108 related articles for article (PubMed ID: 31598935)
1. [Analysis of a patient with early-onset Parkinson's disease and PARK7 gene variation].
Xie F; Zheng X; Cen Z; Luo W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):957-960. PubMed ID: 31598935
[TBL] [Abstract][Full Text] [Related]
2. Familial early onset Parkinson's disease caused by a homozygous frameshift variant in PARK7: Clinical features and literature update.
Stephenson SE; Djaldetti R; Rafehi H; Wilson GR; Gillies G; Bahlo M; Lockhart PJ
Parkinsonism Relat Disord; 2019 Jul; 64():308-311. PubMed ID: 30928208
[TBL] [Abstract][Full Text] [Related]
3. Generation of a human iPSC line (CIBi013-A) from a patient with young-onset Parkinson's disease carrying a novel homozygous PARK7 (DJ-1) mutation.
Li L; Si X; Lei M; Yang J; Ruan J; Liu H; Huang F; Jin X; Xie K; Yang H; Lei X; Liu Y
Stem Cell Res; 2023 Feb; 66():102983. PubMed ID: 36469984
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial LonP1 protease is implicated in the degradation of unstable Parkinson's disease-associated DJ-1/PARK 7 missense mutants.
Sánchez-Lanzas R; Castaño JG
Sci Rep; 2021 Apr; 11(1):7320. PubMed ID: 33795807
[TBL] [Abstract][Full Text] [Related]
5. DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology.
Taipa R; Pereira C; Reis I; Alonso I; Bastos-Lima A; Melo-Pires M; Magalhães M
Brain; 2016 Jun; 139(Pt 6):1680-7. PubMed ID: 27085187
[TBL] [Abstract][Full Text] [Related]
6. DJ-1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7.
Di Nottia M; Masciullo M; Verrigni D; Petrillo S; Modoni A; Rizzo V; Di Giuda D; Rizza T; Niceta M; Torraco A; Bianchi M; Santoro M; Bentivoglio AR; Bertini E; Piemonte F; Carrozzo R; Silvestri G
Clin Genet; 2017 Jul; 92(1):18-25. PubMed ID: 27460976
[TBL] [Abstract][Full Text] [Related]
7. A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family.
Hanagasi HA; Giri A; Kartal E; Guven G; Bilgiç B; Hauser AK; Emre M; Heutink P; Basak N; Gasser T; Simón-Sánchez J; Lohmann E
Parkinsonism Relat Disord; 2016 Aug; 29():117-20. PubMed ID: 26972524
[TBL] [Abstract][Full Text] [Related]
8. Early-Onset Parkinson's Disease and Brain Iron Accumulation Caused by a Novel Homozygous DJ-1 Mutation.
Lin RR; Tao QQ; Wu ZY
J Parkinsons Dis; 2022; 12(3):813-819. PubMed ID: 35124661
[TBL] [Abstract][Full Text] [Related]
9. Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).
Hering R; Strauss KM; Tao X; Bauer A; Woitalla D; Mietz EM; Petrovic S; Bauer P; Schaible W; Müller T; Schöls L; Klein C; Berg D; Meyer PT; Schulz JB; Wollnik B; Tong L; Krüger R; Riess O
Hum Mutat; 2004 Oct; 24(4):321-9. PubMed ID: 15365989
[TBL] [Abstract][Full Text] [Related]
10. Early Onset Parkinson's disease due to DJ1 mutations: An Indian study.
Abbas MM; Govindappa ST; Sudhaman S; Thelma BK; Juyal RC; Behari M; Muthane UB
Parkinsonism Relat Disord; 2016 Nov; 32():20-24. PubMed ID: 27592010
[TBL] [Abstract][Full Text] [Related]
11. DJ-1/PARK7: A New Therapeutic Target for Neurodegenerative Disorders.
Hijioka M; Inden M; Yanagisawa D; Kitamura Y
Biol Pharm Bull; 2017; 40(5):548-552. PubMed ID: 28458339
[TBL] [Abstract][Full Text] [Related]
12. Generation of an induced pluripotent stem cell line (GIBHi004-A) from a Parkinson's disease patient with mutant DJ-1/PARK7 (p.L10P).
Li Y; Ibañez DP; Fan W; Zhao P; Chen S; Md Abdul M; Jiang Y; Fu L; Luo Z; Liu Z; Yang Y; Guo J; Volpe G; Kanwal S; Wang D; Tang B; Li W
Stem Cell Res; 2020 Jul; 46():101845. PubMed ID: 32534165
[TBL] [Abstract][Full Text] [Related]
13. Private variants in PRKN are associated with late-onset Parkinson's disease.
Hopfner F; Mueller SH; Szymczak S; Junge O; Tittmann L; May S; Lohmann K; Grallert H; Lieb W; Strauch K; Müller-Nurasyid M; Berger K; Schormair B; Winkelmann J; Mollenhauer B; Trenkwalder C; Maetzler W; Berg D; Kasten M; Klein C; Höglinger GU; Gasser T; Deuschl G; Franke A; Krawczak M; Dempfle A; Kuhlenbäumer G
Parkinsonism Relat Disord; 2020 Jun; 75():24-26. PubMed ID: 32442813
[No Abstract] [Full Text] [Related]
14. Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil.
Chien HF; Rohé CF; Costa MD; Breedveld GJ; Oostra BA; Barbosa ER; Bonifati V
Neurogenetics; 2006 Mar; 7(1):13-9. PubMed ID: 16328510
[TBL] [Abstract][Full Text] [Related]
15. Unexpected mitochondrial matrix localization of Parkinson's disease-related DJ-1 mutants but not wild-type DJ-1.
Kojima W; Kujuro Y; Okatsu K; Bruno Q; Koyano F; Kimura M; Yamano K; Tanaka K; Matsuda N
Genes Cells; 2016 Jul; 21(7):772-88. PubMed ID: 27270837
[TBL] [Abstract][Full Text] [Related]
16. Inhibition by pesticides of the DJ-1/Park7 protein related to Parkinson disease.
Mathas N; Poncet G; Laurent C; Larigot L; Le-Grand B; Gonis E; Birman S; Galardon E; Sari MA; Tiouaini M; Nioche P; Barouki R; Coumoul X; Mansuy D; Dairou J
Toxicology; 2023 Mar; 487():153467. PubMed ID: 36842454
[TBL] [Abstract][Full Text] [Related]
17. Transient sampling of aggregation-prone conformations causes pathogenic instability of a parkinsonian mutant of DJ-1 at physiological temperature.
Milkovic NM; Catazaro J; Lin J; Halouska S; Kizziah JL; Basiaga S; Cerny RL; Powers R; Wilson MA
Protein Sci; 2015 Oct; 24(10):1671-85. PubMed ID: 26234586
[TBL] [Abstract][Full Text] [Related]
18. Mutation analysis of the PARKIN, PINK1, DJ1, and SNCA genes in Turkish early-onset Parkinson's patients and genotype-phenotype correlations.
Erer S; Egeli U; Zarifoglu M; Tezcan G; Cecener G; Tunca B; Ak S; Demirdogen E; Kenangil G; Kaleagası H; Dogu O; Saka E; Elibol B
Clin Neurol Neurosurg; 2016 Sep; 148():147-53. PubMed ID: 27455133
[TBL] [Abstract][Full Text] [Related]
19. A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion.
Dogu O; Johnson J; Hernandez D; Hanson M; Hardy J; Apaydin H; Özekmekçi S; Sevim S; Gwinn-Hardy K; Singleton A
Mov Disord; 2004 Jul; 19(7):812-816. PubMed ID: 15254940
[TBL] [Abstract][Full Text] [Related]
20. Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease.
Tarantino P; Annesi F; Scornaienchi V; Rocca FE; De Marco EV; Civitelli D; Provenzano G; Sproviero W; Greco V; Annesi G
Hum Genet; 2010 Apr; 127(4):463. PubMed ID: 21506293
[No Abstract] [Full Text] [Related]
[Next] [New Search]
