[HTML][HTML] Retracted: clinical and technical phosphoproteomic research

E Lopez, I Lopez, A Ferreira, J Sequi - Proteome Science, 2011 - Springer
An encouraging approach for the diagnosis and effective therapy of immunological
pathologies, which would include cancer, is the identification of proteins and phosphorylated …

[PDF][PDF] 2 Evaluation of CARMA1/CARD11 and Bob1 as Candidate Genes in Common Variable Immunodeficiency

G Tampella, M Baronio, M Vitali… - Journal of …, 2011 - esmonformacion.com
■ Abstract Background and Objective: The candidate gene approach has led to the
detection of associations between common variable immunodeficiency (CVID) and …

Systemic lupus erythematosus as a first presentation of common variable immunodeficiency associated with infrequent mannose-binding lectin gene polymorphisms

M Torres-Salido, J Cortés-Hernández, E Balada… - Rheumatology …, 2011 - Springer
The association of common variable immunodeficiency (CVID) and systemic lupus
erythematosus (SLE) is infrequent. Mannose-binding lectin (MBL) has been shown to play a …

Клинико-иммунологические особенности, генетические аспекты и эффективность терапии первичных иммунодефицитов с тотальным дефектом продукции …

АВ Караулов, ИВ Сидоренко, ВВ Андросов… - Иммунология, 2011 - elibrary.ru
Наиболее часто встречаемым первичным иммунодефицитом (ПИД) с тотальным
дефектом продукции антител у взрослых является общая вариабельная иммунная …

Первичные иммунодефициты у взрослых: общая вариабельная иммунная недостаточность клинические проявления, иммунологические и генетические …

АВ Караулов, ИВ Сидоренко, ВВ Андросов… - Терапевтический …, 2011 - elibrary.ru
У взрослых наиболее часто встречающейся формой первичного иммунодефицита с
тотальным дефектом продукции антител является общая вариабельная иммунная …

Novel sequencing-based strategies for high-throughput discovery of genetic mutations underlying inherited antibody deficiency disorders

HY Wang, A Jain - Current allergy and asthma reports, 2011 - Springer
Human inherited antibody deficiency disorders are generally caused by mutations in genes
involved in the pathways regulating B-cell class switch recombination; DNA damage repair; …

Stratégie diagnostique devant la découverte d'une hypogammaglobulinemie en rhumatologie

M Samson, S Audia, D Lakomy, B Bonnotte… - Revue du …, 2011 - Elsevier
Résumé La découverte d'une hypogammaglobulinémie qui se définit par un taux
plasmatique d'immunoglobulines inférieur à 5 g/L est rare en pratique clinique. Cependant …

Roles for infections in systemic lupus erythematosus pathogenesis

ES Vista, AD Farris, JA James - Systemic Lupus Erythematosus, 2011 - Elsevier
Publisher Summary This chapter focuses on examining roles for infection in the initiation
and pathogenesis of systemic lupus erythematosus (SLE). It presents accumulating data for …

Yaygin Değişken İMmün Yetmezlikte Oksidatif Stres

ST Başaranoğlu - 2011 - search.proquest.com
Normal hücresel dengede reaktif oksijen radikali oluşumunun artmasıve/veya antioksidan
seviyelerinin azalması sonucu oluşacak değişiklikler oksidatif stres durumuna sebep …

Primary immunodeficiency in adults: total variable immune deficiency clinical manifestations, immunological and genetic defects, treatment

AV Karaulov, IV Sidorenko… - Terapevticheskii …, 2011 - journals.eco-vector.com
The most prevalent form of primary immunodeficiency with a total defect of antibody
production in adults is common variable immunodeficiency (CVID). Compared to other forms …