Business Litigation Personal Injury Medical Malpractice Premises Liability Automobile Accidents Truck Accidents Motorcycle Accidents Products Liability Professional Liability Nursing Home Negligence Estate Litigation Trust Litigation Civil Litigation Commercial Litigation Real Estate Litigation Admiralty and Maritime Law Property Disputes Automobile Injuries Automobile Wrecks Motor Vehicle Injuries
Memberships:
Carteret County Bar; North Carolina Bar Association (Board of Governors, 1978-1981, Member of Sections on Litigation, Health, and Antitrust); American Bar Association (Member of Sections on Litigation and Antitrust); North Carolina Advocates for Justice (Member of Sections on Professional Negligence and Auto Torts).
ISLN:
902269970
Admitted:
1964
University:
Guilford College, B.A., with high honors, 1964
Law School:
Wake Forest University, J.D., with honors, 1964
Links:
Site
Biography:
Certification, AV Rated. Member, Guilford Scholarship Society. Research Assistant, North Carolina Supreme Court, 1964-1965.
Business Litigation Personal Injury Medical Malpractice Premises Liability
Memberships:
Carteret County Bar North Carolina Bar Association (Board of Governors, 1978-1981, Member of Sections on Litigation, Health, and Antitrust) American Bar Association (Member of Sections on Litigation and Antitrust) North Carolina Advocates for Justice (Member of Sections on Professional Negligence and Auto Torts).
ISLN:
902269970
Admitted:
1964, North Carolina 1965, U.S. District Court, Eastern and Middle Districts of North Carolina 1966, U.S. Court of Appeals, Fourth Circuit
University:
Guilford College, B.A., with high honors, 1964
Law School:
Wake Forest University, J.D., with honors, 1964
Links:
Site
Biography:
Certification, AV Rated. Member, Guilford Scholarship Society. Research Assistant, North Carolina Supreme Court, 1964-1965.
Wake Forest University School of Law Degree - JD - Juris Doctor - Law Graduated - 1964 Guilford College Degree - AB Graduated - 1964
Specialties:
Personal Injury - 25% Defective / Dangerous Products - 25% Business - 25% Litigation - 25%
Associations:
North Carolina Bar Association - Board of Governors, 1978-1981 American Bar Association, Antitrust Law Section - Member American Bar Association, Litigation Section - Member Carteret County Bar Association - Member North Carolina Academy of Trial Lawyers - Member North Carolina Bar Association, Antitrust and Trade Regulation Law Section - Member North Carolina Bar Association, Health Law Section - Member North Carolina Bar Association, Litigation Section - Member
Name / Title
Company / Classification
Phones & Addresses
912 Arendell St, Morehead City, NC 28557
Edward L. Murrelle President
Davis, Murrelle & Lyles PA General Practice Attorney Specializing In Personal Injuries and Trial Practice
Joseph Louie MCCLAY - Richmond VA, US Barbara K. ZEDLER - Richmond VA, US Edward Lenn MURRELLE - Midlothian VA, US Edwin J.C.G. VAN DEN OORD - Richmond VA, US Thomas O'CONNELL - Raleigh NC, US Daniel ADKINS - Richmond VA, US
International Classification:
G01N 24/08
US Classification:
424600, 2524081, 514169, 514653, 514304, 73 6141
Abstract:
Chronic obstructive pulmonary disease (COPD), characterized by chronic airflow limitation, is a serious and growing public health concern. The major environmental risk factor for COPD is cigarette smoking, but the biological mechanisms underlying COPD are not well understood. Herein, proton nuclear magnetic resonance (H-NMR) spectroscopy is used in methods to identify metabolites and biomarkers associated with lung function in COPD.
Jason FLORA - Richmond VA, US Barbara K. Zedler - Richmond VA, US Edward Lenn Murrelle - Midlothian VA, US Mark Leppert - Salt Lake City UT, US Edwin J.C.G. van den Oord - Richmond VA, US Bradley Todd Webb - Richmond VA, US Timothy York - Richmond VA, US Gaurav S. J. B. Rana - Richmond VA, US Jeffrey S. Edmiston - Mechanicsville VA, US Willie J. McKinney - Richmond VA, US
International Classification:
G01N 33/68
US Classification:
424600, 435 23, 506 18, 514179
Abstract:
Cigarette smoking is a primary determinant of chronic obstructive pulmonary disease (COPD), which is the fourth leading cause of morbidity and mortality in the United States. Unique proteins associated with COPD capable of differentiating subjects likely to experience rapid (RPD) or slow (SLW) decline in lung function have been identified using comprehensive high-throughput proteomic approaches. Thirty peptides, which mapped to 21 unique proteins, were linearly associated with annualized rates of lung function decline among smokers with COPD characterized as having rapid or slow decline and smokers without COPD. Using three different statistical approaches to assess the data, the RPD and SLW groups are differentiated by 55 peptides, which mapped to 33 unique proteins. A number of the identified peptides are proteolytic fragments of proteins that are involved in the complement and/or coagulation systems, have anti-protease activity, or metabolic functions.
Risk Factors Of Cigarette Smoke-Induced Spirometric Phenotypes
Bradley Todd WEBB - Richmond VA, US Barbara K. Zedler - Richmond VA, US Edward Lenn Murrelle - Midlothian VA, US Mark Leppert - Salt Lake City UT, US Edwin J. C. G. Van Den Oord - Richmond VA, US Daniel E. Adkins - Richmond VA, US Willie J. McKinney - Richmond VA, US
International Classification:
C12Q 1/68
US Classification:
506 2, 506 16, 506 38
Abstract:
The technology provided herein relates to the SNPs identified as described herein, both singly and in combination, as well as to the use of these SNPs, and others in linkage disequilibrium with these SNPs, for diagnosis, prediction of clinical course, and/or treatment response for pulmonary disease such as COPD, development of new treatments for pulmonary disease such as COPD based upon comparison of the variant and normal versions of the gene or gene product, and development of cell-culture based and animal models for research and treatment of pulmonary disease such as COPD. The technology provided herein further relates to novel compounds, pharmaceutical compositions, and kits for use in the diagnosis, treatment, and evaluation of such disorders.
Edward L. Murrelle - Midlothian VA, US Barbara K. Zedler - Richmond VA, US Andrew R. Joyce - Richmond VA, US Edwin J.C.G. van den Oord - Richmond VA, US Tapas K. Sengupta - Springfield VA, US Hailong Meng - New York NY, US Daniel E. Adkins - Richmond VA, US
International Classification:
C12Q 1/68
US Classification:
506 9, 506 16
Abstract:
Biomarkers of lung disease are provided. The biomarkers comprise target genomic DNA sequences having one or more CpG dinucleotides that are differentially methylated in genomic DNA of subjects having lung disease as compared to normal subjects or subjects not having lung disease. In one exemplary embodiment, methylation status profiles of 71 CpG sites mapping to 67 unique genes are significantly associated with at least one of three lung function decline measures associated with lung disease. Other biomarkers significantly associated with cigarette smoking-related lung function decline, with age-related lung function decline, and with the intensifying effects of cigarette smoking on lung function decline with age are also provided.
Jeffery S. Edmiston - Mechanicsville VA, US Barbara K. Zedler - Richmond VA, US Edward Lenn Murrelle - Midlothian VA, US Mark Leppert - Salt Lake City UT, US Kellie J. Archer - Richmond VA, US Mariano J. Scian - Charlottesville VA, US
International Classification:
C12Q 1/68
US Classification:
506 9, 506 17, 506 39
Abstract:
Described herein are a group of 1,013 genes and 1 phenotypic variable are identified as candidate predictors that differentiated smokers (current or former) with or without COPD. The full predictor set can be reduced to a nine-gene classifier (IL6R, CCR2, PPP2CB, RASSF2, WTAP, DNTTIP2, GDAP1, LIPE, and RPL14) with similar performance. Also described herein is the use of the full predictor set and the reduced nine gene set in methods of diagnosing lung disease or an increased risk of developing lung disease, such as COPD, in a subject. Also described herein is the use of the full predictor set and the reduced nine gene set in methods of providing a prognosis for a subject with lung disease, such as COPD.
Risk Factors Of Cigarette Smoke-Induced Spriometric Phenotypes
- Salt Lake City UT, US Barbara K. Zedler - Richmond VA, US Edward Lenn Murrelle - Midlothian VA, US Mark Leppert - Salt Lake City UT, US Edwin J. C. G. van den Oord - Richmond VA, US Daniel E. Adkins - Richmond VA, US Willie J. McKinney - Richmond VA, US
International Classification:
C12Q 1/68 G01N 33/574
Abstract:
The technology provided herein relates to the SNPs identified as described herein, both singly and in combination, as well as to the use of these SNPs, and others in linkage disequilibrium with these SNPs, for diagnosis, prediction of clinical course, and/or treatment response for pulmonary disease such as COPD, development of new treatments for pulmonary disease such as COPD based upon comparison of the variant and normal versions of the gene or gene product, and development of cell-culture based and animal models for research and treatment of pulmonary disease such as COPD. The technology provided herein further relates to novel compounds, pharmaceutical compositions, and kits for use in the diagnosis, treatment, and evaluation of such disorders.
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