Trappe R - Search Results

1

MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin.

Trappe R, Laccone F, Cobilanschi J, Meins M, Huppke P, Hanefeld F, Engel W. Trappe R, et al. Am J Hum Genet. 2001 May;68(5):1093-101. doi: 10.1086/320109. Epub 2001 Apr 17. Am J Hum Genet. 2001. PMID: 11309679 Free PMC article.

2

MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution.

Laccone F, Zoll B, Huppke P, Hanefeld F, Pepinski W, Trappe R. Laccone F, et al. Among authors: trappe r. J Med Genet. 2002 Aug;39(8):586-8. doi: 10.1136/jmg.39.8.586. J Med Genet. 2002. PMID: 12161600 Free PMC article. No abstract available.

3

A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?

Brockmann K, Meins M, Taubert A, Trappe R, Grond M, Hanefeld F. Brockmann K, et al. Among authors: trappe r. Eur Neurol. 2003;50(2):100-5. doi: 10.1159/000072507. Eur Neurol. 2003. PMID: 12944715

4

Targeted expression of SV40 large tumour antigen (TAg) induces a transient enhancement of spermatocyte proliferation and apoptosis.

Tascou S, Nayernia K, Meinhardt A, Schweyer S, Engel W, Trappe R, Burfeind P. Tascou S, et al. Among authors: trappe r. Mol Hum Reprod. 2001 Dec;7(12):1123-31. doi: 10.1093/molehr/7.12.1123. Mol Hum Reprod. 2001. PMID: 11719589

5

Identification and characterization of a novel murine multigene family containing a PHD-finger-like motif.

Trappe R, Ahmed M, Gläser B, Vogel C, Tascou S, Burfeind P, Engel W. Trappe R, et al. Biochem Biophys Res Commun. 2002 May 3;293(2):816-26. doi: 10.1016/S0006-291X(02)00277-2. Biochem Biophys Res Commun. 2002. PMID: 12054543

6

A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis.

Trappe R, Böhm D, Kohlhase J, Weise A, Liehr T, Essers G, Meins M, Zoll B, Bartels I, Burfeind P. Trappe R, et al. Cytogenet Genome Res. 2002;98(1):1-8. doi: 10.1159/000068533. Cytogenet Genome Res. 2002. PMID: 12584434 Review.

7

Identification and characterization of NIF3L1 BP1, a novel cytoplasmic interaction partner of the NIF3L1 protein.

Tascou S, Kang TW, Trappe R, Engel W, Burfeind P. Tascou S, et al. Among authors: trappe r. Biochem Biophys Res Commun. 2003 Sep 19;309(2):440-8. doi: 10.1016/j.bbrc.2003.07.008. Biochem Biophys Res Commun. 2003. PMID: 12951069

8

The Caenorhabditis elegans ortholog of human PHF5a shows a muscle-specific expression domain and is essential for C. elegans morphogenetic development.

Trappe R, Schulze E, Rzymski T, Fröde S, Engel W. Trappe R, et al. Biochem Biophys Res Commun. 2002 Oct 4;297(4):1049-57. doi: 10.1016/s0006-291x(02)02276-3. Biochem Biophys Res Commun. 2002. PMID: 12359262

9

The murine BTB/POZ zinc finger gene Znf131: predominant expression in the developing central nervous system, in adult brain, testis, and thymus.

Trappe R, Buddenberg P, Uedelhoven J, Gläser B, Buck A, Engel W, Burfeind P. Trappe R, et al. Biochem Biophys Res Commun. 2002 Aug 16;296(2):319-27. doi: 10.1016/s0006-291x(02)00850-1. Biochem Biophys Res Commun. 2002. PMID: 12163020

10

TSPY-LTA transgenic mice develop endocrine tumors of the pituitary and adrenal gland.

Tascou S, Trappe R, Nayernia K, Jarry H, König F, Schulz-Schaeffer W, Saeger W, Meinhardt A, Engel W, Schmidtke J, Burfeind P. Tascou S, et al. Among authors: trappe r. Mol Cell Endocrinol. 2003 Feb 28;200(1-2):9-18. doi: 10.1016/s0303-7207(02)00426-4. Mol Cell Endocrinol. 2003. PMID: 12644295

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