Brandau O - Search Results

1

BTKbase, mutation database for X-linked agammaglobulinemia (XLA).

Vihinen M, Brandau O, Brandén LJ, Kwan SP, Lappalainen I, Lester T, Noordzij JG, Ochs HD, Ollila J, Pienaar SM, Riikonen P, Saha BK, Smith CI. Vihinen M, et al. Among authors: brandau o. Nucleic Acids Res. 1998 Jan 1;26(1):242-7. doi: 10.1093/nar/26.1.242. Nucleic Acids Res. 1998. PMID: 9399844 Free PMC article.

2

Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course.

Holinski-Feder E, Weiss M, Brandau O, Jedele KB, Nore B, Bäckesjö CM, Vihinen M, Hubbard SR, Belohradsky BH, Smith CI, Meindl A. Holinski-Feder E, et al. Among authors: brandau o. Pediatrics. 1998 Feb;101(2):276-84. doi: 10.1542/peds.101.2.276. Pediatrics. 1998. PMID: 9445504

3

UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2.

Brandau O, Nyakatura G, Jedele KB, Platzer M, Achatz H, Ross M, Murken J, Rosenthal A, Meindl A. Brandau O, et al. Eur J Hum Genet. 1998 Sep-Oct;6(5):459-66. doi: 10.1038/sj.ejhg.5200207. Eur J Hum Genet. 1998. PMID: 9801870

4

Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP).

Brandau O, Schuster V, Weiss M, Hellebrand H, Fink FM, Kreczy A, Friedrich W, Strahm B, Niemeyer C, Belohradsky BH, Meindl A. Brandau O, et al. Hum Mol Genet. 1999 Dec;8(13):2407-13. doi: 10.1093/hmg/8.13.2407. Hum Mol Genet. 1999. PMID: 10556288

5

X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15.

Bader I, Brandau O, Achatz H, Apfelstedt-Sylla E, Hergersberg M, Lorenz B, Wissinger B, Wittwer B, Rudolph G, Meindl A, Meitinger T. Bader I, et al. Among authors: brandau o. Invest Ophthalmol Vis Sci. 2003 Apr;44(4):1458-63. doi: 10.1167/iovs.02-0605. Invest Ophthalmol Vis Sci. 2003. PMID: 12657579

6

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

Pusch CM, Zeitz C, Brandau O, Pesch K, Achatz H, Feil S, Scharfe C, Maurer J, Jacobi FK, Pinckers A, Andreasson S, Hardcastle A, Wissinger B, Berger W, Meindl A. Pusch CM, et al. Among authors: brandau o. Nat Genet. 2000 Nov;26(3):324-7. doi: 10.1038/81627. Nat Genet. 2000. PMID: 11062472

7

A novel gene, tendin, is strongly expressed in tendons and ligaments and shows high homology with chondromodulin-I.

Brandau O, Meindl A, Fässler R, Aszódi A. Brandau O, et al. Dev Dyn. 2001 May;221(1):72-80. doi: 10.1002/dvdy.1126. Dev Dyn. 2001. PMID: 11357195 Free article.

8

Recurrent B-cell non-Hodgkin's lymphoma in two brothers with X-linked lymphoproliferative disease without evidence for Epstein-Barr virus infection.

Strahm B, Rittweiler K, Duffner U, Brandau O, Orlowska-Volk M, Karajannis MA, Stadt Uz, Tiemann M, Reiter A, Brandis M, Meindl A, Niemeyer CM. Strahm B, et al. Among authors: brandau o. Br J Haematol. 2000 Feb;108(2):377-82. doi: 10.1046/j.1365-2141.2000.01884.x. Br J Haematol. 2000. PMID: 10691868 Free article.

9

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene.

Coffey AJ, Brooksbank RA, Brandau O, Oohashi T, Howell GR, Bye JM, Cahn AP, Durham J, Heath P, Wray P, Pavitt R, Wilkinson J, Leversha M, Huckle E, Shaw-Smith CJ, Dunham A, Rhodes S, Schuster V, Porta G, Yin L, Serafini P, Sylla B, Zollo M, Franco B, Bolino A, Seri M, Lanyi A, Davis JR, Webster D, Harris A, Lenoir G, de St Basile G, Jones A, Behloradsky BH, Achatz H, Murken J, Fassler R, Sumegi J, Romeo G, Vaudin M, Ross MT, Meindl A, Bentley DR. Coffey AJ, et al. Among authors: brandau o. Nat Genet. 1998 Oct;20(2):129-35. doi: 10.1038/2424. Nat Genet. 1998. PMID: 9771704

10

An integrated, functionally annotated gene map of the DXS8026-ELK1 interval on human Xp11.3-Xp11.23: potential hotspot for neurogenetic disorders.

Thiselton DL, McDowall J, Brandau O, Ramser J, d'Esposito F, Bhattacharya SS, Ross MT, Hardcastle AJ, Meindl A. Thiselton DL, et al. Among authors: brandau o. Genomics. 2002 Apr;79(4):560-72. doi: 10.1006/geno.2002.6733. Genomics. 2002. PMID: 11944989

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