Matches in SemOpenAlex for { <https://semopenalex.org/work/W2018251168> ?p ?o ?g. }
Showing items 1 to 62 of
62
with 100 items per page.
- W2018251168 endingPage "90" @default.
- W2018251168 startingPage "89" @default.
- W2018251168 abstract "Correspondence| June 21 2000 The Pro-115 → Gln mutation in peroxisome-proliferator-activated receptor (PPAR) γ2 is extremely rare in a large cohort of U.S. Caucasians Jonathan TERRETT; Jonathan TERRETT *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K. Search for other works by this author on: This Site PubMed Google Scholar John CHAMBERLAIN; John CHAMBERLAIN *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K.†Rayne Institute, Bone and Mineral Centre, Department of Medicine, Royal Free and University College Medical School, London WC1E 6JJ, U.K. Correspondence: Dr J. C. Chamberlain, Roche Products Ltd., 40 Broadwater Road, Welwyn Garden City, Herts., U.K. (e-mail chris.chamberlain@roche.com). Search for other works by this author on: This Site PubMed Google Scholar Sohaila RASTAN; Sohaila RASTAN *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K. Search for other works by this author on: This Site PubMed Google Scholar Richard MARSHALL; Richard MARSHALL *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K. Search for other works by this author on: This Site PubMed Google Scholar Ralph MCGINNIS; Ralph MCGINNIS *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K. Search for other works by this author on: This Site PubMed Google Scholar Nigel SPURR; Nigel SPURR *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K. Search for other works by this author on: This Site PubMed Google Scholar Eamonn O'BRIEN; Eamonn O'BRIEN *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K. Search for other works by this author on: This Site PubMed Google Scholar Catherine EVANS; Catherine EVANS *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K. Search for other works by this author on: This Site PubMed Google Scholar Andrew RUT Andrew RUT *Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, U.K. Search for other works by this author on: This Site PubMed Google Scholar Clin Sci (Lond) (2000) 99 (1): 89–90. https://doi.org/10.1042/cs0990089 Article history Received: October 27 1999 Views Icon Views Article contents Figures & tables Video Audio Supplementary Data Peer Review Share Icon Share MailTo Twitter LinkedIn Cite Icon Cite Get Permissions Citation Jonathan TERRETT, John CHAMBERLAIN, Sohaila RASTAN, Richard MARSHALL, Ralph MCGINNIS, Nigel SPURR, Eamonn O'BRIEN, Catherine EVANS, Andrew RUT; The Pro-115 → Gln mutation in peroxisome-proliferator-activated receptor (PPAR) γ2 is extremely rare in a large cohort of U.S. Caucasians. Clin Sci (Lond) 1 July 2000; 99 (1): 89–90. doi: https://doi.org/10.1042/cs0990089 Download citation file: Ris (Zotero) Reference Manager EasyBib Bookends Mendeley Papers EndNote RefWorks BibTex toolbar search Search Dropdown Menu toolbar search search input Search input auto suggest filter your search All ContentAll JournalsClinical Science Search Advanced Search Keywords: obesity, pharmacogenetics, point mutation, type II diabetes mellitus, transcription factors This content is only available as a PDF. The Biochemical Society and the Medical Research Society © 20002000 Article PDF first page preview Close Modal You do not currently have access to this content." @default.
- W2018251168 created "2016-06-24" @default.
- W2018251168 creator A5000740332 @default.
- W2018251168 creator A5016673645 @default.
- W2018251168 creator A5021679263 @default.
- W2018251168 creator A5050838325 @default.
- W2018251168 creator A5052146722 @default.
- W2018251168 creator A5069023418 @default.
- W2018251168 creator A5073775242 @default.
- W2018251168 creator A5078722690 @default.
- W2018251168 creator A5079152697 @default.
- W2018251168 date "2000-06-21" @default.
- W2018251168 modified "2023-09-27" @default.
- W2018251168 title "The Pro-115 → Gln mutation in peroxisome-proliferator-activated receptor (PPAR) γ2 is extremely rare in a large cohort of U.S. Caucasians" @default.
- W2018251168 cites W1985735647 @default.
- W2018251168 cites W2028661874 @default.
- W2018251168 cites W2078535741 @default.
- W2018251168 cites W2086376157 @default.
- W2018251168 cites W2125344994 @default.
- W2018251168 cites W2333284976 @default.
- W2018251168 doi "https://doi.org/10.1042/cs0990089" @default.
- W2018251168 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10887062" @default.
- W2018251168 hasPublicationYear "2000" @default.
- W2018251168 type Work @default.
- W2018251168 sameAs 2018251168 @default.
- W2018251168 citedByCount "3" @default.
- W2018251168 crossrefType "journal-article" @default.
- W2018251168 hasAuthorship W2018251168A5000740332 @default.
- W2018251168 hasAuthorship W2018251168A5016673645 @default.
- W2018251168 hasAuthorship W2018251168A5021679263 @default.
- W2018251168 hasAuthorship W2018251168A5050838325 @default.
- W2018251168 hasAuthorship W2018251168A5052146722 @default.
- W2018251168 hasAuthorship W2018251168A5069023418 @default.
- W2018251168 hasAuthorship W2018251168A5073775242 @default.
- W2018251168 hasAuthorship W2018251168A5078722690 @default.
- W2018251168 hasAuthorship W2018251168A5079152697 @default.
- W2018251168 hasConcept C161191863 @default.
- W2018251168 hasConcept C41008148 @default.
- W2018251168 hasConceptScore W2018251168C161191863 @default.
- W2018251168 hasConceptScore W2018251168C41008148 @default.
- W2018251168 hasIssue "1" @default.
- W2018251168 hasLocation W20182511681 @default.
- W2018251168 hasLocation W20182511682 @default.
- W2018251168 hasOpenAccess W2018251168 @default.
- W2018251168 hasPrimaryLocation W20182511681 @default.
- W2018251168 hasRelatedWork W2001060508 @default.
- W2018251168 hasRelatedWork W2010066730 @default.
- W2018251168 hasRelatedWork W2039589765 @default.
- W2018251168 hasRelatedWork W2070869476 @default.
- W2018251168 hasRelatedWork W4242188614 @default.
- W2018251168 hasRelatedWork W611717159 @default.
- W2018251168 hasRelatedWork W617126653 @default.
- W2018251168 hasRelatedWork W654893371 @default.
- W2018251168 hasRelatedWork W658636438 @default.
- W2018251168 hasRelatedWork W1564778502 @default.
- W2018251168 hasVolume "99" @default.
- W2018251168 isParatext "false" @default.
- W2018251168 isRetracted "false" @default.
- W2018251168 magId "2018251168" @default.
- W2018251168 workType "article" @default.