Associated Papers
Zinc-Related Proteasome Variants in Type 1 Diabetes: An in Silico-Guided Case-Control Study.
Nasre-Nasser RG et al.
Metabolites, 2025
Influence of PSMB6 and PSMB9 Genetic Polymorphisms on Bortezomib-Based Therapy Response in Newly Diagnosed Multiple Myeloma.
Sood N et al.
Cureus, 2025
Sequence Variants in PSMB8/PSMB9 Immunoproteasome Genes and Risk of Urothelial Bladder Carcinoma.
Elhawary NA et al.
Cureus, 2023
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis.
Han Y et al.
Nature Communications, 2023
Exome variants associated with asthma and allergy.
Wjst M
Scientific Reports, 2022
Genetic Landscape of Rare Autoinflammatory Disease Variants in Qatar and Middle Eastern Populations Through the Integration of Whole-Genome and Exome Datasets.
Sharma P et al.
Frontiers in Genetics, 2021
Variations in TAP1 and PSMB9 Genes Involved in Antigen Processing and Presentation Increase the Risk of Vitiligo in the Saudi Community.
Mufti AH et al.
International Journal of General Medicine, 2021
Integrated Genomic, Functional, and Prognostic Characterization of Atypical Chronic Myeloid Leukemia.
Fontana D et al.
Hemasphere, 2020
Genetic polymorphisms of proteasome subunit genes of the MHC-I antigen-presenting system are associated with cervical cancer in a Chinese Han population.
Li C et al.
Human Immunology, 2020
The LMP2 CfoI polymorphism is associated with ankylosing spondylitis (AS) risk but not with acute anterior uveitis (AAU): A meta-analysis.
Qian Y et al.
Medicine, 2019
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
Transporter TAP1-637G and immunoproteasome PSMB9-60H variants influence the risk of developing vitiligo in the Saudi population.
Elhawary NA et al.
Disease Markers, 2014
Association between putative functional variants in the PSMB9 gene and risk of melanoma--re-analysis of published melanoma genome-wide association studies.
Qian J et al.
Pigment Cell & Melanoma Research, 2013
Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines.
Duan J et al.
Scientific Reports, 2013
PSMB9 codon 60 polymorphisms have no impact on the activity of the immunoproteasome catalytic subunit B1i expressed in multiple types of solid cancer.
Park JE et al.
Plos One, 2013
Radiographic severity of ankylosing spondylitis is associated with polymorphism of the large multifunctional peptidase 2 gene in the Spondyloarthritis Research Consortium of Canada cohort.
Haroon N et al.
Arthritis and Rheumatism, 2012
An update on the genetics of HLA B27-associated acute anterior uveitis.
Martin TM et al.
Ocular Immunology and Inflammation, 2011
PSMB8 (LMP7) but not PSMB9 (LMP2) gene polymorphisms are associated to pigeon breeder's hypersensitivity pneumonitis.
Camarena A et al.
Respiratory Medicine, 2010
Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population.
Mishto M et al.
Plos One, 2010
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
Genetic susceptibility to atopic dermatitis.
Kiyohara C et al.
Allergology International : Official Journal of the Japanese Society of Allergology, 2008
Genes, ageing and longevity in humans: problems, advantages and perspectives.
Salvioli S et al.
Free Radical Research, 2006
A structural model of 20S immunoproteasomes: effect of LMP2 codon 60 polymorphism on expression, activity, intracellular localisation and insight into the regulatory mechanisms.
Mishto M et al.
Biological Chemistry, 2006
Genes of the LMP/TAP cluster are associated with the human autoimmune disease vitiligo.
Casp CB et al.
Genes and Immunity, 2003
Large multifunctional proteasome 2 gene Arg60His variant in autoimmune thyroid disease in Shanghai Chinese.
Ding H et al.
Zhonghua Nei Ke Za Zhi, 2002
ASSOSIATION ANALYSYS OF 11 POLYMORPHISMS OF SNPS WITH ENDOTHELIUM DEPENDENT VASODILATATION IN CHILDREN WITH DIABETES MELLITUS TYPE 1.
Pranik NB et al.
Fiziolohichnyi Zhurnal (kiev, Ukraine : 1994), 0