Schweiger S - Search Results

1

Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing.

Winter J, Lehmann T, Krauss S, Trockenbacher A, Kijas Z, Foerster J, Suckow V, Yaspo ML, Kulozik A, Kalscheuer V, Schneider R, Schweiger S. Winter J, et al. Among authors: schweiger s. Hum Genet. 2004 May;114(6):541-52. doi: 10.1007/s00439-004-1114-x. Epub 2004 Mar 31. Hum Genet. 2004. PMID: 15057556

2

AIRE encodes a nuclear protein co-localizing with cytoskeletal filaments: altered sub-cellular distribution of mutants lacking the PHD zinc fingers.

Rinderle C, Christensen HM, Schweiger S, Lehrach H, Yaspo ML. Rinderle C, et al. Among authors: schweiger s. Hum Mol Genet. 1999 Feb;8(2):277-90. doi: 10.1093/hmg/8.2.277. Hum Mol Genet. 1999. PMID: 9931335

3

Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome.

Winter J, Lehmann T, Suckow V, Kijas Z, Kulozik A, Kalscheuer V, Hamel B, Devriendt K, Opitz J, Lenzner S, Ropers HH, Schweiger S. Winter J, et al. Among authors: schweiger s. Hum Genet. 2003 Mar;112(3):249-54. doi: 10.1007/s00439-002-0901-5. Epub 2003 Jan 24. Hum Genet. 2003. PMID: 12545276

4

The MID1/PP2A complex: a key to the pathogenesis of Opitz BBB/G syndrome.

Schweiger S, Schneider R. Schweiger S, et al. Bioessays. 2003 Apr;25(4):356-66. doi: 10.1002/bies.10256. Bioessays. 2003. PMID: 12655643 Review.

5

Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations.

So J, Suckow V, Kijas Z, Kalscheuer V, Moser B, Winter J, Baars M, Firth H, Lunt P, Hamel B, Meinecke P, Moraine C, Odent S, Schinzel A, van der Smagt JJ, Devriendt K, Albrecht B, Gillessen-Kaesbach G, van der Burgt I, Petrij F, Faivre L, McGaughran J, McKenzie F, Opitz JM, Cox T, Schweiger S. So J, et al. Among authors: schweiger s. Am J Med Genet A. 2005 Jan 1;132A(1):1-7. doi: 10.1002/ajmg.a.30407. Am J Med Genet A. 2005. PMID: 15558842

6

The Opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complex.

Aranda-Orgillés B, Trockenbacher A, Winter J, Aigner J, Köhler A, Jastrzebska E, Stahl J, Müller EC, Otto A, Wanker EE, Schneider R, Schweiger S. Aranda-Orgillés B, et al. Among authors: schweiger s. Hum Genet. 2008 Mar;123(2):163-76. doi: 10.1007/s00439-007-0456-6. Epub 2008 Jan 3. Hum Genet. 2008. PMID: 18172692 Free PMC article.

7

Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy.

Shoichet SA, Duprez L, Hagens O, Waetzig V, Menzel C, Herdegen T, Schweiger S, Dan B, Vamos E, Ropers HH, Kalscheuer VM. Shoichet SA, et al. Among authors: schweiger s. Hum Genet. 2006 Jan;118(5):559-67. doi: 10.1007/s00439-005-0084-y. Epub 2005 Oct 25. Hum Genet. 2006. PMID: 16249883

8

Alternative polyadenylation signals and promoters act in concert to control tissue-specific expression of the Opitz Syndrome gene MID1.

Winter J, Kunath M, Roepcke S, Krause S, Schneider R, Schweiger S. Winter J, et al. Among authors: schweiger s. BMC Mol Biol. 2007 Nov 15;8:105. doi: 10.1186/1471-2199-8-105. BMC Mol Biol. 2007. PMID: 18005432 Free PMC article.

9

Protein phosphatase 2A and rapamycin regulate the nuclear localization and activity of the transcription factor GLI3.

Krauss S, Foerster J, Schneider R, Schweiger S. Krauss S, et al. Among authors: schweiger s. Cancer Res. 2008 Jun 15;68(12):4658-65. doi: 10.1158/0008-5472.CAN-07-6174. Cancer Res. 2008. PMID: 18559511

10

Active transport of the ubiquitin ligase MID1 along the microtubules is regulated by protein phosphatase 2A.

Aranda-Orgillés B, Aigner J, Kunath M, Lurz R, Schneider R, Schweiger S. Aranda-Orgillés B, et al. Among authors: schweiger s. PLoS One. 2008;3(10):e3507. doi: 10.1371/journal.pone.0003507. Epub 2008 Oct 24. PLoS One. 2008. PMID: 18949047 Free PMC article.

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