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491 citation(s) found for "Owen, B A".

Bence Jones Cryoglobulinuria: Characterization of a Urinary κ Light Chain Cryoglobulin
Jaleel, Abdul , Owen, Barbara, Katzmann, Jerry A., Kyle, Robert A. , Abraham, Roshini S. , Manske, Michelle K.

Clinical Chemistry | June 23, 2006 | Volume: 52 | Issue: 7 | Pages: 1435-1436

10.1373/clinchem.2006.066753 | PMID 16798972 Get It

Hirudin as a molecular probe for thrombin in vitro and during systemic coagulation in the pig.
Zoldhelyi, Pierre, Chesebro, James H., Owen, Whyte G.

Proceedings of the National Academy of Sciences | May 31, 2006 | Volume: 90 | Issue: 5 | Pages: 1819-1823

10.1073/pnas.90.5.1819 | PMID 8446595 Get It

The amount of thrombin active in vivo in the intravascular space (blood and endothelial surface), both basally and in experimental intravascular coagulation, is measured by way of the accessibility of thrombin to intravascular hirudin. Blood samples from pigs given intravenous 125I-labeled hirudin contain 125I-labeled hirudin-thrombin complex in concentrations indicative of a basal thrombin concentration in vivo of 0.5 nmol/liter. Intravenous infusion of Salmonella endotoxin elicits an increase in the circulating concentration of hirudin-thrombin complex that begins within 15 min and is 20-30 times basal after 4 hr. Induction of mild intravascular coagulation is evidenced by a modest reduction in plasma fibrinogen concentrations. It is concluded that there is a basal pool of hirudin-accessible thrombin in the intravascular space that, were it free in the plasma phase, would be sufficient in principle to sustain intravascular coagulation.
Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population
Toft, Mathias , Pielsticker, Liza K., Ross, Owen A. , Aasly, Jan , Farrer, Matthew J. , Ross, Owen A , Toft, Mathias

Neurology | February 13, 2006 | Volume: 66 | Issue: 3 | Pages: 415-417

10.1212/01.wnl.0000196492.80676.7c | PMID 16476943 Get It

Systemic Correction of a Fatty Acid Oxidation Defect by Intramuscular Injection of a Recombinant Adeno-Associated Virus Vector
Conlon, Thomas J. , Walter, Glenn A. , Owen, Renius , Cossette, Travis , Erger, Kirsten, Gutierrez, Gregory M. , Matern, Dietrich , Vockley, Jerry , Flotte, Terence R. , Goetzman, Eric S.

Human Gene Therapy | January 12, 2006 | Volume: 17 | Issue: 1 | Pages: 71-80

10.1089/hum.2006.17.71 | PMID 16409126 Get It

Phase I Clinical and Pharmacokinetic Study of Flavopiridol in Children With Refractory Solid Tumors: A Children's Oncology Group Study
Whitlock, James A. , Krailo, Mark , Ruben, Stacie, Ames, Matthew M. , Owen, William F. , Reaman, Gregory H. , Reid, Joel M.

Journal of Clinical Oncology | December 17, 2005 | Volume: 23 | Issue: 36 | Pages: 9179-9186

10.1200/jco.2004.01.0660 | PMID 16361620 Get It

Purpose To determine the dose-limiting toxicities, maximum-tolerated dose, and pharmacokinetics of the cyclin-dependent kinase inhibitor flavopiridol (NSC 649890) when administered as a 1-hour infusion over 3 consecutive days to children with recurrent or refractory solid tumors. Patients and Methods Flavopiridol was administered as a 1-hour intravenous infusion daily for 3 consecutive days every 21 days, or when hematologic toxicity or any grade 2 or greater nonhematologic toxicity resolved. The starting dose was 37.5 mg/m2/d. Dose escalation was in cohorts of three patients in a standard fashion until dose-limiting toxicity and the maximum-tolerated dose were determined. Flavopiridol levels were measured on days 1, 2, and 3. Results Twenty-five children received flavopiridol at doses of 37.5 to 80 mg/m2/day over 3 consecutive days. The maximum-tolerated dose was 62.5 mg/m2/d. The primary dose-limiting toxicities were neutropenia and diarrhea. No antitumor effect was observed in this population. Mean peak plasma concentrations of 3.71 and 9.11 μmol/L were achieved at the end of the 1-hour infusion, following dose escalation from 37.5 mg/m2 to 80 mg/m2, respectively. The median flavopiridol plasma clearance was 8.0 L/h/m2 (range, 2.6 to 17.1 L/h/m2). Conclusion The maximum-tolerated dose of flavopiridol in children, and the recommended phase II dose for pediatric studies, was 62.5 mg/m2/day when administered as a 1-hour infusion for 3 consecutive days. Dose-limiting toxicities of neutropenia and diarrhea were similar to those in adult studies.
Pathophysiology, pleotrophy and paradigm shifts: genetic lessons from Parkinson's disease
Ross, Owen A. , Farrer, Matthew J. , Ross, Owen A

Biochemical Society Transactions | August 3, 2005 | Volume: 33 | Issue: 4 | Pages: 586-590

10.1042/bst0330586 | PMID 16042550 Get It

PD (Parkinson's disease) is an aetiologically heterogeneous disorder characterized by a clinical phenotype consisting of resting tremor, rigidity and bradykinesia. Motor symptoms are associated with a progressive loss of dopaminergic neurons, with Lewy body inclusions within surviving neurons. Although heritability studies have shown evidence of familial aggregation, twin studies have provided limited support for a genetic aetiology. Nevertheless, classical linkage methods have nominated 11 regions of the genome and pathogenic mutations have been identified in several genes, including α-synuclein, parkin, ubiquitin C-ter-minal hydrolase L1, oncogene DJ-1, PTEN-induced protein kinase 1 and microtubule-associated protein tau. Most recently, heterozygous mutations in LRRK2 (leucine-rich repeat kinase 2) were found to cause late-onset, autosomal-dominant PD. Despite their consistent clinical phenotype, family members with LRRK2 mutations can have variable α-synuclein and tau pathologies. Lrrk2 is a member of the Roc (Ras of complex proteins) family, with Ras GTPase and MAPKKK (mitogen-activated protein kinase kinase kinase) catalytic domains. Thus its discovery highlights vesicle dynamics and secondary-messenger signalling in disease pathophysiology. To diagnose a disease accurately and effectively treat it, requires an understanding of its molecular pathogenesis. Herein, we provide an overview of the genetics of PD, how these discoveries are revolutionizing long-held beliefs and more importantly how this knowledge may be translated into patient therapy.
Factors Contributing to Individual Propensity for Arterial Thrombosis
Karnicki, Krzysztof, Owen, Whyte G., Miller, Randall S., McBane, Robert D. , McBane, Robert

Arteriosclerosis, Thrombosis, and Vascular Biology | September 13, 2002 | Volume: 22 | Issue: 9 | Pages: 1495-1499

10.1161/01.atv.0000029968.34056.94 | PMID 12231572 Get It

Objective— Occurrence of arterial thrombosis secondary to vascular disease in an individual is not easily predicted. After establishing that this poor predictability arises at least in part from an intrinsic thrombosis propensity of the individual, we sought to determine whether the propensity for arterial thrombosis is governed by blood or arterial wall factors. Methods and Results— To evaluate the variability arising from the blood, autologous 111 In-labeled platelet deposition was measured after high-shear perfusion of compressed aortic strips, prepared from a single pig, with heparinized blood from 25 pigs. To evaluate the variability arising from the vessel wall, aortic strips from 8 pigs were superfused with blood from a single animal. Blood samples from 25 animals superfused over aortic substrate from a single source yielded a 24-fold range of platelet deposition. In contrast, when aortic substrates from 8 different animals were superfused with blood from a single animal, platelet deposition spanned a 3-fold range. Platelet deposition was significantly correlated with whole-blood lymphocyte counts and with platelet counts . Conclusions— Individual propensity for arterial thrombosis in pigs is more greatly influenced by blood components than by elements within the arterial wall.
Influence of Anatomical Location on Arterial Thrombosis
Karnicki, Krzysztof, Komorowicz, Erzsébet , Fass, David N., Owen, Whyte G., McBane, Robert D. , McBane, Robert

Arteriosclerosis, Thrombosis, and Vascular Biology | July 28, 2002 | Volume: 22 | Issue: 2 | Pages: 342-347

10.1161/hq0202.103999 | PMID 11834539 Get It

Atherosclerosis manifests as a systemic disease with near global involvement of the named segments of the arterial tree. Acute thrombotic arterial occlusion, however, is not equally distributed. To evaluate intra-individual regional differences in arterial thrombogenicity, we compared 111 In-platelet deposition in porcine carotid and femoral arteries after a standardized crush injury. Within the unidirectional flow conditions of elastic carotid arteries, platelet deposition was more than 3-fold higher compared with predominantly muscular femoral arteries with triphasic arterial flow. To determine the influence of rheology on platelet deposition after crush injury, carotid arteries were transplanted into the femoral position and compared with the paired native carotid and femoral arteries. Similarly, femoral arteries transposed to the carotid position were compared with the paired native carotid artery. In each of these experiments, arterial transposition to a new anatomic location imparts a predilection for platelet deposition indigenous to the new location. In the controlled environment of two high-shear thrombin–independent and –dependent flow chambers, porcine carotid and femoral arterial substrates were indistinguishable from one another with respect to platelet deposition. Regional differences in arterial hemodynamics may account for substantial differences in thrombosis arising from deep arterial injury.
Susceptibility Locus for Alzheimer's Disease on Chromosome 10
Holmans, Peter , Marshall, Helen, Kwon, Jennifer M. , Meyer, David , Ramic, Dzanan, Shears, Shantia, DeVriéze, Fabienne Wavrant, Hamshere, Marian L. , Abraham, Richard, Tunstall, Nigel, Rice, Frances , Carty, Stephanie, Lillystone, Sara, Kehoe, Patrick G. , Rudrasingham, Varuni, Jones, Lesley , Lovestone, Simon , Pérez‐Tur, Jordi , Williams, Julie , Hardy, John , Goate, Alison , Myers, Amanda , Booth, Jeremy , Crook, Richard , Owen, Michael J. , Hardy, John , Goate, Alison M

Science | July 27, 2002 | Volume: 290 | Issue: 5500 | Pages: 2304-2305

10.1126/science.290.5500.2304 | PMID 11125144 Get It

The apolipoprotein E ( APOE ) gene is the only genetic risk factor that has so far been linked to risk for late-onset Alzheimer's disease (LOAD). However, 50 percent of Alzheimer's disease cases do not carry an APOE4 allele, suggesting that other risk factors must exist. We performed a two-stage genome-wide screen in sibling pairs with LOAD to detect other susceptibility loci. Here we report evidence for an Alzheimer's disease locus on chromosome 10. Our stage one multipoint lod score (logarithm of the odds ratio for linkage/no linkage) of 2.48 (266 sibling pairs) increased to 3.83 in stage 2 (429 sibling pairs) close to D10S1225 (79 centimorgans). This locus modifies risk for Alzheimer's disease independent of APOE genotype.
Physical Evidence that Yeast Frataxin Is an Iron Storage Protein
Gakh, Oleksandr , Gacy, A. Marquis, Twesten, Ray D., Owen, Whyte G., Isaya, Grazia , Adamec, Jiří

Biochemistry | July 26, 2002 | Volume: 41 | Issue: 21 | Pages: 6798-6804

10.1021/bi025566+ | PMID 12022884 Get It