• A doggy tale: Risk of zoonotic infection with Bordetella bronchiseptica for cystic fibrosis (CF) patients from live licenced bacterial veterinary vaccines for cats and dogs
• A Novel Deletion in FERMT3 Causes LAD-III in a Turkish Family
• A novel ITGB2 variant with long survival in patients with leukocyte adhesion defect type-I
• A Novel Nonsense Mutation in <em>FERMT3</em> Causes LAD-III in a Pakistani Family
• AA Amyloidosis Secondary to Primary Immune Deficiency: About 40 Cases Including 2 New French Cases and a Systematic Literature Review
• Adhesive dynamics simulations quantitatively predict effects of kindlin-3 deficiency on T-cell homing
• Analysis of Clinical, Immunological and Molecular Features of Leukocyte Adhesion Deficiency Type I in Egyptian Children
• Approach to a Child with Primary Immunodeficiency Made Simple
• ArhGAP15, a RacGAP, Acts as a Temporal Signaling Regulator of Mac-1 Affinity in Sterile Inflammation
• Assessment of Arf6 Deletion in PLB-985 Differentiated in Neutrophil-Like Cells and in Mouse Neutrophils: Impact on Adhesion and Migration
• Biallelic variants in SLC35C1 as a cause of isolated short stature with intellectual disability
• Bioreactivity of stent material: Activation of platelets, coagulation, leukocytes and endothelial cell dysfunction in vitro
• Boldine prevents the inflammatory response of cardiac fibroblasts induced by SGK1-NFκB signaling pathway activation
• Carbon monoxide poisoning
• Case Report: A Case of Leukocyte Adhesion Deficiency, Type III Presenting With Impaired Platelet Function, Lymphocytosis and Granulocytosis
• Case report: HLA-haploidentical hematopoietic cell transplant with posttransplant cyclophosphamide in a patient with leukocyte adhesion deficiency type I
• Cerebrovascular Senescence Is Associated With Tau Pathology in Alzheimer's Disease
• Chronic ethanol consumption compromises neutrophil function in acute pulmonary <em>Aspergillus fumigatus</em> infection
• Clinical and functional spectrum of RAC2-related immunodeficiency
• Clinical and Genetic Spectrum of a Large Cohort of Patients With Leukocyte Adhesion Deficiency Type 1 and 3: A Multicentric Study From India
• Clinical and Osteopetrosis-Like Radiological Findings in Patients with Leukocyte Adhesion Deficiency Type III
• Clinical manifestations and expression of CD18 to guide the diagnosis of leukocyte adhesion deficiency type 1: Mexico experience
• Coronin 1A, a novel player in integrin biology, controls neutrophil trafficking in innate immunity
• Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1
• Diagnosis of platelet function disorders: A standardized, rational, and modular flow cytometric approach
• Direct Rap1/Talin1 interaction regulates platelet and neutrophil integrin activity in mice
• Endothelial Dysfunction and Heart Failure with Preserved Ejection Fraction-An Updated Review of the Literature
• Extensive perineal ecthyma gangrenosum in leukocyte adhesion deficiency type 1 associated with Staphylococcus hominis bacteremia
• Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience
• Glucose lowering by SGLT2-inhibitor empagliflozin accelerates atherosclerosis regression in hyperglycemic STZ-diabetic mice
• Haematopoietic Stem Cell Transplantation (HSCT) for Primary Immune System Disorders in Children: A Single Centre Experience
• Health Benefits of Polyphenols and Carotenoids in Age-Related Eye Diseases
• Hematologically important mutations: Leukocyte adhesion deficiency (second update)
• Hematopoietic stem cell Transplantation in Children with very Early Onset Inflammatory Bowel Disease Secondary to Monogenic Disorders of immune-dysregulation
• Human endoglin as a potential new partner involved in platelet-endothelium interactions
• Hyperglycemia and advanced glycation end products disrupt BBB and promote occludin and claudin-5 protein secretion on extracellular microvesicles
• IL-1 induces throboxane-A2 (TxA2) in COVID-19 causing inflammation and micro-thrombi: inhibitory effect of the IL-1 receptor antagonist (IL-1Ra)
• Immunodeficiency
• Immunodeficiency
• Impaired Treg-DC interactions contribute to autoimmunity in leukocyte adhesion deficiency type 1
• Inborn errors of immunity and protozoa
• Incorporation of fucose into glycans independent of the GDP-fucose transporter SLC35C1 preferentially utilizes salvaged over de novo GDP-fucose
• Inflammatory consequences of inherited disorders affecting neutrophil function
• Integrin affinity modulation critically regulates atherogenic endothelial activation in vitro and in vivo
• Ischemia-reperfusion injury to coronary arteries: Comprehensive microscopic study after reperfused myocardial infarction
• Laryngeal Cyst in Children : A Retrospective Analysis
• Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report
• Leucocyte adhesion defect presenting as fulminant sepsis in a new born
• Leucocyte adhesion deficiency-A multicentre national experience
• Leukocyte adhesion defect-I: rare primary immune deficiency
• Leukocyte adhesion defect: An uncommon immunodeficiency
• Leukocyte adhesion defect: Where do we stand circa 2019?
• Leukocyte Adhesion Deficiency
• Leukocyte Adhesion Deficiency
• Leukocyte Adhesion Deficiency Type 1 with Low Expression of CD 11b
• Macrophage β2-Integrins Regulate IL-22 by ILC3s and Protect from Lethal Citrobacter rodentium-Induced Colitis
• Mitofusin-2 regulates leukocyte adhesion and beta2 integrin activation
• Mitofusin-2 regulates leukocyte adhesion and β2 integrin activation
• Molecular Insights Into Neutrophil Biology From the Zebrafish Perspective: Lessons From CD18 Deficiency
• Molecular Mechanisms of Leukocyte Migration and Its Potential Targeting-Lessons Learned From MKL1/SRF-Related Primary Immunodeficiency Diseases
• MRC1 and LYVE1 expressing macrophages in vascular beds of GNAQ p.R183Q driven capillary malformations in Sturge Weber syndrome
• Multifaceted pathomolecular mechanism of a VWF large deletion involved in the pathogenesis of severe VWD
• Multiplex fluorescent amplification-refractory mutation system PCR method for the detection of 10 genetic defects in Holstein cattle and its comparison with the KASP genotyping assay
• Mutations in the SLC35C1 gene, contributing to significant differences in fucosylation patterns, may underlie the diverse phenotypic manifestations observed in leukocyte adhesion deficiency type II patients
• Neutropenia
• Neutropenia
• Neutrophil Defects and Diagnosis Disorders of Neutrophil Function: An Overview
• Neutrophil-Specific Knockdown of β2 Integrins Impairs Antifungal Effector Functions and Aggravates the Course of Invasive Pulmonal Aspergillosis
• Nkx2-5 Is Expressed in Atherosclerotic Plaques and Attenuates Development of Atherosclerosis in Apolipoprotein E-Deficient Mice
• Novel <em>FERMT3</em> and <em>PTPRQ</em> Mutations Associated with Leukocyte Adhesion Deficiency-III and Sensorineural Hearing Loss
• Novel FERMT3 and PTPRQ Mutations Associated with Leukocyte Adhesion Deficiency-III and Sensorineural Hearing Loss
• Novel Mutations in the beta2 Integrin Gene (ITGB2) in a Moderate Leukocyte Adhesion Defect type 1 Patient
• Novel Mutations in the β2 Integrin Gene (ITGB2) in a Moderate Leukocyte Adhesion Defect type 1 Patient
• Novel mutations of ITGB2 induced leukocyte adhesion defect type 1
• Novel variants in FERMT3 and RASGRP2-Genetic linkage in Glanzmann-like bleeding disorders
• Preclinical Evaluation of Foamy Virus Vector-Mediated Gene Addition in Human Hematopoietic Stem/Progenitor Cells for Correction of Leukocyte Adhesion Deficiency Type 1
• Prevalence of nine genetic defects in Chinese Holstein cattle
• Primary immune deficiencies with defects in neutrophil function
• Primary immunodeficiencies reveal the essential role of tissue neutrophils in periodontitis
• Primary Immunodeficiencies With Defects in Innate Immunity: Focus on Orofacial Manifestations
• Primary Immunodeficiency Diseases: Current and Emerging Therapeutics
• Primary Immunodeficiency Disorders Among North Indian Children
• Progressive skeletal defects caused by Kindlin3 deficiency, a model of autosomal recessive osteopetrosis in humans
• Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition
• Rare and heterogeneous manifestations of leucocyte adhesion deficiency type 1: report of two cases with diagnostic dilemmas and novel ITGB2 mutation
• Structural and functional characteristics of the pulmonary hemomicrocirculatory bed in induced systemic sclerosis: an experimental study
• Successful reconstitution of leukocyte adhesion defect after umbilical cord blood stem cell transplant
• Technical note: Development and application of KASP assays for rapid screening of 8 genetic defects in Holstein cattle
• The ideal treatment timing for diabetic retinopathy: the molecular pathological mechanisms underlying early-stage diabetic retinopathy are a matter of concern
• The physiological and pathological roles and applications of sialyl Lewis x, a common carbohydrate ligand of the three selectins
• The Prevalence of Atopic Manifestations in 313 Iranian Patients with Inborn Errors of Immunity
• The Yin and Yang of Tyrosine Kinase Inhibition During Experimental Polymicrobial Sepsis
• Three novel homozygous <em>ITGB2</em> mutations among two patients with leukocyte adhesion defect type-1: Two case reports
• Three novel homozygous ITGB2 mutations among two patients with leukocyte adhesion defect type-1: Two case reports
• TNF-α protects from exacerbated myocarditis and cardiac death by suppressing expansion of activated heart-reactive CD4+ T cells
• Transcriptomic analysis of CFTR-impaired endothelial cells reveals a pro-inflammatory phenotype
• Type I leucocyte adhesion deficiency in Yemenian family managed with appropriate treatment: A case series
• Utility of targeted next generation sequencing for inborn errors of immunity at a tertiary care centre in North India
• Vascular cell-specific roles of mineralocorticoid receptors in pulmonary hypertension
• β2 Integrins-Multi-Functional Leukocyte Receptors in Health and Disease