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Items: 18

1.

MtDNA diversity of Ghana: a forensic and phylogeographic view.

Fendt L, Röck A, Zimmermann B, Bodner M, Thye T, Tschentscher F, Owusu-Dabo E, Göbel TM, Schneider PM, Parson W.

Forensic Sci Int Genet. 2012 Mar;6(2):244-9. doi: 10.1016/j.fsigen.2011.05.011. Epub 2011 Jun 30.

2.

Methylation analysis of several tumour suppressor genes shows a low frequency of methylation of CDKN2A and RARB in uveal melanomas.

Zeschnigk M, Tschentscher F, Lich C, Brandt B, Horsthemke B, Lohmann DR.

Comp Funct Genomics. 2003;4(3):329-36. doi: 10.1002/cfg.295.

3.

Allele frequencies of 11 X-chromosomal loci in a population sample from Ghana.

Poetsch M, El-Mostaqim D, Tschentscher F, Browne EN, Timmann C, Horstmann RD, von Wurmb-Schwark N.

Int J Legal Med. 2009 Jan;123(1):81-3. doi: 10.1007/s00414-008-0251-5. Epub 2008 Jul 8.

PMID:
18607615
4.

Amelogenin sex determination by pyrosequencing of short PCR products.

Tschentscher F, Frey UH, Bajanowski T.

Int J Legal Med. 2008 Jul;122(4):333-5. doi: 10.1007/s00414-008-0228-4. Epub 2008 Mar 20.

PMID:
18351373
5.

NHE3 in the human brainstem: implication for the pathogenesis of the sudden infant death syndrome (SIDS)?

Wiemann M, Frede S, Tschentscher F, Kiwull-Schöne H, Kiwull P, Bingmann D, Brinkmann B, Bajanowski T.

Adv Exp Med Biol. 2008;605:508-13.

PMID:
18085326
6.

Genetic investigation of the TSPYL1 gene in sudden infant death syndrome.

Hering R, Frade-Martinez R, Bajanowski T, Poets CF, Tschentscher F, Riess O.

Genet Med. 2006 Jan;8(1):55-8.

PMID:
16418600
7.

Protocols for ancient DNA typing.

Capelli C, Tschentscher F.

Methods Mol Biol. 2005;297:265-78.

PMID:
15570114
8.

Tumor classification based on gene expression profiling shows that uveal melanomas with and without monosomy 3 represent two distinct entities.

Tschentscher F, Hüsing J, Hölter T, Kruse E, Dresen IG, Jöckel KH, Anastassiou G, Schilling H, Bornfeld N, Horsthemke B, Lohmann DR, Zeschnigk M.

Cancer Res. 2003 May 15;63(10):2578-84.

9.

"Ancient" protocols for the crime scene? Similarities and differences between forensic genetics and ancient DNA analysis.

Capelli C, Tschentscher F, Pascali VL.

Forensic Sci Int. 2003 Jan 9;131(1):59-64.

PMID:
12505472
10.

[Prognostically relevant markers of malignant melanoma of the uvea].

Anastassiou G, Tschentscher F, Zeschnigk M.

Ophthalmologe. 2002 May;99(5):327-32. Review. German.

PMID:
12043285
11.

Cadherin expression in uveal melanoma.

Anastassiou G, Tschentscher F, Zeschnigk M, Bornfeld N.

Exp Eye Res. 2002 Mar;74(3):423-5. No abstract available.

PMID:
12014924
12.

Partial deletions of the long and short arm of chromosome 3 point to two tumor suppressor genes in uveal melanoma.

Tschentscher F, Prescher G, Horsman DE, White VA, Rieder H, Anastassiou G, Schilling H, Bornfeld N, Bartz-Schmidt KU, Horsthemke B, Lohmann DR, Zeschnigk M.

Cancer Res. 2001 Apr 15;61(8):3439-42.

13.

Identification of chromosomes 3, 6, and 8 aberrations in uveal melanoma by microsatellite analysis in comparison to comparative genomic hybridization.

Tschentscher F, Prescher G, Zeschnigk M, Horsthemke B, Lohmann DR.

Cancer Genet Cytogenet. 2000 Oct 1;122(1):13-7.

PMID:
11104026
14.

Genetic analysis of immunomodulating factors in sporadic Parkinson's disease.

Krüger R, Hardt C, Tschentscher F, Jäckel S, Kuhn W, Müller T, Werner J, Woitalla D, Berg D, Kühnl N, Fuchs GA, Santos EJ, Przuntek H, Epplen JT, Schöls L, Riess O.

J Neural Transm (Vienna). 2000;107(5):553-62.

PMID:
11072751
15.

A view of Neandertal genetic diversity.

Krings M, Capelli C, Tschentscher F, Geisert H, Meyer S, von Haeseler A, Grossschmidt K, Possnert G, Paunovic M, Pääbo S.

Nat Genet. 2000 Oct;26(2):144-6. No abstract available.

PMID:
11017066
16.

Identification and efficient genotyping of an (A)n/(T)m polymorphism within the 5' untranslated region of the human IL6 gene.

Tschentscher F, Kalt A, Hoffmann V, Epplen J, Hardt C.

Eur J Immunogenet. 2000 Feb;27(1):1-3. No abstract available.

PMID:
10651844
17.

Too mammoth an undertaking.

Tschentscher F.

Science. 1999 Dec 10;286(5447):2084. No abstract available.

PMID:
10617418
18.

Polymerase chain reaction-single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes.

Jaeckel S, Epplen JT, Kauth M, Miterski B, Tschentscher F, Epplen C.

Electrophoresis. 1998 Dec;19(18):3055-61. Review.

PMID:
9932793

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