1132 Stagecoach Trl, San Marcos, TX 78666 • 512 667-7199
Name / Title
Company / Classification
Phones & Addresses
William Olson Assistant Professional And Interim Chair
Wagner College Colleges, Universities, and Professional Scho...
1 Campus Rd, Staten Island, NY 10301
William Dirk Olson
OLSON HOLDINGS LLC
William D Olson
NOSLO GROUP, LLC
William D Olson Treasurer
SAWTOOTH, INC
William Olson Chief
New Mexico Department of Health Noncommercial Research Organization · Administrative Public Health Programs Ret Drugs/Sundries · Administrative Public Health Programs · General Government · Health Services · Death Birth Records & Health Statistics · Specialty Outpatient Clinic Administrative Public Health Programs
William Olson MD 3400 Dexter Ct STE 118, Davenport, IA 52807 563 344-8333 (phone), 563 344-8334 (fax)
Education:
Medical School University of Illinois, Chicago College of Medicine Graduated: 2000
Procedures:
Appendectomy Endoscopic Retrograde Cholangiopancreatography (ERCP) Laparoscopic Gallbladder Removal Proctosigmoidoscopy Small Bowel Resection Varicose Vein Procedures Bariatric Surgery Breast Biopsy Colonoscopy Destruction of Lesions on the Anus Hemorrhoid Procedures Hernia Repair Laparoscopic Appendectomy Mastectomy Pilonidal Cyst Excision Skin Tags Removal Spleen Surgey Thyroid Gland Removal Tracheostomy Upper Gastrointestinal Endoscopy Vasectomy
Conditions:
Appendicitis Intestinal Obstruction Abdominal Hernia Benign Neoplasm of Breast Breast Disorders
Languages:
English Spanish
Description:
Dr. Olson graduated from the University of Illinois, Chicago College of Medicine in 2000. He works in Davenport, IA and specializes in General Surgery. Dr. Olson is affiliated with Genesis Medical Center Silvis, Trinity Medical Center Moline and Unitypoint Health Trinity.
Brown & Associates Medical Laboratories 2525 W Delfort St STE 120, Houston, TX 77054 713 741-6677 (phone), 713 748-5860 (fax)
Education:
Medical School University of Illinois, Chicago College of Medicine Graduated: 1972
Languages:
English
Description:
Dr. Olson graduated from the University of Illinois, Chicago College of Medicine in 1972. He works in Houston, TX and specializes in Anatomic Pathology & Clinical Pathology. Dr. Olson is affiliated with Memorial Hermann Katy Hospital, Memorial Hermann Sugar Land Hospital, Oak Bend Medical Center and Park Plaza Hospital.
Customer Service Microsoft Word Strategic Planning Research Manufacturing Microsoft Office Negotiation Microsoft Excel Sales Management Powerpoint Team Building Engineering
Tatjana Dragic - Scarsdale NY William C. Olson - Ossining NY
Assignee:
Progenics Pharmaceuticals, Inc. - Tarrytown NY Aaron Diamond AIDS Research Centre - New York NY
International Classification:
A61K 3804
US Classification:
530328, 530324, 530325, 530326, 530327
Abstract:
This invention provides a compound comprising the structure: YDINYYTSE wherein each T represents a threonine, each S represents a serine, each E represents a glutamic acid, each Y represents a tyrosine; each D represents an aspartic acid, each I represents an isoleucine; and each N represents an asparagine; wherein represents from 0 to 9 amino acids, with the proviso that if there are more than 2 amino acids, they are joined by peptide bonds in consecutive order and have a sequence identical to the sequence set forth in SEQ ID NO: 1 beginning with the I at position 9 and extending therefrom in the amino terminal direction; wherein represents from 0 to 13 amino acids, with the proviso that if there are more than 2 amino acids, they are joined by peptide bonds in consecutive order and have a sequence identical to the sequence set forth in SEQ ID NO: 1 beginning with the P at position 19 and extending therefrom in the carboxy terminal direction; wherein represents an amino group or an acetylated amino group; wherein represents a carboxyl group or an amidated carboxyl group; wherein all of , Y,D,I,N,Y,Y,T,S,E and are joined together by peptide bonds; further provided that at least two tyrosines in the compound are sulfated.
Stabilized Viral Envelope Proteins And Uses Thereof
James M. Binley - Brooklyn NY Norbert Schuelke - New City NY William C. Olson - Ossining NY Paul J. Maddon - Scarsdale NY John P. Moore - New York NY
Assignee:
Progenics Pharmaceuticals, Inc. - Tarrytown NY Aaron Diamond AIDS Research Centre (ADARC) - New York NY
International Classification:
C07H 2104
US Classification:
536 2372, 4241881, 4242081
Abstract:
This invention provides an isolated nucleic acid which comprises a nucleotide segment having a sequence encoding a viral envelope protein comprising a viral surface protein and a corresponding viral transmembrane protein wherein the viral envelope protein contains one or more mutations in amino acid sequence that enhance the stability of the complex formed between the viral surface protein and transmembrane protein. This invention also provides a viral envelope protein comprising a viral surface protein and a corresponding viral transmembrane protein wherein the viral envelope protein contains one or more mutations in amino acid sequence that enhance the stability of the complex formed between the viral surface protein and transmembrane protein. This invention further provides methods of treating HIV-1 infection.
This invention provides a compound comprising the structure: θαYDINYYTSEβλ wherein each T represents a threonine, each S represents a serine, each E represents a glutamic acid, each Y represents a tyrosine; each D represents an aspartic acid, each I represents an isoleucine; and each N represents an asparagine; wherein α represents from 0 to 9 amino acids, with the proviso that if there are more than 2 amino acids, they are joined by peptide bonds in consecutive order and have a sequence identical to the sequence set forth in SEQ ID NO: 1 beginning with the I at position 9 and extending therefrom in the amino terminal direction; wherein β represents from 0 to 13 amino acids, with the proviso that if there are more than 2 amino acids, they are joined by peptide bonds in consecutive order and have a sequence identical to the sequence set forth in SEQ ID NO: 1 beginning with the P at position 19 and extending therefrom in the carboxy terminal direction; wherein θ represents an amino group or an acetylated amino group; wherein λ represents a carboxyl group or an amidated carboxyl group; wherein all of α,Y,D,I,N,Y,Y,T,S,E and β are joined together by peptide bonds; further provided that at least two tyrosines in the compound are sulfated.
Stabilized Viral Envelope Proteins And Uses Thereof
James M. Binley - Brooklyn NY, US Norbert Schuelke - New City NY, US William C. Olson - Ossining NY, US Paul J. Maddon - Scarsdale NY, US John P. Moore - New York NY, US
Assignee:
Progenics Pharmaceuticals, Inc. - Tarrytown NY
International Classification:
A61K 39/21
US Classification:
4241881, 4242081
Abstract:
This invention provides an isolated nucleic acid which comprises a nucleotide segment having a sequence encoding a viral envelope protein comprising a viral surface protein and a corresponding viral transmembrane protein wherein the viral envelope protein contains one or more mutations in amino acid sequence that enhance the stability of the complex formed between the viral surface protein and transmembrane protein. This invention also provides a viral envelope protein comprising a viral surface protein and a corresponding viral transmembrane protein wherein the viral envelope protein contains one or more mutations in amino acid sequence that enhance the stability of the complex formed between the viral surface protein and transmembrane protein. This invention further provides methods of treating HIV-1 infection.
Nucleic Acids Encoding Mutant Disulfide Bond-Stabilized Human Immunodeficiency Virus Type 1 (Hiv-1) Gp140 Envelope Glycoproteins
James M. Binley - Brooklyn NY, US Norbert Schuelke - New City NY, US William C. Olson - Ossining NY, US Paul J. Maddon - Scarsdale NY, US John P. Moore - New York NY, US
Assignee:
Progenics Pharmaceuticals, Inc. - Tarrytown NY Aaron Diamond AIDS Research Centre (ADARC) - New York NY
International Classification:
C07H 21/04 A61K 39/21
US Classification:
536 2372, 4242081
Abstract:
This invention provides a DNA which upon transcription produces an RNA encoding a modified HIV-1 gp140 polypeptide, which polypeptide upon cleavage produces a modified gp120 and a modified ectodomain of gp41 which together form a complex exhibiting enhanced binding to HIV-1 neutralizing antibodies and reduced binding to HIV-1 non-neutralizing antibodies, wherein the modifications comprise an A492C mutation in gp120 and a T596C mutation in gp41, said mutations being numbered by reference to the HIV-1 isolate JR-FL, and resulting in a disulfide bond between gp120 and ectodomain gp41 which stabilizes the otherwise non-covalent gp120-gp41 interaction.
Stabilized Viral Envelope Proteins And Uses Thereof
James M. Binley - Brooklyn NY, US Norbert Schuelke - New City NY, US William C. Olson - Ossining NY, US Paul J. Maddon - Scarsdale NY, US John P. Moore - New York NY, US
Assignee:
Progenics Pharmaceuticals Inc. - Tarrytown NY Aaron Diamond Aids Research Centre (ADARC) - New York NY
International Classification:
A61K 39/21
US Classification:
4242081
Abstract:
This invention provides an isolated nucleic acid which comprises a nucleotide segment having a sequence encoding a viral envelope protein comprising a viral surface protein and a corresponding viral transmembrane protein wherein the viral envelope protein contains one or more mutations in amino acid sequence that enhance the stability of the complex formed between the viral surface protein and transmembrane protein. This invention also provides a viral envelope protein comprising a viral surface protein and a corresponding viral transmembrane protein wherein the viral envelope protein contains one or more mutations in amino acid sequence that enhance the stability of the complex formed between the viral surface protein and transmembrane protein. This invention further provides methods of treating HIV-1 infection.
Paul J. Maddon - Scarsdale NY, US Gerald P. Donovan - New York NY, US William C. Olson - Ossining NY, US Norbert Schuelke - Dedham MA, US Jason Gardner - Merseyside, GB Dangshe Ma - Millwood NY, US
The invention includes antibodies or antigen-binding fragments thereof which bind specifically to conformational epitopes on the extracellular domain of PSMA, compositions containing one or a combination of such antibodies or antigen-binding fragments thereof, hybridoma cell lines that produce the antibodies, and methods of using the antibodies or antigen-binding fragments thereof for cancer diagnosis and treatment. The invention also includes oligomeric forms of PSMA proteins, compositions comprising the multimers, and antibodies that selectively bind to the multimers.
Paul J. Maddon - Scarsdale NY, US Gerald P. Donovan - New York NY, US William C. Olson - Ossining NY, US Norbert Schuelke - Dedham MA, US Jason Gardner - Merseyside, GB Dangshe Ma - Milwood NY, US Jaspal S. Kang - Surrey, CA Larry Green - San Francisco CA, US
Assignee:
PSMA Development Company, LLC - Tarrytown NY Amgen Fremont Inc. - Fremont CA
The invention includes antibodies or antigen-binding fragments thereof which bind specifically to conformational epitopes on the extracellular domain of PSMA, compositions containing one or a combination of such antibodies or antigen-binding fragments thereof, hybridoma cell lines that produce the antibodies, and methods of using the antibodies or antigen-binding fragments thereof for cancer diagnosis and treatment. The invention also includes oligomeric forms of PSMA proteins, compositions comprising the multimers, and antibodies that selectively bind to the multimers.
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