Bittner RE - Search Results

1

Proteins implicated in muscular dystrophy and cancer are functional constituents of the centrosome.

Winter L, Kustermann M, Ernhofer B, Höger H, Bittner RE, Schmidt WM. Winter L, et al. Among authors: bittner re. Life Sci Alliance. 2022 Jul 5;5(11):e202201367. doi: 10.26508/lsa.202201367. Print 2022 Nov. Life Sci Alliance. 2022. PMID: 35790299 Free PMC article.

2

DNA damage, somatic aneuploidy, and malignant sarcoma susceptibility in muscular dystrophies.

Schmidt WM, Uddin MH, Dysek S, Moser-Thier K, Pirker C, Höger H, Ambros IM, Ambros PF, Berger W, Bittner RE. Schmidt WM, et al. Among authors: bittner re. PLoS Genet. 2011 Apr;7(4):e1002042. doi: 10.1371/journal.pgen.1002042. Epub 2011 Apr 14. PLoS Genet. 2011. PMID: 21533183 Free PMC article.

3

Oxyradical damage and mitochondrial enzyme activities in the mdx mouse.

Hauser E, Höger H, Bittner R, Widhalm K, Herkner K, Lubec G. Hauser E, et al. Neuropediatrics. 1995 Oct;26(5):260-2. doi: 10.1055/s-2007-979768. Neuropediatrics. 1995. PMID: 8552217

4

Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration.

Schmidt WM, Kraus C, Höger H, Hochmeister S, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Müller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE. Schmidt WM, et al. Among authors: bittner re. EMBO Rep. 2007 Jul;8(7):691-7. doi: 10.1038/sj.embor.7401001. Epub 2007 Jun 15. EMBO Rep. 2007. PMID: 17571074 Free PMC article.

5

Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype-phenotype correlation.

Baumann M, Steichen-Gersdorf E, Krabichler B, Petersen BS, Weber U, Schmidt WM, Zschocke J, Müller T, Bittner RE, Janecke AR. Baumann M, et al. Among authors: bittner re. Eur J Hum Genet. 2017 Feb;25(2):262-266. doi: 10.1038/ejhg.2016.144. Epub 2016 Oct 26. Eur J Hum Genet. 2017. PMID: 27782104 Free PMC article.

6

Coisogenic all-plus-one immunization: a model for identifying missing proteins in null-mutant conditions. Antibodies to dystrophin in mdx mouse after transplantation of muscle from normal coisogenic donor.

Bittner RE, Streubel B, Shorny S, Schaden G, Voit T, Höger H. Bittner RE, et al. Neuropediatrics. 1994 Aug;25(4):176-82. doi: 10.1055/s-2008-1073019. Neuropediatrics. 1994. PMID: 7824089

7

The susceptibility to experimental autoimmune encephalomyelitis is not related to dysferlin-deficiency.

Hochmeister S, Bittner RE, Höger H, Lassmann H, Bradl M. Hochmeister S, et al. Among authors: bittner re. Autoimmunity. 2009 Mar;42(3):235-41. doi: 10.1080/08916930802716542. Autoimmunity. 2009. PMID: 19301206

8

Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia.

Schmidt WM, Rutledge SL, Schüle R, Mayerhofer B, Züchner S, Boltshauser E, Bittner RE. Schmidt WM, et al. Among authors: bittner re. Am J Hum Genet. 2015 Dec 3;97(6):855-61. doi: 10.1016/j.ajhg.2015.10.011. Epub 2015 Nov 12. Am J Hum Genet. 2015. PMID: 26581903 Free PMC article.

9

Dystrophin expression in heterozygous mdx/+ mice indicates imprinting of X chromosome inactivation by parent-of-origin-, tissue-, strain- and position-dependent factors.

Bittner RE, Popoff I, Shorny S, Höger H, Wachtler F. Bittner RE, et al. Anat Embryol (Berl). 1997 Feb;195(2):175-82. doi: 10.1007/s004290050036. Anat Embryol (Berl). 1997. PMID: 9045987

10

The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.

von der Hagen M, Laval SH, Cree LM, Haldane F, Pocock M, Wappler I, Peters H, Reitsamer HA, Hoger H, Wiedner M, Oberndorfer F, Anderson LV, Straub V, Bittner RE, Bushby KM. von der Hagen M, et al. Among authors: bittner re. Neuromuscul Disord. 2005 Dec;15(12):863-77. doi: 10.1016/j.nmd.2005.09.002. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288871

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