HOXB13 is co-localized with androgen receptor to suppress androgen-stimulated prostate-specific antigen expression - Wikidata - wikimedia - TriplyDB

HOXB13 is co-localized with androgen receptor to suppress androgen-stimulated prostate-specific antigen expression

HOXB13 is co-localized with androgen receptor to suppress androgen-stimulated prostate-specific antigen expression

http://www.wikidata.org/entity/Q34517352

about

Getting personal with prostate cancer: adding new pieces to an incomplete jigsaw puzzle.Dysregulation of the homeobox transcription factor gene HOXB13: role in prostate cancer.Dose-dependent effects of small-molecule antagonists on the genomic landscape of androgen receptor binding.HOX genes and their role in the development of human cancers.Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer.HOXB13 overexpression is an independent predictor of early PSA recurrence in prostate cancer treated by radical prostatectomy Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients HOXB13 mutations in a population-based, case-control study of prostate cancer.HOXB13 mutation and prostate cancer: studies of siblings and aggressive disease The role of HOX genes in head and neck squamous cell carcinoma.c-Myc Antagonises the Transcriptional Activity of the Androgen Receptor in Prostate Cancer Affecting Key Gene Networks.Oncogenic mechanisms of HOXB13 missense mutations in prostate carcinogenesis.HOXB13 downregulates intracellular zinc and increases NF-κB signaling to promote prostate cancer metastasis.Confirmation of the HOXB13 G84E germline mutation in familial prostate cancer.Endogenous androgen receptor proteomic profiling reveals genomic subcomplex involved in prostate tumorigenesis.Prevalence of the HOXB13 G84E germline mutation in British men and correlation with prostate cancer risk, tumour characteristics and clinical outcomes.Wedelolactone inhibits adipogenesis through the ERK pathway in human adipose tissue-derived mesenchymal stem cells.Do HOXB13 and P63 have a role in differentiating poorly differentiated prostatic carcinoma from urothelial high-grade carcinoma?HOXB13 as an immunohistochemical marker of prostatic origin in metastatic tumors.

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HOXB13 is co-localized with androgen receptor to suppress androgen-stimulated prostate-specific antigen expression

http://www.wikidata.org/entity/Q34517352

description

2010 nî lūn-bûn

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2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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HOXB13 is co-localized with an ...... te-specific antigen expression

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ACB.2010.43.4.284

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Anatomy & cell biology

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Baik Youn Kim

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Chaeyong Jung

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Choon Sang Bae

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In-Je Kim

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Kyu Youn Ahn

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Ra-Young Park

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Sin Do Kim

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Sung Sik Park

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Taek Won Kang

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Young-Rang Kim

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P2860

HOXA5 regulates expression of the progesterone receptor

Compromised HOXA5 function can limit p53 expression in human breast tumours

The HOX homeodomain proteins block CBP histone acetyltransferase activity

AbdB-like Hox proteins stabilize DNA binding by the Meis1 homeodomain proteins

CBP and histone deacetylase inhibition enhance the transactivation potential of the HOXB7 homeodomain-containing protein

Specificity of HOX protein function depends on DNA-protein and protein-protein interactions, both mediated by the homeo domain

HOXB13 homeodomain protein suppresses the growth of prostate cancer cells by the negative regulation of T-cell factor 4

Hoxb-13: a new Hox gene in a distant region of the HOXB cluster maintains colinearity

HOXB13 induces growth suppression of prostate cancer cells as a repressor of hormone-activated androgen receptor signaling

Hoxb13 mutations cause overgrowth of caudal spinal cord and tail vertebrae

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284-293

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