Below are the most recent publications written about "TATA-Box Binding Protein" by people in Profiles.
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Kelp A, Koeppen AH, Petrasch-Parwez E, Calaminus C, Bauer C, Portal E, Yu-Taeger L, Pichler B, Bauer P, Riess O, Nguyen HP. A novel transgenic rat model for spinocerebellar ataxia type 17 recapitulates neuropathological changes and supplies in vivo imaging biomarkers. J Neurosci. 2013 May 22; 33(21):9068-81.
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Chaturvedi CP, Lodhi N, Ansari SA, Tiwari S, Srivastava R, Sawant SV, Tuli R. Mutated TATA-box/TATA binding protein complementation system for regulated transgene expression in tobacco. Plant J. 2007 Jun; 50(5):917-25.
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Tomiuk J, Bachmann L, Bauer C, Rolfs A, Sch?ls L, Roos C, Zischler H, Schuler MM, Bruntner S, Riess O, Bauer P. Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach. Eur J Hum Genet. 2007 Jan; 15(1):81-7.
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Metzger S, Bauer P, Tomiuk J, Laccone F, Didonato S, Gellera C, Mariotti C, Lange HW, Weirich-Schwaiger H, Wenning GK, Seppi K, Melegh B, Havasi V, Balik? L, Wieczorek S, Zaremba J, Hoffman-Zacharska D, Sulek A, Basak AN, Soydan E, Zidovska J, Kebrdlova V, Pandolfo M, Riba? P, Kadasi L, Kvasnicova M, Weber BH, Kreuz F, Dose M, Stuhrmann M, Riess O. Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease. Hum Genet. 2006 Sep; 120(2):285-92.
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Konieczny M, Bauer P, Tomiuk J, Weisser G, Haan J, Berger K, Riess O, Sch?ls L. CAG repeats in Restless Legs syndrome. Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 05; 141B(2):173-6.
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Grundmann K, Laubis-Herrmann U, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Sch?ls L, Topka H, Riess O. Mutation at the SCA17 locus is not a common cause of primary dystonia. J Neurol. 2004 Oct; 251(10):1232-4.
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Rolfs A, Koeppen AH, Bauer I, Bauer P, Buhlmann S, Topka H, Sch?ls L, Riess O. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17). Ann Neurol. 2003 Sep; 54(3):367-75.