UC Davis Medical GroupUC Davis Medical Center Neurology Clinic 3160 Folsom Blvd STE 2100, Sacramento, CA 95816 (916)7347777 (phone), (916)4512010 (fax)
Education:
Medical School West China Univ of Med Sci, Chengdu City, Sichuan, China Graduated: 1983
Procedures:
Lumbar Puncture Neurological Testing Sleep and EEG Testing
Dr. Zhang graduated from the West China Univ of Med Sci, Chengdu City, Sichuan, China in 1983. He works in Sacramento, CA and specializes in Neurology and Neuromuscular Medicine. Dr. Zhang is affiliated with UC Davis Medical Center.
Dr. Zhang graduated from the West China Univ of Med Sci, Chengdu City, Sichuan, China in 1988. He works in Columbus, OH and 1 other location and specializes in Hematology/Oncology. Dr. Zhang is affiliated with Cincinnati VA Medical Center.
West China University Of Medical Sciences (1988) Montefiore Medical Center *Internal Medicine Wake Forest University Baptist Medical Center *Hematology & Oncology
Kenneth W. Kinzler - Bel Air MD Bert Vogelstein - Baltimore MD Victor E. Velculescu - Baltimore MD Lin Zhang - Baltimore MD
Assignee:
The John Hopkins University School of Medicine - Baltimore MD
International Classification:
C12Q 168
US Classification:
435 6, 435196, 536 231, 702 19
Abstract:
Serial analysis of gene expression, SAGE, a method for the rapid quantitative and qualitative analysis of transcripts is provided. Short defined sequence tags corresponding to expressed genes are isolated and analyzed. Sequencing of over 1,000 defined tags in a short period of time (e. g. , hours) reveals a gene expression pattern characteristic of the function of a cell or tissue. Moreover, SAGE is useful as a gene discovery tool for the identification and isolation of novel sequence tags corresponding to novel transcripts and genes.
Kenneth W. Kinzler - Bel Air MD Bert Vogelstein - Baltimore MD Victor E. Velculescu - Baltimore MD Lin Zhang - Baltimore MD
Assignee:
The Johns Hopkins University - Baltimore MD
International Classification:
C12Q 168
US Classification:
435 6, 435 911, 435 915, 536 231, 536 242
Abstract:
Serial analysis of gene expression, SAGE, a method for the rapid quantitative and qualitative analysis of transcripts is provided. Short defined sequence tags corresponding to expressed genes are isolated and analyzed. Sequencing of over 1,000 defined tags in a short period of time (e. g. , hours) reveals a gene expression pattern characteristic of the function of a cell or tissue. Moreover, SAGE is useful as a gene discovery tool for the identification and isolation of novel sequence tags corresponding to novel transcripts and genes.
High Dose Solid Unit Oral Pharmaceutical Dosage Form Of Amorphous Nelfinavir Mesylate And Process For Making Same
Martin Howard Infeld - Upper Montclair NJ, US Wantanee Phuapradit - Clifton NJ, US Navnit Hargovindas Shah - Clifton NJ, US Lin Zhang - Piscataway NJ, US
Assignee:
Hoffmann-La Roche Inc. - Nutley NJ
International Classification:
A61K 9/20
US Classification:
424464, 424451, 424470, 514772, 5147723
Abstract:
A solid unit oral pharmaceutical dosage form of amorphous nelfinavir mesylate is provided comprising amorphous nelfinavir mesylate in an amount of from about 400 mg to about 700 mg calculated as nelfinavir base, and a pharmaceutically acceptable water soluble, non-ionic synthetic block copolymer of ethylene oxide and propylene oxide, the copolymer having a melting point of at least about 45 C. and an HLB value at 25 C. of from about 18 to about 29, wherein the copolymer is present from about 40% to about 65% by weight of the nelfinavir mesylate. A hot melt granulation process for making the dosage form is provided.
Antonio Albano - Clifton NJ, US Martin Infeld - Upper Montclair NJ, US Wantanee Phuapradit - Montville NJ, US Navnit Shah - Clifton NJ, US Lin Zhang - Bloomfield NJ, US
International Classification:
A61K031/551
US Classification:
514220000
Abstract:
A solid unit oral pharmaceutical dosage form of saquinavir mesylate is provided comprising micronized saquinavir mesylate in an amount of from 250 mg to 800 mg calculated as free base, and a pharmaceutically acceptable binder, disintegrant, and water soluble carrier. A solid unit dosage form of saquinavir mesylate is provided comprising from 60% to 80% micronized saquinavir mesylate based on the mesylate salt, 4% to 8% water soluble binder, a disintegrant and a carrier, wherein each percentage is of the kernel weight.
Pharmaceutical Solid Dosage Forms Comprising Amorphous Compounds Micro-Embedded In Ionic Water-Insoluble Polymers
Antonio Albano - Clifton NJ, US Wantanee Phuapradit - Montville NJ, US Navnit Shah - Clifton NJ, US Zhongshui Yu - Bridgewater NJ, US Lin Zhang - Nutley NJ, US
International Classification:
A61K 9/48 A61K 31/4965
US Classification:
424451000, 514255060
Abstract:
The present invention provides novel pharmaceutical solid dosage forms for oral administration comprising a therapeutically effective amount of an unstable crystalline form or an amorphous form of a therapeutically effective compound micro-embedded into an ionic water-insoluble polymer. The therapeutically effective compounds, which have a tendency to gel, are micro-embedded into an ionic water-insoluble polymer matrix to provide a dosage form having rapid, reproducible, and complete dissolution profiles. These novel solid pharmaceutical dosage forms are useful in the treatment or control of a number of diseases. The present invention also provides a method for treating a disease comprising administering to a subject, in need thereof, a therapeutically effective amount of the novel solid pharmaceutical dosage form. The present invention further provides a method for preparing the pharmaceutical dosage forms.
Antonio A. Albano - Clifton NJ, US Martin Howard Infeld - Upper Montclair NJ, US Wantanee Phuapradit - Montville NJ, US Navnit Hargovindas Shah - Clifton NJ, US Lin Zhang - Bloomfield NJ, US
International Classification:
A61K 31/4725
US Classification:
514307
Abstract:
A solid unit oral pharmaceutical dosage form of saquinavir mesylate is provided comprising micronized saquinavir mesylate in an amount of from 250 mg to 800 mg calculated as free base, and a pharmaceutically acceptable binder, disintegrant, and water soluble carrier. A solid unit dosage form of saquinavir mesylate is provided comprising from 60% to 80% micronized saquinavir mesylate based on the mesylate salt, 4% to 8% water soluble binder, a disintegrant and a carrier, wherein each percentage is of the kernel weight.
Highly Electrically Conductive Surfaces For Electrochemical Applications And Methods To Produce Same
A method to use a novel structured metal-ceramic composite powder to improve the surface electrical conductivity of corrosion resistant metal substrates by thermal spraying the structured powder onto a surface of a metallic substrate is disclosed. The structured powder has a metal core and is wholly or partially surrounded by an electrically conductive ceramic material such as a metal nitride material. The metal cores may have the ceramic material formed on them prior to a thermal spraying process performed in an inert atmosphere, or the thermal spraying may be performed in a reactive atmosphere such that the ceramic coating forms on the cores during the thermal spraying process and/or after deposition. The metal cores will bond conductive ceramic material onto the surface of the substrate through the thermal spray process.
Oct 2005 to May 2011 Senior AccountantTotal Tec Systems, Inc. A company of Bell Micro
Aug 1999 to Oct 2005 AccountantSamsung Electronics America, Inc
Feb 1998 to Aug 1999 Staff Accountant
Education:
Long Island University Brooklyn, NY Jan 1998 M.S in AccountancyUniversity of Baltimore Baltimore, MD Jan 1996 to May 1996 M.S in AccountancyMiddlesex County College Edison, NJ Dec 1994 Accountancy
Skills:
SAP, JDE, Quick books, AS 400, Great plains, MS office