Schackert HK - Search Results

1

Screening for large rearrangements of the BRCA1 gene in German breast or ovarian cancer families using semi-quantitative multiplex PCR method.

Hofmann W, Görgens H, John A, Horn D, Hüttner C, Arnold N, Scherneck S, Schackert HK. Hofmann W, et al. Among authors: schackert hk. Hum Mutat. 2003 Jul;22(1):103-4. doi: 10.1002/humu.9154. Hum Mutat. 2003. PMID: 12815601

2

Identification of six novel MSH2 and MLH1 germline mutations in HNPCC.

Krüger S, Plaschke J, Jeske B, Görgens H, Pistorius SR, Bier A, Kreuz FR, Theissig F, Aust DE, Saeger HD, Schackert HK. Krüger S, et al. Among authors: schackert hk. Hum Mutat. 2003 Apr;21(4):445-6. doi: 10.1002/humu.9121. Hum Mutat. 2003. PMID: 12655562

3

Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines.

Seitz S, Wassmuth P, Plaschke J, Schackert HK, Karsten U, Santibanez-Koref MF, Schlag PM, Scherneck S. Seitz S, et al. Among authors: schackert hk. Genes Chromosomes Cancer. 2003 May;37(1):29-35. doi: 10.1002/gcc.10196. Genes Chromosomes Cancer. 2003. PMID: 12661003

4

One-step analysis of ten functional haplotype combinations of the basic RET promoter with a LightCycler assay.

Görgens H, Fitze G, Roesner D, Schackert HK. Görgens H, et al. Among authors: schackert hk. Clin Chem. 2004 Sep;50(9):1693-5. doi: 10.1373/clinchem.2004.034165. Epub 2004 Jul 20. Clin Chem. 2004. PMID: 15265820 No abstract available.

5

Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.

Pistorius S, Görgens H, Plaschke J, Hoehl R, Krüger S, Engel C, Saeger HD, Schackert HK. Pistorius S, et al. Among authors: schackert hk. Cancer Lett. 2007 Apr 8;248(1):89-95. doi: 10.1016/j.canlet.2006.06.002. Epub 2006 Jul 11. Cancer Lett. 2007. PMID: 16837128

6

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.

Steinke V, Rahner N, Morak M, Keller G, Schackert HK, Görgens H, Schmiegel W, Royer-Pokora B, Dietmaier W, Kloor M, Engel C, Propping P, Aretz S; German HNPCC Consortium. Steinke V, et al. Among authors: schackert hk. Eur J Hum Genet. 2008 May;16(5):587-92. doi: 10.1038/ejhg.2008.26. Epub 2008 Feb 27. Eur J Hum Genet. 2008. PMID: 18301448

7

Analysis of RET, ZEB2, EDN3 and GDNF genomic rearrangements in central congenital hyperventilation syndrome patients by multiplex ligation-dependent probe amplification.

Serra A, Görgens H, Alhadad K, Fitze G, Schackert HK. Serra A, et al. Among authors: schackert hk. Ann Hum Genet. 2010 Jul;74(4):369-74. doi: 10.1111/j.1469-1809.2010.00577.x. Epub 2010 Apr 25. Ann Hum Genet. 2010. PMID: 20456320

8

Analysis of RET, ZEB2, EDN3 and GDNF genomic rearrangements in 80 patients with Hirschsprung disease (using multiplex ligation-dependent probe amplification).

Serra A, Görgens H, Alhadad K, Ziegler A, Fitze G, Schackert HK. Serra A, et al. Among authors: schackert hk. Ann Hum Genet. 2009 Mar;73(2):147-51. doi: 10.1111/j.1469-1809.2008.00503.x. Epub 2009 Jan 14. Ann Hum Genet. 2009. PMID: 19183406

9

Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: a comprehensive analysis of 3,671 families.

Steinke V, Holzapfel S, Loeffler M, Holinski-Feder E, Morak M, Schackert HK, Görgens H, Pox C, Royer-Pokora B, von Knebel-Doeberitz M, Büttner R, Propping P, Engel C; German HNPCC Consortium. Steinke V, et al. Among authors: schackert hk. Int J Cancer. 2014 Jul 1;135(1):69-77. doi: 10.1002/ijc.28650. Epub 2014 Feb 20. Int J Cancer. 2014. PMID: 24493211

10

Analysis of the base excision repair genes MTH1, OGG1 and MUTYH in patients with squamous oral carcinomas.

Görgens H, Müller A, Krüger S, Kuhlisch E, König IR, Ziegler A, Schackert HK, Eckelt U. Görgens H, et al. Among authors: schackert hk. Oral Oncol. 2007 Sep;43(8):791-5. doi: 10.1016/j.oraloncology.2006.10.004. Epub 2007 Jan 4. Oral Oncol. 2007. PMID: 17207658

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