Detalhe da pesquisa
1.
Expression, purification, and characterization of authentic mouse prolactin obtained in Escherichia coli periplasmic space.
Biotechnol Appl Biochem
; 59(3): 178-85, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23586827
2.
Dendritic Cell Differentiation from Human Induced Pluripotent Stem Cells: Challenges and Progress.
Stem Cells Dev
; 31(9-10): 207-220, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35316109
3.
A universal gene correction approach for FKRP-associated dystroglycanopathies to enable autologous cell therapy.
Cell Rep
; 36(2): 109360, 2021 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34260922
4.
Long-term human growth hormone expression and partial phenotypic correction by plasmid-based gene therapy in an animal model of isolated growth hormone deficiency.
J Gene Med
; 12(7): 580-5, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20603861
5.
Efficient engraftment of pluripotent stem cell-derived myogenic progenitors in a novel immunodeficient mouse model of limb girdle muscular dystrophy 2I.
Skelet Muscle
; 10(1): 10, 2020 04 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32321586
6.
Partial correction of the dwarf phenotype by non-viral transfer of the growth hormone gene in mice: Treatment age is critical.
Growth Horm IGF Res
; 26: 1-7, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26774398
7.
A novel homologous model for gene therapy of dwarfism by non-viral transfer of the mouse growth hormone gene into immunocompetent dwarf mice.
Curr Gene Ther
; 14(1): 44-51, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24559069
8.
Growth responses following a single intra-muscular hGH plasmid administration compared to daily injections of hGH in dwarf mice.
Curr Gene Ther
; 12(6): 437-43, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22974419
9.
Feeder-free derivation of induced pluripotent stem cells from human immature dental pulp stem cells.
Cell Transplant
; 20(11-12): 1707-19, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21457612
10.
Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells.
Mol Med
; 13(7-8): 422-42, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17622301
11.
Further evidence of association between mutations in FGFR2 and syndromic craniosynostosis with sacrococcygeal eversion.
Birth Defects Res A Clin Mol Teratol
; 76(8): 629-33, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16955501