PHILIP B PATY, MD
Radiology at York Ave, New York, NY

License number
New York 182002
Category
Radiology
Type
Surgery
Address
Address
1275 York Ave, New York, NY 10021
Phone
(212) 639-2000

Personal information

See more information about PHILIP B PATY at radaris.com
Name
Address
Phone
Philip Paty, age 62
27 Birkdale Ct, Slingerlands, NY 12159
(518) 478-9192
Philip Paty, age 68
345 E 68Th St APT 1C, New York, NY 10065
(212) 288-6754
Philip Paty, age 68
345 E 68Th St APT 1D, New York, NY 10065
Philip Paty
New York, NY
(212) 288-6754
Philip K Paty, age 62
27 Birkdale Ct, Slingerlands, NY 12159
(518) 478-9192

Organization information

See more information about PHILIP B PATY at bizstanding.com

Memorial Sloan Kettering CNCR - Philip B Paty MD

1275 York Ave #1081, New York, NY 10065

Categories:
Proctology Physicians & Surgeons
Phone:
(212) 639-2000 (Phone)

Professional information

See more information about PHILIP B PATY at trustoria.com
Philip Paty Photo 1
Use Of Lecithin:retinol Acyl Transferase Gene Promoter Methylation In Evaluating The Cancer State Of Subject

Use Of Lecithin:retinol Acyl Transferase Gene Promoter Methylation In Evaluating The Cancer State Of Subject

US Patent:
2010014, Jun 10, 2010
Filed:
Dec 19, 2007
Appl. No.:
12/520386
Inventors:
Francis Barany - New York NY, US
Yu-Wei Cheng - Forest Hills NY, US
Philip Paty - New York NY, US
Daniel Notterman - Cranbury NJ, US
Assignee:
CORNELL RESEARCH FOUNDATION, INC. - Ithaca NY
SLOAN KETTERING CANCER CENTER - New York NY
UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY - New Brunswick NJ
International Classification:
A61K 31/27, C12Q 1/68, A61K 31/07, A61K 31/10
US Classification:
514478, 435 6, 514725, 514709
Abstract:
The present invention relates to a method of evaluating the cancer state of a subject using lecithin:retinol acyl transferase (LRAT) gene promoter methylation status. Methods of analyzing and quantifying LRAT gene promoter methylation level are also disclosed. The present invention also relates to methods of determining the prognosis for s subject having cancer by assessing LRAT mRNA expression and LRAT protein expression. Methods of cancer detection, diagnosis, prognosis, and treatment are also disclosed.


Philip B Paty Photo 2
Philip B Paty, New York NY

Philip B Paty, New York NY

Specialties:
Surgery, Vascular Surgery
Work:
Memorial Sloan-Kettering
1275 York Ave, New York, NY 10065
Education:
Stanford University (1983)


Philip B Paty Photo 3
Philip B Paty, New York NY

Philip B Paty, New York NY

Specialties:
Surgeon
Address:
633 3Rd Ave, New York, NY 10017
1275 York Ave, New York, NY 10065
Education:
Stanford University, School of Medicine - Doctor of Medicine
Memorial Sloan-Kettering Cancer Center - Fellowship - Surgical Oncology
UCSF Medical Center - Residency - Surgery
Board certifications:
American Board of Surgery Certification in Surgery


Philip Paty Photo 4
Accelerating Identification Of Single Nucleotide Polymorphisms And Alignment Of Clones In Genomic Sequencing

Accelerating Identification Of Single Nucleotide Polymorphisms And Alignment Of Clones In Genomic Sequencing

US Patent:
6534293, Mar 18, 2003
Filed:
Jan 5, 2000
Appl. No.:
09/478189
Inventors:
Francis Barany - New York NY
Jianzhao Liu - New York NY
Brian W. Kirk - New York NY
Monib Zirvi - New York NY
Norman P. Gerry - New York NY
Philip B. Paty - New York NY
Assignee:
Cornell Research Foundation, Inc. - Ithaca NY
Sloan-Kettering Institute for Cancer Research - New York NY
International Classification:
C12P 1934
US Classification:
435 912, 435 6, 435 911, 4352871, 4352872, 436 94, 536 231
Abstract:
The present invention is directed to a method of assembling genomic maps of an organisms DNA or portions thereof. A library of an organisms DNA is provided where the individual genomic segments or sequences are found on more than one clone in the library. Representations of the genome are created, and nucleic acid sequence information is generated from the representations. The sequence information is analyzed to determine clone overlap from a representation. The clone overlap and sequence information from different representations is combined to assemble a genomic map of the organism. Once the genomic map is obtained, genomic sequence information from multiple individuals can be applied to the map and compared with one another to identify single nucleotide polymorphisms. These single nucleotide polymorphisms can be detected, and alleles quantified, by conducting (1) a global PCR amplification which creates a genome representation, and (2) a ligation detection reaction process whose ligation products are captured by hybridization to a support.


Philip Paty Photo 5
Accelerating Identification Of Single Nucleotide Polymorphisms And Alignment Of Clones In Genomic Sequencing

Accelerating Identification Of Single Nucleotide Polymorphisms And Alignment Of Clones In Genomic Sequencing

US Patent:
8367322, Feb 5, 2013
Filed:
Jul 17, 2002
Appl. No.:
10/198235
Inventors:
Francis Barany - New York NY, US
Jianzhao Kiu - Boston MA, US
Brian W. Kirk - New York NY, US
Monib Zirvi - Willingboro NJ, US
Norman P. Gerry - Boston MA, US
Philip B. Paty - New York NY, US
Assignee:
Cornell Research Foundation, Inc. - Ithaca NY
Sloan-Kettering Institute for Cancer Research - New York NY
International Classification:
C12Q 1/68, C12P 19/34, C07H 21/02, C07H 21/04, C07H 21/00
US Classification:
435 61, 435 611, 435 612, 435 911, 435 912
Abstract:
The present invention is directed to a method of assembling genomic maps of an organism's DNA or portions thereof. A library of an organism's DNA is provided where the individual genomic segments or sequences are found on more than one clone in the library. Representations of the genome are created, and nucleic acid sequence information is generated from the representations. The sequence information is analyzed to determine clone overlap from a representation. The clone overlap and sequence information from different representations is combined to assemble a genomic map of the organism. Once the genomic map is obtained, genomic sequence information from multiple individuals can be applied to the map and compared with one another to identify single nucleotide polymorphisms. These single nucleotide polymorphisms can be detected, and alleles quantified, by conducting (1) a global PCR amplification which creates a genome representation, and (2) a ligation detection reaction process whose ligation products are captured by hybridization to a support.


Philip Paty Photo 6
Methods For Identifying Genes Which Predict Disease Outcome For Patients With Colon Cancer

Methods For Identifying Genes Which Predict Disease Outcome For Patients With Colon Cancer

US Patent:
2011025, Oct 20, 2011
Filed:
Oct 13, 2009
Appl. No.:
13/123689
Inventors:
Francis Barany - New York NY, US
Owen Parker - Brooklyn NY, US
Manny D. Bacolod - Roosevelt Island NY, US
Sarah F. Giardina - New York NY, US
Yu-wei Cheng - Chicago IL, US
Daniel A. Notterman - Cranbury NJ, US
Gunter S. Schemmann - Princeton NJ, US
Philip B. Paty - New York NY, US
Monib Zirvi - Monmouth Junction NJ, US
Assignee:
CORNELL UNIVERSITY - Ithaca NY
THE TRUSTEES OF PRINCETON UNIVERSITY - Princeton NJ
SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH - New York NY
UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY - New Brunswick NJ
International Classification:
C40B 30/04, C40B 40/06, G01N 33/53, C40B 40/08, C12Q 1/68, G01N 33/566
US Classification:
506 9, 435 61, 435 618, 435 617, 436501, 435 612, 435 611, 435 613, 506 17, 506 16
Abstract:
Closures for containers and methods for using same are provided. In a general embodiment/the present disclosure provides a closure having a top portion (), a bottom portion () and a side portion (), an aperture () extending though the closure, a projection () extending from the closure and at least two rib members () on an interior of the projection. The projection may also include a cover (). In another embodiment, a method for using a closure includes inserting a. spike member into a projection, piercing a membrane that hermetically seals a medical container, pushing rib members within the projection to center the spike member inserted into the projection, and tearing the membrane to create a vent hole in the membrane.