Detalhe da pesquisa
1.
Development of MGD007, a gpA33 x CD3-Bispecific DART Protein for T-Cell Immunotherapy of Metastatic Colorectal Cancer.
Mol Cancer Ther;
17(8): 1761-1772, 2018 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29866746
2.
A two-tier approach to mutation detection in the COL4A5 gene for Alport syndrome.
Hum Mutat;
27(10): 1061, 2006 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16941480
3.
Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.
Hum Mutat;
27(1): 44-54, 2006 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16278823
4.
Detection of muramyl dipeptide-sensing pathway defects in patients with Crohn's disease.
Inflamm Bowel Dis;
12(7): 598-605, 2006 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16804397
5.
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates.
Hum Pathol;
36(7): 761-7, 2005 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16084945
6.
Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.
Genomics;
90(4): 493-501, 2007 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17719742
7.
Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome.
Hum Genet;
111(6): 548-54, 2002 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12436246
8.
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.
Gastroenterology;
122(4): 867-74, 2002 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-11910337
9.
Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.
Am J Hum Genet;
72(4): 1018-22, 2003 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12618963