1 ested using a PCR-based assay that detects a W. bancrofti-specific repetitive DNA sequence.

2 relation coefficients were assessed for both W. bancrofti infection and microfilaremia by controlling

3 cide-treated bed nets is a valuable tool for W. bancrofti elimination in areas in which anopheline mo

4 tein appears to be a new ligand of TLR4 from W. bancrofti.

5 ng the same period, the rate of detection of W. bancrofti in anopheline mosquitoes decreased from 1.8

6 ncluding 143 individuals with a diagnosis of W. bancrofti circulating filarial antigens (CFAs) and 44

7 R-based assay will be useful in diagnosis of W. bancrofti infection in a variety of clinical settings

8 bedded sections established the diagnosis of W. bancrofti infection in another 2 cases.

9 us of filarial infection and the presence of W. bancrofti DNA in anopheline mosquitoes before and aft

10 rotein (MfP) was isolated from the sheath of W. bancrofti microfilariae through ultrafiltration, foll

11  Anopheles koliensis are the only vectors of W. bancrofti.

12 s infected with O. volvulus, M. perstans, or W. bancrofti showed positive immunoreactivity.

13 ection increases childhood susceptibility to W. bancrofti and skews filaria-specific immunity toward

14 rial-specific immunity and susceptibility to W. bancrofti infection during childhood.

15 r determinant of childhood susceptibility to W. bancrofti infection.

16 C. quinquefasciatus genes responsive to WNV, W. bancrofti, and non-native bacteria facilitated an unp