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JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY (2011)
Lipid map of the mammalian cell
Gerrit van Meer et al.
JOURNAL OF CELL SCIENCE (2011)
Malformation syndromes caused by disorders of cholesterol synthesis
Forbes D. Porter et al.
JOURNAL OF LIPID RESEARCH (2011)
Hepatitis C Virus Hijacks P-Body and Stress Granule Components around Lipid Droplets
Yasuo Ariumi et al.
JOURNAL OF VIROLOGY (2011)
Poliovirus Unlinks TIA1 Aggregation and mRNA Stress Granule Formation
James P. White et al.
JOURNAL OF VIROLOGY (2011)
Characterizing the RNA targets and position-dependent splicing regulation by TDP-43
James R. Tollervey et al.
NATURE NEUROSCIENCE (2011)
Substance P receptor activation induces downregulation of the AMPA receptor functionality in cortical neurons from a genetic model of Amyotrophic Lateral Sclerosis
Silvia Caioli et al.
NEUROBIOLOGY OF DISEASE (2011)
Sleep Disorders in Spinocerebellar Ataxia Type 2 Patients
Luis Velazquez-Perez et al.
NEURODEGENERATIVE DISEASES (2011)
Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms
A. R. Paciorkowski et al.
NEUROLOGY (2011)
Presymptomatic spinal cord neurometabolic findings in SOD1-positive people at risk for familial ALS
J. D. Carew et al.
NEUROLOGY (2011)
TOLL-LIKE RECEPTOR SIGNALING IN AMYOTROPHIC LATERAL SCLEROSIS SPINAL CORD TISSUE
M. Casula et al.
NEUROSCIENCE (2011)
The Ataxin-2 protein is required for microRNA function and synapse-specific long-term olfactory habituation
Cathal McCann et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA
Noemie Haud et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Calcium dysregulation in amyotrophic lateral sclerosis
Julian Grosskreutz et al.
CELL CALCIUM (2010)
Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis
L. E. Almaguer-Mederos et al.
CLINICAL GENETICS (2010)
A New Kv1.2 Channelopathy Underlying Cerebellar Ataxia
Gang Xie et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Structural Basis of Binding of P-body-associated Proteins GW182 and Ataxin-2 by the Mlle Domain of Poly(A)-binding Protein
Guennadi Kozlov et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
The unique hypusine modification of eIF5A promotes islet β cell inflammation and dysfunction in mice
Bernhard Maier et al.
JOURNAL OF CLINICAL INVESTIGATION (2010)
Progression markers of Spinocerebellar Ataxia 2. A twenty years neurophysiological follow up study
Luis Velazquez-Perez et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2010)
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
Andrew C. Elden et al.
NATURE (2010)
TAR DNA-binding protein 43 in neurodegenerative disease
Alice S. Chen-Plotkin et al.
NATURE REVIEWS NEUROLOGY (2010)
Immunohistochemical localization of calbindin D28-k, parvalbumin, and calretinin in the cerebellar cortex of the circling mouse
Dhiraj Maskey et al.
NEUROSCIENCE LETTERS (2010)
Deletion of TDP-43 down-regulates Tbc1d1, a gene linked to obesity, and alters body fat metabolism
Po-Min Chiang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2
L. Velazquez-Perez et al.
CLINICAL NEUROPHYSIOLOGY (2009)
Amyotrophic Lateral Sclerosis-Like Conditions in Possible Association with Cholesterol-Lowering Drugs An Analysis of Patient Reports to the University of California, San Diego (UCSD) Statin Effects Study
Beatrice A. Golomb et al.
DRUG SAFETY (2009)
Ataxin-2 associates with rough endoplasmic reticulum
Simone van de Loo et al.
EXPERIMENTAL NEUROLOGY (2009)
Deranged Calcium Signaling and Neurodegeneration in Spinocerebellar Ataxia Type 2
Jing Liu et al.
JOURNAL OF NEUROSCIENCE (2009)
Protein Kinase KIS Localizes to RNA Granules and Enhances Local Translation
Serafi Cambray et al.
MOLECULAR AND CELLULAR BIOLOGY (2009)
Peptide neurotransmitters activate a cation channel complex of NALCN and UNC-80
Boxun Lu et al.
NATURE (2009)
RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection
Marco Henneke et al.
NATURE GENETICS (2009)
Ataxin-2 associates with the endocytosis complex and affects EGF receptor trafficking
David Nonis et al.
CELLULAR SIGNALLING (2008)
Insulin receptor and lipid metabolism pathology in ataxin-2 knock-out mice
Isabel Lastres-Becker et al.
HUMAN MOLECULAR GENETICS (2008)
Analyzing real-time PCR data by the comparative C-T method
Thomas D. Schmittgen et al.
NATURE PROTOCOLS (2008)
Liver X receptor β (LXRβ):: A link between β-sitosterol and amyotrophic lateral sclerosis-Parkinson's dementia
Hyun-Jin Kim et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Human immunodeficiency virus type 1 Vif functionally interacts with diverse APOBEC3 cytidine deaminases and moves with them between cytoplasmic sites of mRNA metabolism
Mariana Marin et al.
JOURNAL OF VIROLOGY (2008)
DAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1
Ismael Al-Ramahi et al.
PLOS GENETICS (2007)
Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43
Yong-Jie Zhang et al.
JOURNAL OF NEUROSCIENCE (2007)
Subthalamic-thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor - A unusual clinical benefit
Hans-Joachim Freund et al.
MOVEMENT DISORDERS (2007)
Neuronal growth and survival mediated by eIF5A, a polyamine-modified translation initiation factor
Yunfei Huang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy
Udo Rueb et al.
BRAIN RESEARCH REVIEWS (2007)
Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules
Ute Nonhoff et al.
MOLECULAR BIOLOGY OF THE CELL (2007)
Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7
U. Rueb et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2006)
Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes
Terrence F. Satterfield et al.
HUMAN MOLECULAR GENETICS (2006)
Sodium channel β4 subunit:: down-regulation and possible involvement in neuritic degeneration in Huntington's disease transgenic mice
Fumitaka Oyama et al.
JOURNAL OF NEUROCHEMISTRY (2006)
Transcriptional signatures of cellular plasticity in mice lacking the α1 subunit of GABAA receptors
Igor Ponomarev et al.
JOURNAL OF NEUROSCIENCE (2006)
A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration
Janghoo Lim et al.
CELL (2006)
Brain cholesterol synthesis in mice is affected by high dose of simvastatin but not of pravastatin
KM Thelen et al.
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2006)
Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathways
M Ralser et al.
HUMAN MOLECULAR GENETICS (2005)
Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2)
K Gierga et al.
ACTA NEUROPATHOLOGICA (2005)
An integrative approach to gain insights into the cellular function of human ataxin-2
M Ralser et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
NEDL1, a novel ubiquitin-protein isopeptide ligase for dishevelled-1, targets mutant superoxide dismutase-1
K Miyazaki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2
L Velázquez-Pérez et al.
ANNALS OF NEUROLOGY (2004)
Gene expression profile following stable expression of the cellular prion protein
J Satoh et al.
CELLULAR AND MOLECULAR NEUROBIOLOGY (2004)
Generation of viable cholesterol-free mice
A Wechsler et al.
SCIENCE (2003)
α-synuclein locus triplication causes Parkinson's disease
AB Singleton et al.
SCIENCE (2003)
Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance
U Rüb et al.
BRAIN (2003)
Anatomically based guidelines for systematic investigation of the central somatosensory system and their application to a spinocerebellar ataxia type 2 (SCA2) patient
U Rüb et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2003)
PQBP-1 transgenic mice show a late-onset motor neuron disease-like phenotype
T Okuda et al.
HUMAN MOLECULAR GENETICS (2003)
Effect of allelic variation at the NACP-Rep1 repeat upstream of the α-synuclein gene (SNCA) on transcription in a cell culture luciferase reporter system
O Chiba-Falek et al.
HUMAN MOLECULAR GENETICS (2001)
Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration
B Oosthuyse et al.
NATURE GENETICS (2001)
The cerebellum-specific Munc13 isoform Munc13-3 regulates cerebellar synaptic transmission and motor learning in mice
I Augustin et al.
JOURNAL OF NEUROSCIENCE (2001)
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