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Minecraft: Story Mode, an episodic spin-off game developed by Telltale Games in collaboration with Mojang, was announced in December 2014. [8] [9] [10] Consisting of five episodes plus three additional downloadable episodes, the standalone game is a narrative and player choice-driven, and it was released on Windows, OS X, iOS, PlayStation 3, PlayStation 4, Xbox 360, and Xbox One via download ...
Cinerama at full height (three specially captured 35 mm images projected side by side into one composite widescreen image). 2. 6:1 = 8:3 = 24:9 Full-frame output from Super 16 mm negative when an anamorphic lens system has been used. Effectively, an image that is of the ratio 24:9 is squashed onto the native 15:9 aspect ratio of a Super 16 mm ...
1937 – Snow White and the Seven Dwarfs, the world's first full-length animated feature, premieres at the Carthay Circle Theatre. 1941 – World War II: A Thai-Japanese Pact of Alliance is signed. 1946 – An 8.1 M w earthquake and subsequent tsunami in NankaidÅ, Japan, kills over 1,300 people and destroys over 38,000 homes.
Location of the psa genes in the chloroplast genome of Arabidopsis thaliana.The 21 protein-coding genes involved in photosynthesis are displayed as green boxes. Photosystem I (PSI, or plastocyanin–ferredoxin oxidoreductase) is one of two photosystems in the photosynthetic light reactions of algae, plants, and cyanobacteria.
1981 – Belize is granted full independence from the United Kingdom. 1981 – Sandra Day O'Connor is unanimously approved by the U.S. Senate as the first female Supreme Court justice. 1984 – Brunei joins the United Nations. 1991 – Armenia gains independence from the Soviet Union.
IEEE 802.1 is a working group of the IEEE 802 project of the IEEE Standards Association.. It is concerned with: [1] 802 LAN/MAN architecture; internetworking among 802 LANs, MANs and wide area networks
1q21.1 duplication syndrome, also known as 1q21.1 microduplication, is an uncommon copy number variant associated with several congenital abnormalities, including developmental delay, dysmorphic traits, autism spectrum disorder, and congenital cardiac defects. [1]
1q21.1 deletion syndrome is a rare aberration of chromosome 1.A human cell has one pair of identical chromosomes on chromosome 1.With the 1q21.1 deletion syndrome, one chromosome of the pair is not complete, because a part of the sequence of the chromosome is missing.