Jacobsen NJ - Search Results

1

Charcot-Marie-Tooth disease neurofilament mutations disrupt neurofilament assembly and axonal transport.

Brownlees J, Ackerley S, Grierson AJ, Jacobsen NJ, Shea K, Anderton BH, Leigh PN, Shaw CE, Miller CC. Brownlees J, et al. Among authors: jacobsen nj. Hum Mol Genet. 2002 Nov 1;11(23):2837-44. doi: 10.1093/hmg/11.23.2837. Hum Mol Genet. 2002. PMID: 12393795

2

Axonal transport of neurofilaments in normal and disease states.

Miller CC, Ackerley S, Brownlees J, Grierson AJ, Jacobsen NJ, Thornhill P. Miller CC, et al. Among authors: jacobsen nj. Cell Mol Life Sci. 2002 Feb;59(2):323-30. doi: 10.1007/s00018-002-8425-7. Cell Mol Life Sci. 2002. PMID: 11924605 Free PMC article. Review.

3

ALS2/Alsin regulates Rac-PAK signaling and neurite outgrowth.

Tudor EL, Perkinton MS, Schmidt A, Ackerley S, Brownlees J, Jacobsen NJ, Byers HL, Ward M, Hall A, Leigh PN, Shaw CE, McLoughlin DM, Miller CC. Tudor EL, et al. Among authors: jacobsen nj. J Biol Chem. 2005 Oct 14;280(41):34735-40. doi: 10.1074/jbc.M506216200. Epub 2005 Jul 26. J Biol Chem. 2005. PMID: 16049005 Free article.

4

ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.

Jacobsen NJ, Lyons I, Hoogendoorn B, Burge S, Kwok PY, O'Donovan MC, Craddock N, Owen MJ. Jacobsen NJ, et al. Hum Mol Genet. 1999 Sep;8(9):1631-6. doi: 10.1093/hmg/8.9.1631. Hum Mol Genet. 1999. PMID: 10441325

5

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease.

Sakuntabhai A, Ruiz-Perez V, Carter S, Jacobsen N, Burge S, Monk S, Smith M, Munro CS, O'Donovan M, Craddock N, Kucherlapati R, Rees JL, Owen M, Lathrop GM, Monaco AP, Strachan T, Hovnanian A. Sakuntabhai A, et al. Nat Genet. 1999 Mar;21(3):271-7. doi: 10.1038/6784. Nat Genet. 1999. PMID: 10080178

6

Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's disease.

Jones I, Jacobsen N, Green EK, Elvidge GP, Owen MJ, Craddock N. Jones I, et al. Mol Psychiatry. 2002;7(4):424-7. doi: 10.1038/sj.mp.4000989. Mol Psychiatry. 2002. PMID: 11986988

7

Mutational analysis of phospholipase A2A: a positional candidate susceptibility gene for bipolar disorder.

Jacobsen NJ, Franks EK, Owen MJ, Craddock NJ. Jacobsen NJ, et al. Mol Psychiatry. 1999 May;4(3):274-9. doi: 10.1038/sj.mp.4000476. Mol Psychiatry. 1999. PMID: 10395219

8

Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease.

Green E, Elvidge G, Jacobsen N, Glaser B, Jones I, O'Donovan MC, Kirov G, Owen MJ, Craddock N. Green E, et al. Am J Psychiatry. 2005 Jan;162(1):35-42. doi: 10.1176/appi.ajp.162.1.35. Am J Psychiatry. 2005. PMID: 15625199

9

Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder.

Jacobsen NJ, Franks EK, Elvidge G, Jones I, McCandless F, O'Donovan MC, Owen MJ, Craddock N. Jacobsen NJ, et al. Mol Psychiatry. 2001 Jan;6(1):92-7. doi: 10.1038/sj.mp.4000774. Mol Psychiatry. 2001. PMID: 11244492

10

CUX2, a potential regulator of NCAM expression: genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder.

Jacobsen NJ, Elvidge G, Franks EK, O'Donovan MC, Craddock N, Owen MJ. Jacobsen NJ, et al. Am J Med Genet. 2001 Apr 8;105(3):295-300. doi: 10.1002/ajmg.1325. Am J Med Genet. 2001. PMID: 11353453

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