-
1
-
-
0026708177
-
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
-
Li E, Bestor TH, Jaenisch R: Targeted mutation of the DNA methyltransferase gene results in embryonic lethality. Cell 1992, 69:915-926.
-
(1992)
Cell
, vol.69
, pp. 915-926
-
-
Li, E.1
Bestor, T.H.2
Jaenisch, R.3
-
2
-
-
0023848337
-
Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: The ICF syndrome
-
Maraschio P, Zuffardi O, Dalla Fior T, Tiepolo L: Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome. J Med Genet 1988, 25:173-180.
-
(1988)
J Med Genet
, vol.25
, pp. 173-180
-
-
Maraschio, P.1
Zuffardi, O.2
Dalla Fior, T.3
Tiepolo, L.4
-
3
-
-
0027286618
-
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome
-
Jeanpierre M, Turleau C, Aurias A, Prieur M, Ledeist F, Fischer A, Viegas-Pequignot E: An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. Hum Mol Genet 1993, 2:731-735.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 731-735
-
-
Jeanpierre, M.1
Turleau, C.2
Aurias, A.3
Prieur, M.4
Ledeist, F.5
Fischer, A.6
Viegas-Pequignot, E.7
-
4
-
-
0032231449
-
Localization of the ICF syndrome to chromosome 20 by homozygosity mapping
-
Wijmenga C, van den Heuvel LP, Strengman E, Luyten JA, van der Burgt U, de Groot R, Smeets DF, Draaisma JM, van Dongen JJ, De Abreu RA, et al.: Localization of the ICF syndrome to chromosome 20 by homozygosity mapping. Am J Hum Genet 1998, 63:803-809.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 803-809
-
-
Wijmenga, C.1
Van Den Heuvel, L.P.2
Strengman, E.3
Luyten, J.A.4
Van Der Burgt, U.5
De Groot, R.6
Smeets, D.F.7
Draaisma, J.M.8
Van Dongen, J.J.9
De Abreu, R.A.10
-
5
-
-
0033153303
-
The human DNA methyltransferases (DNMTs) 1, 3a and 3b: Coordinate mRNA expression in normal tissues and overexpression in tumors
-
Robertson KD, Uzvolgyi E, Liang G, Talmadge C, Sumegi J, Gonzales FA, Jones PA: The human DNA methyltransferases (DNMTs) 1, 3a and 3b: coordinate mRNA expression in normal tissues and overexpression in tumors. Nucleic Acids Res 1999, 27:2291-2298.
-
(1999)
Nucleic Acids Res
, vol.27
, pp. 2291-2298
-
-
Robertson, K.D.1
Uzvolgyi, E.2
Liang, G.3
Talmadge, C.4
Sumegi, J.5
Gonzales, F.A.6
Jones, P.A.7
-
6
-
-
0033435205
-
The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome
-
Hansen RS, Wijmenga C, Luo P, Stanek AM, Canfield TK, Weemaes CMR, Gartler SM: The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. Proc Natl Acad Sci USA 1999, 96:14412-14417.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 14412-14417
-
-
Hansen, R.S.1
Wijmenga, C.2
Luo, P.3
Stanek, A.M.4
Canfield, T.K.5
Weemaes, C.M.R.6
Gartler, S.M.7
-
7
-
-
0033615717
-
DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
-
Okano M, Bell DW, Haber DA, Li E: DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell 1999, 99:247-257.
-
(1999)
Cell
, vol.99
, pp. 247-257
-
-
Okano, M.1
Bell, D.W.2
Haber, D.A.3
Li, E.4
-
8
-
-
0033547330
-
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
-
Xu G-L, Bestor TH, Bourc'his D, Hsieh C-L, Tommerup N, Bugge M, Hulten M, Qu X, Russo JJ, Viegas-Péquignot E: Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. Nature 1999, 402:187-191.
-
(1999)
Nature
, vol.402
, pp. 187-191
-
-
Xu, G.-L.1
Bestor, T.H.2
Bourc'His, D.3
Hsieh, C.-L.4
Tommerup, N.5
Bugge, M.6
Hulten, M.7
Qu, X.8
Russo, J.J.9
Viegas-Péquignot, E.10
-
9
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir RE, Van Den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 1999, 23:185-188.
-
(1999)
Nat Genet
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van Den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zoghbi, H.Y.6
-
10
-
-
0033365401
-
Rett Syndrome and beyond: Recurrent spontaneous and familial MECP2 mutations at CpG hotspots
-
Wan M, Lee SSJ, Zhang X, Houwink-Manville I, Song H-R, Amir RE, Budden S, Naidu S, Pereira JLP, Lo IFM, et al.: Rett Syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots. Am J Hum Gene 1999, 65:1520-1529.
-
(1999)
Am J Hum Gene
, vol.65
, pp. 1520-1529
-
-
Wan, M.1
Lee, S.S.J.2
Zhang, X.3
Houwink-Manville, I.4
Song, H.-R.5
Amir, R.E.6
Budden, S.7
Naidu, S.8
Pereira, J.L.P.9
Lo, I.F.M.10
-
11
-
-
0020507697
-
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
-
Hagberg B, Aicardi J, Dias K, Ramos O: A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann Neurol 1983, 14:471-479.
-
(1983)
Ann Neurol
, vol.14
, pp. 471-479
-
-
Hagberg, B.1
Aicardi, J.2
Dias, K.3
Ramos, O.4
-
13
-
-
0023797483
-
Genetic aspects of Rett syndrome
-
Zoghbi H: Genetic aspects of Rett syndrome. J Child Neurol 1988, 3 (suppl):S76-S78.
-
(1988)
J Child Neurol
, vol.3
, Issue.SUPPL.
-
-
Zoghbi, H.1
-
14
-
-
0032133323
-
Workshop on autonomic function in Rett syndrome
-
Engerstrom IW, Kerr A: Workshop on autonomic function in Rett syndrome. Brain Dev 1988, 20:323-326.
-
(1988)
Brain Dev
, vol.20
, pp. 323-326
-
-
Engerstrom, I.W.1
Kerr, A.2
-
15
-
-
0342437491
-
MeCP2 is a transcriptional represser with abundant binding sites in genomic chromatin
-
Nan X, Campoy F, Bird A: MeCP2 is a transcriptional represser with abundant binding sites in genomic chromatin. Cell 1997, 88:471-481.
-
(1997)
Cell
, vol.88
, pp. 471-481
-
-
Nan, X.1
Campoy, F.2
Bird, A.3
-
16
-
-
0030071685
-
The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse
-
Tate P, Skarnes W, Bird A: The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse. Nat Genet 1996, 12:205-208.
-
(1996)
Nat Genet
, vol.12
, pp. 205-208
-
-
Tate, P.1
Skarnes, W.2
Bird, A.3
-
17
-
-
0033520515
-
The solution structure of the domain from MeCP2 that binds to methylated DNA
-
Wakefield RI, Smith BO, Nan X, Free A, Soteriou A, Uhrin D, Bird AP, Barlow PN: The solution structure of the domain from MeCP2 that binds to methylated DNA. J Mol Biol 1999, 291:1055-1065.
-
(1999)
J Mol Biol
, vol.291
, pp. 1055-1065
-
-
Wakefield, R.I.1
Smith, B.O.2
Nan, X.3
Free, A.4
Soteriou, A.5
Uhrin, D.6
Bird, A.P.7
Barlow, P.N.8
|