نتائج البحث - "Gavin P. Spickett"

1

An Atypical Autoinflammatory Disease Due to an LRR Domain NLRP3 Mutation Enhancing Binding to NEK7

المؤلفون: Sinisa Savic, Fatima Nadat, Michael F. McDermott, Samuel Lara-Reyna, Clive Carter, James A. Poulter, Joanne Topping, Gavin P. Spickett, Emily A. Caseley

المصدر: Journal of Clinical Immunology

مصطلحات موضوعية: Chemokine, Immunology, Inflammation, Leucine-rich repeat domain, medicine.disease_cause, 03 medical and health sciences, Mice, 0302 clinical medicine, NLR Family, Pyrin Domain-Containing 3 Protein, medicine, Immunology and Allergy, Animals, Humans, NIMA-Related Kinases, NLRP3-associated autoinflammatory diseases, 030304 developmental biology, 0303 health sciences, Anakinra, Mutation, Innate immune system, biology, integumentary system, business.industry, Hereditary Autoinflammatory Diseases, NF-kappa B, Inflammasome, NIMA-related kinase 7, Phenotype, NLRP3 inflammasome, 3. Good health, Mice, Inbred C57BL, 030220 oncology & carcinogenesis, NACHT domain, biology.protein, Original Article, Female, medicine.symptom, business, medicine.drug

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8cbfe128610f240d089259051a59eb5
http://europepmc.org/articles/PMC8528658

Find this article in full text from Springer Verlag.

Find this article in full text from ProQuest

2

Plasmapheresis as rescue therapy in severe bronchiectasis with blocking anti pseudomonas antibodies

المؤلفون: S Kanagasundaram, Timothy J. Wells, A DeSoyza, Calman A. MacLennan, John M. Davison, Ian R. Henderson, G Davies, Robert A. Stockley, Gavin P. Spickett, E Sheehan

المصدر: Pneumologie. 70

مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Bronchiectasis, biology, Blocking (radio), business.industry, medicine.medical_treatment, medicine.disease, Rescue therapy, Immunology, medicine, biology.protein, Plasmapheresis, Antibody, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::49ce42bbce0e953231baaf0ae2ca09d9
https://doi.org/10.1055/s-0036-1592256

3

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

المساهمون: Univ Hosp Freiburg, Inst Child Hlth, Karolinska Univ Hosp Huddinge, Univ Brescia, Spedali Civil Brescia, Royal Free Hosp, UCL, Allergy Asthma & Immunol Clin, Oxford Radcliffe Hosp, Royal Victoria Infirm, Univ Washington, Childrens Hosp, Univ Munich, Addenbrookes Hosp, Universidade Federal de São Paulo (UNIFESP), Univ Oslo, Univ Antioquia, Charite Humboldt Univ, Univ Lausanne, Natl Lib Med

المصدر: Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Blood; Vol 113

مصطلحات موضوعية: Heterozygote, Transmembrane Activator and CAML Interactor Protein, DNA Mutational Analysis, Immunology, Polymorphism, Single Nucleotide, Biochemistry, Immunoglobulin D, Cohort Studies, Hypogammaglobulinemia, Loss of heterozygosity, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, common variable immunodeficiency, B cells, TACI, autoimmunity, Agammaglobulinemia, Risk Factors, Genotype, medicine, Humans, Genetic Predisposition to Disease, Allele, Alleles, Cells, Cultured, Immunobiology, 030304 developmental biology, 0303 health sciences, biology, Common variable immunodeficiency, Homozygote, Heterozygote advantage, Syndrome, Cell Biology, Hematology, medicine.disease, Pedigree, 3. Good health, Amino Acid Substitution, Case-Control Studies, Mutation, biology.protein, Antibody, 030215 immunology