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of 5
pro vyhledávání: '"Alex J. Carlisle"'
Autor:
Peter J. Munson, James I. Hudson, Abdel G. Elkahloun, Jeffrey M. Trent, Lance A. Liotta, David B. Krizman, Vinay V. Prabhu, W. Marston Linehan, Alex J. Carlisle, Michael R. Emmert-Buck, Elizabeth D. Williams
Publikováno v:
Molecular Carcinogenesis. 28:12-22
A cDNA microarray comprising 5184 different cDNAs spotted onto nylon membrane filters was developed for prostate gene expression studies. The clones used for arraying were identified by cluster analysis of > 35 000 prostate cDNA library‐derived exp
Autor:
Cynthia Winter, Eric F. Rappaport, John M. Maris, Deepa Khazi, Alex J. Carlisle, Marci Laudenslager, Yael P. Mosse
To the Editor: We read with interest the study by Trochet and colleagues (2004), published in the April 2004 issue of The American Journal of Human Genetics, that described germline mutations of the paired-like homeobox 2B gene (PHOX2B [MIM 603851])
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77b64b12dc23c0ad688c3122e0bb53a7
https://europepmc.org/articles/PMC1182065/
https://europepmc.org/articles/PMC1182065/
Publikováno v:
Cancer Research. 73:2108-2108
Purpose: We have previously demonstrated that CXCR4 is widely but heterogeneously expressed in neuroblastoma cells and that the selective CXCR4 drug Plerixafor has preclinical efficacy for reducing growth of ectopic neuroblastomas in mice. Despite th
Autor:
Jayanti Jagannathan, Qun Wang, Daniel Martinez, Huaqing Zhao, Alex J. Carlisle, Kristina A. Cole, Bruce Pawal, Rosalind Y Carlisle, John M. Maris, Christopher A. Lyttle, Nhu Nguyen
Publikováno v:
Cancer Research. 72:5566-5566
ABSTRACT Purpose: Recent evidence suggests that expression of CXCR4 is associated with the growth and progression of neuroblastoma. The purpose of this study was to determine the value of CXCR4 as in independent predictive biomarker and evaluate its
Publikováno v:
Molecular Cancer
Molecular Cancer, Vol 8, Iss 1, p 126 (2009)
Molecular Cancer, Vol 8, Iss 1, p 126 (2009)
BackgroundCXCR4, the receptor for the chemokine stromal-derived factor 1 (SDF-1), has been shown to mediate many of the processes essential for cancer progression such as tumor cell proliferation, metastasis, and angiogenesis. To understand the role