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7716 citation(s) found for "Ma, Daniel".

Two Different Molecular Defects in the Tva Receptor Gene Explain the Resistance of TwotvarLines of Chickens to Infection by Subgroup A Avian Sarcoma and Leukosis Viruses
Melder, Deborah C., Trejbalová, Kateřina , Federspiel, Mark J. , Elleder, Daniel , Svoboda, Jan

Journal of Virology | November 24, 2004 | Volume: 78 | Issue: 24 | Pages: 13489-13500

10.1128/jvi.78.24.13489-13500.2004 | PMID 15564460 Get It

ABSTRACTThe subgroup A to E avian sarcoma and leukosis viruses (ASLVs) are highly related and are thought to have evolved from a common ancestor. These viruses use distinct cell surface proteins as receptors to gain entry into avian cells. Chickens have evolved resistance to infection by the ASLVs. We have identified the mutations responsible for the block to virus entry in chicken lines resistant to infection by subgroup A ASLVs [ASLV(A)]. Thetvagenetic locus determines the susceptibility of chicken cells to ASLV(A) viruses. In quail, the ASLV(A) susceptibility alleletvasencodes two forms of the Tva receptor; these proteins are translated from alternatively spliced mRNAs. The normal cellular function of the Tva receptor is unknown; however, the extracellular domain contains a 40-amino-acid, cysteine-rich region that is homologous to the ligand binding region of the low-density lipoprotein receptor (LDLR) proteins. The chickentvascDNAs had not yet been fully characterized; we cloned the chickentvacDNAs from two lines of subgroup A-susceptible chickens, line H6 and line 0. Two types of chickentvascDNAs were obtained. These cDNAs encode a longer and shorter form of the Tva receptor homologous to the Tva forms in quail. Two different defects were identified in cDNAs cloned from two different ASLV(A)-resistant inbred chickens, line C and line 72. Line Ctvarcontains a single base pair substitution, resulting in a cysteine-to-tryptophan change in the LDLR-like region of Tva. This mutation drastically reduces the binding affinity of TvaRfor the ASLV(A) envelope glycoproteins. Line 72tvar2contains a 4-bp insertion in exon 1 that causes a change in the reading frame, which blocks expression of the Tva receptor.
Increasing Access to Clinical Cancer Trials and Emerging Technologies for Minority Populations: The Native American Project
Petereit, Daniel G. , Rogers, Deborah, Govern, Frank S., Coleman, Norman, Osburn, Christen H., Howard, Steve , Kaur, Judith S. , Burhansstipanov, Linda , Fowler, C. Jack F., Mehta, Minesh P. , Chappell, Richard J. , Mehta, Minesh P

Journal of Clinical Oncology | November 12, 2004 | Volume: 22 | Issue: 22 | Pages: 4452-4455

10.1200/jco.2004.01.119 | PMID 15542797 Get It

Erosion of Endogenous Testosterone-Driven Negative Feedback on Pulsatile Luteinizing Hormone Secretion in Healthy Aging Men
Veldhuis, Johannes D. , Keenan, Daniel M., Iranmanesh, Ali

The Journal of Clinical Endocrinology & Metabolism | November 5, 2004 | Volume: 89 | Issue: 11 | Pages: 5753-5761

10.1210/jc.2004-0399 | PMID 15531539 Get It

Abstract The present study tests the intuition that successful aging in men is marked by: 1) impaired feedforward by endogenous LH concentrations (con) of testosterone (Te) secretion (sec); and/or 2) attenuated feedback by unmanipulated Te con of LH sec. The goal was to assess both implicit linkages analytically without disrupting normal pathway coupling. This strategy required: 1) assay of paired LH and Te con sampled every 10 min for 24 h in 13 older (O) (ages 60–78 yr) and 13 young (Y) (ages 18–30 yr) men; 2) deconvolution-based estimation of LH and Te sec rates; 3) lag-specific cross-correlation analyses of the relationships between LH and Te con and sec; and 4) statistical contrasts by age stratum. Salient outcomes were: 1) O and Y men maintain comparable LH con drive of Te sec, viz maximal r = +0.51 and r = +0.52, respectively, at an optimal time lag of 50 min (both P < 0.001 against random LH and Te associations); 2) elderly subjects exhibit reduced Te con inhibition of LH sec [minimal r = −0.008 (O) vs. r = −0.10 (Y), P < 0.01 at a time lag of 40 min]; 3) mean (24-h) LH con do not differ by age; and 4) molar Te/sex hormone-binding globulin con are lower in the elderly than in Y individuals (P < 0.01). In conclusion, noninvasive analyses predict that attenuation of endogenous Te feedback restraint on the hypothalamo-pituitary unit may be an early biological marker of adaptive changes in the GnRH-LH-Te ensemble axis in the healthy O male.
Medical Costs and Quality of Life 10 to 12 Years After Randomization to Angioplasty or Bypass Surgery for Multivessel Coronary Artery Disease
Hlatky, Mark A. , Boothroyd, Derek , Melsop, Kathryn , Brooks, Maria M. , Mark, Daniel B. , Pitt, Bertram, Reeder, Guy S., Rogers, William J. , Ryan, Thomas J. , Whitlow, Patrick L., Wiens, Robert D., Mark, Daniel B

Circulation | September 28, 2004 | Volume: 110 | Issue: 14 | Pages: 1960-1966

10.1161/01.cir.0000143379.26342.5c | PMID 15451795 Get It

Background— Coronary bypass surgery (CABG) and angioplasty (PTCA) have been compared in several randomized trials, but data about long-term economic and quality-of-life outcomes are limited. Methods and Results— Cost and quality-of-life data were collected prospectively from 934 patients who were randomized in the Bypass Angioplasty Revascularization Investigation (BARI) and followed up for 10 to12 years. CABG had 53% higher costs initially, but the gap closed to <5% during the first 2 years; after 12 years, the mean cumulative cost of CABG patients was $123 000 versus $120 750 for PTCA, yielding a cost-effectiveness ratio of $14 300/life-year added. CABG patients experienced significantly greater improvement in their physical functioning for the first 3 years but not in later follow-up. Recurrent angina substantially reduced all quality-of-life measures throughout follow-up. Cumulative costs were significantly higher among patients with diabetes, heart failure, and comorbid conditions and among women; costs also were increased by angina, by the number of revascularization procedures, and among patients who died. Conclusion— Early differences between CABG and PTCA in costs and quality of life were no longer significant at 10 to 12 years of follow-up. CABG was cost-effective as compared with PTCA for multivessel disease.
CD4+ T Cell Depletion during all Stages of HIV Disease Occurs Predominantly in the Gastrointestinal Tract
Brenchley, Jason M. , Schacker, Timothy W. , Ruff, Laura E., Price, David A. , Taylor, Jodie H., Beilman, Gregory J. , Nguyen, Phuong L., Khoruts, Alexander , Larson, Matthew , Haase, Ashley T. , Douek, Daniel C.

The Journal of Experimental Medicine | September 13, 2004 | Volume: 200 | Issue: 6 | Pages: 749-759

10.1084/jem.20040874 | PMID 15365096 Get It

The mechanisms underlying CD4+ T cell depletion in human immunodeficiency virus (HIV) infection are not well understood. Comparative studies of lymphoid tissues, where the vast majority of T cells reside, and peripheral blood can potentially illuminate the pathogenesis of HIV-associated disease. Here, we studied the effect of HIV infection on the activation and depletion of defined subsets of CD4+ and CD8+ T cells in the blood, gastrointestinal (GI) tract, and lymph node (LN). We also measured HIV-specific T cell frequencies in LNs and blood, and LN collagen deposition to define architectural changes associated with chronic inflammation. The major findings to emerge are the following: the GI tract has the most substantial CD4+ T cell depletion at all stages of HIV disease; this depletion occurs preferentially within CCR5+ CD4+ T cells; HIV-associated immune activation results in abnormal accumulation of effector-type T cells within LNs; HIV-specific T cells in LNs do not account for all effector T cells; and T cell activation in LNs is associated with abnormal collagen deposition. Taken together, these findings define the nature and extent of CD4+ T cell depletion in lymphoid tissue and point to mechanisms of profound depletion of specific T cell subsets related to elimination of CCR5+ CD4+ T cell targets and disruption of T cell homeostasis that accompanies chronic immune activation.
Dual Secretagogue Drive of Burst-Like Growth Hormone Secretion in Postmenopausal Compared with Premenopausal Women Studied under an Experimental Estradiol Clamp
Erickson, Dana , Keenan, Daniel M., Mielke, Kristi L., Bradford, Kandace, Bowers, Cyril Y., Miles, John M., Veldhuis, Johannes D. , Miles, John M.

The Journal of Clinical Endocrinology & Metabolism | September 7, 2004 | Volume: 89 | Issue: 9 | Pages: 4746-4754

10.1210/jc.2004-0424 | PMID 15356089 Get It

Normative Sexual Behavior in Children: A Contemporary Sample
Friedrich, William N., Fisher, Jennifer, Broughton, Daniel D., Houston, Margaret S., Shafran, Constance R.

Pediatrics | August 13, 2004 | Volume: 101 | Issue: 4 | Pages: e9-e9

10.1542/peds.101.4.e9 | PMID 9521975 Get It

Objective. Sexual behavior in children can cause uncertainty in the clinician because of the relationship between sexual abuse and sexual behavior. Consequently, it is important to understand normative childhood sexual behavior. Design. Sexual behavior in 1114 2- to 12-year-old children was rated by primary female caregivers. These children were screened for the absence of sexual abuse. A 38-item scale assessing a broad range of sexual behavior (Child Sexual Behavior Inventory, Third Version) was administered along with the Child Behavior Checklist and a questionnaire assessing family stress, family sexuality, social maturity of the child, maternal attitudes regarding child sexuality, and hours in day care. Results. Sexual behavior was related to the child's age, maternal education, family sexuality, family stress, family violence, and hours/week in day care. Frequencies of sexual behaviors for 2- to 5-, 6- to 9-, and 10- to 12-year-old boys and girls are presented. Conclusions. A broad range of sexual behaviors are exhibited by children who there is no reason to believe have been sexually abused. Their relative frequency is similar to two earlier studies, and this reinforces the validity of these results.
Linkage Disequilibrium Testing When Linkage Phase Is Unknown
Schaid, Daniel J.

Genetics | August 2, 2004 | Volume: 166 | Issue: 1 | Pages: 505-512

10.1534/genetics.166.1.505 | PMID 15020439 Get It

Abstract Linkage disequilibrium, the nonrandom association of alleles from different loci, can provide valuable information on the structure of haplotypes in the human genome and is often the basis for evaluating the association of genomic variation with human traits among unrelated subjects. But, linkage phase of genetic markers measured on unrelated subjects is typically unknown, and so measurement of linkage disequilibrium, and testing whether it differs significantly from the null value of zero, requires statistical methods that can account for the ambiguity of unobserved haplotypes. A common method to test whether linkage disequilibrium differs significantly from zero is the likelihood-ratio statistic, which assumes Hardy-Weinberg equilibrium of the marker phenotype proportions. We show, by simulations, that this approach can be grossly biased, with either extremely conservative or liberal type I error rates. In contrast, we use simulations to show that a composite statistic, proposed by Weir and Cockerham, maintains the correct type I error rates, and, when comparisons are appropriate, has similar power as the likelihood-ratio statistic. We extend the composite statistic to allow for more than two alleles per locus, providing a global composite statistic, which is a strong competitor to the usual likelihood-ratio statistic.
Hemangioblastoma of the Optic Nerve
Kerr, Daniel J., Scheithauer, Bernd W., Miller, Gary M. , Ebersold, Michael J., McPhee, Thomas J.

Neurosurgery | July 30, 2004 | Volume: 36 | Issue: 3 | Pages: 573-581

10.1097/00006123-199503000-00017 Get It

Management of Intracranial Infectious Aneurysms: A Series of 16 Cases
Phuong, Loi K., Link, Michael J. , Barrow, Daniel L. , Wijdicks, Eelco F. M. , Barrow, Daniel L

Neurosurgery | July 30, 2004 | Volume: 51 | Issue: 5 | Pages: 1145-1152

10.1097/00006123-200211000-00008 | PMID 12383359 Get It

Abstract OBJECTIVE The purpose of this study was to better define the management of intracranial infectious aneurysms. METHODS We present a retrospective review of the management of 16 patients with intracranial infectious aneurysms. The mean follow-up period was 86 months. RESULTS None of the patients had a rehemorrhage during antibiotic treatment. The mortality and long-term outcome from ruptured intracranial infectious aneurysms may be better than previously thought. There was no significant difference in long-term outcome between patients with single or multiple infectious aneurysms or between patients who underwent surgical resection and those who were treated only with antibiotics. CONCLUSION Operative treatment should be pursued for patients with ruptured infectious aneurysms. Patients with unruptured intracranial infectious aneurysms should be observed during antibiotic therapy and followed up with cerebral angiography. Surgical resection should be considered if the aneurysm enlarges and the patient's general medical condition allows general anesthesia to be tolerated.