EP 1100962 A1 20010523 - GENETIC POLYMORPHISMS IN THE HUMAN NEUROKININ 1 RECEPTOR GENE AND THEIR USES IN DIAGNOSIS AND TREATMENT OF DISEASES
Title (en)
GENETIC POLYMORPHISMS IN THE HUMAN NEUROKININ 1 RECEPTOR GENE AND THEIR USES IN DIAGNOSIS AND TREATMENT OF DISEASES
Title (de)
GENETISCHE POLYMORPHISMEN DES HUMANEN NEUROKININ-1-RECEPTOR-GENS UND DEREN VERWENDUNG ZUR DIAGNOSE UND BEHANDLUNG VON KRANKHEITEN
Title (fr)
POLYMORPHISMES GENETIQUES DU GENE DU RECEPTEUR NEUROKININIQUE 1 DE L'HOMME ET LEURS UTILISATIONS POUR LE DIAGNOSTIC ET LE TRAITEMENT D'AFFECTIONS
Publication
Application
Priority
- GB 9902340 W 19990720
- GB 9816192 A 19980725
- GB 9818280 A 19980822
Abstract (en)
[origin: WO0006768A1] This invention relates to nine single nucleotide polymorphisms in the human NK1R gene (1 in the regulatory region, 2 in coding regions, 2 in flanking intron sequence, 4 in the 3' UTR region) and corresponding novel allelic polypeptides encoded thereby. The invention also relates to methods and materials for analysing allelic variation in the NK1R gene and to the use of said polymorphism in the diagnosis and treatment of NK1R ligand mediated diseases, such as asthma.
IPC 1-7
IPC 8 full level
A61K 45/00 (2006.01); A61P 11/06 (2006.01); A61P 43/00 (2006.01); C07K 14/705 (2006.01); C12M 1/00 (2006.01); C12N 15/09 (2006.01); C12Q 1/68 (2006.01); G01N 33/50 (2006.01); G01N 33/53 (2006.01); G01N 33/566 (2006.01)
CPC (source: EP)
A61P 11/06 (2017.12); A61P 43/00 (2017.12); C07K 14/70571 (2013.01); C12Q 1/6883 (2013.01); C12Q 2600/156 (2013.01); C12Q 2600/172 (2013.01)
Citation (search report)
See references of WO 0006768A1
Designated contracting state (EPC)
AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE
DOCDB simple family (publication)
WO 0006768 A1 20000210; AU 5052899 A 20000221; EP 1100962 A1 20010523; JP 2002521062 A 20020716
DOCDB simple family (application)
GB 9902340 W 19990720; AU 5052899 A 19990720; EP 99934895 A 19990720; JP 2000562550 A 19990720