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Items: 10

1.

The Loop of the TPR1 Subdomain of Phi29 DNA Polymerase Plays a Pivotal Role in Primer-Terminus Stabilization at the Polymerization Active Site.

Del Prado A, Santos E, Lázaro JM, Salas M, de Vega M.

Biomolecules. 2019 Oct 24;9(11). pii: E648. doi: 10.3390/biom9110648.

2.

Role of the LEXE motif of protein-primed DNA polymerases in the interaction with the incoming nucleotide.

Santos E, Lázaro JM, Pérez-Arnaiz P, Salas M, de Vega M.

J Biol Chem. 2014 Jan 31;289(5):2888-98. doi: 10.1074/jbc.M113.530980. Epub 2013 Dec 9.

3.

Compensatory T-cell regulation in unaffected relatives of SLE patients, and opposite IL-2/CD25-mediated effects suggested by coreferentiality modeling.

Fesel C, Barreto M, Ferreira RC, Costa N, Venda LL, Pereira C, Carvalho C, Morães-Fontes MF, Ferreira CM, Vasconcelos C, Viana JF, Santos E, Martins B, Demengeot J, Vicente AM.

PLoS One. 2012;7(3):e33992. doi: 10.1371/journal.pone.0033992. Epub 2012 Mar 29.

4.

Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFbeta gene variants.

Barreto M, Ferreira RC, Lourenço L, Moraes-Fontes MF, Santos E, Alves M, Carvalho C, Martins B, Andreia R, Viana JF, Vasconcelos C, Mota-Vieira L, Ferreira C, Demengeot J, Vicente AM.

BMC Immunol. 2009 Jan 27;10:5. doi: 10.1186/1471-2172-10-5.

5.

Heritable factors shape natural human IgM reactivity to Ro60/SS-A and may predispose for SLE-associated IgG anti-Ro and anti-La autoantibody production.

Ferreira R, Barreto M, Santos E, Pereira C, Martins B, Andreia R, Crespo F, Viana JF, Vasconcelos C, Ferreira C, Vicente AM, Fesel C.

J Autoimmun. 2005 Sep;25(2):155-63. Epub 2005 Jul 11.

PMID:
16006098
6.

Lymphadenopathy after BCG vaccination in a child with chronic granulomatous disease.

Vieira AP, Vasconcelos J, Fernandes JC, Antunes H, Basto AS, Macedo C, Zaman A, Santos E, Melo JC, Roos D.

Pediatr Dermatol. 2004 Nov-Dec;21(6):646-51.

PMID:
15575848
7.

Evidence for CTLA4 as a susceptibility gene for systemic lupus erythematosus.

Barreto M, Santos E, Ferreira R, Fesel C, Fontes MF, Pereira C, Martins B, Andreia R, Viana JF, Crespo F, Vasconcelos C, Ferreira C, Vicente AM.

Eur J Hum Genet. 2004 Aug;12(8):620-6.

8.

Adrenal involvement in the antiphospholipid syndrome: clinical and immunologic characteristics of 86 patients.

Espinosa G, Santos E, Cervera R, Piette JC, de la Red G, Gil V, Font J, Couch R, Ingelmo M, Asherson RA.

Medicine (Baltimore). 2003 Mar;82(2):106-18. Review.

9.

A new case of autosomal recessive agammaglobulinaemia with impaired pre-B cell differentiation due to a large deletion of the IGH locus.

Milili M, Antunes H, Blanco-Betancourt C, Nogueiras A, Santos E, Vasconcelos J, Castro e Melo J, Schiff C.

Eur J Pediatr. 2002 Sep;161(9):479-84. Epub 2002 Jul 12.

PMID:
12200606
10.

Neutrophil dysfunction in a case of glucose-6-phosphate dehydrogenase deficiency.

Costa E, Vasconcelos J, Santos E, Laranjeira A, Castro e Melo J, Barbot J.

J Pediatr Hematol Oncol. 2002 Feb;24(2):164-5. No abstract available.

PMID:
11990707

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