86
, pp. 240-247
-
-
Nikopoulos, K.1
Gilissen, C.2
Hoischen, A.3
Van Nouhuys, C.E.4
Boonstra, F.N.5
Blokland, E.A.6
Arts, P.7
Wieskamp, N.8
Strom, T.M.9
Ayuso, C.10
Tilanus, M.A.11
Bouwhuis, S.12
Mukhopadhyay, A.13
Scheffer, H.14
Hoefsloot, L.H.15
Veltman, J.A.16
Cremers, F.P.17
Collin, R.W.18
-
9
-
-
76049125294
-
Mutations in TSPAN 12 cause autosomal dominant familial exudative vitreoretinopathy
-
10.1016/j.ajhg.2010.01.012. 20159112
-
Mutations in TSPAN 12 cause autosomal dominant familial exudative vitreoretinopathy. JA Poulter M Ali DF Gilmour A Rice H Kondo K Hayashi DA Mackey LS Kearns JB Ruddle JE Craig EA Pierce LM Downey MD Mohamed AF Markham CF Inglehearn C Toomes, Am J Hum Genet 2010 86 248 253 10.1016/j.ajhg.2010.01.012 20159112
-
(2010)
Am J Hum Genet
, vol.86
, pp. 248-253
-
-
Poulter, J.A.1
Ali, M.2
Gilmour, D.F.3
Rice, A.4
Kondo, H.5
Hayashi, K.6
MacKey, D.A.7
Kearns, L.S.8
Ruddle, J.B.9
Craig, J.E.10
Pierce, E.A.11
Downey, L.M.12
Mohamed, M.D.13
Markham, A.F.14
Inglehearn, C.F.15
Toomes, C.16
-
10
-
-
0030919857
-
Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity
-
9152134
-
Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity. BS Shastry D Pendergast MK Hartzer X Liu MT Trese, Arch Ophthalmol 1997 115 651 656 9152134
-
(1997)
Arch Ophthalmol
, vol.115
, pp. 651-656
-
-
Shastry, B.S.1
Pendergast, D.2
Hartzer, M.K.3
Liu, X.4
Trese, M.T.5
-
11
-
-
33748541935
-
Mutations in the NDP gene: Contribution to Norrie disease, Familial Exudative Vitreoretinopathy and Retinopathy of Prematurity
-
10.1111/j.1442-9071.2006.01314.x
-
Mutations in the NDP gene: contribution to Norrie disease, Familial Exudative Vitreoretinopathy and Retinopathy of Prematurity. JL Dickinson MM Sale A Passmore LM FitzGerald CM Wheatley KP Burdon JE Craig S Tengtrisorn SM Carden H Maclean DA Mackey, Clin Exp Ophthalmol 2006 34 682 688 10.1111/j.1442-9071. 2006.01314.x
-
(2006)
Clin Exp Ophthalmol
, vol.34
, pp. 682-688
-
-
Dickinson, J.L.1
Sale, M.M.2
Passmore, A.3
Fitzgerald, L.M.4
Wheatley, C.M.5
Burdon, K.P.6
Craig, J.E.7
Tengtrisorn, S.8
Carden, S.M.9
MacLean, H.10
MacKey, D.A.11
-
12
-
-
0033490961
-
Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency
-
10.1016/S0161-6420(99)90448-7
-
Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency. HA Mintz-Hittner MJ Miyashiro KM Knight-Nanan RE O'Malley RA Marlar, Ophthalmol 1999 106 1525 1530 10.1016/S0161-6420(99)90448-7
-
(1999)
Ophthalmol
, vol.106
, pp. 1525-1530
-
-
Mintz-Hittner, H.A.1
Miyashiro, M.J.2
Knight-Nanan, K.M.3
O'Malley, R.E.4
Marlar, R.A.5
-
13
-
-
0035036976
-
Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematurity
-
10.1007/s100380170085. 11322656
-
Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematurity. M Hiraoka DM Beristein MT Trese BS Shastry, J Hum Genet 2001 46 178 181 10.1007/s100380170085 11322656
-
(2001)
J Hum Genet
, vol.46
, pp. 178-181
-
-
Hiraoka, M.1
Beristein, D.M.2
Trese, M.T.3
Shastry, B.S.4
-
14
-
-
17144469069
-
De novo mutation in the 5'-regulatory region of the Norrie disease gene in retinopathy of prematurity
-
10.1136/jmg.38.12.e46. 11748312
-
De novo mutation in the 5'-regulatory region of the Norrie disease gene in retinopathy of prematurity. SJ Talks N Ebenezer P Hykin G Adams F Yang E Schulenberg K Gregory-Evans Y Gregory-Evans, J Med Genet 2001 38 46 10.1136/jmg.38.12.e46 11748312
-
(2001)
J Med Genet
, vol.38
, pp. 546
-
-
Talks, S.J.1
Ebenezer, N.2
Hykin, P.3
Adams, G.4
Yang, F.5
Schulenberg, E.6
Gregory-Evans, K.7
Gregory-Evans, Y.8
-
15
-
-
0036654418
-
C597A polymorphism in the Norrie disease gene is associated with advanced retinopathy of prematurity in Kuwaiti infants
-
12145535
-
C597A polymorphism in the Norrie disease gene is associated with advanced retinopathy of prematurity in Kuwaiti infants. MZ Haider LV Devarajan M Al-Essa HA Kumar, J Biomed Sci 2002 9 365 370 12145535
-
(2002)
J Biomed Sci
, vol.9
, pp. 365-370
-
-
Haider, M.Z.1
Devarajan, L.V.2
Al-Essa, M.3
Kumar, H.A.4
-
16
-
-
0035993044
-
Angiotensin-converting enzyme gene insertion/deletion polymorphism in Kuwaiti children with retinopathy of prematurity
-
10.1159/000063092. 12169829
-
Angiotensin-converting enzyme gene insertion/deletion polymorphism in Kuwaiti children with retinopathy of prematurity. MZ Haider LV Devarajan M Al-Essa H Kumar, Biol Neonate 2002 82 84 88 10.1159/000063092 12169829
-
(2002)
Biol Neonate
, vol.82
, pp. 84-88
-
-
Haider, M.Z.1
Devarajan, L.V.2
Al-Essa, M.3
Kumar, H.4
-
17
-
-
26244442311
-
Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity
-
16052165
-
Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity. KA Hutcheson PC Paluru SL Bernstein J Koh EF Rappaport RA Leach TL Young, Mol Vis 2005 11 501 508 16052165
-
(2005)
Mol Vis
, vol.11
, pp. 501-508
-
-
Hutcheson, K.A.1
Paluru, P.C.2
Bernstein, S.L.3
Koh, J.4
Rappaport, E.F.5
Leach, R.A.6
Young, T.L.7
-
18
-
-
15844369018
-
Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity
-
10.1111/j.1399-0004.2005.00408.x. 15733276
-
Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity. MLE MacDonald YP Goldberg J MacFarlane ME Samuels MT Trese BS Shastry, Clin Genet 2005 67 363 366 10.1111/j.1399-0004.2005.00408.x 15733276
-
(2005)
Clin Genet
, vol.67
, pp. 363-366
-
-
MacDonald, M.L.E.1
Goldberg, Y.P.2
MacFarlane, J.3
Samuels, M.E.4
Trese, M.T.5
Shastry, B.S.6
-
19
-
-
76649121524
-
Severe retinopathy of prematurity associated with FZD4 mutations
-
10.3109/13816810903479834. 20141357
-
Severe retinopathy of prematurity associated with FZD4 mutations. A Ells DL Guemsey K Wallace B Zheng M Vincer A Allen A Ingram O Da Silva L Siebert T Sheidow J Beis JM Robitaille, Ophthalmic Genet 2010 31 37 43 10.3109/13816810903479834 20141357
-
(2010)
Ophthalmic Genet
, vol.31
, pp. 37-43
-
-
Ells, A.1
Guemsey, D.L.2
Wallace, K.3
Zheng, B.4
Vincer, M.5
Allen, A.6
Ingram, A.7
Da Silva, O.8
Siebert, L.9
Sheidow, T.10
Beis, J.11
Robitaille, J.M.12
-
20
-
-
33750958906
-
Genetic susceptibility to retinopathy of prematurity
-
10.1542/peds.2006-1088. 17079555
-
Genetic susceptibility to retinopathy of prematurity. MJ Bizzarro N Hussain B Jonsson R Feng LR Ment JR Gruen H Zhang V Bhandari, Pediatrics 2006 118 1858 1863 10.1542/peds.2006-1088 17079555
-
(2006)
Pediatrics
, vol.118
, pp. 1858-1863
-
-
Bizzarro, M.J.1
Hussain, N.2
Jonsson, B.3
Feng, R.4
Ment, L.R.5
Gruen, J.R.6
Zhang, H.7
Bhandari, V.8
-
21
-
-
23744513886
-
Is specific race a retinopathy prematurity risk factor
-
10.1001/archpedi.159.8.771. 16061786
-
Is specific race a retinopathy prematurity risk factor. DM Lang J Backledege RW Arnold, Arch Pediatr Adolesc Med 2005 159 771 773 10.1001/archpedi.159.8.771 16061786
-
(2005)
Arch Pediatr Adolesc Med
, vol.159
, pp. 771-773
-
-
Lang, D.M.1
Backledege, J.2
Arnold, R.W.3
-
24
-
-
36749026344
-
Genetic susceptibility to retinopathy of prematurity: The evidence from clinical and experimental animal studies
-
10.1136/bjo.2007.117283
-
Genetic susceptibility to retinopathy of prematurity: the evidence from clinical and experimental animal studies. G Holmstrom P Van Wijngaarden DJ Coster KA Williams, Br J Ophthalmol 2007 97 1704 1708 10.1136/bjo.2007.117283
-
(2007)
Br J Ophthalmol
, vol.97
, pp. 1704-1708
-
-
Holmstrom, G.1
Van Wijngaarden, P.2
Coster, D.J.3
Williams, K.A.4
-
25
-
-
0029816808
-
Regulation of Vascular endothelial growth factor by oxygen in a model of retinopathy of prematurity
-
8859081
-
Regulation of Vascular endothelial growth factor by oxygen in a model of retinopathy of prematurity. EA Pierce ED Foley LEH Smith, Arch Ophthalmol 1996 114 1219 1228 8859081
-
(1996)
Arch Ophthalmol
, vol.114
, pp. 1219-1228
-
-
Pierce, E.A.1
Foley, E.D.2
Smith, L.E.H.3
-
26
-
-
0028803509
-
Vascular endothelial growth factor acts as a survival factor for newly formed retinal vessels and has implications for retinopathy of prematurity
-
10.1038/nm1095-1024. 7489357
-
Vascular endothelial growth factor acts as a survival factor for newly formed retinal vessels and has implications for retinopathy of prematurity. T Alon I Hemo A Itin J Peer J Stone E Keshet, Nat Med 1995 1 1024 1028 10.1038/nm1095-1024 7489357
-
(1995)
Nat Med
, vol.1
, pp. 1024-1028
-
-
Alon, T.1
Hemo, I.2
Itin, A.3
Peer, J.4
Stone, J.5
Keshet, E.6
-
27
-
-
77952123817
-
Increased angiogenic factors associated with peripheral avascular retina and intravitreous neovascularization: A model of retinopathy of prematurity
-
10.1001/archophthalmol.2010.65. 20457980
-
Increased angiogenic factors associated with peripheral avascular retina and intravitreous neovascularization: a model of retinopathy of prematurity. SJ Budd ME Hartnett, Arch Ophthalmol 2010 128 589 595 10.1001/archophthalmol.2010. 65 20457980
-
(2010)
Arch Ophthalmol
, vol.128
, pp. 589-595
-
-
Budd, S.J.1
Hartnett, M.E.2
-
28
-
-
0033865580
-
Identification of polymorphisms within the vascular endothelial growth factor gene (VEGF): Correlation with variation in VEGF protein production
-
10.1006/cyto.2000.0692. 10930302
-
Identification of polymorphisms within the vascular endothelial growth factor gene (VEGF): correlation with variation in VEGF protein production. CJ Watson NJ Webb MJ Bottomley PE Brenchley, Cytokine 2000 12 1232 1235 10.1006/cyto.2000.0692 10930302
-
(2000)
Cytokine
, vol.12
, pp. 1232-1235
-
-
Watson, C.J.1
Webb, N.J.2
Bottomley, M.J.3
Brenchley, P.E.4
-
29
-
-
0034509524
-
A common 936 C/T mutation in the gene for vascular endothelial growth factor is associated with vascular endothelial growth factor plasma levels
-
10.1159/000054076
-
A common 936 C/T mutation in the gene for vascular endothelial growth factor is associated with vascular endothelial growth factor plasma levels. W Renner S Kotschan C Hoffmann B Obermayer-Pietsch E Pilger, J Vas Res 2000 37 443 448 10.1159/000054076
-
(2000)
J Vas Res
, vol.37
, pp. 443-448
-
-
Renner, W.1
Kotschan, S.2
Hoffmann, C.3
Obermayer-Pietsch, B.4
Pilger, E.5
-
30
-
-
3042577725
-
Genetic polymorphisms and retinopathy of prematurity
-
10.1167/iovs.03-1303. 15161830
-
Genetic polymorphisms and retinopathy of prematurity. RW Cooke JA Drury R Mountford D Clark, Invest Ophthalmol Vis Sci 2004 45 1712 1715 10.1167/iovs.03-1303 15161830
-
(2004)
Invest Ophthalmol Vis Sci
, vol.45
, pp. 1712-1715
-
-
Cooke, R.W.1
Drury, J.A.2
Mountford, R.3
Clark, D.4
-
31
-
-
14344249625
-
Association of genetic polymorphisms of vascular endothelial growth factor and risk of proliferative retinopathy of prematurity
-
10.1203/01.PDR.0000153867.80238.E0. 15635051
-
Association of genetic polymorphisms of vascular endothelial growth factor and risk of proliferative retinopathy of prematurity. AV Vannay G Dunai I Banyasz M Szabo R Vamos A Treszl J Hajdu T Tulassay YI Vasarhel, Pediatr Res 2005 57 396 398 10.1203/01.PDR.0000153867.80238.E0 15635051
-
(2005)
Pediatr Res
, vol.57
, pp. 396-398
-
-
Vannay, A.V.1
Dunai, G.2
Banyasz, I.3
Szabo, M.4
Vamos, R.5
Treszl, A.6
Hajdu, J.7
Tulassay, T.8
Vasarhel, Y.I.9
-
32
-
-
34250763299
-
Lack of association of the VEGF gene promoter (-634 G to C and -460 C to T) polymorphism and the risk of advanced retinopathy of prematurity
-
10.1007/s00417-006-0480-6. 17119993
-
Lack of association of the VEGF gene promoter (-634 G to C and -460 C to T) polymorphism and the risk of advanced retinopathy of prematurity. BS Shastry X Qu, Graefes Arch Clin Exp Ophthalmol 2007 245 741 743 10.1007/s00417-006-0480- 6 17119993
-
(2007)
Graefes Arch Clin Exp Ophthalmol
, vol.245
, pp. 741-743
-
-
Shastry, B.S.1
Qu, X.2
-
33
-
-
67349221743
-
Lack of association of VEGF (-2578 C to A) and ANG2 (-35 G to C) gene polymorphisms with the progression of retinopathy of prematurity
-
10.1007/s00417-008-0988-z. 19018553
-
Lack of association of VEGF (-2578 C to A) and ANG2 (-35 G to C) gene polymorphisms with the progression of retinopathy of prematurity. BS Shastry, Graefes Arch Clin Exp Ophthalmol 2009 247 859 860 10.1007/s00417-008-0988-z 19018553
-
(2009)
Graefes Arch Clin Exp Ophthalmol
, vol.247
, pp. 859-860
-
-
Shastry, B.S.1
-
34
-
-
51649126694
-
The clinical role of vascular endothelial growth factor (VEGF) system in the pathogenesis of retinopathy of prematurity
-
10.1007/s00417-008-0865-9. 18546007
-
The clinical role of vascular endothelial growth factor (VEGF) system in the pathogenesis of retinopathy of prematurity. P Kwinta M Bik-Multanowski Z Mitkowska T Tomasik JJ Pietrzyk, Graefes Arch Clin Exp Ophthalmol 2008 246 1467 1475 10.1007/s00417-008-0865-9 18546007
-
(2008)
Graefes Arch Clin Exp Ophthalmol
, vol.246
, pp. 1467-1475
-
-
Kwinta, P.1
Bik-Multanowski, M.2
Mitkowska, Z.3
Tomasik, T.4
Pietrzyk, J.J.5
-
35
-
-
33746858957
-
Genetic polymorphisms of vascular endothelial growth factor and angiopoietin 2 in retinopathy of prematurity
-
10.1080/02713680600801123. 16877277
-
Genetic polymorphisms of vascular endothelial growth factor and angiopoietin 2 in retinopathy of prematurity. I Banyasz G Bokodl A Vannay B Szebenl A Treszl B Vasarhelyi T Tulassay A Szabo, Curr Eye Res 2006 31 685 690 10.1080/02713680600801123 16877277
-
(2006)
Curr Eye Res
, vol.31
, pp. 685-690
-
-
Banyasz, I.1
Bokodl, G.2
Vannay, A.3
Szebenl, B.4
Treszl, A.5
Vasarhelyi, B.6
Tulassay, T.7
Szabo, A.8
-
36
-
-
47349119395
-
Published genetic variants in retinopathy of prematurity: Random forest analysis suggests a negligible contribution to risk and severity
-
10.1080/02713680802018427. 18568888
-
Published genetic variants in retinopathy of prematurity: random forest analysis suggests a negligible contribution to risk and severity. G Dunai B Vasarhelyi M Szabo J Hajdu G Meszaros T Tulassay A Treszl, Curr Eye Res 2008 33 501 505 10.1080/02713680802018427 18568888
-
(2008)
Curr Eye Res
, vol.33
, pp. 501-505
-
-
Dunai, G.1
Vasarhelyi, B.2
Szabo, M.3
Hajdu, J.4
Meszaros, G.5
Tulassay, T.6
Treszl, A.7
-
37
-
-
0242300678
-
Postnatal serum insulin-like growth factor - I deficiency is associated with retinopathy of prematurity and other complications of premature birth
-
10.1542/peds.112.5.1016. 14595040
-
Postnatal serum insulin-like growth factor - I deficiency is associated with retinopathy of prematurity and other complications of premature birth. A Hellstrom E Engstrom AL Hard K Albertsson-Wildand B Carlsson A Niklasson C Lofqvist E Svensson S Holm U Ewald G Holmstrom LE Smith, Pediatrics 2003 112 1016 1020 10.1542/peds.112.5.1016 14595040
-
(2003)
Pediatrics
, vol.112
, pp. 1016-1020
-
-
Hellstrom, A.1
Engstrom, E.2
Hard, A.L.3
Albertsson-Wildand, K.4
Carlsson, B.5
Niklasson, A.6
Lofqvist, C.7
Svensson, E.8
Holm, S.9
Ewald, U.10
Holmstrom, G.11
Smith, L.E.12
-
38
-
-
39349084337
-
Assessment of the contribution of insulin-like growth factor -I receptor 3174 G to A polymorphism to the progression of advanced retinopathy of prematurity
-
18050122
-
Assessment of the contribution of insulin-like growth factor -I receptor 3174 G to A polymorphism to the progression of advanced retinopathy of prematurity. BS Shastry, Eur J Ophthalmol 2007 17 950 953 18050122
-
(2007)
Eur J Ophthalmol
, vol.17
, pp. 950-953
-
-
Shastry, B.S.1
-
39
-
-
33746926708
-
Lack of association between insulin-like growth factor - I receptor G3174A polymorphism and retinoapthy of prematurity
-
10.1007/s00417-005-0203-4. 16362313
-
Lack of association between insulin-like growth factor - I receptor G3174A polymorphism and retinoapthy of prematurity. A Balogh L Derzbach A Vannay B Vasarhelyi, Graefes Arch Clin Exp Ophthalmol 2006 244 1035 1038 10.1007/s00417-005-0203-4 16362313
-
(2006)
Graefes Arch Clin Exp Ophthalmol
, vol.244
, pp. 1035-1038
-
-
Balogh, A.1
Derzbach, L.2
Vannay, A.3
Vasarhelyi, B.4
-
40
-
-
67649418108
-
Polymorphism in the renin-angiotensin system and outcome of very low birth weight infants
-
10.1159/000226602. 19571582
-
Polymorphism in the renin-angiotensin system and outcome of very low birth weight infants. J Spiegler A Gilhaus IR Konig E Kattner M Vochem H Kuster J Moller D Muller A Kribs H Segerer C Weig W Nikischin A Van der Wense C Gebauer E Herting W Gopel, Neonatology 2009 97 10 14 10.1159/000226602 19571582
-
(2009)
Neonatology
, vol.97
, pp. 10-14
-
-
Spiegler, J.1
Gilhaus, A.2
Konig, I.R.3
Kattner, E.4
Vochem, M.5
Kuster, H.6
Moller, J.7
Muller, D.8
Kribs, A.9
Segerer, H.10
Weig, C.11
Nikischin, W.12
Van Der Wense, A.13
Gebauer, C.14
Herting, E.15
Gopel, W.16
-
41
-
-
16244416225
-
Angiotensin converting enzyme insertion/deletion polymorphism does not alter sepsis outcome in ventilated very low birth weight infants
-
10.1038/sj.jp.7211231. 15549142
-
Angiotensin converting enzyme insertion/deletion polymorphism does not alter sepsis outcome in ventilated very low birth weight infants. BR John J Loggins K Yanamandra, J Perinatol 2005 25 205 209 10.1038/sj.jp.7211231 15549142
-
(2005)
J Perinatol
, vol.25
, pp. 205-209
-
-
John, B.R.1
Loggins, J.2
Yanamandra, K.3
-
42
-
-
60449105560
-
Genetic contributions to the development of retinopathy of prematurity
-
10.1203/PDR.0b013e31818d1dbd. 18787502
-
Genetic contributions to the development of retinopathy of prematurity. S Mohamed K Schaa ME Cooper E Ahrens A Alvarado T Colaizy ML Marazita JC Murray JM Dagle, Pediatr Res 2009 65 193 197 10.1203/PDR.0b013e31818d1dbd 18787502
-
(2009)
Pediatr Res
, vol.65
, pp. 193-197
-
-
Mohamed, S.1
Schaa, K.2
Cooper, M.E.3
Ahrens, E.4
Alvarado, A.5
Colaizy, T.6
Marazita, M.L.7
Murray, J.C.8
Dagle, J.M.9
-
43
-
-
70349816655
-
Norrin, frizzled 4 and LRP5 signaling in endothelial cells controls a genetic program for retinal vascularization
-
10.1016/j.cell.2009.07.047. 19837032
-
Norrin, frizzled 4 and LRP5 signaling in endothelial cells controls a genetic program for retinal vascularization. X Ye YS Wang H Cahill MZ Yu TC Badea PM Smallwood NS Peachey J Nathans, Cell 2009 139 285 298 10.1016/j.cell.2009.07.047 19837032
-
(2009)
Cell
, vol.139
, pp. 285-298
-
-
Ye, X.1
Wang, Y.S.2
Cahill, H.3
Yu, M.Z.4
Badea, T.C.5
Smallwood, P.M.6
Peachey, N.S.7
Nathans, J.8
-
44
-
-
37749020529
-
Moderate reduction of norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy
-
10.1007/s00439-007-0438-8. 17955262
-
Moderate reduction of norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy. M Qin H Kondo T Tahira K Hayashi, Hum Genet 2008 122 615 623 10.1007/s00439-007-0438-8 17955262
-
(2008)
Hum Genet
, vol.122
, pp. 615-623
-
-
Qin, M.1
Kondo, H.2
Tahira, T.3
Hayashi, K.4
-
45
-
-
0030044029
-
An animal model for Norrie disease: Gene targeting of mouse ND gene
-
10.1093/hmg/5.1.51. 8789439
-
An animal model for Norrie disease: gene targeting of mouse ND gene. W Berger D Van de Pool D Bachner F Oerlemans H Winkens H Hameister B Wieringa W Hendricks H-H Ropers, Hum Mol Genet 1996 5 51 59 10.1093/hmg/5.1.51 8789439
-
(1996)
Hum Mol Genet
, vol.5
, pp. 51-59
-
-
Berger, W.1
Van De Pool, D.2
Bachner, D.3
Oerlemans, F.4
Winkens, H.5
Hameister, H.6
Wieringa, B.7
Hendricks, W.8
Ropers, H.-H.9
-
46
-
-
0035399638
-
Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled- 4 gene
-
11425903
-
Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled- 4 gene. Y Wang D Huso H Cahill D Ruygo J Nathans, J Neurosci 2001 21 4761 4771 11425903
-
(2001)
J Neurosci
, vol.21
, pp. 4761-4771
-
-
Wang, Y.1
Huso, D.2
Cahill, H.3
Ruygo, D.4
Nathans, J.5
-
47
-
-
44349149348
-
A model for familial exudative vitreoretinopathy caused by LRP5 mutations
-
10.1093/hmg/ddn047. 18263894
-
A model for familial exudative vitreoretinopathy caused by LRP5 mutations. CH Xia H Liu D Cheung M Wang C Cheng X Du B Chang B Beutler X Gong, Hum Mol Genet 2008 17 1605 1612 10.1093/hmg/ddn047 18263894
-
(2008)
Hum Mol Genet
, vol.17
, pp. 1605-1612
-
-
Xia, C.H.1
Liu, H.2
Cheung, D.3
Wang, M.4
Cheng, C.5
Du, X.6
Chang, B.7
Beutler, B.8
Gong, X.9
-
48
-
-
70349838225
-
TSPAN12 regulates retinal vascular development by promoting norrin but not Wnt induced FZD4/beta-catenin signaling
-
10.1016/j.cell.2009.07.048. 19837033
-
TSPAN12 regulates retinal vascular development by promoting norrin but not Wnt induced FZD4/beta-catenin signaling. HJ Junge S Yang JR Burton K Paes X Shu DM French M Costa DS Rice W Ye, Cell 2009 139 299 311 10.1016/j.cell.2009. 07.048 19837033
-
(2009)
Cell
, vol.139
, pp. 299-311
-
-
Junge, H.J.1
Yang, S.2
Burton, J.R.3
Paes, K.4
Shu, X.5
French, D.M.6
Costa, M.7
Rice, D.S.8
Ye, W.9
-
49
-
-
33846543218
-
A potential biomarker in the cord blood of preterm infants who develop retinopathy of prematurity
-
10.1203/pdr.0b013e31802d776d. 17237725
-
A potential biomarker in the cord blood of preterm infants who develop retinopathy of prematurity. A Madan G El-Ferzli SM Carlson JC Whitin J Schilling A Najmi TT Yu K Lau RA Dimmitt HJ Cohen, Pediatr Res 2007 61 215 221 10.1203/pdr.0b013e31802d776d 17237725
-
(2007)
Pediatr Res
, vol.61
, pp. 215-221
-
-
Madan, A.1
El-Ferzli, G.2
Carlson, S.M.3
Whitin, J.C.4
Schilling, J.5
Najmi, A.6
Yu, T.T.7
Lau, K.8
Dimmitt, R.A.9
Cohen, H.J.10
|