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http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_12/B3598D6B5BF17CBEE053120B220A90C5/authorship/6
http://hub.abes.fr/bmj/periodical/jmedgenet/1988/volume_25/issue_12/B3591CB9650B14CDE053120B220A6689/authorship/1
http://hub.abes.fr/bmj/periodical/jmg/2000/volume_37/issue_3/B3598D6B5C247CBEE053120B220A90C5/authorship/8
http://hub.abes.fr/oup/periodical/hmg/2005/volume_14/issue_4/101093hmgddi047/authorship/10
http://hub.abes.fr/oup/periodical/hmg/2005/volume_14/issue_suppl1/101093hmgddi114/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2003/volume_13/issue_2/101093hmgddh013/authorship/8
http://hub.abes.fr/oup/periodical/humrep/2010/volume_25/issue_9/101093humrepdeq151/authorship/6
http://hub.abes.fr/oup/periodical/hmg/1997/volume_6/issue_9/101093hmg691543/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1998/volume_7/issue_7/101093hmg771149/authorship/14
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_3/101093hmgddg022/authorship/11
http://hub.abes.fr/oup/periodical/humrep/2009/volume_24/issue_3/101093humrepden406/authorship/11
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_18/101093hmg9182691/authorship/7
http://hub.abes.fr/oup/periodical/hmg/2006/volume_15/issue_8/101093hmgddl041/authorship/9
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_12/101093hmg9121829/authorship/8
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_23/101093hmgddg338/authorship/8
http://hub.abes.fr/oup/periodical/humupd/2001/volume_7/issue_4/101093humupd74419/authorship/3
http://hub.abes.fr/springer/periodical/335/1993/volume_4/issue_2/B8CA678C368366D6E053120B220A2E8F/authorship/2
http://hub.abes.fr/springer/periodical/335/1992/volume_3/issue_11/B8CA678C356A66D6E053120B220A2E8F/authorship/1
http://hub.abes.fr/springer/periodical/335/1991/volume_2/issue_1/B8CA678C35E066D6E053120B220A2E8F/authorship/2
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Evaluation of epigenetic marks in human embryos derived from IVF and ICSI
Syntenic Organization of the Mouse Distal Chromosome 7 Imprinting Cluster and the Beckwith-Wiedemann Syndrome Region in Chromosome 11p15.5
Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting
Epigenetic modifications in an imprinting cluster are controlled by a hierarchy of DMRs suggesting long-range chromatin interactions
Epigenetic reprogramming in mammals
Imprinting of IGF2 and H19: Lack of Reciprocity in Sporadic Beckwith-Wiedemann Syndrome
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster
Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA
An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype
Culture of preimplantation embryos and its long-term effects on gene expression and phenotype
Mapping of two human homologs of a Drosophila heterochromatin protein gene to the X Chromosome
Mapping of a mouse homolog of a Heterochromatin protein gene to the X Chromosome
Chromosomal localization of human homologs of the Drosophila heterochromatin protein 1 (HP1) gene
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