SFX by Ex Libris Inc.

Title:	Erratum: Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11
Source:	Nature Genetics [1061-4036] Houlden, Henry yr:2008

Basic

Full text

Full text available via Nature

Year:

Volume:

Issue:

Start Page:

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Wood, T. "Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11." Nature genetics 39.12 (2008): 1434-6.
description	2.	Reiman, Eric M M. "GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers." Neuron 54.5 (2007): 713-20.
description	3.	Waters, Michael F F. "Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes." Nature genetics 38.4: 447-51.
description	4.	Taatjes, Douglas J. "Morphological and cytochemical determination of cell death by apoptosis." Histochemistry and Cell Biology 129.1 (2008): 33-43.
description	5.	Imbert, G. "Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats." Nature genetics 14.3 (1996): 285-291.
description	6.	Rockenstein, E. "Neuroprotective effects of regulators of the glycogen synthase kinase-3beta signaling pathway in a transgenic model of Alzheimer's disease are associated with reduced amyloid precursor protein phosphorylation." The journal of neuroscience 27.8 (2007): 1981-1991.
description	7.	Rhodes, R. "Genetic links, family ties, and social bonds: Rights and responsibilities in the face of genetic knowledge." The Journal of medicine and philosophy 23.1 (1998): 10-30.
description	8.	Thorburn, A. "Apoptosis and autophagy: regulatory connections between two supposedly different processes." Apoptosis 13.1 (2007): 1-9.
description	9.	Jacobsen, Jessie C. "An ovine transgenic Huntington's disease model." Human Molecular Genetics 19.10 (2010): 1873-82.
description	10.	Pulst, Alex M. "Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2." Nature Genetics 14.3 (1996): 269-76.
description	11.	Sahba, S. "Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1." Genomics (1998): 359-364.
description	12.	Liu, W. "Linking SNPs to CAG repeat length in Huntington's disease patients." Nature methods 5.11 (2008): 951-953.
description	13.	Martinez, A. "Preclinical efficacy on GSK-3 inhibitors: towards a future generation of powerful drugs." Medicinal research reviews 28.5 (2008): 773-96.
description	14.	Ittner, Lars M M. "Animal models of Alzheimer's disease and frontotemporal dementia." Nature reviews. Neuroscience 9.7 (2008): 532-44.
description	15.	Kawaguchi, Y. "CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1." Nature genetics 8.3: 221-228.
description	16.	LeGuern, E. "First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene." Nature genetics 28.1 (2001): 46-8.
description	17.	Zhuchenko, O. "Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha(1A)-voltage-dependent calcium channel." Nature genetics 15.1 (1997): 62-69.
description	18.	Biervert, C. "A potassium channel mutation in neonatal human epilepsy." Science 279.5349 (1997): 403-6.
description	19.	Kim, J. "Regulation of Dendritic Excitability by Activity-Dependent Trafficking of the A-Type K Channel Subunit Kv4. 2 in Hippocampal Neurons." Neuron 54.6 (2007): 933-47.
description	20.	Elmore, S. "Apoptosis: A Review of Programmed Cell Death." Toxicologic pathology 35.4 (2007): 495-516.