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7 articles, 4 other pages.

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  1. sv:Klorofyll a
    |Systematiskt namn= Magnesium [metyl (3S,4S,21R)-14-etyl-4,8,13,18-tetrametyl-20-oxo-3-(3-oxo-3-{[(2E,7R,11R)-3,7,11,15-tetrametyl-2-hexadecen-1-yl]oxy}propyl)-9-vinyl-21-forbinkarboxylatato(2-)-κ2N,N']
  2. sv:Klorofyll b
    |Systematiskt namn= Magnesium [metyl (3S,4S,21R)-14-etyl-13-formyl-4,8,18-trimetyl-20-oxo-3-(3-oxo-3-{[(2E,7R,11R)-3,7,11,15-tetrametyl-2-hexadecen-1-yl]oxy}propyl)-9-vinyl-21-forbinekarboxylatato(2-)-κ2N,N']
  3. sv:Cykloheximid
    |Systematiskt namn = 4-{(2''R'')-2-[(1''S'',3''S'',5''S'')-3,5-dimetyl<br/>-2-oxocyklohexyl]-2-hydroxietyl}<br/>piperidin-2,6-dion
  4. sv:Imidakloprid
    |Systematiskt namn = ''N''-{1-[(6-Chloro-3-pyridyl)methyl]-4,5-dihydroimidazol-2-yl}nitramide
  5. sv:Aulacaspis kenyae
    <ref name = "col80172">Oloo, G.W. (1975) Sugarcane. 1.-{Aulacaspis} spp. and other scales., </ref>
  6. sv:Tymidinkinas
    Införlivande av en tymidinanalog med bor har föreslagits och prövats i djurmodeller för borneutroninfångningsterapi av hjärntumörer<ref name="pmid16942024">{{cite journal |author=Byun Y, Thirumamagal BT, Yang W, Eriksson S, Barth RF, Tjarks W |title=Preparation and biological evaluation of 10B-enriched 3-[5-{2-(2,3-dihydroxyprop-1-yl)-o-carboran-1-yl}pentan-1-yl]thymidine (N5-2OH), a new boron delivery agent for boron neutron capture therapy of brain tumors |journal=Journal of Medicinal Chemistry |volume=49 |issue=18 |pages=5513–23 |year=2006 |month=September |pmid=16942024 |doi=10.1021/jm060413w |url=}}</ref><ref name="pmid16901817">{{cite journal |author=Thirumamagal BT, Johnsamuel J, Cosquer GY, ''et al.'' |title=Boronated thymidine analogues for boron neutron capture therapy |journal=Nucleosides Nucleotides Nucleic Acids |volume=25 |issue=8 |pages=861–6 |year=2006 |pmid=16901817 |doi=10.1080/15257770600793844 |url=}}</ref><ref name="pmid16831554">{{cite journal |author=Narayanasamy S, Thirumamagal BT, Johnsamuel J, ''et al.'' |title=Hydrophilically enhanced 3-carboranyl thymidine analogues (3CTAs) for boron neutron capture therapy (BNCT) of cancer |journal=Bioorg. Med. Chem. |volume=14 |issue=20 |pages=6886–99 |date=October 2006 |pmid=16831554 |doi=10.1016/j.bmc.2006.06.039|url=}}</ref><ref name="pmid=16529536">{{cite journal |author=Byun Y, Narayanasamy S, Johnsamuel J, ''et al.'' |title=3-Carboranyl thymidine analogues (3CTAs) and other boronated nucleosides for boron neutron capture therapy |journal=Anticancer Agents Med Chem |volume=6 |issue=2 |pages=127–44 |date=March 2006 |pmid=16529536 |doi= 10.2174/187152006776119171|url=http://www.bentham-direct.org/pages/content.php?ACAMC/2006/00000006/00000002/0004W.SGM}}</ref><ref name="pmid15715485">{{cite journal |author=Byun Y, Yan J, Al-Madhoun AS, ''et al.'' |title=Synthesis and biological evaluation of neutral and zwitterionic 3-carboranyl thymidine analogues for boron neutron capture therapy |journal=Journal of Medicinal Chemistry |volume=48 |issue=4 |pages=1188–98 |date=February 2005 |pmid=15715485 |doi=10.1021/jm0491896 |url=}}</ref><ref name="pmid15342417">{{cite journal |author=Barth RF, Yang W, Al-Madhoun AS, ''et al.'' |title=Boron-containing nucleosides as potential delivery agents for neutron capture therapy of brain tumors |journal=Cancer Res. |volume=64 |issue=17 |pages=6287–95 |date=September 2004 |pmid=15342417 |doi=10.1158/0008-5472.CAN-04-0437 |url=}}</ref><ref name="pmid15342416">{{cite journal |author=Al-Madhoun AS, Johnsamuel J, Barth RF, Tjarks W, Eriksson S |title=Evaluation of human thymidine kinase 1 substrates as new candidates for boron neutron capture therapy |journal=Cancer Res. |volume=64 |issue=17 |pages=6280–6 |date=September 2004 |pmid=15342416 |doi=10.1158/0008-5472.CAN-04-0197 |url=}}</ref><ref name="pmid15336255">{{cite journal |author=Johnsamuel J, Lakhi N, Al-Madhoun AS, ''et al.'' |title=Synthesis of ethyleneoxide modified 3-carboranyl thymidine analogues and evaluation of their biochemical, physicochemical, and structural properties |journal=Bioorg. Med. Chem. |volume=12 |issue=18 |pages=4769–81 |date=September 2004 |pmid=15336255|doi=10.1016/j.bmc.2004.07.032 |url=}}</ref><ref name="pmid15308203">{{cite journal |author=Byun Y, Yan J, Al-Madhoun AS, ''et al.'' |title=The synthesis and biochemical evaluation of thymidine analogues substituted with nido carborane at the N-3 position |journal=Appl Radiat Isot |volume=61 |issue=5 |pages=1125–30 |date=November 2004 |pmid=15308203 |doi=10.1016/j.apradiso.2004.05.023 |url=}}</ref><ref name="pmid12127539">{{cite journal |author=Yan J, Naeslund C, Al-Madhoun AS, ''et al.'' |title=Synthesis and biological evaluation of 3'-carboranyl thymidine analogues |journal=Bioorg. Med. Chem. Lett. |volume=12 |issue=16 |pages=2209–12 |date=August 2002 |pmid=12127539 |doi= 10.1016/S0960-894X(02)00357-8|url=http://linkinghub.elsevier.com/retrieve/pii/S0960894X02003578}}</ref><ref name="pmid18981415">{{cite journal |author=Barth RF, Yang W, Wu G, ''et al.'' |title=Thymidine kinase 1 as a molecular target for boron neutron capture therapy of brain tumors |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=105 |issue=45 |pages=17493–7 |date=November 2008 |pmid=18981415 |doi=10.1073/pnas.0809569105 |url= |pmc=2582264|bibcode = 2008PNAS..10517493B }}</ref>.
  7. sv:Pigment Yellow 154
    Pigmentet heter i den internationella färgdatabasen [[Colour Index]] (C.I.) ''Pigment Yellow 154'' och har nummer ''11781''.<ref name="Myers"/> Det är ett bensimidazolon-derivat och dess kemiska struktur kan beskrivas som 3-oxo-''N''-(2-oxo-2,3-dihydro-1''H''-bensimidazol-5-yl)-2-{(''E'')-[2-(trifluormetyl)fenyl]diazenyl}butanamid.<ref>[https://pubchem.ncbi.nlm.nih.gov/compound/109160 Pigment Yellow 154] PubChem Compound Database. Läst 21 mars 2016.</ref>

Matches not in article namespace

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  1. sv:Wikipedia:Sidor föreslagna för radering/Alex Kelly
    :Röster kan ändras om artikeln har förändrats under omröstningen. Skriv till dem som du vill ska ändra sin röst i stället för att dra igång en ny omröstning. --{Saber 2 mars 2007 kl. 16.32 (CET)
  2. sv:Mall:GeoTemplate
    *[http://beta.mapy.atlas.cz/#appName=atlasof@mapType=2@centerX=-{osgb36easting}@centerY=-{osgb36northing}@mapScale={scale}@geoType=1 Find this location] on Mapy Atlas Beta . [http://beta.mapy.atlas.cz/]
  3. sv:Mall:Convert/numdisp
    -- negative amounts, the &minus with inverse -{1} is padded
  4. sv:Mall:Colevel/process item
    The '''[[Mall:Colevel/process_item]]''' is used by [[Mall:Autonumbered_list]] to display the parameters {alpha} and {beta} by {alphawidth}. The width of the first column is set by the data in {alpha}, or by {alphawidth}% which defaults to 1%; the second column (containing {beta}{{ns|1}}) has width = 100-{alphawidth}% (or 99%).
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