Jia J Li

US Patent:

6764822, Jul 20, 2004

Filed:

Apr 3, 2000

Appl. No.:

09/541210

Inventors:

John M. Butler - Menlo Park CA
Jia Li - Union City CA
Joseph A. Monforte - Berkeley CA
Christopher H. Becker - Palo Alto CA

Assignee:

Sequenom, Inc. - San Diego CA

International Classification:

C12Q 168

US Classification:

435 6, 435 912, 436 94, 436173, 536 253, 536 254

Abstract:

The present invention is related to the fields of genetic mapping and genetic identity detection, including forensic identification and paternity testing. This invention is more specifically directed to the use of mass spectrometry to detect length variation in DNA nucleotide sequence repeats (including variants of common alleles), such as microsatellites and short tandem repeats, and to DNA sequences provided as primers for the analysis of DNA tandem nucleotide repeat polymorphisms at specific loci on specific chromosomes.

US Patent:

7790371, Sep 7, 2010

Filed:

Apr 20, 2004

Appl. No.:

10/552641

Inventors:

Russell Gene Higuchi - Alameda CA, US
Gary Allen Peltz - Redwood City CA, US
Bonnie Fijal - Hillsborough NJ, US
Sunhee Kwon Ro - Foster City CA, US
Jia Li - Union City CA, US

Assignee:

Roche Molecular Systems, Inc. - Pleasanton CA

International Classification:

C12Q 1/68
C12P 19/34

US Classification:

435 6, 435 912

Abstract:

The present invention relates to polymorphisms of the FRZB gene and the analysis of nucleic acids thereof. The invention further relates to methods of predicting risks of certain conditions in individual and kits for the determination of such risks.

US Patent:

20030158187, Aug 21, 2003

Filed:

Jan 30, 2003

Appl. No.:

10/354693

Inventors:

Dorothee Foernzler - Lenzburg, CH
Lara Hashimoto - Basle, CH
Jia Li - Union City CA, US
Eric Luedin - Liestal, CH
Andrew Sleight - Riedisheim, FR
Pierre Vankan - Basle, CH

International Classification:

C12Q001/68
A61K031/44
A61K031/541
A61K031/5377

US Classification:

514/227500, 435/006000, 514/235500, 514/357000

Abstract:

The present invention relates to a method for correlating single nucleotide polymorphisms in the preprotachykinin (NKNA) gene with the efficacy and compatibility of a pharmaceutically active compound administered to a human being. The invention further relates to a method for determining the efficacy and compatibility of a pharmaceutically active compound administered to a human being which method comprises determining at least one single nucleotide polymorphism in the NKNA gene. Said methods are based on determining specific single nucleotide polymorphisms in the NKNA gene and determining the efficacy and compatibility of a pharmaceutically active compound in the human by reference to polymorphism in NKNA. The invention further relates to isolated nucleic acids comprising within their sequence the polymorphisms as defined herein, to nucleic acid primers and oligonucleotide probes capable of hybridizing to such nucleic acids and to a diagnostic kit comprising one or more of such primers and probes for detecting a polymorphism in the NKNA gene, to a pharmaceutical pack comprising NK-1 receptor antagonists and instructions for administration of the drug to human beings tested for the polymorphisms as well as to a computer readable medium with the stored sequence information for the polymorphisms in the NKNA gene.

US Patent:

20060014187, Jan 19, 2006

Filed:

Jun 28, 2005

Appl. No.:

11/170717

Inventors:

Jia Li - Union City CA, US
Russell Higuchi - Alameda CA, US
Sunhee Ro - Foster City CA, US
Gary Peltz - Redmond City CA, US

Assignee:

Roche Molecular Systems., Inc. - Alameda CA

International Classification:

C12Q 1/68
C12P 19/34

US Classification:

435006000, 435091200

Abstract:

The current invention is based on the discovery that the Prol2Ala and VN102 single nucleotide polymorphisms in the PPARγ2 provides a method of determining a susceptibility to osteoporosis by detecting the presence of PPARγ of the alleles.

US Patent:

20060228752, Oct 12, 2006

Filed:

Jun 21, 2006

Appl. No.:

11/472083

Inventors:

Dorothee Foernzler - Lenzburg, CH
Lara Hashimoto - Basle, CH
Jia Li - Union City CA, US
Eric Luedin - Liestal, CH
Andrew Sleight - Riedisheim, FR
Pierre Vankan - Basle, CH

International Classification:

C12Q 1/68
A61K 31/5377
C07H 21/04

US Classification:

435006000, 514235200, 536023500

Abstract:

The present invention relates to a method for correlating single nucleotide polymorphisms in the preprotachykinin (NKNA) gene with the efficacy and compatibility of a pharmaceutically active compound administered to a human being. The invention further relates to a method for determining the efficacy and compatibility of a pharmaceutically active compound administered to a human being which method comprises determining at least one single nucleotide polymorphism in the NKNA gene. Said methods are based on determining specific single nucleotide polymorphisms in the NKNA gene and determining the efficacy and compatibility of a pharmaceutically active compound in the human by reference to polymorphism in NKNA. The invention further relates to isolated nucleic acids comprising within their sequence the polymorphisms as defined herein, to nucleic acid primers and oligonucleotide probes capable of hybridizing to such nucleic acids and to a diagnostic kit comprising one or more of such primers and probes for detecting a polymorphism in the NKNA gene, to a pharmaceutical pack comprising NK-1 receptor antagonists and instructions for administration of the drug to human beings tested for the polymorphisms as well as to a computer readable medium with the stored sequence information for the polymorphisms in the NKNA gene.

US Patent:

60905581, Jul 18, 2000

Filed:

Sep 18, 1998

Appl. No.:

9/157177

Inventors:

John M. Butler - Menlo Park CA
Jia Li - Union City CA
Joseph A. Monforte - Berkeley CA
Christopher H. Becker - Palo Alto CA

Assignee:

Genetrace Systems, Inc. - Alameda CA

International Classification:

C07H 2104
C12P 1934
C12Q 168

US Classification:

435 6

Abstract:

The present invention is related to the fields of genetic mapping and genetic identity detection, including forensic identification and paternity testing. This invention is more specifically directed to the use of mass spectrometry to detect length variation in DNA nucleotide sequence repeats (including variants of common alleles), such as microsatellites and short tandem repeats, and to DNA sequences provided as primers for the analysis of DNA tandem nucleotide repeat polymorphisms at specific loci on specific chromosomes.

US Patent:

20220369706, Nov 24, 2022

Filed:

Aug 3, 2022

Appl. No.:

17/880531

Inventors:

- San Francisco CA, US
Jia Li - Burlingame CA, US
Maurizio Tarsia - San Carlos CA, US

International Classification:

A24F 40/40
A24F 40/51
A24F 40/10

Abstract:

A vaporizer device includes a cartridge and a vaporizer body. The cartridge includes reservoir configured to hold a vaporizable material. The cartridge further includes a channel extending from the reservoir and having an opening at an end of the channel. The vaporizer body includes a movable block. The vaporizer body further includes a controller configured to actuate the movable block, the actuating of the movable block moving the movable block towards the channel to compress the channel, and the compression of the channel ejects, from the opening, at least a portion of the vaporizable material. The vaporizer body further includes a heating element positioned toward the opening of the channel when the cartridge is coupled with the vaporizer body, the heating element configured to vaporize the portion of the vaporizable material.

US Patent:

20230063920, Mar 2, 2023

Filed:

Oct 24, 2022

Appl. No.:

18/049098

Inventors:

- Santa Monica CA, US
Yuke Zhu - Stanford CA, US
Ning Xu - Irvine CA, US
Kevin Dechau Tang - Los Angeles CA, US
Jia Li - Marina Del Rey CA, US

International Classification:

H04L 51/10
G06F 16/22
G06F 16/51
G06F 16/583
G06N 20/00
G06F 16/9535
G06F 16/954
G06F 16/2457
G06F 16/951
G06N 3/04
G06N 3/08
G06V 20/00
H04L 51/52

Abstract:

Systems, devices, methods, media, and instructions for automated image processing and content curation are described. In one embodiment a server computer system communicates at least a portion of a first content collection to a first client device, and receives a first selection communication in response, the first selection communication identifying a first piece of content of the first plurality of pieces of content. The server analyzes analyzing the first piece of content to identify a set of context values for the first piece of content, and accesses accessing a second content collection comprising pieces of content sharing at least a portion of the set of context values of the first piece of content. In various embodiments, different content values, image processing operations, and content selection operations are used to curate the content collections.