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Although vaccine was offered to all girls from age 13 17 during the catch-up programme, there was a statistically significant effect of deprivation on HPV positivity which existed at the baseline examination of HPV prevalence, where the most deprived girls were more likely to have HPV infection (Kavanagh et al, 2013).
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Just over a quarter of all women in this study had a cervical HR-HPV infection, which is very similar to the prevalence found in the WHINURS, the largest examination of cervical HPV genotype prevalence in Australian women (cervical HR-HPV prevalence 30.0% in non-Indigenous women and 31.3% in Indigenous women aged <41 years) [ 19].
Fig. 4 Confocal fluorescent microscopic examinations (×400) of HPV-E6 (red) and caspase-3 (green) in HeLa, C33a and HK cells after a 48-h treatment.
A thorough examination and follow-up of HPV mothers' newborns may be vital for the selection of a group of children prone to HPV-related entities.
A major limitation is the cross-sectional nature of the survey, which prevented the examination of temporal associations between HPV infection and cancers, and the fact that only antibodies to L1, the HPV structural proteins, were assessed in NHANES.
Clearance of HPV infections since baseline examination was 80.6% (95% CI: 67.6 93.5), and did not differ between high-risk and low-risk HPV types or between single- and multiple-type infections.
In this study, we found a 4.8% prevalence of HPV infection in women seeking cervical Papanicolaou examination of Durango City, Mexico.
We concluded that prevalence of HPV infection in women seeking cervical Papanicolaou examination in Durango City, Mexico was low.
Analysis of an endocervical swab for Chlamydia trachomatis, analysis of a cervical scrape for HPV, and morphological examination of cervical biopsy specimens were also performed.
A closer examination of these data shows that most HPV-16-positive VIN 2/3 (11/12) do not have methylated p16INK4a, whereas in HPV-negative lesions, 8/11 VIN 3, 2/5 VIN 2 and 0/4 VIN 1 show p16 methylation.
Study design: Parallel with the routine histological examination, Southern blot hybridisation and multiplex PCRs were used to detect type/physical state of HPV DNA in primary tumours and in regional lymph nodes combined with p53 genotyping of 83 patients.
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