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Items: 24

1.

Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.

Rodriguez-Jato S, Shan J, Khadake J, Heggestad AD, Ma X, Johnstone KA, Resnick JL, Yang TP.

PLoS One. 2013;8(2):e52390. doi: 10.1371/journal.pone.0052390. Epub 2013 Feb 4.

2.

Identification of olfactory receptor genes in Atlantic salmon Salmo salar.

Johnstone KA, Lubieniecki KP, Koop BF, Davidson WS.

J Fish Biol. 2012 Jul;81(2):559-75. doi: 10.1111/j.1095-8649.2012.03368.x. Review.

PMID:
22803724
3.

Temporal and developmental requirements for the Prader-Willi imprinting center.

DuBose AJ, Smith EY, Johnstone KA, Resnick JL.

Proc Natl Acad Sci U S A. 2012 Feb 28;109(9):3446-50. doi: 10.1073/pnas.1115057109. Epub 2012 Feb 13.

4.

Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus.

Smith EY, Futtner CR, Chamberlain SJ, Johnstone KA, Resnick JL.

PLoS Genet. 2011 Dec;7(12):e1002422. doi: 10.1371/journal.pgen.1002422. Epub 2011 Dec 29.

5.

Expression of olfactory receptors in different life stages and life histories of wild Atlantic salmon (Salmo salar).

Johnstone KA, Lubieniecki KP, Koop BF, Davidson WS.

Mol Ecol. 2011 Oct;20(19):4059-69. doi: 10.1111/j.1365-294X.2011.05251.x. Epub 2011 Aug 29.

PMID:
21883590
6.

A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center.

Dubose AJ, Smith EY, Yang TP, Johnstone KA, Resnick JL.

Hum Mol Genet. 2011 Sep 1;20(17):3461-6. doi: 10.1093/hmg/ddr262. Epub 2011 Jun 9.

7.

Physiological effects of Type 2 diabetes on mRNA processing and gene expression.

Morrison FS, Johnstone KA, Harries LW.

Expert Rev Endocrinol Metab. 2011 Mar;6(2):255-267. doi: 10.1586/eem.10.76.

PMID:
30290446
8.

Dysregulation of Hnf1b gene expression in cultured beta-cells in response to cytotoxic fatty acid.

Johnstone KA, Diakogiannaki E, Dhayal S, Morgan NG, Harries LW.

JOP. 2011 Jan 5;12(1):6-10.

9.

Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitro.

Wirsing A, Johnstone KA, Harries LW, Ellard S, Ryffel GU, Stanik J, Gasperikova D, Klimes I, Murphy R.

Diabet Med. 2010 Jun;27(6):631-5. doi: 10.1111/j.1464-5491.2010.03003.x.

PMID:
20546279
10.

Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome.

Relkovic D, Doe CM, Humby T, Johnstone KA, Resnick JL, Holland AJ, Hagan JJ, Wilkinson LS, Isles AR.

Eur J Neurosci. 2010 Jan;31(1):156-64. doi: 10.1111/j.1460-9568.2009.07048.x. Epub 2009 Dec 23.

PMID:
20092561
11.

Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.

DuBose AJ, Johnstone KA, Smith EY, Hallett RA, Resnick JL.

Neurogenetics. 2010 May;11(2):145-51. doi: 10.1007/s10048-009-0226-9. Epub 2009 Nov 6.

PMID:
19894069
12.

HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.

Adalat S, Woolf AS, Johnstone KA, Wirsing A, Harries LW, Long DA, Hennekam RC, Ledermann SE, Rees L, van't Hoff W, Marks SD, Trompeter RS, Tullus K, Winyard PJ, Cansick J, Mushtaq I, Dhillon HK, Bingham C, Edghill EL, Shroff R, Stanescu H, Ryffel GU, Ellard S, Bockenhauer D.

J Am Soc Nephrol. 2009 May;20(5):1123-31. doi: 10.1681/ASN.2008060633. Epub 2009 Apr 23.

13.

Genomic organization and evolution of the vomeronasal type 2 receptor-like (OlfC) gene clusters in Atlantic salmon, Salmo salar.

Johnstone KA, Ciborowski KL, Lubieniecki KP, Chow W, Phillips RB, Koop BF, Jordan WC, Davidson WS.

Mol Biol Evol. 2009 May;26(5):1117-25. doi: 10.1093/molbev/msp027. Epub 2009 Feb 12.

14.

Genomic organization and characterization of two vomeronasal 1 receptor-like genes (ora1 and ora2) in Atlantic salmon Salmo salar.

Johnstone KA, Lubieniecki KP, Chow W, Phillips RB, Koop BF, Davidson WS.

Mar Genomics. 2008 Mar;1(1):23-31. doi: 10.1016/j.margen.2008.04.003. Epub 2008 Apr 28.

PMID:
21798150
15.

Phylogeographic genomics of mitochondrial DNA: Highly-resolved patterns of intraspecific evolution and a multi-species, microarray-based DNA sequencing strategy for biodiversity studies.

Carr SM, Marshall HD, Duggan AT, Flynn SM, Johnstone KA, Pope AM, Wilkerson CD.

Comp Biochem Physiol Part D Genomics Proteomics. 2008 Mar;3(1):1-11. doi: 10.1016/j.cbd.2006.12.005. Epub 2007 Feb 24.

PMID:
20483203
16.

A targeted deletion upstream of Snrpn does not result in an imprinting defect.

Peery EG, Elmore MD, Resnick JL, Brannan CI, Johnstone KA.

Mamm Genome. 2007 Apr;18(4):255-62. Epub 2007 May 19.

PMID:
17514346
17.
18.

A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects.

Johnstone KA, DuBose AJ, Futtner CR, Elmore MD, Brannan CI, Resnick JL.

Hum Mol Genet. 2006 Feb 1;15(3):393-404. Epub 2005 Dec 20.

PMID:
16368707
19.

Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice.

Chamberlain SJ, Johnstone KA, DuBose AJ, Simon TA, Bartolomei MS, Resnick JL, Brannan CI.

Hum Mol Genet. 2004 Dec 1;13(23):2971-7. Epub 2004 Sep 30.

PMID:
15459179
20.
21.

A muscleblind knockout model for myotonic dystrophy.

Kanadia RN, Johnstone KA, Mankodi A, Lungu C, Thornton CA, Esson D, Timmers AM, Hauswirth WW, Swanson MS.

Science. 2003 Dec 12;302(5652):1978-80.

22.
23.

How to tell a sea monster: molecular discrimination of large marine animals of the North Atlantic.

Carr SM, Marshall HD, Johnstone KA, Pynn LM, Stenson GB.

Biol Bull. 2002 Feb;202(1):1-5.

PMID:
11842010
24.

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.

Sutherland HF, Wadey R, McKie JM, Taylor C, Atif U, Johnstone KA, Halford S, Kim UJ, Goodship J, Baldini A, Scambler PJ.

Am J Hum Genet. 1996 Jul;59(1):23-31.

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