-
1
-
-
0036779497
-
Developmental dyslexia: Genetic dissection of a complex cognitive trait
-
Fisher SE, DeFries JC (2002) Developmental dyslexia: genetic dissection of a complex cognitive trait. Nat Rev Neurosci 3: 767-780.
-
(2002)
Nat Rev Neurosci
, vol.3
, pp. 767-780
-
-
Fisher, S.E.1
DeFries, J.C.2
-
2
-
-
0032576678
-
Dyslexia
-
Shaywitz SE (1998) Dyslexia. N EnglJ Med 338: 307-312.
-
(1998)
N EnglJ Med
, vol.338
, pp. 307-312
-
-
Shaywitz, S.E.1
-
3
-
-
0025181072
-
Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study
-
Shaywitz SE, Shaywitz BA, Fletcher JM, Escobar MD (1990) Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study. JAMA 264: 998-1002.
-
(1990)
JAMA
, vol.264
, pp. 998-1002
-
-
Shaywitz, S.E.1
Shaywitz, B.A.2
Fletcher, J.M.3
Escobar, M.D.4
-
4
-
-
0023179955
-
Evidence for a genetic aetiology in reading disability of twins
-
DeFries JC, Fulker DW, LaBuda MC (1987) Evidence for a genetic aetiology in reading disability of twins. Nature 329: 537-539.
-
(1987)
Nature
, vol.329
, pp. 537-539
-
-
DeFries, J.C.1
Fulker, D.W.2
LaBuda, M.C.3
-
6
-
-
0017107298
-
The genetics of specific reading disability
-
Finucci Jm, Guthrie JT, Childs AL, Abbey H, Childs B (1976) The genetics of specific reading disability. Ann Hum Genet 40: 1-23.
-
(1976)
Ann Hum Genet
, vol.40
, pp. 1-23
-
-
Finucci, J.1
Guthrie, J.T.2
Childs, A.L.3
Abbey, H.4
Childs, B.5
-
7
-
-
0026591562
-
Reading disability, immune disorders and non-right-handedness: Twin and family studies of their relations
-
Gilger JW, Pennington BF, Green P, Smith SM, Smith SD (1992) Reading disability, immune disorders and non-right-handedness: twin and family studies of their relations. Neuropsychologia 30: 209-227.
-
(1992)
Neuropsychologia
, vol.30
, pp. 209-227
-
-
Gilger, J.W.1
Pennington, B.F.2
Green, P.3
Smith, S.M.4
Smith, S.D.5
-
9
-
-
0141482054
-
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
-
Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, et al. (2003) A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci USA 100: 11553-11558.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 11553-11558
-
-
Taipale, M.1
Kaminen, N.2
Nopola-Hemmi, J.3
Haltia, T.4
Myllyluoma, B.5
-
10
-
-
8744255235
-
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
-
Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, et al. (2004) Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. J Med Genet 41: 853-857.
-
(2004)
J Med Genet
, vol.41
, pp. 853-857
-
-
Scerri, T.S.1
Fisher, S.E.2
Francks, C.3
MacPhie, I.L.4
Paracchini, S.5
-
11
-
-
19944428926
-
Support for EKN1 as the susceptibility locus for dyslexia on 15q21
-
Wigg KG, Couto JM, Feng Y, Anderson B, Cate-Carter TD, et al. (2004) Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Mol Psychiatry 9: 1111-1121.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 1111-1121
-
-
Wigg, K.G.1
Couto, J.M.2
Feng, Y.3
Anderson, B.4
Cate-Carter, T.D.5
-
12
-
-
33745343959
-
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia
-
doi:10.1371/journal.pgen.0010050
-
Hannula-Jouppi K, Kaminen-Ahola N, Taipale M, Eklund R, Nopola-Hemmi J, et al. (2005) The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet 1: e50. doi:10.1371/journal.pgen.0010050.
-
(2005)
PLoS Genet
, vol.1
-
-
Hannula-Jouppi, K.1
Kaminen-Ahola, N.2
Taipale, M.3
Eklund, R.4
Nopola-Hemmi, J.5
-
13
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
Meng H, Smith SD, Hager K, Held M, Liu J, et al. (2005) DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 102: 17053-17058.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 17053-17058
-
-
Meng, H.1
Smith, S.D.2
Hager, K.3
Held, M.4
Liu, J.5
-
14
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
Schumacher J, Anthoni H, Dahdouh F, Konig IR, Hillmer AM, et al. (2006) Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 78: 52-62.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 52-62
-
-
Schumacher, J.1
Anthoni, H.2
Dahdouh, F.3
Konig, I.R.4
Hillmer, A.M.5
-
15
-
-
8844258018
-
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
-
Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, et al. (2004) A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet 75: 1046-1058.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1046-1058
-
-
Francks, C.1
Paracchini, S.2
Smith, S.D.3
Richardson, A.J.4
Scerri, T.S.5
-
16
-
-
15944372645
-
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
-
Cope N, Harold D, Hill G, Moskvina V, Stevenson J, et al. (2005) Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. Am J Hum Genet 76: 581-591.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 581-591
-
-
Cope, N.1
Harold, D.2
Hill, G.3
Moskvina, V.4
Stevenson, J.5
-
17
-
-
33845246158
-
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
-
1085-1091
-
Harold D, Paracchini S, Scerri T, Dennis M, Cope N, et al. (2006) Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Mol Psychiatry 11: 1085-1091, 1061.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 1061
-
-
Harold, D.1
Paracchini, S.2
Scerri, T.3
Dennis, M.4
Cope, N.5
-
18
-
-
34548473808
-
A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability
-
Luciano M, Lind PA, Duffy DL, Castles A, Wright MJ, et al. (2007) A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biol Psychiatry 62: 811-817.
-
(2007)
Biol Psychiatry
, vol.62
, pp. 811-817
-
-
Luciano, M.1
Lind, P.A.2
Duffy, D.L.3
Castles, A.4
Wright, M.J.5
-
19
-
-
57349157021
-
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population
-
Paracchini S, Steer CD, Buckingham LL, Morris AP, Ring S, et al. (2008) Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am JPsychiatry 12: 1576-1584.
-
(2008)
Am JPsychiatry
, vol.12
, pp. 1576-1584
-
-
Paracchini, S.1
Steer, C.D.2
Buckingham, L.L.3
Morris, A.P.4
Ring, S.5
-
20
-
-
34247092473
-
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
-
Anthoni H, Zucchelli M, Matsson H, Muller-Myhsok B, Fransson I, et al. (2007) A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia. Hum Mol Genet 16: 667-677.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 667-677
-
-
Anthoni, H.1
Zucchelli, M.2
Matsson, H.3
Muller-Myhsok, B.4
Fransson, I.5
-
21
-
-
33749071999
-
From genes to behavior in developmental dyslexia
-
Galaburda AM, LoTurco J, Ramus F, Fitch RH, Rosen GD (2006) From genes to behavior in developmental dyslexia. Nat Neurosci 9: 1213-1217.
-
(2006)
Nat Neurosci
, vol.9
, pp. 1213-1217
-
-
Galaburda, A.M.1
LoTurco, J.2
Ramus, F.3
Fitch, R.H.4
Rosen, G.D.5
-
22
-
-
35148851563
-
Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations
-
Rosen GD, Bai J, Wang Y, Fiondella CG, Threlkeld SW, et al. (2007) Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations. Cereb Cortex 17: 2562-2572.
-
(2007)
Cereb Cortex
, vol.17
, pp. 2562-2572
-
-
Rosen, G.D.1
Bai, J.2
Wang, Y.3
Fiondella, C.G.4
Threlkeld, S.W.5
-
23
-
-
33846440958
-
Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1
-
Threlkeld SW, McClure MM, Bai J, Wang Y, LoTurco JJ, et al. (2007) Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1. Brain Res Bull 71: 508-514.
-
(2007)
Brain Res Bull
, vol.71
, pp. 508-514
-
-
Threlkeld, S.W.1
McClure, M.M.2
Bai, J.3
Wang, Y.4
LoTurco, J.J.5
-
24
-
-
33751251057
-
DYX1C1 functions in neuronal migration in developing neocortex
-
Wang Y, Paramasivam M, Thomas A, Bai J, Kaminen-Ahola N, et al. (2006) DYX1C1 functions in neuronal migration in developing neocortex. Neuroscience 143: 515-522.
-
(2006)
Neuroscience
, vol.143
, pp. 515-522
-
-
Wang, Y.1
Paramasivam, M.2
Thomas, A.3
Bai, J.4
Kaminen-Ahola, N.5
-
25
-
-
40949114128
-
Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat
-
Burbridge TJ, Wang Y, Volz AJ, Peschansky VJ, Lisann L, et al. (2008) Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat. Neuroscience 3: 723-733.
-
(2008)
Neuroscience
, vol.3
, pp. 723-733
-
-
Burbridge, T.J.1
Wang, Y.2
Volz, A.J.3
Peschansky, V.J.4
Lisann, L.5
-
26
-
-
33744920683
-
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
-
Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, et al. (2006) The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet 15: 1659-1666.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1659-1666
-
-
Paracchini, S.1
Thomas, A.2
Castro, S.3
Lai, C.4
Paramasivam, M.5
-
27
-
-
0021832834
-
Developmental dyslexia: Four consecutive patients with cortical anomalies
-
Galaburda AM, Sherman GF, Rosen GD, Aboitiz F, Geschwind N (1985) Developmental dyslexia: four consecutive patients with cortical anomalies. Ann Neurol 18: 222-233.
-
(1985)
Ann Neurol
, vol.18
, pp. 222-233
-
-
Galaburda, A.M.1
Sherman, G.F.2
Rosen, G.D.3
Aboitiz, F.4
Geschwind, N.5
-
28
-
-
0034863552
-
Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK
-
Marlow AJ, Fisher SE, Richardson AJ, Francks C, Talcott JB, et al. (2001) Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK. Behav Genet 31: 219-230.
-
(2001)
Behav Genet
, vol.31
, pp. 219-230
-
-
Marlow, A.J.1
Fisher, S.E.2
Richardson, A.J.3
Francks, C.4
Talcott, J.B.5
-
29
-
-
18544365699
-
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia
-
Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, et al. (2002) Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet 30: 86-91.
-
(2002)
Nat Genet
, vol.30
, pp. 86-91
-
-
Fisher, S.E.1
Francks, C.2
Marlow, A.J.3
MacPhie, I.L.4
Newbury, D.F.5
-
30
-
-
0033909546
-
A general test ofassociation for quantitative traits in nuclear families
-
Abecasis GR, Cardon LR, Cookson WO (2000) A general test ofassociation for quantitative traits in nuclear families. Am J Hum Genet 66: 279-292.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.3
-
31
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ (2005) Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21: 263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
32
-
-
0034020416
-
PipMaker-a web server for aligning two genomic DNA sequences
-
Schwartz S, Zhang Z, Frazer KA, Smit A, Riemer C, et al. (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
-
33
-
-
0035487293
-
Recombineering: A powerful new tool for mouse functional genomics
-
Copeland NG, Jenkins NA, Court DL (2001) Recombineering: a powerful new tool for mouse functional genomics. Nat Rev Genet 2: 769-779.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 769-779
-
-
Copeland, N.G.1
Jenkins, N.A.2
Court, D.L.3
-
34
-
-
26644453335
-
Simple and highly efficient BAC recombineering using galK selection
-
Warming S, Costantino N, Court DL, Jenkins NA, Copeland NG (2005) Simple and highly efficient BAC recombineering using galK selection. Nucleic Acids Res 33: e36.
-
(2005)
Nucleic Acids Res
, vol.33
-
-
Warming, S.1
Costantino, N.2
Court, D.L.3
Jenkins, N.A.4
Copeland, N.G.5
-
35
-
-
63449095587
-
-
Totowa, N.J, Humana Press ix
-
Perdew GH, Vanden Heuvel JP, Peters JM (2006) Regulation of gene expression: molecular mechanisms. Totowa, N.J.: Humana Press ix, 333: 77-78.
-
(2006)
Regulation of gene expression: Molecular mechanisms
, vol.333
, pp. 77-78
-
-
Perdew, G.H.1
Vanden Heuvel, J.P.2
Peters, J.M.3
-
36
-
-
23744493161
-
Evaluation of regulatory potential and conservation scores for detecting cis-regulatory modules in aligned mammalian genome sequences
-
King DC, Taylor J, Elnitski L, Chiaromonte F, Miller W, et al. (2005) Evaluation of regulatory potential and conservation scores for detecting cis-regulatory modules in aligned mammalian genome sequences. Genome Res 15: 1051-1060.
-
(2005)
Genome Res
, vol.15
, pp. 1051-1060
-
-
King, D.C.1
Taylor, J.2
Elnitski, L.3
Chiaromonte, F.4
Miller, W.5
-
37
-
-
33845303175
-
ESPERR: Learning strong and weak signals in genomic sequence alignments to identify functional elements
-
Taylor J, Tyekucheva S, King DC, Hardison RC, Miller W, et al. (2006) ESPERR: learning strong and weak signals in genomic sequence alignments to identify functional elements. Genome Res 16: 1596-1604.
-
(2006)
Genome Res
, vol.16
, pp. 1596-1604
-
-
Taylor, J.1
Tyekucheva, S.2
King, D.C.3
Hardison, R.C.4
Miller, W.5
-
38
-
-
0041465867
-
Comparative analyses of multi-species sequences from targeted genomic regions
-
Thomas JW, Touchman JW, Blakesley RW, Bouffard GG, Beckstrom-Sternberg SM, et al. (2003) Comparative analyses of multi-species sequences from targeted genomic regions. Nature 424: 788-793.
-
(2003)
Nature
, vol.424
, pp. 788-793
-
-
Thomas, J.W.1
Touchman, J.W.2
Blakesley, R.W.3
Bouffard, G.G.4
Beckstrom-Sternberg, S.M.5
-
40
-
-
0036079158
-
The human genome browser at UCSC
-
Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, et al. (2002) The human genome browser at UCSC. Genome Res 12: 996-1006.
-
(2002)
Genome Res
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
Sugnet, C.W.2
Furey, T.S.3
Roskin, K.M.4
Pringle, T.H.5
-
41
-
-
0041853625
-
MATCH: A tool for searching transcription factor binding sites in DNA sequences
-
Kel AE, Gossling E, Reuter I, Cheremushkin E, Kel-Margoulis OV, et al. (2003) MATCH: A tool for searching transcription factor binding sites in DNA sequences. Nucleic Acids Res 31: 3576-3579.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3576-3579
-
-
Kel, A.E.1
Gossling, E.2
Reuter, I.3
Cheremushkin, E.4
Kel-Margoulis, O.V.5
-
42
-
-
0024437754
-
Nuclear factor ETF specifically stimulates transcription from promoters without a TATA box
-
Kageyama R, Merlino GT, Pastan I (1989) Nuclear factor ETF specifically stimulates transcription from promoters without a TATA box. J Biol Chem 264: 15508-15514.
-
(1989)
J Biol Chem
, vol.264
, pp. 15508-15514
-
-
Kageyama, R.1
Merlino, G.T.2
Pastan, I.3
-
46
-
-
0033713259
-
The RFX-type transcription factor DAF-19 regulates sensory neuron cilium formation in C. elegans
-
Swoboda P, Adler HT, Thomas JH (2000) The RFX-type transcription factor DAF-19 regulates sensory neuron cilium formation in C. elegans. Mol Cell 5: 411-421.
-
(2000)
Mol Cell
, vol.5
, pp. 411-421
-
-
Swoboda, P.1
Adler, H.T.2
Thomas, J.H.3
-
47
-
-
0036910278
-
Drosophila regulatory factor X is necessary for ciliated sensory neuron differentiation
-
Dubruille R, Laurencon A, Vandaele C, Shishido E, Coulon-Bublex M, et al. (2002) Drosophila regulatory factor X is necessary for ciliated sensory neuron differentiation. Development 129: 5487-5498.
-
(2002)
Development
, vol.129
, pp. 5487-5498
-
-
Dubruille, R.1
Laurencon, A.2
Vandaele, C.3
Shishido, E.4
Coulon-Bublex, M.5
-
48
-
-
0032215091
-
Pax6 controls radial glia differentiation in the cerebral cortex
-
Gotz M, Stoykova A, Gruss P (1998) Pax6 controls radial glia differentiation in the cerebral cortex. Neuron 21: 1031-1044.
-
(1998)
Neuron
, vol.21
, pp. 1031-1044
-
-
Gotz, M.1
Stoykova, A.2
Gruss, P.3
-
49
-
-
0034711293
-
Functional domains of the cone-rod homeobox (CRX) transcription factor
-
Chau KY, Chen S, Zack DJ, Ono SJ(2000) Functional domains of the cone-rod homeobox (CRX) transcription factor. J Biol Chem 275: 37264-37270.
-
(2000)
J Biol Chem
, vol.275
, pp. 37264-37270
-
-
Chau, K.Y.1
Chen, S.2
Zack, D.J.3
Ono, S.J.4
-
50
-
-
0028200262
-
Crystal structure of the Oct-1 POU domain bound to an octamer site: DNA recognition with tethered DNA-binding modules
-
Klemm JD, Rould MA, Aurora R, Herr W, Pabo CO (1994) Crystal structure of the Oct-1 POU domain bound to an octamer site: DNA recognition with tethered DNA-binding modules. Cell 77: 21-32.
-
(1994)
Cell
, vol.77
, pp. 21-32
-
-
Klemm, J.D.1
Rould, M.A.2
Aurora, R.3
Herr, W.4
Pabo, C.O.5
-
51
-
-
0024251459
-
The ubiquitous octamer-binding protein Oct- 1 contains a POU domain with a homeo box subdomain
-
Sturm RA, Das G, Herr W (1988) The ubiquitous octamer-binding protein Oct- 1 contains a POU domain with a homeo box subdomain. Genes Dev 2: 1582-1599.
-
(1988)
Genes Dev
, vol.2
, pp. 1582-1599
-
-
Sturm, R.A.1
Das, G.2
Herr, W.3
-
52
-
-
39949084307
-
The POU homeobox protein Oct-1 regulates radial glia formation downstream of Notch signaling
-
Kiyota T, Kato A, Altmann CR, Kato Y (2008) The POU homeobox protein Oct-1 regulates radial glia formation downstream of Notch signaling. Dev Biol 315: 579-592.
-
(2008)
Dev Biol
, vol.315
, pp. 579-592
-
-
Kiyota, T.1
Kato, A.2
Altmann, C.R.3
Kato, Y.4
-
53
-
-
0029953723
-
A soluble transcription factor, Oct-1, is also found in the insoluble nuclear matrix and possesses silencing activity in its alanine-rich domain
-
Kim MK, Lesoon-Wood LA, Weintraub BD, Chung JH (1996) A soluble transcription factor, Oct-1, is also found in the insoluble nuclear matrix and possesses silencing activity in its alanine-rich domain. Mol Cell Biol 16: 4366-4377.
-
(1996)
Mol Cell Biol
, vol.16
, pp. 4366-4377
-
-
Kim, M.K.1
Lesoon-Wood, L.A.2
Weintraub, B.D.3
Chung, J.H.4
-
54
-
-
0026597313
-
Biological significance of unwinding capability of nuclear matrix-associating DNAs
-
Bode J, Kohwi Y, Dickinson L, Joh T, Klehr D, et al. (1992) Biological significance of unwinding capability of nuclear matrix-associating DNAs. Science 255: 195-197.
-
(1992)
Science
, vol.255
, pp. 195-197
-
-
Bode, J.1
Kohwi, Y.2
Dickinson, L.3
Joh, T.4
Klehr, D.5
-
55
-
-
34250305146
-
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
-
Birney E, Stamatoyannopoulos JA, Dutta A, Guigo R, Gingeras TR, et al. (2007) Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature 447: 799-816.
-
(2007)
Nature
, vol.447
, pp. 799-816
-
-
Birney, E.1
Stamatoyannopoulos, J.A.2
Dutta, A.3
Guigo, R.4
Gingeras, T.R.5
-
56
-
-
15044364239
-
Regulatory polymorphisms underlying complex disease traits
-
Knight JC (2005) Regulatory polymorphisms underlying complex disease traits. J Mol Med 83: 97-109.
-
(2005)
J Mol Med
, vol.83
, pp. 97-109
-
-
Knight, J.C.1
-
57
-
-
33746393852
-
Influence ofhuman genome polymorphism on gene expression
-
Pastinen T, Ge B, Hudson TJ(2006) Influence ofhuman genome polymorphism on gene expression. Hum Mol Genet 15 Spec No 1: R9-16.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.SPEC 1
-
-
Pastinen, T.1
Ge, B.2
Hudson, T.J.3
|