|1.||Krobitsch, Sylvia: 6 articles (05/2015 - 02/2005)|
|2.||Lehrach, Hans: 5 articles (01/2012 - 02/2005)|
|3.||Auburger, Georg: 5 articles (01/2012 - 05/2008)|
|4.||Pulst, Stefan M: 5 articles (07/2009 - 07/2003)|
|5.||Huynh, Duong P: 5 articles (07/2009 - 07/2003)|
|6.||Nonhoff, Ute: 4 articles (01/2012 - 02/2005)|
|7.||Nowock, Joachim: 4 articles (01/2009 - 01/2003)|
|8.||Pulst, S M: 4 articles (08/2001 - 05/2000)|
|9.||Kaehler, Christian: 3 articles (05/2015 - 01/2012)|
|10.||Wszolek, Zbigniew K: 3 articles (10/2014 - 01/2002)|
|1.||Spinocerebellar Ataxias (Spinocerebellar Ataxia)
01/01/2014 - "Ataxin-2 is an evolutionarily conserved protein first identified in humans as responsible for spinocerebellar ataxia type 2 (SCA2). "
01/01/2013 - "Pathogenic CAG repeat expansion in the ataxin-2 gene (ATXN2) is the genetic cause of spinocerebellar ataxia type 2 (SCA2). "
01/01/2012 - "For the disease-causing protein in spinocerebellar ataxia type 2, ataxin-2, a paralog of unknown function, termed ataxin-2-like, has been described. "
01/01/2012 - "The role of short, large or intermediate normal alleles (ANs) of the ataxin-2 gene in generating expanded alleles (EAs) causing spinocerebellar ataxia type 2 (SCA2) is poorly understood. "
01/01/2004 - "Spinocerebellar ataxia type 2 (SCA2) is caused by a CAG trinucleotide repeat expansion within the coding region of the ataxin-2 gene. "
|2.||Neurodegenerative Diseases (Neurodegenerative Disease)
06/01/2009 - "Spinocerebellar ataxia type 2 is a neurodegenerative disease caused by a CAG repeat expansion in the ataxin-2 gene. "
08/01/2004 - "Spinocerebellar ataxia types 2 (SCA2) and 3 (SCA3) are autosomal-dominantly inherited, neurodegenerative diseases caused by CAG repeat expansions in the coding regions of the genes encoding ataxin-2 and ataxin-3, respectively. "
12/01/2003 - "Spinocerebellar ataxia type 2 (SCA2) is a human neurodegenerative disease caused by mutation in the ataxin-2 gene on human chromosome 12. "
05/17/2013 - "We found that the Drosophila homolog of ATAXIN-2 (ATX2)--an RNA-binding protein implicated in human neurodegenerative diseases--was required for circadian locomotor behavior. "
05/17/2013 - "We found that ATAXIN-2 (ATX2), an RNA-associated protein involved in neurodegenerative disease, is a translational activator of the rate-limiting clock component PERIOD (PER) in Drosophila. "
|3.||Progressive Myoclonic Epilepsies (Progressive Myoclonic Epilepsy)
|4.||Angelman Syndrome (Syndrome, Angelman)
|5.||Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)
01/01/2014 - "Taking a risk: a therapeutic focus on ataxin-2 in amyotrophic lateral sclerosis?"
03/06/2014 - "Ataxin-2 (ATXN2) plays vital roles in cell proliferation and growth, and functional mutations of ATXN2 cause neurodegenerative phenotypes, including spinocerebellar ataxia type 2 (SCA2) and amyotrophic lateral sclerosis (ALS). "
02/15/2013 - "Ataxin-2 interacts with FUS and intermediate-length polyglutamine expansions enhance FUS-related pathology in amyotrophic lateral sclerosis."
12/11/2012 - "Recent evidence suggests that intermediate-length polyglutamine (PolyQ) expansions in the ataxin-2 (ATXN-2) gene are a risk factor for amyotrophic lateral sclerosis (ALS). "
05/01/2012 - "A higher prevalence of intermediate ataxin-2 CAG repeats in amyotrophic lateral sclerosis (ALS) patients has raised the possibility that CAG expansions in other polyglutamine disease genes could contribute to ALS neurodegeneration. "
|2.||Staphylococcal Protein A (A, Protein)
|3.||protein TDP-43 (TDP-43)
|4.||TATA-Box Binding Protein (TATA-Binding Protein)
|6.||tributyl phosphate (TBP)
|7.||RNA (Ribonucleic Acid)
|8.||Proteins (Proteins, Gene)
|9.||RNA-Binding Proteins (RNA-Binding Protein)
|10.||Poly(A)-Binding Proteins (Poly(A)-Binding Protein)