Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
8 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Association of a common TLR-6 polymorphism with coronary artery disease - implications for healthy ageing?
Immun Ageing. 2013 Oct 30;10(1):43. doi: 10.1186/1742-4933-10-43.
Immun Ageing. 2013.
PMID: 24498948
Free PMC article.
A micro RNA-146a polymorphism is associated with coronary restenosis.
Hamann L, Glaeser C, Schulz S, Gross M, Franke A, Nöthlings U, Schumann RR.
Hamann L, et al. Among authors: glaeser c.
Int J Immunogenet. 2014 Oct;41(5):393-6. doi: 10.1111/iji.12136. Epub 2014 Jul 22.
Int J Immunogenet. 2014.
PMID: 25053223
Item in Clipboard
A frequent toll-like receptor (TLR)-2 polymorphism is a risk factor for coronary restenosis.
Hamann L, Gomma A, Schröder NW, Stamme C, Glaeser C, Schulz S, Gross M, Anker SD, Fox K, Schumann RR.
Hamann L, et al. Among authors: glaeser c.
J Mol Med (Berl). 2005 Jun;83(6):478-85. doi: 10.1007/s00109-005-0643-7. Epub 2005 May 4.
J Mol Med (Berl). 2005.
PMID: 15875151
Item in Clipboard
Toll-like receptor (TLR)-9 promotor polymorphisms and atherosclerosis.
Hamann L, Glaeser C, Hamprecht A, Gross M, Gomma A, Schumann RR.
Hamann L, et al. Among authors: glaeser c.
Clin Chim Acta. 2006 Feb;364(1-2):303-7. doi: 10.1016/j.cca.2005.07.017. Epub 2005 Aug 24.
Clin Chim Acta. 2006.
PMID: 16125159
Item in Clipboard
Gene symbol: JAG1. Disease: tetralogy of Fallot.
Glaeser C, Kotzot D, Caliebe A, Kottke R, Schulz S, Schweigmann U, Hansmann I.
Glaeser C, et al.
Hum Genet. 2006 Jul;119(6):674.
Hum Genet. 2006.
PMID: 17128462
No abstract available.
Item in Clipboard
Gene symbol: JAG1. Disease: Alagille syndrome.
Glaeser C.
Glaeser C.
Hum Genet. 2005 May;116(6):533.
Hum Genet. 2005.
PMID: 15988824
No abstract available.
Item in Clipboard
Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome.
Fischer A, Klamt B, Schumacher N, Glaeser C, Hansmann I, Fenge H, Gessler M.
Fischer A, et al. Among authors: glaeser c.
Mamm Genome. 2004 Sep;15(9):711-6. doi: 10.1007/s00335-004-2389-x.
Mamm Genome. 2004.
PMID: 15389319
Item in Clipboard
Detection and molecular characterization of Cryptosporidium spp. isolated from diarrheic children in Switzerland.
Glaeser C, Grimm F, Mathis A, Weber R, Nadal D, Deplazes P.
Glaeser C, et al.
Pediatr Infect Dis J. 2004 Apr;23(4):359-61. doi: 10.1097/00006454-200404000-00018.
Pediatr Infect Dis J. 2004.
PMID: 15071295
Item in Clipboard
Cite
Cite