GPR6sb polypeptides and polynucleotides and methods for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for utilizing GPR6sb polypeptides and polynucleotides in therapy, and diagnostic assays for such.
Nabil Elshourbagy - West Chester PA, US Pamela Lane - Norristown PA, US Ping Tsui - Berwyn PA, US
International Classification:
C12P021/02 C12N005/06 C07K014/705 C07H021/04
US Classification:
435/069100, 435/325000, 530/350000, 536/023500
Abstract:
Rattus norvegus AXOR29 polypeptides and polynucleotides and method for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for screening for compounds that either agonize or antagonize rattus norvegus AXOR29. Such compounds are expected to be useful in treatment of human diseases, including, but not limited to: infections such as bacterial, fungal, protozoan and viral infections, particularly infections caused by HIV-1 or HIV-2; pain; cancers; diabetes, obesity; anorexia; bulimia; asthma; Parkinson's disease; acute heart failure; hypotension; hypertension; urinary retention; osteoporosis; angina pectoris; myocardial infarction; stroke; ulcers; asthma; allergies; benign prostatic hypertrophy; migraine; vomiting; psychotic and neurological disorders, including anxiety, schizophrenia, manic depression, depression, delirium, dementia, and severe mental retardation; and dyskinesias, such as Huntington's disease or Gilles dela Tourett's syndrome.
Mus Musculus FMRL-3 polypeptides and polynucleotides and method for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for screening for compounds that either agonize or antagonize Mus Musculus FMRL-3. Such compounds are expected to be useful in treatment of human diseases, including, but not limited to: infections such as bacterial, fungal, protozoan and viral infections, particularly infections caused by HIV-1 or HIV-2; pain; cancers; diabetes, obesity; anorexia; bulimia; asthma; Parkinson's disease; acute heart failure; hypotension; hypertension; urinary retention; osteoporosis; angina pectoris; myocardial infarction; stroke; ulcers; asthma; allergies; benign prostatic hypertrophy; migraine; vomiting; psychotic and neurological disorders, including anxiety, schizophrenia, manic depression, depression, delirium, dementia, and severe mental retardation; and dyskinesias, such as Huntington's disease or Gilles dela Tourett's syndrome.
Mus musculus EDG7 polypeptides and polynucleotides and method for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for screening for compounds that either agonize or antagonize Mus musculus EDG7. Such compounds are expected to be useful in treatment of human diseases, including, but not limited to: infections such as bacterial, fungal, protozoan and viral infections, particularly infections caused by HIV-1 or HIV-2; pain; cancers; diabetes, obesity; anorexia; bulimia; asthma; Parkinson's disease; acute heart failure; hypotension; hypertension; urinary retention; osteoporosis; angina pectoris; myocardial infarction; stroke; ulcers; asthma; allergies; benign prostatic hypertrophy; migraine; vomiting; psychotic and neurological disorders, including anxiety, schizophrenia, manic depression, depression, delirium, dementia, and severe mental retardation; and dyskinesias, such as Huntington's disease or Gilles dela Tourett's syndrome.
Mus musculus EDG4 polypeptides and polynucleotides and method for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for screening for compounds that either agonize or antagonize Mus musculus EDG4. Such compounds are expected to be useful in treatment of human diseases, including, but not limited to: infections such as bacterial, fungal, protozoan and viral infections, particularly infections caused by HIV-1 or HIV-2; pain; cancers; diabetes, obesity; anorexia; bulimia; asthma; Parkinson's disease; acute heart failure; hypotension; hypertension; urinary retention; osteoporosis; angina pectoris; myocardial infarction; stroke; ulcers; asthma; allergies; benign prostatic hypertrophy; migraine; vomiting; psychotic and neurological disorders, including anxiety, schizophrenia, manic depression, depression, delirium, dementia, and severe mental retardation; and dyskinesias, such as Huntington's disease or Gilles dela Tourett's syndrome.
Polynucleotide Encoding A Mouse 7-Transmembrane Gpr43 Receptor
Nabil Elshourbagy - West Chester PA Pamela Lane - Norristown PA Ping Tsui - Berwyn PA Lisa Vawter - Coopersburg PA
Assignee:
SmithKline Beecham Corporation - Philadelphia PA
International Classification:
C12P 2106 C12P 2104 C12N 120 C12N 1500 C07H 2104
US Classification:
435 691
Abstract:
The mouse GPR43 polypeptides and polynucleotides and methods for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for utilizing mouse GPR43 polypeptides and polynucleotides in therapy, and diagnostic assays for such.
Name / Title
Company / Classification
Phones & Addresses
Pamela Lane Partner
Coldwell Banker Res Brokerage
1879 N Hwy 25, Travelers Rest, SC 29690 7816318610
Aug 2013 to 2000 AREA RESOURCE COORDINATOREnersys Richmond, KY Mar 2000 to Aug 2013 Production Planning ClerkA.C.S Berea, KY Aug 1983 to Mar 2000 Data entry operator
Education:
Sullivan University eLearning Louisville, KY Jun 2012 Supply Chain DemandNational College of Business & Technology Richmond, KY May 1999 to May 2001 Vocational in businessMadison Central High School Richmond, KY May 1979 to May 1982 Diploma
License Records
Pamela A. Lane
License #:
PST.011551 - Expired
Issued Date:
Feb 8, 1979
Expiration Date:
Dec 31, 1995
Type:
Pharmacist
Pamela A Lane
License #:
202843 - Expired
Issued Date:
Apr 27, 1981
Expiration Date:
Oct 1, 1990
Type:
Licensed Certified Social Worker
Isbn (Books And Publications)
Learning for Life: Creating Classrooms for Self-Directed Learning