337 related articles for article (PubMed ID: 31432357)
1. Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients.
Narain P; Padhi AK; Dave U; Mishra D; Bhatia R; Vivekanandan P; Gomes J
Neurogenetics; 2019 Oct; 20(4):197-208. PubMed ID: 31432357
[TBL] [Abstract][Full Text] [Related]
2. Rare Angiogenin and Ribonuclease 4 variants associated with amyotrophic lateral sclerosis exhibit loss-of-function: a comprehensive in silico study.
Padhi AK; Narain P; Gomes J
Metab Brain Dis; 2019 Dec; 34(6):1661-1677. PubMed ID: 31368019
[TBL] [Abstract][Full Text] [Related]
3. Targeted next-generation sequencing reveals novel and rare variants in Indian patients with amyotrophic lateral sclerosis.
Narain P; Pandey A; Gupta S; Gomes J; Bhatia R; Vivekanandan P
Neurobiol Aging; 2018 Nov; 71():265.e9-265.e14. PubMed ID: 29895397
[TBL] [Abstract][Full Text] [Related]
4. Four novel optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in Mainland China.
Yang L; Cheng Y; Jia X; Liu X; Li X; Zhang K; Shen D; Liu M; Guan Y; Liu Q; Cui L; Li X
Neurobiol Aging; 2021 Jan; 97():149.e1-149.e8. PubMed ID: 32893042
[TBL] [Abstract][Full Text] [Related]
5. Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis.
Nishiyama A; Niihori T; Warita H; Izumi R; Akiyama T; Kato M; Suzuki N; Aoki Y; Aoki M
Neurobiol Aging; 2017 May; 53():194.e1-194.e8. PubMed ID: 28160950
[TBL] [Abstract][Full Text] [Related]
6. A molecular dynamics based investigation reveals the role of rare Ribonuclease 4 variants in amyotrophic lateral sclerosis susceptibility.
Padhi AK; Gomes J
Mutat Res; 2019 Jan; 813():1-12. PubMed ID: 30544007
[TBL] [Abstract][Full Text] [Related]
7. Mechanisms of loss of functions of human angiogenin variants implicated in amyotrophic lateral sclerosis.
Padhi AK; Kumar H; Vasaikar SV; Jayaram B; Gomes J
PLoS One; 2012; 7(2):e32479. PubMed ID: 22384259
[TBL] [Abstract][Full Text] [Related]
8. Angiogenin mutations in Hungarian patients with amyotrophic lateral sclerosis: Clinical, genetic, computational, and functional analyses.
Tripolszki K; Danis J; Padhi AK; Gomes J; Bozó R; Nagy ZF; Nagy D; Klivényi P; Engelhardt JI; Széll M
Brain Behav; 2019 Jun; 9(6):e01293. PubMed ID: 31025543
[TBL] [Abstract][Full Text] [Related]
9. Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis.
Fernández-Santiago R; Hoenig S; Lichtner P; Sperfeld AD; Sharma M; Berg D; Weichenrieder O; Illig T; Eger K; Meyer T; Anneser J; Münch C; Zierz S; Gasser T; Ludolph A
J Neurol; 2009 Aug; 256(8):1337-42. PubMed ID: 19363631
[TBL] [Abstract][Full Text] [Related]
10. Some pathogenic SETX variants are partially conserved during evolution.
Tariq H; Tariq I; Bourinaris T; Houlden H; Naz S
Gene; 2021 Mar; 771():145360. PubMed ID: 33333218
[TBL] [Abstract][Full Text] [Related]
11. Evidence of synergism among three genetic variants in a patient with LMNA-related lipodystrophy and amyotrophic lateral sclerosis leading to a remarkable nuclear phenotype.
Volkening K; Farhan SMK; Kao J; Leystra-Lantz C; Ang LC; McIntyre A; Wang J; Hegele RA; Strong MJ
Mol Cell Biochem; 2021 Jul; 476(7):2633-2650. PubMed ID: 33661429
[TBL] [Abstract][Full Text] [Related]
12. Computational and functional characterization of Angiogenin mutations, and correlation with amyotrophic lateral sclerosis.
Padhi AK; Banerjee K; Gomes J; Banerjee M
PLoS One; 2014; 9(11):e111963. PubMed ID: 25372031
[TBL] [Abstract][Full Text] [Related]
13. High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis.
Tripolszki K; Török D; Goudenège D; Farkas K; Sulák A; Török N; Engelhardt JI; Klivényi P; Procaccio V; Nagy N; Széll M
Brain Behav; 2017 Apr; 7(4):e00669. PubMed ID: 28413711
[TBL] [Abstract][Full Text] [Related]
14. MATR3 mutation analysis in a Chinese cohort with sporadic amyotrophic lateral sclerosis.
Xu L; Li J; Tang L; Zhang N; Fan D
Neurobiol Aging; 2016 Feb; 38():218.e3-218.e4. PubMed ID: 26708275
[TBL] [Abstract][Full Text] [Related]
15. A distant angiogenin variant causes amyotrophic lateral sclerosis through loss-of-function mechanisms: Insights from long-timescale atomistic simulations and conformational dynamics.
Padhi AK; Shukla R; Narain P; Gomes J
Comput Biol Med; 2021 Aug; 135():104602. PubMed ID: 34214939
[TBL] [Abstract][Full Text] [Related]
16. Accuracy of a machine learning method based on structural and locational information from AlphaFold2 for predicting the pathogenicity of TARDBP and FUS gene variants in ALS.
Hatano Y; Ishihara T; Onodera O
BMC Bioinformatics; 2023 May; 24(1):206. PubMed ID: 37208601
[TBL] [Abstract][Full Text] [Related]
17. Matrin 3 variants are frequent in Italian ALS patients.
Marangi G; Lattante S; Doronzio PN; Conte A; Tasca G; Monforte M; Patanella AK; Bisogni G; Meleo E; La Spada S; Zollino M; Sabatelli M
Neurobiol Aging; 2017 Jan; 49():218.e1-218.e7. PubMed ID: 28029397
[TBL] [Abstract][Full Text] [Related]
18. Angiogenin loss-of-function mutations in amyotrophic lateral sclerosis.
Wu D; Yu W; Kishikawa H; Folkerth RD; Iafrate AJ; Shen Y; Xin W; Sims K; Hu GF
Ann Neurol; 2007 Dec; 62(6):609-17. PubMed ID: 17886298
[TBL] [Abstract][Full Text] [Related]
19. Genetic variability in sporadic amyotrophic lateral sclerosis.
Van Daele SH; Moisse M; van Vugt JJFA; Zwamborn RAJ; van der Spek R; van Rheenen W; Van Eijk K; Kenna K; Corcia P; Vourc'h P; Couratier P; Hardiman O; McLaughin R; Gotkine M; Drory V; Ticozzi N; Silani V; Ratti A; de Carvalho M; Mora Pardina JS; Povedano M; Andersen PM; Weber M; Başak NA; Shaw C; Shaw PJ; Morrison KE; Landers JE; Glass JD; van Es MA; van den Berg LH; Al-Chalabi A; Veldink J; Van Damme P
Brain; 2023 Sep; 146(9):3760-3769. PubMed ID: 37043475
[TBL] [Abstract][Full Text] [Related]
20. Genetic landscape of ALS in Malta based on a quinquennial analysis.
Farrugia Wismayer M; Farrugia Wismayer A; Borg R; Bonavia K; Abela A; Chircop C; Aquilina J; Soler D; Pace A; Vella M; Vassallo N; Cauchi RJ
Neurobiol Aging; 2023 Mar; 123():200-207. PubMed ID: 36549973
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
