Detalhe da pesquisa
1.
EVI1 drives leukemogenesis through aberrant ERG activation.
Blood
; 141(5): 453-466, 2023 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36095844
2.
Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans.
N Engl J Med
; 384(25): 2406-2417, 2021 06 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34161705
3.
Senescence-associated reprogramming promotes cancer stemness.
Nature
; 553(7686): 96-100, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29258294
4.
Loss-of-Function Myeloperoxidase Mutations Are Associated with Increased Neutrophil Counts and Pustular Skin Disease.
Am J Hum Genet
; 107(3): 539-543, 2020 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32758448
5.
Nonadherence to systemic immune-modifying therapy in people with psoriasis during the COVID-19 pandemic: findings from a global cross-sectional survey.
Br J Dermatol
; 188(5): 610-617, 2023 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36763806
6.
Biomarkers of systemic treatment response in people with psoriasis: a scoping review.
Br J Dermatol
; 187(4): 494-506, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35606928
7.
Biomarkers of disease progression in people with psoriasis: a scoping review.
Br J Dermatol
; 187(4): 481-493, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35482474
8.
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
Am J Hum Genet
; 102(3): 494-504, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29478781
9.
The neurotrophic factor receptor RET drives haematopoietic stem cell survival and function.
Nature
; 514(7520): 98-101, 2014 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25079320
10.
Loss-of-function myeloperoxidase mutations are associated with increased neutrophil counts and pustular skin disease.
Am J Hum Genet
; 108(4): 757, 2021 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33798446
11.
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number.
Am J Hum Genet
; 99(4): 860-876, 2016 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27693233
12.
TRAP1 regulates autophagy in lung cancer cells.
Eur J Clin Invest
; 48(4)2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29383696
13.
Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits.
Neurogenetics
; 18(4): 227-235, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29075935
14.
Pathogenic variants in HTRA2 cause an early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduria.
J Inherit Metab Dis
; 40(1): 121-130, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27696117
15.
LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population.
Brain
; 138(Pt 12): 3503-19, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26510951
16.
Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number.
Am J Hum Genet
; 99(6): 1405, 2016 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27912046
17.
Direct and selective pharmacological disruption of the YAP-TEAD interface by IAG933 inhibits Hippo-dependent and RAS-MAPK-altered cancers.
Nat Cancer
; 2024 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38565920
18.
Mitochondrial remodeling in cancer metabolism and survival: potential for new therapies.
Biochim Biophys Acta
; 1826(1): 238-54, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22554970
19.
Cancer lineage-specific regulation of YAP responsive elements revealed through large-scale functional epigenomic screens.
Nat Commun
; 14(1): 3907, 2023 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37400441
20.
Development of antidrug antibodies against adalimumab maps to variation within the HLA-DR peptide-binding groove.
JCI Insight
; 8(4)2023 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36810251