ataxin 1 ; Homo sapiens






237 Article(s)
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1 1372030 Transforming growth factor beta inhibits the action of stem cell factor on mouse and human hematopoietic progenitors. Int J Cell Cloning 1992 Mar 1
2 7477379 Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias. Nature 1995 Nov 23 1
3 7543989 Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan. Neurology 1995 Aug 6
4 7614095 Spinocerebellar ataxia type 1. Clin Neurosci 1995 2
5 7647801 Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals. Nat Genet 1995 May 6
6 7741996 Triplet repeats in neuromuscular disorders. Ann Med 1995 Feb 1
7 7922453 The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias. Brain 1994 Aug 3
8 7951322 Identification and characterization of the gene causing type 1 spinocerebellar ataxia. Nat Genet 1994 Aug 4
9 7952848 Molecular genetics of hereditary ataxias. Baillieres Clin Neurol 1994 Aug 4
10 7998766 Trinucleotide repeat expansion in neurological disease. Ann Neurol 1994 Dec 2
11 8037204 Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset. Am J Hum Genet 1994 Aug 2
12 8190020 Trinucleotide repeats in neurologic diseases: an hypothesis concerning the pathogenesis of Huntington's disease, Kennedy's disease, and spinocerebellar ataxia type I. Life Sci 1994 3
13 8198139 Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I. Am J Hum Genet 1994 Jun 1
14 8559378 Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients. Neurology 1996 Jan 2
15 8677716 [The molecular genetic approach to the study of dominant spinocerebellar ataxias]. Zh Nevrol Psikhiatr Im S S Korsakova 1996 1
16 8731379 Immunoreactive levels of alpha-ketoglutarate dehydrogenase subunits in Friedreich's ataxia and spinocerebellar ataxia type 1. Neurodegeneration 1996 Mar 1
17 8813226 Brain levels of thiamine and its phosphate esters in Friedreich's ataxia and spinocerebellar ataxia type 1. Mov Disord 1996 Jul 1
18 8815156 Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease. J Neurol Sci 1996 Mar 1
19 8836939 Spinocerebellar ataxia type 1 in Russia. J Neurol 1996 Jul 4
20 8872471 Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase. Hum Mol Genet 1996 Sep 4
21 8912795 Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions. Ann Hum Genet 1996 Sep 1
22 9017980 A simple and rapid nonisotopic method for sizing CAG repeats in the SCA1 gene. Hum Hered 1997 Jan-Feb 1
23 9046258 Ocular changes in patients with spinocerebellar degeneration and repeated trinucleotide expansion of spinocerebellar ataxia type 1 gene. Arch Ophthalmol 1997 Feb 5
24 9048937 Transmission distortion of the mutant alleles in spinocerebellar ataxia. Hum Genet 1997 Feb 1
25 9097953 Identification of a self-association region within the SCA1 gene product, ataxin-1. Hum Mol Genet 1997 Apr 4
26 9109912 Striatal dopamine nerve terminal markers but not nigral cellularity are reduced in spinocerebellar ataxia type 1. Neurology 1997 Apr 6
27 9109985 Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1. Arq Neuropsiquiatr 1996 Sep 1
28 9187671 Analysis of amino-acid and nucleotide variants in the spinocerebellar ataxia type 1 (SCA1) gene in schizophrenic patients. Hum Genet 1997 Jun 2
29 9273319 [Presymptomatic DNA diagnosis of spinocerebellar ataxia type 1]. Genetika 1997 May 1
30 9353120 Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures. Nature 1997 Oct 30 3
31 9353121 The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1. Nature 1997 Oct 30 3
32 9443466 Reduced immunoreactivity to calcium-binding proteins in Purkinje cells precedes onset of ataxia in spinocerebellar ataxia-1 transgenic mice. Neurology 1998 Jan 1
33 9485066 Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1. Ann Neurol 1998 Feb 7
34 9629425 [Hereditary cerebellar ataxias: from hammer to genetics]. Arq Neuropsiquiatr 1997 Sep 1
35 9630233 The hereditary ataxias. J Neuropathol Exp Neurol 1998 Jun 1
36 9756151 Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1. Mov Disord 1998 Sep 5
37 9790729 Sca1(+)/Mac1(+) nitric oxide-producing cells in the spleens of recipients early following bone marrow transplant suppress T cell responses in vitro. Cell Immunol 1998 Nov 1 1
38 9801928 Rapid touchdown PCR assay for the molecular diagnosis of spinocerebellar ataxia type 2. Int J Clin Lab Res 1998 1
39 9860298 Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1. Hum Genet 1998 Nov 7
40 10066385 Pathogenesis of polyglutamine-induced disease: A model for SCA1. Mol Genet Metab 1999 Mar 1
41 10222768 [Clinical and genetic characteristics of SCA1]. Nihon Rinsho 1999 Apr 4
42 10222769 [Unstable expansion of CAG repeat and molecular mechanism of neurodegeneration in SCA1]. Nihon Rinsho 1999 Apr 1
43 10369884 Evidence that allelic variants of the spinocerebellar ataxia type 2 gene influence susceptibility to multiple sclerosis. Neurogenetics 1999 Apr 1
44 10374379 Trinucleotide repeat expansion of spinocerebellar ataxia (SCA1) found in a Chinese family. Chin Med J (Engl) 1998 Feb 2
45 10424816 The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1). J Med Genet 1999 Jul 5
46 10434309 Progress in pathogenesis studies of spinocerebellar ataxia type 1. Philos Trans R Soc Lond B Biol Sci 1999 Jun 29 1
47 10452554 Peptide models for inherited neurodegenerative disorders: conformation and aggregation properties of long polyglutamine peptides with and without interruptions. FEBS Lett 1999 Jul 30 4
48 10453742 Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group. Hum Genet 1999 Jun 1
49 10500422 [Clinico-genetic study of type I spinocerebelllar ataxia]. Srp Arh Celok Lek 1999 May-Jun 2
50 10514531 [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 1999 Oct 1