Jing Lu MD OBGYN 500 N Garfield Ave STE 205, Monterey Park, CA 91754 (626)2811198 (phone), (626)2808656 (fax)
Education:
Medical School Shanghai Second Med Univ, Shanghai City, Shanghai, China Graduated: 1990
Procedures:
D & C Dilation and Curettage Ovarian Surgery Vaginal Repair
Conditions:
Abnormal Vaginal Bleeding Genital HPV Uterine Leiomyoma Breast Disorders Candidiasis of Vulva and Vagina
Languages:
Chinese English Spanish
Description:
Dr. Lu graduated from the Shanghai Second Med Univ, Shanghai City, Shanghai, China in 1990. She works in Monterey Park, CA and specializes in Obstetrics & Gynecology. Dr. Lu is affiliated with Garfield Medical Center and San Gabriel Valley Medical Center.
Dr. Lu graduated from the Tongji Med Univ, Wuhan City, Hubei, China in 1983. She works in Riverside, CA and specializes in Psychiatry. Dr. Lu is affiliated with Riverside County Regional Medical Center.
Name / Title
Company / Classification
Phones & Addresses
Jing Lu Postdoctoral Associate
Yale Univ Medical School of Medicine National Commercial Banks
333 Cedar St Ste Lmp5031, New York, NY 10012
Jing Lu President
QUEENS DEALER CAREER CENTER INC Job Training/Related Services
136-77 Roosevelt Ave #300, Flushing, NY 11354 13677 Roosevelt Ave, Flushing, NY 11354 (718)8880136
Jing Lu PRESIDENT
Green Bay Property Inc ANY BIZ ALLOWED BY THE CODES, APT. BUILING HOLDING, PUBLISHING · Nonresidential Building Operator
160 Broad St, Providence, RI 02907 1356 Broad St, Providence, RI 02905 257 W 30, New York, NY 10001
Jing Lu Principal
XIN XING BEAUTY WORLD INC Beauty Shop
133-55 Roosevelt Ave, Flushing, NY 11354 3707 Main St, Flushing, NY 11354
Jing Lu Secretary
China Housing & Land Development, Inc
Jing Lu Medical Doctor
Joseph Saint Hospital Foundation Health/Allied Services
1835 Franklin St, Denver, CO 80218
Us Patents
Rotary Electric Motor Having Controller And Power Supply Integrated Therein
Boris A. Maslov - Reston VA Alexander V. Pyntikov - Ashburn VA Jing Lu - Herndon VA
Assignee:
Wavecrest Laboratories, LLC - Dulles VA
International Classification:
H02K 1100
US Classification:
310 67R, 310216, 310218, 310259
Abstract:
A rotary electric motor is formed within a cylindrical rotor housing structure that surrounds an annular stator ring. The permanent magnet rotor is configured in an annular ring coaxial with, and outside of, the stator. The stator ring contains a plurality of wound core segments that are ferromagnetically isolated from each other. The core segments are secured to a rigid skeletal structure that is centrally fixed to a stationary shaft. The stator support structure is formed of spine members that extend radially away from the center. U-shaped plates at the outer ends of the spine members engage adjacent pair of stator segments. Within the inner periphery of the stator ring, space is provided within which motor control circuitry and battery power supply may be incorporated.
Detection Of Nucleic Acid Differences Using Combined Endonuclease Cleavage And Ligation Reactions
Francis Barany - New York NY, US Weiguo Cao - Central SC, US Jianmin Huang - Jackson Heights NY, US Jing Lu - Central SC, US
Assignee:
Cornell Research Foundation, Inc. - Ithaca NY
International Classification:
C12Q 1/68 C12P 19/34
US Classification:
435 6, 435 911, 435 912, 435 9152, 204450
Abstract:
The present invention is a method for detecting DNA sequence differences including single nucleotide mutations or polymorphisms, one or more nucleotide insertions, and one or more nucleotide deletions. Labeled heteroduplex PCR fragments containing base mismatches are prepared. Endonuclease cleaves the heteroduplex PCR fragments both at the position containing the variation (one or more mismatched bases) and to a lesser extent, at non-variant (perfectly matched) positions. Ligation of the cleavage products with a DNA ligase corrects non-variant cleavages and thus substantially reduces background. This is then followed by a detection step in which the reaction products are detected, and the position of the sequence variations are determined.
Detection Of Nucleic Acid Differences Using Combined Endonuclease Cleavage And Ligation Reactions
Francis Barany - New York NY, US Weiguo Cao - Central SC, US Jianmin Huang - Jackson Heights NY, US Jing Lu - Tucker GA, US
Assignee:
Cornell Research Foundation, Inc. - Ithaca NY
International Classification:
C12N 9/22
US Classification:
435199, 536 232
Abstract:
The present invention is a method for detecting DNA sequence differences including single nucleotide mutations or polymorphisms, one or more nucleotide insertions, and one or more nucleotide deletions. Labeled heteroduplex PCR fragments containing base mismatches are prepared. Endonuclease cleaves the heteroduplex PCR fragments both at the position containing the variation (one or more mismatched bases) and to a lesser extent, at non-variant (perfectly matched) positions. Ligation of the cleavage products with a DNA ligase corrects non-variant cleavages and thus substantially reduces background. This is then followed by a detection step in which the reaction products are detected, and the position of the sequence variations are determined.
Detection Of Nucleic Acid Differences Using Combined Endonuclease Cleavage And Ligation Reactions
Francis Barany - New York NY, US Weiguo Cao - Central SC, US Jianmin Huang - Jackson Heights NY, US Jing Lu - Tucker GA, US
Assignee:
Corneil Research Foundation, Inc. - Ithaca NY
International Classification:
C12N 9/22
US Classification:
435199, 536 232
Abstract:
The present invention is a method for detecting DNA sequence differences including single nucleotide mutations or polymorphisms, one or more nucleotide insertions, and one or more nucleotide deletions. Labeled heteroduplex PCR fragments containing base mismatches are prepared. Endonuclease cleaves the heteroduplex PCR fragments both at the position containing the variation (one or more mismatched bases) and to a lesser extent, at non-variant (perfectly matched) positions. Ligation of the cleavage products with a DNA ligase corrects non-variant cleavages and thus substantially reduces background. This is then followed by a detection step in which the reaction products are detected, and the position of the sequence variations are determined.