Detalhe da pesquisa
1.
CCL5 is a potential bridge between type 1 and type 2 inflammation in asthma.
J Allergy Clin Immunol
; 152(1): 94-106.e12, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-36893862
2.
A rationally designed A34R mutant oncolytic poxvirus: improved efficacy in peritoneal carcinomatosis.
Mol Ther
; 21(5): 1024-33, 2013 May.
Artigo
Inglês
| MEDLINE | ID: mdl-23439499
3.
High-dimensional profiling clusters asthma severity by lymphoid and non-lymphoid status.
Cell Rep
; 35(2): 108974, 2021 04 13.
Artigo
Inglês
| MEDLINE | ID: mdl-33852838
4.
Development of flow cytometry assays for measuring cell-membrane enzyme activity on individual cells.
J Cancer
; 11(3): 702-715, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-31942194
5.
Three epigenetic drugs up-regulate homeobox gene Rhox5 in cancer cells through overlapping and distinct molecular mechanisms.
Mol Pharmacol
; 76(5): 1072-81, 2009 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-19679824
6.
ADAM10 Sheddase Activity is a Potential Lung-Cancer Biomarker.
J Cancer
; 9(14): 2559-2570, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-30026855
7.
Modification of proteolytic activity matrix analysis (PrAMA) to measure ADAM10 and ADAM17 sheddase activities in cell and tissue lysates.
J Cancer
; 8(19): 3916-3932, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-29187866
8.
Renal manifestations of a mutation in the uromodulin (Tamm Horsfall protein) gene.
Am J Kidney Dis
; 42(2): E20-6, 2003 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-12900848
9.
Clinico-pathologic findings in medullary cystic kidney disease type 2.
Pediatr Nephrol
; 20(6): 824-7, 2005 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-15844001
10.
Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.
Eur J Oral Sci
; 111(4): 326-31, 2003 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-12887398
11.
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1.
Am J Hum Genet
; 70(4): 943-54, 2002 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-11868160
12.
Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene.
Kidney Int
; 64(1): 36-42, 2003 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-12787393