Detalhe da pesquisa
1.
Vitamin A mediates conversion of monocyte-derived macrophages into tissue-resident macrophages during alternative activation.
Nat Immunol
; 18(6): 642-653, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28436955
2.
Material Flow Analysis and Occupational Exposure Assessment in Additive Manufacturing End-of-Life Material Management.
Environ Sci Technol
; 58(20): 9000-9012, 2024 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38710661
3.
Review of generic scenario environmental release and occupational exposure models used in chemical risk assessment.
J Occup Environ Hyg
; 20(11): 545-562, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37526475
4.
The helminth glycoprotein omega-1 improves metabolic homeostasis in obese mice through type 2 immunity-independent inhibition of food intake.
FASEB J
; 35(2): e21331, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33476078
5.
Temporal and spatial goal-directed reaching in upper limb prosthesis users.
Exp Brain Res
; 240(11): 3011-3021, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36222884
6.
Supporting contaminated sites management with Multiple Criteria Decision Analysis: Demonstration of a regulation-consistent approach.
J Clean Prod
; 316: 1-10, 2021 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35087262
7.
Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey.
Neurol Neurochir Pol
; 54(2): 176-184, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32242913
8.
Emergency Etoposide-Cisplatin (Em-EP) for patients with germ cell tumours (GCT) and trophoblastic neoplasia (TN).
BMC Cancer
; 19(1): 770, 2019 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31382912
9.
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
Brain
; 140(6): 1561-1578, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28459997
10.
Absence of BiP co-chaperone DNAJC3 causes diabetes mellitus and multisystemic neurodegeneration.
Am J Hum Genet
; 95(6): 689-97, 2014 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25466870
11.
Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.
Am J Hum Genet
; 94(2): 268-77, 2014 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24388663
12.
Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease.
J Neurol Neurosurg Psychiatry
; 88(7): 575-585, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28501821
13.
De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
Brain
; 139(Pt 6): 1649-56, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27009151
14.
Rapid in vivo forward genetic approach for identifying axon death genes in Drosophila.
Proc Natl Acad Sci U S A
; 111(27): 9965-70, 2014 Jul 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24958874
15.
Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia.
Am J Hum Genet
; 92(2): 238-44, 2013 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23332916
16.
Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia.
Am J Hum Genet
; 93(1): 118-23, 2013 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23746551
17.
Mining Available Data from the United States Environmental Protection Agency to Support Rapid Life Cycle Inventory Modeling of Chemical Manufacturing.
Environ Sci Technol
; 50(17): 9013-25, 2016 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27517866
18.
Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2.
Brain
; 138(Pt 2): 293-310, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25497877
19.
A novel mutation in VCP causes Charcot-Marie-Tooth Type 2 disease.
Brain
; 137(Pt 11): 2897-902, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25125609
20.
Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier.
Brain
; 137(Pt 8): 2164-77, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24970096