Lista de obras - Rebeca Perez de Diego - Dominio Público Uruguay

A genotype-phenotype correlation study in a group of 54 patients with X-linked agammaglobulinemia.

artículo científico publicado en 2005

A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon

scientific article published on 01 November 2018

Actin polymerisation after FCγR stimulation of human fibroblasts is BCL10 independent.

artículo científico publicado en 2016

Anti-CXCR4 Antibody Combined With Activated and Expanded Natural Killer Cells for Sarcoma Immunotherapy

artículo científico publicado en 2019

Bruton's tyrosine kinase is not essential for LPS-induced activation of human monocytes

scientific article published on 31 March 2006

Chronic lymphocytic leukemia: a paradigm of innate immune cross-tolerance.

artículo científico publicado en 2014

Clinical and Immunological Features of Human BCL10 Deficiency

artículo científico publicado en 2021

Crystallization and preliminary X-ray diffraction analysis of the beta subunit Yke2 of the Gim complex from Saccharomyces cerevisiae

artículo científico publicado en 2008

Double-strand break repair through homologous recombination in autosomal-recessive BCL10 deficiency

artículo científico publicado en 2019

Evaluation of Polysaccharide Typhim Vi Antibody Response as a predictor of Humoral Immunodeficiency in Haematological Malignancies

scientific article published on 21 November 2019

Extending the clinical horizons of mucosal bacterial vaccines: current evidence and future prospects

artículo científico publicado en 2014

Gain-of-function mutation in PIK3R1 in a patient with a narrow clinical phenotype of respiratory infections.

artículo científico publicado en 2016

Genetic errors of the human caspase recruitment domain-B-cell lymphoma 10-mucosa-associated lymphoid tissue lymphoma-translocation gene 1 (CBM) complex: Molecular, immunologic, and clinical heterogeneity

artículo científico publicado en 2015

Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

artículo científico publicado en 2011

Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity

artículo científico publicado en 2011

Heterozygous TBK1 mutations impair TLR3 immunity and underlie herpes simplex encephalitis of childhood

artículo científico publicado en 2012

High frequency in the delay in primary tooth loss in X-linked chronic granulomatous disease

artículo científico publicado en 2012

Human BCL10 Deficiency due to Homozygosity for a Rare Allele

scientific article published on 01 February 2020

Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis

artículo científico publicado en 2010

Ibrutinib as an antitumor immunomodulator in patients with refractory chronic lymphocytic leukemia

artículo científico publicado en 2016

Identification of novel non-pathogenic mutation in SH3 domain of Btk in an XLA patient

Immunodeficiency and CARD-BCL10-MALT1.

artículo científico publicado en 2015

Inborn errors of anti-viral interferon immunity in humans

artículo científico publicado en 2011

Inherited BCL10 deficiency impairs hematopoietic and nonhematopoietic immunity

artículo científico publicado en 2014

Kinase activity and XLA phenotypic variability.

artículo científico publicado en 2005

Measurement of Typhim Vi IgG as a Diagnostic Tool to Determine Anti-polysaccharide Antibody Production Deficiency in Children

artículo científico publicado en 2019

Multimarker risk stratification approach at multiple sclerosis onset.

artículo científico publicado en 2017

NFκB2/p100 is a key factor for endotoxin tolerance in human monocytes: a demonstration using primary human monocytes from patients with sepsis.

artículo científico publicado en 2014

Naturally occurring Bruton's tyrosine kinase mutations have no dominant negative effect in an X-linked agammaglobulinaemia cellular model.

artículo científico publicado en 2008

New Biological Insights in the Immunomodulatory Effects of Mucosal Polybacterial Vaccines in Clinical Practice.

artículo científico publicado en 2016

Proteomics in immunity and herpes simplex encephalitis

artículo científico publicado en 2013

Similar percentages in most abundant chronic granulomatous disease autosomal recessive forms in a Spanish cohort

article

TLR3 immunity to infection in mice and humans

artículo científico publicado en 2013

The proteome of Toll-like receptor 3-stimulated human immortalized fibroblasts: implications for susceptibility to herpes simplex virus encephalitis

artículo científico publicado en 2013

Toll-like receptor 3 deficiency in autoimmune encephalitis post-herpes simplex encephalitis

artículo científico publicado en 2019

Unexpected Relevant Role of Gene Mosaicism in Primary Immunodeficiency Diseases

article

Lista de obras de Rebeca Perez de Diego

A genotype-phenotype correlation study in a group of 54 patients with X-linked agammaglobulinemia.

A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon

Actin polymerisation after FCγR stimulation of human fibroblasts is BCL10 independent.

Anti-CXCR4 Antibody Combined With Activated and Expanded Natural Killer Cells for Sarcoma Immunotherapy

Bruton's tyrosine kinase is not essential for LPS-induced activation of human monocytes

Chronic lymphocytic leukemia: a paradigm of innate immune cross-tolerance.

Clinical and Immunological Features of Human BCL10 Deficiency

Crystallization and preliminary X-ray diffraction analysis of the beta subunit Yke2 of the Gim complex from Saccharomyces cerevisiae

Double-strand break repair through homologous recombination in autosomal-recessive BCL10 deficiency

Evaluation of Polysaccharide Typhim Vi Antibody Response as a predictor of Humoral Immunodeficiency in Haematological Malignancies

Extending the clinical horizons of mucosal bacterial vaccines: current evidence and future prospects

Gain-of-function mutation in PIK3R1 in a patient with a narrow clinical phenotype of respiratory infections.

Genetic errors of the human caspase recruitment domain-B-cell lymphoma 10-mucosa-associated lymphoid tissue lymphoma-translocation gene 1 (CBM) complex: Molecular, immunologic, and clinical heterogeneity

Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity

Heterozygous TBK1 mutations impair TLR3 immunity and underlie herpes simplex encephalitis of childhood

High frequency in the delay in primary tooth loss in X-linked chronic granulomatous disease

Human BCL10 Deficiency due to Homozygosity for a Rare Allele

Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis

Ibrutinib as an antitumor immunomodulator in patients with refractory chronic lymphocytic leukemia

Identification of novel non-pathogenic mutation in SH3 domain of Btk in an XLA patient

Immunodeficiency and CARD-BCL10-MALT1.

Inborn errors of anti-viral interferon immunity in humans

Inherited BCL10 deficiency impairs hematopoietic and nonhematopoietic immunity

Kinase activity and XLA phenotypic variability.

Measurement of Typhim Vi IgG as a Diagnostic Tool to Determine Anti-polysaccharide Antibody Production Deficiency in Children

Multimarker risk stratification approach at multiple sclerosis onset.

NFκB2/p100 is a key factor for endotoxin tolerance in human monocytes: a demonstration using primary human monocytes from patients with sepsis.

Naturally occurring Bruton's tyrosine kinase mutations have no dominant negative effect in an X-linked agammaglobulinaemia cellular model.

New Biological Insights in the Immunomodulatory Effects of Mucosal Polybacterial Vaccines in Clinical Practice.

Proteomics in immunity and herpes simplex encephalitis

Similar percentages in most abundant chronic granulomatous disease autosomal recessive forms in a Spanish cohort

TLR3 immunity to infection in mice and humans

The proteome of Toll-like receptor 3-stimulated human immortalized fibroblasts: implications for susceptibility to herpes simplex virus encephalitis

Toll-like receptor 3 deficiency in autoimmune encephalitis post-herpes simplex encephalitis

Unexpected Relevant Role of Gene Mosaicism in Primary Immunodeficiency Diseases