Simpson EM - Search Results

1

Novel vertebrate genes and putative regulatory elements identified at kidney disease and NR2E1/fierce loci.

Abrahams BS, Mak GM, Berry ML, Palmquist DL, Saionz JR, Tay A, Tan YH, Brenner S, Simpson EM, Venkatesh B. Abrahams BS, et al. Among authors: simpson em. Genomics. 2002 Jul;80(1):45-53. doi: 10.1006/geno.2002.6795. Genomics. 2002. PMID: 12079282

2

Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent.

Young KA, Berry ML, Mahaffey CL, Saionz JR, Hawes NL, Chang B, Zheng QY, Smith RS, Bronson RT, Nelson RJ, Simpson EM. Young KA, et al. Among authors: simpson em. Behav Brain Res. 2002 May 14;132(2):145-58. doi: 10.1016/s0166-4328(01)00413-2. Behav Brain Res. 2002. PMID: 11997145 Free PMC article.

3

Metaphase FISHing of transgenic mice recommended: FISH and SKY define BAC-mediated balanced translocation.

Abrahams BS, Chong AC, Nisha M, Milette D, Brewster DA, Berry ML, Muratkhodjaev F, Mai S, Rajcan-Separovic E, Simpson EM. Abrahams BS, et al. Among authors: simpson em. Genesis. 2003 Jul;36(3):134-41. doi: 10.1002/gene.10205. Genesis. 2003. PMID: 12872244

4

Retroposon compensatory mechanism hypothesis not supported: Zfa knockout mice are fertile.

Banks KG, Johnson KA, Lerner CP, Mahaffey CL, Bronson RT, Simpson EM. Banks KG, et al. Among authors: simpson em. Genomics. 2003 Sep;82(3):254-60. doi: 10.1016/s0888-7543(03)00155-1. Genomics. 2003. PMID: 12906850

5

Unexpected embryonic stem (ES) cell mutations represent a concern in gene targeting: lessons from "fierce" mice.

Kumar RA, Chan KL, Wong AH, Little KQ, Rajcan-Separovic E, Abrahams BS, Simpson EM. Kumar RA, et al. Among authors: simpson em. Genesis. 2004 Feb;38(2):51-7. doi: 10.1002/gene.20001. Genesis. 2004. PMID: 14994267

6

Pathological aggression in "fierce" mice corrected by human nuclear receptor 2E1.

Abrahams BS, Kwok MC, Trinh E, Budaghzadeh S, Hossain SM, Simpson EM. Abrahams BS, et al. Among authors: simpson em. J Neurosci. 2005 Jul 6;25(27):6263-70. doi: 10.1523/JNEUROSCI.4757-04.2005. J Neurosci. 2005. PMID: 16000615 Free PMC article.

7

Mutation and evolutionary analyses identify NR2E1-candidate-regulatory mutations in humans with severe cortical malformations.

Kumar RA, Leach S, Bonaguro R, Chen J, Yokom DW, Abrahams BS, Seaver L, Schwartz CE, Dobyns W, Brooks-Wilson A, Simpson EM. Kumar RA, et al. Among authors: simpson em. Genes Brain Behav. 2007 Aug;6(6):503-16. doi: 10.1111/j.1601-183X.2006.00277.x. Epub 2006 Nov 29. Genes Brain Behav. 2007. PMID: 17054721 Free PMC article.

8

Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes.

Kumar RA, Everman DB, Morgan CT, Slavotinek A, Schwartz CE, Simpson EM. Kumar RA, et al. Among authors: simpson em. BMC Med Genet. 2007 Jul 26;8:48. doi: 10.1186/1471-2350-8-48. BMC Med Genet. 2007. PMID: 17655765 Free PMC article.

9

Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing.

Kumar RA, McGhee KA, Leach S, Bonaguro R, Maclean A, Aguirre-Hernandez R, Abrahams BS, Coccaro EF, Hodgins S, Turecki G, Condon A, Muir WJ, Brooks-Wilson AR, Blackwood DH, Simpson EM. Kumar RA, et al. Among authors: simpson em. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):880-9. doi: 10.1002/ajmg.b.30696. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18205168

10

Next generation tools for high-throughput promoter and expression analysis employing single-copy knock-ins at the Hprt1 locus.

Yang GS, Banks KG, Bonaguro RJ, Wilson G, Dreolini L, de Leeuw CN, Liu L, Swanson DJ, Goldowitz D, Holt RA, Simpson EM. Yang GS, et al. Among authors: simpson em. Genomics. 2009 Mar;93(3):196-204. doi: 10.1016/j.ygeno.2008.09.014. Epub 2008 Dec 3. Genomics. 2009. PMID: 18950699 Free article.

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