Detalhe da pesquisa
1.
Exploring the Diverse Biological Properties of Cannabidiol: A Focus on Plant Growth Stimulation.
Chem Biodivers
; 21(5): e202400274, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38466647
2.
Use of Thermoluminescence Dosimetry for QA in High-Dose-Rate Skin Surface Brachytherapy with Custom-Flap Applicator.
Sensors (Basel)
; 23(7)2023 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37050652
3.
Chemical Composition, Phytotoxic and Antibiofilm Activity of Seven Eucalyptus Species from Tunisia.
Molecules
; 27(23)2022 Nov 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36500316
4.
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastoma.
J Cell Mol Med
; 24(11): 6459-6471, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32336043
5.
Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway.
Am J Hematol
; 95(2): 188-197, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31737919
6.
RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway.
Int J Mol Sci
; 21(15)2020 Aug 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32759740
7.
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant.
Am J Hematol
; 94(11): 1227-1235, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31400017
8.
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.
Am J Hematol
; 93(12): 1509-1517, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30187933
9.
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.
Am J Hematol
; 93(5): 672-682, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29396846
10.
Kinome expression profiling of human neuroblastoma tumors identifies potential drug targets for ultra high-risk patients.
Carcinogenesis
; 38(10): 1011-1020, 2017 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28968651
11.
Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia.
Haematologica
; 101(8): 909-17, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27151991
12.
Arterio-Venous Malformations of the Nose: Combined Approach for a Successful Strategy.
J Craniofac Surg
; 27(6): 1524-6, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27607121
13.
Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus.
Haematologica
; 105(12): 2883-2886, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33256393
14.
Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene.
Am J Hematol
; 95(11): 1423-1426, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32720728
15.
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).
Am J Hematol
; 90(10): 921-6, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26178367
16.
Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II.
Blood
; 128(14): 1899-1902, 2016 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27540014
17.
PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis.
Haematologica
; 103(3): e94-e97, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29191841
18.
GATA1 erythroid-specific regulation of SEC23B expression and its implication in the pathogenesis of congenital dyserythropoietic anemia type II.
Haematologica
; 102(9): e371-e374, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28550189
19.
Targeted next generation sequencing identifies a novel ß-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis.
Am J Hematol
; 92(10): E607-E609, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28699249
20.
Lingual schwannoma in pediatric patients.
J Craniofac Surg
; 23(5): e454-6, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22976705