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Results: 1-25/26
Authors:
Reik, W
Walter, J
Citation: W. Reik et J. Walter, Genomic imprinting: Parental influence on the genome, NAT REV GEN, 2(1), 2001, pp. 21-32
Authors:
Khosla, S
Dean, W
Reik, W
Feil, R
Citation: S. Khosla et al., Epigenetic and experimental modifications in early mammalian development: Part II - Culture of preimplantation embryos and its long-term effects on gene expression and phenotype, HUM REP UPD, 7(4), 2001, pp. 419-427
Authors:
Valenza-Schaerly, P
Pickard, B
Walter, J
Jung, M
Pourcel, L
Reik, W
Gauguier, D
Vergnaud, G
Pourcel, C
Citation: P. Valenza-schaerly et al., A dominant modifier of transgene methylation is mapped by QTL analysis to mouse chromosome 13, GENOME RES, 11(3), 2001, pp. 382-388
Authors:
Reik, W
Walter, J
Citation: W. Reik et J. Walter, Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote, NAT GENET, 27(3), 2001, pp. 255-256
Authors:
Engemann, S
Strodicke, M
Paulsen, M
Franck, O
Reinhardt, R
Lane, N
Reik, W
Walter, J
Citation: S. Engemann et al., Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting (vol 9, pg 2691, 2000), HUM MOL GEN, 10(9), 2001, pp. 1003-1003
Authors:
Pickard, B
Dean, W
Engemann, S
Bergmann, K
Fuermann, M
Jung, M
Reis, A
Allen, N
Reik, W
Walter, J
Citation: B. Pickard et al., Epigenetic targeting in the mouse zygote marks DNA for later methylation: a mechanism for maternal effects in development, MECH DEVEL, 103(1-2), 2001, pp. 35-47
Authors:
Thompson, SL
Konfortova, G
Gregory, RI
Reik, W
Dean, W
Feil, R
Citation: Sl. Thompson et al., Environmental effects on genomic imprinting in mammals, TOX LETT, 120(1-3), 2001, pp. 143-150
Authors:
Schofield, PN
Joyce, JA
Lam, WK
Grandjean, V
Ferguson-Smith, A
Reik, W
Maher, ER
Citation: Pn. Schofield et al., Genomic imprinting and cancer; new paradigms in the genetics of neoplasia, TOX LETT, 120(1-3), 2001, pp. 151-160
Authors:
Eden, S
Constancia, M
Hashimshony, T
Dean, W
Goldstein, B
Johnson, AC
Keshet, I
Reik, W
Cedar, H
Citation: S. Eden et al., An upstream repressor element plays a role in Igf2 imprinting, EMBO J, 20(13), 2001, pp. 3518-3525
Authors:
Reik, W
Dean, W
Citation: W. Reik et W. Dean, DNA methylation and mammalian epigenetics, ELECTROPHOR, 22(14), 2001, pp. 2838-2843
Authors:
Reik, W
Dean, W
Walter, J
Citation: W. Reik et al., Epigenetic reprogramming in mammalian development, SCIENCE, 293(5532), 2001, pp. 1089-1093
Authors:
Dean, W
Santos, F
Stojkovic, M
Zakhartchenko, V
Walter, J
Wolf, E
Reik, W
Citation: W. Dean et al., Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos, P NAS US, 98(24), 2001, pp. 13734-13738
Authors:
Khosla, S
Dean, W
Brown, D
Reik, W
Feil, R
Citation: S. Khosla et al., Culture of preimplantation mouse embryos affects fetal development and theexpression of imprinted genes, BIOL REPROD, 64(3), 2001, pp. 918-926
Authors:
Constancia, M
Dean, W
Lopes, S
Moore, T
Kelsey, G
Reik, W
Citation: M. Constancia et al., Deletion of a silencer element in lgf2 results in loss of imprinting independent of H19, NAT GENET, 26(2), 2000, pp. 203-206
Authors:
Engemann, S
Strodicke, M
Paulsen, M
Franck, O
Reinhardt, R
Lane, N
Reik, W
Walter, J
Citation: S. Engemann et al., Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting, HUM MOL GEN, 9(18), 2000, pp. 2691-2706
Authors:
Paulsen, M
El-Maarri, O
Engemann, S
Strodicke, M
Franck, O
Davies, K
Reinhardt, R
Reik, W
Walter, J
Citation: M. Paulsen et al., Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse, HUM MOL GEN, 9(12), 2000, pp. 1829-1841
Authors:
Oswald, J
Engemann, S
Lane, N
Mayer, W
Olek, A
Fundele, R
Dean, W
Reik, W
Walter, J
Citation: J. Oswald et al., Active demethylation of the paternal genome in the mouse zygote, CURR BIOL, 10(8), 2000, pp. 475-478
Authors:
Reik, W
Constancia, M
Dean, W
Davies, K
Bowden, L
Murrell, A
Feil, R
Walter, J
Kelsey, G
Citation: W. Reik et al., Igf2 imprinting in development and disease, INT J DEV B, 44(1), 2000, pp. 145-150
Authors:
Reik, W
Murrell, A
Citation: W. Reik et A. Murrell, Genomic imprinting - Silence across the border, NATURE, 405(6785), 2000, pp. 408-409
Authors:
Catchpoole, D
Smallwood, AV
Joyce, JA
Murrell, A
Lam, W
Tang, T
Munroe, D
Reik, W
Schofield, PN
Maher, ER
Citation: D. Catchpoole et al., Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome, J MED GENET, 37(3), 2000, pp. 212-215
Authors:
Maher, ER
Reik, W
Citation: Er. Maher et W. Reik, The two-domain hypothesis in Beckwith-Wiedemann syndrome - Reply, J CLIN INV, 106(6), 2000, pp. 740-740
Authors:
Maher, ER
Reik, W
Citation: Er. Maher et W. Reik, Beckwith-Wiedemann syndrome: imprinting in clusters revisited, J CLIN INV, 105(3), 2000, pp. 247-252
Authors:
Reik, W
Kelsey, G
Walter, J
Citation: W. Reik et al., Dissecting de novo methylation, NAT GENET, 23(4), 1999, pp. 380-382
Authors:
Smilinich, NJ
Day, CD
Fitzpatrick, GV
Caldwell, GM
Lossie, AC
Cooper, PR
Smallwood, AC
Joyce, JA
Schofield, PN
Reik, W
Nicholls, RD
Weksberg, R
Driscoll, DJ
Maher, ER
Shows, TB
Higgins, MJ
Citation: Nj. Smilinich et al., A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome, P NAS US, 96(14), 1999, pp. 8064-8069
Authors:
Lam, WWK
Hatada, I
Ohishi, S
Mukai, T
Joyce, JA
Cole, TRP
Donnai, D
Reik, W
Schofield, PN
Maher, ER
Citation: Wwk. Lam et al., Analysis of germline CDKN1C (p57(KIP2)) mutations in familial and sporadicBeckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation, J MED GENET, 36(7), 1999, pp. 518-523