Anne R Greenlee
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Explore the profile of Anne R Greenlee including associated specialties, affiliations and a list of published articles.
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19
Citations
386
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Recent Articles
1.
Chakraborty P, Buaas F, Sharma M, Smith B, Greenlee A, Eacker S, et al.
Mol Endocrinol
. 2014 May;
28(7):1055-72.
PMID: 24825397
Sertoli cell tight junctions (SCTJs) of the seminiferous epithelium create a specialized microenvironment in the testis to aid differentiation of spermatocytes and spermatids from spermatogonial stem cells. SCTJs must be...
2.
Greenlee A, Shiao M, Snyder E, Buaas F, Gu T, Stearns T, et al.
PLoS One
. 2012 Oct;
7(10):e46359.
PMID: 23056286
MicroRNAs (miRNAs) are a class of endogenous, non-coding RNAs that mediate post-transcriptional gene silencing by inhibiting mRNA translation and promoting mRNA decay. DICER1, an RNase III endonuclease encoded by Dicer1,...
3.
Zhao Y, Liu H, Li Y, Wu J, Greenlee A, Yang C, et al.
Toxicol Lett
. 2011 Jul;
205(3):320-6.
PMID: 21726609
Growing evidence indicates that the alteration of microRNA (miRNA) expression in tumors that is induced by chemical carcinogens plays an important role in tumor development and progression. However, the mechanism...
4.
Meng J, Greenlee A, Taub C, Braun R
Biol Reprod
. 2011 May;
85(2):254-60.
PMID: 21543771
In the mammalian testis, meiotic and postmeiotic germ cell antigens are granted immune privilege. Both local immune suppression and specialized intercellular junctions between somatic Sertoli cells have been proposed to...
5.
Yang Q, Jie Z, Cao H, Greenlee A, Yang C, Zou F, et al.
Carcinogenesis
. 2011 Feb;
32(5):713-22.
PMID: 21349817
Gastric cancer is the fourth most common cancer and the second leading cause of cancer mortality worldwide but the underlying molecular mechanism is not entirely clear. The objective of this...
6.
Jiang Y, Wu Y, Greenlee A, Wu J, Han Z, Li X, et al.
Toxicol Sci
. 2010 Oct;
119(1):50-60.
PMID: 20889678
microRNAs (miRNAs) are an abundant class of small noncoding RNAs that function primarily as oncogenes and tumor suppressors by mediating translational repression or mRNA degradation via binding target genes. In...
7.
Liu L, Jiang Y, Zhang H, Greenlee A, Yu R, Yang Q
Toxicol In Vitro
. 2010 Feb;
24(4):1168-75.
PMID: 20170724
MicroRNAs (miRNAs) are small non-coding RNA molecules that negatively control the expression of target genes post-transcriptionally. In this study, transformed human bronchial epithelial cells induced by anti-benzo[a]pyrene-7,8-diol-9,10-epoxide were characterized for...
8.
Liu L, Jiang Y, Zhang H, Greenlee A, Han Z
Life Sci
. 2009 Dec;
86(5-6):192-8.
PMID: 20006626
Aims: We investigated the functionality of miR-494 in anti-benzo(a)pyrene-trans-7,8-dihydrodiol-9,10-epoxide (anti-BPDE)-transformed human bronchial epithelial cell 16HBE to reveal its potential target coding-gene. Main Methods: The expression of mature miR-494 in cells...
9.
Shen Y, Jiang Y, Greenlee A, Zhou L, Liu L
Biomed Environ Sci
. 2009 May;
22(1):14-21.
PMID: 19462682
Objective: To screen miRNA profiles of malignantly transformed human bronchial epithelial cells, 16HBE-T, induced by anti-benzo[a]pyrene-trans-7,8-diol-9,10-epoxide (anti-BPDE), and to analyze putative miR-10a targets in 16HBE-T. Methods: A novel microarray platform...
10.
Jiang Y, Fu J, Greenlee A, Shen Y, Duan H, Chen X
Toxicol In Vitro
. 2008 Nov;
23(1):53-9.
PMID: 18992321
Anti-benzo[a]pyrene-7,8-diol-9,10-epoxide (anti-BPDE) is a metabolite of benzo[a]pyrene (B[a]P) and acts as a potent mutagen in mammalian systems. However, the molecular mechanisms related to anti-BPDE-induced carcinogenesis are poorly understood. We have...