Редактирование: BICD1

Protein bicaudal D homolog 1 (Bic-D 1)

==Publications==

{{medline-entry
|title=Kidney Allograft Telomere Length Is Not Associated with Sex, Recipient Comorbid Conditions, Post-Transplant Infections, or CMV Reactivation.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27350315
|abstract=BACKGROUND Immunosenescence is closely linked to chromosome telomere erosion and telomerase activity alterations. The aim of this study was to analyze the associations of relative telomere length (RTL) of a graft with sex, comorbid conditions, post-transplant infections, and CMV reactivation among transplanted kidney recipients. Additionally, the associations of donor and recipient hTERT, [[BICD1]] genes and chromosome 18 polymorphisms with post-transplant infections were analyzed, including the analysis of donor-recipient genotype pairs. MATERIAL AND METHODS The study enrolled 119 white Polish kidney allograft recipients (64M/55F, mean age 47.3±14.0). The RTL was assessed by modification of a method developed by Cawthon, using a qPCR system. To identify genotypes of the studied polymorphisms, real-time PCR was performed. RESULTS There were no significant associations between graft RTL and sex of donor and recipient, comorbid DM and AH, as well as post-transplant infections and CMV reactivation. There were no statistically significant differences in distribution of hTERT, [[BICD1]] genes and chromosome 18 graft and recipient polymorphisms genotypes between individuals with post-transplant infection and those without infection. The rs2735940 CX-TT hTERT gene donor-recipient genotypes combination was associated with higher risk of post-transplant infection on the border of statistical significance (OR=4.632, 95%CI (0.853-25.14); p=0.067). CONCLUSIONS Assessment of kidney allograft RTL does not show its association with sex, DM, AH, post-transplant infection, or CMV reactivation in the recipients, suggesting that other factors, probably directly related to the transplantation procedure, have a greater effect on telomere length. 
|mesh-terms=* Adaptor Proteins, Signal Transducing
* Adult
* Allografts
* Cytomegalovirus Infections
* Cytoskeletal Proteins
* Female
* Humans
* Immunosenescence
* Kidney Transplantation
* Male
* Middle Aged
* Polymorphism, Single Nucleotide
* Sex Factors
* Telomerase
* Telomere
* Virus Activation

|full-text-url=https://sci-hub.do/10.12659/aot.898007
}}