-
1
-
-
0027394822
-
Fetal growth retardation: associated malformations and chromosomal abnormalities
-
PID: 8438926, COI: 1:STN:280:DyaK3s7nsFGmtQ%3D%3D
-
Snijders RJ, Sherrod C, Gosden CM, Nicolaides KH. Fetal growth retardation: associated malformations and chromosomal abnormalities. Am J Obstet Gynecol. 1993;168(2):547–55.
-
(1993)
Am J Obstet Gynecol
, vol.168
, Issue.2
, pp. 547-555
-
-
Snijders, R.J.1
Sherrod, C.2
Gosden, C.M.3
Nicolaides, K.H.4
-
2
-
-
84878107771
-
-
The role of imprinted genes in humans, Molecular aspects of medicine:
-
Ishida M, Moore GE. The role of imprinted genes in humans. Molecular aspects of medicine. 2012. doi:10.1016/j.mam.2012.06.009.
-
(2012)
Moore GE
-
-
Ishida, M.1
-
3
-
-
8544273687
-
Resourceful imprinting
-
PID: 15525980, COI: 1:CAS:528:DC%2BD2cXpt1eit74%3D
-
Constancia M, Kelsey G, Reik W. Resourceful imprinting. Nature. 2004;432(7013):53–7. doi:10.1038/432053a.
-
(2004)
Nature
, vol.432
, Issue.7013
, pp. 53-57
-
-
Constancia, M.1
Kelsey, G.2
Reik, W.3
-
4
-
-
0029007625
-
Causes of intrauterine growth restriction
-
PID: 7671543, COI: 1:STN:280:DyaK2MvgtFGhsA%3D%3D
-
Neerhof MG. Causes of intrauterine growth restriction. Clin Perinatol. 1995;22(2):375–85.
-
(1995)
Clin Perinatol
, vol.22
, Issue.2
, pp. 375-385
-
-
Neerhof, M.G.1
-
5
-
-
84867189881
-
IGF2 DNA methylation is a modulator of newborn’s fetal growth and development
-
7 (10)
-
St-Pierre J, Hivert MF, Perron P, Poirier P, Guay SP, Brisson D et al. IGF2 DNA methylation is a modulator of newborn’s fetal growth and development. Epigenetics: official journal of the DNA Methylation Society. 2012;7 (10).
-
(2012)
Epigenetics : official journal of the DNA Methylation Society
-
-
St-Pierre, J.1
Hivert, M.F.2
Perron, P.3
Poirier, P.4
Guay, S.P.5
Brisson, D.6
-
6
-
-
14044261317
-
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster
-
PID: 15640248, COI: 1:CAS:528:DC%2BD2MXhtV2qs7s%3D
-
Cerrato F, Sparago A, Di Matteo I, Zou X, Dean W, Sasaki H, et al. The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster. Hum Mol Genet. 2005;14(4):503–11. doi:10.1093/hmg/ddi047.
-
(2005)
Hum Mol Genet
, vol.14
, Issue.4
, pp. 503-511
-
-
Cerrato, F.1
Sparago, A.2
Di Matteo, I.3
Zou, X.4
Dean, W.5
Sasaki, H.6
-
7
-
-
84862980829
-
Gain of function in CDKN1C
-
PID: 22735584, COI: 1:CAS:528:DC%2BC38Xpt1Shsb4%3D
-
Riccio A, Cubellis MV. Gain of function in CDKN1C. Nat Genet. 2012;44(7):737–8. doi:10.1038/ng.2336.
-
(2012)
Nat Genet
, vol.44
, Issue.7
, pp. 737-738
-
-
Riccio, A.1
Cubellis, M.V.2
-
8
-
-
84883789858
-
Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth
-
PID: 23495910, COI: 1:CAS:528:DC%2BC3sXhsVCrtb3L
-
Jacob KJ, Robinson WP, Lefebvre L. Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth. Clin Genet. 2013;84(4):326–34. doi:10.1111/cge.12143.
-
(2013)
Clin Genet
, vol.84
, Issue.4
, pp. 326-334
-
-
Jacob, K.J.1
Robinson, W.P.2
Lefebvre, L.3
-
9
-
-
84859496664
-
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight
-
PID: 22444668, COI: 1:CAS:528:DC%2BC38XksFejt7c%3D
-
Ishida M, Monk D, Duncan AJ, Abu-Amero S, Chong J, Ring SM, et al. Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight. Am J Hum Genet. 2012;90(4):715–9. doi:10.1016/j.ajhg.2012.02.021.
-
(2012)
Am J Hum Genet
, vol.90
, Issue.4
, pp. 715-719
-
-
Ishida, M.1
Monk, D.2
Duncan, A.J.3
Abu-Amero, S.4
Chong, J.5
Ring, S.M.6
-
10
-
-
34250160167
-
Mechanisms regulating imprinted genes in clusters
-
PID: 17467259, COI: 1:CAS:528:DC%2BD2sXmsFKmsrc%3D
-
Edwards CA, Ferguson-Smith AC. Mechanisms regulating imprinted genes in clusters. Curr Opin Cell Biol. 2007;19(3):281–9. doi:10.1016/j.ceb.2007.04.013.
-
(2007)
Curr Opin Cell Biol
, vol.19
, Issue.3
, pp. 281-289
-
-
Edwards, C.A.1
Ferguson-Smith, A.C.2
-
11
-
-
83455213564
-
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases
-
PID: 21920939
-
Chiesa N, De Crescenzo A, Mishra K, Perone L, Carella M, Palumbo O, et al. The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases. Hum Mol Genet. 2012;21(1):10–25. doi:10.1093/hmg/ddr419.
-
(2012)
Hum Mol Genet
, vol.21
, Issue.1
, pp. 10-25
-
-
Chiesa, N.1
De Crescenzo, A.2
Mishra, K.3
Perone, L.4
Carella, M.5
Palumbo, O.6
-
12
-
-
42649101672
-
MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment
-
PID: 18212817, COI: 1:CAS:528:DC%2BD1cXltFeit7Y%3D
-
Priolo M, Sparago A, Mammi C, Cerrato F, Lagana C, Riccio A. MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment. European journal of human genetics: EJHG. 2008;16(5):565–71.
-
(2008)
European journal of human genetics : EJHG
, vol.16
, Issue.5
, pp. 565-571
-
-
Priolo, M.1
Sparago, A.2
Mammi, C.3
Cerrato, F.4
Lagana, C.5
Riccio, A.6
-
13
-
-
77954909570
-
Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns
-
PID: 20194112, COI: 1:CAS:528:DC%2BC3cXotlCjtLY%3D
-
Schneider E, Pliushch G, El Hajj N, Galetzka D, Puhl A, Schorsch M, et al. Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns. Nucleic Acids Res. 2010;38(12):3880–90. doi:10.1093/nar/gkq126.
-
(2010)
Nucleic Acids Res
, vol.38
, Issue.12
, pp. 3880-3890
-
-
Schneider, E.1
Pliushch, G.2
El Hajj, N.3
Galetzka, D.4
Puhl, A.5
Schorsch, M.6
-
14
-
-
0035710746
-
Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) Method
-
COI: 1:CAS:528:DC%2BD38XhtFelt7s%3D
-
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) Method. Methods (San Diego, Calif). 2001;25(4):402–8. doi:10.1006/meth.2001.1262.
-
(2001)
Methods (San Diego, Calif)
, vol.25
, Issue.4
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
-
15
-
-
48949115579
-
Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae
-
PID: 18550048, COI: 1:CAS:528:DC%2BD1cXptVCnsro%3D
-
Guo L, Choufani S, Ferreira J, Smith A, Chitayat D, Shuman C, et al. Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae. Dev Biol. 2008;320(1):79–91. doi:10.1016/j.ydbio.2008.04.025.
-
(2008)
Dev Biol
, vol.320
, Issue.1
, pp. 79-91
-
-
Guo, L.1
Choufani, S.2
Ferreira, J.3
Smith, A.4
Chitayat, D.5
Shuman, C.6
-
16
-
-
33645902182
-
Unbalanced placental expression of imprinted genes in human intrauterine growth restriction
-
PID: 16125225, COI: 1:CAS:528:DC%2BD28XjvVagsLg%3D
-
McMinn J, Wei M, Schupf N, Cusmai J, Johnson EB, Smith AC, et al. Unbalanced placental expression of imprinted genes in human intrauterine growth restriction. Placenta. 2006;27(6–7):540–9. doi:10.1016/j.placenta.2005.07.004.
-
(2006)
Placenta
, vol.27
, Issue.6-7
, pp. 540-549
-
-
McMinn, J.1
Wei, M.2
Schupf, N.3
Cusmai, J.4
Johnson, E.B.5
Smith, A.C.6
-
17
-
-
37749034611
-
Placental IGF2 expression in normal and intrauterine growth restricted (IUGR) pregnancies
-
PID: 17919721, COI: 1:CAS:528:DC%2BD1cXls1Chtw%3D%3D
-
Antonazzo P, Alvino G, Cozzi V, Grati FR, Tabano S, Sirchia S, et al. Placental IGF2 expression in normal and intrauterine growth restricted (IUGR) pregnancies. Placenta. 2008;29(1):99–101. doi:10.1016/j.placenta.2007.06.010.
-
(2008)
Placenta
, vol.29
, Issue.1
, pp. 99-101
-
-
Antonazzo, P.1
Alvino, G.2
Cozzi, V.3
Grati, F.R.4
Tabano, S.5
Sirchia, S.6
-
18
-
-
33947398439
-
Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight
-
COI: 1:CAS:528:DC%2BD2sXjt1Kktb0%3D
-
Apostolidou S, Abu-Amero S, O'Donoghue K, Frost J, Olafsdottir O, Chavele KM. Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight. Journal of molecular medicine (Berlin, Germany). 2007;85(4):379–87. doi:10.1007/s00109-006-0131-8.
-
(2007)
Journal of molecular medicine (Berlin, Germany)
, vol.85
, Issue.4
, pp. 379-387
-
-
Apostolidou, S.1
Abu-Amero, S.2
O'Donoghue, K.3
Frost, J.4
Olafsdottir, O.5
Chavele, K.M.6
-
19
-
-
2542555066
-
Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta
-
PID: 15150410, COI: 1:CAS:528:DC%2BD2cXkslCitLo%3D
-
Sibley CP, Coan PM, Ferguson-Smith AC, Dean W, Hughes J, Smith P, et al. Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta. Proc Natl Acad Sci U S A. 2004;101(21):8204–8. doi:10.1073/pnas.0402508101.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, Issue.21
, pp. 8204-8208
-
-
Sibley, C.P.1
Coan, P.M.2
Ferguson-Smith, A.C.3
Dean, W.4
Hughes, J.5
Smith, P.6
-
20
-
-
77954680732
-
Gene expression pattern of IGF2, PHLDA2, PEG10 and CDKN1C imprinted genes in spontaneous miscarriages or fetal deaths
-
COI: 1:CAS:528:DC%2BC3cXht1egt73K
-
Doria S, Sousa M, Fernandes S, Ramalho C, Brandao O, Matias A, et al. Gene expression pattern of IGF2, PHLDA2, PEG10 and CDKN1C imprinted genes in spontaneous miscarriages or fetal deaths. Epigenetics: official journal of the DNA Methylation Society. 2010;5(5):444–50.
-
(2010)
Epigenetics : official journal of the DNA Methylation Society
, vol.5
, Issue.5
, pp. 444-450
-
-
Doria, S.1
Sousa, M.2
Fernandes, S.3
Ramalho, C.4
Brandao, O.5
Matias, A.6
-
21
-
-
79961147541
-
The role of imprinted genes in fetal growth abnormalities
-
PID: 21648055, COI: 1:CAS:528:DC%2BC3MXpvVyhtL8%3D
-
Piedrahita JA. The role of imprinted genes in fetal growth abnormalities. Birth defects research Part A, Clinical and molecular teratology. 2011;91(8):682–92. doi:10.1002/bdra.20795.
-
(2011)
Birth defects research Part A, Clinical and molecular teratology
, vol.91
, Issue.8
, pp. 682-692
-
-
Piedrahita, J.A.1
-
22
-
-
33847080501
-
Bacterial infection promotes DNA hypermethylation
-
PID: 17251518, COI: 1:CAS:528:DC%2BD2sXitVCru7w%3D
-
Bobetsis YA, Barros SP, Lin DM, Weidman JR, Dolinoy DC, Jirtle RL, et al. Bacterial infection promotes DNA hypermethylation. J Dent Res. 2007;86(2):169–74.
-
(2007)
J Dent Res
, vol.86
, Issue.2
, pp. 169-174
-
-
Bobetsis, Y.A.1
Barros, S.P.2
Lin, D.M.3
Weidman, J.R.4
Dolinoy, D.C.5
Jirtle, R.L.6
-
23
-
-
79958177916
-
Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues
-
PID: 20738330, COI: 1:STN:280:DC%2BC3MjhtFGrsg%3D%3D
-
Begemann M, Spengler S, Kanber D, Haake A, Baudis M, Leisten I, et al. Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues. Clin Genet. 2011;80(1):83–8. doi:10.1111/j.1399-0004.2010.01514.x.
-
(2011)
Clin Genet
, vol.80
, Issue.1
, pp. 83-88
-
-
Begemann, M.1
Spengler, S.2
Kanber, D.3
Haake, A.4
Baudis, M.5
Leisten, I.6
-
24
-
-
70450162112
-
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci
-
PID: 19755383, COI: 1:CAS:528:DC%2BD1MXhsVGltbvO
-
Azzi S, Rossignol S, Steunou V, Sas T, Thibaud N, Danton F, et al. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Hum Mol Genet. 2009;18(24):4724–33. doi:10.1093/hmg/ddp435.
-
(2009)
Hum Mol Genet
, vol.18
, Issue.24
, pp. 4724-4733
-
-
Azzi, S.1
Rossignol, S.2
Steunou, V.3
Sas, T.4
Thibaud, N.5
Danton, F.6
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