Vous avez cherché: pn (Anglais - Croate)

(pn) -
(qb)

pn limit).
ograničenje pn).

all grade pn
svi stupnjevi pn

incidence of pn (%)
incidencija pn (%)

 grade 2 pn
≥ stupanj 2 pn

discontinuation due to pn (%)
prekid radi pn (%)

the active moiety of velphoro, pn-feooh, is not metabolised.
aktivni dio lijeka velphoro, pn­feooh, se ne metabolizira.

the active moiety of velphoro, pn-feooh, is practically insoluble and therefore not absorbed.
aktivni dio lijeka velphoro, pn­feooh, praktički je netopljiv i zato se ne apsorbira.

a where a, b and n are constants and pn is the rate engine power in kw and the emissions are measured in accordance with the harmonised standards.
a kad su a, b i n konstante, a pn je snaga motora u kw, emisije se mjere u skladu s usklađenim normama.

its degradation product, mononuclear iron species, can however be released from the surface of pn-feooh and be absorbed.
međutim, njegov razgradni produkt, mononuklearni željezovi spojevi, može se otpuštati s površine pn­feooh­a i zatim apsorbirati.

the jrc further supported the analytical work with a research project on the effects of particulate number (pn) limits for certain engine categories.
jrc je dodatno potpomogao analitički rad istraživačkim projektom o učincima graničnih vrijednosti broja čestica za određene kategorije motora.

an in vitro general receptor activity screen showed that plerixafor, at a concentration (5 µg/ml) several fold higher than the maximum human systemic level, has moderate or strong binding affinity for a number of different receptors predominantly located on pre-synaptic nerve endings in the central nervous system (cns) and/or the peripheral nervous system (pns) (n-type calcium channel, potassium channel skca, histamine h3, acetylcholine muscarinic m1 and m2, adrenergic α1b and α2c, neuropeptide y/y1 and glutamate nmda polyamine receptors).
općeniti in vitro probir na aktivnost receptora pokazao je da pleriksafor pri koncentraciji (5 µg/ml) nekoliko puta višoj od maksimalne sustavne razine u ljudi ima umjeren ili jak afinitet vezanja za različite receptore, pretežno smještene na presinaptičkim krajevima živaca u središnjem živčanom sustavu i/ili perifernom živčanom sustavu (kalcijev kanal n-tipa, kalijev kanal skca, histaminski receptor h3, muskarinski acetilkolinski receptori m1 i m2, adrenergički receptori α1b i α2c, neuropeptidni receptori yy1 i glutamatni nmda poliaminski receptor).