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POU5F1B wt Allele
Known as:
OCT4-PG1
, POU Domain Transcription Factor OCT4-Pg1 Gene
, Octamer Binding Protein 3-Like Sequence Gene
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Human POU5F1B wild-type allele is located in the vicinity of 8q24.21 and is approximately 6 kb in length. This allele, which encodes putative POU…
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National Institutes of Health
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Related topics
Related topics
6 relations
Cell Differentiation process
Homo sapiens
POU5F1B gene
Pattern Formation
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Silencing the OCT4-PG1 pseudogene reduces OCT-4 protein levels and changes characteristics of the multidrug resistance phenotype in chronic myeloid leukemia
Aline Portantiolo Lettnin
,
E. F. Wagner
,
+5 authors
Ana Paula de Souza Votto
Molecular Biology Reports
2019
Corpus ID: 59603760
Cancer stem cells show epigenetic plasticity and intrinsic resistance to anti-cancer therapy, rendering capable of initiating…
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2014
2014
Clinical Significance of POU5F1P1 rs10505477 Polymorphism in Chinese Gastric Cancer Patients Receving Cisplatin-Based Chemotherapy after Surgical Resection
Lili Shen
,
Mulong Du
,
+11 authors
Zhengdong Zhang
International Journal of Molecular Sciences
2014
Corpus ID: 12233617
This study aimed to investigate the association between POU class5 homeobox 1 pseudogene 1 gene (POU5F1P1) rs10505477…
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Highly Cited
2009
Highly Cited
2009
POU5F1P1, a putative cancer susceptibility gene, is overexpressed in prostatic carcinoma
S. Kastler
,
Lisa Honold
,
+6 authors
Guenter Assum
The Prostate
2009
Corpus ID: 25200647
Association between genetic variants located on human chromosome 8q24.21 with an increased risk for prostatic carcinoma has been…
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Highly Cited
2008
Highly Cited
2008
The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1.
I. Panagopoulos
,
Emely Möller
,
A. Collin
,
F. Mertens
Oncology Report
2008
Corpus ID: 19448542
POU5F1, which encodes a transcriptional factor, has two alternatively spliced transcripts, 1 and 2, as well as six pseudogenes…
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Highly Cited
2004
Highly Cited
2004
Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.
C. Storlazzi
,
T. Fioretos
,
+7 authors
B. Johansson
Human Molecular Genetics
2004
Corpus ID: 13576017
Double minutes (dmin), the cytogenetic hallmark of genomic amplification, are found in approximately 1% of karyotypically…
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