Detalhe da pesquisa
1.
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications.
Am J Hum Genet
; 109(8): 1421-1435, 2022 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35830857
2.
Biochemical characterization of chamomile essential oil: Antioxidant, antibacterial, anticancer and neuroprotective activity and potential treatment for Alzheimer's disease.
Saudi J Biol Sci
; 31(2): 103912, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38229887
3.
Anticandidal Activity of a Siderophore from Marine Endophyte Pseudomonas aeruginosa Mgrv7.
Antibiotics (Basel)
; 13(4)2024 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38667023
4.
A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay.
Neurobiol Aging
; 106: 351.e1-351.e6, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34272080
5.
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.
JAMA Neurol
; 78(10): 1236-1248, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34459874
6.
Frequency and methylation status of selected retrotransposition competent L1 loci in amyotrophic lateral sclerosis.
Mol Brain
; 13(1): 154, 2020 11 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33187550