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Kamen Rider Revice is the eponymous duo of Ikki Igarashi and his inner demon partner Vice whose arsenal revolves around Vistamps (バイスタンプ, Baisutanpu), a series of rubber stamp-like items reverse-engineered from the Giff Stamp (ギフスタンプ, Gifu Sutanpu) and designed to harness the power of inner demons as well as channel the human user's genetic memory. [1]
Tategami Hyoujuu Senki (タテガミ氷獣戦記, Tategami Hyōjū Senki, Mane Ice Beast War Chronicle): Rintaro's ultimate form accessed from the eponymous Wonder Ride Book that grants cryokinesis and the ability to summon the souls of deceased swordsmen, such as his teacher, to aid him in battle.
Shindo or Shindō may refer to: Japan Meteorological Agency seismic intensity scale ( 震度 , shindo ) Shindo (religion) (신도), an alternative name of Korean Shamanism used by Shamanic associations in modern South Korea.
In 2012, in celebration of Image Comics' then 20 years as a publisher and Spawn being one of their longest running titles, Spawn Compendium was released, reprinting Spawn issues #1–50 at 1136 pages in black and white, though this volume does not collect the individual issues' covers. The book went to a second printing in March 2016.
Ice from a theorized superionic water may possess two crystalline structures. At pressures in excess of 50 GPa (7,300,000 psi) such superionic ice would take on a body-centered cubic structure. However, at pressures in excess of 100 GPa (15,000,000 psi) the structure may shift to a more stable face-centered cubic lattice.
The CDK4 gene is located on chromosome 12 in humans. [7] The gene is composed of 4,583 base pairs which together code for the 303 amino acid protein with a molecular mass of 33,730 Da. [7] [8] All CDK proteins, including CDK4, have two lobes: the smaller N-terminal lobe (which contains an inhibitory G-loop), and the C terminal lobe (which contains an activation domain and a T-loop).
CDK13-related disorder, also known as congenital heart defects, dysmorphic facial features and intellectual developmental disorder (CHDFIDD), is a very rare autosomal dominant genetic condition characterised by congenital heart defects, intellectual disability and characteristic facial features.