W Reik

发表

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

W. Reik, W. Bickmore, Y. Le Bouc, 1995, Human molecular genetics.

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

W. Reik, S. Bowdin, J. Sampson, 2003, Journal of medical genetics.

Mammalian epigenomics: reprogramming the genome for development and therapy.

W Dean, W. Reik, W. Dean, 2003, Theriogenology.

Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos

W Dean, W. Reik, M. Stojkovic, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome.

W. Reik, E. Maher, W Reik, 1997, Trends in genetics : TIG.

Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human.

S Apostolidou, P Stanier, D Monk, 2006, Human molecular genetics.

Imprinting mechanisms.

B Pickard, W Reik, M Constância, 1998, Genome research.

Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes.

W. Reik, J. Walter, N. Allen, 1994, Development.

DNA methylation and mammalian epigenetics

W Dean, W. Reik, W. Dean, 2001, Electrophoresis.

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

T. Moore, W. Reik, H. Sasaki, 1997, Proceedings of the National Academy of Sciences of the United States of America.

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

A. Bird, W. Reik, J. Walter, 1994, Nucleic acids research.