140 related articles for article (PubMed ID: 15618281)
1. Protein kinase C gamma mutations in spinocerebellar ataxia 14 increase kinase activity and alter membrane targeting.
Verbeek DS; Knight MA; Harmison GG; Fischbeck KH; Howell BW
Brain; 2005 Feb; 128(Pt 2):436-42. PubMed ID: 15618281
[TBL] [Abstract][Full Text] [Related]
2. PKC gamma mutations in spinocerebellar ataxia type 14 affect C1 domain accessibility and kinase activity leading to aberrant MAPK signaling.
Verbeek DS; Goedhart J; Bruinsma L; Sinke RJ; Reits EA
J Cell Sci; 2008 Jul; 121(Pt 14):2339-49. PubMed ID: 18577575
[TBL] [Abstract][Full Text] [Related]
3. SCA14 mutation V138E leads to partly unfolded PKCγ associated with an exposed C-terminus, altered kinetics, phosphorylation and enhanced insolubilization.
Jezierska J; Goedhart J; Kampinga HH; Reits EA; Verbeek DS
J Neurochem; 2014 Mar; 128(5):741-51. PubMed ID: 24134140
[TBL] [Abstract][Full Text] [Related]
4. Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.
Stevanin G; Hahn V; Lohmann E; Bouslam N; Gouttard M; Soumphonphakdy C; Welter ML; Ollagnon-Roman E; Lemainque A; Ruberg M; Brice A; Durr A
Arch Neurol; 2004 Aug; 61(8):1242-8. PubMed ID: 15313841
[TBL] [Abstract][Full Text] [Related]
5. Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin.
Asai H; Hirano M; Shimada K; Kiriyama T; Furiya Y; Ikeda M; Iwamoto T; Mori T; Nishinaka K; Konishi N; Udaka F; Ueno S
Hum Mol Genet; 2009 Oct; 18(19):3533-43. PubMed ID: 19561170
[TBL] [Abstract][Full Text] [Related]
6. Enzymological analysis of mutant protein kinase Cgamma causing spinocerebellar ataxia type 14 and dysfunction in Ca2+ homeostasis.
Adachi N; Kobayashi T; Takahashi H; Kawasaki T; Shirai Y; Ueyama T; Matsuda T; Seki T; Sakai N; Saito N
J Biol Chem; 2008 Jul; 283(28):19854-63. PubMed ID: 18499672
[TBL] [Abstract][Full Text] [Related]
7. The clinical and genetic spectrum of spinocerebellar ataxia 14.
Chen DH; Cimino PJ; Ranum LP; Zoghbi HY; Yabe I; Schut L; Margolis RL; Lipe HP; Feleke A; Matsushita M; Wolff J; Morgan C; Lau D; Fernandez M; Sasaki H; Raskind WH; Bird TD
Neurology; 2005 Apr; 64(7):1258-60. PubMed ID: 15824357
[TBL] [Abstract][Full Text] [Related]
8. Increased biological activity of protein Kinase C gamma is not required in Spinocerebellar ataxia 14.
Shimobayashi E; Kapfhammer JP
Mol Brain; 2017 Jul; 10(1):34. PubMed ID: 28738819
[TBL] [Abstract][Full Text] [Related]
9. Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.
Hiramoto K; Kawakami H; Inoue K; Seki T; Maruyama H; Morino H; Matsumoto M; Kurisu K; Sakai N
Mov Disord; 2006 Sep; 21(9):1355-60. PubMed ID: 16763984
[TBL] [Abstract][Full Text] [Related]
10. Mutant gammaPKC found in spinocerebellar ataxia type 14 induces aggregate-independent maldevelopment of dendrites in primary cultured Purkinje cells.
Seki T; Shimahara T; Yamamoto K; Abe N; Amano T; Adachi N; Takahashi H; Kashiwagi K; Saito N; Sakai N
Neurobiol Dis; 2009 Feb; 33(2):260-73. PubMed ID: 19041943
[TBL] [Abstract][Full Text] [Related]
11. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
Tonelli A; D'Angelo MG; Salati R; Villa L; Germinasi C; Frattini T; Meola G; Turconi AC; Bresolin N; Bassi MT
J Neurol Sci; 2006 Feb; 241(1-2):13-7. PubMed ID: 16325861
[TBL] [Abstract][Full Text] [Related]
12. Spinocerebellar ataxia type 14 caused by a nonsense mutation in the PRKCG gene.
Shirafuji T; Shimazaki H; Miyagi T; Ueyama T; Adachi N; Tanaka S; Hide I; Saito N; Sakai N
Mol Cell Neurosci; 2019 Jul; 98():46-53. PubMed ID: 31158466
[TBL] [Abstract][Full Text] [Related]
13. Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14.
Klebe S; Faivre L; Forlani S; Dussert C; Tourbah A; Brice A; Stevanin G; Durr A
Arch Neurol; 2007 Jun; 64(6):913-4. PubMed ID: 17562946
[No Abstract] [Full Text] [Related]
14. Calcium Signaling, PKC Gamma, IP3R1 and CAR8 Link Spinocerebellar Ataxias and Purkinje Cell Dendritic Development.
Shimobayashi E; Kapfhammer JP
Curr Neuropharmacol; 2018 Jan; 16(2):151-159. PubMed ID: 28554312
[TBL] [Abstract][Full Text] [Related]
15. A New Mouse Model Related to SCA14 Carrying a Pseudosubstrate Domain Mutation in PKCγ Shows Perturbed Purkinje Cell Maturation and Ataxic Motor Behavior.
Shimobayashi E; Kapfhammer JP
J Neurosci; 2021 Mar; 41(9):2053-2068. PubMed ID: 33478986
[TBL] [Abstract][Full Text] [Related]
16. New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.
Klebe S; Durr A; Rentschler A; Hahn-Barma V; Abele M; Bouslam N; Schöls L; Jedynak P; Forlani S; Denis E; Dussert C; Agid Y; Bauer P; Globas C; Wüllner U; Brice A; Riess O; Stevanin G
Ann Neurol; 2005 Nov; 58(5):720-9. PubMed ID: 16193476
[TBL] [Abstract][Full Text] [Related]
17. Aggregate formation of mutant protein kinase C gamma found in spinocerebellar ataxia type 14 impairs ubiquitin-proteasome system and induces endoplasmic reticulum stress.
Seki T; Takahashi H; Adachi N; Abe N; Shimahara T; Saito N; Sakai N
Eur J Neurosci; 2007 Dec; 26(11):3126-40. PubMed ID: 18005063
[TBL] [Abstract][Full Text] [Related]
18. Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
Yabe I; Sasaki H; Chen DH; Raskind WH; Bird TD; Yamashita I; Tsuji S; Kikuchi S; Tashiro K
Arch Neurol; 2003 Dec; 60(12):1749-51. PubMed ID: 14676051
[TBL] [Abstract][Full Text] [Related]
19. Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death.
Seki T; Adachi N; Ono Y; Mochizuki H; Hiramoto K; Amano T; Matsubayashi H; Matsumoto M; Kawakami H; Saito N; Sakai N
J Biol Chem; 2005 Aug; 280(32):29096-106. PubMed ID: 15964845
[TBL] [Abstract][Full Text] [Related]
20. Pharmacological induction of heat shock proteins ameliorates toxicity of mutant PKCγ in spinocerebellar ataxia type 14.
Nakazono A; Adachi N; Takahashi H; Seki T; Hamada D; Ueyama T; Sakai N; Saito N
J Biol Chem; 2018 Sep; 293(38):14758-14774. PubMed ID: 30093405
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
