Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
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A Mouse Model for Imprinting of the Human Retinoblastoma GeneEvolutionary origin and methylation status of human intronic CpG islands that are not present in mouse.Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.Genome-wide methylation analysis of retrocopy-associated CpG islands and their genomic environment.
P2860
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
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2013 nî lūn-bûn
@nan
2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年論文
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2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
@ast
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
@en
type
label
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
@ast
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
@en
prefLabel
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
@ast
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
@en
P2093
P2860
P1433
P1476
Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.
@en
P2093
Bernhard Horsthemke
Deniz Kanber
Dietmar Lohmann
Laura Steenpass
Michaela Hiber
P2860
P304
P356
10.1371/JOURNAL.PONE.0074159
P407
P577
2013-09-03T00:00:00Z