Lista de obras -

A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia

scientific article published on 10 April 2020

A novel case of homozygous IFNAR1 deficiency with haemophagocytic lymphohistiocytosis

artículo científico publicado en 2020

Aberrantly expressed CEACAM6 is involved in the signaling leading to apoptosis of acute lymphoblastic leukemia cells.

artículo científico publicado en 2010

An automated analysis of highly complex flow cytometry-based proteomic data.

artículo científico publicado en 2011

CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID

artículo científico publicado en 2018

Characterization of lymphocyte subsets in patients with common variable immunodeficiency reveals subsets of naive human B cells marked by CD24 expression.

artículo científico publicado en 2010

Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia.

artículo científico publicado en 2017

Comprehensive Molecular Profiling for Relapsed/Refractory Pediatric Burkitt Lymphomas-Retrospective Analysis of Three Real-Life Clinical Cases-Addressing Issues on Randomization and Customization at the Bedside

artículo científico publicado en 2019

Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK

artículo científico publicado en 2022

Erratum: Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia.

artículo científico publicado en 2017

EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children

scientific article published on 19 March 2020

High-resolution Antibody Array Analysis of Childhood Acute Leukemia Cells

artículo científico publicado en 2016

Lymphoproliferation, immunodeficiency and early-onset inflammatory bowel disease associated with a novel mutation in Caspase 8

artículo científico publicado en 2018

Multiplexed immuno-precipitation with 1725 commercially available antibodies to cellular proteins

artículo científico publicado en 2011

Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement

scientific article published on 18 September 2019

Novel XIAP mutation causing enhanced spontaneous apoptosis and disturbed NOD2 signalling in a patient with atypical adult-onset Crohn's disease

artículo científico publicado en 2020

Optimization and testing of dried antibody tube: The EuroFlow LST and PIDOT tubes as examples

artículo científico publicado en 2017

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects

artículo científico publicado en 2018

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised?

Somatic Mutations in Oncogenes Are in Chronic Myeloid Leukemia Acquired De Novo via Deregulated Base-Excision Repair and Alternative Non-Homologous End Joining

artículo científico publicado en 2021

The adaptor protein NTAL enhances proximal signaling and potentiates corticosteroid-induced apoptosis in T-ALL.

artículo científico publicado en 2012

Transmembrane adaptor protein WBP1L regulates CXCR4 signalling and murine haematopoiesis

scientific article published on 17 December 2019

Utility of Ruxolitinib in a Child with Chronic Mucocutaneous Candidiasis Caused by a Novel STAT1 Gain-of-Function Mutation

scientific article published on 22 June 2018

Lista de obras de

A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia

A novel case of homozygous IFNAR1 deficiency with haemophagocytic lymphohistiocytosis

Aberrantly expressed CEACAM6 is involved in the signaling leading to apoptosis of acute lymphoblastic leukemia cells.

An automated analysis of highly complex flow cytometry-based proteomic data.

CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID

Characterization of lymphocyte subsets in patients with common variable immunodeficiency reveals subsets of naive human B cells marked by CD24 expression.

Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia.

Comprehensive Molecular Profiling for Relapsed/Refractory Pediatric Burkitt Lymphomas-Retrospective Analysis of Three Real-Life Clinical Cases-Addressing Issues on Randomization and Customization at the Bedside

Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK

Erratum: Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia.

EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children

High-resolution Antibody Array Analysis of Childhood Acute Leukemia Cells

Lymphoproliferation, immunodeficiency and early-onset inflammatory bowel disease associated with a novel mutation in Caspase 8

Multiplexed immuno-precipitation with 1725 commercially available antibodies to cellular proteins

Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement

Novel XIAP mutation causing enhanced spontaneous apoptosis and disturbed NOD2 signalling in a patient with atypical adult-onset Crohn's disease

Optimization and testing of dried antibody tube: The EuroFlow LST and PIDOT tubes as examples

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised?

Somatic Mutations in Oncogenes Are in Chronic Myeloid Leukemia Acquired De Novo via Deregulated Base-Excision Repair and Alternative Non-Homologous End Joining

The adaptor protein NTAL enhances proximal signaling and potentiates corticosteroid-induced apoptosis in T-ALL.

Transmembrane adaptor protein WBP1L regulates CXCR4 signalling and murine haematopoiesis

Utility of Ruxolitinib in a Child with Chronic Mucocutaneous Candidiasis Caused by a Novel STAT1 Gain-of-Function Mutation