-
1
-
-
0035885192
-
Inheritance of open-angle glaucoma in the Barbados family study
-
Nemesure, B., He, Q., Mendell, N., Wu, S.Y., Hejtmancik, J.F., Hennis, A. and Leske, M.C. (2001) Inheritance of open-angle glaucoma in the Barbados family study. Am. J. Med. Genet., 103, 36-43.
-
(2001)
Am. J. Med. Genet.
, vol.103
, pp. 36-43
-
-
Nemesure, B.1
He, Q.2
Mendell, N.3
Wu, S.Y.4
Hejtmancik, J.F.5
Hennis, A.6
Leske, M.C.7
-
2
-
-
0029980777
-
Number of people with glaucoma worldwide
-
Quigley, H.A. (1996) Number of people with glaucoma worldwide. Br. J. Ophthalmol., 80, 389-393.
-
(1996)
Br. J. Ophthalmol.
, vol.80
, pp. 389-393
-
-
Quigley, H.A.1
-
3
-
-
0029268389
-
Available data on blindness (update 1994)
-
Thylefors, B., Negrel, A.D., Pararajasegaram, R. and Dadzie, K.Y. (1995) Available data on blindness (update 1994). Ophthalmic Epidemiol., 2, 5-39.
-
(1995)
Ophthalmic Epidemiol.
, vol.2
, pp. 5-39
-
-
Thylefors, B.1
Negrel, A.D.2
Pararajasegaram, R.3
Dadzie, K.Y.4
-
4
-
-
0033941238
-
Accuracy and implications of a reported family history of glaucoma: Experience from the Glaucoma Inheritance Study in Tasmania
-
McNaught, A.I., Allen, J.G., Healey, D.L., McCartney, P.J., Coote, M.A., Wong, T.L., Craig, J.E., Green, C.M., Rait, J.L. and Mackey, D.A. (2000) Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in Tasmania. Arch. Ophthalmol., 118, 900-904.
-
(2000)
Arch. Ophthalmol.
, vol.118
, pp. 900-904
-
-
McNaught, A.I.1
Allen, J.G.2
Healey, D.L.3
McCartney, P.J.4
Coote, M.A.5
Wong, T.L.6
Craig, J.E.7
Green, C.M.8
Rait, J.L.9
Mackey, D.A.10
-
5
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
-
Semina, E.V., Reiter, R., Leysens, N.J., Alward, W.L., Small, K.W., Datson, N.A., Siegel-Bartelt, J., Bierke-Nelson, D., Bitoun, P., Zabel, B.U. et al. (1996) Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat. Genet., 14, 392-399.
-
(1996)
Nat. Genet.
, vol.14
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
Alward, W.L.4
Small, K.W.5
Datson, N.A.6
Siegel-Bartelt, J.7
Bierke-Nelson, D.8
Bitoun, P.9
Zabel, B.U.10
-
6
-
-
17344368672
-
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
-
Nishimura, D.Y., Swiderski, R.E., Alward, W.L., Searby, C.C., Patil, S.R., Bennet, S.R., Kanis, A.B., Gastier, J.M., Stone, E.M. and Sheffield, V.C. (1998) The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25. Nat. Genet., 19, 140-147.
-
(1998)
Nat. Genet.
, vol.19
, pp. 140-147
-
-
Nishimura, D.Y.1
Swiderski, R.E.2
Alward, W.L.3
Searby, C.C.4
Patil, S.R.5
Bennet, S.R.6
Kanis, A.B.7
Gastier, J.M.8
Stone, E.M.9
Sheffield, V.C.10
-
7
-
-
0032231330
-
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly
-
Mears, A.J., Jordan, T., Mirzayans, F., Dubois, S., Kume, T., Parlee, M., Ritch, R., Koop, B., Kuo, W.L., Collins, C. et al. (1998) Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly. Am. J. Hum. Genet., 63, 1316-1328.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1316-1328
-
-
Mears, A.J.1
Jordan, T.2
Mirzayans, F.3
Dubois, S.4
Kume, T.5
Parlee, M.6
Ritch, R.7
Koop, B.8
Kuo, W.L.9
Collins, C.10
-
8
-
-
0029762015
-
A second locus for Rieger syndrome maps to chromosome 13q14
-
Phillips, J.C., del Bono, E.A., Haines, J.L., Pralea, A.M., Cohen, J.S., Greff, L.J. and Wiggs, J.L. (1996) A second locus for Rieger syndrome maps to chromosome 13q14. Am. J. Hum. Genet., 59, 613-619.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 613-619
-
-
Phillips, J.C.1
del Bono, E.A.2
Haines, J.L.3
Pralea, A.M.4
Cohen, J.S.5
Greff, L.J.6
Wiggs, J.L.7
-
9
-
-
0030900462
-
A small deletion of 16q23.1- >16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies
-
Werner, W., Kraft, S., Callen, D.F., Bartsch, O. and Hinkel, G.K. (1997) A small deletion of 16q23.1- >16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies. Am. J. Med. Genet., 70, 371-376.
-
(1997)
Am. J. Med. Genet.
, vol.70
, pp. 371-376
-
-
Werner, W.1
Kraft, S.2
Callen, D.F.3
Bartsch, O.4
Hinkel, G.K.5
-
10
-
-
0029572447
-
Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12)
-
Larsson, C., Hellqvist, M., Pierrou, S., White, I., Enerback, S. and Carlsson, P. (1995) Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12). Genomics, 30, 464-469.
-
(1995)
Genomics
, vol.30
, pp. 464-469
-
-
Larsson, C.1
Hellqvist, M.2
Pierrou, S.3
White, I.4
Enerback, S.5
Carlsson, P.6
-
11
-
-
0342614209
-
Unified nomenclature for the winged helix/forkhead transcription factors
-
Kaestner, K.H., Knochel, W. and Martinez, D.E. (2000) Unified nomenclature for the winged helix/forkhead transcription factors. Genes Dev., 14, 142-146.
-
(2000)
Genes Dev.
, vol.14
, pp. 142-146
-
-
Kaestner, K.H.1
Knochel, W.2
Martinez, D.E.3
-
12
-
-
0027270989
-
Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5
-
Clark, K.L., Halay, E.D., Lai, E. and Burley, S.K. (1993) Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5. Nature, 364, 412-420.
-
(1993)
Nature
, vol.364
, pp. 412-420
-
-
Clark, K.L.1
Halay, E.D.2
Lai, E.3
Burley, S.K.4
-
13
-
-
0035092384
-
Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1
-
Saleem, R.A., Banerjee-Basu, S., Berry, F.B., Baxevanis, A.D. and Walter, M.A. (2001) Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1. Am. J. Hum. Genet., 68, 627-641.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 627-641
-
-
Saleem, R.A.1
Banerjee-Basu, S.2
Berry, F.B.3
Baxevanis, A.D.4
Walter, M.A.5
-
14
-
-
0344443182
-
Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1
-
Saleem, R.A., Banerjee-Basu, S., Berry, F.B., Baxevanis, A.D. and Walter, M.A. (2003) Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1. Hum. Mol. Genet., 12, 2993-3005.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2993-3005
-
-
Saleem, R.A.1
Banerjee-Basu, S.2
Berry, F.B.3
Baxevanis, A.D.4
Walter, M.A.5
-
15
-
-
0142169915
-
Identification and analysis of a novel mutation in the FOXC1 forkhead domain
-
Saleem, R.A., Murphy, T.C., Liebmann, J.M. and Walter, M.A. (2003) Identification and analysis of a novel mutation in the FOXC1 forkhead domain. Invest. Ophthalmol. Vis. Sci., 44, 4608-4612.
-
(2003)
Invest. Ophthalmol. Vis. Sci.
, vol.44
, pp. 4608-4612
-
-
Saleem, R.A.1
Murphy, T.C.2
Liebmann, J.M.3
Walter, M.A.4
-
16
-
-
0032511231
-
The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus
-
Kume, T., Deng, K.Y., Winfrey, V., Gould, D.B., Walter, M.A. and Hogan, B.L. (1998) The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus. Cell, 93, 985-996.
-
(1998)
Cell
, vol.93
, pp. 985-996
-
-
Kume, T.1
Deng, K.Y.2
Winfrey, V.3
Gould, D.B.4
Walter, M.A.5
Hogan, B.L.6
-
17
-
-
0033566179
-
The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye
-
Kidson, S.H., Kume, T., Deng, K., Winfrey, V. and Hogan, B.L. (1999) The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye. Dev. Biol., 211, 306-322.
-
(1999)
Dev. Biol.
, vol.211
, pp. 306-322
-
-
Kidson, S.H.1
Kume, T.2
Deng, K.3
Winfrey, V.4
Hogan, B.L.5
-
18
-
-
0033568038
-
Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles
-
Winnier, G.E., Kume, T., Deng, K., Rogers, R., Bundy, J., Raines, C., Walter, M.A., Hogan, B.L. and Conway, S.J. (1999) Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles. Dev. Biol., 213, 418-431.
-
(1999)
Dev. Biol.
, vol.213
, pp. 418-431
-
-
Winnier, G.E.1
Kume, T.2
Deng, K.3
Rogers, R.4
Bundy, J.5
Raines, C.6
Walter, M.A.7
Hogan, B.L.8
Conway, S.J.9
-
19
-
-
6944252087
-
Identification of target genes regulated by FOXC1 using nickel agarose-based chromatin enrichment
-
Tamimi, Y., Lines, M., Coca-Prados, M. and Walter, M.A. (2004) Identification of target genes regulated by FOXC1 using nickel agarose-based chromatin enrichment. Invest. Ophthalmol. Vis. Sci., 45, 3904-3913.
-
(2004)
Invest. Ophthalmol. Vis. Sci.
, vol.45
, pp. 3904-3913
-
-
Tamimi, Y.1
Lines, M.2
Coca-Prados, M.3
Walter, M.A.4
-
20
-
-
0032822672
-
FGF-19, a novel fibroblast growth factor with unique specificity for FGFR4
-
Xie, M.H., Holcomb, I., Deuel, B., Dowd, P., Huang, A., Vagts, A., Foster, J., Liang, J., Brush, J., Gu, Q. et al. (1999) FGF-19, a novel fibroblast growth factor with unique specificity for FGFR4. Cytokine, 11, 729-735.
-
(1999)
Cytokine
, vol.11
, pp. 729-735
-
-
Xie, M.H.1
Holcomb, I.2
Deuel, B.3
Dowd, P.4
Huang, A.5
Vagts, A.6
Foster, J.7
Liang, J.8
Brush, J.9
Gu, Q.10
-
21
-
-
0034020416
-
PipMaker - A web server for aligning two genomic DNA sequences
-
Schwartz, S., Zhang, Z., Frazer, K.A., Smit, A., Riemer, C., Bouck, J., Gibbs, R., Hardison, R. and Miller, W. (2000) PipMaker - a web server for aligning two genomic DNA sequences. Genome Res., 10, 577-586.
-
(2000)
Genome Res.
, vol.10
, pp. 577-586
-
-
Schwartz, S.1
Zhang, Z.2
Frazer, K.A.3
Smit, A.4
Riemer, C.5
Bouck, J.6
Gibbs, R.7
Hardison, R.8
Miller, W.9
-
22
-
-
1842816370
-
Mouse FGF15 is the ortholog of human and chick FGF19, but is not uniquely required for otic induction
-
Wright, T.J., Ladher, R., McWhirter, J., Murre, C., Schoenwolf, G.C. and Mansour, S.L. (2004) Mouse FGF15 is the ortholog of human and chick FGF19, but is not uniquely required for otic induction. Dev. Biol., 269, 264-275.
-
(2004)
Dev. Biol.
, vol.269
, pp. 264-275
-
-
Wright, T.J.1
Ladher, R.2
McWhirter, J.3
Murre, C.4
Schoenwolf, G.C.5
Mansour, S.L.6
-
23
-
-
0028046675
-
Cloning and characterization of seven human forkhead proteins: Binding site specificity and DNA bending
-
Pierrou, S., Hellqvist, M., Samuelsson, L., Enerback, S. and Carlsson, P. (1994) Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending. EMBO J., 13, 5002-5012.
-
(1994)
EMBO J.
, vol.13
, pp. 5002-5012
-
-
Pierrou, S.1
Hellqvist, M.2
Samuelsson, L.3
Enerback, S.4
Carlsson, P.5
-
24
-
-
33750206693
-
Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations
-
in press
-
Strungaru, M.H., Dinu, I. and Walter, M.A. (2006) Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations. IOVS, in press.
-
(2006)
IOVS
-
-
Strungaru, M.H.1
Dinu, I.2
Walter, M.A.3
-
25
-
-
7944231499
-
Using zebrafish to study the complex genetics of glaucoma
-
McMahon, C., Semina, E.V. and Link, B.A. (2004) Using zebrafish to study the complex genetics of glaucoma. Comp. Biochem. Physiol. C Toxicol. Pharmacol., 138, 343-350.
-
(2004)
Comp. Biochem. Physiol. C Toxicol. Pharmacol.
, vol.138
, pp. 343-350
-
-
McMahon, C.1
Semina, E.V.2
Link, B.A.3
-
26
-
-
0035883747
-
The winged helix transcription factor Foxc1a is essential for somitogenesis in zebrafish
-
Topczewska, J.M., Topczewski, J., Shostak, A., Kume, T., Solnica-Krezel, L. and Hogan, B.L. (2001) The winged helix transcription factor Foxc1a is essential for somitogenesis in zebrafish. Genes Dev., 15, 2483-2493.
-
(2001)
Genes Dev.
, vol.15
, pp. 2483-2493
-
-
Topczewska, J.M.1
Topczewski, J.2
Shostak, A.3
Kume, T.4
Solnica-Krezel, L.5
Hogan, B.L.6
-
27
-
-
28244468141
-
Fgf19 regulated by Hh signaling is required for zebrafish forebrain development
-
Miyake, A., Nakayama, Y., Konishi, M. and Itoh, N. (2005) Fgf19 regulated by Hh signaling is required for zebrafish forebrain development. Dev. Biol., 288, 259-275.
-
(2005)
Dev. Biol.
, vol.288
, pp. 259-275
-
-
Miyake, A.1
Nakayama, Y.2
Konishi, M.3
Itoh, N.4
-
28
-
-
33750214319
-
Expression and functional analysis of foxc1.1 and foxc1.2 during ocular development in zebrafish
-
Skarie, J.M., Berry, F.B., Walter, M.A. and Link, B.A. (2006). Expression and functional analysis of foxc1.1 and foxc1.2 during ocular development in zebrafish. Invest. Ophthalmol. Vis. Sci., 47, 3118.
-
(2006)
Invest. Ophthalmol. Vis. Sci.
, vol.47
, pp. 3118
-
-
Skarie, J.M.1
Berry, F.B.2
Walter, M.A.3
Link, B.A.4
-
29
-
-
0034612592
-
Transformation and Stat activation by derivatives of FGFR1, FGFR3 and FGFR4
-
Hart, K.C., Robertson, S.C., Kanemitsu, M.Y., Meyer, A.N., Tynan, J.A. and Donoghue, D.J. (2000) Transformation and Stat activation by derivatives of FGFR1, FGFR3 and FGFR4. Oncogene, 19, 3309-3320.
-
(2000)
Oncogene
, vol.19
, pp. 3309-3320
-
-
Hart, K.C.1
Robertson, S.C.2
Kanemitsu, M.Y.3
Meyer, A.N.4
Tynan, J.A.5
Donoghue, D.J.6
-
30
-
-
0036884167
-
The use and analysis of microarray data
-
Butte, A. (2002) The use and analysis of microarray data. Nat. Rev. Drug Discov., 1, 951-960.
-
(2002)
Nat. Rev. Drug Discov.
, vol.1
, pp. 951-960
-
-
Butte, A.1
-
31
-
-
0035809197
-
PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: Implications for the pathology of Rieger syndrome
-
Hjalt, T.A., Amendt, B.A. and Murray, J.C. (2001) PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: Implications for the pathology of Rieger syndrome. J. Cell Biol., 152, 545-552.
-
(2001)
J. Cell Biol.
, vol.152
, pp. 545-552
-
-
Hjalt, T.A.1
Amendt, B.A.2
Murray, J.C.3
-
32
-
-
3242875213
-
MotifViz: An analysis and visualization tool for motif discovery
-
Fu, Y., Frith, M.C., Haverty, P.M. and Weng, Z. (2004) MotifViz: An analysis and visualization tool for motif discovery. Nucleic Acids Res., 32, W420-W423.
-
(2004)
Nucleic Acids Res.
, vol.32
-
-
Fu, Y.1
Frith, M.C.2
Haverty, P.M.3
Weng, Z.4
-
33
-
-
0033579972
-
Structure and expression of a novel human FGF, FGF-19, expressed in the fetal brain
-
Nishimura, T., Utsunomiya, Y., Hoshikawa, M., Ohuchi, H. and Itoh, N. (1999) Structure and expression of a novel human FGF, FGF-19, expressed in the fetal brain. Biochim. Biophys. Acta, 1444, 148-151.
-
(1999)
Biochim. Biophys. Acta
, vol.1444
, pp. 148-151
-
-
Nishimura, T.1
Utsunomiya, Y.2
Hoshikawa, M.3
Ohuchi, H.4
Itoh, N.5
-
34
-
-
1342328598
-
Differential distribution of fibroblast growth factor receptors (FGFRs) on foveal cones: FGFR-4 is an early marker of cone photoreceptors
-
Cornish, E.E., Natoli, R.C., Hendrickson, A. and Provis, J.M. (2004) Differential distribution of fibroblast growth factor receptors (FGFRs) on foveal cones: FGFR-4 is an early marker of cone photoreceptors. Mol. Vis., 10, 1-14.
-
(2004)
Mol. Vis.
, vol.10
, pp. 1-14
-
-
Cornish, E.E.1
Natoli, R.C.2
Hendrickson, A.3
Provis, J.M.4
-
35
-
-
0035976138
-
Signaling by fibroblast growth factors: The inside story
-
2001
-
Goldfarb, M. (2001) Signaling by fibroblast growth factors: The inside story. Sci. STKE, 2001, E37.
-
(2001)
Sci. STKE
-
-
Goldfarb, M.1
-
36
-
-
0035081241
-
Fibroblast growth factors
-
REVIEWS3005
-
Ornitz, D.M. and Itoh, N. (2001) Fibroblast growth factors. Genome Biol., 2, REVIEWS3005.
-
(2001)
Genome Biol.
, vol.2
-
-
Ornitz, D.M.1
Itoh, N.2
-
37
-
-
0034673214
-
Inhibition of MAP kinase (MEK) results in an anti-inflammatory response in vivo
-
Jaffee, B.D., Manos, E.J., Collins, R.J., Czerniak, P.M., Favata, M.F., Magolda, R.L., Scherle, P.A. and Trzaskos, J.M. (2000) Inhibition of MAP kinase (MEK) results in an anti-inflammatory response in vivo. Biochem. Biophys. Res. Commun., 268, 647-651.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.268
, pp. 647-651
-
-
Jaffee, B.D.1
Manos, E.J.2
Collins, R.J.3
Czerniak, P.M.4
Favata, M.F.5
Magolda, R.L.6
Scherle, P.A.7
Trzaskos, J.M.8
-
38
-
-
0036845687
-
Signaling mechanism of TGF-beta1-induced collagen contraction mediated by bovine trabecular meshwork cells
-
Nakamura, Y., Hirano, S., Suzuki, K., Seki, K., Sagara, T. and Nishida, T. (2002) Signaling mechanism of TGF-beta1-induced collagen contraction mediated by bovine trabecular meshwork cells. Invest. Ophthalmol. Vis. Sci., 43, 3465-3472.
-
(2002)
Invest. Ophthalmol. Vis. Sci.
, vol.43
, pp. 3465-3472
-
-
Nakamura, Y.1
Hirano, S.2
Suzuki, K.3
Seki, K.4
Sagara, T.5
Nishida, T.6
-
39
-
-
0344688189
-
Activation of ERK1/2 MAP kinase pathway induces tight junction disruption in human corneal epithelial cells
-
Wang, Y., Zhang, J., Yi, X.J. and Yu, F.S. (2004) Activation of ERK1/2 MAP kinase pathway induces tight junction disruption in human corneal epithelial cells. Exp. Eye Res., 78, 125-136.
-
(2004)
Exp. Eye Res.
, vol.78
, pp. 125-136
-
-
Wang, Y.1
Zhang, J.2
Yi, X.J.3
Yu, F.S.4
-
40
-
-
0038485740
-
Novel anterior segment phenotypes resulting from forkhead gene alterations: Evidence for cross-species conservation of function
-
Lehmann, O.J., Tuft, S., Brice, G., Smith, R., Blixt, A., Bell, R., Johansson, B., Jordan, T., Hitchings, R.A., Khaw, P.T. et al. (2003) Novel anterior segment phenotypes resulting from forkhead gene alterations: Evidence for cross-species conservation of function. Invest. Ophthalmol. Vis. Sci., 44, 2627-2633.
-
(2003)
Invest. Ophthalmol. Vis. Sci.
, vol.44
, pp. 2627-2633
-
-
Lehmann, O.J.1
Tuft, S.2
Brice, G.3
Smith, R.4
Blixt, A.5
Bell, R.6
Johansson, B.7
Jordan, T.8
Hitchings, R.A.9
Khaw, P.T.10
-
41
-
-
0037080674
-
Isolating human transcription factor targets by coupling chromatin immunoprecipitation and CpG island microarray analysis
-
Weinmann, A.S., Yan, P.S., Oberley, M.J., Huang, T.H. and Farnham, P.J. (2002) Isolating human transcription factor targets by coupling chromatin immunoprecipitation and CpG island microarray analysis. Genes Dev., 16, 235-244.
-
(2002)
Genes Dev.
, vol.16
, pp. 235-244
-
-
Weinmann, A.S.1
Yan, P.S.2
Oberley, M.J.3
Huang, T.H.4
Farnham, P.J.5
-
42
-
-
0036024955
-
Identification of unknown target genes of human transcription factors using chromatin immunoprecipitation
-
Weinmann, A.S. and Farnham, P.J. (2002) Identification of unknown target genes of human transcription factors using chromatin immunoprecipitation. Methods (Duluth), 26, 37-47.
-
(2002)
Methods (Duluth)
, vol.26
, pp. 37-47
-
-
Weinmann, A.S.1
Farnham, P.J.2
-
43
-
-
0033562350
-
Development and validation of real-time quantitative reverse transcriptase-polymerase chain reaction for monitoring gene expression in cardiac myocytes in vitro
-
Winer, J., Jung, C.K., Shackel, I. and Williams, P.M. (1999) Development and validation of real-time quantitative reverse transcriptase-polymerase chain reaction for monitoring gene expression in cardiac myocytes in vitro. Anal. Biochem., 270, 41-49.
-
(1999)
Anal. Biochem.
, vol.270
, pp. 41-49
-
-
Winer, J.1
Jung, C.K.2
Shackel, I.3
Williams, P.M.4
-
44
-
-
16644391747
-
Spatial and temporal expression of the zebrafish genome by large-scale in situ hybridization screening
-
Thisse, B., Heyer, V., Lux, A., Alunni, V., Degrave, A., Seiliez, I., Kirchner, J., Parkhill, J.P. and Thisse, C. (2004) Spatial and temporal expression of the zebrafish genome by large-scale in situ hybridization screening. Methods Cell Biol., 77, 505-519.
-
(2004)
Methods Cell Biol.
, vol.77
, pp. 505-519
-
-
Thisse, B.1
Heyer, V.2
Lux, A.3
Alunni, V.4
Degrave, A.5
Seiliez, I.6
Kirchner, J.7
Parkhill, J.P.8
Thisse, C.9
-
45
-
-
23944494639
-
Morphogenesis of the anterior segment in the zebrafish eye
-
Soules, K.A. and Link, B.A. (2005) Morphogenesis of the anterior segment in the zebrafish eye. BMC Dev. Biol., 5, 12.
-
(2005)
BMC Dev. Biol.
, vol.5
, pp. 12
-
-
Soules, K.A.1
Link, B.A.2
|