Foernzler D[au] - Search Results

Year	Number of Results
1997	1
1999	3
2001	3
2002	3
2003	2
2004	1
2005	1
2006	1
2008	2
2022	1
2024	0

1

Comparison of Two Illumina Whole Transcriptome RNA Sequencing Library Preparation Methods Using Human Cancer FFPE Specimens.

Wang D, Rolfe PA, Foernzler D, O'Rourke D, Zhao S, Scheuenpflug J, Feng Z. Wang D, et al. Among authors: foernzler d. Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221076304. doi: 10.1177/15330338221076304. Technol Cancer Res Treat. 2022. PMID: 35138205 Free PMC article.

2

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. Liao G, et al. Among authors: foernzler d. Science. 2004 Oct 22;306(5696):690-5. doi: 10.1126/science.1100636. Science. 2004. PMID: 15499019

3

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. Fleming MD, et al. Among authors: foernzler d. Nat Genet. 1997 Aug;16(4):383-6. doi: 10.1038/ng0897-383. Nat Genet. 1997. PMID: 9241278

4

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. Rao C, et al. Among authors: foernzler d. Development. 2003 Oct;130(19):4665-72. doi: 10.1242/dev.00668. Development. 2003. PMID: 12925592

5

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. Miksch S, et al. Among authors: foernzler d. Hum Mutat. 2005 Sep;26(3):235-48. doi: 10.1002/humu.20206. Hum Mutat. 2005. PMID: 16086317

6

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. Bertrand-Thiébault C, et al. Among authors: foernzler d. Ann Hum Genet. 2008 Mar;72(Pt 2):178-83. doi: 10.1111/j.1469-1809.2007.00417.x. Epub 2008 Jan 20. Ann Hum Genet. 2008. PMID: 18205890

7

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

Foernzler D, Beier DR. Foernzler D, et al. Methods Cell Biol. 1999;60:185-93. doi: 10.1016/s0091-679x(08)61901-9. Methods Cell Biol. 1999. PMID: 9891338 Review. No abstract available.

8

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. Balemans W, et al. Among authors: foernzler d. Hum Mol Genet. 2001 Mar 1;10(5):537-43. doi: 10.1093/hmg/10.5.537. Hum Mol Genet. 2001. PMID: 11181578

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. Balemans W, et al. Among authors: foernzler d. J Med Genet. 2002 Feb;39(2):91-7. doi: 10.1136/jmg.39.2.91. J Med Genet. 2002. PMID: 11836356 Free PMC article.

10

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. Balemans W, et al. Among authors: foernzler d. Bone. 2002 Oct;31(4):515-9. doi: 10.1016/s8756-3282(02)00844-x. Bone. 2002. PMID: 12398949

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