WordNet

relying on or requiring a person or thing for support, supply, or what is needed; "dependent children"; "dependent on moisture"
addicted to a drug (同)dependant, drug-addicted, hooked, strung-out
contingent on something else (同)dependant, qualified
(of a clause) unable to stand alone syntactically as a complete sentence; "a subordinate (or dependent) clause functions as a noun or adjective or adverb within a sentence" (同)subordinate
a light soft silver-white metallic element of the alkali metal group; oxidizes rapidly in air and reacts violently with water; is abundant in nature in combined forms occurring in sea water and in carnallite and kainite and sylvite (同)K, atomic number 19
the rate at which energy is drawn from a source that produces a flow of electricity in a circuit; expressed in volts (同)electromotive_force, emf

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1. 成人における高カリウム血症の原因および評価 causes and evaluation of hyperkalemia in adults
2. 腎尿細管性アシドーシスの概要と病態生理、およびカリウムバランスへの影響 overview and pathophysiology of renal tubular acidosis and the effect on potassium balance
3. 赤血球水分量の制御 control of red blood cell hydration
4. 心筋活動電位および抗不整脈剤の作用 myocardial action potential and action of antiarrhythmic drugs
5. 抗てんかん剤：作用機序、薬理学、および有害事象 antiepileptic drugs mechanism of action pharmacology and adverse effects

Martínez-Mármol R1,2, Comes N1, Styrczewska K1, Pérez-Verdaguer M1, Vicente R3, Pujadas L2, Soriano E2,4,5, Sorkin A6, Felipe A7,8.
Cellular and molecular life sciences : CMLS.Cell Mol Life Sci.2015 Nov 5. [Epub ahead of print]
The potassium channel Kv1.3 plays roles in immunity, neuronal development and sensory discrimination. Regulation of Kv1.3 by kinase signaling has been studied. In this context, EGF binds to specific receptors (EGFR) and triggers tyrosine kinase-dependent signaling, which down-regulates Kv1.3 current
PMID 26542799

Ke Q1, He F1, Lu L2, Yu P2, Jiang Y3, Weng C4, Huang H5, Yi X5, Qi M6.
Neuromuscular disorders : NMD.Neuromuscul Disord.2015 Sep 9. pii: S0960-8966(15)00732-4. doi: 10.1016/j.nmd.2015.09.006. [Epub ahead of print]
Primary hypokalemic periodic paralysis is an autosomal dominant skeletal muscle channelopathy. In the present study, we investigated the genotype and phenotype of a Chinese hypokalemic periodic paralysis family. We used whole-exome next-generation sequencing to identify a mutation in the calcium cha
PMID 26433613

Abnormal excitability and episodic low-frequency oscillations in the cerebral cortex of the tottering mouse.

Cramer SW1, Popa LS1, Carter RE1, Chen G1, Ebner TJ2.
The Journal of neuroscience : the official journal of the Society for Neuroscience.J Neurosci.2015 Apr 8;35(14):5664-79. doi: 10.1523/JNEUROSCI.3107-14.2015.
The Ca(2+) channelopathies caused by mutations of the CACNA1A gene that encodes the pore-forming subunit of the human Cav2.1 (P/Q-type) voltage-gated Ca(2+) channel include episodic ataxia type 2 (EA2). Although, in EA2 the emphasis has been on cerebellar dysfunction, patients also exhibit episodic,
PMID 25855180