PubMed=3821905; DOI=10.1038/326292a0
Hooper M.L., Hardy K., Handyside A., Hunter S., Monk M.
HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells.
Nature 326:292-295(1987)

PubMed=19581487; DOI=10.1101/gr.092643.109; PMCID=PMC2720191
Marks H., Chow J.C., Denissov S., Francoijs K.-J., Brockdorff N., Heard E., Stunnenberg H.G.
High-resolution analysis of epigenetic changes associated with X inactivation.
Genome Res. 19:1361-1373(2009)

PubMed=23850244; DOI=10.1016/j.stem.2013.06.002
Habibi E., Brinkman A.B., Arand J., Kroeze L.I., Kerstens H.H.D., Matarese F., Lepikhov K., Gut M., Brun-Heath I., Hubner N.C., Benedetti R., Altucci L., Jansen J.H., Walter J., Gut I.G., Marks H., Stunnenberg H.G.
Whole-genome bisulfite sequencing of two distinct interconvertible DNA methylomes of mouse embryonic stem cells.
Cell Stem Cell 13:360-369(2013)

PubMed=25004115; DOI=10.1016/j.ygeno.2014.06.007
Incarnato D., Krepelova A., Neri F.
High-throughput single nucleotide variant discovery in E14 mouse embryonic stem cells provides a new reference genome assembly.
Genomics 104:121-127(2014)

PubMed=26484140; DOI=10.1016/j.gdata.2014.10.023; PMCID=PMC4535964
Incarnato D., Neri F.
High-throughput whole-genome sequencing of E14 mouse embryonic stem cells.
Genom. Data 3:6-7(2015)