Haaf T - Search Results

1

Lack of F8 mRNA: a novel mechanism leading to hemophilia A.

El-Maarri O, Singer H, Klein C, Watzka M, Herbiniaux U, Brackmann HH, Schröder J, Graw J, Müller CR, Schramm W, Schwaab R, Haaf T, Hanfland P, Oldenburg J. El-Maarri O, et al. Among authors: haaf t. Blood. 2006 Apr 1;107(7):2759-65. doi: 10.1182/blood-2005-09-3702. Epub 2005 Dec 8. Blood. 2006. PMID: 16339403 Free article.

2

Epigenetic reprogramming in mouse primordial germ cells.

Hajkova P, Erhardt S, Lane N, Haaf T, El-Maarri O, Reik W, Walter J, Surani MA. Hajkova P, et al. Among authors: haaf t. Mech Dev. 2002 Sep;117(1-2):15-23. doi: 10.1016/s0925-4773(02)00181-8. Mech Dev. 2002. PMID: 12204247 Free article.

3

Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA.

Pezeshkpoor B, Zimmer N, Marquardt N, Nanda I, Haaf T, Budde U, Oldenburg J, El-Maarri O. Pezeshkpoor B, et al. Among authors: haaf t. J Thromb Haemost. 2013 Sep;11(9):1679-87. doi: 10.1111/jth.12339. J Thromb Haemost. 2013. PMID: 23809411 Free article.

4

Methylation analysis of the promoter region and intron 1 of the factor VIII gene in haemophilia A patients.

Zimmermann MA, Hansmann T, Haaf T, Oldenburg J, Müller CR, Rost S. Zimmermann MA, et al. Among authors: haaf t. Hamostaseologie. 2013;33 Suppl 1:S46-9. Hamostaseologie. 2013. PMID: 24170290

5

Berenil-induced undercondensation in human heterochromatin.

Haaf T, Feichtinger W, Guttenbach M, Sanchez L, Müller CR, Schmid M. Haaf T, et al. Cytogenet Cell Genet. 1989;50(1):27-33. doi: 10.1159/000132713. Cytogenet Cell Genet. 1989. PMID: 2472933

6

Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6.

Rost S, Bach E, Neuner C, Nanda I, Dysek S, Bittner RE, Keller A, Bartsch O, Mlynski R, Haaf T, Müller CR, Kunstmann E. Rost S, et al. Among authors: haaf t. Eur J Hum Genet. 2014 Feb;22(2):208-15. doi: 10.1038/ejhg.2013.108. Epub 2013 May 29. Eur J Hum Genet. 2014. PMID: 23714752 Free PMC article.

7

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.

Vona B, Müller T, Nanda I, Neuner C, Hofrichter MA, Schröder J, Bartsch O, Läßig A, Keilmann A, Schraven S, Kraus F, Shehata-Dieler W, Haaf T. Vona B, et al. Among authors: haaf t. Genet Med. 2014 Dec;16(12):945-53. doi: 10.1038/gim.2014.65. Epub 2014 May 29. Genet Med. 2014. PMID: 24875298 Free PMC article.

8

Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

Vona B, Nanda I, Neuner C, Schröder J, Kalscheuer VM, Shehata-Dieler W, Haaf T. Vona B, et al. Among authors: haaf t. BMC Med Genet. 2014 Jun 25;15:72. doi: 10.1186/1471-2350-15-72. BMC Med Genet. 2014. PMID: 24962056 Free PMC article. Review.

9

A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment.

Hofrichter MA, Nanda I, Gräf J, Schröder J, Shehata-Dieler W, Vona B, Haaf T. Hofrichter MA, et al. Among authors: haaf t. Mol Syndromol. 2015 Oct;6(4):156-63. doi: 10.1159/000439576. Epub 2015 Sep 3. Mol Syndromol. 2015. PMID: 26648831 Free PMC article.

10

Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation-negative early-onset and high-risk breast cancer patients.

Böck J, Appenzeller S, Haertle L, Schneider T, Gehrig A, Schröder J, Rost S, Wolf B, Bartram CR, Sutter C, Haaf T. Böck J, et al. Among authors: haaf t. Int J Cancer. 2018 Sep 15;143(6):1416-1425. doi: 10.1002/ijc.31526. Epub 2018 Apr 25. Int J Cancer. 2018. PMID: 29659014 Free PMC article.

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