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Inventor

John N. Feder

Inventor
Belle Mead, NJ, US

Overview

67→
Patents
1998–2013
Patent span
Chemistry
Primary field (CPC C)

Patents· 67 as inventor

Public. Assignee & technology derived from the patent record. Each patent links to its LexDana page.

C07Kprimary
C07KPeptides28%
A61KPreparations for medical, dental or toiletry purposes23%
C12QMeasuring or testing processes involving enzymes, nucleic acids or microorganisms10%
A61PSpecific therapeutic activity of chemical compounds or medicinal preparations9%
C12NMicroorganisms or enzymes8%
G01NInvestigating or analysing materials by determining their chemical or physical properties5%
Y10STechnical subjects covered by former uspc cross-reference art collections [xracs] and digests5%
C07HSugars4%
A01KAnimal husbandry2%
C12YEnzymes2%
PatentTitleYear
8,354,264'Polynucleotides encoding novel PCSK9 variants'20138,257,927'Hereditary hemochromatosis gene'20128,124,729'Splice variants of human G-protein coupled receptor HGPRBMY29 (HGPRMBY29SV2)'20128,105,804'Polynucleotides encoding novel PCSK9 variants'20127,998,680'Determining genotype of a polymorphic site in the hereditary hemochromatosis gene'20117,846,706'PCSK9 polypeptides'20107,767,418'Polynucleotide encoding a novel TRP channel family member, LTRPC3, and splice variants thereof'20107,741,025'Method of diagnosing lung cancer using BGS42'20107,713,699'Methods of diagnosing colon adenocarcinoma using mRNA encoding the human g-protein coupled receptor, HGPRBMY23'20107,705,134'Antibodies that bind to BGS-4'20107,635,758'Antibodies directed to G-protein coupled receptor HGPRBMY29sv1'20097,579,169'Hereditary hemochromatosis gene'20097,531,310'Methods of diagnosing Crohn\'s disease by measuring expression level of RNA encoding human G-protein coupled receptor, HGPRBMY11'20097,521,044'Human histone deacetylase, HDAC9c'20097,517,652'Methods of diagnosing tumors using the G-protein coupled receptor (GPCR), RAI-3'20097,504,481'TRP channel family member, LTRPC3 polypeptides'20097,456,256'BGS 4'20087,374,892'Methods and compositions for diagnosis and treatment of iron overload diseases and iron deficiency diseases'20087,374,765'Methods and compositions for diagnosis and treatment of iron misregulation diseases'20087,371,822'Human G-protein coupled receptor variant of HM74, HGPRBMY74'20087,348,149'Methods of diagnosing Parkinson\'s disease by measuring expression level of RNA encoding human protein HLLRCR-1'20087,344,860'Polynucleotide encoding a novel human P2X7 splice variant, HBMYP2X7v'20087,345,148'Human G-protein coupled receptor, HGPRBMY29sv1 polypeptides'20087,339,032'Human relaxin receptor HGPRBMY5v1'20087,329,650'Peptides and peptide analogues designed from HFE protein and their uses in the treatment of iron overload diseases'20087,326,781'Polynucleotides encoding the human citron kinase polypeptide, BMSNKC—0020/0021'20087,312,086'Methods of diagnosing colon adenocarcinoma using the human g-protein coupled receptor hgprbmy23'20077,309,779'Antibodies directed to the testis-specific tubulin tyrosine-ligase-like protein, BGS42'20077,304,141'Human leucine-rich repeat containing protein expressed predominately in bone marrow, HLRRBM1'20077,285,633'Metalloprotease highly expressed in the testis, MMP-29'20077,276,354'Polynucleotides encoding a novel human G-protein coupled receptor splice variant, HGPRBMY29SV2'20077,273,706'Method of diagnosing testicular tumors using polynucleotides encoding a novel testis-specific tubulin tyrosine-ligase-like protein, BGS42'20077,259,002'Polynucleotide encoding a novel acyl coenzyme A, monoacylglycerol acyltransferase-3 (MGAT3), and uses thereof'20077,223,558'Polynucleotides encoding three novel human cell surface proteins with leucine rich repeats and immunologobulin folds, BGS2, 3, and 4 and variants thereof'20077,223,557'Polynucleotide encoding a TRP channel family member, TRP-PLIK2'20077,211,423'Acetyl CoA carboxylase 2 sequences and methods'20077,202,056'Polynucleotides encoding a human cell surface protein with immunoglobulin folds, BGS-19'20077,199,227'Polynucleotides encoding human histone deacetylase HDAC9c'20077,189,539'Polynucleotide encoding a human relaxin receptor, HGPRBMY5v1'20077,183,379'Human leucine-rich repeat containing protein expressed predominately in small intestine, HLRRSI1'20077,153,678'Polynucleotides encoding the novel human phosphatase, RET31, and variants thereof'20067,141,381'Human leucine-rich repeat-containing proteins specifically expressed in the nervous system'20067,129,085'Polynucleotides encoding a human leucine-rich repeat domain containing protein, HLLRCR-1'20067,122,358'Testis-specific tubulin tyrosine-ligase-like protein, BGS42'20067,119,170'Methods and compositions for diagnosis and treatment of iron overload diseases and iron deficiency diseases'20067,115,375'Methods of diagnosing renal tumors by determining the expression level of RNA encoding the HGPRBMY18 polypeptide'20067,115,402'Polynucleotides encoding a novel testis-specific tubulin tyrosine-ligase-like protein, BGS42'20067,094,572'Polynucleotide encoding a novel human G-protein coupled receptor variant of HM74, HGPRBMY74'20067,078,513'Plasmids comprising nucleic acids from the hereditary hemochromatosis gene'20067,067,255'Hereditary hemochromatosis gene'20067,056,737'Polynucleotides encoding a novel glycine receptor alpha subunit expressed in the gastrointestinal tract, HGRA4, and splice variant thereof'20067,049,096'Polynucleotides encoding a novel human G-protein coupled receptor splice variant HGPRBMY29sv1'20066,949,363'Polynucleotides encoding novel human leucine-rich repeat containing protein expressed predominately in bone marrow, HLRRBM1'20056,924,265'Peptides and peptide analogues designed from HFE protein and their uses in the treatment of iron overload diseases'20056,858,407'Human leucine-rich repeat containing protein expressed predominately in small intestine, HLRRSI1'20056,849,399'Methods and compositions for diagnosis and treatment of iron misregulation diseases'20056,706,513'Adenosine deaminase homolog'20046,642,041'Polynucleotides encoding a novel metalloprotease, MP-1'20036,391,852'Methods and compositions for diagnosis and treatment of iron overload diseases and iron deficiency diseases'20026,284,732'Peptides and peptide analogues designed from HFE protein and their uses in the treatment of iron overload diseases'20016,228,594'Method for determining the presence or absence of a hereditary hemochromatosis gene mutation'20016,140,305'Hereditary hemochromatosis gene products'20006,025,130'Hereditary hemochromatosis gene'20005,872,237'Megabase transcript map: novel sequences and antibodies thereto'19995,753,438'Method to diagnose hereditary hemochromatosis'19985,712,098'Hereditary hemochromatosis diagnostic markers and diagnostic methods'19985,705,343'Method to diagnose hereditary hemochromatosis'1998

Career & activity timeline

Assembled from patent assignee/location history and declaration credentials.

1998–2000Patents assigned to MERCATOR GENETICS INC (4)· patent assignee history
1998–2012Based in Mountain View, CA, US· patent location history
1998Based in San Bernardino, CA, US· patent location history
1999–2008Based in San Carlos, CA, US· patent location history
2000–2012Patents assigned to BIO RAD LABORATORIES (12)· patent assignee history
2001–2008Patents assigned to CALIFORNIA INST OF TECHN (6)· patent assignee history
2003–2013Based in Belle Mead, NJ, US· patent location history
2004–2013Patents assigned to BRISTOL MYERS SQUIBB CO (42)· patent assignee history
2007Based in Belle Meade, NJ, US· patent location history
2012–2013Patents assigned to FEDER JOHN N (4)· patent assignee history

Inventor activity

Assignee and location history derived from the patent record.

Assignees
AssigneePatentsSpan
BRISTOL MYERS SQUIBB CO422004–2013
BIO RAD LABORATORIES122000–2012
CALIFORNIA INST OF TECHN62001–2008
FEDER JOHN Nself42012–2013
MERCATOR GENETICS INC41998–2000
Locations
LocationPatentsSpan
Belle Mead, New Jersey, US462003–2013
Mountain View, California, US101998–2012
San Carlos, California, US91999–2008
Belle Meade, New Jersey, US12007
San Bernardino, California, US11998