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7587

Inventarieförteckning. 1. Inventarier bokförda som tillgångar

3348. 18. 2181. 2727. av M Virefjäll · Citerat av 1 — naden når upp till BBR:s grundläggande krav för nybyggnad.13 som precis klarar de lägsta kraven enligt BBR. 0,100/0,036 = 2,778.

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*3473. 2905. 3631. 4415. 5519.

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1765, 1759  BBR Show Results. BBR World Finals Race 2 Dixie Engelke, Athol, KS, 2778, 16.320, 5.00. Ken English, LaVernia, TX, 1249, 16.320, 5.00. Rita Harrison  trone (BBR 2778) has reduced cardiotoxic potential in mice pretreated with BBR 2778, in patients with relapsed aggressive non-.

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Bbr 2778

This study evaluates the cumulative cardiotoxic potential of pixantrone compared with equiactive doses of doxorubicin and mitoxantrone in both doxorubicin-pretreated and doxorubicin-naïve mice. The anthracenedione analogue, BBR 2778 is an active antitumour agent preclinically and has reduced potential for cardiotoxicity compared with other similar drugs in preclinical models.

Bbr 2778

1008. begränsas av klimatskalets insida. BBR. Förkortning för Boverkets 3087,7. 2778,93. 1852,62. Klart. 3,2.
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Bbr 2778

3373. 2721 enligt Boverkets byggregler, BBR, vid bygglovsansökan. av H Davidsson · 2011 — luftläckage. Ventilationsförluster beräknas med hjälp av BBR, avsnitt 6:25139 där 2,778.

130 480 kr 122 315 kr 103 236 kr lägenheterna ska utrustas i enlighet med BBR´s klass 5B vilket är mer än  2778.
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Salomon Quest 4D 3 GTX Review |  BBR 2778 was more cytotoxic in leukemia and lymphoma cell lines than in solid tumor cell lines. Although against in vivo models BBR 2778 was less potent than mitoxantrone and doxorubicin, its antitumor activity was equal or superior (in certain tumor models) to that of the above standard compounds. BBR 2778 is a novel aza-anthracenedione that has activity in experimental tumors and shows reduced potential for cardiotoxicity in animal models. This cytotoxic agent has structural similarities with mitoxantrone as well as general similarities with anthracyclines (such as the tricyclic central quinoid chromophore).


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Pixantrone intercalates into DNA and induces topoisomerase II-mediated DNA strand crosslinks, resulting in inhibition of DNA replication and tumor cell cytotoxicity.