280 related articles for article (PubMed ID: 26668131)
1. Disruption of Golgi morphology and altered protein glycosylation in PLA2G6-associated neurodegeneration.
Davids M; Kane MS; He M; Wolfe LA; Li X; Raihan MA; Chao KR; Bone WP; Boerkoel CF; Gahl WA; Toro C
J Med Genet; 2016 Mar; 53(3):180-9. PubMed ID: 26668131
[TBL] [Abstract][Full Text] [Related]
2. Catalytic function of PLA2G6 is impaired by mutations associated with infantile neuroaxonal dystrophy but not dystonia-parkinsonism.
Engel LA; Jing Z; O'Brien DE; Sun M; Kotzbauer PT
PLoS One; 2010 Sep; 5(9):e12897. PubMed ID: 20886109
[TBL] [Abstract][Full Text] [Related]
3. Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations.
Paisán-Ruiz C; Li A; Schneider SA; Holton JL; Johnson R; Kidd D; Chataway J; Bhatia KP; Lees AJ; Hardy J; Revesz T; Houlden H
Neurobiol Aging; 2012 Apr; 33(4):814-23. PubMed ID: 20619503
[TBL] [Abstract][Full Text] [Related]
4. Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.
Kapoor S; Shah MH; Singh N; Rather MI; Bhat V; Gopinath S; Bindu PS; Taly AB; Sinha S; Nagappa M; Bharath RD; Mahadevan A; Narayanappa G; Chickabasaviah YT; Kumar A
PLoS One; 2016; 11(5):e0155605. PubMed ID: 27196560
[TBL] [Abstract][Full Text] [Related]
5. Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.
Dehnavi AZ; Bemanalizadeh M; Kahani SM; Ashrafi MR; Rohani M; Toosi MB; Heidari M; Hosseinpour S; Amini B; Zokaei S; Rezaei Z; Aryan H; Amanat M; Vahidnezhad H; Mohammadi P; Garshasbi M; Tavasoli AR
Orphanet J Rare Dis; 2023 Jul; 18(1):177. PubMed ID: 37403138
[TBL] [Abstract][Full Text] [Related]
6. Loss of PLA2G6 leads to elevated mitochondrial lipid peroxidation and mitochondrial dysfunction.
Kinghorn KJ; Castillo-Quan JI; Bartolome F; Angelova PR; Li L; Pope S; Cochemé HM; Khan S; Asghari S; Bhatia KP; Hardy J; Abramov AY; Partridge L
Brain; 2015 Jul; 138(Pt 7):1801-16. PubMed ID: 26001724
[TBL] [Abstract][Full Text] [Related]
7. A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy.
Iannello G; Graziano C; Cenacchi G; Cordelli DM; Zuntini R; Papa V; Magistà AM; Gagliardi M; Procopio R; Quattrone A; Annesi G
J Neurol Sci; 2017 Oct; 381():209-212. PubMed ID: 28991683
[TBL] [Abstract][Full Text] [Related]
8. The role of the PLA2G6 gene in neurodegenerative diseases.
Deng X; Yuan L; Jankovic J; Deng H
Ageing Res Rev; 2023 Aug; 89():101957. PubMed ID: 37236368
[TBL] [Abstract][Full Text] [Related]
9. Neuroaxonal dystrophy in PLA2G6 knockout mice.
Sumi-Akamaru H; Beck G; Kato S; Mochizuki H
Neuropathology; 2015 Jun; 35(3):289-302. PubMed ID: 25950622
[TBL] [Abstract][Full Text] [Related]
10. Mouse models of human INAD by Pla2g6 deficiency.
Wada H; Kojo S; Seino K
Histol Histopathol; 2013 Aug; 28(8):965-9. PubMed ID: 23467909
[TBL] [Abstract][Full Text] [Related]
11. PLA2G6-associated neurodegeneration in four different populations-case series and literature review.
Hanna Al-Shaikh R; Milanowski LM; Holla VV; Kurihara K; Yadav R; Kamble N; Muthusamy B; Bellad A; Koziorowski D; Szlufik S; Hoffman-Zacharska D; Fujioka S; Tsuboi Y; Ross OA; Wierenga K; Uitti RJ; Wszolek Z; Pal PK
Parkinsonism Relat Disord; 2022 Aug; 101():66-74. PubMed ID: 35803092
[TBL] [Abstract][Full Text] [Related]
12. Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN).
Kurian MA; Morgan NV; MacPherson L; Foster K; Peake D; Gupta R; Philip SG; Hendriksz C; Morton JE; Kingston HM; Rosser EM; Wassmer E; Gissen P; Maher ER
Neurology; 2008 Apr; 70(18):1623-9. PubMed ID: 18443314
[TBL] [Abstract][Full Text] [Related]
13. Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: case series and literature review.
Chu YT; Lin HY; Chen PL; Lin CH
BMC Neurol; 2020 Mar; 20(1):101. PubMed ID: 32183746
[TBL] [Abstract][Full Text] [Related]
14. Neurons and astrocytes in an infantile neuroaxonal dystrophy (INAD) mouse model show characteristic alterations in glutamate-induced Ca
Strokin M; Reiser G
Neurochem Int; 2017 Sep; 108():121-132. PubMed ID: 28279750
[TBL] [Abstract][Full Text] [Related]
15. PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia.
Koh K; Ichinose Y; Ishiura H; Nan H; Mitsui J; Takahashi J; Sato W; Itoh Y; Hoshino K; Tsuji S; Takiyama Y;
J Hum Genet; 2019 Jan; 64(1):55-59. PubMed ID: 30302010
[TBL] [Abstract][Full Text] [Related]
16. Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis.
Iodice A; Spagnoli C; Salerno GG; Frattini D; Bertani G; Bergonzini P; Pisani F; Fusco C
Brain Dev; 2017 Feb; 39(2):93-100. PubMed ID: 27884548
[TBL] [Abstract][Full Text] [Related]
17. Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6.
Strokin M; Seburn KL; Cox GA; Martens KA; Reiser G
Hum Mol Genet; 2012 Jun; 21(12):2807-14. PubMed ID: 22442204
[TBL] [Abstract][Full Text] [Related]
18. Exploring therapeutic strategies for infantile neuronal axonal dystrophy (INAD/PARK14).
Lin G; Tepe B; McGrane G; Tipon RC; Croft G; Panwala L; Hope A; Liang AJH; Zuo Z; Byeon SK; Wang L; Pandey A; Bellen HJ
Elife; 2023 Jan; 12():. PubMed ID: 36645408
[TBL] [Abstract][Full Text] [Related]
19. Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysis.
Al-Maawali A; Yoon G; Feigenbaum AS; Halliday WC; Clarke JT; Branson HM; Banwell BL; Chitayat D; Blaser SI
Neuroradiology; 2016 Oct; 58(10):1035-1042. PubMed ID: 27516098
[TBL] [Abstract][Full Text] [Related]
20. Establishment of an improved mouse model for infantile neuroaxonal dystrophy that shows early disease onset and bears a point mutation in Pla2g6.
Wada H; Yasuda T; Miura I; Watabe K; Sawa C; Kamijuku H; Kojo S; Taniguchi M; Nishino I; Wakana S; Yoshida H; Seino K
Am J Pathol; 2009 Dec; 175(6):2257-63. PubMed ID: 19893029
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
