Kalscheuer V - Search Results

1

Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion.

Tzschach A, Krause-Plonka I, Menzel C, Knoblauch A, Toennies H, Hoeltzenbein M, Radke M, Ropers HH, Kalscheuer V. Tzschach A, et al. Among authors: kalscheuer v. Am J Med Genet A. 2006 May 15;140(10):1108-10. doi: 10.1002/ajmg.a.31226. Am J Med Genet A. 2006. PMID: 16619204

2

The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans.

Kalscheuer VM, Mariman EC, Schepens MT, Rehder H, Ropers HH. Kalscheuer VM, et al. Nat Genet. 1993 Sep;5(1):74-8. doi: 10.1038/ng0993-74. Nat Genet. 1993. PMID: 8220428

3

The MAS proto-oncogene is not imprinted in humans.

Riesewijk AM, Schepens MT, Mariman EM, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: kalscheuer vm. Genomics. 1996 Jul 15;35(2):380-2. doi: 10.1006/geno.1996.0372. Genomics. 1996. PMID: 8661154 Free article.

4

Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription.

Riesewijk AM, Schepens MT, Welch TR, van den Berg-Loonen EM, Mariman EM, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: kalscheuer vm. Genomics. 1996 Jan 15;31(2):158-66. doi: 10.1006/geno.1996.0027. Genomics. 1996. PMID: 8824797

5

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses.

Riesewijk AM, Hu L, Schulz U, Tariverdian G, Höglund P, Kere J, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: kalscheuer vm. Genomics. 1997 Jun 1;42(2):236-44. doi: 10.1006/geno.1997.4731. Genomics. 1997. PMID: 9192843 Free article.

6

Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression.

Riesewijk AM, Xu YQ, Schepens MT, Mariman EM, Polychronakos C, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: kalscheuer vm. Biochem Biophys Res Commun. 1998 Apr 7;245(1):272-7. doi: 10.1006/bbrc.1998.8414. Biochem Biophys Res Commun. 1998. PMID: 9535821

7

Evidence against a major role of PEG1/MEST in Silver-Russell syndrome.

Riesewijk AM, Blagitko N, Schinzel AA, Hu L, Schulz U, Hamel BC, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: kalscheuer vm. Eur J Hum Genet. 1998 Mar-Apr;6(2):114-20. doi: 10.1038/sj.ejhg.5200164. Eur J Hum Genet. 1998. PMID: 9781054

8

Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1.

Brunner B, Todt T, Lenzner S, Stout K, Schulz U, Ropers HH, Kalscheuer VM. Brunner B, et al. Among authors: kalscheuer vm. Genome Res. 1999 May;9(5):437-48. Genome Res. 1999. PMID: 10330123 Free PMC article.

9

gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome.

Blagitko N, Schulz U, Schinzel AA, Ropers HH, Kalscheuer VM. Blagitko N, et al. Among authors: kalscheuer vm. Hum Mol Genet. 1999 Dec;8(13):2387-96. doi: 10.1093/hmg/8.13.2387. Hum Mol Genet. 1999. PMID: 10556286

10

Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion.

Blagitko N, Mergenthaler S, Schulz U, Wollmann HA, Craigen W, Eggermann T, Ropers HH, Kalscheuer VM. Blagitko N, et al. Among authors: kalscheuer vm. Hum Mol Genet. 2000 Jul 1;9(11):1587-95. doi: 10.1093/hmg/9.11.1587. Hum Mol Genet. 2000. PMID: 10861285

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