-
1
-
-
0038497542
-
Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid
-
Watson JD, Crick FH. Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid. Nature 1953; 171: 737-8.
-
(1953)
Nature
, vol.171
, pp. 737-738
-
-
Watson, J.D.1
Crick, F.H.2
-
2
-
-
0017837314
-
The compaction of DNA helices into either continuous supercoils or folded-fiber rods and toroids
-
Eickbush TH, Moudrianakis EN. The compaction of DNA helices into either continuous supercoils or folded-fiber rods and toroids. Cell 1978; 13: 295-306.
-
(1978)
Cell
, vol.13
, pp. 295-306
-
-
Eickbush, T.H.1
Moudrianakis, E.N.2
-
3
-
-
55949134303
-
DNA methylomes, histone codes and miRNAs: Tying it all together
-
Guil S, Esteller M. DNA methylomes, histone codes and miRNAs: tying it all together. Int J Biochem Cell Biol 2009; 41: 87-95.
-
(2009)
Int J Biochem Cell Biol
, vol.41
, pp. 87-95
-
-
Guil, S.1
Esteller, M.2
-
4
-
-
79955060261
-
Regulation of expression and activity of DNA (cytosine-5) methyltransferases in mammalian cells
-
Kinney SR, Pradhan S. Regulation of expression and activity of DNA (cytosine-5) methyltransferases in mammalian cells. Prog Mol Biol Transl Sci 2011; 101: 311-33.
-
(2011)
Prog Mol Biol Transl Sci
, vol.101
, pp. 311-333
-
-
Kinney, S.R.1
Pradhan, S.2
-
6
-
-
79955538247
-
Hydroxylation of 5- methylcytosine by TET1 promotes active DNA demethylation in the adult brain
-
Guo JU, Su Y, Zhong C, Ming GL, Song H. Hydroxylation of 5- methylcytosine by TET1 promotes active DNA demethylation in the adult brain. Cell 2011; 145: 423-34.
-
(2011)
Cell
, vol.145
, pp. 423-434
-
-
Guo, J.U.1
Su, Y.2
Zhong, C.3
Ming, G.L.4
Song, H.5
-
7
-
-
84859265962
-
Active DNA demethylation by Gadd45 and DNA repair
-
Niehrs C, Schafer A. Active DNA demethylation by Gadd45 and DNA repair. Trends Cell Biol 2012; 22: 220-7.
-
(2012)
Trends Cell Biol
, vol.22
, pp. 220-227
-
-
Niehrs, C.1
Schafer, A.2
-
8
-
-
79952763586
-
Reprogramming of the paternal genome upon fertilization involves genome-wide oxidation of 5-methylcytosine
-
Iqbal K, Jin SG, Pfeifer GP, Szabo PE. Reprogramming of the paternal genome upon fertilization involves genome-wide oxidation of 5-methylcytosine. Proc Natl Acad Sci USA 2011; 108: 3642-7.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 3642-3647
-
-
Iqbal, K.1
Jin, S.G.2
Pfeifer, G.P.3
Szabo, P.E.4
-
9
-
-
37249059981
-
Computational and experimental identification of novel human imprinted genes
-
Luedi PP, Dietrich FS, Weidman JR, Bosko JM, Jirtle RL, Hartemink AJ. Computational and experimental identification of novel human imprinted genes. Genome Res 2007; 17: 1723-30.
-
(2007)
Genome Res
, vol.17
, pp. 1723-1730
-
-
Luedi, P.P.1
Dietrich, F.S.2
Weidman, J.R.3
Bosko, J.M.4
Jirtle, R.L.5
Hartemink, A.J.6
-
10
-
-
84866098740
-
A genome-wide approach reveals novel imprinted genes expressed in the human placenta
-
in press
-
Barbaux S, Gascoin-Lachambre G, Buffat C, et al. A genome-wide approach reveals novel imprinted genes expressed in the human placenta. Epigenetics 2012: in press.
-
(2012)
Epigenetics
-
-
Barbaux, S.1
Gascoin-Lachambre, G.2
Buffat, C.3
-
11
-
-
48249141249
-
Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians
-
Smits G, Mungall AJ, Griffiths-Jones S, et al. Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians. Nat Genet 2008; 40: 971-6.
-
(2008)
Nat Genet
, vol.40
, pp. 971-976
-
-
Smits, G.1
Mungall, A.J.2
Griffiths-Jones, S.3
-
12
-
-
12344284062
-
Imprinting and looping: Epigenetic marks control interactions between regulatory elements
-
Kato Y, Sasaki H. Imprinting and looping: epigenetic marks control interactions between regulatory elements. Bioessays 2005; 27: 1-4.
-
(2005)
Bioessays
, vol.27
, pp. 1-4
-
-
Kato, Y.1
Sasaki, H.2
-
13
-
-
33750959900
-
Raising the curtains on interchromosomal interactions
-
Krueger C, Osborne CS. Raising the curtains on interchromosomal interactions. Trends Genet 2006; 22: 637-9.
-
(2006)
Trends Genet
, vol.22
, pp. 637-639
-
-
Krueger, C.1
Osborne, C.S.2
-
14
-
-
0017696835
-
Androgenetic origin of hydatidiform mole
-
Kajii T, Ohama K. Androgenetic origin of hydatidiform mole. Nature 1977; 268: 633-4.
-
(1977)
Nature
, vol.268
, pp. 633-634
-
-
Kajii, T.1
Ohama, K.2
-
15
-
-
33644615366
-
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans
-
Murdoch S, Djuric U, Mazhar B, et al. Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans. Nat Genet 2006; 38: 300-2.
-
(2006)
Nat Genet
, vol.38
, pp. 300-302
-
-
Murdoch, S.1
Djuric, U.2
Mazhar, B.3
-
16
-
-
33644622619
-
Genetics and epigenetics of hydatidiform moles
-
Bestor TH, Bourc'his D. Genetics and epigenetics of hydatidiform moles. Nat Genet 2006; 38: 274-6.
-
(2006)
Nat Genet
, vol.38
, pp. 274-276
-
-
Bestor, T.H.1
Bourc'his, D.2
-
17
-
-
0016439429
-
DNA modification mechanisms and gene activity during development
-
Holliday R, Pugh JE. DNA modification mechanisms and gene activity during development. Science 1975; 187: 226-32.
-
(1975)
Science
, vol.187
, pp. 226-232
-
-
Holliday, R.1
Pugh, J.E.2
-
18
-
-
0016692220
-
X inactivation, differentiation, and DNA methylation
-
Riggs AD. X inactivation, differentiation, and DNA methylation. Cytogenet Cell Genet 1975; 14: 9-25.
-
(1975)
Cytogenet Cell Genet
, vol.14
, pp. 9-25
-
-
Riggs, A.D.1
-
19
-
-
0017841507
-
Use of restriction enzymes to study eukaryotic DNA methylation: I. The methylation pattern in ribosomal DNA from Xenopus laevis
-
Bird AP, Southern EM. Use of restriction enzymes to study eukaryotic DNA methylation: I. The methylation pattern in ribosomal DNA from Xenopus laevis. J Mol Biol 1978; 118: 27-47.
-
(1978)
J Mol Biol
, vol.118
, pp. 27-47
-
-
Bird, A.P.1
Southern, E.M.2
-
20
-
-
0018370141
-
Direct detection of methylated cytosine in DNA by use of the restriction enzyme MspI
-
Cedar H, Solage A, Glaser G, Razin A. Direct detection of methylated cytosine in DNA by use of the restriction enzyme MspI. Nucleic Acids Res 1979; 6: 2125-32.
-
(1979)
Nucleic Acids Res
, vol.6
, pp. 2125-2132
-
-
Cedar, H.1
Solage, A.2
Glaser, G.3
Razin, A.4
-
21
-
-
0022212315
-
The accessibility of 5-methylcytosine to specific antibodies in double- stranded DNA of Xanthomonas phage XP12
-
Adouard V, Dante R, Niveleau A, Delain E, Revet B, Ehrlich M. The accessibility of 5-methylcytosine to specific antibodies in double- stranded DNA of Xanthomonas phage XP12. Eur J Biochem 1985; 152: 115-21.
-
(1985)
Eur J Biochem
, vol.152
, pp. 115-121
-
-
Adouard, V.1
Dante, R.2
Niveleau, A.3
Delain, E.4
Revet, B.5
Ehrlich, M.6
-
22
-
-
0031792779
-
Identification and characterization of a family of mammalian methyl-CpG binding proteins
-
Hendrich B, Bird A. Identification and characterization of a family of mammalian methyl-CpG binding proteins. Mol Cell Biol 1998; 18: 6538-47.
-
(1998)
Mol Cell Biol
, vol.18
, pp. 6538-6547
-
-
Hendrich, B.1
Bird, A.2
-
23
-
-
0014936031
-
Reaction of sodium bisulfite with uracil, cytosine, and their derivatives
-
Hayatsu H, Wataya Y, Kai K, Iida S. Reaction of sodium bisulfite with uracil, cytosine, and their derivatives. Biochemistry 1970; 9: 2858-65.
-
(1970)
Biochemistry
, vol.9
, pp. 2858-2865
-
-
Hayatsu, H.1
Wataya, Y.2
Kai, K.3
Iida, S.4
-
24
-
-
0014940938
-
The addition of sodium bisulfite to uracil and to cytosine
-
Hayatsu H, Wataya Y, Kazushige K. The addition of sodium bisulfite to uracil and to cytosine. J Am Chem Soc 1970; 92: 724-6.
-
(1970)
J Am Chem Soc
, vol.92
, pp. 724-726
-
-
Hayatsu, H.1
Wataya, Y.2
Kazushige, K.3
-
25
-
-
0019332015
-
Comparison of bisulfite modification of 5-methyldeoxycytidine and deoxycytidine residues
-
Wang RY, Gehrke CW, Ehrlich M. Comparison of bisulfite modification of 5-methyldeoxycytidine and deoxycytidine residues. Nucleic Acids Res 1980; 8: 4777-90.
-
(1980)
Nucleic Acids Res
, vol.8
, pp. 4777-4790
-
-
Wang, R.Y.1
Gehrke, C.W.2
Ehrlich, M.3
-
26
-
-
0026546877
-
A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands
-
Frommer M, McDonald LE, Millar DS, et al. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proc Natl Acad Sci USA 1992; 89: 1827-31.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 1827-1831
-
-
Frommer, M.1
McDonald, L.E.2
Millar, D.S.3
-
27
-
-
66449121652
-
Finding the fifth base: Genome-wide sequencing of cytosine methylation
-
Lister R, Ecker JR. Finding the fifth base: genome-wide sequencing of cytosine methylation. Genome Res 2009; 19: 959-66.
-
(2009)
Genome Res
, vol.19
, pp. 959-966
-
-
Lister, R.1
Ecker, J.R.2
-
28
-
-
77957937011
-
Quantitative comparison of genome-wide DNA methylation mapping technologies
-
Bock C, Tomazou EM, Brinkman AB, et al. Quantitative comparison of genome-wide DNA methylation mapping technologies. Nat Biotechnol 2010; 28: 1106-14.
-
(2010)
Nat Biotechnol
, vol.28
, pp. 1106-1114
-
-
Bock, C.1
Tomazou, E.M.2
Brinkman, A.B.3
-
29
-
-
77957932941
-
Comparison of sequencingbased methods to profile DNA methylation and identification of monoallelic epigenetic modifications
-
Harris RA, Wang T, Coarfa C, et al. Comparison of sequencingbased methods to profile DNA methylation and identification of monoallelic epigenetic modifications. Nat Biotechnol 2010; 28: 1097-105.
-
(2010)
Nat Biotechnol
, vol.28
, pp. 1097-1105
-
-
Harris, R.A.1
Wang, T.2
Coarfa, C.3
-
30
-
-
64349106730
-
Targeted bisulfite sequencing reveals changes in DNA methylation associated with nuclear reprogramming
-
Deng J, Shoemaker R, Xie B, et al. Targeted bisulfite sequencing reveals changes in DNA methylation associated with nuclear reprogramming. Nat Biotechnol 2009; 27: 353-60.
-
(2009)
Nat Biotechnol
, vol.27
, pp. 353-360
-
-
Deng, J.1
Shoemaker, R.2
Xie, B.3
-
31
-
-
0036193520
-
Human gene mutations causing infertility
-
Layman LC. Human gene mutations causing infertility. J Med Genet 2002; 39: 153-61.
-
(2002)
J Med Genet
, vol.39
, pp. 153-161
-
-
Layman, L.C.1
-
32
-
-
55549115368
-
The biology of infertility: Research advances and clinical challenges
-
Matzuk MM, Lamb DJ. The biology of infertility: research advances and clinical challenges. Nat Med 2008; 14: 1197-213.
-
(2008)
Nat Med
, vol.14
, pp. 1197-1213
-
-
Matzuk, M.M.1
Lamb, D.J.2
-
33
-
-
0142091380
-
A multitude of genes expressed solely in meiotic or postmeiotic spermatogenic cells offers a myriad of contraceptive targets
-
Schultz N, Hamra FK, Garbers DL. A multitude of genes expressed solely in meiotic or postmeiotic spermatogenic cells offers a myriad of contraceptive targets. Proc Natl Acad Sci USA 2003; 100: 12201-6.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 12201-12206
-
-
Schultz, N.1
Hamra, F.K.2
Garbers, D.L.3
-
34
-
-
42449115398
-
Epigenetic reprogramming of the male genome during gametogenesis and in the zygote
-
Rousseaux S, Reynoird N, Escoffier E, Thevenon J, Caron C, Khochbin S. Epigenetic reprogramming of the male genome during gametogenesis and in the zygote. Reprod Biomed Online 2008; 16: 492-503.
-
(2008)
Reprod Biomed Online
, vol.16
, pp. 492-503
-
-
Rousseaux, S.1
Reynoird, N.2
Escoffier, E.3
Thevenon, J.4
Caron, C.5
Khochbin, S.6
-
35
-
-
0042031173
-
The structural organization of sperm chromatin
-
Wykes SM, Krawetz SA. The structural organization of sperm chromatin. J Biol Chem 2003; 278: 29471-7.
-
(2003)
J Biol Chem
, vol.278
, pp. 29471-29477
-
-
Wykes, S.M.1
Krawetz, S.A.2
-
36
-
-
34250189494
-
Germline histone dynamics and epigenetics
-
Ooi SL, Henikoff S. Germline histone dynamics and epigenetics. Curr Opin Cell Biol 2007; 19: 257-65.
-
(2007)
Curr Opin Cell Biol
, vol.19
, pp. 257-265
-
-
Ooi, S.L.1
Henikoff, S.2
-
37
-
-
34347213437
-
Developmental acquisition of genome-wide DNA methylation occurs prior to meiosis in male germ cells
-
Oakes CC, La Salle S, Smiraglia DJ, Robaire B, Trasler JM. Developmental acquisition of genome-wide DNA methylation occurs prior to meiosis in male germ cells. Dev Biol 2007; 307: 368-79.
-
(2007)
Dev Biol
, vol.307
, pp. 368-379
-
-
Oakes, C.C.1
la Salle, S.2
Smiraglia, D.J.3
Robaire, B.4
Trasler, J.M.5
-
38
-
-
0141992792
-
Quantitation by image analysis of global DNA methylation in human spermatozoa and its prognostic value in in vitro fertilization: A preliminary study
-
Benchaib M, Ajina M, Lornage J, Niveleau A, Durand P, Guerin JF. Quantitation by image analysis of global DNA methylation in human spermatozoa and its prognostic value in in vitro fertilization: a preliminary study. Fertil Steril 2003; 80: 947-53.
-
(2003)
Fertil Steril
, vol.80
, pp. 947-953
-
-
Benchaib, M.1
Ajina, M.2
Lornage, J.3
Niveleau, A.4
Durand, P.5
Guerin, J.F.6
-
39
-
-
77956897397
-
Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm
-
Navarro-Costa P, Nogueira P, Carvalho M, et al. Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm. Hum Reprod 2010; 25: 2647-54.
-
(2010)
Hum Reprod
, vol.25
, pp. 2647-2654
-
-
Navarro-Costa, P.1
Nogueira, P.2
Carvalho, M.3
-
40
-
-
84861787169
-
Routine diagnostic testing of Y chromosome deletions in male infertile and subfertile
-
Ghorbian S. Routine diagnostic testing of Y chromosome deletions in male infertile and subfertile. Gene 2012; 503: 160-4.
-
(2012)
Gene
, vol.503
, pp. 160-164
-
-
Ghorbian, S.1
-
41
-
-
77249112916
-
Lack of association between DAZ gene methylation patterns and spermatogenic failure
-
Wu W, Lu C, Xia Y, et al. Lack of association between DAZ gene methylation patterns and spermatogenic failure. Clin Chem Lab Med 2010; 48: 355-60.
-
(2010)
Clin Chem Lab Med
, vol.48
, pp. 355-360
-
-
Wu, W.1
Lu, C.2
Xia, Y.3
-
42
-
-
61649125853
-
An epigenetic mechanism regulates germ cell-specific expression of the porcine Deleted in Azoospermia-Like (DAZL) gene
-
Linher K, Cheung Q, Baker P, Bedecarrats G, Shiota K, Li J. An epigenetic mechanism regulates germ cell-specific expression of the porcine Deleted in Azoospermia-Like (DAZL) gene. Differentiation 2009; 77: 335-49.
-
(2009)
Differentiation
, vol.77
, pp. 335-349
-
-
Linher, K.1
Cheung, Q.2
Baker, P.3
Bedecarrats, G.4
Shiota, K.5
Li, J.6
-
43
-
-
69349086991
-
Tissue-specific differentially methylated regions of the human VASA gene are potentially associated with maturation arrest phenotype in the testis
-
Sugimoto K, Koh E, Sin HS, et al. Tissue-specific differentially methylated regions of the human VASA gene are potentially associated with maturation arrest phenotype in the testis. J Hum Genet 2009; 54: 450-6.
-
(2009)
J Hum Genet
, vol.54
, pp. 450-456
-
-
Sugimoto, K.1
Koh, E.2
Sin, H.S.3
-
44
-
-
84857485975
-
Divergent RNA-binding proteins, DAZL and VASA, induce meiotic progression in human germ cells derived in vitro
-
Medrano JV, Ramathal C, Nguyen HN, Simon C, Reijo Pera RA. Divergent RNA-binding proteins, DAZL and VASA, induce meiotic progression in human germ cells derived in vitro. Stem Cells 2012; 30: 441-51.
-
(2012)
Stem Cells
, vol.30
, pp. 441-451
-
-
Medrano, J.V.1
Ramathal, C.2
Nguyen, H.N.3
Simon, C.4
Reijo, P.R.A.5
-
45
-
-
2442686408
-
Genomic imprinting in disruptive spermatogenesis
-
Marques CJ, Carvalho F, Sousa M, Barros A. Genomic imprinting in disruptive spermatogenesis. Lancet 2004; 363: 1700-2.
-
(2004)
Lancet
, vol.363
, pp. 1700-1702
-
-
Marques, C.J.1
Carvalho, F.2
Sousa, M.3
Barros, A.4
-
46
-
-
40049100483
-
Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia
-
Marques CJ, Costa P, Vaz B, et al. Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia. Mol Hum Reprod 2008; 14: 67-74.
-
(2008)
Mol Hum Reprod
, vol.14
, pp. 67-74
-
-
Marques, C.J.1
Costa, P.2
Vaz, B.3
-
47
-
-
77953712614
-
Methylation defects of imprinted genes in human testicular spermatozoa
-
Marques CJ, Francisco T, Sousa S, Carvalho F, Barros A, Sousa M. Methylation defects of imprinted genes in human testicular spermatozoa. Fertil Steril 2010; 94: 585-94.
-
(2010)
Fertil Steril
, vol.94
, pp. 585-594
-
-
Marques, C.J.1
Francisco, T.2
Sousa, S.3
Carvalho, F.4
Barros, A.5
Sousa, M.6
-
48
-
-
79957968811
-
Integrative DNA methylation and gene expression analyses identify DNA packaging and epigenetic regulatory genes associated with low motility sperm
-
Pacheco SE, Houseman EA, Christensen BC, et al. Integrative DNA methylation and gene expression analyses identify DNA packaging and epigenetic regulatory genes associated with low motility sperm. PLoS One 2011; 6: e20280.
-
(2011)
PLoS One
, vol.6
-
-
Pacheco, S.E.1
Houseman, E.A.2
Christensen, B.C.3
-
49
-
-
70450252294
-
DNA methylation errors at imprinted loci after assisted conception originate in the parental sperm
-
Kobayashi H, Hiura H, John RM, et al. DNA methylation errors at imprinted loci after assisted conception originate in the parental sperm. Eur J Hum Genet 2009; 17: 1582-91.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1582-1591
-
-
Kobayashi, H.1
Hiura, H.2
John, R.M.3
-
50
-
-
77449113500
-
Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men
-
Boissonnas CC, Abdalaoui HE, Haelewyn V, et al. Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men. Eur J Hum Genet 2010; 18: 73-80.
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 73-80
-
-
Boissonnas, C.C.1
Abdalaoui, H.E.2
Haelewyn, V.3
-
51
-
-
37549033497
-
Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Con trol Region methylation and H19 gene expression in individual mouse embryos
-
Fauque P, Jouannet P, Lesaffre C, et al. Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Con trol Region methylation and H19 gene expression in individual mouse embryos. BMC Dev Biol 2007; 7: 116.
-
(2007)
BMC Dev Biol
, vol.7
, pp. 116
-
-
Fauque, P.1
Jouannet, P.2
Lesaffre, C.3
-
52
-
-
77950160019
-
In vitro fertilization and embryo culture strongly impact the placental transcriptome in the mouse model
-
Fauque P, Mondon F, Letourneur F, et al. In vitro fertilization and embryo culture strongly impact the placental transcriptome in the mouse model. PLoS One 2010; 5: e9218.
-
(2010)
PLoS One
, vol.e9218
, pp. 5
-
-
Fauque, P.1
Mondon, F.2
Letourneur, F.3
-
53
-
-
78049243483
-
Aberrant DNA methylation of imprinted H19 gene in human preimplantation embryos
-
Chen SL, Shi XY, Zheng HY, Wu FR, Luo C. Aberrant DNA methylation of imprinted H19 gene in human preimplantation embryos. Fertil Steril 2010; 94: 2356-8, 2358 e1.
-
Fertil Steril 2010; 94: 2356-8
-
-
Chen, S.L.1
Shi, X.Y.2
Zheng, H.Y.3
Wu, F.R.4
Luo, C.5
-
54
-
-
0035930660
-
Dnmt3L and the establishment of maternal genomic imprints
-
Bourc'his D, Xu GL, Lin CS, Bollman B, Bestor TH. Dnmt3L and the establishment of maternal genomic imprints. Science 2001; 294: 2536-9.
-
(2001)
Science
, vol.294
, pp. 2536-2539
-
-
Bourc'his, D.1
Xu, G.L.2
Lin, C.S.3
Bollman, B.4
Bestor, T.H.5
-
55
-
-
34548603504
-
Structure of Dnmt3a bound to Dnmt3L suggests a model for de novo DNA methylation
-
Jia D, Jurkowska RZ, Zhang X, Jeltsch A, Cheng X. Structure of Dnmt3a bound to Dnmt3L suggests a model for de novo DNA methylation. Nature 2007; 449: 248-51.
-
(2007)
Nature
, vol.449
, pp. 248-251
-
-
Jia, D.1
Jurkowska, R.Z.2
Zhang, X.3
Jeltsch, A.4
Cheng, X.5
-
56
-
-
20344385787
-
Epigenetic transgenerational actions of endocrine disruptors and male fertility
-
Anway MD, Cupp AS, Uzumcu M, Skinner MK. Epigenetic transgenerational actions of endocrine disruptors and male fertility. Science 2005; 308: 1466-9.
-
(2005)
Science
, vol.308
, pp. 1466-1469
-
-
Anway, M.D.1
Cupp, A.S.2
Uzumcu, M.3
Skinner, M.K.4
-
57
-
-
33847673965
-
Endothelial dysfunction: A link among preeclampsia, recurrent pregnancy loss, and future cardiovascular events?
-
Germain AM, Romanik MC, Guerra I, et al. Endothelial dysfunction: a link among preeclampsia, recurrent pregnancy loss, and future cardiovascular events? Hypertension 2007; 49: 90-5.
-
(2007)
Hypertension
, vol.49
, pp. 90-95
-
-
Germain, A.M.1
Romanik, M.C.2
Guerra, I.3
-
58
-
-
0346186090
-
Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS)
-
ESHRE/ASRM
-
ESHRE/ASRM. Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS). Hum Reprod 2004; 19: 41-7.
-
(2004)
Hum Reprod
, vol.19
, pp. 41-47
-
-
-
59
-
-
0036146428
-
The androgen receptor CAG repeat polymorphism and X-chromosome inactivation in Australian Caucasian women with infertility related to polycystic ovary syndrome
-
Hickey T, Chandy A, Norman RJ. The androgen receptor CAG repeat polymorphism and X-chromosome inactivation in Australian Caucasian women with infertility related to polycystic ovary syndrome. J Clin Endocrinol Metab 2002; 87: 161-5.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 161-165
-
-
Hickey, T.1
Chandy, A.2
Norman, R.J.3
-
60
-
-
77957883552
-
Androgen receptor CAG repeat polymorphism and epigenetic influence among the south Indian women with Polycystic Ovary Syndrome
-
Dasgupta S, Sirisha PV, Neelaveni K, et al. Androgen receptor CAG repeat polymorphism and epigenetic influence among the south Indian women with Polycystic Ovary Syndrome. PLoS One 2010; 5: e12401.
-
(2010)
PLoS One
, vol.5
-
-
Dasgupta, S.1
Sirisha, P.V.2
Neelaveni, K.3
-
61
-
-
0034528599
-
Epigenetic regulation of androgen receptor gene expression in human prostate cancers
-
Nakayama T, Watanabe M, Suzuki H, et al. Epigenetic regulation of androgen receptor gene expression in human prostate cancers. Lab Invest 2000; 80: 1789-96.
-
(2000)
Lab Invest
, vol.80
, pp. 1789-1796
-
-
Nakayama, T.1
Watanabe, M.2
Suzuki, H.3
-
62
-
-
77953709665
-
Epigenetics in polycystic ovary syndrome: A pilot study of global DNA methylation
-
Xu N, Azziz R, Goodarzi MO. Epigenetics in polycystic ovary syndrome: a pilot study of global DNA methylation. Fertil Steril 2010; 94: 781-3 e1.
-
(2010)
Fertil Steril
, vol.94
, pp. 781
-
-
Xu, N.1
Azziz, R.2
Goodarzi, M.O.3
-
63
-
-
77952779185
-
Demethylation of LHR in dehydroepiandrosterone-induced mouse model of polycystic ovary syndrome
-
Zhu JQ, Zhu L, Liang XW, Xing FQ, Schatten H, Sun QY. Demethylation of LHR in dehydroepiandrosterone-induced mouse model of polycystic ovary syndrome. Mol Hum Reprod 2010; 16: 260-6.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 260-266
-
-
Zhu, J.Q.1
Zhu, L.2
Liang, X.W.3
Xing, F.Q.4
Schatten, H.5
Sun, Q.Y.6
-
64
-
-
80455156236
-
Epigenetic mechanism underlying the development of polycystic ovary syndrome (PCOS)-like phenotypes in prenatally androgenized rhesus monkeys
-
Xu N, Kwon S, Abbott DH, et al. Epigenetic mechanism underlying the development of polycystic ovary syndrome (PCOS)-like phenotypes in prenatally androgenized rhesus monkeys. PLoS One 2011; 6: e27286.
-
(2011)
PLoS One
, vol.6
-
-
Xu, N.1
Kwon, S.2
Abbott, D.H.3
-
65
-
-
0344099497
-
Fertility, sex determination, and the X chromosome
-
Vaiman D. Fertility, sex determination, and the X chromosome. Cytogenet Genome Res 2002; 99: 224-8.
-
(2002)
Cytogenet Genome Res
, vol.99
, pp. 224-228
-
-
Vaiman, D.1
-
66
-
-
69749125027
-
Epigenetic analysis of the critical region I for premature ovarian failure: Demonstration of a highly heterochromatic domain on the long arm of the mammalian X chromosome
-
Rizzolio F, Pramparo T, Sala C, et al. Epigenetic analysis of the critical region I for premature ovarian failure: demonstration of a highly heterochromatic domain on the long arm of the mammalian X chromosome. J Med Genet 2009; 46: 585-92.
-
(2009)
J Med Genet
, vol.46
, pp. 585-592
-
-
Rizzolio, F.1
Pramparo, T.2
Sala, C.3
-
67
-
-
78649244092
-
Androgen receptor epigenetic variations influence early follicular phase gonadotropin levels
-
Laisk T, Haller-Kikkatalo K, Laanpere M, et al. Androgen receptor epigenetic variations influence early follicular phase gonadotropin levels. Acta Obstet Gynecol Scand 2010; 89: 1557-63.
-
(2010)
Acta Obstet Gynecol Scand
, vol.89
, pp. 1557-1563
-
-
Laisk, T.1
Haller-Kikkatalo, K.2
Laanpere, M.3
-
68
-
-
34247855875
-
Skewed Xchromosome inactivation is associated with primary but not secondary ovarian failure
-
Bretherick KL, Metzger DL, Chanoine JP, et al. Skewed Xchromosome inactivation is associated with primary but not secondary ovarian failure. Am J Med Genet A 2007; 143A: 945-51.
-
(2007)
Am J Med Genet A
, vol.143 A
, pp. 945-951
-
-
Bretherick, K.L.1
Metzger, D.L.2
Chanoine, J.P.3
-
69
-
-
56049095961
-
Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure
-
Mansouri MR, Schuster J, Badhai J, et al. Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure. Hum Mol Genet 2008; 17: 3776-83.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3776-3783
-
-
Mansouri, M.R.1
Schuster, J.2
Badhai, J.3
-
70
-
-
0000929470
-
Peritoneal endometriosis due to menstrual dissemination of endometrial tissue into the peritoneal cavity
-
Sampson J. Peritoneal endometriosis due to menstrual dissemination of endometrial tissue into the peritoneal cavity. Am J Obstet Gynecol 1927; 14: 422-469.
-
(1927)
Am J Obstet Gynecol
, vol.14
, pp. 422-469
-
-
Sampson, J.1
-
71
-
-
79959768605
-
The steroidogenic factor-1 protein is not expressed in various forms of endometriosis but is strongly present in ovarian cortical or medullary mesenchymatous cells adjacent to endometriotic foci
-
in press
-
Noel JC, Anaf V, Borghese B, Vaiman D, Fayt I, Chapron C. The steroidogenic factor-1 protein is not expressed in various forms of endometriosis but is strongly present in ovarian cortical or medullary mesenchymatous cells adjacent to endometriotic foci. Fertil Steril 2011: in press.
-
(2011)
Fertil Steril
-
-
Noel, J.C.1
Anaf, V.2
Borghese, B.3
Vaiman, D.4
Fayt, I.5
Chapron, C.6
-
72
-
-
77956115251
-
Endometriosis and infertility: Pathophysiology and management
-
de Ziegler D, Borghese B, Chapron C. Endometriosis and infertility: pathophysiology and management. Lancet 2010; 376: 730-8.
-
(2010)
Lancet
, vol.376
, pp. 730-738
-
-
de Ziegler, D.1
Borghese, B.2
Chapron, C.3
-
73
-
-
84863588059
-
Combined mRNA microarray and proteomic analysis of eutopic endometrium of women with and without endometriosis
-
Fassbender A, Verbeeck N, Bornigen D, et al. Combined mRNA microarray and proteomic analysis of eutopic endometrium of women with and without endometriosis. Hum Reprod 2012; 27: 2020-9.
-
(2012)
Hum Reprod
, vol.27
, pp. 2020-2029
-
-
Fassbender, A.1
Verbeeck, N.2
Bornigen, D.3
-
74
-
-
84859905212
-
Nuclear receptor, coregulator signaling, and chromatin remodeling pathways suggest involvement of the epigenome in the steroid hormone response of endometrium and abnormalities in endometriosis
-
Zelenko Z, Aghajanova L, Irwin JC, Giudice LC. Nuclear receptor, coregulator signaling, and chromatin remodeling pathways suggest involvement of the epigenome in the steroid hormone response of endometrium and abnormalities in endometriosis. Reprod Sci 2012; 19: 152-62.
-
(2012)
Reprod Sci
, vol.19
, pp. 152-162
-
-
Zelenko, Z.1
Aghajanova, L.2
Irwin, J.C.3
Giudice, L.C.4
-
75
-
-
58149479755
-
Experimental murine endometriosis induces DNA methylation and altered gene expression in eutopic endometrium
-
Lee B, Du H, Taylor HS. Experimental murine endometriosis induces DNA methylation and altered gene expression in eutopic endometrium. Biol Reprod 2009; 80: 79-85.
-
(2009)
Biol Reprod
, vol.80
, pp. 79-85
-
-
Lee, B.1
Du, H.2
Taylor, H.S.3
-
76
-
-
23844520882
-
Aberrant methylation at HOXA10 may be responsible for its aberrant expression in the endometrium of patients with endometriosis
-
Wu Y, Halverson G, Basir Z, Strawn E, Yan P, Guo SW. Aberrant methylation at HOXA10 may be responsible for its aberrant expression in the endometrium of patients with endometriosis. Am J Obstet Gynecol 2005; 193: 371-80.
-
(2005)
Am J Obstet Gynecol
, vol.193
, pp. 371-380
-
-
Wu, Y.1
Halverson, G.2
Basir, Z.3
Strawn, E.4
Yan, P.5
Guo, S.W.6
-
77
-
-
78649887722
-
Reduced expression of HOXA10 in the midluteal endometrium from infertile women with minimal endometriosis
-
Szczepanska M, Wirstlein P, Luczak M, Jagodzinski PP, Skrzypczak J. Reduced expression of HOXA10 in the midluteal endometrium from infertile women with minimal endometriosis. Biomed Pharmacother 2010; 64: 697-705.
-
(2010)
Biomed Pharmacother
, vol.64
, pp. 697-705
-
-
Szczepanska, M.1
Wirstlein, P.2
Luczak, M.3
Jagodzinski, P.P.4
Skrzypczak, J.5
-
78
-
-
55049090208
-
Gene expression profile for ectopic versus eutopic endometrium provides new insights into endometriosis oncogenic potential
-
Borghese B, Mondon F, Noel JC, et al. Gene expression profile for ectopic versus eutopic endometrium provides new insights into endometriosis oncogenic potential. Mol Endocrinol 2008; 22: 2557-62.
-
(2008)
Mol Endocrinol
, vol.22
, pp. 2557-2562
-
-
Borghese, B.1
Mondon, F.2
Noel, J.C.3
-
79
-
-
84871451979
-
DNA hypomethylation of the COX-2 gene promoter is associated with up-regulation of its mRNA expression in eutopic endometrium of endometriosis
-
Wang D, Chen Q, Zhang C, Ren F, Li T. DNA hypomethylation of the COX-2 gene promoter is associated with up-regulation of its mRNA expression in eutopic endometrium of endometriosis. Eur J Med Res 2012; 17: 12.
-
(2012)
Eur J Med Res
, vol.17
, pp. 12
-
-
Wang, D.1
Chen, Q.2
Zhang, C.3
Ren, F.4
Li, T.5
-
80
-
-
84856750827
-
Expression of HOXA11 in the mid-luteal endometrium from women with endometriosis-associated infertility
-
Szczepanska M, Wirstlein P, Skrzypczak J, Jagodzinski PP. Expression of HOXA11 in the mid-luteal endometrium from women with endometriosis-associated infertility. Reprod Biol Endocrinol 2012; 10: 1.
-
(2012)
Reprod Biol Endocrinol
, vol.10
, pp. 1
-
-
Szczepanska, M.1
Wirstlein, P.2
Skrzypczak, J.3
Jagodzinski, P.P.4
-
81
-
-
84858724823
-
Paired-box gene 2 is down-regulated in endometriosis and correlates with low epidermal growth factor receptor expression
-
de Graaff AA, Delvoux B, Van de Vijver KK, Kyama CM, D'Hooghe TM, Dunselman GA, Romano A. Paired-box gene 2 is down-regulated in endometriosis and correlates with low epidermal growth factor receptor expression. Hum Reprod 2012; 27: 1676-84.
-
(2012)
Hum Reprod
, vol.27
, pp. 1676-1684
-
-
de Graaff, A.A.1
Delvoux, B.2
Van de Vijver, K.K.3
Kyama, C.M.4
D'hooghe, T.M.5
Dunselman, G.A.6
Romano, A.7
-
82
-
-
77957976878
-
Promoter hypermethylation of progesterone receptor isoform B (PR-B) in adenomyosis and its rectification by a histone deacetylase inhibitor and a demethylation agent
-
Jichan N, Xishi L, Guo SW. Promoter hypermethylation of progesterone receptor isoform B (PR-B) in adenomyosis and its rectification by a histone deacetylase inhibitor and a demethylation agent. Reprod Sci 2010; 17: 995-1005.
-
(2010)
Reprod Sci
, vol.17
, pp. 995-1005
-
-
Jichan, N.1
Xishi, L.2
Guo, S.W.3
-
83
-
-
34848857939
-
Promoter methylation regulates estrogen receptor 2 in human endometrium and endometriosis
-
Xue Q, Lin Z, Cheng YH, et al. Promoter methylation regulates estrogen receptor 2 in human endometrium and endometriosis. Biol Reprod 2007; 77: 681-7.
-
(2007)
Biol Reprod
, vol.77
, pp. 681-687
-
-
Xue, Q.1
Lin, Z.2
Cheng, Y.H.3
-
84
-
-
80054979013
-
Hypermethylation of the CpG island spanning from exon II to intron III is associated with steroidogenic factor 1 expression in stromal cells of endometriosis
-
Xue Q, Zhou YF, Zhu SN, Bulun SE. Hypermethylation of the CpG island spanning from exon II to intron III is associated with steroidogenic factor 1 expression in stromal cells of endometriosis. Reprod Sci 2011; 18: 1080-4.
-
(2011)
Reprod Sci
, vol.18
, pp. 1080-1084
-
-
Xue, Q.1
Zhou, Y.F.2
Zhu, S.N.3
Bulun, S.E.4
-
85
-
-
78650415868
-
Demethylation of a nonpromoter cytosine-phosphate-guanine island in the aromatase gene may cause the aberrant up-regulation in endometriotic tissues
-
Izawa M, Taniguchi F, Uegaki T, et al. Demethylation of a nonpromoter cytosine-phosphate-guanine island in the aromatase gene may cause the aberrant up-regulation in endometriotic tissues. Fertil Steril 2010; 95: 33-9.
-
(2010)
Fertil Steril
, vol.95
, pp. 33-39
-
-
Izawa, M.1
Taniguchi, F.2
Uegaki, T.3
-
86
-
-
33751112809
-
Promoter hypermethylation of progesterone receptor isoform B (PR-B) in endometriosis
-
Wu Y, Strawn E, Basir Z, Halverson G, Guo SW. Promoter hypermethylation of progesterone receptor isoform B (PR-B) in endometriosis. Epigenetics 2006; 1: 106-11.
-
(2006)
Epigenetics
, vol.1
, pp. 106-111
-
-
Wu, Y.1
Strawn, E.2
Basir, Z.3
Halverson, G.4
Guo, S.W.5
-
87
-
-
84860790124
-
Epigenetic inactivation of hMLH1 in the malignant transformation of ovarian endometriosis
-
Ren F, Wang D, Jiang Y. Epigenetic inactivation of hMLH1 in the malignant transformation of ovarian endometriosis. Arch Gynecol Obstet 2012; 285: 215-21.
-
(2012)
Arch Gynecol Obstet
, vol.285
, pp. 215-221
-
-
Ren, F.1
Wang, D.2
Jiang, Y.3
-
88
-
-
0036888656
-
Possible involvement of hMLH1 p16(INK4a) and PTEN in the malignant transformation of endometriosis
-
Martini M, Ciccarone M, Garganese G, et al. Possible involvement of hMLH1 p16(INK4a) and PTEN in the malignant transformation of endometriosis. Int J Cancer 2002; 102: 398-406.
-
(2002)
Int J Cancer
, vol.102
, pp. 398-406
-
-
Martini, M.1
Ciccarone, M.2
Garganese, G.3
-
89
-
-
0343362705
-
The number of nephrons in the mammalian kidney: Environmental influences play a determining role
-
Lelievre-Pegorier M, Merlet-Benichou C. The number of nephrons in the mammalian kidney: environmental influences play a determining role. Exp Nephrol 2000; 8: 63-5.
-
(2000)
Exp Nephrol
, vol.8
, pp. 63-65
-
-
Lelievre-Pegorier, M.1
Merlet-Benichou, C.2
-
90
-
-
34547784612
-
Transcriptional activation of steroidogenic factor-1 by hypomethylation of the 5' CpG island in endometriosis
-
Xue Q, Lin Z, Yin P, et al. Transcriptional activation of steroidogenic factor-1 by hypomethylation of the 5' CpG island in endometriosis. J Clin Endocrinol Metab 2007; 92: 3261-7.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 3261-3267
-
-
Xue, Q.1
Lin, Z.2
Yin, P.3
-
91
-
-
77951741621
-
Steroidogenic factor-1 expression in ovarian endometriosis
-
Noel JC, Borghese B, Vaiman D, Fayt I, Anaf V, Chapron C. Steroidogenic factor-1 expression in ovarian endometriosis. Appl Immunohistochem Mol Morphol 2010; 18: 258-61.
-
(2010)
Appl Immunohistochem Mol Morphol
, vol.18
, pp. 258-261
-
-
Noel, J.C.1
Borghese, B.2
Vaiman, D.3
Fayt, I.4
Anaf, V.5
Chapron, C.6
-
92
-
-
58349090850
-
Endometriosis
-
Bulun SE. Endometriosis. N Engl J Med 2009; 360: 268-79.
-
(2009)
N Engl J Med
, vol.360
, pp. 268-279
-
-
Bulun, S.E.1
-
93
-
-
45849085801
-
Prolonged stimulation with tumor necrosis factor-alpha induced partial methylation at PR-B promoter in immortalized epithelial-like endometriotic cells
-
Wu Y, Starzinski-Powitz A, Guo SW. Prolonged stimulation with tumor necrosis factor-alpha induced partial methylation at PR-B promoter in immortalized epithelial-like endometriotic cells. Fertil Steril 2008; 90: 234-7.
-
(2008)
Fertil Steril
, vol.90
, pp. 234-237
-
-
Wu, Y.1
Starzinski-Powitz, A.2
Guo, S.W.3
-
94
-
-
81255147796
-
Oncogenic events associated with endometrial and ovarian cancers are rare in endometriosis
-
Vestergaard AL, Thorup K, Knudsen UB, et al. Oncogenic events associated with endometrial and ovarian cancers are rare in endometriosis. Mol Hum Reprod 2011; 17: 758-61.
-
(2011)
Mol Hum Reprod
, vol.17
, pp. 758-761
-
-
Vestergaard, A.L.1
Thorup, K.2
Knudsen, U.B.3
-
95
-
-
77956109563
-
Research resource: Genome- wide profiling of methylated promoters in endometriosis re veals a subtelomeric location of hypermethylation
-
Borghese B, Barbaux S, Mondon F, et al. Research resource: genome- wide profiling of methylated promoters in endometriosis re veals a subtelomeric location of hypermethylation. Mol Endocrinol 2010; 24: 1872-85.
-
(2010)
Mol Endocrinol
, vol.24
, pp. 1872-1885
-
-
Borghese, B.1
Barbaux, S.2
Mondon, F.3
-
96
-
-
65449186589
-
A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation
-
El-Maarri O, Kareta MS, Mikeska T, et al. A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation. Hum Mol Genet 2009; 18: 1755-68.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1755-1768
-
-
El-Maarri, O.1
Kareta, M.S.2
Mikeska, T.3
-
97
-
-
84860247326
-
Genetic polymorphisms of DNMT3L involved in hypermethylation of chromosomal ends are associated with greater risk of developing ovarian endometriosis
-
Borghese B, Santulli P, Hequet D, et al. Genetic polymorphisms of DNMT3L involved in hypermethylation of chromosomal ends are associated with greater risk of developing ovarian endometriosis. Am J Pathol 2012; 180: 1781-6.
-
(2012)
Am J Pathol
, vol.180
, pp. 1781-1786
-
-
Borghese, B.1
Santulli, P.2
Hequet, D.3
-
98
-
-
33845762310
-
Aberrant expression of deoxyribonucleic acid methyltransferases DNMT1, DNMT3A, and DNMT3B in women with endometriosis
-
Wu Y, Strawn E, Basir Z, Halverson G, Guo SW. Aberrant expression of deoxyribonucleic acid methyltransferases DNMT1, DNMT3A, and DNMT3B in women with endometriosis. Fertil Steril 2007; 87: 24-32.
-
(2007)
Fertil Steril
, vol.87
, pp. 24-32
-
-
Wu, Y.1
Strawn, E.2
Basir, Z.3
Halverson, G.4
Guo, S.W.5
-
99
-
-
0033230419
-
Fertilizing ability of DNA-damaged spermatozoa
-
Ahmadi A, Ng SC. Fertilizing ability of DNA-damaged spermatozoa. J Exp Zool 1999; 284: 696-704.
-
(1999)
J Exp Zool
, vol.284
, pp. 696-704
-
-
Ahmadi, A.1
Ng, S.C.2
-
100
-
-
77954968463
-
Assisted reproductive technology in Europe, 2006: Results generated from European registers by ESHRE
-
de Mouzon J, Goossens V, Bhattacharya S, et al. Assisted reproductive technology in Europe, 2006: results generated from European registers by ESHRE. Hum Reprod 2010; 25: 1851-62.
-
(2010)
Hum Reprod
, vol.25
, pp. 1851-1862
-
-
de Mouzon, J.1
Goossens, V.2
Bhattacharya, S.3
-
101
-
-
72849113308
-
Increased risk of blastogenesis birth defects, arising in the first 4 weeks of pregnancy, after assisted reproductive technologies
-
Halliday JL, Ukoumunne OC, Baker HW, et al. Increased risk of blastogenesis birth defects, arising in the first 4 weeks of pregnancy, after assisted reproductive technologies. Hum Reprod 2010; 25: 59-65.
-
(2010)
Hum Reprod
, vol.25
, pp. 59-65
-
-
Halliday, J.L.1
Ukoumunne, O.C.2
Baker, H.W.3
-
102
-
-
70349573301
-
DNA methylation and gene expression differences in children conceived in vitro or in vivo
-
Katari S, Turan N, Bibikova M, et al. DNA methylation and gene expression differences in children conceived in vitro or in vivo. Hum Mol Genet 2009; 18: 3769-78.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3769-3778
-
-
Katari, S.1
Turan, N.2
Bibikova, M.3
-
103
-
-
84858405593
-
Assisted reproductive technology in Europe, 2007: Results generated from European registers by ESHRE
-
de Mouzon J, Goossens V, Bhattacharya S, et al. Assisted reproductive technology in Europe, 2007: results generated from European registers by ESHRE. Hum Reprod 2012; 27: 954-66.
-
(2012)
Hum Reprod
, vol.27
, pp. 954-966
-
-
de Mouzon, J.1
Goossens, V.2
Bhattacharya, S.3
-
105
-
-
77649289429
-
Dual effects of superovulation: Loss of maternal and paternal imprinted methylation in a dose-dependent manner
-
Market-Velker BA, Zhang L, Magri LS, Bonvissuto AC, Mann MR. Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner. Hum Mol Genet 2010; 19: 36-51.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 36-51
-
-
Market-Velker, B.A.1
Zhang, L.2
Magri, L.S.3
Bonvissuto, A.C.4
Mann, M.R.5
-
106
-
-
0034112603
-
Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo
-
Doherty AS, Mann MR, Tremblay KD, Bartolomei MS, Schultz RM. Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo. Biol Reprod 2000; 62: 1526-35.
-
(2000)
Biol Reprod
, vol.62
, pp. 1526-1535
-
-
Doherty, A.S.1
Mann, M.R.2
Tremblay, K.D.3
Bartolomei, M.S.4
Schultz, R.M.5
-
107
-
-
77952516401
-
Modulation of imprinted gene network in placenta results in normal development of in vitro manipulated mouse embryos
-
Fauque P, Ripoche MA, Tost J, et al. Modulation of imprinted gene network in placenta results in normal development of in vitro manipulated mouse embryos. Hum Mol Genet 2010; 19: 1779-90.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 1779-1790
-
-
Fauque, P.1
Ripoche, M.A.2
Tost, J.3
-
108
-
-
33845630826
-
methylation of imprinted loci in superovulated oocytes
-
Sato A, Otsu E, Negishi H, Utsunomiya T, Arima T. Aberrant DNA methylation of imprinted loci in superovulated oocytes. Hum Reprod 2007; 22: 26-35.
-
(2007)
Hum Reprod
, vol.22
, pp. 26-35
-
-
Sato, A.1
Otsu, E.2
Negishi, H.3
Utsunomiya, T.4
Arima, T.5
Aberrant, D.N.A.6
-
109
-
-
0842265436
-
Perinatal outcome of singletons and twins after assisted conception: A systematic review of controlled studies
-
Helmerhorst FM, Perquin DA, Donker D, Keirse MJ. Perinatal outcome of singletons and twins after assisted conception: a systematic review of controlled studies. BMJ 2004; 328: 261.
-
(2004)
BMJ
, vol.328
, pp. 261
-
-
Helmerhorst, F.M.1
Perquin, D.A.2
Donker, D.3
Keirse, M.J.4
-
110
-
-
1842458446
-
Perinatal outcomes in singletons following in vitro fertilization: A meta-analysis
-
Jackson RA, Gibson KA, Wu YW, Croughan MS. Perinatal outcomes in singletons following in vitro fertilization: a meta-analysis. Obstet Gynecol 2004; 103: 551-63.
-
(2004)
Obstet Gynecol
, vol.103
, pp. 551-563
-
-
Jackson, R.A.1
Gibson, K.A.2
Wu, Y.W.3
Croughan, M.S.4
-
111
-
-
27444439562
-
Assisted reproductive technology and pregnancy outcome
-
Shevell T, Malone FD, Vidaver J, et al. Assisted reproductive technology and pregnancy outcome. Obstet Gynecol 2005; 106: 1039-45.
-
(2005)
Obstet Gynecol
, vol.106
, pp. 1039-1045
-
-
Shevell, T.1
Malone, F.D.2
Vidaver, J.3
-
112
-
-
60749100951
-
In vitro fertilization is associated with an increased risk for preeclampsia
-
Chen XK, Wen SW, Bottomley J, Smith GN, Leader A, Walker MC. In vitro fertilization is associated with an increased risk for preeclampsia. Hypertens Pregnancy 2009; 28: 1-12.
-
(2009)
Hypertens Pregnancy
, vol.28
, pp. 1-12
-
-
Chen, X.K.1
Wen, S.W.2
Bottomley, J.3
Smith, G.N.4
Leader, A.5
Walker, M.C.6
-
113
-
-
50149106551
-
Effects of technology or maternal factors on perinatal outcome after assisted fertilisation: A population-based cohort study
-
Romundstad LB, Romundstad PR, Sunde A, et al. Effects of technology or maternal factors on perinatal outcome after assisted fertilisation: a population-based cohort study. Lancet 2008; 372: 737-43.
-
(2008)
Lancet
, vol.372
, pp. 737-743
-
-
Romundstad, L.B.1
Romundstad, P.R.2
Sunde, A.3
-
114
-
-
84874114810
-
Assisted reproductive technology and pregnancy-related hypertensive complications: A systematic review
-
Thomopoulos C, Tsioufis C, Michalopoulou H, Makris T, Papademetriou V, Stefanadis C. Assisted reproductive technology and pregnancy-related hypertensive complications: a systematic review. J Hum Hypertens 2013; 27(3): 148-57.
-
(2013)
J Hum Hypertens
, vol.27
, Issue.3
, pp. 148-157
-
-
Thomopoulos, C.1
Tsioufis, C.2
Michalopoulou, H.3
Makris, T.4
Papademetriou, V.5
Stefanadis, C.6
-
115
-
-
0037222510
-
Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19
-
DeBaun MR, Niemitz EL, Feinberg AP. Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. Am J Hum Genet 2003; 72: 156-60.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 156-160
-
-
Debaun, M.R.1
Niemitz, E.L.2
Feinberg, A.P.3
-
116
-
-
0346777377
-
Epigenetic risks related to assisted reproductive technologies: Epigenetics, imprinting, ART and icebergs?
-
Maher ER, Afnan M, Barratt CL. Epigenetic risks related to assisted reproductive technologies: epigenetics, imprinting, ART and icebergs? Hum Reprod 2003; 18: 2508-11.
-
(2003)
Hum Reprod
, vol.18
, pp. 2508-2511
-
-
Maher, E.R.1
Afnan, M.2
Barratt, C.L.3
-
117
-
-
0038644577
-
In vitro fertilization may increase the risk of Beckwith- Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene
-
Gicquel C, Gaston V, Mandelbaum J, Siffroi JP, Flahault A, Le Bouc Y. In vitro fertilization may increase the risk of Beckwith- Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene. Am J Hum Genet 2003; 72: 1338-41.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1338-1341
-
-
Gicquel, C.1
Gaston, V.2
Mandelbaum, J.3
Siffroi, J.P.4
Flahault, A.5
Le Bouc, Y.6
-
118
-
-
0036304235
-
Intracytoplasmic sperm injection may increase the risk of imprinting defects
-
Cox GF, Burger J, Lip V, et al. Intracytoplasmic sperm injection may increase the risk of imprinting defects. Am J Hum Genet 2002; 71: 162-4.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 162-164
-
-
Cox, G.F.1
Burger, J.2
Lip, V.3
-
119
-
-
0037221929
-
Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection
-
Orstavik KH, Eiklid K, van der Hagen CB, et al. Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection. Am J Hum Genet 2003; 72: 218-9.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 218-219
-
-
Orstavik, K.H.1
Eiklid, K.2
van der Hagen, C.B.3
-
120
-
-
17144413341
-
Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples
-
Ludwig M, Katalinic A, Gross S, Sutcliffe A, Varon R, Horsthemke B. Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples. J Med Genet 2005; 42: 289-91.
-
(2005)
J Med Genet
, vol.42
, pp. 289-291
-
-
Ludwig, M.1
Katalinic, A.2
Gross, S.3
Sutcliffe, A.4
Varon, R.5
Horsthemke, B.6
-
121
-
-
33645312361
-
Assisted reproductive therapies and imprinting disorders--a preliminary British survey
-
Sutcliffe AG, Peters CJ, Bowdin S, et al. Assisted reproductive therapies and imprinting disorders--a preliminary British survey. Hum Reprod 2006; 21: 1009-11.
-
(2006)
Hum Reprod
, vol.21
, pp. 1009-1011
-
-
Sutcliffe, A.G.1
Peters, C.J.2
Bowdin, S.3
-
122
-
-
33645463808
-
Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype
-
Bliek J, Terhal P, van den Bogaard MJ, et al. Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype. Am J Hum Genet 2006; 78: 604-14.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 604-614
-
-
Bliek, J.1
Terhal, P.2
van den Bogaard, M.J.3
-
123
-
-
34247395327
-
Silver- Russell syndrome in a girl born after in vitro fertilization: Partial hypermethylation at the differentially methylated region of PEG1/MEST
-
Kagami M, Nagai T, Fukami M, Yamazawa K, Ogata T. Silver- Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST. J Assist Reprod Genet 2007; 24: 131-6.
-
(2007)
J Assist Reprod Genet
, vol.24
, pp. 131-136
-
-
Kagami, M.1
Nagai, T.2
Fukami, M.3
Yamazawa, K.4
Ogata, T.5
-
124
-
-
0037464771
-
Incidence of retinoblastoma in children born after in-vitro fertilisation
-
Moll AC, Imhof SM, Cruysberg JR, et al. Incidence of retinoblastoma in children born after in-vitro fertilisation. Lancet 2003; 361: 309-10.
-
(2003)
Lancet
, vol.361
, pp. 309-310
-
-
Moll, A.C.1
Imhof, S.M.2
Cruysberg, J.R.3
-
125
-
-
84858427863
-
Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: A cross-sectional study
-
Puumala SE, Nelson HH, Ross JA, Nguyen RH, Damario MA, Spector LG. Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: a cross-sectional study. BMC Pediatr 2012; 12: 33.
-
(2012)
BMC Pediatr
, vol.12
, pp. 33
-
-
Puumala, S.E.1
Nelson, H.H.2
Ross, J.A.3
Nguyen, R.H.4
Damario, M.A.5
Spector, L.G.6
-
126
-
-
20444409135
-
Latest advances in understanding preeclampsia
-
Redman CW, Sargent IL. Latest advances in understanding preeclampsia. Science 2005; 308: 1592-4.
-
(2005)
Science
, vol.308
, pp. 1592-1594
-
-
Redman, C.W.1
Sargent, I.L.2
-
127
-
-
27944467137
-
Excess syncytiotrophoblast microparticle shedding is a feature of early-onset preeclampsia, but not normotensive intrauterine growth restriction
-
Goswami D, Tannetta DS, Magee LA, et al. Excess syncytiotrophoblast microparticle shedding is a feature of early-onset preeclampsia, but not normotensive intrauterine growth restriction. Placenta 2006; 27: 56-61.
-
(2006)
Placenta
, vol.27
, pp. 56-61
-
-
Goswami, D.1
Tannetta, D.S.2
Magee, L.A.3
-
128
-
-
52449124640
-
Changes in microparticle numbers and cellular origin during pregnancy and preeclampsia
-
Lok CA, Van Der Post JA, Sargent IL, et al. Changes in microparticle numbers and cellular origin during pregnancy and preeclampsia. Hypertens Pregnancy 2008; 27: 344-60.
-
(2008)
Hypertens Pregnancy
, vol.27
, pp. 344-360
-
-
Lok, C.A.1
van der Post, J.A.2
Sargent, I.L.3
-
129
-
-
34247099770
-
Microarray analysis of differentially expressed fetal genes in placental tissue derived from early and late onset severe pre-eclampsia
-
Nishizawa H, Pryor-Koishi K, Kato T, Kowa H, Kurahashi H, Udagawa Y. Microarray analysis of differentially expressed fetal genes in placental tissue derived from early and late onset severe pre-eclampsia. Placenta 2007; 28: 487-97.
-
(2007)
Placenta
, vol.28
, pp. 487-497
-
-
Nishizawa, H.1
Pryor-Koishi, K.2
Kato, T.3
Kowa, H.4
Kurahashi, H.5
Udagawa, Y.6
-
130
-
-
40549121961
-
Whole-genome microarray and targeted analysis of angiogenesis-regulating gene expression (ENG, FLT1, VEGF, PlGF) in placentas from pre-eclamptic and smallfor- gestational-age pregnancies
-
Toft JH, Lian IA, Tarca AL, et al. Whole-genome microarray and targeted analysis of angiogenesis-regulating gene expression (ENG, FLT1, VEGF, PlGF) in placentas from pre-eclamptic and smallfor- gestational-age pregnancies. J Matern Fetal Neonatal Med 2008; 21: 267-73.
-
(2008)
J Matern Fetal Neonatal Med
, vol.21
, pp. 267-273
-
-
Toft, J.H.1
Lian, I.A.2
Tarca, A.L.3
-
131
-
-
79151481145
-
Microarray profiling reveals that placental transcriptomes of early-onset HELLP syndrome and preeclampsia are similar
-
Varkonyi T, Nagy B, Fule T, et al. Microarray profiling reveals that placental transcriptomes of early-onset HELLP syndrome and preeclampsia are similar. Placenta 2011; 32 Suppl: S21-9.
-
(2011)
Placenta
, Issue.32 SUPPL.
-
-
Varkonyi, T.1
Nagy, B.2
Fule, T.3
-
132
-
-
84862506779
-
Differential gene expression analysis of placentas with increased vascular resistance and pre-eclampsia using whole-genome microarrays
-
Centlow M, Wingren C, Borrebaeck C, Brownstein MJ, Hansson SR. Differential gene expression analysis of placentas with increased vascular resistance and pre-eclampsia using whole-genome microarrays. J Pregnancy 2011; 2011: 472354.
-
J Pregnancy
, vol.2011
, pp. 2011
-
-
Centlow, M.1
Wingren, C.2
Borrebaeck, C.3
Brownstein, M.J.4
Hansson, S.R.5
-
133
-
-
79951510445
-
Transcriptional profiling of human placentas from pregnancies complicated by preeclampsia reveals disregulation of sialic acid acetylesterase and immune signalling pathways
-
Tsai S, Hardison NE, James AH, et al. Transcriptional profiling of human placentas from pregnancies complicated by preeclampsia reveals disregulation of sialic acid acetylesterase and immune signalling pathways. Placenta 2011; 32: 175-82.
-
(2011)
Placenta
, vol.32
, pp. 175-182
-
-
Tsai, S.1
Hardison, N.E.2
James, A.H.3
-
134
-
-
78650684089
-
A transcriptional profile of the decidua in preeclampsia
-
Loset M, Mundal SB, Johnson MP, et al. A transcriptional profile of the decidua in preeclampsia. Am J Obstet Gynecol 2011; 204: 84 e1-27.
-
(2011)
Am J Obstet Gynecol
, vol.204
, Issue.84
-
-
Loset, M.1
Mundal, S.B.2
Johnson, M.P.3
-
135
-
-
39149127564
-
Genetic and epigenetic factors contribute to the onset of preeclampsia
-
Chelbi ST, Vaiman D. Genetic and epigenetic factors contribute to the onset of preeclampsia. Mol Cell Endocrinol 2008; 282: 120-129.
-
(2008)
Mol Cell Endocrinol
, vol.282
, pp. 120-129
-
-
Chelbi, S.T.1
Vaiman, D.2
-
136
-
-
84861464009
-
Screening for differential methylation status in human placenta in preeclampsia using a CpG island plus promoter microarray
-
Jia RZ, Zhang X, Hu P, et al. Screening for differential methylation status in human placenta in preeclampsia using a CpG island plus promoter microarray. Int J Mol Med 2012; 30: 133-41.
-
(2012)
Int J Mol Med
, vol.30
, pp. 133-141
-
-
Jia, R.Z.1
Zhang, X.2
Hu, P.3
-
137
-
-
77955980639
-
DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia
-
Yuen RK, Penaherrera MS, von Dadelszen P, McFadden DE, Robinson WP. DNA methylation profiling of human placentas reveals promoter hypomethylation of multiple genes in early-onset preeclampsia. Eur J Hum Genet 2010; 18: 1006-12.
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 1006-1012
-
-
Yuen, R.K.1
Penaherrera, M.S.2
von Dadelszen, P.3
McFadden, D.E.4
Robinson, W.P.5
-
138
-
-
37349014758
-
Quantitative aberrations of hypermethylated RASSF1A gene sequences in maternal plasma in pre-eclampsia
-
Tsui DW, Chan KC, Chim SS, et al. Quantitative aberrations of hypermethylated RASSF1A gene sequences in maternal plasma in pre-eclampsia. Prenat Diagn 2007; 27: 1212-8.
-
(2007)
Prenat Diagn
, vol.27
, pp. 1212-1218
-
-
Tsui, D.W.1
Chan, K.C.2
Chim, S.S.3
-
139
-
-
77953849706
-
MALDI-TOF mass array analysis of RASSF1A and SERPINB5 methylation patterns in human placenta and plasma
-
Bellido ML, Radpour R, Lapaire O, et al. MALDI-TOF mass array analysis of RASSF1A and SERPINB5 methylation patterns in human placenta and plasma. Biol Reprod 2010; 82: 745-50.
-
(2010)
Biol Reprod
, vol.82
, pp. 745-750
-
-
Bellido, M.L.1
Radpour, R.2
Lapaire, O.3
-
140
-
-
33847635589
-
Expressional and epigenetic alterations of placental serine protease inhibitors: SERPINA3 is a potential marker of preeclampsia
-
Chelbi ST, Mondon F, Jammes H, et al. Expressional and epigenetic alterations of placental serine protease inhibitors: SERPINA3 is a potential marker of preeclampsia. Hypertension 2007; 49: 76-83.
-
(2007)
Hypertension
, vol.49
, pp. 76-83
-
-
Chelbi, S.T.1
Mondon, F.2
Jammes, H.3
-
141
-
-
75449113017
-
Expressional and epigenetic alterations of placental matrix metalloproteinase 9 in preeclampsia
-
Wang Z, Lu S, Liu C, Zhao B, Pei K, Tian L, Ma X. Expressional and epigenetic alterations of placental matrix metalloproteinase 9 in preeclampsia. Gynecol Endocrinol 2010; 26: 96-102.
-
(2010)
Gynecol Endocrinol
, vol.26
, pp. 96-102
-
-
Wang, Z.1
Lu, S.2
Liu, C.3
Zhao, B.4
Pei, K.5
Tian, L.6
Ma, X.7
-
142
-
-
75049083513
-
Cullins in human intra-uterine growth restriction: Expressional and epigenetic alterations
-
Gascoin-Lachambre G, Buffat C, Rebourcet R, et al. Cullins in human intra-uterine growth restriction: expressional and epigenetic alterations. Placenta 2010; 31: 151-7.
-
(2010)
Placenta
, vol.31
, pp. 151-157
-
-
Gascoin-Lachambre, G.1
Buffat, C.2
Rebourcet, R.3
-
143
-
-
84859138763
-
Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases
-
Chelbi ST, Wilson ML, Veillard AC, et al. Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases. Hum Mol Genet 2012; 21: 1968-78.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 1968-1978
-
-
Chelbi, S.T.1
Wilson, M.L.2
Veillard, A.C.3
-
144
-
-
79951472544
-
Combination of promoter hypomethylation and PDX1 overexpression leads to TBX15 decrease in vascular IUGR placentas
-
Chelbi ST, Doridot L, Mondon F, et al. Combination of promoter hypomethylation and PDX1 overexpression leads to TBX15 decrease in vascular IUGR placentas. Epigenetics 2011; 6: 247-55.
-
(2011)
Epigenetics
, vol.6
, pp. 247-255
-
-
Chelbi, S.T.1
Doridot, L.2
Mondon, F.3
-
145
-
-
79551633322
-
Global DNA methylation patterns in placenta and its association with maternal hypertension in pre-eclampsia
-
Kulkarni A, Chavan-Gautam P, Mehendale S, Yadav H, Joshi S. Global DNA methylation patterns in placenta and its association with maternal hypertension in pre-eclampsia. DNA Cell Biol 2011; 30: 79-84.
-
(2011)
DNA Cell Biol
, vol.30
, pp. 79-84
-
-
Kulkarni, A.1
Chavan-Gautam, P.2
Mehendale, S.3
Yadav, H.4
Joshi, S.5
-
146
-
-
15544369982
-
Developmental origins of the metabolic syndrome: Prediction, plasticity, and programming
-
McMillen IC, Robinson JS. Developmental origins of the metabolic syndrome: prediction, plasticity, and programming. Physiol Rev 2005; 85: 571-633.
-
(2005)
Physiol Rev
, vol.85
, pp. 571-633
-
-
McMillen, I.C.1
Robinson, J.S.2
-
147
-
-
0142084634
-
Uteroplacental insufficiency increases apoptosis and alters p53 gene methylation in the full-term IUGR rat kidney
-
Pham TD, MacLennan NK, Chiu CT, Laksana GS, Hsu JL, Lane RH. Uteroplacental insufficiency increases apoptosis and alters p53 gene methylation in the full-term IUGR rat kidney. Am J Physiol Regul Integr Comp Physiol 2003; 285: R962-70.
-
(2003)
Am J Physiol Regul Integr Comp Physiol
, vol.285
-
-
Pham, T.D.1
Maclennan, N.K.2
Chiu, C.T.3
Laksana, G.S.4
Hsu, J.L.5
Lane, R.H.6
-
148
-
-
4844229628
-
Uteroplacental insufficiency alters DNA methylation, one-carbon metabolism, and histone acetylation in IUGR rats
-
MacLennan NK, James SJ, Melnyk S, et al. Uteroplacental insufficiency alters DNA methylation, one-carbon metabolism, and histone acetylation in IUGR rats. Physiol Genomics 2004; 18: 43-50.
-
(2004)
Physiol Genomics
, vol.18
, pp. 43-50
-
-
Maclennan, N.K.1
James, S.J.2
Melnyk, S.3
-
149
-
-
79959485990
-
The Intensity of IUGR-Induced Transcriptome Deregulations Is Inversely Correlated with the Onset of Organ Function in a Rat Model
-
Vaiman D, Gascoin-Lachambre G, Boubred F, et al. The Intensity of IUGR-Induced Transcriptome Deregulations Is Inversely Correlated with the Onset of Organ Function in a Rat Model. PLoS One 2011; 6: e21222.
-
(2011)
PLoS One
, vol.6
-
-
Vaiman, D.1
Gascoin-Lachambre, G.2
Boubred, F.3
-
150
-
-
33845662610
-
Growth retardation alters the epigenetic characteristics of hepatic dual specificity phosphatase 5
-
Fu Q, McKnight RA, Yu X, Callaway CW, Lane RH. Growth retardation alters the epigenetic characteristics of hepatic dual specificity phosphatase 5. FASEB J 2006; 20: 2127-9.
-
(2006)
FASEB J
, vol.20
, pp. 2127-2129
-
-
Fu, Q.1
McKnight, R.A.2
Yu, X.3
Callaway, C.W.4
Lane, R.H.5
-
151
-
-
69249107768
-
Chronic dietary exposure to a low-dose mixture of genistein and vinclozolin modifies the reproductive axis, testis transcriptome, and fertility
-
Eustache F, Mondon F, Canivenc-Lavier MC, et al. Chronic dietary exposure to a low-dose mixture of genistein and vinclozolin modifies the reproductive axis, testis transcriptome, and fertility. Environ Health Perspect 2009; 117: 1272-9.
-
(2009)
Environ Health Perspect
, vol.117
, pp. 1272-1279
-
-
Eustache, F.1
Mondon, F.2
Canivenc-Lavier, M.C.3
-
152
-
-
33645755191
-
Uteroplacental insufficiency affects epigenetic determinants of chromatin structure in brains of neonatal and juvenile IUGR rats
-
Ke X, Lei Q, James SJ, et al. Uteroplacental insufficiency affects epigenetic determinants of chromatin structure in brains of neonatal and juvenile IUGR rats. Physiol Genomics 2006; 25: 16-28.
-
(2006)
Physiol Genomics
, vol.25
, pp. 16-28
-
-
Ke, X.1
Lei, Q.2
James, S.J.3
-
153
-
-
74949087038
-
Nutritional programming affects hypothalamic organization and early response to leptin
-
Coupe B, Amarger V, Grit I, Benani A, Parnet P. Nutritional programming affects hypothalamic organization and early response to leptin. Endocrinology 2010; 151: 702-13.
-
(2010)
Endocrinology
, vol.151
, pp. 702-713
-
-
Coupe, B.1
Amarger, V.2
Grit, I.3
Benani, A.4
Parnet, P.5
-
154
-
-
80755130075
-
Dietary methyl donor deficiency during pregnancy in rats shapes learning and anxiety in offspring
-
Konycheva G, Dziadek MA, Ferguson LR, et al. Dietary methyl donor deficiency during pregnancy in rats shapes learning and anxiety in offspring. Nutr Res 2011; 31: 790-804.
-
(2011)
Nutr Res
, vol.31
, pp. 790-804
-
-
Konycheva, G.1
Dziadek, M.A.2
Ferguson, L.R.3
-
155
-
-
80054817669
-
Intrauterine growth restriction affects hippocampal dual specificity phosphatase 5 gene expression and epigenetic characteristics
-
Ke X, McKnight RA, Caprau D, et al. Intrauterine growth restriction affects hippocampal dual specificity phosphatase 5 gene expression and epigenetic characteristics. Physiol Genomics 2011; 43: 1160-9.
-
(2011)
Physiol Genomics
, vol.43
, pp. 1160-1169
-
-
Ke, X.1
McKnight, R.A.2
Caprau, D.3
-
156
-
-
45549097738
-
Development of type 2 diabetes following intrauterine growth retardation in rats is associated with progressive epigenetic silencing of Pdx1
-
Park JH, Stoffers DA, Nicholls RD, Simmons RA. Development of type 2 diabetes following intrauterine growth retardation in rats is associated with progressive epigenetic silencing of Pdx1. J Clin Invest 2008; 118: 2316-24.
-
(2008)
J Clin Invest
, vol.118
, pp. 2316-2324
-
-
Park, J.H.1
Stoffers, D.A.2
Nicholls, R.D.3
Simmons, R.A.4
-
157
-
-
80054098357
-
Exendin-4 increases histone acetylase activity and reverses epigenetic modifications that silence Pdx1 in the intrauterine growth retarded rat
-
Pinney SE, Jaeckle Santos LJ, Han Y, Stoffers DA, Simmons RA. Exendin-4 increases histone acetylase activity and reverses epigenetic modifications that silence Pdx1 in the intrauterine growth retarded rat. Diabetologia 2011; 54: 2606-14.
-
(2011)
Diabetologia
, vol.54
, pp. 2606-2614
-
-
Pinney, S.E.1
Jaeckle, S.L.J.2
Han, Y.3
Stoffers, D.A.4
Simmons, R.A.5
-
158
-
-
77952061606
-
Experimental intrauterine growth restriction induces alterations in DNA methylation and gene expression in pancreatic islets of rats
-
Thompson RF, Fazzari MJ, Niu H, Barzilai N, Simmons RA, Greally JM. Experimental intrauterine growth restriction induces alterations in DNA methylation and gene expression in pancreatic islets of rats. J Biol Chem 2010; 285: 15111-8.
-
(2010)
J Biol Chem
, vol.285
, pp. 15111-15118
-
-
Thompson, R.F.1
Fazzari, M.J.2
Niu, H.3
Barzilai, N.4
Simmons, R.A.5
Greally, J.M.6
-
159
-
-
0344196938
-
Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation- sensitive representational difference analysis
-
Monk D, Smith R, Arnaud P, et al. Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation- sensitive representational difference analysis. Mamm Genome 2003; 14: 805-16.
-
(2003)
Mamm Genome
, vol.14
, pp. 805-816
-
-
Monk, D.1
Smith, R.2
Arnaud, P.3
-
160
-
-
0028023046
-
Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation
-
Eggerding FA, Schonberg SA, Chehab FF, Norton ME, Cox VA, Epstein CJ. Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation. Am J Hum Genet 1994; 55: 253-65.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 253-265
-
-
Eggerding, F.A.1
Schonberg, S.A.2
Chehab, F.F.3
Norton, M.E.4
Cox, V.A.5
Epstein, C.J.6
-
161
-
-
77958592153
-
Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality
-
Lee DH, Singh P, Tsark WM, Szabo PE. Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality. PLoS One 2010; 5: e12630.
-
(2010)
PLoS One
, vol.5
-
-
Lee, D.H.1
Singh, P.2
Tsark, W.M.3
Szabo, P.E.4
-
162
-
-
79952525753
-
Antenatal maternal hypoxic stress: Adaptations in fetal lung Renin- Angiotensin system
-
Goyal R, Leitzke A, Goyal D, Gheorghe CP, Longo LD. Antenatal maternal hypoxic stress: adaptations in fetal lung Renin- Angiotensin system. Reprod Sci 2011; 18: 180-9.
-
(2011)
Reprod Sci
, vol.18
, pp. 180-189
-
-
Goyal, R.1
Leitzke, A.2
Goyal, D.3
Gheorghe, C.P.4
Longo, L.D.5
-
163
-
-
79961135015
-
Cellular DNA methylation program during neurulation and its alteration by alcohol exposure
-
Zhou FC, Chen Y, Love A. Cellular DNA methylation program during neurulation and its alteration by alcohol exposure. Birth Defects Res A Clin Mol Teratol 2011; 91: 703-15.
-
(2011)
Birth Defects Res a Clin Mol Teratol
, vol.91
, pp. 703-715
-
-
Zhou, F.C.1
Chen, Y.2
Love, A.3
-
164
-
-
78650555097
-
Subtle decreases in DNA methylation and gene expression at the mouse Igf2 locus following prenatal alcohol exposure: Effects of a methyl-supplemented diet
-
Downing C, Johnson TE, Larson C, et al. Subtle decreases in DNA methylation and gene expression at the mouse Igf2 locus following prenatal alcohol exposure: effects of a methyl-supplemented diet. Alcohol 2011; 45: 65-71.
-
(2011)
Alcohol
, vol.45
, pp. 65-71
-
-
Downing, C.1
Johnson, T.E.2
Larson, C.3
-
165
-
-
73449131530
-
Alcohol exposure alters DNA methylation profiles in mouse embryos at early neurulation
-
Liu Y, Balaraman Y, Wang G, Nephew KP, Zhou FC. Alcohol exposure alters DNA methylation profiles in mouse embryos at early neurulation. Epigenetics 2009; 4: 500-11.
-
(2009)
Epigenetics
, vol.4
, pp. 500-511
-
-
Liu, Y.1
Balaraman, Y.2
Wang, G.3
Nephew, K.P.4
Zhou, F.C.5
-
166
-
-
67650704762
-
Exposure of mouse embryos to ethanol during preimplantation development: Effect on DNA methylation in the h19 imprinting control region
-
Haycock PC, Ramsay M. Exposure of mouse embryos to ethanol during preimplantation development: effect on DNA methylation in the h19 imprinting control region. Biol Reprod 2009; 81: 618-27.
-
(2009)
Biol Reprod
, vol.81
, pp. 618-627
-
-
Haycock, P.C.1
Ramsay, M.2
-
167
-
-
78650848373
-
Adenoviral delivery of VEGF121 early in pregnancy prevents spontaneous development of preeclampsia in BPH/5 mice
-
Woods AK, Hoffmann DS, Weydert CJ, et al. Adenoviral delivery of VEGF121 early in pregnancy prevents spontaneous development of preeclampsia in BPH/5 mice. Hypertension 2011; 57: 94-102.
-
(2011)
Hypertension
, vol.57
, pp. 94-102
-
-
Woods, A.K.1
Hoffmann, D.S.2
Weydert, C.J.3
-
168
-
-
59449105284
-
Identification of quantitative trait loci controlling rice mature seed culturability using chromosomal segment substitution lines
-
Zhao L, Zhou H, Lu L, et al. Identification of quantitative trait loci controlling rice mature seed culturability using chromosomal segment substitution lines. Plant Cell Rep 2009; 28: 247-56.
-
(2009)
Plant Cell Rep
, vol.28
, pp. 247-256
-
-
Zhao, L.1
Zhou, H.2
Lu, L.3
-
169
-
-
33847080501
-
Bacterial infection promotes DNA hypermethylation
-
Bobetsis YA, Barros SP, Lin DM, et al. Bacterial infection promotes DNA hypermethylation. J Dent Res 2007; 86: 169-74.
-
(2007)
J Dent Res
, vol.86
, pp. 169-174
-
-
Bobetsis, Y.A.1
Barros, S.P.2
Lin, D.M.3
-
170
-
-
25144454048
-
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver- Russell syndrome
-
Gicquel C, Rossignol S, Cabrol S, et al. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver- Russell syndrome. Nat Genet 2005; 37: 1003-7.
-
(2005)
Nat Genet
, vol.37
, pp. 1003-1007
-
-
Gicquel, C.1
Rossignol, S.2
Cabrol, S.3
-
171
-
-
33745903915
-
Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain
-
Eggermann T, Schonherr N, Meyer E, et al. Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain. J Med Genet 2006; 43: 615-6.
-
(2006)
J Med Genet
, vol.43
, pp. 615-616
-
-
Eggermann, T.1
Schonherr, N.2
Meyer, E.3
-
172
-
-
33846461696
-
The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome
-
Schonherr N, Meyer E, Roos A, Schmidt A, Wollmann HA, Eggermann T. The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome. J Med Genet 2007; 44: 59-63.
-
(2007)
J Med Genet
, vol.44
, pp. 59-63
-
-
Schonherr, N.1
Meyer, E.2
Roos, A.3
Schmidt, A.4
Wollmann, H.A.5
Eggermann, T.6
-
173
-
-
34547764390
-
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: Clinical scoring system and epigenetic-phenotypic correlations
-
Netchine I, Rossignol S, Dufourg MN, et al. 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations. J Clin Endocrinol Metab 2007; 92: 3148-54.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 3148-3154
-
-
Netchine, I.1
Rossignol, S.2
Dufourg, M.N.3
-
174
-
-
40449100468
-
ICR1 epimutations in llp15 are restricted to patients with Silver- Russell syndrome features
-
Eggermann T, Meyer E, Caglayan AO, Dundar M, Schonherr N. ICR1 epimutations in llp15 are restricted to patients with Silver- Russell syndrome features. J Pediatr Endocrinol Metab 2008; 21: 59-62.
-
(2008)
J Pediatr Endocrinol Metab
, vol.21
, pp. 59-62
-
-
Eggermann, T.1
Meyer, E.2
Caglayan, A.O.3
Dundar, M.4
Schonherr, N.5
-
175
-
-
42049122139
-
The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alteration
-
Binder G, Seidel AK, Martin DD, et al. The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alteration. J Clin Endocrinol Metab 2008; 93: 1402-7.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 1402-1407
-
-
Binder, G.1
Seidel, A.K.2
Martin, D.D.3
-
176
-
-
53949102226
-
Segmental maternal UPD(7q) in Silver-Russell syndrome
-
Eggermann T, Schonherr N, Jager S, et al. Segmental maternal UPD(7q) in Silver-Russell syndrome. Clin Genet 2008; 74: 486-9.
-
(2008)
Clin Genet
, vol.74
, pp. 486-489
-
-
Eggermann, T.1
Schonherr, N.2
Jager, S.3
-
177
-
-
55349119907
-
Rapid detection of methylation change at H19 in human imprinting disorders using methylation- sensitive high-resolution melting
-
Wojdacz TK, Dobrovic A, Algar EM. Rapid detection of methylation change at H19 in human imprinting disorders using methylation- sensitive high-resolution melting. Hum Mutat 2008; 29: 1255-60.
-
(2008)
Hum Mutat
, vol.29
, pp. 1255-1260
-
-
Wojdacz, T.K.1
Dobrovic, A.2
Algar, E.M.3
-
178
-
-
62149105139
-
Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): Results from a large cohort of patients with SRS and SRS-like phenotypes
-
Bartholdi D, Krajewska-Walasek M, Ounap K, et al. Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes. J Med Genet 2009; 46: 192-7.
-
(2009)
J Med Genet
, vol.46
, pp. 192-197
-
-
Bartholdi, D.1
Krajewska-Walasek, M.2
Ounap, K.3
-
179
-
-
66749154227
-
Silver-Russell and Beckwith-Wiedemann syndromes: Opposite (epi)mutations in 11p15 result in opposite clinical pictures
-
Eggermann T. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures. Horm Res 2009; 71 Suppl 2: 30-5.
-
(2009)
Horm Res
, Issue.71 SUPPL. 2
, pp. 30-35
-
-
Eggermann, T.1
-
180
-
-
77952779338
-
Chromosome 11p15 duplication in Silver-Russell syndrome due to a maternally inherited translocation t(11;15)
-
Eggermann T, Spengler S, Bachmann N, et al. Chromosome 11p15 duplication in Silver-Russell syndrome due to a maternally inherited translocation t(11;15). Am J Med Genet A 2010; 152A: 1484-7.
-
(2010)
Am J Med Genet A
, vol.152 A
, pp. 1484-1487
-
-
Eggermann, T.1
Spengler, S.2
Bachmann, N.3
-
181
-
-
77950523023
-
Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders
-
Demars J, Shmela ME, Rossignol S, et al. Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders. Hum Mol Genet 2010; 19: 803-14.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 803-814
-
-
Demars, J.1
Shmela, M.E.2
Rossignol, S.3
-
182
-
-
77952671659
-
Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci
-
Turner CL, Mackay DM, Callaway JL, et al. Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. Eur J Hum Genet 2010; 18: 648-55.
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 648-655
-
-
Turner, C.L.1
Mackay, D.M.2
Callaway, J.L.3
-
183
-
-
33645902182
-
Unbalanced placental expression of imprinted genes in human intrauterine growth restriction
-
McMinn J, Wei M, Schupf N, Cusmai J, Johnson EB, Smith AC, Weksberg R, Thaker HM, Tycko B. Unbalanced placental expression of imprinted genes in human intrauterine growth restriction. Placenta 2006; 27: 540-9.
-
(2006)
Placenta
, vol.27
, pp. 540-549
-
-
McMinn, J.1
Wei, M.2
Schupf, N.3
Cusmai, J.4
Johnson, E.B.5
Smith, A.C.6
Weksberg, R.7
Thaker, H.M.8
Tycko, B.9
-
184
-
-
78650512418
-
Hypomethylation along with increased H19 expression in placentas from pregnancies complicated with fetal growth restriction
-
Koukoura O, Sifakis S, Zaravinos A, et al. Hypomethylation along with increased H19 expression in placentas from pregnancies complicated with fetal growth restriction. Placenta 2011; 32: 51-7.
-
(2011)
Placenta
, vol.32
, pp. 51-57
-
-
Koukoura, O.1
Sifakis, S.2
Zaravinos, A.3
-
185
-
-
76749161350
-
Decreased placental methylation at the H19/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia
-
Bourque DK, Avila L, Penaherrera M, von Dadelszen P, Robinson WP. Decreased placental methylation at the H19/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia. Placenta 2010; 31: 197-202.
-
(2010)
Placenta
, vol.31
, pp. 197-202
-
-
Bourque, D.K.1
Avila, L.2
Penaherrera, M.3
von Dadelszen, P.4
Robinson, W.P.5
-
186
-
-
77954678397
-
Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extraembryonic compartments and its possible role in fetal growth restriction
-
Tabano S, Colapietro P, Cetin I, et al. Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extraembryonic compartments and its possible role in fetal growth restriction. Epigenetics 2010; 5: 313-24.
-
(2010)
Epigenetics
, vol.5
, pp. 313-324
-
-
Tabano, S.1
Colapietro, P.2
Cetin, I.3
-
187
-
-
80054997205
-
Differential methylation of imprinted genes in growth-restricted placentas
-
Lambertini L, Lee TL, Chan WY, et al. Differential methylation of imprinted genes in growth-restricted placentas. Reprod Sci 2011; 18: 1111-7.
-
(2011)
Reprod Sci
, vol.18
, pp. 1111-1117
-
-
Lambertini, L.1
Lee, T.L.2
Chan, W.Y.3
-
188
-
-
79960120705
-
Infant growth restriction is associated with distinct patterns of DNA methylation in human placentas
-
Banister CE, Koestler DC, Maccani MA, Padbury JF, Houseman EA, Marsit CJ. Infant growth restriction is associated with distinct patterns of DNA methylation in human placentas. Epigenetics 2011; 6: 920-7.
-
(2011)
Epigenetics
, vol.6
, pp. 920-927
-
-
Banister, C.E.1
Koestler, D.C.2
Maccani, M.A.3
Padbury, J.F.4
Houseman, E.A.5
Marsit, C.J.6
-
189
-
-
80053289302
-
Birthweight, maternal weight trajectories and global DNA methylation of LINE-1 repetitive elements
-
Michels KB, Harris HR, Barault L. Birthweight, maternal weight trajectories and global DNA methylation of LINE-1 repetitive elements. PLoS One 2011; 6: e25254.
-
(2011)
PLoS One
, vol.6
-
-
Michels, K.B.1
Harris, H.R.2
Barault, L.3
-
190
-
-
33646271627
-
Evidence for a role of developmental genes in the origin of obesity and body fat distribution
-
Gesta S, Bluher M, Yamamoto Y, et al. Evidence for a role of developmental genes in the origin of obesity and body fat distribution. Proc Natl Acad Sci USA 2006; 103: 6676-81.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 6676-6681
-
-
Gesta, S.1
Bluher, M.2
Yamamoto, Y.3
-
191
-
-
84861305389
-
Newborn umbilical cord blood DNA methylation and gene expression levels exhibit limited association with birth weight
-
Adkins RM, Tylavsky FA, Krushkal J. Newborn umbilical cord blood DNA methylation and gene expression levels exhibit limited association with birth weight. Chem Biodivers 2012; 9: 888-99.
-
(2012)
Chem Biodivers
, vol.9
, pp. 888-899
-
-
Adkins, R.M.1
Tylavsky, F.A.2
Krushkal, J.3
-
192
-
-
79951486887
-
DNA methylation of IGF2, GNASAS, INSIGF and LEP and being born small for gestational age
-
Tobi EW, Heijmans BT, Kremer D, et al. DNA methylation of IGF2, GNASAS, INSIGF and LEP and being born small for gestational age. Epigenetics 2011; 6: 171-6.
-
(2011)
Epigenetics
, vol.6
, pp. 171-176
-
-
Tobi, E.W.1
Heijmans, B.T.2
Kremer, D.3
-
193
-
-
41849101659
-
Genetic and epigenetic mechanisms combine to control MMP1 expression and its association with preterm premature rupture of membranes
-
Wang H, Ogawa M, Wood JR, et al. Genetic and epigenetic mechanisms combine to control MMP1 expression and its association with preterm premature rupture of membranes. Hum Mol Genet 2008; 17: 1087-96.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 1087-1096
-
-
Wang, H.1
Ogawa, M.2
Wood, J.R.3
|