Mark R Gray
Overview
Explore the profile of Mark R Gray including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
130
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Recent Articles
1.
Smith A, Gray M, Del Campo S, Shlapak D, Ganeshan B, Zhang X, et al.
AJR Am J Roentgenol
. 2015 Aug;
205(3):W283-93.
PMID: 26295664
Objective: The purpose of this study was to use CT texture analysis to predict overall survival (OS) in patients with metastatic melanoma and stable disease (SD) according to the Response...
2.
Gray M, Del Campo S, Zhang X, Zhang H, Souza F, Carson 3rd W, et al.
Radiology
. 2013 Sep;
270(2):425-34.
PMID: 24072776
Purpose: To predict survival in patients with metastatic melanoma by evaluating a combination of serum lactate dehydrogenase (LDH) level and initial computed tomographic (CT) findings of tumor devascularization after antiangiogenic...
3.
Wiesman K, Wei L, Baughman C, Russo J, Gray M, Castellot J
J Cell Commun Signal
. 2010 Jun;
4(2):91-8.
PMID: 20531984
CCN5, a member of the CCN family of growth factors, inhibits the proliferation and migration of smooth muscle cells in cell culture and animal models. Expressed in both embryonic and...
4.
Gray M, Malmquist J, Sullivan M, Blea M, Castellot Jr J
J Cell Commun Signal
. 2008 May;
1(2):145-58.
PMID: 18481204
CCN5 is a secreted heparin- and estrogen-regulated matricellular protein that inhibits vertebrate smooth muscle cell proliferation and motility. CCN5 is expressed throughout murine embryonic development in most organs and tissues....
5.
Jones J, Gray M, Oliveira B, Koch M, Castellot Jr J
J Cell Commun Signal
. 2008 May;
1(2):127-43.
PMID: 18481203
The six proteins of the CCN family have important roles in development, angiogenesis, cell motility, proliferation, and other fundamental cell processes. To date, CCN5 distribution in developing rodents and humans...
6.
Lalwani S, Wu H, Reindollar R, Gray M
Fertil Steril
. 2007 May;
89(2):325-30.
PMID: 17482600
Objective: To analyze the HOXA10 genes in CAUV patients for mutations. Congenital absence of the uterus and vagina (CAUV) is the most extreme female reproductive tract developmental defect known. The...
7.
Laprise S, Gray M
Gene
. 2007 Feb;
391(1-2):45-52.
PMID: 17276628
Several approaches are used to survey genomic DNA methylation patterns, including Southern blot, PCR, and microarray strategies. All of these methods are based on the use of methylation-sensitive isoschizomer restriction...
8.
Ryley D, Wu H, Leader B, Zimon A, Reindollar R, Gray M
Fertil Steril
. 2005 May;
83(5):1363-71.
PMID: 15866570
Objective: Formin-2 (Fmn2) mutant mice produce oocytes with meiosis I arrest. Our aim was to describe the human FORMIN-2 (FMN2) gene and to identify DNA sequence polymorphisms in patients with...
9.
Timmreck L, Gray M, Handelin B, Allito B, Rohlfs E, Davis A, et al.
Am J Med Genet A
. 2003 Jun;
120A(1):72-6.
PMID: 12794695
The relationship between cystic fibrosis transmembrane conductance regulator gene (CFTR) mutations and congenital absence of the uterus and vagina (CAUV) was examined. CFTR mutations have previously been associated with congenital...