(Q30881530)

27 June 2017

1 reference

title

Why is SCA12 different from other SCAs? (English)

1 reference

27 June 2017

1 reference

17 March 2024

author name string

S. E. Holmes

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14526180

17 March 2024

E. O'Hearn

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14526180

17 March 2024

R. L. Margolis

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14526180

17 March 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14526180

17 March 2024

publication date

1 January 2003

1 reference

full work available at URL

27 June 2017

https://www.karger.com/Article/Pdf/72854

1 reference

Cytogenetics and Genome Research

17 March 2024

published in

1 reference

27 June 2017

volume

100

1 reference

27 June 2017

issue

1-4

1 reference

27 June 2017

page(s)

189-197

1 reference

Human immunodeficiency virus type 1 Vpr-mediated G(2) cell cycle arrest: Vpr interferes with cell cycle signaling cascades by interacting with the B subunit of serine/threonine protein phosphatase 2A

27 June 2017

cites work

1 reference

30 December 2023

https://opencitations.net/index/api/v1/citations/10.1093/EMBOJ/19.15.3956

The SCA12 mutation as a rare cause of spinocerebellar ataxia

1

1 reference

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

17 March 2024

2

1 reference

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family

17 March 2024

3

1 reference

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

17 March 2024

4

1 reference

SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia

17 March 2024

5

1 reference

A conserved downstream element defines a new class of RNA polymerase II promoters

17 March 2024

7

1 reference

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

17 March 2024

8

1 reference

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

17 March 2024

9

1 reference

Interaction between protein phosphatase 5 and the A subunit of protein phosphatase 2A: evidence for a heterotrimeric form of protein phosphatase 5

17 March 2024

10

1 reference

Deconstructing myotonic dystrophy

17 March 2024

11

1 reference

Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients

17 March 2024

12

1 reference

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

17 March 2024

13

1 reference

The 55 kd regulatory subunit of Drosophila protein phosphatase 2A is required for anaphase.

17 March 2024

14

1 reference

The B56 family of protein phosphatase 2A (PP2A) regulatory subunits encodes differentiation-induced phosphoproteins that target PP2A to both nucleus and cytoplasm

17 March 2024

15

1 reference

Regulation of protein kinase cascades by protein phosphatase 2A.

17 March 2024

16

1 reference

Friedreich ataxia: from GAA triplet-repeat expansion to frataxin deficiency

17 March 2024

17

1 reference

Regulation of protein phosphatase 2A activity by caspase-3 during apoptosis

17 March 2024

18

1 reference

Genetic background of apparently idiopathic sporadic cerebellar ataxia

17 March 2024

19

1 reference

Protein serine/threonine phosphatases--new avenues for cell regulation

17 March 2024

20

1 reference

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

17 March 2024

21

1 reference

Regulation of the phosphorylation state and microtubule-binding activity of Tau by protein phosphatase 2A.

17 March 2024

22

1 reference

Molecular interactions among protein phosphatase 2A, tau, and microtubules. Implications for the regulation of tau phosphorylation and the development of tauopathies

17 March 2024

23

1 reference

Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12

17 March 2024

24

1 reference

Brain protein phosphatase 2A: developmental regulation and distinct cellular and subcellular localization by B subunits

17 March 2024

25

1 reference

Protein phosphatase 2A holoenzyme assembly: identification of contacts between B-family regulatory and scaffolding A subunits

17 March 2024

26

1 reference

Identification of a novel protein phosphatase 2A regulatory subunit highly expressed in muscle

17 March 2024

27

1 reference

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

17 March 2024

28

1 reference

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

17 March 2024

29

1 reference

Glutamine repeats and neurodegeneration

17 March 2024

30

1 reference

17 March 2024

Identifiers

DOI

10.1159/000072854

1 reference

release_tcqjwsygergqrnf3kjbnkidf2a

27 June 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tcqjwsygergqrnf3kjbnkidf2a

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference