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Items: 17


A phase II pharmacodynamic study of erlotinib in patients with advanced non-small cell lung cancer previously treated with platinum-based chemotherapy.

Felip E, Rojo F, Reck M, Heller A, Klughammer B, Sala G, Cedres S, Peralta S, Maacke H, Foernzler D, Parera M, Möcks J, Saura C, Gatzemeier U, Baselga J.

Clin Cancer Res. 2008 Jun 15;14(12):3867-74. doi: 10.1158/1078-0432.CCR-07-5186.


Genetic Polymorphism of CYP2C19 gene in the Stanislas cohort. A link with inflammation.

Bertrand-Thiébault C, Berrahmoune H, Thompson A, Marie B, Droesch S, Siest G, Foernzler D, Visvikis-Siest S.

Ann Hum Genet. 2008 Mar;72(Pt 2):178-83. doi: 10.1111/j.1469-1809.2007.00417.x. Epub 2008 Jan 20.


Interaction between CYP1A1 T3801C and AHR G1661A polymorphisms according to smoking status on blood pressure in the Stanislas cohort.

Gambier N, Marteau JB, Batt AM, Marie B, Thompson A, Siest G, Foernzler D, Visvikis-Siest S.

J Hypertens. 2006 Nov;24(11):2199-205.


Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6.

Miksch S, Lumsden A, Guenther UP, Foernzler D, Christen-Zäch S, Daugherty C, Ramesar RK, Lebwohl M, Hohl D, Neldner KH, Lindpaintner K, Richards RI, Struk B.

Hum Mutat. 2005 Sep;26(3):235-48.


In silico genetics: identification of a functional element regulating H2-Ealpha gene expression.

Liao G, Wang J, Guo J, Allard J, Cheng J, Ng A, Shafer S, Puech A, McPherson JD, Foernzler D, Peltz G, Usuka J.

Science. 2004 Oct 22;306(5696):690-5.


A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation.

Rao C, Foernzler D, Loftus SK, Liu S, McPherson JD, Jungers KA, Apte SS, Pavan WJ, Beier DR.

Development. 2003 Oct;130(19):4665-72.


Which are the best tools for specific clinical application (chips, multiplex, mass spec profile, etc.)?

Ferrari M, Michel G, Foernzler D, Leininger-Muller B, Noyer-Weidner M, Frueh F, Visvikis S, Lambert C, Shenoi H, Hinnen A, Siest G.

Clin Chem Lab Med. 2003 Apr;41(4):492-5. No abstract available.


Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity.

Acuña G, Foernzler D, Leong D, Rabbia M, Smit R, Dorflinger E, Gasser R, Hoh J, Ott J, Borroni E, To Z, Thompson A, Li J, Hashimoto L, Lindpaintner K.

Pharmacogenomics J. 2002;2(5):327-34.


Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphisms.

Balemans W, Foernzler D, Parsons C, Ebeling M, Thompson A, Reid DM, Lindpaintner K, Ralston SH, Van Hul W.

Bone. 2002 Oct;31(4):515-9.


Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease.

Balemans W, Patel N, Ebeling M, Van Hul E, Wuyts W, Lacza C, Dioszegi M, Dikkers FG, Hildering P, Willems PJ, Verheij JB, Lindpaintner K, Vickery B, Foernzler D, Van Hul W.

J Med Genet. 2002 Feb;39(2):91-7.


Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis.

Heinimann K, Thompson A, Locher A, Furlanetto T, Bader E, Wolf A, Meier R, Walter K, Bauerfeind P, Marra G, Müller H, Foernzler D, Dobbie Z.

Cancer Res. 2001 Oct 15;61(20):7616-22.


A semi-automated system for analysis and storage of SNPs.

Lehnert V, Holzwarth J, Ott M, Thompson A, Demmak S, Foernzler D.

Hum Mutat. 2001 Apr;17(4):243-54.


Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).

Balemans W, Ebeling M, Patel N, Van Hul E, Olson P, Dioszegi M, Lacza C, Wuyts W, Van Den Ende J, Willems P, Paes-Alves AF, Hill S, Bueno M, Ramos FJ, Tacconi P, Dikkers FG, Stratakis C, Lindpaintner K, Vickery B, Foernzler D, Van Hul W.

Hum Mol Genet. 2001 Mar 1;10(5):537-43.


The spontaneous coat color mutant white nose (wn) maps to murine chromosome 15.

Marks PW, Bandura JL, Shieh DB, Foernzler D, Beier DR, Kwiatkowski DJ.

Mamm Genome. 1999 Jul;10(7):750-2. No abstract available.


Isolation of zebrafish gdf7 and comparative genetic mapping of genes belonging to the growth/differentiation factor 5, 6, 7 subgroup of the TGF-beta superfamily.

Davidson AJ, Postlethwait JH, Yan YL, Beier DR, van Doren C, Foernzler D, Celeste AJ, Crosier KE, Crosier PS.

Genome Res. 1999 Feb;9(2):121-9.


Gene mapping in zebrafish using single-strand conformation polymorphism analysis.

Foernzler D, Beier DR.

Methods Cell Biol. 1999;60:185-93. Review. No abstract available.


Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene.

Fleming MD, Trenor CC 3rd, Su MA, Foernzler D, Beier DR, Dietrich WF, Andrews NC.

Nat Genet. 1997 Aug;16(4):383-6.


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