-
1
-
-
40849139208
-
Epigenetics in Cancer
-
PMID:18337604
-
Esteller M. Epigenetics in Cancer. N Eng J Med 2008; 358:1148-59; PMID:18337604.
-
(2008)
N Eng J Med
, vol.358
, pp. 1148-1159
-
-
Esteller, M.1
-
2
-
-
78049419464
-
Orphan CpG islands identity numerous conserved promoter in the mammalian genome
-
PMID: 20885785
-
Illingworth RS, Gruenewald-Schneider U, Webb S, Kerr AR, James KD, Turner DJ, et al. Orphan CpG islands identity numerous conserved promoter in the mammalian genome. PLoS Genet 2010; 6:1001134; PMID: 20885785.
-
(2010)
PLoS Genet
, vol.6
, pp. 1001134
-
-
Illingworth, R.S.1
Gruenewald-Schneider, U.2
Webb, S.3
Kerr, A.R.4
James, K.D.5
Turner, D.J.6
-
3
-
-
46249117780
-
Genomic survey by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methyation
-
PMID: 18568024
-
Kerkel K, Spadola A, Yuan E, Kosek J, Jiang L, Hod E, et al. Genomic survey by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methyation. Nat Genet 2008; 40:904-8; PMID: 18568024.
-
(2008)
Nat Genet
, vol.40
, pp. 904-908
-
-
Kerkel, K.1
Spadola, A.2
Yuan, E.3
Kosek, J.4
Jiang, L.5
Hod, E.6
-
4
-
-
63449103531
-
DNA methylation analysis of chromosome 21 gene promoters at single base pair and single allele resolution
-
PMID: 19325872
-
Zhang Y, Rohde C, Tierling S, Jurkowski TP, Bock C, Santacruz D, et al. DNA methylation analysis of chromosome 21 gene promoters at single base pair and single allele resolution. PLoS Genet 2009; 5:1000438; PMID: 19325872.
-
(2009)
PLoS Genet
, vol.5
, pp. 1000438
-
-
Zhang, Y.1
Rohde, C.2
Tierling, S.3
Jurkowski, T.P.4
Bock, C.5
Santacruz, D.6
-
5
-
-
76249089640
-
Non-imprinted allele-specific DNA methylation on human autosomes
-
PMID: 19958531
-
Zhang Y, Rohde C, Reinhardt R, Voelcker-Rehage C, Jeltsch A. Non-imprinted allele-specific DNA methylation on human autosomes. Genome Biol 2009; 10:138; PMID: 19958531.
-
(2009)
Genome Biol
, vol.10
, pp. 138
-
-
Zhang, Y.1
Rohde, C.2
Reinhardt, R.3
Voelcker-Rehage, C.4
Jeltsch, A.5
-
6
-
-
77953223693
-
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
-
PMID: 20485568
-
Gibbs JR, van der Brug MP, Hernandez DG, Traynor BJ, Nalls MA, Lai SL, et al. Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain. PLoS Genet 2010; 6:1000952; PMID: 20485568.
-
(2010)
PLoS Genet
, vol.6
, pp. 1000952
-
-
Gibbs, J.R.1
van der, B.M.P.2
Hernandez, D.G.3
Traynor, B.J.4
Nalls, M.A.5
Lai, S.L.6
-
7
-
-
77649204292
-
Genetic control of individual differences in gene-specific methylation in human brain
-
PMID: 20215007
-
Zhang D, Cheng L, Badner JA, Chen C, Chen Q, Luo W, et al. Genetic control of individual differences in gene-specific methylation in human brain. Am J Hum Genet 2010; 86:411-9; PMID: 20215007.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 411-419
-
-
Zhang, D.1
Cheng, L.2
Badner, J.A.3
Chen, C.4
Chen, Q.5
Luo, W.6
-
8
-
-
78651276230
-
Allele-specific DNA methylation: Beyond imprinting
-
PMID: 20855472
-
Tycko B. Allele-specific DNA methylation: beyond imprinting. Hum Mol Genet 2010; 19:210-20; PMID: 20855472.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 210-220
-
-
Tycko, B.1
-
10
-
-
14744277207
-
Molecular cloning of TRPC3a, an N-terminally extended, store-operated variant of the human C3 transient receptor potential channel
-
PMID: 15728370
-
Yildirim E, Kawasaki BT, Birnbaumer L. Molecular cloning of TRPC3a, an N-terminally extended, store-operated variant of the human C3 transient receptor potential channel. Proc Natl Acad Sci USA 2005; 102:3307-11; PMID: 15728370.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 3307-3311
-
-
Yildirim, E.1
Kawasaki, B.T.2
Birnbaumer, L.3
-
11
-
-
79960804327
-
Methylation screening of reciprocal genome-wide UPDs identifies novel human specific imprinted genes
-
PMID:21593219
-
Nakabayashi K, Martin-Trujillo A, Tayama C, Camprubi C, Yoshida W, Lapunzina P, et al. Methylation screening of reciprocal genome-wide UPDs identifies novel human specific imprinted genes. Hum Mol Genet 2011; 20:3188-97; PMID:21593219.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3188-3197
-
-
Nakabayashi, K.1
Martin-Trujillo, A.2
Tayama, C.3
Camprubi, C.4
Yoshida, W.5
Lapunzina, P.6
-
12
-
-
0037203329
-
MRNA distribution analysis of human TRPC family in CNS and peripheral tissues
-
PMID: 12531519
-
Riccio A, Medhurst AD, Mattei C, Kelsell RE, Calver AR, Randall AD, et al. mRNA distribution analysis of human TRPC family in CNS and peripheral tissues. Brain Res Mol Brain Res 2002; 109:95-104; PMID: 12531519.
-
(2002)
Brain Res Mol Brain Res
, vol.109
, pp. 95-104
-
-
Riccio, A.1
Medhurst, A.D.2
Mattei, C.3
Kelsell, R.E.4
Calver, A.R.5
Randall, A.D.6
-
13
-
-
41049094414
-
TrpC3 regulates hypertrophy-associated gene expression without affecting myocyte beating or cell size
-
PMID: 17726532
-
Brenner JS, Dolmetsch RE. TrpC3 regulates hypertrophy-associated gene expression without affecting myocyte beating or cell size. PLos One 2007; 2:802; PMID: 17726532.
-
(2007)
PLos One
, vol.2
, pp. 802
-
-
Brenner, J.S.1
Dolmetsch, R.E.2
-
14
-
-
1642433144
-
An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: Interaction between genotype and epigenotype
-
PMID: 14645199
-
Murrell A, Heeson S, Cooper WN, Douglas E, Apostolidou S, Moore GE, et al. An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype. Hum Mol Genet 2004; 13:247-55; PMID: 14645199.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 247-255
-
-
Murrell, A.1
Heeson, S.2
Cooper, W.N.3
Douglas, E.4
Apostolidou, S.5
Moore, G.E.6
-
15
-
-
78649969065
-
The DNA methylome of human peripheral blood mononuclear cells
-
PMID: 21085693
-
Li Y, Zhu J, Tian G, Li N, Li Q, Ye M, et al. The DNA methylome of human peripheral blood mononuclear cells. PLoS Biol 2010; 8:1000533; PMID: 21085693.
-
(2010)
PLoS Biol
, vol.8
, pp. 1000533
-
-
Li, Y.1
Zhu, J.2
Tian, G.3
Li, N.4
Li, Q.5
Ye, M.6
-
16
-
-
0028104109
-
Sp1 elements protect a CpG island from de novo methylation
-
PMID: 8090226
-
Brandeis M, Frank D, Keshet I, Siegfried Z, Mendelsohn M, Nemes A, et al. Sp1 elements protect a CpG island from de novo methylation. Nature 1994; 371:435-8; PMID: 8090226.
-
(1994)
Nature
, vol.371
, pp. 435-438
-
-
Brandeis, M.1
Frank, D.2
Keshet, I.3
Siegfried, Z.4
Mendelsohn, M.5
Nemes, A.6
-
17
-
-
0027960055
-
Sp1 sites in the mouse aprt gene promoter are required to prevent methylation of the CpG island
-
PMID: 7958895
-
Macleod D, Charlton J, Mullins J, Bird AP Sp1 sites in the mouse aprt gene promoter are required to prevent methylation of the CpG island. Genes Dev 1994; 8:2282-92; PMID: 7958895.
-
(1994)
Genes Dev
, vol.8
, pp. 2282-2292
-
-
Macleod, D.1
Charlton, J.2
Mullins, J.3
Bird, A.P.4
-
18
-
-
50849141092
-
An Sp1/Sp3 binding polymorphism confers methylation protection
-
PMID: 18725933
-
Boumber YA, Kondo Y, Chen X, Shen L, Guo Y, Tellez C, et al. An Sp1/Sp3 binding polymorphism confers methylation protection. PLos Genet 2008; 4:1000162; PMID: 18725933.
-
(2008)
PLos Genet
, vol.4
, pp. 1000162
-
-
Boumber, Y.A.1
Kondo, Y.2
Chen, X.3
Shen, L.4
Guo, Y.5
Tellez, C.6
-
19
-
-
66149097030
-
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice
-
PMID: 19351902
-
Becker EB, Oliver PL, Glitsch MD, Banks GT, Achilli F, Hardy A, et al. A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice. Proc Natl Acad Sci USA 2009; 106:6706-11; PMID: 19351902.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 6706-6711
-
-
Becker, E.B.1
Oliver, P.L.2
Glitsch, M.D.3
Banks, G.T.4
Achilli, F.5
Hardy, A.6
-
20
-
-
80051788858
-
Candidate screening of the TRPC3 gene in cerebellar ataxia
-
PMID: 21321808
-
Becker EB, Fogel BL, Rajakulendran S, Dulneva A, Hanna MG, Perlman SL, et al. Candidate screening of the TRPC3 gene in cerebellar ataxia. Cerebellum 2011; 10:296-9; PMID: 21321808.
-
(2011)
Cerebellum
, vol.10
, pp. 296-299
-
-
Becker, E.B.1
Fogel, B.L.2
Rajakulendran, S.3
Dulneva, A.4
Hanna, M.G.5
Perlman, S.L.6
-
21
-
-
33749338744
-
Calcineurin-dependent cardiomyopathy is activated by TRPC in the adult mouse heart
-
PMID: 16873889
-
Nakayama H, Wilkin BJ, Bodi I, Molkentin JD. Calcineurin-dependent cardiomyopathy is activated by TRPC in the adult mouse heart. FASEB J 2006; 20:1660-70; PMID: 16873889.
-
(2006)
FASEB J
, vol.20
, pp. 1660-1670
-
-
Nakayama, H.1
Wilkin, B.J.2
Bodi, I.3
Molkentin, J.D.4
-
22
-
-
33845597014
-
Canonical transient receptor potential channels promote cardiomyocyte hypertrophy through activation of calcineurin signaling
-
PMID: 16950785
-
Bush EW, Hood DB, Papst PJ, Chapo JA, Minobe W, Bristow MR, et al. Canonical transient receptor potential channels promote cardiomyocyte hypertrophy through activation of calcineurin signaling. J Biol Chem 2006; 281:33487-96; PMID: 16950785.
-
(2006)
J Biol Chem
, vol.281
, pp. 33487-33496
-
-
Bush, E.W.1
Hood, D.B.2
Papst, P.J.3
Chapo, J.A.4
Minobe, W.5
Bristow, M.R.6
-
23
-
-
44649128517
-
Ito HTRP channel and cardiovascular disease
-
PMID: 18508125
-
Watanabe H, Murakami M, Ohba T, Takahashi Y, Ito HTRP channel and cardiovascular disease. Pharmacol Ther 2008; 118:337-51; PMID: 18508125.
-
(2008)
Pharmacol Ther
, vol.118
, pp. 337-351
-
-
Watanabe, H.1
Murakami, M.2
Ohba, T.3
Takahashi, Y.4
-
24
-
-
41749094096
-
Genetic determinants of cardiac hypertrophy
-
PMID: 18382207
-
Marian AJ. Genetic determinants of cardiac hypertrophy. Curr Opin Cardiol 2008; 23:199-205; PMID: 18382207.
-
(2008)
Curr Opin Cardiol
, vol.23
, pp. 199-205
-
-
Marian, A.J.1
-
25
-
-
33646265537
-
Limited evolutionary conservation of imprinting in the human placenta
-
PMID: 16614068
-
Monk D, Arnaud P, Apostolidou S, Hills FA, Kelsey G, Stanier P, et al. Limited evolutionary conservation of imprinting in the human placenta. Proc Natl Acad Sci USA 2006; 103:6623-8; PMID: 16614068.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 6623-6628
-
-
Monk, D.1
Arnaud, P.2
Apostolidou, S.3
Hills, F.A.4
Kelsey, G.5
Stanier, P.6
-
26
-
-
59749096283
-
Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3 and TPM1 in patients with hypertrophic cardiomyopathy
-
PMID: 19161138
-
García-Castro M, Coto E, Reguero JR, Berrazueta JR, Álvarez, Alonso B, et al. Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3 and TPM1 in patients with hypertrophic cardiomyopathy. Rev Esp Cardiol 2009; 62:48-56; PMID: 19161138.
-
(2009)
Rev Esp Cardiol
, vol.62
, pp. 48-56
-
-
García-Castro, M.1
Coto, E.2
Reguero, J.R.3
Berrazueta, J.R.4
Álvarez, A.B.5
-
27
-
-
33745088678
-
Molecular pathogenesis of spinocerebellar ataxias
-
PMID: 18418661
-
Matilla-Dueñas A, Goold R, Giunti P. Molecular pathogenesis of spinocerebellar ataxias. Brain 2006; 129:1357-70; PMID: 18418661.
-
(2006)
Brain
, vol.129
, pp. 1357-1370
-
-
Matilla-Dueñas, A.1
Goold, R.2
Giunti, P.3
-
28
-
-
77955480316
-
Cellular and molecular pathways triggering neurodegeneration in the spinocerebellar ataxias
-
PMID: 19890685
-
Matilla-Dueñas A, Sanchez I, Corral-Juan M, Davalos A, Alvarez R, Latorre P. Cellular and molecular pathways triggering neurodegeneration in the spinocerebellar ataxias. Cerebellum 2010; 9:148-66; PMID: 19890685.
-
(2010)
Cerebellum
, vol.9
, pp. 148-166
-
-
Matilla-Dueñas, A.1
Sanchez, I.2
Corral-Juan, M.3
Davalos, A.4
Alvarez, R.5
Latorre, P.6
|