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Team Win Recovery Project (TWRP), pronounced "twerp", [4] is an open-source software custom recovery image for Android-based devices. [ 5 ] [ 6 ] It provides a touchscreen -enabled interface that allows users to install third-party firmware and back up the current system, functions usually not supported by stock recovery images.
iPhone OS 3 (stylized as iPhone OS 3.0) is the third major release of the iOS mobile operating system developed by Apple Inc., succeeding iPhone OS 2. It was announced on March 17, 2009, and was released on June 17, 2009.
This list contains a list of EC numbers for the third group, EC 3, hydrolases, placed in numerical order as determined by the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology.
OpenSSL clients are vulnerable in all versions of OpenSSL before the versions 0.9.8za, 1.0.0m and 1.0.1h. Servers are only known to be vulnerable in OpenSSL 1.0.1 and 1.0.2-beta1. Users of OpenSSL servers earlier than 1.0.1 are advised to upgrade as a precaution.
This is an accepted version of this page This is the latest accepted revision, reviewed on 18 January 2025. Extension of the HTTP communications protocol to support TLS encryption Internet protocol suite Application layer BGP DHCP (v6) DNS FTP HTTP (HTTP/3) HTTPS IMAP IRC LDAP MGCP MQTT NNTP NTP OSPF POP PTP ONC/RPC RTP RTSP RIP SIP SMTP SNMP SSH Telnet TLS/SSL XMPP more... Transport layer TCP ...
T6 armored recovery vehicle; Armoured recovery vehicle based on the chassis of an M5A1. Project was discontinued in 1943 in favor of the M24 Chaffee-based T6E1. [51] T16 4.5-inch gun motor carriage; Self-propelled 4.5-inch gun based on the chassis of an M5. Project was discontinued in 1943. [52] T18 howitzer motor carriage
K Desktop Environment 3.0. K Desktop Environment 3.0 introduced better support for restricted usage, a feature demanded by certain environments such as kiosks, Internet cafes and enterprise deployments, which disallows the user from having full access to all capabilities of a piece of software. [3]
3-Hydroxytetrahydrofuran was prepared in 1910 by Pariselle [5] via cyclization and hydrolysis of 3,4-Dibromo-1-methoxybutane. Chiral 3-hydroxytetrahydrofuran (both (S) – and (R)-forms) has been synthesized in high enantiomeric purity from (S)- and (R)-1,2,4-butanetriol, respectively, obtained from chiral feedstocks.