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Lista de obras de Lennart Hammarström

4 Primary immunodeficiency mutation databases

article

A New IL-2RG Gene Mutation in an X-linked SCID Identified through TREC/KREC Screening: a Case Report

artículo científico publicado en 2015

A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency.

artículo científico publicado en 2014

A heterodimeric antibody fragment for passive immunotherapy against norovirus infection

scientific article published on 25 March 2020

A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency.

artículo científico publicado en 2014

A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside

artículo científico publicado en 2013

A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination

scientific article published on 21 October 2013

AID from bony fish catalyzes class switch recombination

artículo científico publicado en 2005

ATM is not required in somatic hypermutation of VH, but is involved in the introduction of mutations in the switch mu region

artículo científico publicado en 2003

ATM mutations in B-cell chronic lymphocytic leukemia

artículo científico publicado en 2004

Alteration of the N-glycome of bovine milk glycoproteins during early lactation

artículo científico publicado en 2011

Alternative end joining during switch recombination in patients with ataxia-telangiectasia

artículo científico publicado en 2002

An Exopolysaccharide-Deficient Mutant of Lactobacillus rhamnosus GG Efficiently Displays a Protective Llama Antibody Fragment against Rotavirus on Its Surface

artículo científico publicado en 2015

Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q

artículo científico publicado en 2005

Analysis of immunoglobulin transcripts in the ostrich Struthio camelus, a primitive avian species

artículo científico publicado en 2012

Anti-rotavirus protein reduces stool output in infants with diarrhea: a randomized placebo-controlled trial

artículo científico publicado en 2013

Antibody deficiency diseases.

artículo científico publicado en 2008

Artiodactyl IgD: the missing link

artículo científico publicado en 2002

Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing

artículo científico publicado en 2017

Association between IgA deficiency & other autoimmune conditions: a population-based matched cohort study

artículo científico publicado en 2014

Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells

artículo científico publicado en 2015

Association of FcRn Heavy Chain Encoding Gene (FCGRT) Polymorphisms with IgG Content in Bovine Colostrum

article

Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency

artículo científico publicado en 2010

Association of elevated rotavirus-specific antibody titers with HBGA secretor status in Swedish individuals: The FUT2 gene as a putative susceptibility determinant for infection

artículo científico publicado en 2015

Association of immunoglobulin A deficiency and elevated thyrotropin-receptor autoantibodies in two Nordic countries

scientific article published on 25 October 2010

Autoantibodies against BAFF, APRIL or IL21 - an alternative pathogenesis for antibody-deficiencies?

artículo científico publicado en 2017

B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.

scholarly article

Biosensor Based Protein Profiling on Reverse Phase Serum Microarray

Both Lewis and secretor status mediate susceptibility to rotavirus infections in a rotavirus genotype-dependent manner

artículo científico publicado en 2014

Carbohydrate phenotyping of human and animal milk glycoproteins

artículo científico publicado en 2005

Carbohydrate-dependent inhibition of Helicobacter pylori colonization using porcine milk

artículo científico publicado en 2005

Caucasian origin of disease associated HLA haplotypes in chinese blood donors with IgA deficiency

artículo científico publicado en 2014

Characterization and complete genome sequences of L. rhamnosus DSM 14870 and L. gasseri DSM 14869 contained in the EcoVag® probiotic vaginal capsules

artículo científico publicado en 2017

Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

artículo científico publicado en 2020

Class switch recombination: a comparison between mouse and human.

artículo científico publicado en 2007

Clinical and laboratory findings in hyper-IgM syndrome with novel CD40L and AICDA mutations.

artículo científico publicado en 2009

Clinical and molecular analysis of patients with defects in micro heavy chain gene.

artículo científico publicado en 2002

Clinical implications of experimental analyses of AID function on predictive computational tools: Challenge of missense variants

artículo científico publicado en 2020

Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency

artículo científico publicado en 2018

Clinical, Immunological and Genetic Spectrum of 696 Patients with Combined Immunodeficiency.

artículo científico publicado en 2017

Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study.

artículo científico publicado en 2017

Cloning and characterization of the dromedary (Camelus dromedarius) neonatal Fc receptor (drFcRn).

artículo científico publicado en 2006

Cloning of the complete rat immunoglobulin delta gene: evolutionary implications

artículo científico publicado en 2003

Co-expression of anti-rotavirus proteins (llama VHH antibody fragments) in Lactobacillus: development and functionality of vectors containing two expression cassettes in tandem

artículo científico publicado en 2014

Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects

artículo científico publicado en 2016

Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency

scientific article published on 23 December 2016

Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B-cell immunodeficiencies.

artículo científico publicado en 2014

Comment on "Reassessment of the role of mut S homolog 5 in Ig class switch recombination shows lack of involvement in cis- and trans-switching".

artículo científico publicado en 2009

Common variable immunodeficiency disorders: division into distinct clinical phenotypes.

artículo científico publicado en 2008

Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

artículo científico publicado en 2016

Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort

artículo científico publicado en 2018

Compound Heterozygous Mutations of IL2-Inducible T cell Kinase in a Swedish Patient: the Importance of Early Genetic Diagnosis

scientific article published on 12 February 2019

Concomitant autoimmunity in myasthenia gravis--lack of association with IgA deficiency

artículo científico publicado en 2011

Construction of a High Efficiency PCR Products Cloning T Vector Using pGEM-5zf (+)

artículo científico publicado en 2009

Correction: Genome-Wide Analyses Suggest Mechanisms Involving Early B-Cell Development in Canine IgA Deficiency

artículo científico publicado en 2015

Correction: Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis

artículo científico publicado en 2015

Correction: Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis.

artículo científico publicado en 2013

Correction: Table II

article by Qiang Pan-Hammarström et al published 17 January 2006 in Journal of Experimental Medicine

Costs associated with treatment of severe combined immunodeficiency-rationale for newborn screening in Sweden

artículo científico publicado en 2016

Current genetic landscape in common variable immune deficiency

artículo científico publicado en 2020

Cytokine gene expression profiles in human lymphocytes induced by a formula of traditional Chinese medicine, vigconic VI-28.

artículo científico publicado en 2006

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency.

artículo científico publicado en 2015

DNA-PKcs Is Involved in Ig Class Switch Recombination in Human B Cells

artículo científico publicado en 2015

Deconstructing common variable immunodeficiency by genetic analysis

artículo científico publicado en 2007

Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease

artículo científico publicado en 2016

Defective TLR9-driven STAT3 activation in B cells of patients with CVID

artículo científico publicado en 2018

Defective formation of IgA memory B cells, Th1 and Th17 cells in symptomatic patients with selective IgA deficiency

artículo científico publicado en 2020

Defects in plasma cell differentiation are associated with primary immunodeficiency in human subjects.

artículo científico publicado en 2017

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity

artículo científico publicado en 2012

Development of passive immunity against SARS-CoV-2 for management of immunodeficient patients - a perspective

scientific article published on 12 May 2020

Different brands of intravenous immunoglobulin for primary immunodeficiencies: how to choose the best option for the patient?

artículo científico

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

artículo científico publicado en 2018

Disparate roles of ATR and ATM in immunoglobulin class switch recombination and somatic hypermutation

artículo científico publicado en 2006

Effective prophylaxis against rotavirus diarrhea using a combination of Lactobacillus rhamnosus GG and antibodies

artículo científico publicado en 2007

Effects of fucosylated milk of goat and mouse on Helicobacter pylori binding to Lewis b antigen

artículo científico publicado en 2004

Engineered Lactobacillus rhamnosus GG expressing IgG-binding domains of protein G: Capture of hyperimmune bovine colostrum antibodies and protection against diarrhea in a mouse pup rotavirus infection model

artículo científico publicado en 2013

Environmental and genetic factors in the development of anticitrullinated protein antibodies (ACPAs) and ACPA-positive rheumatoid arthritis: an epidemiological investigation in twins

artículo científico publicado en 2013

European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups

artículo científico publicado en 2009

Evaluation of Known Defective Signaling-Associated Molecules in Patients Who Primarily Diagnosed as Common Variable Immunodeficiency

artículo científico publicado en 2016

Evidence of IgY subclass diversification in snakes: evolutionary implications

artículo científico publicado en 2012

Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency

scientific article published on 20 December 2019

Expression of IgM, IgD, and IgY in a reptile, Anolis carolinensis

artículo científico publicado en 2009

Extended antimicrobial treatment of bacterial vaginosis combined with human lactobacilli to find the best treatment and minimize the risk of relapses.

artículo científico publicado en 2011

Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

artículo científico publicado en 2020

Extensive diversification of IgD-, IgY-, and truncated IgY(δFc)-encoding genes in the red-eared turtle (Trachemys scripta elegans).

artículo científico publicado en 2012

Extensive diversification of IgH subclass-encoding genes and IgM subclass switching in crocodilians.

artículo científico publicado en 2013

Familial aggregation of IgAD and autoimmunity

artículo científico publicado en 2009

FcRn mediates elongated serum half-life of human IgG in cattle

artículo científico publicado en 2006

Fine-scale mapping at IGAD1 and genome-wide genetic linkage analysis implicate HLA-DQ/DR as a major susceptibility locus in selective IgA deficiency and common variable immunodeficiency

artículo científico publicado en 2003

Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis

scientific article published on 09 October 2018

Fucosyltransferase Gene Polymorphisms and Lewisb-Negative Status Are Frequent in Swedish Newborns, With Implications for Infectious Disease Susceptibility and Personalized Medicine

artículo científico publicado en 2019

Fusion of the mouse IgG1 Fc domain to the VHH fragment (ARP1) enhances protection in a mouse model of rotavirus

artículo científico publicado en 2016

Generation of human induced pluripotent stem cell lines from patients with selective IgA deficiency

artículo científico publicado en 2019

Genome-Wide Analyses Suggest Mechanisms Involving Early B-Cell Development in Canine IgA Deficiency

artículo científico publicado en 2015

Genome-wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A, and Identification of ZBTB10 and Three Distinct HLA Associations

artículo científico publicado en 2015

Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis

artículo científico publicado en 2013

Genomic organization of the immunoglobulin light chain gene loci in Xenopus tropicalis: evolutionary implications

artículo científico publicado en 2007

Global systematic review of primary immunodeficiency registries

artículo científico publicado en 2020

Guidelines for newborn screening of primary immunodeficiency diseases

artículo científico

Heat differentiated complement factor profiling

Helicobacter pylori SabA adhesin in persistent infection and chronic inflammation

artículo científico publicado en 2002

Heterozygosity for transmembrane activator and calcium modulator ligand interactor A144E causes haploinsufficiency and pneumococcal susceptibility in mice

artículo científico publicado en 2016

High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency.

artículo científico publicado en 2012

Histocompatibility Complex Status and Mendelian Randomization Analysis in Unsolved Antibody Deficiency

artículo científico publicado en 2020

Host-derived pentapeptide affecting adhesion, proliferation, and local pH in biofilm communities composed of Streptococcus and Actinomyces species

artículo científico publicado en 2006

Human Sera Collected between 1979 and 2010 Possess Blocking-Antibody Titers to Pandemic GII.4 Noroviruses Isolated over Three Decades

artículo científico publicado en 2017

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

artículo científico publicado en 2015

Human estrogen receptor beta 548 is not a common variant in three distinct populations

artículo científico publicado en 2003

Human genetic and immunological determinants of critical COVID-19 pneumonia

artículo científico publicado en 2022

Human leukocyte antigens (HLA) associated with selective IgA deficiency in Iran and Sweden

scientific article published on 01 December 2008

ICOS deficiency in patients with common variable immunodeficiency.

artículo científico publicado en 2004

Identification and characterisation of vaginal lactobacilli from South African women

artículo científico publicado en 2013

Identification of IgF, a hinge-region-containing Ig class, and IgD in Xenopus tropicalis

artículo científico publicado en 2006

Identification of a functional variant of estrogen receptor beta in an African population

artículo científico publicado en 2004

Identification of the activation-induced cytidine deaminase gene from zebrafish: an evolutionary analysis

artículo científico publicado en 2005

IgA deficiency and risk of cancer: a population-based matched cohort study

artículo científico publicado en 2015

IgA deficiency and the MHC: assessment of relative risk and microheterogeneity within the HLA A1 B8, DR3 (8.1) haplotype.

artículo científico publicado en 2009

IgA deficiency in wolves

scientific article published on 22 January 2013

IgA deficiency in wolves from Canada and Scandinavia

artículo científico publicado en 2014

IgA deficiency, autoimmunity & pregnancy: a population-based matched cohort study

artículo científico publicado en 2014

IgA deficiency: what is new?

artículo científico

IgA measurements in over 12 000 Swedish twins reveal sex differential heritability and regulatory locus near CD30L.

artículo científico publicado en 2014

Impact of DNA ligase IV on nonhomologous end joining pathways during class switch recombination in human cells.

artículo científico publicado en 2005

Impact of Down syndrome on the performance of neonatal screening assays for severe primary immunodeficiency diseases.

artículo científico publicado en 2013

Impact of a 3-Months Vegetarian Diet on the Gut Microbiota and Immune Repertoire.

artículo científico publicado en 2018

Important differences in the diagnostic spectrum of primary immunodeficiency in adults versus children

artículo científico

In situ delivery of passive immunity by lactobacilli producing single-chain antibodies

scientific article published on 01 July 2002

In situ gastrointestinal protection against anthrax edema toxin by single-chain antibody fragment producing lactobacilli

artículo científico publicado en 2011

In vivo mucosal delivery of bioactive human interleukin 1 receptor antagonist produced by Streptococcus gordonii

artículo científico publicado en 2003

Individuals with selective IgA deficiency resolve rotavirus disease and develop higher antibody titers (IgG, IgG1) than IgA competent individuals

artículo científico publicado en 2008

Inducible Plasmid Self-Destruction (IPSD) Assisted Genome Engineering in Lactobacilli and Bifidobacteria

scientific article published on 12 July 2019

Integrative expression system for delivery of antibody fragments by lactobacilli.

artículo científico publicado en 2011

Interleukin-21 restores immunoglobulin production ex vivo in patients with common variable immunodeficiency and selective IgA deficiency

artículo científico publicado en 2009

Internal Duplications of DH, JH, and C Region Genes Create an Unusual IgH Gene Locus in Cattle.

artículo científico publicado en 2016

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders

artículo científico publicado en 2016

Isolation of the gene encoding the bovine neonatal Fc receptor.

artículo científico publicado en 2005

Kappa-deleting recombination excision circle levels remain low or undetectable throughout life in patients with X-linked agammaglobulinemia

artículo científico publicado en 2018

Lack of IgA in C(mu)-deficient patients

artículo científico publicado en 2002

Lack of association between human switch recombination breakpoints and the secondary structure of targeted DNA regions.

artículo científico publicado en 2004

Lack of association of the CIITA -168A→G promoter SNP with myasthenia gravis and its role in autoimmunity

artículo científico publicado en 2010

Lack of correlation between the reduction of serum immunoglobulin concentration and the CTG repeat expansion in patients with type 1 dystrophia [correction of Dystrofia] myotonica

scientific article published on 01 November 2003

Lactobacilli expressing variable domain of llama heavy-chain antibody fragments (lactobodies) confer protection against rotavirus-induced diarrhea

artículo científico publicado en 2006

Lactobacilli producing bispecific llama-derived anti-rotavirus proteins in vivo for rotavirus-induced diarrhea

artículo científico publicado en 2011

Lactobacillli expressing llama VHH fragments neutralise Lactococcus phages

artículo científico publicado en 2007

Lactobacillus delivery of bioactive interleukin-22.

artículo científico publicado en 2017

Lactobacillus paracasei strain ST11 has no effect on rotavirus but ameliorates the outcome of nonrotavirus diarrhea in children from Bangladesh

artículo científico publicado en 2005

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.

artículo científico publicado en 2006

Localization of the sheep FcRn in the mammary gland

scientific article published on 01 September 2002

Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients

artículo científico publicado en 2014

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score

scientific article published on 27 December 2019

Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

artículo científico publicado en 2009

Molecular diagnosis of primary immunodeficiency diseases in a developing country: Iran as an example.

artículo científico

Monogenic mutations associated with IgA deficiency

artículo científico publicado en 2016

Monozygotic Twins Concordant for Common Variable Immunodeficiency: Strikingly Similar Clinical and Immune Profile Associated With a Polygenic Burden

artículo científico publicado en 2019

Multiple IgH Isotypes Including IgD, Subclasses of IgM, and IgY Are Expressed in the Common Ancestors of Modern Birds.

artículo científico publicado en 2016

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

artículo científico publicado en 2010

Mutations in toll-like receptor 3 are associated with elevated levels of rotavirus-specific IgG antibodies in IgA-deficient but not IgA-sufficient individuals

artículo científico publicado en 2013

NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion.

artículo científico publicado en 2017

NFκB induces overexpression of bovine FcRn: a novel mechanism that further contributes to the enhanced immune response in genetically modified animals carrying extra copies of FcRn.

artículo científico publicado en 2013

Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.

artículo científico publicado en 2011

Neutralization of Clostridium difficile Toxin B Mediated by Engineered Lactobacilli That Produce Single-Domain Antibodies

artículo científico publicado en 2015

New facets of antibody deficiencies

artículo científico

Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

scientific article published on 17 March 2020

Newborn Screening for Primary Immunodeficiency Diseases: History, Current and Future Practice

artículo científico publicado en 2017

Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden-a 2-Year Pilot TREC and KREC Screening Study

artículo científico publicado en 2016

Newborn screening for primary immunodeficiencies: beyond SCID and XLA.

artículo científico

Newborn screening for severe T and B cell lymphopenia identifies a fraction of patients with Wiskott-Aldrich syndrome.

artículo científico publicado en 2014

Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran

scientific article published on 26 June 2018

Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders - Future Directions

artículo científico publicado en 2016

Noncoding RNA transcription alters chromosomal topology to promote isotype-specific class switch recombination

artículo científico publicado en 2020

Normalized immunoglobulin patterns in adults with recurrent acute otitis media and low IgG2 levels during early childhood.

artículo científico publicado en 2014

Novel Leb-like Helicobacter pylori-binding glycosphingolipid created by the expression of human alpha-1,3/4-fucosyltransferase in FVB/N mouse stomach

artículo científico publicado en 2008

Novel Mutations in TACI (TNFRSF13B) Causing Common Variable Immunodeficiency

artículo científico publicado en 2009

Novel NLRP12 mutations associated with intestinal amyloidosis in a patient diagnosed with common variable immunodeficiency

artículo científico publicado en 2014

Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.

artículo científico publicado en 2008

Novel genetic loci associated HLA-B*08:01 positive myasthenia gravis

artículo científico publicado en 2017

Novel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome.

artículo científico publicado en 2012

Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency

artículo científico

Onychomadesis in a patient with immunoglobulin class switch recombination deficiency

artículo científico publicado en 2008

Oral Delivery of Pentameric Glucagon-Like Peptide-1 by Recombinant Lactobacillus in Diabetic Rats

artículo científico publicado en 2016

Ornithorhynchus anatinus (platypus) links the evolution of immunoglobulin genes in eutherian mammals and nonmammalian tetrapods.

artículo científico publicado en 2009

Over-expression of the bovine FcRn in the mammary gland results in increased IgG levels in both milk and serum of transgenic mice

scientific article published on 03 July 2007

PTPN22 R620W promotes production of anti-AChR autoantibodies and IL-2 in myasthenia gravis

artículo científico publicado en 2008

Passive immunization by lactobacilli expressing single-chain antibodies against Streptococcus mutans

artículo científico publicado en 2005

Phylogeny, genomic organization and expression of lambda and kappa immunoglobulin light chain genes in a reptile, Anolis carolinensis

artículo científico publicado en 2010

Physical mapping of the bovine immunoglobulin heavy chain constant region gene locus

artículo científico publicado en 2003

Physical mapping of the giant panda immunoglobulin heavy chain constant region genes.

artículo científico publicado en 2007

Placental transfer of maternally-derived IgA precludes the use of guthrie card eluates as a screening tool for primary immunodeficiency diseases.

artículo científico publicado en 2012

Polyautoimmunity in Patients with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency.

artículo científico publicado en 2018

Position independent and copy-number-related expression of the bovine neonatal Fc receptor alpha-chain in transgenic mice carrying a 102 kb BAC genomic fragment.

artículo científico publicado en 2007

Predictive markers for humoral influenza vaccine response in patients with common variable immunodeficiency (CVID).

artículo científico publicado en 2018

Presence of the di-leucine motif in the cytoplasmic tail of the pig FcRn α chain ⬇️

artículo científico publicado el 15 de diciembre de 2003

Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

artículo científico publicado en 2007

Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency

artículo científico publicado en 2011

Progression of Selective IgA Deficiency to Common Variable Immunodeficiency

artículo científico publicado en 2008

Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects.

artículo científico publicado en 2011

RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency

artículo científico publicado en 2014

Redistribution of the sheep neonatal Fc receptor in the mammary gland around the time of parturition in ewes and its localization in the small intestine of neonatal lambs

artículo científico publicado en 2002

Reduced BAFF-R and Increased TACI Expression in Common Variable Immunodeficiency

artículo científico publicado en 2014

Reduced immunoglobulin gene diversity in patients with Cornelia de Lange syndrome.

artículo científico publicado en 2017

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency

artículo científico publicado en 2007

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

artículo científico publicado en 2008

Reply

Restricted immunoglobulin constant heavy G chain genes in primary immunodeficiencies

artículo científico publicado en 2008

Retrospective analysis of TREC based newborn screening results and clinical phenotypes in infants with the 22q11 deletion syndrome

artículo científico publicado en 2014

Reversal of Immunoglobulin A Deficiency in Children

artículo científico publicado en 2014

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia

artículo científico publicado en 2013

Rice-based oral antibody fragment prophylaxis and therapy against rotavirus infection.

artículo científico publicado en 2013

Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08

scientific journal article

Risk of Infections Among 2100 Individuals with IgA Deficiency: a Nationwide Cohort Study

artículo científico publicado en 2016

Role for Msh5 in the regulation of Ig class switch recombination

artículo científico publicado en 2007

Screening and evaluation of human intestinal lactobacilli for the development of novel gastrointestinal probiotics

artículo científico publicado en 2010

Screening for C3 deficiency in newborns using microarrays.

artículo científico publicado en 2009

Screening of functional and positional candidate genes in families with common variable immunodeficiency

artículo científico publicado en 2008

Selective IgA deficiency in autoimmune diseases

artículo científico publicado en 2011

Selective IgA deficiency in early life: Association to infections and allergic diseases during childhood

article

Selective IgG2 deficiency due to a point mutation causing abnormal splicing of the Cgamma2 gene

artículo científico publicado en 2004

Serological assessment for celiac disease in IgA deficient adults

artículo científico publicado en 2014

Serum microarrays for large scale screening of protein levels.

artículo científico publicado en 2005

Severe congenital neutropenia or hyper-IgM syndrome? A novel mutation of CD40 ligand in a patient with severe neutropenia.

artículo científico publicado en 2008

Small for gestational age and risk of childhood mortality: A Swedish population study

Spectrum of Phenotypes Associated with Mutations in LRBA.

artículo científico

Structural Insights into Polymorphic ABO Glycan Binding by Helicobacter pylori

artículo científico publicado en 2016

Study of an extended family with CTLA-4 deficiency suggests a CD28/CTLA-4 independent mechanism responsible for differences in disease manifestations and severity

artículo científico publicado en 2018

Successful treatment of rotavirus-induced diarrhoea in suckling mice with egg yolk immunoglobulin.

artículo científico publicado en 2007

Surge of immune cell formation at birth differs by mode of delivery and infant characteristics-A population-based cohort study

artículo científico publicado en 2017

Targeted antibodies in dairy-based products

artículo científico publicado en 2008

Targeted next-generation sequencing for genetic diagnosis of 160 patients with primary immunodeficiency in south China

scientific article published on 01 December 2018

The CD45 77C/G allele is not associated with myasthenia gravis - a reassessment of the potential role of CD45 in autoimmunity

artículo científico publicado en 2010

The Immunoglobulins: New Insights, Implications, and Applications

scientific article published on 17 December 2019

The dog as a genetic model for immunoglobulin A (IgA) deficiency: identification of several breeds with low serum IgA concentrations

artículo científico publicado en 2014

The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993.

artículo científico publicado en 2012

The immunoglobulin δ gene in jawed vertebrates: A comparative overview ⬇️

artículo científico publicado el 21 de diciembre de 2010

The neonatal Fc receptor (FcRn) is expressed in the bovine lung.

artículo científico publicado en 2004

The porcine Ig delta gene: unique chimeric splicing of the first constant region domain in its heavy chain transcripts.

artículo científico publicado en 2003

The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies

artículo científico publicado en 2022

Therapeutic effect of llama derived VHH fragments against Streptococcus mutans on the development of dental caries

artículo científico publicado en 2006

Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation

artículo científico publicado en 2017

Tuberculosis and impaired IL-23-dependent IFN-γ immunity in humans homozygous for a common missense variant

scientific article published on 01 December 2018

Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID

artículo científico publicado en 2010

Utilizing twins concordance rates to infer the predisposition to myasthenia gravis

artículo científico publicado en 2011

Vaginal colonisation by probiotic lactobacilli and clinical outcome in women conventionally treated for bacterial vaginosis and yeast infection

artículo científico publicado en 2015

[Study on immunoglobulin A Deficiency(IgAD) in Chinese Shanghai Blood Donors]

scientific article published on 01 August 2016

hypomorphic mutation: identification of a novel pathogenic mutation in exon 8 and a review of the literature

scientific article published on 05 January 2019

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