Disease: Wiskott Aldrich syndrome
- <em>Brucella</em> NpeA is a secreted Type IV effector containing an N-WASP-binding short linear motif that promotes niche formation
- A first-in-class Wiskott-Aldrich syndrome protein activator with anti-tumor activity in hematologic cancers
- A mutation in F-actin polymerization factor suppresses the distal arthrogryposis type 5 PIEZO2 pathogenic variant in Caenorhabditis elegans
- A Novel Splicing Mutation Leading to Wiskott-Aldrich Syndrome from a Family
- A single-cell atlas of immunocytes in the spleen of a mouse model of Wiskott-Aldrich syndrome
- Accelerated death of megakaryocytes from Wiskott-Aldrich syndrome patients
- Actin-nucleation promoting factor N-WASP influences alpha-synuclein condensates and pathology
- Advances in gene therapy for inborn errors of immunity
- Allogeneic hematopoietic stem cell transplantation outcome in oldest known surviving patients with Wiskott-Aldrich syndrome
- An independent regulator of global release pathways in astrocytes generates a subtype of extracellular vesicles required for postsynaptic function
- Association of Wiskott-Aldrich syndrome protein (WASp) in epigenetic regulation of B cell differentiation in non-small-cell lung cancer (NSCLC)
- B cell mediated CD4 T cell co-stimulation via CD86 exacerbates pro-inflammatory cytokine production during autoimmune intestinal inflammation
- B cell-mediated CD4 T-cell costimulation via CD86 exacerbates pro-inflammatory cytokine production during autoimmune intestinal inflammation
- Both Las17-binding sites on Arp2/3 complex are important for branching nucleation and assembly of functional endocytic actin networks in S. cerevisiae
- Case report: A novel <em>WASHC5</em> variant altering mRNA splicing causes spastic paraplegia in a patient
- Case report: Allogeneic stem cell transplantation for type B insulin resistance
- Changes in bile acid composition are correlated with reduced intestinal cholesterol uptake in intestine-specific WASH-deficient mice
- Conditional Knockout of N-WASP Enhanced the Formation of Keratinizing Squamous Cell Carcinoma Induced by KRas<sup>G12D</sup>
- Controlled WASp activity regulates the proliferative response for Treg cell differentiation in the thymus
- Differential analysis of immune reconstitution after allogeneic hematopoietic stem cell transplantation in children with Wiskott-Aldrich syndrome and chronic granulomatous disease
- Differential Diagnosis and Interdisciplinary Workup of a Pediatric Patient With an Unknown Immune Condition: Chronic Respiratory Distress Secondary to Viral Illness and Developmental Consequences
- Differential Role of the RAC1-Binding Proteins FAM49b (CYRI-B) and CYFIP1 in Platelets
- Drug resistance related genes in lung adenocarcinoma predict patient prognosis and influence the tumor microenvironment
- Dupilumab for Post-Hematopoietic Cell Transplantation Dermatitis in Wiskott-Aldrich Syndrome
- Estrogen receptors differentially modifies lamellipodial and focal adhesion dynamics in airway smooth muscle cell migration
- Facial Skin Lesions in a Boy With Wiskott-Aldrich Syndrome
- FAM21 interacts with Ku to promote the localization of WASH to DNA double strand break sites
- Gene editing-based targeted integration for correction of Wiskott-Aldrich syndrome
- GTP-dependent regulation of heterochromatin fluctuations at subtelomeric regions in Saccharomyces cerevisiae
- Haploidentical bone marrow transplantation in a pediatric patient with Wiskott-Aldrich syndrome. A case report
- Hematopoietic reconstitution dynamics of mobilized- and bone marrow-derived human hematopoietic stem cells after gene therapy
- HIV-1 Mediated Cortical Actin Disruption Mirrors ARP2/3 Defects Found in Primary T Cell Immunodeficiencies
- IMD2, located near the boundary of heterochromatin regions, is regulated by multiple HAT-related factors
- Immunodeficiency
- Inhibitory effects of estetrol on the invasion and migration of immortalized human endometrial stromal cells
- Interleukin-1 blockade in patients with Wiskott-Aldrich Syndrome: a retrospective multinational case series
- IQGAP1 and NWASP promote human cancer cell dissemination and metastasis by regulating β1-integrin via FAK and MRTF/SRF
- It's all about location: Targeting the right spot for Wiskott-Aldrich syndrome
- Kawasaki Disease and Inborn Errors of Immunity: Exploring the Link and Implications
- LINC00869 Promotes Hepatocellular Carcinoma Metastasis via Protrusion Formation
- LncRNA MYLK antisense RNA 1 activates cell division cycle 42/Neutal Wiskott-Aldrich syndrome protein pathway via microRNA-101-5p to accelerate epithelial-to-mesenchymal transition of colon cancer cells
- Lymphoproliferative Disorders
- Mechanism of synergistic activation of Arp2/3 complex by cortactin and WASP-family proteins
- Mechanisms of actin filament severing and elongation by formins
- Mechanisms regulating the intracellular trafficking and release of CLN5 and CTSD
- Membrane curvature catalyzes actin nucleation through nano-scale condensation of N-WASP-FBP17
- Modulating Liquid-Liquid Phase Separation of Nck Adaptor Protein against Enteropathogenic <em>Escherichia coli</em> Infection
- Mutation in F-actin Polymerization Factor Suppresses Distal Arthrogryposis Type 5 (DA5) PIEZO2 Pathogenic Variant in <em>Caenorhabditis elegans</em>
- Myelin oligodendrocyte glycoprotein antibody-associated disease as a novel presentation of central nervous system autoimmunity in a pediatric patient with Wiskott-Aldrich syndrome
- Neural Wiskott-Aldrich syndrome protein (N-WASP) promotes distant metastasis in pancreatic ductal adenocarcinoma via activation of LOXL2
- Normal mean platelet volume and thrombocytopenia: It may still be Wiskott-Aldrich syndrome
- Orchestration of synaptic functions by WAVE regulatory complex-mediated actin reorganization
- Outcomes of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome
- Pan-Cancer Proteomics Analysis Reveals Wiskott-Aldrich Syndrome Protein as a Potential Regulator of Programmed Death-Ligand 1
- Phosphorylation of PACSIN2 at S313 Regulates Podocyte Architecture in Coordination with N-WASP
- Polyglutamine binding protein 1 regulates neurite outgrowth through recruiting N-WASP
- Production of Humanized Mice through Stem Cell Transfer
- Progress in the field of hematopoietic stem cell-based therapies for inborn errors of immunity
- PSIP1 promotes gefitinib resistance in lung adenocarcinoma by inducing the expression of WASF3 and its downstream ITGB3/AKT signaling
- Rare solid tumors in a patient with Wiskott-Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature
- Role of WAVE3 as an of actin binding protein in the pathology of triple negative breast cancer
- Role of Wiskott Aldrich syndrome protein in haematological malignancies: genetics, molecular mechanisms and therapeutic strategies
- Severe eczema in Wiskott-Aldrich syndrome-related disorder successfully treated with dupilumab
- SOX4 induces cytoskeleton remodeling and promotes cell motility via N-wasp/ARP2/3 pathway in colorectal cancer cells
- Spectrum of WAS gene mutations in Vietnamese patients with Wiskott-Aldrich syndrome
- Structural basis for coupling of the WASH subunit FAM21 with the endosomal SNX27-Retromer complex
- Strumpellin/WASHC5 regulates the structural plasticity of cortical neurons involved in gait coordination
- Successful T replete haploidentical HSCT with post-transplant cyclophosphamide in two patients with Wiskott-Aldrich syndrome
- The mutated cytoplasmic fragile X mental retardation 1 (FMR1)-interacting protein 2 (CYFIP2 S968F) regulates cocaine-induced reward behaviour and plasticity in the nucleus accumbens
- The mutated cytoplasmic fragile X messenger ribonucleoprotein 1 (FMR1)-interacting protein 2 (CYFIP2 S968F) regulates cocaine-induced reward behaviour and plasticity in the nucleus accumbens
- The NADPH oxidase 2 subunit p47<sup>phox</sup> binds to the WAVE regulatory complex and p22<sup>phox</sup> in a mutually exclusive manner
- The recurrent WASF1 nonsense variant identified in two unaffected Chinese families with neurodevelopmental disorder: case report and review of the literatures
- The SH3 binding site in front of the WH1 domain contributes to the membrane binding of the BAR domain protein endophilin A2
- The sufficiency of genetic diagnosis in managing patients with inborn errors of immunity during prenatal care and childbearing
- The Wiskott-Aldrich syndrome protein is required for positive selection during T-cell lineage differentiation
- TRANSPARENT TESTA GLABRA2 defines trichome cell shape by modulating actin cytoskeleton in Arabidopsis thaliana
- Tuftelin1 drives experimental pulmonary fibrosis progression by facilitating stress fiber assembly
- Unusual infection in a haploidentical transplant of Wiskott - Aldrich syndrome
- Update on the Use of Thrombopoietin-Receptor Agonists in Pediatrics
- Vaccination against respiratory tract pathogens in primary immune deficiency patients receiving immunoglobulin replacement therapy
- Viral-specific T cells for Cytomegalovirus retinitis following hematopoietic stem cell transplantation: A success story
- WASF3 disrupts mitochondrial respiration and may mediate exercise intolerance in myalgic encephalomyelitis/chronic fatigue syndrome
- WASP facilitates tumor mechanosensitivity in T lymphocytes
- WAVE2 Is a Vital Regulator in Myogenic Differentiation of Progenitor Cells through the Mechanosensitive MRTFA-SRF Axis
- WAVE3 Facilitates the Tumorigenesis and Metastasis of Tongue Squamous Cell Carcinoma via EMT
- Who's your data? Primary immune deficiency differential diagnosis prediction via machine learning and data mining of the USIDNET registry
- Whole-genome DNA methylation profiling reveals epigenetic signatures in developing muscle in Tan and Hu sheep and their offspring
- WIPF1 promotes gastric cancer progression by regulating PI3K/Akt signaling in a myocardin-dependent manner
- Wiskott Aldrich syndrome protein (WASp)-deficient Th1 cells promote R-loop-driven transcriptional insufficiency and transcription-coupled nucleotide excision repair factor (TC-NER)-driven genome-instability in the pathogenesis of T cell acute lymphoblasti
- Wiskott-Aldrich syndrome
- Wiskott-Aldrich Syndrome
- Wiskott-Aldrich syndrome diagnosed after cellulitis at the BCG vaccination site
- Wiskott-Aldrich syndrome protein expression in female WAS carriers: A flow cytometry study from North India
- Wiskott-Aldrich syndrome with platelets of normal size and c.295C>T mutation of the WAS gene. Case report
- Wiskott-Aldrich syndrome with platelets of normal size and c.295C>T mutation of the WAS gene. Case report
- Wiskott-Aldrich syndrome: A new synonym mutation in the WAS gene
- Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival
- Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity
- WNK1 controls endosomal trafficking through TRIM27-dependent regulation of actin assembly
- X-Linked Immunodeficiency