Detalhe da pesquisa
1.
Transcriptomic Analysis of Mineralized Adipose-Derived Stem Cell Tissues for Calcific Valve Disease Modelling.
Int J Mol Sci
; 25(4)2024 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38396969
2.
Heterozygous NF1 dermal fibroblasts modulate exosomal content to promote angiogenesis in a tissue-engineered skin model of neurofibromatosis type-1.
J Neurochem
; 167(4): 556-570, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37837197
3.
Moyamoya Disease Susceptibility Gene RNF213 Regulates Endothelial Barrier Function.
Stroke
; 53(4): 1263-1275, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34991336
4.
Persisting chemosensory impairments in 366 healthcare workers following COVID-19: an 11-month follow-up.
Chem Senses
; 472022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35522081
5.
Tissue-engineered in vitro modeling of the impact of Schwann cells in amyotrophic lateral sclerosis.
Biotechnol Bioeng
; 119(7): 1938-1948, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35289393
6.
Impact of Exosomes Released by Different Corneal Cell Types on the Wound Healing Properties of Human Corneal Epithelial Cells.
Int J Mol Sci
; 23(20)2022 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36293057
7.
Chemosensory Dysfunctions Induced by COVID-19 Can Persist up to 7 Months: A Study of Over 700 Healthcare Workers.
Chem Senses
; 462021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34423831
8.
Diagnosis of idiopathic amyotrophic lateral sclerosis using Fourier-transform infrared spectroscopic analysis of patient-derived skin.
Analyst
; 145(10): 3678-3685, 2020 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32307493
9.
Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis.
Hum Mol Genet
; 25(21): 4771-4786, 2016 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28175304
10.
LMNB1-duplication mediated nuclear architecture alteration and demyelination of cerebral white matter in a patient with ADLD.
Neuropathol Appl Neurobiol
; : e12947, 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38102845
11.
Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
Nat Genet
; 39(1): 80-5, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17159980
12.
Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis.
Hum Mol Genet
; 22(12): 2350-60, 2013 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23446633
13.
Spherical rotary cell seeding system for production of small-caliber tissue-engineered blood vessels with complex geometry.
Sci Rep
; 13(1): 3001, 2023 02 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36810756
14.
In Vitro Characterization of Motor Neurons and Purkinje Cells Differentiated from Induced Pluripotent Stem Cells Generated from Patients with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
Stem Cells Int
; 2023: 1496597, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37096129
15.
An oligodendrocyte silencer element underlies the pathogenic impact of lamin B1 structural variants.
bioRxiv
; 2023 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37609196
16.
Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.
Proc Natl Acad Sci U S A
; 106(51): 21777-82, 2009 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-20007371
17.
RNF213 Loss-of-Function Promotes Angiogenesis of Cerebral Microvascular Endothelial Cells in a Cellular State Dependent Manner.
Cells
; 12(1)2022 12 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36611871
18.
Generation of three induced pluripotent stem cell lines (UQACi003-A, UQACi004-A, and UQACi006-A) from three patients with KRT5 epidermolysis bullosa simplex mutations.
Stem Cell Res
; 60: 102726, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35247839
19.
Generation of two induced pluripotent stem cell lines (UQACi002-A and UQACi005-A) from two patients with KRT14 epidermolysis bullosa simplex mutations.
Stem Cell Res
; 61: 102750, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35334406
20.
Tridimensional cell culture of dermal fibroblasts promotes exosome-mediated secretion of extracellular matrix proteins.
Sci Rep
; 12(1): 19786, 2022 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36396670