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Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin.
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The present study did not show any significant association of the EVER1/2 polymorphisms (rs2290907and rs16970849) with cervical cancer.
There were no differences in Ever1 SNPs between head and neck squamous cell carcinoma patients with human papilloma virus (HPV)-positive and HPV-negative tumors, and healthy controls.
Findings suggest that SNP in EVER 1 may be involved in the development of premalignant skin lesions that harbour beta-HPV, perhaps giving rise to SCC (Montrer CYP11A1 Anticorps) tumours that have lost beta-HPV gene expression during progression
TMC6/EVER1 and TMC8/EVER2 (Montrer TMC8 Anticorps) are known to be involved in the development of EV.
TMC6 variants are associated with diminished age-of-onset of P. aeruginosa airway infection in children with cystic fibrosis (Montrer S100A8 Anticorps).
EV is also a rare autosomal recessive genodermatosis involving susceptibility to human papillomavirus (HPV) infections and squamous cell carcinoma, caused in most cases by homozygous mutations in EVER1 or EVER2 (Montrer TMC8 Anticorps).
Expression of both EVER1 and EVER2 (Montrer TMC8 Anticorps) in B cells is activated immediately after Epstein-Barr virus (EBV) infection, whereas at later stages, it is strongly repressed by latent membrane protein 1-activated NF-kappaB (Montrer NFKB1 Anticorps) signaling.
Data support the involvement of the TMC6/8 region in cervix cancer susceptibility.
Mutations in EVER1 are associated with epidermodysplasia verruciformis.
four mutations in recurrent respiratory papillomatosis patients might indicate that EVER 1 alleles are not associated with susceptibility to RRP (Montrer RRBP1 Anticorps)
Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25.3. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane channels. This gene encodes a transmembrane channel-like protein with 10 transmembrane domains and 2 leucine zipper motifs.
transmembrane channel-like 6
, epidermodysplasia verruciformis 1
, transmembrane channel-like protein 6
, transmembrane channel-like protein 6-like
, epidermodysplasia verruciformis protein 1
, expressed in activated T/LAK lymphocytes
, protein LAK-4