Müller I - Search Results

1

Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesis.

Herr A, Meunier D, Müller I, Rump A, Fundele R, Ropers HH, Nuber UA. Herr A, et al. Among authors: muller i. Dev Dyn. 2003 Apr;226(4):579-86. doi: 10.1002/dvdy.10260. Dev Dyn. 2003. PMID: 12666195 Free article.

2

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.

Ullmann R, Turner G, Kirchhoff M, Chen W, Tonge B, Rosenberg C, Field M, Vianna-Morgante AM, Christie L, Krepischi-Santos AC, Banna L, Brereton AV, Hill A, Bisgaard AM, Müller I, Hultschig C, Erdogan F, Wieczorek G, Ropers HH. Ullmann R, et al. Among authors: muller i. Hum Mutat. 2007 Jul;28(7):674-82. doi: 10.1002/humu.20546. Hum Mutat. 2007. PMID: 17480035

3

The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation.

Abdelkhalek HB, Beckers A, Schuster-Gossler K, Pavlova MN, Burkhardt H, Lickert H, Rossant J, Reinhardt R, Schalkwyk LC, Müller I, Herrmann BG, Ceolin M, Rivera-Pomar R, Gossler A. Abdelkhalek HB, et al. Among authors: muller i. Genes Dev. 2004 Jul 15;18(14):1725-36. doi: 10.1101/gad.303504. Epub 2004 Jul 1. Genes Dev. 2004. PMID: 15231714 Free PMC article.

4

An integrative approach for analyzing the interplay of genetic and epigenetic changes in tumors.

Muradyan A, Boldt V, Steininger A, Stabentheiner S, Tebel K, Kreutzberger J, Müller I, Madle H, Popper HH, Ullmann R. Muradyan A, et al. Among authors: muller i. Arch Pathol Lab Med. 2008 Oct;132(10):1557-61. doi: 10.5858/2008-132-1557-AIAFAT. Arch Pathol Lab Med. 2008. PMID: 18834209 Free article.

5

Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome.

So J, Müller I, Kunath M, Herrmann S, Ullmann R, Schweiger S. So J, et al. Among authors: muller i. Am J Med Genet A. 2008 Jan 1;146A(1):103-9. doi: 10.1002/ajmg.a.32055. Am J Med Genet A. 2008. PMID: 18074389

6

Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization.

Shoichet SA, Waibel S, Endruhn S, Sperfeld AD, Vorwerk B, Müller I, Erdogan F, Ludolph AC, Ropers HH, Ullmann R. Shoichet SA, et al. Among authors: muller i. Amyotroph Lateral Scler. 2009 Jun;10(3):162-9. doi: 10.1080/17482960802535001. Amyotroph Lateral Scler. 2009. PMID: 18985462

7

The genomic sequence and comparative analysis of the rat major histocompatibility complex.

Hurt P, Walter L, Sudbrak R, Klages S, Müller I, Shiina T, Inoko H, Lehrach H, Günther E, Reinhardt R, Himmelbauer H. Hurt P, et al. Among authors: muller i. Genome Res. 2004 Apr;14(4):631-9. doi: 10.1101/gr.1987704. Genome Res. 2004. PMID: 15060004 Free PMC article.

8

Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation.

Erdogan F, Chen W, Kirchhoff M, Kalscheuer VM, Hultschig C, Müller I, Schulz R, Menzel C, Bryndorf T, Ropers HH, Ullmann R. Erdogan F, et al. Among authors: muller i. Cytogenet Genome Res. 2006;115(3-4):247-53. doi: 10.1159/000095921. Cytogenet Genome Res. 2006. PMID: 17124407

9

Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.

Thorwarth A, Schnittert-Hübener S, Schrumpf P, Müller I, Jyrch S, Dame C, Biebermann H, Kleinau G, Katchanov J, Schuelke M, Ebert G, Steininger A, Bönnemann C, Brockmann K, Christen HJ, Crock P, deZegher F, Griese M, Hewitt J, Ivarsson S, Hübner C, Kapelari K, Plecko B, Rating D, Stoeva I, Ropers HH, Grüters A, Ullmann R, Krude H. Thorwarth A, et al. Among authors: muller i. J Med Genet. 2014 Jun;51(6):375-87. doi: 10.1136/jmedgenet-2013-102248. Epub 2014 Apr 8. J Med Genet. 2014. PMID: 24714694 Free PMC article.

10

The genome of Erwinia tasmaniensis strain Et1/99, a non-pathogenic bacterium in the genus Erwinia.

Kube M, Migdoll AM, Müller I, Kuhl H, Beck A, Reinhardt R, Geider K. Kube M, et al. Among authors: muller i. Environ Microbiol. 2008 Sep;10(9):2211-22. doi: 10.1111/j.1462-2920.2008.01639.x. Epub 2008 May 6. Environ Microbiol. 2008. PMID: 18462403

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