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<channel>
<title>Journal Articles</title>
<copyright>Copyright (c) 2013 Texas Medical Center Library All rights reserved.</copyright>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs</link>
<description>Recent documents in Journal Articles</description>
<language>en-us</language>
<lastBuildDate>Wed, 23 Jan 2013 22:28:22 PST</lastBuildDate>
<ttl>3600</ttl>








<item>
<title>Myositis ossificans circumscripta of the buccinator muscle: first report of a rare complication of mandibular third molar extraction.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/27</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/27</guid>
<pubDate>Wed, 15 Jun 2011 16:07:38 PDT</pubDate>
<description>
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</description>

<author>Raymond L Wiggins et al.</author>


<category>Adolescent</category>

<category>Facial Muscles</category>

<category>Humans</category>

<category>Male</category>

<category>Mandible</category>

<category>Molar, Third</category>

<category>Myositis Ossificans</category>

<category>Postoperative Complications</category>

<category>Tooth Extraction</category>

</item>






<item>
<title>Incidental detection of an occult oral malignancy with autofluorescence imaging: a case report.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/26</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/26</guid>
<pubDate>Wed, 15 Jun 2011 16:07:36 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Autofluorescence imaging is used widely for diagnostic evaluation of various epithelial malignancies. Cancerous lesions display loss of autofluorescence due to malignant changes in epithelium and subepithelial stroma. Carcinoma of unknown primary site presents with lymph node or distant metastasis, for which the site of primary tumour is not detectable. We describe here the use of autofluorescence imaging for detecting a clinically innocuous appearing occult malignancy of the palate which upon pathological examination was consistent with a metastatic squamous cell carcinoma.</p>
<p>CASE DESCRIPTION: A submucosal nodule was noted on the right posterior hard palate of a 59-year-old white female during clinical examination. Examination of this lesion using a multispectral oral cancer screening device revealed loss of autofluorescence at 405 nm illumination. An excisional biopsy of this nodule, confirmed the presence of a metastatic squamous cell carcinoma. Four years ago, this patient was diagnosed with metastatic squamous cell carcinoma of the right mid-jugular lymph node of unknown primary. She was treated with external beam irradiation and remained disease free until current presentation.</p>
<p>CONCLUSION: This case illustrates the important role played by autofluorescence tissue imaging in diagnosing a metastatic palatal tumour that appeared clinically innocuous and otherwise would not have been biopsied.</p>

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</description>

<author>Nadarajah Vigneswaran et al.</author>


<category>Carcinoma, Squamous Cell</category>

<category>Diagnosis, Differential</category>

<category>Female</category>

<category>Fluorescence</category>

<category>Humans</category>

<category>Lymphatic Metastasis</category>

<category>Middle Aged</category>

<category>Neoplasms, Unknown Primary</category>

<category>Palatal Neoplasms</category>

</item>






<item>
<title>Influence of blood contamination on bond strength of a self-etching system.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/25</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/25</guid>
<pubDate>Wed, 15 Jun 2011 16:07:35 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVES: To detect the influence of blood contamination (BC) on the bond strength (BS) of a self-etching bonding system (SES) to enamel and dentine.</p>
<p>METHODS: 25 human molars were longitudinally sectioned on the mesio-distal axis in order to obtain 50 specimens, which were embedded in acrylic resin. At first, the specimens were ground to expose a flat surface of enamel, and a bond strength test was performed. Afterwards, the samples were ground again in order to obtain a flat surface of dentine. Ten groups (total: n=100) were assigned according to substrate (enamel and dentine), step in the bonding sequence when contamination occurred (before the acidic primer and after the bonding resin), and contamination treatment (dry or rinse and dry procedure). Fresh human blood was introduced either before or after SES application (Clearfil SE Bond) and treated with air drying, or by rinsing and drying following application. Composite resin (Filtek Z-250,3M ESPE) was applied as inverted, truncated cured cones that were debonded in tension.</p>
<p>RESULTS: The mean tensile BS values (MPa) for enamel/dentine were 19.4/23.0 and 17.1/10.0 for rinse-and-dry treatment (contamination before and after SES, respectively); while the measurements for the dry treatment, 16.2/23.3 and 0.0/0.0 contamination before and after SES, respectively.</p>
<p>CONCLUSIONS: It was determined that blood contamination impaired adhesion to enamel and dentine when it occurred after bond light curing. Among the tested contamination treatments, the rinse-and-dry treatment produced the highest bond strength with BC after SES application, but it was not sufficient to recover the BS in the contamination-free group.</p>

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</description>

<author>Ellen Cristina de Carvalho Mendonça et al.</author>


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<item>
<title>MMP-9/TIMP-1 imbalance induced in human dendritic cells by Porphyromonas gingivalis.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/24</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/24</guid>
<pubDate>Wed, 15 Jun 2011 16:07:34 PDT</pubDate>
<description>
	<![CDATA[
	<p>Matrix metalloproteinase-9 (MMP-9) cleaves collagen, allowing leukocytes to traffic toward the vasculature and the lymphatics. When MMP-9 is unregulated by tissue inhibitor of metalloproteinase-1 (TIMP-1), this can lead to tissue destruction. Dendritic cells (DCs) infiltrate the oral mucosa increasingly in chronic periodontitis, characterized by infection with several pathogens including Porphyromonas gingivalis. In this study, human monocyte-derived DCs were pulsed with different doses of lipopolysaccharide of P. gingivalis 381 and of Escherichia coli type strain 25922, as well as whole live isogenic fimbriae-deficient mutant strains of P. gingivalis 381. Levels of induction of MMP-9 and TIMP-1, as well as interleukin-10 (IL-10), which reportedly inhibits MMP-9 induction, were measured by several approaches. Our results reveal that lipopolysaccharide of P. gingivalis, compared with lipopolysaccharide from E. coli type strain 25922, is a relatively potent inducer of MMP-9, but a weak inducer of TIMP-1, contributing to a high MMP-9/TIMP-1 ratio.Whole live P. gingivalis strain 381, major fimbriae mutant DPG-3 and double mutant MFB were potent inducers of MMP-9, but minor fimbriae mutant MFI was not. MMP-9 induction was inversely proportional to IL-10 induction. These results suggest that lipopolysaccharide and the minor and the major fimbriae of P. gingivalis may play distinct roles in induction by DCs of MMP-9, a potent mediator of local tissue destruction and leukocyte trafficking.</p>

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</description>

<author>Ravi Jotwani et al.</author>


<category>Cells, Cultured</category>

<category>Dendritic Cells</category>

<category>Escherichia coli</category>

<category>Humans</category>

<category>Interleukin-10</category>

<category>Lipopolysaccharides</category>

<category>Matrix Metalloproteinase 9</category>

<category>Monocytes</category>

<category>Porphyromonas gingivalis</category>

<category>Tissue Inhibitor of Metalloproteinase-1</category>

<category>Up-Regulation</category>

</item>






<item>
<title>The performance of human papillomavirus high-risk DNA testing in the screening and diagnostic settings.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/23</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/23</guid>
<pubDate>Wed, 15 Jun 2011 16:07:32 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVE: We sought to evaluate the performance of the human papillomavirus high-risk DNA test in patients 30 years and older.</p>
<p>MATERIALS AND METHODS: Screening (n=835) and diagnosis (n=518) groups were defined based on prior Papanicolaou smear results as part of a clinical trial for cervical cancer detection. We compared the Hybrid Capture II (HCII) test result with the worst histologic report. We used cervical intraepithelial neoplasia (CIN) 2/3 or worse as the reference of disease. We calculated sensitivities, specificities, positive and negative likelihood ratios (LR+ and LR-), receiver operating characteristic (ROC) curves, and areas under the ROC curves for the HCII test. We also considered alternative strategies, including Papanicolaou smear, a combination of Papanicolaou smear and the HCII test, a sequence of Papanicolaou smear followed by the HCII test, and a sequence of the HCII test followed by Papanicolaou smear.</p>
<p>RESULTS: For the screening group, the sensitivity was 0.69 and the specificity was 0.93; the area under the ROC curve was 0.81. The LR+ and LR- were 10.24 and 0.34, respectively. For the diagnosis group, the sensitivity was 0.88 and the specificity was 0.78; the area under the ROC curve was 0.83. The LR+ and LR- were 4.06 and 0.14, respectively. Sequential testing showed little or no improvement over the combination testing.</p>
<p>CONCLUSIONS: The HCII test in the screening group had a greater LR+ for the detection of CIN 2/3 or worse. HCII testing may be an additional screening tool for cervical cancer in women 30 years and older.</p>

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</description>

<author>Marylou Cárdenas-Turanzas et al.</author>


<category>Adult</category>

<category>DNA, Viral</category>

<category>Female</category>

<category>Humans</category>

<category>Mass Screening</category>

<category>Middle Aged</category>

<category>Papillomaviridae</category>

<category>Predictive Value of Tests</category>

<category>ROC Curve</category>

<category>Sensitivity and Specificity</category>

<category>Uterine Cervical Neoplasms</category>

<category>Vaginal Smears</category>

</item>






<item>
<title>Funding crisis in Title VII diversity programs.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/22</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/22</guid>
<pubDate>Wed, 15 Jun 2011 16:07:31 PDT</pubDate>
<description>
	<![CDATA[
	
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</description>

<author>Paula N O&apos;Neill et al.</author>


<category>Career Choice</category>

<category>Cultural Diversity</category>

<category>Financing, Government</category>

<category>Forecasting</category>

<category>Health Occupations</category>

<category>Humans</category>

<category>Minority Groups</category>

<category>Schools, Health Occupations</category>

<category>Training Support</category>

<category>United States</category>

<category>Vulnerable Populations</category>

</item>






<item>
<title>A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/21</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/21</guid>
<pubDate>Wed, 15 Jun 2011 16:07:29 PDT</pubDate>
<description>
	<![CDATA[
	<p>The molecular mechanisms controlling bone extracellular matrix (ECM) deposition by differentiated osteoblasts in postnatal life, called hereafter bone formation, are unknown. This contrasts with the growing knowledge about the genetic control of osteoblast differentiation during embryonic development. Cbfa1, a transcriptional activator of osteoblast differentiation during embryonic development, is also expressed in differentiated osteoblasts postnatally. The perinatal lethality occurring in Cbfa1-deficient mice has prevented so far the study of its function after birth. To determine if Cbfa1 plays a role during bone formation we generated transgenic mice overexpressing Cbfa1 DNA-binding domain (DeltaCbfa1) in differentiated osteoblasts only postnatally. DeltaCbfa1 has a higher affinity for DNA than Cbfa1 itself, has no transcriptional activity on its own, and can act in a dominant-negative manner in DNA cotransfection assays. DeltaCbfa1-expressing mice have a normal skeleton at birth but develop an osteopenic phenotype thereafter. Dynamic histomorphometric studies show that this phenotype is caused by a major decrease in the bone formation rate in the face of a normal number of osteoblasts thus indicating that once osteoblasts are differentiated Cbfa1 regulates their function. Molecular analyses reveal that the expression of the genes expressed in osteoblasts and encoding bone ECM proteins is nearly abolished in transgenic mice, and ex vivo assays demonstrated that DeltaCbfa1-expressing osteoblasts were less active than wild-type osteoblasts. We also show that Cbfa1 regulates positively the activity of its own promoter, which has the highest affinity Cbfa1-binding sites characterized. This study demonstrates that beyond its differentiation function Cbfa1 is the first transcriptional activator of bone formation identified to date and illustrates that developmentally important genes control physiological processes postnatally.</p>

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</description>

<author>P Ducy et al.</author>


<category>Amino Acid Sequence</category>

<category>Animals</category>

<category>Animals, Newborn</category>

<category>Base Sequence</category>

<category>Biological Evolution</category>

<category>Bone Development</category>

<category>Bone Diseases, Metabolic</category>

<category>COS Cells</category>

<category>Cell Differentiation</category>

<category>Core Binding Factor Alpha 1 Subunit</category>

<category>DNA, Complementary</category>

<category>Down-Regulation</category>

<category>Gene Expression</category>

<category>Humans</category>

<category>Mice</category>

<category>Mice, Transgenic</category>

<category>Molecular Sequence Data</category>

<category>Neoplasm Proteins</category>

<category>Osteoblasts</category>

<category>Phenotype</category>

<category>Transcription Factors</category>

<category>Transcriptional Activation</category>

</item>






<item>
<title>The future of dental education.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/20</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/20</guid>
<pubDate>Wed, 15 Jun 2011 16:07:28 PDT</pubDate>
<description>
	<![CDATA[
	
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</description>

<author>D L Allen</author>


<category>American Dental Association</category>

<category>Anesthesiology</category>

<category>Curriculum</category>

<category>Education, Dental</category>

<category>Forecasting</category>

<category>Humans</category>

<category>Specialties, Dental</category>

<category>United States</category>

</item>






<item>
<title>Identification and characterization of the herpes simplex virus type 2 gene encoding the essential capsid protein ICP32/VP19c.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/19</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/19</guid>
<pubDate>Wed, 15 Jun 2011 16:07:26 PDT</pubDate>
<description>
	<![CDATA[
	<p>We describe the characterization of the herpes simplex virus type 2 (HSV-2) gene encoding infected cell protein 32 (ICP32) and virion protein 19c (VP19c). We also demonstrate that the HSV-1 UL38/ORF.553 open reading frame (ORF), which has been shown to specify a viral protein essential for capsid formation (B. Pertuiset, M. Boccara, J. Cebrian, N. Berthelot, S. Chousterman, F. Puvian-Dutilleul, J. Sisman, and P. Sheldrick, J. Virol. 63: 2169-2179, 1989), must encode the cognate HSV type 1 (HSV-1) ICP32/VP19c protein. The region of the HSV-2 genome deduced to contain the gene specifying ICP32/VP19c was isolated and subcloned, and the nucleotide sequence of 2,158 base pairs of HSV-2 DNA mapping immediately upstream of the gene encoding the large subunit of the viral ribonucleotide reductase was determined. This region of the HSV-2 genome contains a large ORF capable of encoding two related 50,538- and 49,472-molecular-weight polypeptides. Direct evidence that this ORF encodes HSV-2 ICP32/VP19c was provided by immunoblotting experiments that utilized antisera directed against synthetic oligopeptides corresponding to internal portions of the predicted polypeptides encoded by the HSV-2 ORF or antisera directed against a TrpE/HSV-2 ORF fusion protein. The type-common immunoreactivity of the two antisera and comparison of the primary amino acid sequences of the predicted products of the HSV-2 ORF and the equivalent genomic region of HSV-1 provided evidence that the HSV-1 UL38 ORF encodes the HSV-1 ICP32/VP19c. Analysis of the expression of the HSV-1 and HSV-2 ICP32/VP19c cognate proteins indicated that there may be differences in their modes of synthesis. Comparison of the predicted structure of the HSV-2 ICP32/VP19c protein with the structures of related proteins encoded by other herpes viruses suggested that the internal capsid architecture of the herpes family of viruses varies substantially.</p>

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</description>

<author>S P Yei et al.</author>


<category>Amino Acid Sequence</category>

<category>Base Sequence</category>

<category>Capsid</category>

<category>Capsid Proteins</category>

<category>Cell Line</category>

<category>DNA Replication</category>

<category>DNA, Viral</category>

<category>Genes, Viral</category>

<category>Humans</category>

<category>Molecular Sequence Data</category>

<category>Peptides</category>

<category>Phosphonoacetic Acid</category>

<category>Protein Conformation</category>

<category>Restriction Mapping</category>

<category>Sequence Homology, Nucleic Acid</category>

<category>Simplexvirus</category>

<category>Viral Structural Proteins</category>

</item>






<item>
<title>In vitro staining effects of stannous fluoride and sodium fluoride on ceramic material.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/18</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/18</guid>
<pubDate>Thu, 29 Apr 2010 15:39:58 PDT</pubDate>
<description>
	<![CDATA[
	<p>STATEMENT OF PROBLEM: Long-term fluoride application on the teeth of patients receiving radiation therapy for head and neck tumors results in excessive staining and roughening of ceramic restorations. PURPOSE: The purpose of this in vitro study was to compare the staining effects of 2 fluoride treatments on ceramic disks by simulating 1 year of clinical exposure at 10 minutes per day. In addition, 2 different surface preparations were tested. MATERIAL AND METHODS: Eighty ceramic disks (IPS Empress), 20 x 2 mm, were fabricated. Half of the disks were glazed, and the remaining disks were polished. All disks were brushed for 3 minutes with a soft-bristle power toothbrush and mild dentifrice (baseline) and were immersed in 1 of the 2 fluoride products (0.4% SnF(2), Gel-Kam Gel, or 1.1% NaF, Prevident 5000) for 10 days (n=20). Means and standard deviations of color change (Delta E), surface roughness (Ra, um), and surface gloss (GU) of the ceramic material were measured with a reflection spectrophotometer, a profilometer, and a gloss meter, respectively, at baseline and after fluoride treatment. Two- and 3-way ANOVA (alpha=.05), with surface preparation (polished vs. glazed) and fluoride treatment (0.4% SnF(2) or 1.1% NaF) as independent variables and condition (baseline vs. after fluoride treatment) as a repeated measure, was used to analyze the data. Fisher's PLSD intervals (alpha=.05) were calculated for comparisons among the means. RESULTS: The polished specimens had significantly higher Delta E values, significantly higher surface gloss values, and significantly lower surface roughness values than the glazed specimens before fluoride treatment (P<.001). After both fluoride treatments, ceramic disks exhibited significantly higher surface roughness values when polished and significantly lower surface gloss values when glazed or polished (P<.001). The glazed specimens presented significantly higher surface roughness (P<.001) and lower surface gloss values (P<.001) when treated with 0.4% SnF(2) as compared to NaF. For the polished specimens, there was no significant difference in surface roughness and surface gloss values between the 2 fluoride treatments. CONCLUSIONS: Use of 0.4% SnF(2) and 1.1% NaF gels, in vitro, caused significant color change in the polished IPS Empress ceramic disks. Polishing of the ceramic surface before immersion in either fluoride agent caused the ceramic tested to be more resistant to etching by the 2 solutions tested. The NaF caused less deterioration of the porcelain surface and was less stain inducing than SnF(2).</p>

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</description>

<author>Ioli Ioanna Artopoulou et al.</author>


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<item>
<title>Comparative efficacy of 2 topical anesthetics for the placement of orthodontic temporary anchorage devices.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/17</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/17</guid>
<pubDate>Thu, 29 Apr 2010 15:39:56 PDT</pubDate>
<description>
	<![CDATA[
	<p>This study compared the effectiveness of topical benzocaine 20% versus a combination of lidocaine, tetracaine, and phenylephrine in providing sufficient analgesia for the placement of orthodontic temporary anchorage devices (TADs). The 2 topical anesthetics were tested against each other bilaterally using a randomized, double-blind, crossover design. The agents were left in place for the amount of time prescribed by the manufacturer. The TAD was then placed, and each subject rated the degree of pain on a Heft-Parker visual analogue scale. A pulse oximeter was used to record the preoperative and postoperative pulse rates. Statistically significant differences in perceived pain (P < .05) and success rate (P < .01) between drugs were seen, but no significant difference in pulse rate change between the topical anesthetics was observed (P > .05). It was concluded that when the efficacy of topical benzocaine and of a combination product was compared as the sole anesthetic to facilitate acceptable pain control for placement of orthodontic temporary anchorage devices, the combination product was considerably more efficacious.</p>

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</description>

<author>Derek S Reznik et al.</author>


<category>Adolescent</category>

<category>Adult</category>

<category>Aged</category>

<category>Anesthesia, Dental</category>

<category>Anesthetics, Combined</category>

<category>Anesthetics, Local</category>

<category>Benzocaine</category>

<category>Child</category>

<category>Cross-Over Studies</category>

<category>Double-Blind Method</category>

<category>Female</category>

<category>Heart Rate</category>

<category>Humans</category>

<category>Lidocaine</category>

<category>Male</category>

<category>Middle Aged</category>

<category>Orthodontic Anchorage Procedures</category>

<category>Orthodontic Appliances</category>

<category>Oximetry</category>

<category>Pain</category>

<category>Pain Measurement</category>

<category>Phenylephrine</category>

<category>Tetracaine</category>

<category>Time Factors</category>

<category>Vasoconstrictor Agents</category>

<category>Young Adult</category>

</item>






<item>
<title>Bond strength of adhesives to dentin contaminated with smoker&apos;s saliva.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/16</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/16</guid>
<pubDate>Thu, 29 Apr 2010 15:21:18 PDT</pubDate>
<description>
	<![CDATA[
	<p>The purpose of this study was to determine the effects of contamination with smoker's and non-smoker's saliva on the bond strength of resin composite to superficial dentin using different adhesive systems. The interfacial structure between the resin and dentin was evaluated for each treatment using environmental scanning electron microscopy (ESEM). Freshly extracted human molars were ground with 600-grit SiC paper to expose the superficial dentin. Adhesives [One-Up-Bond-F-Plus (OUFP) and Adper-Prompt-L-Pop (APLP)] and resin composite (TPHSpectrum) were bonded to the dentin (n = 8/group, 180 total specimens) under five surface conditions: control (adhesive applied following manufacturers' instructions); saliva, then 5-s air dry, then adhesive; adhesive, saliva, 5-s air dry; adhesive, saliva, 5-s water rinse, 5-s air dry (ASW group); and adhesive, saliva, 5-s water rinse, 5-s air dry, reapply adhesive (ASWA group). After storage in water at 37 degrees C for 24 h, the specimens were debonded under tension at a speed of 0.5 mm/min. ESEM photomicrographs of the dentin/adhesive interfaces were taken. Mean bond strength ranged from 8.1 to 24.1 MPa. Fisher's protected least significant difference (P = 0.05) intervals for critical adhesive, saliva, and surface condition differences were 1.3, 1.3, and 2.1 MPa, respectively. There were no significant differences in bond strength to dentin between contamination by smoker's and nonsmoker's saliva, but bond strengths were significantly different between adhesive systems, with OUFP twice as strong as APLP under almost all conditions. After adhesive application and contamination with either smoker's or nonsmoker's saliva followed by washing and reapplication of the adhesive (ASWA group), the bond strength of both adhesive systems was the same as that of the control group.</p>

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</description>

<author>Lilliam M Pinzon et al.</author>


</item>






<item>
<title>T-786C polymorphism of the endothelial nitric oxide synthase gene and neuralgia-inducing cavitational osteonecrosis of the jaws.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/15</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/15</guid>
<pubDate>Thu, 29 Apr 2010 15:17:39 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECTIVE: We hypothesized that, similar to idiopathic hip osteonecrosis, the T-786C mutation of the endothelial nitric oxide synthase (eNOS) gene affecting nitric oxide (NO) production was associated with neuralgia-inducing cavitational osteonecrosis of the jaws (NICO). DESIGN: In 22 NICO patients, not having taken bisphosphonates, mutations affecting NO production (eNOS T-786C, stromelysin 5A6A) were measured by polymerase chain reaction. Two healthy normal control subjects were matched per case by race and gender. RESULTS: Homozygosity for the mutant eNOS allele (TT) was present in 6 out of 22 patients (27%) with NICO compared with 0 out of 44 (0%) race and gender-matched control subjects; heterozygosity (TC) was present in 8 patients (36%) versus 15 control subjects (34%); and the wild-type normal genotype (CC) was present in 9 patients (36%) versus 29 controls (66%) (P = .0008). The mutant eNOS T-786C allele was more common in cases (20 out of 44 [45%]) than in control subjects (15 out of 88 [17%]) (P = .0005). The distribution of the stromelysin 5A6A genotype in cases did not differ from control subjects (P = .13). CONCLUSIONS: The eNOS T-786C polymorphism affecting NO production is associated with NICO, may contribute to the pathogenesis of NICO, and may open therapeutic medical approaches to treatment of NICO through provision of L-arginine, the amino-acid precursor of NO.</p>

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</description>

<author>Charles J Glueck et al.</author>


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<item>
<title>Collagenous Myofibroblastic Tumor of the Mandible: Case Report of a Unique Locally Aggressive Neoplasm Journal	Head and Neck Pathology</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/14</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/14</guid>
<pubDate>Thu, 14 Jan 2010 11:47:49 PST</pubDate>
<description>
	<![CDATA[
	<p>We report a locally aggressive collagenous myofibroblastic neoplasm of the mandible in an 18-year-old male. Clinically, the lesion presented with rapid growth and irregular mandibular bone destruction. Grossly, the tumor was 10 cm in greatest dimension, light-tan, firm, and involving the posterior one-thirds of the body and inferior half of the left mandibular ramus. Histologically, the lesion was composed of a loose spindle cell proliferation interspersed with periodic dense bands of collagen. The spindle cells reacted positively to smooth muscle actin, calponin, and focally to desmin and were negative for S-100, pan-cytokeratin, CD99, CD34 and caldesmon, supporting myofibroblastic derivation. At our 4 year follow-up, the patient remained free of local recurrence and surgery related complications. The clinicopathologic findings and the differential diagnosis of this lesion is presented and discussed.</p>

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</description>

<author>Jason W. Nash et al.</author>


</item>






<item>
<title>Shear bond strength of four different esthetic brackets.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/13</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/13</guid>
<pubDate>Thu, 04 Jun 2009 08:58:57 PDT</pubDate>
<description>
	<![CDATA[
	<p>Citation only</p>

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</description>

<author>Gustavo A. Salas et al.</author>


<category>Acid Etching, Dental</category>

<category>Animals</category>

<category>Cattle</category>

<category>Ceramics</category>

<category>Curing Lights, Dental</category>

<category>Dental Bonding</category>

<category>Dental Materials</category>

<category>Dental Stress Analysis</category>

<category>Esthetics, Dental</category>

<category>Materials Testing</category>

<category>Orthodontic Appliance Design</category>

<category>Orthodontic Brackets</category>

<category>Resin Cements</category>

<category>Shear Strength</category>

<category>Stress, Mechanical</category>

<category>Time Factors</category>

</item>






<item>
<title>GSTM1 and GSTT1 null polymorphisms and risk of salivary gland carcinoma.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/12</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/12</guid>
<pubDate>Thu, 04 Jun 2009 08:50:45 PDT</pubDate>
<description>
	<![CDATA[
	<p>Glutathione S-transferase (GST) genes detoxify and metabolize carcinogens, including oxygen free radicals which may contribute to salivary gland carcinogenesis. This cancer center-based case-control association study included 166 patients with incident salivary gland carcinoma (SGC) and 511 cancer-free controls. We performed multiplex polymerase chain reaction-based polymorphism genotyping assays for GSTM1 and GSTT1 null genotypes. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated with multivariable logistic regression analyses adjusted for age, sex, ethnicity, tobacco use, family history of cancer, alcohol use and radiation exposure. In our results, 27.7% of the SGC cases and 20.6% of the controls were null for the GSTT1 (P = 0.054), and 53.0% of the SGC cases and 50.9% of the controls were null for the GSTM1 (P = 0.633). The results of the adjusted multivariale regression analysis suggested that having GSTT1 null genotype was associated with a significantly increased risk for SGC (odds ratio 1.5, 95% confidence interval 1.0-2.3). Additionally, 13.9% of the SGC cases but only 8.4% of the controls were null for both genes and the results of the adjusted multivariable regression analysis suggested that having both null genotypes was significantly associated with an approximately 2-fold increased risk for SGC (odds ratio 1.9, 95% confidence interval 1.0-3.5). The presence of GSTT1 null genotype and the simultaneous presence of GSTM1 and GSTT1 null genotypes appear associated with significantly increased SGC risk. These findings warrant further study with larger sample sizes.</p>

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</description>

<author>Sayaka Kondo et al.</author>


</item>






<item>
<title>Persistent Productive Epstein‐Barr Virus Replication in Normal Epithelial Cells In Vivo</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/11</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/11</guid>
<pubDate>Mon, 04 May 2009 09:11:39 PDT</pubDate>
<description>
	<![CDATA[
	<p>Productive Epstein‐Barr virus (EBV) replication characterizes hairy leukoplakia, an oral epithelial lesion typically occurring in individuals infected with human immunodeficiency virus (HIV). Serial tongue biopsy specimens were obtained from HIV‐infected subjects before, during, and after valacyclovir treatment. EBV replication was detected by Southern hybridization to linear terminal EBV genome fragments, reverse‐transcriptase polymerase chain reaction amplification of EBV replicative gene transcripts, immunohistochemical detection of EBV replicative protein, and in situ hybridization to EBV DNA. EBV replication was detected in both hairy leukoplakia and normal tongue tissues. Valacyclovir treatment completely abrogated EBV replication in vivo, resulting in resolution of hairy leukoplakia when it was present. EBV replication returned in normal tongue epithelial cells after valacyclovir treatment. These data suggest that normal oral epithelium supports persistent EBV infection in individuals infected with HIV and that productive EBV replication is necessary but not sufficient for the pathogenesis of oral hairy leukoplakia.</p>

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</description>

<author>Dennis M. Walling et al.</author>


</item>






<item>
<title>Oral Pathology Report System: Improving an Existing Database System</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/10</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/10</guid>
<pubDate>Tue, 28 Apr 2009 15:46:35 PDT</pubDate>
<description>
	<![CDATA[
	
	]]>
</description>

<author>Yanko Michea et al.</author>


</item>






<item>
<title>Double-blind comparison of rectally administered diazepam to placebo for pediatric sedation: the cardiovascular response.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/9</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/9</guid>
<pubDate>Tue, 28 Apr 2009 15:46:34 PDT</pubDate>
<description>
	<![CDATA[
	<p>The sedative and cardiovascular effects of rectally administered diazepam (0.6 mg/kg) were compared to placebo in uncooperative children who required sedation during dental treatment. Twelve healthy preschool children, who required amalgam restorations, were treated during two standardized restorative appointments in a double-blind, crossover study. Blood pressure and pulse were obtained during four specified intervals during the appointment. The behavior of the children during the treatment visits was videotaped and later statistically analyzed using a kinesics/vocalization instrument. Behavioral ratings of cooperation were significantly improved during the treatment visit following diazepam. All interfering bodily movements, patient vocalizations and operator commands for the diazepam group were reduced significantly (p≤0.0001). No significant differences were observed for noninterfering behavioral response. Rectally administered diazepam did not alter blood pressure or pulse significantly in these sedated children when compared to the placebo. These findings indicate that rectal diazepam is an effective sedative agent with minimal effect on the cardiovascular system for the management of the young pediatric dental patient.</p>

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</description>

<author>Catherine M. Flaitz et al.</author>


<category>Anesthesia, Dental</category>

<category>Anesthesia, Rectal</category>

<category>Child, Preschool</category>

<category>Diazepam</category>

<category>Double-Blind Method</category>

<category>Heart</category>

<category>Hemodynamics</category>

<category>Humans</category>

<category>Placebos</category>

</item>






<item>
<title>Absolute quantitative real-time polymerase chain reaction for the measurement of human papillomavirus E7 mRNA in cervical cytobrush specimens.</title>
<link>http://digitalcommons.library.tmc.edu/uthdb_docs/8</link>
<guid isPermaLink="true">http://digitalcommons.library.tmc.edu/uthdb_docs/8</guid>
<pubDate>Tue, 28 Apr 2009 15:46:33 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Few reports of the utilization of an accurate, cost-effective means for measuring HPV oncogene transcripts have been published. Several papers have reported the use of relative quantitation or more expensive Taqman methods. Here, we report a method of absolute quantitative real-time PCR utilizing SYBR-green fluorescence for the measurement of HPV E7 expression in cervical cytobrush specimens. RESULTS: The construction of a standard curve based on the serial dilution of an E7-containing plasmid was the key for being able to accurately compare measurements between cervical samples. The assay was highly reproducible with an overall coefficient of variation of 10.4%. CONCLUSION: The use of highly reproducible and accurate SYBR-based real-time polymerase chain reaction (PCR) assays instead of performing Taqman-type assays allows low-cost, high-throughput analysis of viral mRNA expression. The development of such assays will help in refining the current screening programs for HPV-related carcinomas.</p>

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</description>

<author>Michael E. Scheurer et al.</author>


</item>





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