about
Primordial germ cells: the first cell lineage or the last cells standing?Epigenetic reprogramming of breast cancer cells with oocyte extracts.5-Carboxylcytosine is localized to euchromatic regions in the nuclei of follicular cells in axolotl ovary.Evolution of the germ line-soma relationship in vertebrate embryos.Mechanisms of Vertebrate Germ Cell Determination.Axolotl Nanog activity in mouse embryonic stem cells demonstrates that ground state pluripotency is conserved from urodele amphibians to mammals.Evolution of germ cell development in tetrapods: comparison of urodeles and amniotes.Stepwise evolution of Elk-1 in early deuterostomes.Stochastic specification of primordial germ cells from mesoderm precursors in axolotl embryos.Semi-quantitative immunohistochemical detection of 5-hydroxymethyl-cytosine reveals conservation of its tissue distribution between amphibians and mammals.Detection of Modified Forms of Cytosine Using Sensitive Immunohistochemistry.5-Carboxylcytosine levels are elevated in human breast cancers and gliomas.Acquisition of germ plasm accelerates vertebrate evolution.Expression of Dazl and Vasa in turtle embryos and ovaries: evidence for inductive specification of germ cells.A conserved mechanism for vertebrate mesoderm specification in urodele amphibians and mammals.The POU-er of gene nomenclature.Epigenetic marks in somatic chromatin are remodelled to resemble pluripotent nuclei by amphibian oocyte extracts.Transient accumulation of 5-carboxylcytosine indicates involvement of active demethylation in lineage specification of neural stem cells.5-hydroxymethyl-cytosine enrichment of non-committed cells is not a universal feature of vertebrate development.
P50
Q26796680-B880075D-4F87-4D7E-8944-08243D122CBAQ34556223-1FCBF5CE-4AE6-4E08-88F2-09BC1A9D7171Q36448575-53F714AB-876E-4FFF-9D2F-92EC62A0F4CDQ37828007-4C016AE5-1FE3-4A0A-9802-3E8EC15860BFQ39038829-960EEF71-518D-4272-8905-0961FF862B6DQ39663796-0010E914-01C7-46C8-8AFF-FBFFD655E341Q39947050-26CFD4E9-DAF8-4FCA-AE24-17BBA4BB22C2Q40268196-10602A3F-2E65-44D2-A8C6-7B4D58B19793Q40484534-ACEE33E9-A019-4849-85E1-DD425183465DQ41810113-CC025302-12AD-4246-B1AA-1CDAD62E3F4DQ41822813-E5F1375B-158A-4F90-9BD2-FC4E87C07ED2Q41984930-708E9A32-26D7-4AD3-9F48-3038F97B9DE3Q42457295-D71734D9-3829-4275-9A0D-60A0247B621CQ42459839-6A5EEC13-56A9-422C-9A58-6D3D264DD85EQ42470297-2ECBAB68-678A-49F2-B6ED-D0F41E2FF98BQ45968908-2CA68580-65BB-4D7D-98EA-ADE06F92E5B8Q47806262-937C21A0-7E7C-4FB3-BA6F-00F025A965A2Q48746126-B2C79F6C-01C0-4B66-8C15-E344959BE4A6Q51803600-1F1C8D25-A622-4C7A-93D7-CC5D634BA7B9
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Andrew D Johnson
@ast
Andrew D Johnson
@en
Andrew D Johnson
@es
Andrew D Johnson
@nl
type
label
Andrew D Johnson
@ast
Andrew D Johnson
@en
Andrew D Johnson
@es
Andrew D Johnson
@nl
prefLabel
Andrew D Johnson
@ast
Andrew D Johnson
@en
Andrew D Johnson
@es
Andrew D Johnson
@nl
P106
P31
P496
0000-0002-5183-2072