Briggs CE - Search Results

1

A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5.

Briggs CE, Guo CY, Schoettler C, Rosoklija I, Silva A, Bauer SB, Retik AB, Kunkel L, Nguyen HT. Briggs CE, et al. Eur J Hum Genet. 2010 Feb;18(2):245-50. doi: 10.1038/ejhg.2009.142. Epub 2009 Aug 19. Eur J Hum Genet. 2010. PMID: 19690587 Free PMC article.

2

A novel mutation in two families with limb-girdle muscular dystrophy type 2C.

Duncan DR, Kang PB, Rabbat JC, Briggs CE, Lidov HG, Darras BT, Kunkel LM. Duncan DR, et al. Among authors: briggs ce. Neurology. 2006 Jul 11;67(1):167-9. doi: 10.1212/01.wnl.0000223600.78363.dd. Neurology. 2006. PMID: 16832103

3

Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy.

Mehta SG, Watts GD, McGillivray B, Mumm S, Hamilton SJ, Ramdeen S, Novack D, Briggs C, Whyte MP, Kimonis VE. Mehta SG, et al. Am J Med Genet A. 2006 Feb 15;140(4):322-30. doi: 10.1002/ajmg.a.31008. Am J Med Genet A. 2006. PMID: 16419137

4

Spectrum of heart disease associated with murine and human GATA4 mutation.

Rajagopal SK, Ma Q, Obler D, Shen J, Manichaikul A, Tomita-Mitchell A, Boardman K, Briggs C, Garg V, Srivastava D, Goldmuntz E, Broman KW, Benson DW, Smoot LB, Pu WT. Rajagopal SK, et al. J Mol Cell Cardiol. 2007 Dec;43(6):677-85. doi: 10.1016/j.yjmcc.2007.06.004. Epub 2007 Jun 21. J Mol Cell Cardiol. 2007. PMID: 17643447 Free PMC article.

5

DNA degradation test predicts success in whole-genome amplification from diverse clinical samples.

Wang F, Wang L, Briggs C, Sicinska E, Gaston SM, Mamon H, Kulke MH, Zamponi R, Loda M, Maher E, Ogino S, Fuchs CS, Li J, Hader C, Makrigiorgos GM. Wang F, et al. J Mol Diagn. 2007 Sep;9(4):441-51. doi: 10.2353/jmoldx.2007.070004. Epub 2007 Aug 9. J Mol Diagn. 2007. PMID: 17690213 Free PMC article.

6

Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.

Briggs CE, Rucinski D, Rosenfeld PJ, Hirose T, Berson EL, Dryja TP. Briggs CE, et al. Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2229-36. Invest Ophthalmol Vis Sci. 2001. PMID: 11527935

7

Compound heterozygous mutation of Rag1 leading to Omenn syndrome.

Matthews AG, Briggs CE, Yamanaka K, Small TN, Mooster JL, Bonilla FA, Oettinger MA, Butte MJ. Matthews AG, et al. Among authors: briggs ce. PLoS One. 2015 Apr 7;10(4):e0121489. doi: 10.1371/journal.pone.0121489. eCollection 2015. PLoS One. 2015. PMID: 25849362 Free PMC article.

8

Unliganded estrogen receptor alpha regulates vascular cell function and gene expression.

Lu Q, Schnitzler GR, Vallaster CS, Ueda K, Erdkamp S, Briggs CE, Iyer LK, Jaffe IZ, Karas RH. Lu Q, et al. Among authors: briggs ce. Mol Cell Endocrinol. 2017 Feb 15;442:12-23. doi: 10.1016/j.mce.2016.11.019. Epub 2016 Nov 22. Mol Cell Endocrinol. 2017. PMID: 27888004

9

Midbrain dopamine neurons in Parkinson's disease exhibit a dysregulated miRNA and target-gene network.

Briggs CE, Wang Y, Kong B, Woo TU, Iyer LK, Sonntag KC. Briggs CE, et al. Brain Res. 2015 Aug 27;1618:111-21. doi: 10.1016/j.brainres.2015.05.021. Epub 2015 Jun 3. Brain Res. 2015. PMID: 26047984 Free PMC article.

10

Transcriptional changes induced by the tumor dormancy-associated microRNA-190.

Almog N, Briggs C, Beheshti A, Ma L, Wilkie KP, Rietman E, Hlatky L. Almog N, et al. Transcription. 2013 Jul-Aug;4(4):177-91. doi: 10.4161/trns.25558. Epub 2013 Jul 1. Transcription. 2013. PMID: 23863200 Free PMC article.

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