WordNet

the quality of not moving
not able or intended to be moved; "the immovable hills" (同)immoveable, stabile, unmovable
not capable of movement or of being moved

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2017/02/18 09:02:24」(JST)

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Sleep in prenatally restraint stressed rats, a model of mixed anxiety-depressive disorder.

Mairesse J1, Van Camp G, Gatta E, Marrocco J, Reynaert ML, Consolazione M, Morley-Fletcher S, Nicoletti F, Maccari S.
Advances in neurobiology.Adv Neurobiol.2015;10:27-44. doi: 10.1007/978-1-4939-1372-5_2.
Prenatal restraint stress (PRS) can induce persisting changes in individual's development. PRS increases anxiety and depression-like behaviors and induces changes in the hypothalamo-pituitary-adrenal (HPA) axis in adult PRS rats after exposure to stress. Since adaptive capabilities also depend on te
PMID 25287534

Løvlie H1, Immonen E2, Gustavsson E2, Kazancioğlu E2, Arnqvist G2.
Proceedings. Biological sciences / The Royal Society.Proc Biol Sci.2014 Dec 7;281(1796). pii: 20141039. doi: 10.1098/rspb.2014.1039.
There is a growing awareness of the influence of mitochondrial genetic variation on life-history phenotypes, particularly via epistatic interactions with nuclear genes. Owing to their direct effect on traits such as metabolic and growth rates, mitonuclear interactions may also affect variation in be
PMID 25320161

Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.

Corrochano S1, Männikkö R2, Joyce PI1, McGoldrick P2, Wettstein J3, Lassi G4, Raja Rayan DL2, Blanco G5, Quinn C6, Liavas A2, Lionikas A7, Amior N2, Dick J2, Healy EG2, Stewart M1, Carter S1, Hutchinson M1, Bentley L1, Fratta P2, Cortese A8, Cox R1, Brown SD1, Tucci V4, Wackerhage H7, Amato AA6, Greensmith L2, Koltzenburg M2, Hanna MG2, Acevedo-Arozena A1.
Brain : a journal of neurology.Brain.2014 Dec;137(Pt 12):3171-85. doi: 10.1093/brain/awu292. Epub 2014 Oct 27.
Mutations in the skeletal muscle channel (SCN4A), encoding the Nav1.4 voltage-gated sodium channel, are causative of a variety of muscle channelopathies, including non-dystrophic myotonias and periodic paralysis. The effects of many of these mutations on channel function have been characterized both
PMID 25348630