Gene expression meta-analysis supports existence of molecular apocrine breast cancer with a role for androgen receptor and implies interactions with ErbB family
about
Prolactin-induced protein mediates cell invasion and regulates integrin signaling in estrogen receptor-negative breast cancerPhase II trial of bicalutamide in patients with androgen receptor-positive, estrogen receptor-negative metastatic Breast CancerLarge-scale integration of microarray data reveals genes and pathways common to multiple cancer typesIntegration of VDR genome wide binding and GWAS genetic variation data reveals co-occurrence of VDR and NF-κB binding that is linked to immune phenotypes.Importance of Breast Cancer Subtype in the Development of Androgen Receptor Directed Therapy.Asymmetric microarray data produces gene lists highly predictive of research literature on multiple cancer types.Identification of a novel luminal molecular subtype of breast cancer.Gross cystic disease fluid protein 15 (GCDFP-15) expression in breast cancer subtypesFABP7 and HMGCS2 are novel protein markers for apocrine differentiation categorizing apocrine carcinoma of the breast.A feedback loop between androgen receptor and ERK signaling in estrogen receptor-negative breast cancer.Mutational profiles in triple-negative breast cancer defined by ultradeep multigene sequencing show high rates of PI3K pathway alterations and clinically relevant entity subgroup specific differences.Androgen receptor driven transcription in molecular apocrine breast cancer is mediated by FoxA1.Synergy between inhibitors of androgen receptor and MEK has therapeutic implications in estrogen receptor-negative breast cancer.Comprehensive literature review and statistical considerations for microarray meta-analysisMinireview: The androgen receptor in breast tissues: growth inhibitor, tumor suppressor, oncogene?An "elite hacker": breast tumors exploit the normal microenvironment program to instruct their progression and biological diversity.AR Signaling in Breast Cancer.Benign and malignant apocrine lesions of the breast.Molecular and diagnostic features of apocrine breast lesions.Coexpression of androgen receptor and FOXA1 in nonmetastatic triple-negative breast cancer: ancillary study from PACS08 trial.Targeting the androgen receptor in triple-negative breast cancer.Heat shock protein 27 and gross cystic disease fluid protein 15 play critical roles in molecular apocrine breast cancer.Androgen receptor-positive, triple-negative breast cancer.Androgen receptor expression is significantly associated with better outcomes in estrogen receptor-positive breast cancers.
P2860
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P2860
Gene expression meta-analysis supports existence of molecular apocrine breast cancer with a role for androgen receptor and implies interactions with ErbB family
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Gene expression meta-analysis ...... interactions with ErbB family
@ast
Gene expression meta-analysis ...... interactions with ErbB family
@en
Gene expression meta-analysis ...... interactions with ErbB family
@nl
type
label
Gene expression meta-analysis ...... interactions with ErbB family
@ast
Gene expression meta-analysis ...... interactions with ErbB family
@en
Gene expression meta-analysis ...... interactions with ErbB family
@nl
prefLabel
Gene expression meta-analysis ...... interactions with ErbB family
@ast
Gene expression meta-analysis ...... interactions with ErbB family
@en
Gene expression meta-analysis ...... interactions with ErbB family
@nl
P2093
P2860
P356
P1433
P1476
Gene expression meta-analysis ...... interactions with ErbB family
@en
P2093
Bradley M Broom
Mary E Edgerton
Sandeep Sanga
Vittorio Cristini
P2860
P2888
P356
10.1186/1755-8794-2-59
P407
P577
2009-09-11T00:00:00Z
P5875
P6179
1038849240