Detalhe da pesquisa
1.
Recurrent de-novo gain-of-function mutation in SPTLC2 confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis.
J Neurol Neurosurg Psychiatry
; 95(3): 201-205, 2024 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38041684
2.
Multiple poloxamers increase plasma membrane repair capacity in muscle and nonmuscle cells.
Am J Physiol Cell Physiol
; 318(2): C253-C262, 2020 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31747313
3.
Genetic Causes of Vascular Malformations and Common Signaling Pathways Involved in Their Formation.
Dermatol Clin
; 40(4): 449-459, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36243432
4.
Genetic Risk Factors for Alzheimer's Disease in Racial/Ethnic Minority Populations in the U.S.: A Scoping Review.
Front Public Health
; 9: 784958, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35004586
5.
Enhancing membrane repair increases regeneration in a sciatic injury model.
PLoS One
; 15(4): e0231194, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32271817
6.
Lipidomic Adaptations in White and Brown Adipose Tissue in Response to Exercise Demonstrate Molecular Species-Specific Remodeling.
Cell Rep
; 18(6): 1558-1572, 2017 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28178530