-
1
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
10.1038/35057062, 11237011
-
Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, Kann L, Lehoczky J, LeVine R, McEwann P, McKernan K, Meldrim J, Mesirov JP, Miranda C, Morris W, Naylor J, Raymond C, Rosetti M, Santos R, Sheridan A, Sougnex C, et al. Initial sequencing and analysis of the human genome. Nature 2001, 409:860-921. 10.1038/35057062, 11237011.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
Devon, K.7
Dewar, K.8
Doyle, M.9
FitzHugh, W.10
Funke, R.11
Gage, D.12
Harris, K.13
Heaford, A.14
Howland, J.15
Kann, L.16
Lehoczky, J.17
LeVine, R.18
McEwann, P.19
McKernan, K.20
Meldrim, J.21
Mesirov, J.P.22
Miranda, C.23
Morris, W.24
Naylor, J.25
Raymond, C.26
Rosetti, M.27
Santos, R.28
Sheridan, A.29
Sougnex, C.30
more..
-
2
-
-
57049118443
-
Analysis of the largest tandemly repeated DNA families in the human genome
-
10.1186/1471-2164-9-533, 2588610, 18992157
-
Warburton PE, Hasson D, Guillem F, Lescale C, Jin X, Abrusan G. Analysis of the largest tandemly repeated DNA families in the human genome. BMC Genomics 2008, 9:533. 10.1186/1471-2164-9-533, 2588610, 18992157.
-
(2008)
BMC Genomics
, vol.9
, pp. 533
-
-
Warburton, P.E.1
Hasson, D.2
Guillem, F.3
Lescale, C.4
Jin, X.5
Abrusan, G.6
-
3
-
-
0036556278
-
Unstable transmission of the RS447 human megasatellite tandem repetitive sequence that contains the USP17 deubiquitinating enzyme gene
-
10.1007/s00439-002-0698-2, 11941478
-
Okada T, Gondo Y, Goto J, Kanazawa I, Hadano S, Ikeda JE. Unstable transmission of the RS447 human megasatellite tandem repetitive sequence that contains the USP17 deubiquitinating enzyme gene. Hum Genet 2002, 110:302-313. 10.1007/s00439-002-0698-2, 11941478.
-
(2002)
Hum Genet
, vol.110
, pp. 302-313
-
-
Okada, T.1
Gondo, Y.2
Goto, J.3
Kanazawa, I.4
Hadano, S.5
Ikeda, J.E.6
-
4
-
-
0027744223
-
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
-
10.1093/hmg/2.12.2037, 8111371
-
van Deutekom JC, Wijmenga C, van Tienhoven EA, Gruter AM, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit. Hum Mol Genet 1993, 2:2037-2042. 10.1093/hmg/2.12.2037, 8111371.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 2037-2042
-
-
van Deutekom, J.C.1
Wijmenga, C.2
van Tienhoven, E.A.3
Gruter, A.M.4
Hewitt, J.E.5
Padberg, G.W.6
van Ommen, G.J.7
Hofker, M.H.8
Frants, R.R.9
-
5
-
-
0026922062
-
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
-
10.1038/ng0992-26, 1363881
-
Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ, Dauwerse HG, Gruter AM, Hofker MH, Moerer P, Williamson R, van Ommen GJ, Padberg GW, Frants RR. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nat Genet 1992, 2:26-30. 10.1038/ng0992-26, 1363881.
-
(1992)
Nat Genet
, vol.2
, pp. 26-30
-
-
Wijmenga, C.1
Hewitt, J.E.2
Sandkuijl, L.A.3
Clark, L.N.4
Wright, T.J.5
Dauwerse, H.G.6
Gruter, A.M.7
Hofker, M.H.8
Moerer, P.9
Williamson, R.10
van Ommen, G.J.11
Padberg, G.W.12
Frants, R.R.13
-
6
-
-
0026865003
-
A novel GC-rich human macrosatellite VNTR in Xq24 is differentially methylated on active and inactive X chromosomes
-
10.1038/ng0592-137, 1302007
-
Giacalone J, Friedes J, Francke U. A novel GC-rich human macrosatellite VNTR in Xq24 is differentially methylated on active and inactive X chromosomes. Nat Genet 1992, 1:137-143. 10.1038/ng0592-137, 1302007.
-
(1992)
Nat Genet
, vol.1
, pp. 137-143
-
-
Giacalone, J.1
Friedes, J.2
Francke, U.3
-
7
-
-
30044449656
-
The evolutionary dynamics of alpha-satellite
-
10.1101/gr.3810906, 1356132, 16344556
-
Rudd MK, Wray GA, Willard HF. The evolutionary dynamics of alpha-satellite. Genome Res 2006, 16:88-96. 10.1101/gr.3810906, 1356132, 16344556.
-
(2006)
Genome Res
, vol.16
, pp. 88-96
-
-
Rudd, M.K.1
Wray, G.A.2
Willard, H.F.3
-
8
-
-
0013462065
-
A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes
-
10.1073/pnas.85.18.6622, 282029, 3413114
-
Moyzis RK, Buckingham JM, Cram LS, Dani M, Deaven LL, Jones MD, Meyne J, Ratliff RL, Wu JR. A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes. Proc Natl Acad Sci USA 1988, 85:6622-6626. 10.1073/pnas.85.18.6622, 282029, 3413114.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 6622-6626
-
-
Moyzis, R.K.1
Buckingham, J.M.2
Cram, L.S.3
Dani, M.4
Deaven, L.L.5
Jones, M.D.6
Meyne, J.7
Ratliff, R.L.8
Wu, J.R.9
-
9
-
-
55949083347
-
Epigenetic mechanisms of facioscapulohumeral muscular dystrophy
-
2650037, 18723032
-
de Greef JC, Frants RR, van der Maarel SM. Epigenetic mechanisms of facioscapulohumeral muscular dystrophy. Mutat Res 2008, 647:94-102. 2650037, 18723032.
-
(2008)
Mutat Res
, vol.647
, pp. 94-102
-
-
de Greef, J.C.1
Frants, R.R.2
van der Maarel, S.M.3
-
10
-
-
0028040601
-
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy
-
10.1093/hmg/3.8.1287, 7987304
-
Hewitt JE, Lyle R, Clark LN, Valleley EM, Wright TJ, Wijmenga C, van Deutekom JC, Francis F, Sharpe PT, Hofker M, Frants RR, Williamson R. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Hum Mol Genet 1994, 3:1287-1295. 10.1093/hmg/3.8.1287, 7987304.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1287-1295
-
-
Hewitt, J.E.1
Lyle, R.2
Clark, L.N.3
Valleley, E.M.4
Wright, T.J.5
Wijmenga, C.6
van Deutekom, J.C.7
Francis, F.8
Sharpe, P.T.9
Hofker, M.10
Frants, R.R.11
Williamson, R.12
-
11
-
-
69149087644
-
Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation
-
10.1186/1741-7007-7-41, 2719609, 19607661
-
Bodega B, Ramirez GD, Grasser F, Cheli S, Brunelli S, Mora M, Meneveri R, Marozzi A, Mueller S, Battaglioli E, Ginelli E. Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation. BMC Biol 2009, 7:41. 10.1186/1741-7007-7-41, 2719609, 19607661.
-
(2009)
BMC Biol
, vol.7
, pp. 41
-
-
Bodega, B.1
Ramirez, G.D.2
Grasser, F.3
Cheli, S.4
Brunelli, S.5
Mora, M.6
Meneveri, R.7
Marozzi, A.8
Mueller, S.9
Battaglioli, E.10
Ginelli, E.11
-
12
-
-
0037047439
-
Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle
-
10.1016/S0092-8674(02)00826-7, 12176321
-
Gabellini D, Green MR, Tupler R. Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle. Cell 2002, 110:339-348. 10.1016/S0092-8674(02)00826-7, 12176321.
-
(2002)
Cell
, vol.110
, pp. 339-348
-
-
Gabellini, D.1
Green, M.R.2
Tupler, R.3
-
13
-
-
70450275779
-
Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
-
10.1038/ejhg.2009.62, 19809486
-
Klooster R, Straasheijm K, Shah B, Sowden J, Frants R, Thornton C, Tawil R, van der Maarel S. Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level. Eur J Hum Genet 2009, 17:1615-1624. 10.1038/ejhg.2009.62, 19809486.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1615-1624
-
-
Klooster, R.1
Straasheijm, K.2
Shah, B.3
Sowden, J.4
Frants, R.5
Thornton, C.6
Tawil, R.7
van der Maarel, S.8
-
14
-
-
8744240156
-
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients
-
10.1136/jmg.2004.019364, 1735617, 15520407
-
Rijkers T, Deidda G, van Koningsbruggen S, van Geel M, Lemmers RJ, van Deutekom JC, Figlewicz D, Hewitt JE, Padberg GW, Frants RR, van der Maarel SM. FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients. J Med Genet 2004, 41:826-836. 10.1136/jmg.2004.019364, 1735617, 15520407.
-
(2004)
J Med Genet
, vol.41
, pp. 826-836
-
-
Rijkers, T.1
Deidda, G.2
van Koningsbruggen, S.3
van Geel, M.4
Lemmers, R.J.5
van Deutekom, J.C.6
Figlewicz, D.7
Hewitt, J.E.8
Padberg, G.W.9
Frants, R.R.10
van der Maarel, S.M.11
-
15
-
-
33749605124
-
Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes
-
10.1002/pmic.200600056, 17013991
-
Celegato B, Capitanio D, Pescatori M, Romualdi C, Pacchioni B, Cagnin S, Vigano A, Colantoni L, Begum S, Ricci E, Wait R, Lanfranchi G, Gelfi C. Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes. Proteomics 2006, 6:5303-5321. 10.1002/pmic.200600056, 17013991.
-
(2006)
Proteomics
, vol.6
, pp. 5303-5321
-
-
Celegato, B.1
Capitanio, D.2
Pescatori, M.3
Romualdi, C.4
Pacchioni, B.5
Cagnin, S.6
Vigano, A.7
Colantoni, L.8
Begum, S.9
Ricci, E.10
Wait, R.11
Lanfranchi, G.12
Gelfi, C.13
-
16
-
-
0345227304
-
Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q
-
10.1093/hmg/ddg323, 14506132
-
Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, Ehrlich M. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q. Hum Mol Genet 2003, 12:2909-2921. 10.1093/hmg/ddg323, 14506132.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2909-2921
-
-
Jiang, G.1
Yang, F.2
van Overveld, P.G.3
Vedanarayanan, V.4
van der Maarel, S.5
Ehrlich, M.6
-
17
-
-
77949656794
-
Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei
-
10.1038/ejhg.2009.183, 2843500, 19888305
-
Masny PS, Chan OY, de Greef JC, Bengtsson U, Ehrlich M, Tawil R, Lock LF, Hewitt JE, Stocksdale J, Martin JH, van der Maarel SM, Winokur ST. Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei. Eur J Hum Genet 2010, 18:448-456. 10.1038/ejhg.2009.183, 2843500, 19888305.
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 448-456
-
-
Masny, P.S.1
Chan, O.Y.2
de Greef, J.C.3
Bengtsson, U.4
Ehrlich, M.5
Tawil, R.6
Lock, L.F.7
Hewitt, J.E.8
Stocksdale, J.9
Martin, J.H.10
van der Maarel, S.M.11
Winokur, S.T.12
-
18
-
-
33847234593
-
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
-
10.1212/01.wnl.0000251269.31442.d9, 17151338
-
Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology 2007, 68:569-577. 10.1212/01.wnl.0000251269.31442.d9, 17151338.
-
(2007)
Neurology
, vol.68
, pp. 569-577
-
-
Osborne, R.J.1
Welle, S.2
Venance, S.L.3
Thornton, C.A.4
Tawil, R.5
-
19
-
-
0344875044
-
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation
-
10.1093/hmg/ddg327, 14519683
-
Winokur ST, Chen YW, Masny PS, Martin JH, Ehmsen JT, Tapscott SJ, van der Maarel SM, Hayashi Y, Flanigan KM. Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Hum Mol Genet 2003, 12:2895-2907. 10.1093/hmg/ddg327, 14519683.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2895-2907
-
-
Winokur, S.T.1
Chen, Y.W.2
Masny, P.S.3
Martin, J.H.4
Ehmsen, J.T.5
Tapscott, S.J.6
van der Maarel, S.M.7
Hayashi, Y.8
Flanigan, K.M.9
-
20
-
-
0034253950
-
The RS447 human megasatellite tandem repetitive sequence encodes a novel deubiquitinating enzyme with a functional promoter
-
10.1006/geno.2000.6261, 10936051
-
Saitoh Y, Miyamoto N, Okada T, Gondo Y, Showguchi-Miyata J, Hadano S, Ikeda JE. The RS447 human megasatellite tandem repetitive sequence encodes a novel deubiquitinating enzyme with a functional promoter. Genomics 2000, 67:291-300. 10.1006/geno.2000.6261, 10936051.
-
(2000)
Genomics
, vol.67
, pp. 291-300
-
-
Saitoh, Y.1
Miyamoto, N.2
Okada, T.3
Gondo, Y.4
Showguchi-Miyata, J.5
Hadano, S.6
Ikeda, J.E.7
-
21
-
-
36749026295
-
DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1
-
10.1073/pnas.0708659104, 2084313, 17984056
-
Dixit M, Ansseau E, Tassin A, Winokur S, Shi R, Qian H, Sauvage S, Matteotti C, van Acker AM, Leo O, Figlewicz D, Barro M, Laoudj-Chenivesse D, Belayew A, Coppee F, Chen YW. DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1. Proc Natl Acad Sci USA 2007, 104:18157-18162. 10.1073/pnas.0708659104, 2084313, 17984056.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 18157-18162
-
-
Dixit, M.1
Ansseau, E.2
Tassin, A.3
Winokur, S.4
Shi, R.5
Qian, H.6
Sauvage, S.7
Matteotti, C.8
van Acker, A.M.9
Leo, O.10
Figlewicz, D.11
Barro, M.12
Laoudj-Chenivesse, D.13
Belayew, A.14
Coppee, F.15
Chen, Y.W.16
-
22
-
-
70349621645
-
Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats
-
10.1371/journal.pone.0007003, 2737622, 19756142
-
Bosnakovski D, Daughters RS, Xu Z, Slack JM, Kyba M. Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats. PLoS One 2009, 4:e7003. 10.1371/journal.pone.0007003, 2737622, 19756142.
-
(2009)
PLoS One
, vol.4
-
-
Bosnakovski, D.1
Daughters, R.S.2
Xu, Z.3
Slack, J.M.4
Kyba, M.5
-
23
-
-
67249104052
-
RNA Transcripts, miRNA-sized Fragments, and Proteins Produced from D4Z4 Units: New Candidates for the Pathophysiology of Facioscapulohumeral Dystrophy
-
2694690, 19359275
-
Snider L, Asawachaicharn A, Tyler AE, Geng LN, Petek LM, Maves L, Miller DG, Lemmers RJ, Winokur ST, Tawil R, van der Maarel SM, Fillippova GN, Tapscott SJ. RNA Transcripts, miRNA-sized Fragments, and Proteins Produced from D4Z4 Units: New Candidates for the Pathophysiology of Facioscapulohumeral Dystrophy. Hum Mol Genet 2009, 2694690, 19359275.
-
(2009)
Hum Mol Genet
-
-
Snider, L.1
Asawachaicharn, A.2
Tyler, A.E.3
Geng, L.N.4
Petek, L.M.5
Maves, L.6
Miller, D.G.7
Lemmers, R.J.8
Winokur, S.T.9
Tawil, R.10
van der Maarel, S.M.11
Fillippova, G.N.12
Tapscott, S.J.13
-
24
-
-
77957327192
-
A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy
-
Lemmers RJ, van der Vliet PJ, Klooster R, Sacconi S, Camano P, Dauwerse JG, Snider L, Straasheijm KR, Jan van Ommen G, Padberg GW, Miller DG, Tapscott SJ, Tawil R, Frants RR, van der Maarel SM. A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy. Science 2010,
-
(2010)
Science
-
-
Lemmers, R.J.1
van der Vliet, P.J.2
Klooster, R.3
Sacconi, S.4
Camano, P.5
Dauwerse, J.G.6
Snider, L.7
Straasheijm, K.R.8
Jan van Ommen, G.9
Padberg, G.W.10
Miller, D.G.11
Tapscott, S.J.12
Tawil, R.13
Frants, R.R.14
van der Maarel, S.M.15
-
25
-
-
48949102889
-
DXZ4 chromatin adopts an opposing conformation to that of the surrounding chromosome and acquires a novel inactive X-specific role involving CTCF and antisense transcripts
-
10.1101/gr.075713.107, 2493436, 18456864
-
Chadwick BP. DXZ4 chromatin adopts an opposing conformation to that of the surrounding chromosome and acquires a novel inactive X-specific role involving CTCF and antisense transcripts. Genome Res 2008, 18:1259-1269. 10.1101/gr.075713.107, 2493436, 18456864.
-
(2008)
Genome Res
, vol.18
, pp. 1259-1269
-
-
Chadwick, B.P.1
-
26
-
-
58549109636
-
X Chromosome Dosage Compensation: How Mammals Keep the Balance
-
Payer B, Lee JT. X Chromosome Dosage Compensation: How Mammals Keep the Balance. Annu Rev Genet 2008,
-
(2008)
Annu Rev Genet
-
-
Payer, B.1
Lee, J.T.2
-
27
-
-
0037166937
-
Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome
-
10.1083/jcb.200112074, 2173542, 12082075
-
Chadwick BP, Willard HF. Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome. J Cell Biol 2002, 157:1113-1123. 10.1083/jcb.200112074, 2173542, 12082075.
-
(2002)
J Cell Biol
, vol.157
, pp. 1113-1123
-
-
Chadwick, B.P.1
Willard, H.F.2
-
28
-
-
35348924169
-
Genetics and epigenetics of the multifunctional protein CTCF
-
full_text, 17950379
-
Filippova GN. Genetics and epigenetics of the multifunctional protein CTCF. Curr Top Dev Biol 2008, 80:337-360. full_text, 17950379.
-
(2008)
Curr Top Dev Biol
, vol.80
, pp. 337-360
-
-
Filippova, G.N.1
-
29
-
-
70450224476
-
Macrosatellite epigenetics: the two faces of DXZ4 and D4Z4
-
10.1007/s00412-009-0233-5, 19690880
-
Chadwick BP. Macrosatellite epigenetics: the two faces of DXZ4 and D4Z4. Chromosoma 2009, 118:675-681. 10.1007/s00412-009-0233-5, 19690880.
-
(2009)
Chromosoma
, vol.118
, pp. 675-681
-
-
Chadwick, B.P.1
-
30
-
-
61449143604
-
The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in facio-scapulo-humeral dystrophy
-
10.1371/journal.pgen.1000394, 2639723, 19247430
-
Ottaviani A, Rival-Gervier S, Boussouar A, Foerster AM, Rondier D, Sacconi S, Desnuelle C, Gilson E, Magdinier F. The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in facio-scapulo-humeral dystrophy. PLoS Genet 2009, 5:e1000394. 10.1371/journal.pgen.1000394, 2639723, 19247430.
-
(2009)
PLoS Genet
, vol.5
-
-
Ottaviani, A.1
Rival-Gervier, S.2
Boussouar, A.3
Foerster, A.M.4
Rondier, D.5
Sacconi, S.6
Desnuelle, C.7
Gilson, E.8
Magdinier, F.9
-
31
-
-
76249101086
-
Abundance of ribosomal RNA gene copies maintains genome integrity
-
10.1126/science.1179044, 20133573
-
Ide S, Miyazaki T, Maki H, Kobayashi T. Abundance of ribosomal RNA gene copies maintains genome integrity. Science 2010, 327:693-696. 10.1126/science.1179044, 20133573.
-
(2010)
Science
, vol.327
, pp. 693-696
-
-
Ide, S.1
Miyazaki, T.2
Maki, H.3
Kobayashi, T.4
-
32
-
-
0034831138
-
Segmental duplications: organization and impact within the current human genome project assembly
-
10.1101/gr.GR-1871R, 311093, 11381028
-
Bailey JA, Yavor AM, Massa HF, Trask BJ, Eichler EE. Segmental duplications: organization and impact within the current human genome project assembly. Genome Res 2001, 11:1005-1017. 10.1101/gr.GR-1871R, 311093, 11381028.
-
(2001)
Genome Res
, vol.11
, pp. 1005-1017
-
-
Bailey, J.A.1
Yavor, A.M.2
Massa, H.F.3
Trask, B.J.4
Eichler, E.E.5
-
33
-
-
0023650628
-
A new moderately repetitive DNA sequence family of novel organization
-
10.1093/nar/15.5.2327, 340637, 3562229
-
Epstein ND, Karlsson S, O'Brien S, Modi W, Moulton A, Nienhuis AW. A new moderately repetitive DNA sequence family of novel organization. Nucleic Acids Res 1987, 15:2327-2341. 10.1093/nar/15.5.2327, 340637, 3562229.
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 2327-2341
-
-
Epstein, N.D.1
Karlsson, S.2
O'Brien, S.3
Modi, W.4
Moulton, A.5
Nienhuis, A.W.6
-
34
-
-
38049162608
-
Chromosome fragile sites
-
10.1146/annurev.genet.41.042007.165900, 17608616
-
Durkin SG, Glover TW. Chromosome fragile sites. Annu Rev Genet 2007, 41:169-192. 10.1146/annurev.genet.41.042007.165900, 17608616.
-
(2007)
Annu Rev Genet
, vol.41
, pp. 169-192
-
-
Durkin, S.G.1
Glover, T.W.2
-
35
-
-
0029827344
-
Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1
-
10.1093/hmg/5.12.1997, 8968754
-
van Deutekom JC, Bakker E, Lemmers RJ, van der Wielen MJ, Bik E, Hofker MH, Padberg GW, Frants RR. Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1. Hum Mol Genet 1996, 5:1997-2003. 10.1093/hmg/5.12.1997, 8968754.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1997-2003
-
-
van Deutekom, J.C.1
Bakker, E.2
Lemmers, R.J.3
van der Wielen, M.J.4
Bik, E.5
Hofker, M.H.6
Padberg, G.W.7
Frants, R.R.8
-
36
-
-
63149156282
-
Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations
-
10.1097/YPG.0b013e3283207ff6, 19672138
-
Bruce HA, Sachs N, Rudnicki DD, Lin SG, Willour VL, Cowell JK, Conroy J, McQuaid DE, Rossi M, Gaile DP, Norwak NJ, Holmes SE, Sklar P, Ross CA, Delisi LE, Margolis RL. Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations. Psychiatr Genet 2009, 19:64-71. 10.1097/YPG.0b013e3283207ff6, 19672138.
-
(2009)
Psychiatr Genet
, vol.19
, pp. 64-71
-
-
Bruce, H.A.1
Sachs, N.2
Rudnicki, D.D.3
Lin, S.G.4
Willour, V.L.5
Cowell, J.K.6
Conroy, J.7
McQuaid, D.E.8
Rossi, M.9
Gaile, D.P.10
Norwak, N.J.11
Holmes, S.E.12
Sklar, P.13
Ross, C.A.14
Delisi, L.E.15
Margolis, R.L.16
-
37
-
-
0036533610
-
Identification of cancer/testis genes by database mining and mRNA expression analysis
-
10.1002/ijc.10276, 11920606
-
Scanlan MJ, Gordon CM, Williamson B, Lee SY, Chen YT, Stockert E, Jungbluth A, Ritter G, Jager D, Jager E, Knuth A, Old LJ. Identification of cancer/testis genes by database mining and mRNA expression analysis. Int J Cancer 2002, 98:485-492. 10.1002/ijc.10276, 11920606.
-
(2002)
Int J Cancer
, vol.98
, pp. 485-492
-
-
Scanlan, M.J.1
Gordon, C.M.2
Williamson, B.3
Lee, S.Y.4
Chen, Y.T.5
Stockert, E.6
Jungbluth, A.7
Ritter, G.8
Jager, D.9
Jager, E.10
Knuth, A.11
Old, L.J.12
-
38
-
-
33644756521
-
Identification of a new cancer/testis gene family, CT47, among expressed multicopy genes on the human X chromosome
-
10.1002/gcc.20298, 16382448
-
Chen YT, Iseli C, Venditti CA, Old LJ, Simpson AJ, Jongeneel CV. Identification of a new cancer/testis gene family, CT47, among expressed multicopy genes on the human X chromosome. Genes Chromosomes Cancer 2006, 45:392-400. 10.1002/gcc.20298, 16382448.
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 392-400
-
-
Chen, Y.T.1
Iseli, C.2
Venditti, C.A.3
Old, L.J.4
Simpson, A.J.5
Jongeneel, C.V.6
-
39
-
-
38849162916
-
An overview of the GAGE cancer/testis antigen family with the inclusion of newly identified members
-
10.1111/j.1399-0039.2007.00997.x, 18179644
-
Gjerstorff MF, Ditzel HJ. An overview of the GAGE cancer/testis antigen family with the inclusion of newly identified members. Tissue Antigens 2008, 71:187-192. 10.1111/j.1399-0039.2007.00997.x, 18179644.
-
(2008)
Tissue Antigens
, vol.71
, pp. 187-192
-
-
Gjerstorff, M.F.1
Ditzel, H.J.2
-
40
-
-
52449122070
-
Distinct GAGE and MAGE-A expression during early human development indicate specific roles in lineage differentiation
-
10.1093/humrep/den262, 18611917
-
Gjerstorff MF, Harkness L, Kassem M, Frandsen U, Nielsen O, Lutterodt M, Mollgard K, Ditzel HJ. Distinct GAGE and MAGE-A expression during early human development indicate specific roles in lineage differentiation. Hum Reprod 2008, 23:2194-2201. 10.1093/humrep/den262, 18611917.
-
(2008)
Hum Reprod
, vol.23
, pp. 2194-2201
-
-
Gjerstorff, M.F.1
Harkness, L.2
Kassem, M.3
Frandsen, U.4
Nielsen, O.5
Lutterodt, M.6
Mollgard, K.7
Ditzel, H.J.8
-
41
-
-
34347245601
-
MAGE-A1, GAGE and NY-ESO-1 cancer/testis antigen expression during human gonadal development
-
10.1093/humrep/del494, 17208940
-
Gjerstorff MF, Kock K, Nielsen O, Ditzel HJ. MAGE-A1, GAGE and NY-ESO-1 cancer/testis antigen expression during human gonadal development. Hum Reprod 2007, 22:953-960. 10.1093/humrep/del494, 17208940.
-
(2007)
Hum Reprod
, vol.22
, pp. 953-960
-
-
Gjerstorff, M.F.1
Kock, K.2
Nielsen, O.3
Ditzel, H.J.4
-
42
-
-
0029987931
-
Zfp-37 is a member of the KRAB zinc finger gene family and is expressed in neurons of the developing and adult CNS
-
10.1006/geno.1996.0189, 8660973
-
Mazarakis N, Michalovich D, Karis A, Grosveld F, Galjart N. Zfp-37 is a member of the KRAB zinc finger gene family and is expressed in neurons of the developing and adult CNS. Genomics 1996, 33:247-257. 10.1006/geno.1996.0189, 8660973.
-
(1996)
Genomics
, vol.33
, pp. 247-257
-
-
Mazarakis, N.1
Michalovich, D.2
Karis, A.3
Grosveld, F.4
Galjart, N.5
-
43
-
-
1842536305
-
The DNA sequence and biology of human chromosome 19
-
10.1038/nature02399, 15057824
-
Grimwood J, Gordon LA, Olsen A, Terry A, Schmutz J, Lamerdin J, Hellsten U, Goodstein D, Couronne O, Tran-Gyamfi M, Aerts A, Altherr M, Ashworth L, Bajorek E, Black S, Branscomb E, Caenepeel S, Carrano A, Caolie C, Chan YM, Chritensen M, Cleland CA, Copeland A, Dalin E, Dehal P, Denys M, Detter JC, Escobar J, Flowers D, Fotopulos D, et al. The DNA sequence and biology of human chromosome 19. Nature 2004, 428:529-535. 10.1038/nature02399, 15057824.
-
(2004)
Nature
, vol.428
, pp. 529-535
-
-
Grimwood, J.1
Gordon, L.A.2
Olsen, A.3
Terry, A.4
Schmutz, J.5
Lamerdin, J.6
Hellsten, U.7
Goodstein, D.8
Couronne, O.9
Tran-Gyamfi, M.10
Aerts, A.11
Altherr, M.12
Ashworth, L.13
Bajorek, E.14
Black, S.15
Branscomb, E.16
Caenepeel, S.17
Carrano, A.18
Caolie, C.19
Chan, Y.M.20
Chritensen, M.21
Cleland, C.A.22
Copeland, A.23
Dalin, E.24
Dehal, P.25
Denys, M.26
Detter, J.C.27
Escobar, J.28
Flowers, D.29
Fotopulos, D.30
more..
-
44
-
-
0031686366
-
Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12
-
Eichler EE, Hoffman SM, Adamson AA, Gordon LA, McCready P, Lamerdin JE, Mohrenweiser HW. Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12. Genome Res 1998, 8:791-808.
-
(1998)
Genome Res
, vol.8
, pp. 791-808
-
-
Eichler, E.E.1
Hoffman, S.M.2
Adamson, A.A.3
Gordon, L.A.4
McCready, P.5
Lamerdin, J.E.6
Mohrenweiser, H.W.7
-
45
-
-
85027945007
-
Kruppel-like factors: three fingers in control
-
Swamynathan SK. Kruppel-like factors: three fingers in control. Hum Genomics 2010, 4:263-270.
-
(2010)
Hum Genomics
, vol.4
, pp. 263-270
-
-
Swamynathan, S.K.1
-
46
-
-
0038141095
-
Differential expansion of zinc-finger transcription factor loci in homologous human and mouse gene clusters
-
10.1101/gr.963903, 403638, 12743021
-
Shannon M, Hamilton AT, Gordon L, Branscomb E, Stubbs L. Differential expansion of zinc-finger transcription factor loci in homologous human and mouse gene clusters. Genome Res 2003, 13:1097-1110. 10.1101/gr.963903, 403638, 12743021.
-
(2003)
Genome Res
, vol.13
, pp. 1097-1110
-
-
Shannon, M.1
Hamilton, A.T.2
Gordon, L.3
Branscomb, E.4
Stubbs, L.5
-
47
-
-
0004136246
-
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, Second
-
Sambrook J, Fritsch EF, Maniatis T. Molecular Cloning: A laboratory manual 1989, Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, Second.
-
(1989)
Molecular Cloning: A laboratory manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
|