Group Health Bellevue Medical Center Otolaryngology 11511 NE 10 St STE 2A, Bellevue, WA 98004 (425)5023770 (phone), (425)5023771 (fax)
Education:
Medical School University of California, Los Angeles David Geffen School of Medicine Graduated: 1980
Procedures:
Myringotomy and Tympanotomy Rhinoplasty Sinus Surgery Tonsillectomy or Adenoidectomy Tracheostomy Tympanoplasty
Conditions:
Acute Upper Respiratory Tract Infections Chronic Sinusitis Deviated Nasal Septum Hearing Loss Otitis Media
Languages:
English Spanish
Description:
Dr. Short graduated from the University of California, Los Angeles David Geffen School of Medicine in 1980. He works in Bellevue, WA and specializes in Otolaryngology.
Dr. Short graduated from the A.T. Still University of Health Sciences/ Kirksville College of Osteopathic Medicine in 1983. He works in Marysville, KS and 1 other location and specializes in Pulmonary Critical Care Medicine and Pulmonary Disease. Dr. Short is affiliated with Community Memorial Healthcare, Manhattan Surgical Hospital and Via Christi Hospital Manhattan.
- Pleasanton CA, US Anthony MAKAREWICZ - Livermore CA, US Steven SHORT - Pleasanton CA, US
International Classification:
B01L 3/00 G01N 15/10 G01N 15/14
Abstract:
Methods and systems for sorting particles are provided. Methods and systems for sorting cell beads are provided. In some cases, cell beads may be sorted from particles unoccupied with cell derivatives. In some cases, singularly occupied cell beads may be sorted from unoccupied particles and multiply occupied cell beads.
Capturing Specific Nucleic Acid Materials From Individual Biological Cells In A Micro-Fluidic Device
- Emeryville CA, US Eric D. Hobbs - Livermore CA, US Steven W. Short - Pleasanton CA, US Mark P. White - San Francisco CA, US Daniele Malleo - San Jose CA, US
International Classification:
B03C 5/00 B03C 5/02 B03C 11/00 B01L 3/00
Abstract:
Individual biological cells can be selected in a micro-fluidic device and moved into isolation pens in the device. The cells can then be lysed in the pens, releasing nucleic acid material, which can be captured by one or more capture objects in the pens. The capture objects with the captured nucleic acid material can then be removed from the pens. The capture objects can include unique identifiers, allowing each capture object to be correlated to the individual cell from which the nucleic acid material captured by the object originated.
- Pleasanton CA, US Denis PRISTINSKI - Dublin CA, US Preyas SHAH - Milpitas CA, US Steven William SHORT - Pleasanton CA, US Dieter WILK - San Jose CA, US Siyuan XING - Newark CA, US
International Classification:
C12Q 1/6874 C12N 15/10
Abstract:
Provided in some aspects are methods for light-controlled in situ surface patterning of a substrate. Compositions such as nucleic acid arrays produced by the methods are also disclosed. In some embodiments, a method disclosed herein comprises using photoresist for photocontrollable hybridization and/or ligation of nucleic acid molecules, wherein photoresist removal allows hybridization and/or ligation of nucleic acid molecules at the exposed area. A large diversity of barcodes can be created in molecules on the substrate via sequential rounds of light exposure, hybridization, and ligation.
Methods And Systems For Sorting Droplets And Beads
Methods and systems for sorting droplets are provided. In some cases, occupied droplets may be sorted from unoccupied droplets. In some cases, singularly occupied droplets may be sorted from unoccupied droplets and multiply occupied droplets. Methods and systems for sorting cell beads are provided. In some cases, cell beads may be sorted from particles unoccupied with cell derivatives. In some cases, singularly occupied cell beads may be sorted from unoccupied particles and multiply occupied cell beads. Methods and systems for selectively polymerizing droplets based on occupancy and size of the droplets are provided.
Methods And Systems For Sorting Droplets And Beads
- Pleasanton CA, US Anthony Makarewicz - Livermore CA, US Steven Short - Pleasanton CA, US
International Classification:
C12N 15/10 G01N 15/14 B01L 3/00 G01N 21/64
Abstract:
Methods and systems for sorting droplets are provided. In some cases, occupied droplets may be sorted from unoccupied droplets. In some cases, singularly occupied droplets may be sorted from unoccupied droplets and multiply occupied droplets. Methods and systems for sorting cell beads are provided. In some cases, cell beads may be sorted from particles unoccupied with cell derivatives. In some cases, singularly occupied cell beads may be sorted from unoccupied particles and multiply occupied cell beads. Methods and systems for selectively polymerizing droplets based on occupancy and size of the droplets are provided.
Capturing Specific Nucleic Acid Materials From Individual Biological Cells In A Micro-Fluidic Device
- Emeryville CA, US Eric D. Hobbs - Livermore CA, US Steven W. Short - Pleasanton CA, US Mark P. White - San Francisco CA, US Daniele Malleo - San Jose CA, US
Assignee:
Berkeley Lights, Inc. - Emeryville CA
International Classification:
B03C 5/00 B03C 11/00 B01L 3/00 B03C 5/02
Abstract:
Individual biological cells can be selected in a micro-fluidic device and moved into isolation pens in the device. The cells can then be lysed in the pens, releasing nucleic acid material, which can be captured by one or more capture objects in the pens. The capture objects with the captured nucleic acid material can then be removed from the pens. The capture objects can include unique identifiers, allowing each capture object to be correlated to the individual cell from which the nucleic acid material captured by the object originated.
Capturing Specific Nucleic Acid Materials From Individual Biological Cells In A Micro-Fluidic Device
- Emeryville CA, US Eric D. Hobbs - Livermore CA, US Steven W. Short - Pleasanton CA, US Mark P. White - San Francisco CA, US
Assignee:
Berkeley Lights, Inc. - Emeryville CA
International Classification:
B81B 1/00 B03C 5/02 B03C 5/00
Abstract:
Individual biological cells can be selected in a micro-fluidic device and moved into isolation pens in the device. The cells can then be lysed in the pens, releasing nucleic acid material, which can be captured by one or more capture objects in the pens. The capture objects with the captured nucleic acid material can then be removed from the pens. The capture objects can include unique identifiers, allowing each capture object to be correlated to the individual cell from which the nucleic acid material captured by the object originated.
Name / Title
Company / Classification
Phones & Addresses
Steven B. Short
LIVING THE DREAM, LLC
Steven E Short
S & L GENERAL CONTRACTORS, INC
Steven P Short
PLOW ME NOW, LLC
Steven P Short
ALASKA WEB CREATIONS, LLC Business Services at Non-Commercial Site
5031 Mayflower Ln, Wasilla, AK 99654 7000 E Beechcraft Rd, Wasilla, AK 99654