-
1
-
-
0025204569
-
Position-effect variegation after 60 years
-
10.1016/0168-9525(90)90304-O 2087785
-
Henikoff S Position-effect variegation after 60 years. Trends Genet 1990, 6:422-426. 10.1016/0168-9525(90)90304-O 2087785
-
(1990)
Trends Genet
, vol.6
, pp. 422-426
-
-
Henikoff, S.1
-
2
-
-
0000563999
-
Parental control of position-effect variegation. II. Effect of sex of parent contributing white-mottled rearrangement in Drosophila melanogaster
-
1210265 13915890
-
Spofford JB Parental control of position-effect variegation. II. Effect of sex of parent contributing white-mottled rearrangement in Drosophila melanogaster. Genetics 1961, 46:1151-1167. 1210265 13915890
-
(1961)
Genetics
, vol.46
, pp. 1151-1167
-
-
Spofford, J.B.1
-
3
-
-
0017844230
-
Influence of maternal phenotype on metabolic differentiation of agouti locus mutants in the mouse
-
1224599 640377
-
Wolff GL Influence of maternal phenotype on metabolic differentiation of agouti locus mutants in the mouse. Genetics 1978, 88:529-539. 1224599 640377
-
(1978)
Genetics
, vol.88
, pp. 529-539
-
-
Wolff, G.L.1
-
5
-
-
0043093697
-
Transposable elements: Targets for early nutritional effects on epigenetic gene regulation
-
165709 12861015 10.1128/MCB.23.15.5293-5300.2003
-
Waterland RA Jirtle RL Transposable elements: Targets for early nutritional effects on epigenetic gene regulation. Mol Cell Biol 2003, 23:5293-5300. 165709 12861015 10.1128/MCB.23.15.5293-5300.2003
-
(2003)
Mol Cell Biol
, vol.23
, pp. 5293-5300
-
-
Waterland, R.A.1
Jirtle, R.L.2
-
6
-
-
0032751471
-
Epigenetic inheritance at the agouti locus in the mouse
-
10.1038/15490 10545949
-
Morgan HD Sutherland HG Martin DI Whitelaw E Epigenetic inheritance at the agouti locus in the mouse. Nat Genet 1999, 23:314-318. 10.1038/15490 10545949
-
(1999)
Nat Genet
, vol.23
, pp. 314-318
-
-
Morgan, H.D.1
Sutherland, H.G.2
Martin, D.I.3
Whitelaw, E.4
-
7
-
-
0026928683
-
Position effect variegation and chromatin proteins
-
10.1002/bies.950140907 1365916
-
Reuter G Spierer P Position effect variegation and chromatin proteins. Bioessays 1992, 14:605-612. 10.1002/bies.950140907 1365916
-
(1992)
Bioessays
, vol.14
, pp. 605-612
-
-
Reuter, G.1
Spierer, P.2
-
8
-
-
0037324675
-
Position-effect variegation and the genetic dissection of chromatin regulation in Drosophila
-
10.1016/S1084-9521(02)00138-6 12524009
-
Schotta G Ebert A Dorn R Reuter G Position-effect variegation and the genetic dissection of chromatin regulation in Drosophila. Semin Cell Dev Biol 2003, 14:67-75. 10.1016/S1084-9521(02)00138-6 12524009
-
(2003)
Semin Cell Dev Biol
, vol.14
, pp. 67-75
-
-
Schotta, G.1
Ebert, A.2
Dorn, R.3
Reuter, G.4
-
9
-
-
0027496506
-
The enhancer of position-effect variegation of Drosophila, E(var)3-93D, codes for a chromatin protein containing a conserved domain common to several transcriptional regulators
-
47985 8248257 10.1073/pnas.90.23.11376
-
Dorn R Krauss V Reuter G Saumweber H The enhancer of position-effect variegation of Drosophila, E(var)3-93D, codes for a chromatin protein containing a conserved domain common to several transcriptional regulators. Proc Natl Acad Sci USA 1993, 90:11376-11380. 47985 8248257 10.1073/pnas.90.23.11376
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 11376-11380
-
-
Dorn, R.1
Krauss, V.2
Reuter, G.3
Saumweber, H.4
-
10
-
-
19644376762
-
An N-ethyl-N-nitrosourea screen for genes involved in variegation in the mouse
-
1140414 15890782 10.1073/pnas.0409375102
-
Blewitt ME Vickaryous NK Hemley SJ Ashe A Bruxner TJ Preis JI Arkell R Whitelaw E An N-ethyl-N-nitrosourea screen for genes involved in variegation in the mouse. Proc Natl Acad Sci USA 2005, 102:7629-7634. 1140414 15890782 10.1073/pnas.0409375102
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 7629-7634
-
-
Blewitt, M.E.1
Vickaryous, N.K.2
Hemley, S.J.3
Ashe, A.4
Bruxner, T.J.5
Preis, J.I.6
Arkell, R.7
Whitelaw, E.8
-
11
-
-
42649100978
-
SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation
-
10.1038/ng.142 18425126
-
Blewitt ME Gendrel AV Pang Z Sparrow DB Whitelaw N Craig JM Apedaile A Hilton DJ Dunwoodie SL Brockdorff N Kay GF Whitelaw E SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation. Nat Genet 2008, 40:663-669. 10.1038/ng.142 18425126
-
(2008)
Nat Genet
, vol.40
, pp. 663-669
-
-
Blewitt, M.E.1
Gendrel, A.V.2
Pang, Z.3
Sparrow, D.B.4
Whitelaw, N.5
Craig, J.M.6
Apedaile, A.7
Hilton, D.J.8
Dunwoodie, S.L.9
Brockdorff, N.10
Kay, G.F.11
Whitelaw, E.12
-
12
-
-
34247641746
-
Modifiers of epigenetic reprogramming show paternal effects in the mouse
-
10.1038/ng2031 17450140
-
Chong S Vickaryous N Ashe A Zamudio N Youngson N Hemley S Stopka T Skoultchi A Matthews J Scott HS de Kretser D O'Bryan M Blewitt M Whitelaw E Modifiers of epigenetic reprogramming show paternal effects in the mouse. Nat Genet 2007, 39:614-622. 10.1038/ng2031 17450140
-
(2007)
Nat Genet
, vol.39
, pp. 614-622
-
-
Chong, S.1
Vickaryous, N.2
Ashe, A.3
Zamudio, N.4
Youngson, N.5
Hemley, S.6
Stopka, T.7
Skoultchi, A.8
Matthews, J.9
Scott, H.S.10
de Kretser, D.11
O'Bryan, M.12
Blewitt, M.13
Whitelaw, E.14
-
13
-
-
0031984304
-
Repeat-induced gene silencing in mammals
-
10.1038/ng0198-56 9425901
-
Garrick D Fiering S Martin DI Whitelaw E Repeat-induced gene silencing in mammals. Nat Genet 1998, 18:56-59. 10.1038/ng0198-56 9425901
-
(1998)
Nat Genet
, vol.18
, pp. 56-59
-
-
Garrick, D.1
Fiering, S.2
Martin, D.I.3
Whitelaw, E.4
-
14
-
-
0037850970
-
Sensitive flow cytometric analysis reveals a novel type of parent-of-origin effect in the mouse genome
-
10.1016/S0960-9822(03)00335-X 12781134
-
Preis JI Downes M Oates NA Rasko JE Whitelaw E Sensitive flow cytometric analysis reveals a novel type of parent-of-origin effect in the mouse genome. Curr Biol 2003, 13:955-959. 10.1016/S0960-9822(03)00335-X 12781134
-
(2003)
Curr Biol
, vol.13
, pp. 955-959
-
-
Preis, J.I.1
Downes, M.2
Oates, N.A.3
Rasko, J.E.4
Whitelaw, E.5
-
15
-
-
33947235559
-
Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: Revisited
-
10.1007/s00335-006-0065-z 17347895
-
Keays DA Clark TG Campbell TG Broxholme J Valdar W Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: Revisited. Mamm Genome 2007, 18:123-124. 10.1007/s00335-006-0065-z 17347895
-
(2007)
Mamm Genome
, vol.18
, pp. 123-124
-
-
Keays, D.A.1
Clark, T.G.2
Campbell, T.G.3
Broxholme, J.4
Valdar, W.5
-
16
-
-
33644639082
-
Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens
-
10.1007/s00335-005-0101-4 16518690
-
Keays DA Clark TG Flint J Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens. Mamm Genome 2006, 17:230-238. 10.1007/s00335-005-0101-4 16518690
-
(2006)
Mamm Genome
, vol.17
, pp. 230-238
-
-
Keays, D.A.1
Clark, T.G.2
Flint, J.3
-
18
-
-
3142562372
-
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases
-
10.1016/j.str.2004.04.012 15242608
-
Somoza JR Skene RJ Katz BA Mol C Ho JD Jennings AJ Luong C Arvai A Buggy JJ Chi E Tang J Sang BC Verner E Wynands R Leahy EM Dougan DR Snell G Navre M Knuth MW Swanson RV McRee DE Tari LW Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases. Structure 2004, 12:1325-1334. 10.1016/j.str.2004.04.012 15242608
-
(2004)
Structure
, vol.12
, pp. 1325-1334
-
-
Somoza, J.R.1
Skene, R.J.2
Katz, B.A.3
Mol, C.4
Ho, J.D.5
Jennings, A.J.6
Luong, C.7
Arvai, A.8
Buggy, J.J.9
Chi, E.10
Tang, J.11
Sang, B.C.12
Verner, E.13
Wynands, R.14
Leahy, E.M.15
Dougan, D.R.16
Snell, G.17
Navre, M.18
Knuth, M.W.19
Swanson, R.V.20
McRee, D.E.21
Tari, L.W.22
more..
-
19
-
-
6344222799
-
Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor
-
524051 15477595 10.1073/pnas.0404603101
-
Vannini A Volpari C Filocamo G Casavola EC Brunetti M Renzoni D Chakravarty P Paolini C De Francesco R Gallinari P Steinkühler C Di Marco S Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor. Proc Natl Acad Sci USA 2004, 101:15064-15069. 524051 15477595 10.1073/ pnas.0404603101
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 15064-15069
-
-
Vannini, A.1
Volpari, C.2
Filocamo, G.3
Casavola, E.C.4
Brunetti, M.5
Renzoni, D.6
Chakravarty, P.7
Paolini, C.8
De Francesco, R.9
Gallinari, P.10
Steinkühler, C.11
Di Marco, S.12
-
20
-
-
0037189568
-
SUMO-1 modification of histone deacetylase 1 (HDAC1) modulates its biological activities
-
10.1074/jbc.M203690200 11960997
-
David G Neptune MA DePinho RA SUMO-1 modification of histone deacetylase 1 (HDAC1) modulates its biological activities. J Biol Chem 2002, 277:23658-23663. 10.1074/jbc.M203690200 11960997
-
(2002)
J Biol Chem
, vol.277
, pp. 23658-23663
-
-
David, G.1
Neptune, M.A.2
DePinho, R.A.3
-
21
-
-
18444414332
-
Essential function of histone deacetylase 1 in proliferation control and CDK inhibitor repression
-
126040 12032080 10.1093/emboj/21.11.2672
-
Lagger G O'Carroll D Rembold M Khier H Tischler J Weitzer G Schuettengruber B Hauser C Brunmeir R Jenuwein T Seiser C Essential function of histone deacetylase 1 in proliferation control and CDK inhibitor repression. EMBO J 2002, 21:2672-2681. 126040 12032080 10.1093/ emboj/21.11.2672
-
(2002)
EMBO J
, vol.21
, pp. 2672-2681
-
-
Lagger, G.1
O'Carroll, D.2
Rembold, M.3
Khier, H.4
Tischler, J.5
Weitzer, G.6
Schuettengruber, B.7
Hauser, C.8
Brunmeir, R.9
Jenuwein, T.10
Seiser, C.11
-
22
-
-
33750324764
-
Negative and positive regulation of gene expression by mouse histone deacetylase 1
-
1636735 16940178 10.1128/MCB.01220-06
-
Zupkovitz G Tischler J Posch M Sadzak I Ramsauer K Egger G Grausenburger R Schweifer N Chiocca S Decker T Seiser C Negative and positive regulation of gene expression by mouse histone deacetylase 1. Mol Cell Biol 2006, 26:7913-7928. 1636735 16940178 10.1128/MCB.01220-06
-
(2006)
Mol Cell Biol
, vol.26
, pp. 7913-7928
-
-
Zupkovitz, G.1
Tischler, J.2
Posch, M.3
Sadzak, I.4
Ramsauer, K.5
Egger, G.6
Grausenburger, R.7
Schweifer, N.8
Chiocca, S.9
Decker, T.10
Seiser, C.11
-
23
-
-
0036565656
-
WSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci
-
125993 11980720 10.1093/emboj/21.9.2231
-
Bozhenok L Wade PA Varga-Weisz P WSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci. EMBO J 2002, 21:2231-2241. 125993 11980720 10.1093/emboj/21.9.2231
-
(2002)
EMBO J
, vol.21
, pp. 2231-2241
-
-
Bozhenok, L.1
Wade, P.A.2
Varga-Weisz, P.3
-
24
-
-
0038046628
-
The chromatin-remodeling complex WINAC targets a nuclear receptor to promoters and is impaired in Williams syndrome
-
10.1016/S0092-8674(03)00436-7 12837248
-
Kitagawa H Fujiki R Yoshimura K Mezaki Y Uematsu Y Matsui D Ogawa S Unno K Okubo M Tokita A Nakagawa T Ito T Ishimi Y Nagasawa H Matsumoto T Yanagisawa J Kato S The chromatin-remodeling complex WINAC targets a nuclear receptor to promoters and is impaired in Williams syndrome. Cell 2003, 113:905-917. 10.1016/S0092-8674(03)00436-7 12837248
-
(2003)
Cell
, vol.113
, pp. 905-917
-
-
Kitagawa, H.1
Fujiki, R.2
Yoshimura, K.3
Mezaki, Y.4
Uematsu, Y.5
Matsui, D.6
Ogawa, S.7
Unno, K.8
Okubo, M.9
Tokita, A.10
Nakagawa, T.11
Ito, T.12
Ishimi, Y.13
Nagasawa, H.14
Matsumoto, T.15
Yanagisawa, J.16
Kato, S.17
-
25
-
-
33644869971
-
The chromatin remodelling complex WSTF-SNF2h interacts with nuclear myosin 1 and has a role in RNA polymerase I transcription
-
1479564 16514417
-
Percipalle P Fomproix N Cavellan E Voit R Reimer G Kruger T Thyberg J Scheer U Grummt I Farrants AK The chromatin remodelling complex WSTF-SNF2h interacts with nuclear myosin 1 and has a role in RNA polymerase I transcription. EMBO Rep 2006, 7:525-530. 1479564 16514417
-
(2006)
EMBO Rep
, vol.7
, pp. 525-530
-
-
Percipalle, P.1
Fomproix, N.2
Cavellan, E.3
Voit, R.4
Reimer, G.5
Kruger, T.6
Thyberg, J.7
Scheer, U.8
Grummt, I.9
Farrants, A.K.10
-
26
-
-
0025323887
-
Epigenetic control of transgene expression and imprinting by genotype-specific modifiers
-
10.1016/0092-8674(90)90195-K 2111735
-
Allen ND Norris ML Surani MA Epigenetic control of transgene expression and imprinting by genotype-specific modifiers. Cell 1990, 61:853-861. 10.1016/0092-8674(90)90195-K 2111735
-
(1990)
Cell
, vol.61
, pp. 853-861
-
-
Allen, N.D.1
Norris, M.L.2
Surani, M.A.3
-
27
-
-
0024758382
-
Cellular mosaicism in the methylation and expression of hemizygous loci in the mouse
-
10.1101/gad.3.11.1669 2606343
-
McGowan R Campbell R Peterson A Sapienza C Cellular mosaicism in the methylation and expression of hemizygous loci in the mouse. Genes Dev 1989, 3:1669-1676. 10.1101/gad.3.11.1669 2606343
-
(1989)
Genes Dev
, vol.3
, pp. 1669-1676
-
-
McGowan, R.1
Campbell, R.2
Peterson, A.3
Sapienza, C.4
-
28
-
-
0030458054
-
Variegated expression of a globin transgene correlates with chromatin accessibility but not methylation status
-
146354 9016659 10.1093/nar/24.24.4902
-
Garrick D Sutherland H Robertson G Whitelaw E Variegated expression of a globin transgene correlates with chromatin accessibility but not methylation status. Nucleic Acids Res 1996, 24:4902-4909. 146354 9016659 10.1093/nar/24.24.4902
-
(1996)
Nucleic Acids Res
, vol.24
, pp. 4902-4909
-
-
Garrick, D.1
Sutherland, H.2
Robertson, G.3
Whitelaw, E.4
-
29
-
-
0026747665
-
Cis-acting sequences regulating expression of the human alpha-globin cluster lie within constitutively open chromatin
-
10.1016/0092-8674(92)90290-S 1591777
-
Vyas P Vickers MA Simmons DL Ayyub H Craddock CF Higgs DR Cis-acting sequences regulating expression of the human alpha-globin cluster lie within constitutively open chromatin. Cell 1992, 69:781-793. 10.1016/ 0092-8674(92)90290-S 1591777
-
(1992)
Cell
, vol.69
, pp. 781-793
-
-
Vyas, P.1
Vickers, M.A.2
Simmons, D.L.3
Ayyub, H.4
Craddock, C.F.5
Higgs, D.R.6
-
30
-
-
0034254857
-
NuRD and SIN3 histone deacetylase complexes in development
-
10.1016/S0168-9525(00)02066-7 10904264
-
Ahringer J NuRD and SIN3 histone deacetylase complexes in development. Trends Genet 2000, 16:351-356. 10.1016/S0168-9525(00)02066-7 10904264
-
(2000)
Trends Genet
, vol.16
, pp. 351-356
-
-
Ahringer, J.1
-
31
-
-
0029932598
-
A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p
-
10.1126/science.272.5260.408 8602529
-
Taunton J Hassig CA Schreiber SL A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p. Science 1996, 272:408-411. 10.1126/science.272.5260.408 8602529
-
(1996)
Science
, vol.272
, pp. 408-411
-
-
Taunton, J.1
Hassig, C.A.2
Schreiber, S.L.3
-
32
-
-
27844520157
-
Ligand-induced transrepression by VDR through association of WSTF with acetylated histones
-
1283952 16252006 10.1038/sj.emboj.7600853
-
Fujiki R Kim MS Sasaki Y Yoshimura K Kitagawa H Kato S Ligand-induced transrepression by VDR through association of WSTF with acetylated histones. EMBO J 2005, 24:3881-3894. 1283952 16252006 10.1038/ sj.emboj.7600853
-
(2005)
EMBO J
, vol.24
, pp. 3881-3894
-
-
Fujiki, R.1
Kim, M.S.2
Sasaki, Y.3
Yoshimura, K.4
Kitagawa, H.5
Kato, S.6
-
33
-
-
25444442079
-
Chromatin remodeling by WSTF-ISWI at the replication site: Opening a window of opportunity for epigenetic inheritance?
-
15753658
-
Poot RA Bozhenok L Berg van den DL Hawkes N Varga-Weisz PD Chromatin remodeling by WSTF-ISWI at the replication site: Opening a window of opportunity for epigenetic inheritance? Cell Cycle 2005, 4:543-546. 15753658
-
(2005)
Cell Cycle
, vol.4
, pp. 543-546
-
-
Poot, R.A.1
Bozhenok, L.2
Berg, D.L.3
Hawkes, N.4
Varga-Weisz, P.D.5
-
34
-
-
0037265835
-
Williams-Beuren syndrome: A model of recurrent genomic mutation
-
10.1159/000067836 12638521
-
Perez Jurado AL Williams-Beuren syndrome: A model of recurrent genomic mutation. Horm Res 2003, 59(Suppl 1):106-113. 10.1159/000067836 12638521
-
(2003)
Horm Res
, vol.59
, Issue.SUPPL. 1
, pp. 106-113
-
-
Perez Jurado, A.L.1
-
35
-
-
0035113116
-
Analysis of cerebral shape in Williams syndrome
-
10.1001/archneur.58.2.283 11176967
-
Schmitt JE Eliez S Bellugi U Reiss AL Analysis of cerebral shape in Williams syndrome. Arch Neurol 2001, 58:283-287. 10.1001/ archneur.58.2.283 11176967
-
(2001)
Arch Neurol
, vol.58
, pp. 283-287
-
-
Schmitt, J.E.1
Eliez, S.2
Bellugi, U.3
Reiss, A.L.4
-
36
-
-
0032999601
-
Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes
-
1734394 10874638
-
Botta A Novelli G Mari A Novelli A Sabani M Korenberg J Osborne LR Digilio MC Giannotti A Dallapiccola B Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes. J Med Genet 1999, 36:478-480. 1734394 10874638
-
(1999)
J Med Genet
, vol.36
, pp. 478-480
-
-
Botta, A.1
Novelli, G.2
Mari, A.3
Novelli, A.4
Sabani, M.5
Korenberg, J.6
Osborne, L.R.7
Digilio, M.C.8
Giannotti, A.9
Dallapiccola, B.10
-
37
-
-
0036021044
-
The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome
-
10.1038/sj.ejhg.5200812 12080386
-
Duba HC Doll A Neyer M Erdel M Mann C Hammerer I Utermann G Grzeschik KH The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome. Eur J Hum Genet 2002, 10:351-361. 10.1038/ sj.ejhg.5200812 12080386
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 351-361
-
-
Duba, H.C.1
Doll, A.2
Neyer, M.3
Erdel, M.4
Mann, C.5
Hammerer, I.6
Utermann, G.7
Grzeschik, K.H.8
-
38
-
-
33847271581
-
An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism
-
10.1136/jmg.2006.044537 16971481
-
Edelmann L Prosnitz A Pardo S Bhatt J Cohen N Lauriat T Ouchanov L González PJ Manghi ER Bondy P Esquivel M Monge S Delgado MF Splendore A Francke U Burton BK McInnes LA An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism. J Med Genet 2007, 44:136-143. 10.1136/jmg.2006.044537 16971481
-
(2007)
J Med Genet
, vol.44
, pp. 136-143
-
-
Edelmann, L.1
Prosnitz, A.2
Pardo, S.3
Bhatt, J.4
Cohen, N.5
Lauriat, T.6
Ouchanov, L.7
González, P.J.8
Manghi, E.R.9
Bondy, P.10
Esquivel, M.11
Monge, S.12
Delgado, M.F.13
Splendore, A.14
Francke, U.15
Burton, B.K.16
McInnes, L.A.17
-
39
-
-
10744229701
-
Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23
-
12865760
-
Hirota H Matsuoka R Chen XN Salandanan LS Lincoln A Rose FE Sunahara M Osawa M Bellugi U Korenberg JR Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23. Genet Med 2003, 5:311-321. 12865760
-
(2003)
Genet Med
, vol.5
, pp. 311-321
-
-
Hirota, H.1
Matsuoka, R.2
Chen, X.N.3
Salandanan, L.S.4
Lincoln, A.5
Rose, F.E.6
Sunahara, M.7
Osawa, M.8
Bellugi, U.9
Korenberg, J.R.10
-
40
-
-
33645117093
-
Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions
-
10.1136/jmg.2005.034009 15994861
-
Howald C Merla G Digilio MC Amenta S Lyle R Deutsch S Choudhury U Bottani A Antonarakis SE Fryssira H Dallapiccola B Reymond A Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions. J Med Genet 2006, 43:266-273. 10.1136/jmg.2005.034009 15994861
-
(2006)
J Med Genet
, vol.43
, pp. 266-273
-
-
Howald, C.1
Merla, G.2
Digilio, M.C.3
Amenta, S.4
Lyle, R.5
Deutsch, S.6
Choudhury, U.7
Bottani, A.8
Antonarakis, S.E.9
Fryssira, H.10
Dallapiccola, B.11
Reymond, A.12
-
41
-
-
0035179436
-
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome
-
10.1038/ng753 11685205
-
Osborne LR Li M Pober B Chitayat D Bodurtha J Mandel A Costa T Grebe T Cox S Tsui LC Scherer SW A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome. Nat Genet 2001, 29:321-325. 10.1038/ng753 11685205
-
(2001)
Nat Genet
, vol.29
, pp. 321-325
-
-
Osborne, L.R.1
Li, M.2
Pober, B.3
Chitayat, D.4
Bodurtha, J.5
Mandel, A.6
Costa, T.7
Grebe, T.8
Cox, S.9
Tsui, L.C.10
Scherer, S.W.11
-
42
-
-
27944486491
-
GTF2IRD1 in craniofacial development of humans and mice
-
10.1126/science.1116142 16293761
-
Tassabehji M Hammond P Karmiloff-Smith A Thompson P Thorgeirsson SS Durkin ME Popescu NC Hutton T Metcalfe K Rucka A Stewart H Read AP Maconochie M Donnai D GTF2IRD1 in craniofacial development of humans and mice. Science 2005, 310:1184-1187. 10.1126/science.1116142 16293761
-
(2005)
Science
, vol.310
, pp. 1184-1187
-
-
Tassabehji, M.1
Hammond, P.2
Karmiloff-Smith, A.3
Thompson, P.4
Thorgeirsson, S.S.5
Durkin, M.E.6
Popescu, N.C.7
Hutton, T.8
Metcalfe, K.9
Rucka, A.10
Stewart, H.11
Read, A.P.12
Maconochie, M.13
Donnai, D.14
-
43
-
-
0035309316
-
Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome
-
10.1006/geno.2001.6507 11352562
-
Durkin ME Keck-Waggoner CL Popescu NC Thorgeirsson SS Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome. Genomics 2001, 73:20-27. 10.1006/ geno.2001.6507 11352562
-
(2001)
Genomics
, vol.73
, pp. 20-27
-
-
Durkin, M.E.1
Keck-Waggoner, C.L.2
Popescu, N.C.3
Thorgeirsson, S.S.4
-
44
-
-
33846587038
-
Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development
-
10.1016/j.modgep.2006.11.008 17239664
-
Palmer SJ Tay ES Santucci N Cuc Bach TT Hook J Lemckert FA Jamieson RV Gunnning PW Hardeman EC Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development. Gene Expr Patterns 2007, 7:396-404. 10.1016/j.modgep.2006.11.008 17239664
-
(2007)
Gene Expr Patterns
, vol.7
, pp. 396-404
-
-
Palmer, S.J.1
Tay, E.S.2
Santucci, N.3
Cuc Bach, T.T.4
Hook, J.5
Lemckert, F.A.6
Jamieson, R.V.7
Gunnning, P.W.8
Hardeman, E.C.9
-
45
-
-
0030298416
-
The vagaries of variegating transgenes
-
10.1002/bies.950181111 8939070
-
Martin DI Whitelaw E The vagaries of variegating transgenes. Bioessays 1996, 18:919-923. 10.1002/bies.950181111 8939070
-
(1996)
Bioessays
, vol.18
, pp. 919-923
-
-
Martin, D.I.1
Whitelaw, E.2
-
46
-
-
52249087966
-
Analysis of DNA content and green fluorescent protein expression
-
Unit 7.16. 18770728 Chapter 7
-
Schmid I Sakamoto KM Analysis of DNA content and green fluorescent protein expression. Curr Protoc Cytom 2001 Chapter 7 Unit 7.16. 18770728
-
(2001)
Curr Protoc Cytom
-
-
Schmid, I.1
Sakamoto, K.M.2
-
47
-
-
33644750203
-
Effects of histone deacetylase inhibitor (HDACi); Trichostatin-A (TSA) on the expression of housekeeping genes
-
10.1016/j.mcp.2005.09.008 16326072
-
Mogal A Abdulkadir SA Effects of histone deacetylase inhibitor (HDACi); Trichostatin-A (TSA) on the expression of housekeeping genes. Mol Cell Probes 2006, 20:81-86. 10.1016/j.mcp.2005.09.008 16326072
-
(2006)
Mol Cell Probes
, vol.20
, pp. 81-86
-
-
Mogal, A.1
Abdulkadir, S.A.2
-
48
-
-
0037418193
-
Fu allele occurs after maternal and paternal transmission
-
151376 12601169 10.1073/pnas.0436776100
-
Fu allele occurs after maternal and paternal transmission. Proc Natl Acad Sci USA 2003, 100:2538-2543. 151376 12601169 10.1073/ pnas.0436776100
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 2538-2543
-
-
Rakyan, V.K.1
Chong, S.2
Champ, M.E.3
Cuthbert, P.C.4
Morgan, H.D.5
Luu, K.V.K.6
Whitelaw, E.7
-
50
-
-
0037296209
-
Genomic screen for genes involved in mammalian craniofacial development
-
10.1002/gene.10165 12533789
-
Fowles LF Bennetts JS Berkman JL Williams E Koopman P Teasdale RD Wicking C Genomic screen for genes involved in mammalian craniofacial development. Genesis 2003, 35:73-87. 10.1002/gene.10165 12533789
-
(2003)
Genesis
, vol.35
, pp. 73-87
-
-
Fowles, L.F.1
Bennetts, J.S.2
Berkman, J.L.3
Williams, E.4
Koopman, P.5
Teasdale, R.D.6
Wicking, C.7
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