Rong P Liu, 60Brandon, FL

7129055, Oct 31, 2006

Dec 11, 2000

09/734221

Dan R. Littman - New York NY, US
Hongkui Deng - Worcester MA, US
Wilfried Ellmeier - New York NY, US
Nathaniel R. Landau - New York NY, US
Rong Liu - New York NY, US

New York University - New York NY

C01N 33/53
C01N 33/533
C12N 15/00
C12N 15/48
C12N 15/07
C12N 15/09
C12N 5/28
C07K 16/28

435 72, 435 721, 435 724, 435 78, 435 793, 435325, 435 691, 435440, 53038822

Entry of HIV-1 into target cells requires cell surface CD4 as well as additional host cell cofactors. A cofactor required for infection with virus adapted for growth in transformed T cell lines was recently identified and named fusin. Fusin, however, does not promote entry of macrophage-tropic viruses that are believed to be the key pathogenic strains in vivo. It has now been determined that the principal cofactor for entry mediated by the envelope glycoproteins of primary macrophage-tropic strains of HIV-1 is CC-CKR5, a receptor for the β-chemokines RANTES, MIP-1α, and MIP-1β.

7592315, Sep 22, 2009

Nov 1, 2005

11/264509

Rong Liu - Scotch Plains NJ, US
Rumin Zhang - Edison NJ, US
Rong Kong - Scotch Plains NJ, US

Schering Corporation - Kenilworth NJ

A01N 37/18
A61K 38/16
A61K 38/21
A61K 39/42
G01N 33/00

514 13, 514 8, 514 11, 514 5, 514 6, 514 9, 514 7, 436 87, 530317, 530326, 435 691

The present invention provides, inter alia, peptide compositions and methods for treating and preventing Flaviviridae virus (e. g. , hepatitis C virus) infections.

2010011, May 13, 2010

Jul 23, 2009

12/508095

Rong Liu - Scotch Plains NJ, US
Rumin Zhang - Edison NJ, US
Rong Kong - Scotch Plains NJ, US

A61K 38/21
C07K 2/00
A61K 38/02
A61K 39/395
C07H 21/00
C12N 15/74
C12N 5/071
C12P 21/02
A61P 31/12
A61P 31/14
A61P 31/18
A61P 37/04

424 857, 530300, 514 2, 4241301, 424 854, 536 231, 4353201, 435325, 435 691

The present invention provides, inter alia, peptide compositions and methods for treating and preventing Flaviviridae virus (e.g., HCV) infections.

2010025, Sep 30, 2010

Mar 30, 2009

12/413749

David Cohn - Dobbs Ferry NY, US
Pankaj Dhoolia - New Delhi, IN
Hemesh Kumar - New Delhi, IN
Santhosh Kumaran - Peekskill NY, US
Rong Liu - Sterling VA, US
Florian Pinel - New York NY, US

International Business Machines Corporation - Armonk NY

G06F 9/45

703 22, 718100

Techniques for modeling a composite application are provided. The techniques include identifying one or more entities that are processed in a user enterprise, identifying one or more actions to be performed during a lifecycle of the one or more entities, and modeling a composite application based on the one or more actions to be performed during a lifecycle of the one or more entities.

6258527, Jul 10, 2001

May 21, 1997

8/861105

Dan R. Littman - New York NY
Hongkui Deng - Worcester MA
Wilfried Ellmeier - New York NY
Nathaniel R. Landau - New York NY
Rong Liu - New York NY

The Aaron Diamond Aids Research Center - New York NY
New York University - New York NY

C12Q 170
G01N 33567
C12N 510

435 5

Entry of HIV-1 into target cells requires cell surface CD4 as well as additional host cell cofactors. A cofactor required for infection with virus adapted for growth in transformed T cell lines was recently identified and named fusin. Fusin, however, does not promote entry of macrophage-tropic viruses that are believed to be the key pathogenic strains in vivo. It has now been determined that the principal cofactor for entry mediated by the envelope glycoproteins of primary macrophage-tropic strains of HIV-1 is CC-CKR5, a receptor for the. beta. -chemokines RANTES, MIP-1. alpha. , and MIP-1. beta.

6057102, May 2, 2000

Aug 8, 1997

8/907468

Nathaniel R. Landau - New York NY
Richard A. Koup - Southlake TX
Rong Liu - New York NY
William Paxton - Amsterdam, NL

The Aaron Diamond Aids Research Center - New York NY

C12Q 168
C12Q 170

435 6

Entry of HIV-1 into target cells requires cell surface CD4 as well as additional host cell cofactors. A cofactor required for infection with virus adapted for growth in transformed T cell lines was recently identified and named fusin. Fusin, however, does not promote entry of macrophage-tropic viruses that are believed to be the key pathogenic strains in vivo. It has now been determined that the principal cofactor for entry mediated by the envelope glycoproteins of primary macrophage-tropic strains of HIV-1 is CC-CKR5, a receptor for the. beta. -chemokines RANTES, MIP-1. alpha. , and MIP-1. beta. It has also been found that individuals who are homozygous for a mutation of the CKR-5 receptor are resistent to HIV infection; in vitro infection requires a 1000-fold higher dose of HIV than normal cells. The mutation results in complete suppression of CKR-5 expression.

5939320, Aug 17, 1999

Jun 19, 1996

8/666020

Dan R. Littman - New York NY
Hongkui Deng - New York NY
Wilfried Ellmeier - New York NY
Nathaniel R. Landau - New York NY
Rong Liu - New York NY

New York University - New York NY
The Aaron Diamond Aids Research Center - New York NY

C12N 506
C12N 510
C12N 508

435325

Entry of HIV-1 into target cells requires cell surface CD4 as well as additional host cell cofactors. A cofactor required for infection with virus adapted for growth in transformed T cell lines was recently identified and named fusin. Fusin, however, does not promote entry of macrophage-tropic viruses that are believed to be the key pathogenic strains in vivo. It has now been determined that the principal cofactor for entry mediated by the envelope glycoproteins of primary macrophage-tropic strains of HIV-1 is CC-CKR5, a receptor for the. beta. -chemokines RANTES, MIP-1. alpha. , and MIP-1. beta.

2020007, Mar 5, 2020

Nov 6, 2019

16/676396

- ARMONK NY, US
Ashish Jagmohan - Irvington NY, US
Ravindranath Kokku - Yorktown Heights NY, US
Rong Liu - Sterling VA, US
Satyanarayana V. Nitta - Westchester NY, US

H04N 21/84
H04N 21/234
H04N 21/266
H04N 21/439
H04N 21/44
H04N 21/278
H04N 21/61
H04N 21/482
H04N 21/845
H04N 21/25
H04N 21/466
H04N 21/258
H04N 21/45
G06F 16/78

A computer system, method, and computer-readable product for automatically generating a hierarchy of concepts described in a video using semantic concept matching that assists persons in searching for specific types of content within videos. A video segment is obtained, with the segment having a distinct running time with discrete information related to one or more topics within its content. The discrete information of the video segment is then parsed out and related to a predetermined relevant topic, and then one or more attributes for weighting each discrete information relevant topic within the video segment are determined. A hierarchy of concepts of the video segments is then created, based upon, at least, the weighting of the information topic within the running time of the video segment based upon the presence of the one or more attributes. Other information related to the video segment can also be used to modify the hierarchy.