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Results: 1 to 20 of 41

1.

StemBANCC: Governing Access to Material and Data in a Large Stem Cell Research Consortium.

Morrison M, Klein C, Clemann N, Collier DA, Hardy J, Heiβerer B, Cader MZ, Graf M, Kaye J.

Stem Cell Rev. 2015 May 30. [Epub ahead of print]

PMID:
26024842
2.

Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathology.

Grice SJ, Sleigh JN, Motley WW, Liu JL, Burgess RW, Talbot K, Cader MZ.

Hum Mol Genet. 2015 Aug 1;24(15):4397-406. doi: 10.1093/hmg/ddv176. Epub 2015 May 13.

3.

EBNA2 binds to genomic intervals associated with multiple sclerosis and overlaps with vitamin D receptor occupancy.

Ricigliano VA, Handel AE, Sandve GK, Annibali V, Ristori G, Mechelli R, Cader MZ, Salvetti M.

PLoS One. 2015 Apr 8;10(4):e0119605. doi: 10.1371/journal.pone.0119605. eCollection 2015.

4.

Altered neurochemical coupling in the occipital cortex in migraine with visual aura.

Bridge H, Stagg CJ, Near J, Lau CI, Zisner A, Cader MZ.

Cephalalgia. 2015 Jan 28. pii: 0333102414566860. [Epub ahead of print]

PMID:
25631169
5.

Diagnostic outcomes associated with ankle synovitis in early inflammatory arthritis: a cohort study.

Abhishek A, de Pablo P, Cader MZ, Buckley CD, Raza K, Filer A.

Clin Exp Rheumatol. 2014 Jul-Aug;32(4):533-8. Epub 2014 Jul 1.

PMID:
24983292
6.

Morphological analysis of neuromuscular junction development and degeneration in rodent lumbrical muscles.

Sleigh JN, Burgess RW, Gillingwater TH, Cader MZ.

J Neurosci Methods. 2014 Apr 30;227:159-65. doi: 10.1016/j.jneumeth.2014.02.005. Epub 2014 Feb 14.

7.

Cloxyquin (5-chloroquinolin-8-ol) is an activator of the two-pore domain potassium channel TRESK.

Wright PD, Weir G, Cartland J, Tickle D, Kettleborough C, Cader MZ, Jerman J.

Biochem Biophys Res Commun. 2013 Nov 15;441(2):463-8.

PMID:
24383077
8.

Neuromuscular junction maturation defects precede impaired lower motor neuron connectivity in Charcot-Marie-Tooth type 2D mice.

Sleigh JN, Grice SJ, Burgess RW, Talbot K, Cader MZ.

Hum Mol Genet. 2014 May 15;23(10):2639-50. doi: 10.1093/hmg/ddt659. Epub 2013 Dec 23.

9.

Recent advances in inflammatory bowel disease: mucosal immune cells in intestinal inflammation.

Cader MZ, Kaser A.

Gut. 2013 Nov;62(11):1653-64. doi: 10.1136/gutjnl-2012-303955. Review.

PMID:
24104886
10.

Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development.

Lise S, Clarkson Y, Perkins E, Kwasniewska A, Sadighi Akha E, Schnekenberg RP, Suminaite D, Hope J, Baker I, Gregory L, Green A, Allan C, Lamble S, Jayawant S, Quaghebeur G, Cader MZ, Hughes S, Armstrong RJ, Kanapin A, Rimmer A, Lunter G, Mathieson I, Cazier JB, Buck D, Taylor JC, Bentley D, McVean G, Donnelly P, Knight SJ, Jackson M, Ragoussis J, Németh AH.

PLoS Genet. 2012;8(12):e1003074. doi: 10.1371/journal.pgen.1003074. Epub 2012 Dec 6.

11.

Neuropilins lock secreted semaphorins onto plexins in a ternary signaling complex.

Janssen BJ, Malinauskas T, Weir GA, Cader MZ, Siebold C, Jones EY.

Nat Struct Mol Biol. 2012 Dec;19(12):1293-9. doi: 10.1038/nsmb.2416. Epub 2012 Oct 28.

12.

Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene.

Dyment DA, Cader MZ, Chao MJ, Lincoln MR, Morrison KM, Disanto G, Morahan JM, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC, Ramagopalan SV.

Neurology. 2012 Jul 31;79(5):406-11. doi: 10.1212/WNL.0b013e3182616fc4. Epub 2012 Jun 27.

13.

Rare variants in the CYP27B1 gene are associated with multiple sclerosis.

Ramagopalan SV, Dyment DA, Cader MZ, Morrison KM, Disanto G, Morahan JM, Berlanga-Taylor AJ, Handel A, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC.

Ann Neurol. 2011 Dec;70(6):881-6. doi: 10.1002/ana.22678.

PMID:
22190362
14.

New directions in migraine.

Weir GA, Cader MZ.

BMC Med. 2011 Oct 25;9:116. doi: 10.1186/1741-7015-9-116. Review.

15.

Performance of the 2010 ACR/EULAR criteria for rheumatoid arthritis: comparison with 1987 ACR criteria in a very early synovitis cohort.

Cader MZ, Filer A, Hazlehurst J, de Pablo P, Buckley CD, Raza K.

Ann Rheum Dis. 2011 Jun;70(6):949-55. doi: 10.1136/ard.2010.143560. Epub 2011 Feb 1. Erratum in: Ann Rheum Dis. 2011 Jul;70(7):1349. Ann Rheum Dis. 2012 Sep;71(9):1592.

PMID:
21285117
16.

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.

Lafrenière RG, Cader MZ, Poulin JF, Andres-Enguix I, Simoneau M, Gupta N, Boisvert K, Lafrenière F, McLaughlan S, Dubé MP, Marcinkiewicz MM, Ramagopalan S, Ansorge O, Brais B, Sequeiros J, Pereira-Monteiro JM, Griffiths LR, Tucker SJ, Ebers G, Rouleau GA.

Nat Med. 2010 Oct;16(10):1157-60. doi: 10.1038/nm.2216. Epub 2010 Sep 26.

PMID:
20871611
17.

The relationship between the presence of anti-cyclic citrullinated peptide antibodies and clinical phenotype in very early rheumatoid arthritis.

Cader MZ, Filer AD, Buckley CD, Raza K.

BMC Musculoskelet Disord. 2010 Aug 23;11:187. doi: 10.1186/1471-2474-11-187.

18.

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.

Achilli F, Bros-Facer V, Williams HP, Banks GT, AlQatari M, Chia R, Tucci V, Groves M, Nickols CD, Seburn KL, Kendall R, Cader MZ, Talbot K, van Minnen J, Burgess RW, Brandner S, Martin JE, Koltzenburg M, Greensmith L, Nolan PM, Fisher EM.

Dis Model Mech. 2009 Jul-Aug;2(7-8):359-73. doi: 10.1242/dmm.002527. Epub 2009 May 26.

19.

Inverse regulation of plasticity-related immediate early genes by calcineurin in hippocampal neurons.

Lam BY, Zhang W, Enticknap N, Haggis E, Cader MZ, Chawla S.

J Biol Chem. 2009 May 1;284(18):12562-71. doi: 10.1074/jbc.M901121200. Epub 2009 Mar 6.

20.

A first stage genome-wide screen for regions shared identical-by-descent in Hutterite families with multiple sclerosis.

Dyment DA, Cader MZ, Datta A, Broxholme SJ, Cherny SS, Willer CJ, Ramagopalan S, Herrera BM, Orton S, Chao M, Sadovnick AD, Hader M, Hader W, Ebers GC.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):467-72.

PMID:
18081025
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