Phage display screening reveals an association between germline-specific transcription factor Oct-4 and multiple cellular proteins
about
Association of chromatin proteins high mobility group box (HMGB) 1 and HMGB2 with mitotic chromosomesBorna disease virus phosphoprotein represses p53-mediated transcriptional activity by interference with HMGB1Upregulation of HMG1 leads to melanoma inhibitory activity expression in malignant melanoma cells and contributes to their malignancy phenotypeUse of altered-specificity binding Oct-4 suggests an absence of pluripotent cell-specific cofactor usageHigh mobility group protein 1: A collaborator in nucleosome dynamics and estrogen-responsive gene expressionMénage à Trois in stress: DAMPs, redox and autophagyHMGB1 interacts with many apparently unrelated proteins by recognizing short amino acid sequencesOct4 interaction with Hmgb2 regulates Akt signaling and pluripotencySelecting open reading frames from DNAMicroarray profiling of phage-display selections for rapid mapping of transcription factor-DNA interactions.Oct-4 controls cell-cycle progression of embryonic stem cells.Silencing BRE expression in human umbilical cord perivascular (HUCPV) progenitor cells accelerates osteogenic and chondrogenic differentiation.Live-cell imaging reveals multiple interactions between Epstein-Barr virus nuclear antigen 1 and cellular chromatin during interphase and mitosisNucleosome dynamics: HMGB1 relaxes canonical nucleosome structure to facilitate estrogen receptor binding.Cooperative recruitment of HMGB1 during V(D)J recombination through interactions with RAG1 and DNA.Quantitative proteomics analysis demonstrates post-transcriptional regulation of embryonic stem cell differentiation to hematopoiesis.Mechanism of high-mobility group protein B enhancement of progesterone receptor sequence-specific DNA binding.Phenotypic complementation establishes requirements for specific POU domain and generic transactivation function of Oct-3/4 in embryonic stem cells.The human OCT-4 isoforms differ in their ability to confer self-renewal.The reprogramming factor nuclear receptor subfamily 5, group A, member 2 cannot replace octamer-binding transcription factor 4 function in the self-renewal of embryonic stem cells.
P2860
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P2860
Phage display screening reveals an association between germline-specific transcription factor Oct-4 and multiple cellular proteins
description
2000 nî lūn-bûn
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2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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Phage display screening reveal ...... and multiple cellular proteins
@ast
Phage display screening reveal ...... and multiple cellular proteins
@en
Phage display screening reveal ...... and multiple cellular proteins
@en-gb
Phage display screening reveal ...... and multiple cellular proteins
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label
Phage display screening reveal ...... and multiple cellular proteins
@ast
Phage display screening reveal ...... and multiple cellular proteins
@en
Phage display screening reveal ...... and multiple cellular proteins
@en-gb
Phage display screening reveal ...... and multiple cellular proteins
@nl
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Phage display screening reveal ...... and multiple cellular proteins
@ast
Phage display screening reveal ...... and multiple cellular proteins
@en
Phage display screening reveal ...... and multiple cellular proteins
@en-gb
Phage display screening reveal ...... and multiple cellular proteins
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P2093
P356
P1476
Phage display screening reveal ...... and multiple cellular proteins
@en
P2093
C Butteroni
H R Schöler
M De Felici
P304
P356
10.1006/JMBI.2000.4238
P407
P577
2000-12-08T00:00:00Z