Detalhe da pesquisa
1.
AAV1.NT-3 gene therapy for X-linked Charcot-Marie-Tooth neuropathy type 1.
Gene Ther
; 29(3-4): 127-137, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33542455
2.
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach.
Neurogenetics
; 16(1): 33-42, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25231362
3.
AAV1.NT-3 gene therapy in the SOD1KO mouse model of accelerated sarcopenia.
J Cachexia Sarcopenia Muscle
; 14(5): 2204-2215, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37553101
4.
AAV1.NT-3 gene therapy prevents age-related sarcopenia.
Aging (Albany NY)
; 15(5): 1306-1329, 2023 03 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36897179
5.
AAV1.NT-3 gene therapy in a CMT2D model: phenotypic improvements in GarsP278KY/+ mice.
Brain Commun
; 3(4): fcab252, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34755111
6.
Systemic delivery of AAVrh74.tMCK.hCAPN3 rescues the phenotype in a mouse model for LGMD2A/R1.
Mol Ther Methods Clin Dev
; 22: 401-414, 2021 Sep 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34514031
7.
Gene therapy to promote regeneration in Charcot-Marie-Tooth disease.
Brain Res
; 1727: 146533, 2020 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31669284
8.
SIK2 attenuates proliferation and survival of breast cancer cells with simultaneous perturbation of MAPK and PI3K/Akt pathways.
Oncotarget
; 9(31): 21876-21892, 2018 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-29774109
9.
Ultrasonographic findings in hereditary neuropathy with liability to pressure palsies.
Neurol Res
; 37(2): 106-11, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25005138
10.
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy.
Cell Rep
; 12(7): 1169-83, 2015 Aug 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-26257172
11.
Motor protein mutations cause a new form of hereditary spastic paraplegia.
Neurology
; 82(22): 2007-16, 2014 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24808017