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Items: 11

1.

Interference of common haemoglobin variants with the Tosoh G7 standard mode HbA1c method.

Piehler AP, Grimholt RM, Bjerner J, Buchmann MS.

Scand J Clin Lab Invest. 2015 Sep;75(5):362-6. doi: 10.3109/00365513.2015.1031687. Epub 2015 Apr 10.

PMID:
25858015
2.

Methylation of bone SOST, its mRNA, and serum sclerostin levels correlate strongly with fracture risk in postmenopausal women.

Reppe S, Noer A, Grimholt RM, Halldórsson BV, Medina-Gomez C, Gautvik VT, Olstad OK, Berg JP, Datta H, Estrada K, Hofman A, Uitterlinden AG, Rivadeneira F, Lyle R, Collas P, Gautvik KM.

J Bone Miner Res. 2015 Feb;30(2):249-56. doi: 10.1002/jbmr.2342.

3.

Serum bilirubin concentration in healthy adult North-Europeans is strictly controlled by the UGT1A1 TA-repeat variants.

Kringen MK, Piehler AP, Grimholt RM, Opdal MS, Haug KB, Urdal P.

PLoS One. 2014 Feb 28;9(2):e90248. doi: 10.1371/journal.pone.0090248. eCollection 2014.

4.

Rapid and reliable detection of α-globin copy number variations by quantitative real-time PCR.

Grimholt RM, Urdal P, Klingenberg O, Piehler AP.

BMC Hematol. 2014 Jan 24;14(1):4. doi: 10.1186/2052-1839-14-4.

5.

Hb Ullevaal [β78(EF2)Leu→Val; HBB: c.235C>G], a new hemoglobin variant interfering with Hb A1c measurement using a cation exchange high performance liquid chromatography method.

Grimholt RM, Sudmann ÅA, Piehler AP, Urdal P, Klingenberg O.

Hemoglobin. 2014;38(2):130-2. doi: 10.3109/03630269.2013.858640. Epub 2013 Nov 25.

PMID:
24274186
6.

Discrepancy between HbA1c and fasting glucose results due to HbD.

Piehler AP, Grimholt RM, Bjerner J, Urdal P, Buchmann M.

Scand J Clin Lab Invest. 2013 Mar;73(2):186-8. doi: 10.3109/00365513.2012.744089. Epub 2012 Dec 3. No abstract available.

PMID:
23198773
7.

Associations between serotonin transporter polymorphisms and cognitive processing applying the Emo 1-back task.

Jonassen R, Foss Haug KB, Endestad T, Bentsen H, Grimholt RM, Landrø NI.

Cogn Emot. 2013;27(3):465-73. doi: 10.1080/02699931.2012.726213. Epub 2012 Sep 27.

PMID:
23017007
8.

A novel 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) splice variant with an alternative exon 1 potentially encoding an extended N-terminus.

Stormo C, Kringen MK, Grimholt RM, Berg JP, Piehler AP.

BMC Mol Biol. 2012 Sep 18;13:29. doi: 10.1186/1471-2199-13-29.

9.

Copy number variations of the ATP-binding cassette transporter ABCC6 gene and its pseudogenes.

Kringen MK, Stormo C, Grimholt RM, Berg JP, Piehler AP.

BMC Res Notes. 2012 Aug 9;5:425. doi: 10.1186/1756-0500-5-425.

10.

Genetic variation of VKORC1 and CYP4F2 genes related to warfarin maintenance dose in patients with myocardial infarction.

Kringen MK, Haug KB, Grimholt RM, Stormo C, Narum S, Opdal MS, Fosen JT, Piehler AP, Johansen PW, Seljeflot I, Berg JP, Brørs O.

J Biomed Biotechnol. 2011;2011:739751. doi: 10.1155/2011/739751. Epub 2010 Nov 24.

11.

Gene expression results in lipopolysaccharide-stimulated monocytes depend significantly on the choice of reference genes.

Piehler AP, Grimholt RM, Ovstebø R, Berg JP.

BMC Immunol. 2010 May 4;11:21. doi: 10.1186/1471-2172-11-21.

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