Genomic imprinting: a possible mechanism for the parental origin effect in Huntington's chorea.

Por Reik, W
Publicado em 1988

Replication-competent Moloney murine leukemia virus carrying a bacterial suppressor tRNA gene: selective cloning of proviral and flanking host sequences.

Por Reik, W, Weiher, H, Jaenisch, R
Publicado em 1985

Retrovirus integration and chromatin structure: Moloney murine leukemia proviral integration sites map near DNase I-hypersensitive sites.

Por Rohdewohld, H, Weiher, H, Reik, W, Jaenisch, R, Breindl, M
Publicado em 1987

Methylation analysis on individual chromosomes: improved protocol for bisulphite genomic sequencing.

Por Feil, R, Charlton, J, Bird, A P, Walter, J, Reik, W
Publicado em 1994

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2

Por Moore, T., Constancia, M., Zubair, M., Bailleul, B., Feil, R., Sasaki, H., Reik, W.
Publicado em 1997

Age at onset in Huntington's disease and methylation at D4S95.

Por Reik, W, Maher, E R, Morrison, P J, Harding, A E, Simpson, S A
Publicado em 1993

Dynamic methylation adjustment and counting as part of imprinting mechanisms.

Por Shemer, R, Birger, Y, Dean, W L, Reik, W, Riggs, A D, Razin, A
Publicado em 1996

Instability of long inverted repeats within mouse transgenes.

Por Collick, A, Drew, J, Penberth, J, Bois, P, Luckett, J, Scaerou, F, Jeffreys, A, Reik, W
Publicado em 1996

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Por Engel, J., Smallwood, A., Harper, A., Higgins, M., Oshimura, M., Reik, W., Schofield, P., Maher, E.
Publicado em 2000

Analysis of germline CDKN1C (p57(KIP2)) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

Por Lam, W., Hatada, I., Ohishi, S., Mukai, T., Joyce, J., Cole, T., Donnai, D., Reik, W., Schofield, P., Maher, E.
Publicado em 1999

Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans

Por Forné, T., Oswald, J., Dean, W., Saam, J. R., Bailleul, B., Dandolo, L., Tilghman, S. M., Walter, J., Reik, W.
Publicado em 1997

Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

Por CATCHPOOLE, D., SMALLWOOD, A., JOYCE, J., MURRELL, A., LAM, W., TANG, T., MUNROE, D., REIK, W., SCHOFIELD, P., MAHER, E.
Publicado em 2000

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

Por Maher, E, Brueton, L, Bowdin, S, Luharia, A, Cooper, W, Cole, T, Macdonald, F, Sampson, J, Barratt, C, Reik, W, Hawkins, M
Publicado em 2003

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Por Catchpoole, D, Lam, W W, Valler, D, Temple, I K, Joyce, J A, Reik, W, Schofield, P N, Maher, E R
Publicado em 1997

Silencing of CDKN1C (p57(KIP2)) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome

Por Diaz-Meyer, N, Day, C, Khatod, K, Maher, E, Cooper, W, Reik, W, Junien, C, Graham, G, Algar, E, Der Kaloustian, V M, Higgins, M
Publicado em 2003

Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta

Por Sibley, C. P., Coan, P. M., Ferguson-Smith, A. C., Dean, W., Hughes, J., Smith, P., Reik, W., Burton, G. J., Fowden, A. L., Constância, M.
Publicado em 2004