Patent Assignment
Reel/Frame 025656/0581
Assignment of Assignor's Interest
Recorded: 2011-01-19
Pages: 32
Assignor
GENZYME CORPORATION
Executed: 2010-11-30
Assignee
ESOTERIX GENETIC LABORATORIES, LLC
358 SOUTH MAIN STREET, BURLINGTON, NORTH CAROLINA, 27215
Covered Properties
(112)
Methods for Detecting Mutations Using Primer Extension for Detecting Disease
PCT:
PCT/US2002/000935 ↗
Method for Alteration Detection
PCT:
PCT/US2002/007926 ↗
Molecular Characteristics of Non-Small Cell Lung Cancer
PCT:
PCT/US2002/026027 ↗
Methods for Detecting Abnormally Methylated Nucleic Acid in Heterogeneous Biological Samples
PCT:
PCT/US2003/011023 ↗
Method for Detecting a Mutant Nucleic Acid
PCT:
PCT/US2005/016518 ↗
Method for Detecting a Recombinant Event
PCT:
PCT/US2005/030942 ↗
Method for Monitoring Disease Progression or Recurrence
PCT:
PCT/US2005/039670 ↗
Analysis of Heterogeneous Nucleic Acid Samples
PCT:
PCT/US2006/015062 ↗
Copy Number Analysis of Genetic Locus
PCT:
PCT/US2010/056494 ↗
Method for Obtaining Informative Cells
Patent:
5,627,029 →
Application:
08/243,647 →
Method of Detecting Cellular Material
Patent:
5,501,954 →
Application:
08/259,224 →
High - Throughout Screening Method for Sequence or Genetic Alterations in Nucleic Acids Using Elution and Sequences of Complementary Oligo- Nucleotides
Patent:
5,589,330 →
Application:
08/281,940 →
Method for Simultaneously Detecting Multiple Mutations in a Dna Sample
Patent:
5,633,134 →
Application:
08/308,638 →
Polycystic Kidney Disease Gene
Patent:
5,654,170 →
Application:
08/323,443 →
Method for Nucleotide Sequence Amplification
Patent:
5,545,539 →
Application:
08/326,432 →
Universal Primer Sequence for Multiplex Dna Amplification
Patent:
5,882,856 →
Application:
08/474,450 →
High Through Put Screening Method for Sequences or Genetic Alterations in Nucleic Acids
Patent:
5,849,483 →
Application:
08/485,885 →
Method for Mismatch-Directed in Vitro Dna Sequencing
Patent:
5,571,676 →
Application:
08/487,986 →
Direct Sequence Identification of Mutations by Cleavage- and Ligation- Associated Mutation-Specific Sequencing
Patent:
5,707,806 →
Application:
08/488,013 →
Method for Nucleotide Sequence Amplification
Patent:
5,846,716 →
Application:
08/592,145 →
Polycystic Kidney Disease Gene and Protein
Patent:
6,071,717 →
Application:
08/658,136 →
Method for the Detection of Clonal Populations of Transformed Cells in a Genomically Heterogeneous Cellular Sample
Patent:
5,670,325 →
Application:
08/700,583 →
High Throughput Screening Method for Sequences or Genetic Alterations in Nucleic Acids
Patent:
5,834,181 →
Application:
08/710,134 →
KVLQT1- a Long Qt Syndrome Gene Which Encodes KVLQT1 Which Coassembles with Mink to Form Cardiac I Ks Potassium Channels
Application:
08/739,383 →
Contiguous Genomic Sequence Scanning
Patent:
5,830,665 →
Application:
08/808,763 →
Improved Methods for the Detection of Loss of Heterozygosity
Patent:
5,928,870 →
Application:
08/876,857 →
High-Throughput Screening Method for Identification of Genetic Mutations or Disease-Causing Microorganisms Using Segmented Primers
Patent:
5,888,778 →
Application:
08/877,333 →
Mutations in the KCNE1 Gene Encoding Human Mink Which Cause Arrhythmia Susceptibility Thereby Establishing KCNE1 as an Lqt Gene
Application:
08/921,068 →
Universal Primer Sequence for Multiplex Dna Amplification
Patent:
6,207,372 →
Application:
08/983,466 →
Methods for the Detection of Chromosomal Aberrations
Patent:
6,100,029 →
Application:
08/984,856 →
Method for Detecting and Identifying Mutations
Patent:
6,297,010 →
Application:
09/016,542 →
Primer Extension Methods for Detecting Nucleic Acids
Patent:
6,566,101 →
Application:
09/067,212 →
Methods for the Detection of Nucleic Acids
Application:
09/098,180 →
Methods for Detecting Differences in Rna Expression Levels and Uses Therefor
Patent:
6,146,828 →
Application:
09/110,759 →
Kvlqti - a Long Qt Syndrome Gene
Patent:
6,277,978 →
Application:
09/135,010 →
Methods for Detecting Contamination in Molecular Diagnostics Using Pcr
Application:
09/177,243 →
Methods for the Detection of Loss of Heterozygosity
Patent:
6,020,137 →
Application:
09/198,091 →
Methods for Improving Sensitivity and Specificity of Screening Assays
Patent:
6,143,529 →
Application:
09/277,016 →
Methods for Detecting Mutations Using Primer Extension
Patent:
6,280,947 →
Application:
09/371,991 →
Methods for Disease Detection
Patent:
6,586,177 →
Application:
09/455,950 →
Methods for the detection of loss of heterozygosity
Application:
09/495,527 →
Methods for Disease Detection
Patent:
6,919,174 →
Application:
09/514,865 →
Methods for the Detection of Nucleic Acids
Patent:
6,203,993 →
Application:
09/542,103 →
Methods for the Detection of Nucleic Acids
Patent:
6,300,077 →
Application:
09/542,377 →
Methods for Detecting Nucleic Acids Indicative of Cancer
Patent:
6,964,846 →
Application:
09/545,162 →
KVLQT1 - a Long Qt Syndrome Gene
Patent:
6,582,913 →
Application:
09/597,731 →
KVLQT1-A Long Qt Syndrome Gene
Patent:
6,451,534 →
Application:
09/597,732 →
KVLQT1 - a Long Qt Syndrome Gene
Patent:
6,420,124 →
Application:
09/597,735 →
Methods for the detection of chromosomal aberrations
Patent:
6,214,558 →
Application:
09/626,809 →
Methods for the diagnosis and treatment of lung cancer
Application:
09/646,478 →
Apparatus and Methods for Drug Screening
Patent:
6,849,403 →
Application:
09/724,274 →
Methods for the detection of loss of heterozygosity
Application:
09/747,355 →
Publication:
US 2002/0004201
Methods for Detecting Mutations Using Primer Extension for Detecting Disease
Method for Alteration Detection
Patent:
6,428,964 →
Application:
09/809,713 →
Methods for Detecting Contamination in Molecular Diagnostics Using Pcr
Methods for Detecting Mutations Using Primer Extension for Detecting Disease
Methods for Detecting Mutations Using Primer Extension for Detecting Disease
Methods for Detecting Mutations Using Primer Extension
Methods for the detection of nucleic acids
Application:
09/972,767 →
Publication:
US 2002/0119469
Method for Alteration Detection
Methods for Detecting Hypermethylated Nucleic Acid in Heterogeneous Biological Samples
Primer extension methods for detecting nucleic acids
Application:
10/358,989 →
Publication:
US 2004/0110162
KVLQT1 - a Long Qt Syndrome Gene
Methods for Analysis of Molecular Events
Methods for disease detection
Application:
10/434,482 →
Publication:
US 2004/0014104
Method for alteration detection
Application:
10/471,306 →
Publication:
US 2004/0110179
Molecular Characteristics of Non-Small Cell Lung Cancer
Methods for detecting nucleic acids indicative of cancer
Application:
11/090,479 →
Publication:
US 2005/0260638
Methods for disease detection
Application:
11/114,917 →
Publication:
US 2006/0121495
Signal Message Compression
Methods for the diagnosis and treatment of lung cancer
Application:
11/504,260 →
Publication:
US 2007/0218511
Methods for Disease Detection
Methods For Detecting A Mutant Nucleic Acid
Application:
11/596,107 →
Publication:
US 2008/0241827
Method for Detecting Recombinant Event
Method For Monitoring Disease Progression or Recurrence
Methods of detecting cancer based on DNA methylation analysis
Application:
11/732,509 →
Molecular Characteristics of Non-Small Cell Lung Cancer
Methods for disease detection
Application:
11/881,138 →
Publication:
US 2008/0248471
Analysis of Heterogeneous Nucleic Acid Samples
Methods for Detecting Nucleic Acids Indicative of Cancer
Application:
11/960,313 →
Publication:
US 2009/0291436
Methods for the Diagnosis and Treatment of Lung Cancer
Methods of Detecting Hypermethylation
Application:
12/572,813 →
Publication:
US 2010/0092981
Methods for Disease Detection
Application:
12/710,798 →
Publication:
US 2010/0151478
Methods for Detecting Nucleic Acids Indicative of Cancer
Application:
12/729,051 →
Publication:
US 2010/0173320
Methods for Analysis of Molecular Events
Copy Number Analysis of Genetic Locus
Methods for the Diagnosis and Treatment of Lung Cancer
High Throughput Screening Method for Sequences or Genetics Alterations in Nucleic Acids
Application:
60/003,788 →
KVLQT1 - a Long Qt Syndrome Gene
Application:
60/019,014 →
Methods for Reducing the Effects of Contamination in Molecular Diagnostics Using Pcr
Application:
60/063,219 →
Genomic Structure of KVLQT1 and KCNE1 and Mutations in These Genes Associated with Long Qt Syndrome
Application:
60/094,477 →
Methods for Detecting Nucleic Acids Indicative of Cancer
Application:
60/128,629 →
Molecular Weight Profiling
Application:
60/152,847 →
Methods for Disease Detection
Application:
60/169,457 →
Molecular characteristics of non-small cell lung cancer
Application:
60/312,400 →
Methods for analysis of molecular events
Application:
60/357,585 →
Method for detecting a mutant nucleic acid
Application:
60/569,736 →
Method for detecting a recombinant event
Application:
60/604,870 →
Method of monitoring the progression of cancer
Application:
60/623,005 →
Method for monitoring tumor growth
Application:
60/627,248 →
Method for detecting a mutant nucleic acid
Application:
60/631,214 →
Analysis of heterogeneous nucleic acid samples
Application:
60/673,436 →
Methods of detecting cancer based on DNA methylation analysis
Application:
60/788,994 →
Copy Number Analysis of Genetic Locus
Application:
61/260,804 →
Mutations Associated with Cystic Fibrosis
Application:
61/316,321 →
Determination of Tumor Origin
Application:
61/324,618 →
Gc Wave Correction for Array-Based Comparative Genomic Hybridization
Application:
61/329,264 →
Enumeration of Nucleic Acids
Application:
61/352,062 →
Mutations Associated with Cystic Fibrosis
Application:
61/359,029 →
Gc Wave Correction for Array-Based Comparative Genomic Hybridization
Application:
61/362,491 →
Identification of Differentially Represented Fetal or Maternal Genomic Regions and Uses Thereof
Application:
61/367,254 →
Enrichment of Low Molecular Weight DNA
Application:
61/389,042 →
Related Assignments
(13)
Other recorded transfers of the patents in this record — the chain of ownership.
Recording to Correct the Assignee's Name to Johns Hopkins University Previosly Recorded at REEL7370, Frame 0083.
Oct 22, 1996
From: GERMINO, GREGORY; QIAN, FENG
To: JOHNS HOPKINS UNIVERSITY
Reel/Frame 008196/0962 →
Change of Name
Jan 25, 2008
From: EXACT LABORATORIES, INC.
To: EXACT SCIENCES CORPORATION
Reel/Frame 020417/0268 →
Confirmatory License
Jul 18, 2008
From: UNIVERSITY OF UTAH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021261/0978 →
Assignment of Assignor's Interest
Mar 25, 2009
From: EXACT SCIENCES CORPORATION
To: GENZYME CORPORATION
Reel/Frame 022460/0934 →
Merger
Oct 21, 2010
From: IG LABORATORIES, INC.
To: GENZYME CORPORATION
Reel/Frame 025169/0524 →
Assignment of Assignor's Interest
Oct 21, 2010
From: SHUBER, TONY; KLINGER, KATHERINE W.
To: IG LABORATORIES, INC.
Reel/Frame 025169/0547 →
Assignment of Assignor's Interest
Jun 10, 2011
From: GENZYME CORPORATION
To: ESOTERIX GENETIC LABORATORIES, LLC
Reel/Frame 026422/0848 →
Assignment of Assignor's Interest
Mar 28, 2012
From: AKMAEV, VIATCHESLAV R.; HENDRICKSON, BRANT; SCHOLL, THOMAS
To: GENZYME CORPORATION
Reel/Frame 027948/0007 →
Assignment of Assignor's Interest
May 6, 2013
From: IG LABORATORIES, INC.
To: GENZYME CORPORATION
Reel/Frame 030352/0940 →
Assignment of Assignor's Interest
May 6, 2013
From: SHUBER, ANTHONY P.
To: IG LABORATORIES, INC.
Reel/Frame 030352/0903 →
Confirmatory License
May 19, 2015
From: UNIVERSITY OF UTAH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035731/0393 →
Confirmatory License
Mar 29, 2016
From: UNIVERSITY OF UTAH
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 038126/0274 →
Confirmatory License
Nov 4, 2017
From: UNIVERSITY OF UTAH
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 044034/0582 →