Detalhe da pesquisa
1.
Identification of exosomal muscle-specific miRNAs in serum of myotonic dystrophy patients relating to muscle disease progress.
Hum Mol Genet
; 26(17): 3285-3302, 2017 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28637233
2.
Mouse Stbd1 is N-myristoylated and affects ER-mitochondria association and mitochondrial morphology.
J Cell Sci
; 130(5): 903-915, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28137759
3.
Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy.
Proc Natl Acad Sci U S A
; 113(17): E2421-9, 2016 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27035961
4.
Transgenic replacement of Cx32 in gap junction-deficient oligodendrocytes rescues the phenotype of a hypomyelinating leukodystrophy model.
Hum Mol Genet
; 24(7): 2049-64, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25524707
5.
Clinical features of primary ciliary dyskinesia in Cyprus with emphasis on lobectomized patients.
Respir Med
; 109(3): 347-56, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25698650