lecollege.org valuation and analysis

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Title Small molecule inhibitors of HCV
Description Small molecule inhibitors of HCV replication 07 May / 2023 2 The progesterone-PGR axis is necessary for efficient innate antiviral response in vivo 2 Th
Keywords N/A
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WebSite lecollege faviconlecollege.org
Host IP 144.217.119.29
Location United States
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lecollege.org Valuation
US$398,263
Last updated: 2023-05-08 15:45:06

lecollege.org has Semrush global rank of 26,576,177. lecollege.org has an estimated worth of US$ 398,263, based on its estimated Ads revenue. lecollege.org receives approximately 45,954 unique visitors each day. Its web server is located in United States, with IP address 144.217.119.29. According to SiteAdvisor, lecollege.org is safe to visit.

Traffic & Worth Estimates
Purchase/Sale Value US$398,263
Daily Ads Revenue US$368
Monthly Ads Revenue US$11,029
Yearly Ads Revenue US$132,346
Daily Unique Visitors 3,064
Note: All traffic and earnings values are estimates.
DNS Records
Host Type TTL Data
lecollege.org. A 3600 IP: 144.217.119.29
lecollege.org. NS 3600 NS Record: ns1.zonomi.com.
lecollege.org. NS 3600 NS Record: ns6.zonomi.com.
lecollege.org. MX 3600 MX Record: 0 mail.lecollege.org.
HtmlToTextCheckTime:2023-05-08 15:45:06
Small molecule inhibitors of HCV replication 07 May / 2023 2 The progesterone-PGR axis is necessary for efficient innate antiviral response in vivo 2 The progesterone-PGR axis is necessary for efficient innate antiviral response in vivo. of and genes. e. Ramifications of SeV infections on progesterone secretion in JEG-3 cells. JEG-3 cells had been cultured in simple RPMI medium and still left uninfected or contaminated with SeV for the indicated situations. The culture media were collected for progesterone measurement by ELISA assays then. *but not really (a non-rate-limiting metabolic enzyme for P4 biosynthesis) gene was elevated in the adrenal gland of virus-infected compared LY2452473 to control mice (Fig. ?(Fig.1c1c and S1b). In the same tests, the mRNA degrees of enzyme genes involved with biosynthesis of various other sex steroid human hormones was also analyzed50,51 (Fig. S1b). The outcomes demonstrated that transcription of (the rate-limiting metabolic enzyme for
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