Ropers HH - Search Results

1

Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation.

Singh U, Fohn LE, Wakayama T, Ohgane J, Steinhoff C, Lipkowitz B, Schulz R, Orth A, Ropers HH, Behringer RR, Tanaka S, Shiota K, Yanagimachi R, Nuber UA, Fundele R. Singh U, et al. Among authors: ropers hh. Dev Dyn. 2004 May;230(1):149-64. doi: 10.1002/dvdy.20024. Dev Dyn. 2004. PMID: 15108320 Free article.

2

Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome.

Nuber UA, Kriaucionis S, Roloff TC, Guy J, Selfridge J, Steinhoff C, Schulz R, Lipkowitz B, Ropers HH, Holmes MC, Bird A. Nuber UA, et al. Among authors: ropers hh. Hum Mol Genet. 2005 Aug 1;14(15):2247-56. doi: 10.1093/hmg/ddi229. Epub 2005 Jul 7. Hum Mol Genet. 2005. PMID: 16002417

3

Comparative study of methyl-CpG-binding domain proteins.

Roloff TC, Ropers HH, Nuber UA. Roloff TC, et al. Among authors: ropers hh. BMC Genomics. 2003 Jan 16;4(1):1. doi: 10.1186/1471-2164-4-1. Epub 2003 Jan 16. BMC Genomics. 2003. PMID: 12529184 Free PMC article.

4

Differences in the pattern of X-linked gene expression between fetal bovine muscle and fibroblast cultures derived from the same muscle biopsies.

Nino-Soto MI, Nuber UA, Basrur PK, Ropers HH, King WA. Nino-Soto MI, et al. Among authors: ropers hh. Cytogenet Genome Res. 2005;111(1):57-64. doi: 10.1159/000085671. Cytogenet Genome Res. 2005. PMID: 16093722

5

BRCA1-mediated repression of select X chromosome genes.

Jazaeri AA, Chandramouli GV, Aprelikova O, Nuber UA, Sotiriou C, Liu ET, Ropers HH, Yee CJ, Boyd J, Barrett JC. Jazaeri AA, et al. Among authors: ropers hh. J Transl Med. 2004 Sep 21;2(1):32. doi: 10.1186/1479-5876-2-32. J Transl Med. 2004. PMID: 15383145 Free PMC article.

6

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: ropers hh. Cytogenet Genome Res. 2006;115(3-4):247-53. doi: 10.1159/000095921. Cytogenet Genome Res. 2006. PMID: 17124407

7

High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.

Erdogan F, Larsen LA, Zhang L, Tümer Z, Tommerup N, Chen W, Jacobsen JR, Schubert M, Jurkatis J, Tzschach A, Ropers HH, Ullmann R. Erdogan F, et al. Among authors: ropers hh. J Med Genet. 2008 Nov;45(11):704-9. doi: 10.1136/jmg.2008.058776. Epub 2008 Aug 19. J Med Genet. 2008. PMID: 18713793

8

Hypergonadotropic hypogonadism in a patient with inv ins (2;4).

Tzschach A, Ramel C, Kron A, Seipel B, Wüster C, Cordes U, Liehr T, Hoeltzenbein M, Menzel C, Ropers HH, Ullmann R, Kalscheuer V, Decker J, Steinberger D. Tzschach A, et al. Among authors: ropers hh. Int J Androl. 2009 Jun;32(3):226-30. doi: 10.1111/j.1365-2605.2007.00839.x. Epub 2007 Nov 27. Int J Androl. 2009. PMID: 18042180

9

Molecular characterisation of antidepressant effects in the mouse brain using gene expression profiling.

Landgrebe J, Welzl G, Metz T, van Gaalen MM, Ropers H, Wurst W, Holsboer F. Landgrebe J, et al. J Psychiatr Res. 2002 May-Jun;36(3):119-29. doi: 10.1016/s0022-3956(01)00061-9. J Psychiatr Res. 2002. PMID: 11886689

10

High rate of constitutional chromosomal rearrangements in apparently sporadic ALS.

Meyer T, Alber B, Roemer K, Martin T, Kalscheuer VM, Göttert E, Zang KD, Ludolph AC, Ropers HH, Prudlo J. Meyer T, et al. Among authors: ropers hh. Neurology. 2003 Apr 22;60(8):1348-50. doi: 10.1212/01.wnl.0000055088.52681.f1. Neurology. 2003. PMID: 12707441

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