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The present study illustrated that the carriage of LMP7 rs2071543-AA and TAP2 rs1800454-AA had a negative effect on treatment response to pegIFN-alpha/RBV among genotype 1 patient with chronic hepatitis C (CHC) in a Chinese Han population
In a meta-analyses of 6 studies with 415 cases and 659 controls, a significant association was found between TAP1-333Val, TAP1-637Gly, and TAP2-565Thr and ankylosing spondylitis compared with combined control group.
Both TAP1 and TAP2 overexpression in breast cancer might be an indicator of an aggressive breast tumor
We replicated the association between the rs2071473 genotype and TAP2 expression by using GTEx data and demonstrated that TAP2 is expressed by decidual stromal cells at the maternal-fetal interface.
Two eSNPs were associated with fecundability at a FDR of 5%; both were in the HLA region and were eQTLs for the TAP2 gene (P = 1.3x10-4) and the HLA-F gene (P = 4.0x10-4), respectively.
there was no significant difference with respect to the genotypic frequencies of the SNPs in PSMB8, TAP1, and TAP2 loci in Parkinson's disease patients
These results suggest that TAP2 polymorphisms influence TB susceptibility in a Japanese population.
TAP1 (Montrer TAP1 Protéines)/2 gene polymorphisms might be associated with pulmonary tuberculosis susceptibility among patients in Zahedan, southeast Iran.
Deletions of ABCB3 predict good tumor response to neoadjuvant chemotherapy in breast cancer.
TAP/TPN complex formation is driven by hydrophobic interactions via leucine zipper-like motifs.
this study show that a new mouse strain with a single point mutation (Tap2 knock-out strain) shows impaired survival of macrophage survival following peritoneal iflammation
The Rose strain has an A to T substitution in exon 10 of TAP1 (Montrer TAP1 Protéines), resulting in an asparagine to valine substitution at position 643; defective TAP expression mice have very low major histocompatibility complex-I cell-surface expression, and few CD8 (Montrer CD8A Protéines) T cells.
A major role for tapasin as a stabilizer of the TAP peptide transporter and consequences for MHC class I expression
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces two products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules.
ABC transporter, MHC 2
, ATP-binding cassette, sub-family B (MDR/TAP), member 3
, antigen peptide transporter 2
, peptide supply factor 2
, peptide transporter PSF2
, peptide transporter involved in antigen processing 2
, really interesting new gene 11 protein
, transporter 2, ABC (ATP binding cassette)
, ATP dependent transport protein family member
, ATP-binding cassette sub-family B member 3
, histocompatibility antigen modifier 2
, Transporter 2 ABC (ATP binding cassette)
, transporter 2, ABC(ATP binding cassette)
, transporter 2, ATP-binding cassette, sub-family B