Detalhe da pesquisa
1.
Dissecting KMT2D missense mutations in Kabuki syndrome patients.
Hum Mol Genet
; 27(21): 3651-3668, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30107592
2.
TRIM50 regulates Beclin 1 proautophagic activity.
Biochim Biophys Acta Mol Cell Res
; 1865(6): 908-919, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29604308
3.
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.
Am J Hum Genet
; 99(3): 704-710, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27523599
4.
gene2drug: a computational tool for pathway-based rational drug repositioning.
Bioinformatics
; 34(9): 1498-1505, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29236977
5.
The Role of Cytotoxic Chemotherapy in Well-Differentiated Gastroenteropancreatic and Lung Neuroendocrine Tumors.
Curr Treat Options Oncol
; 20(9): 72, 2019 07 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31346813
6.
BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomalies.
Genome Res
; 25(2): 155-66, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25561519
7.
TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survival.
BMC Cancer
; 15: 470, 2015 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26077989
8.
Cutting edge: the NLRP3 inflammasome links complement-mediated inflammation and IL-1ß release.
J Immunol
; 191(3): 1006-10, 2013 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23817414
9.
TBC1D7 mutations are associated with intellectual disability, macrocrania, patellar dislocation, and celiac disease.
Hum Mutat
; 35(4): 447-51, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24515783
10.
Molecular analysis, pathogenic mechanisms, and readthrough therapy on a large cohort of Kabuki syndrome patients.
Hum Mutat
; 35(7): 841-50, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24633898
11.
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.
Am J Hum Genet
; 99(3): 786, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27588455
12.
De novo variants in PLCG1 are associated with hearing impairment, ocular pathology, and cardiac defects.
medRxiv
; 2024 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38260438
13.
BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomalies.
Genome Res
; 25(4): 609, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25834187
14.
Angiogenesis in NENs, with a focus on gastroenteropancreatic NENs: from biology to current and future therapeutic implications.
Front Oncol
; 12: 957068, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36059642
15.
Development of anti-somatostatin receptors CAR T cells for treatment of neuroendocrine tumors.
J Immunother Cancer
; 10(6)2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35764366
16.
Adoptive T-cell immunotherapy in digestive tract malignancies: Current challenges and future perspectives.
Cancer Treat Rev
; 100: 102288, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34525422
17.
The psychological impact of COVID-19 pandemic on patients with neuroendocrine tumors: Between resilience and vulnerability.
J Neuroendocrinol
; 33(10): e13041, 2021 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34596289
18.
DAXX mutations as potential genomic markers of malignant evolution in small nonfunctioning pancreatic neuroendocrine tumors.
Sci Rep
; 9(1): 18614, 2019 12 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31819132
19.
Identification of p53-target genes in Danio rerio.
Sci Rep
; 6: 32474, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27581768
20.
HDAC6 mediates the acetylation of TRIM50.
Cell Signal
; 26(2): 363-9, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24308962