Detalhe da pesquisa
1.
Human dermal microvascular endothelial cell morphological response to fluid shear stress.
Microvasc Res
; 143: 104377, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35561754
2.
Multiethnic PDX models predict a possible immune signature associated with TNBC of African ancestry.
Breast Cancer Res Treat
; 186(2): 391-401, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33576900
3.
Somatic inactivating PTPRJ mutations and dysregulated pathways identified in canine malignant melanoma by integrated comparative genomic analysis.
PLoS Genet
; 14(9): e1007589, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30188888
4.
Comprehensive molecular profiling of 718 Multiple Myelomas reveals significant differences in mutation frequencies between African and European descent cases.
PLoS Genet
; 13(11): e1007087, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29166413
5.
E6201, an intravenous MEK1 inhibitor, achieves an exceptional response in BRAF V600E-mutated metastatic malignant melanoma with brain metastases.
Invest New Drugs
; 37(4): 636-645, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30264293
6.
Non-Invasive Electromagnetic Skin Patch Sensor to Measure Intracranial Fluid-Volume Shifts.
Sensors (Basel)
; 18(4)2018 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-29596338
7.
Case report: whole exome sequencing of primary cardiac angiosarcoma highlights potential for targeted therapies.
BMC Cancer
; 17(1): 17, 2017 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28056866
8.
Integrated genomic characterization reveals novel, therapeutically relevant drug targets in FGFR and EGFR pathways in sporadic intrahepatic cholangiocarcinoma.
PLoS Genet
; 10(2): e1004135, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24550739
9.
Long insert whole genome sequencing for copy number variant and translocation detection.
Nucleic Acids Res
; 42(2): e8, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24071583
10.
Simultaneous characterization of somatic events and HPV-18 integration in a metastatic cervical carcinoma patient using DNA and RNA sequencing.
Int J Gynecol Cancer
; 24(2): 329-38, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24418928
11.
Drug Delivery Strategies and Nanozyme Technologies to Overcome Limitations for Targeting Oxidative Stress in Osteoarthritis.
Pharmaceuticals (Basel)
; 16(7)2023 Jul 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37513955
12.
Hypertension contributes to exacerbated osteoarthritis pathophysiology in rats in a sex-dependent manner.
Arthritis Res Ther
; 25(1): 7, 2023 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36635774
13.
Multi-omic molecular profiling guide's efficacious treatment selection in refractory metastatic breast cancer: a prospective phase II clinical trial.
Mol Oncol
; 16(1): 104-115, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34437759
14.
Analytic validation and clinical utilization of the comprehensive genomic profiling test, GEM ExTra®.
Oncotarget
; 12(8): 726-739, 2021 Apr 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33889297
15.
Identifying treatment options for BRAFV600 wild-type metastatic melanoma: A SU2C/MRA genomics-enabled clinical trial.
PLoS One
; 16(4): e0248097, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33826614
16.
In situ fixation and subsequent collection of cultured endothelial cells in a shear flow.
MethodsX
; 6: 1164-1173, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31193472
17.
Canine osteosarcoma genome sequencing identifies recurrent mutations in DMD and the histone methyltransferase gene SETD2.
Commun Biol
; 2: 266, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31341965
18.
Extramedullary myeloma whole genome sequencing reveals novel mutations in Cereblon, proteasome subunit G2 and the glucocorticoid receptor in multi drug resistant disease.
Br J Haematol
; 161(5): 748-751, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23480694
19.
A prospective pilot study of genome-wide exome and transcriptome profiling in patients with small cell lung cancer progressing after first-line therapy.
PLoS One
; 12(6): e0179170, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28586388
20.
A method to reduce ancestry related germline false positives in tumor only somatic variant calling.
BMC Med Genomics
; 10(1): 61, 2017 10 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29052513