Detalhe da pesquisa
1.
Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6.
Nature
; 561(7722): E7, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29977062
2.
RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6.
Nature
; 557(7706): 564-569, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29769720
3.
A roadmap from research to clinical testing of mesenchymal stromal cell exosomes in the treatment of psoriasis.
Cytotherapy
; 25(8): 815-820, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37115163
4.
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita.
Am J Hum Genet
; 100(4): 659-665, 2017 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28318499
5.
Practical considerations in transforming MSC therapy for neurological diseases from cell to EV.
Exp Neurol
; 349: 113953, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34921846
6.
Assessment of Tumorigenic Potential in Mesenchymal-Stem/Stromal-Cell-Derived Small Extracellular Vesicles (MSC-sEV).
Pharmaceuticals (Basel)
; 14(4)2021 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33918628
7.
A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental Defects.
Adv Sci (Weinh)
; 8(5): 2001100, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33717833
8.
A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling.
J Exp Med
; 217(12)2020 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32845958
9.
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.
Nat Commun
; 11(1): 595, 2020 01 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32001716
10.
Efficient expansion of clinical-grade human fibroblasts on microcarriers: cells suitable for ex vivo expansion of clinical-grade hESCs.
J Biotechnol
; 134(1-2): 79-87, 2008 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-18261818
11.
Katanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamics.
Sci Rep
; 7: 39902, 2017 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28079116
12.
A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental Defects.
Adv Sci (Weinh)
; 8(13): e2101786, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34231333
13.
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
Neuron
; 84(6): 1240-57, 2014 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-25521379
14.
Unexpected X chromosome skewing during culture and reprogramming of human somatic cells can be alleviated by exogenous telomerase.
Cell Stem Cell
; 9(2): 156-65, 2011 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-21816366