Hamilton BA - Search Results

1

Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated mice.

Concepcion D, Seburn KL, Wen G, Frankel WN, Hamilton BA. Concepcion D, et al. Among authors: hamilton ba. Genetics. 2004 Oct;168(2):953-9. doi: 10.1534/genetics.104.029843. Genetics. 2004. PMID: 15514066 Free PMC article.

2

A natural allele of Nxf1 suppresses retrovirus insertional mutations.

Floyd JA, Gold DA, Concepcion D, Poon TH, Wang X, Keithley E, Chen D, Ward EJ, Chinn SB, Friedman RA, Yu HT, Moriwaki K, Shiroishi T, Hamilton BA. Floyd JA, et al. Among authors: hamilton ba. Nat Genet. 2003 Nov;35(3):221-8. doi: 10.1038/ng1247. Epub 2003 Sep 28. Nat Genet. 2003. PMID: 14517553 Free PMC article.

3

Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology.

Wen G, Mahata SK, Cadman P, Mahata M, Ghosh S, Mahapatra NR, Rao F, Stridsberg M, Smith DW, Mahboubi P, Schork NJ, O'Connor DT, Hamilton BA. Wen G, et al. Among authors: hamilton ba. Am J Hum Genet. 2004 Feb;74(2):197-207. doi: 10.1086/381399. Epub 2004 Jan 12. Am J Hum Genet. 2004. PMID: 14740315 Free PMC article.

4

Multipotent genetic suppression of retrotransposon-induced mutations by Nxf1 through fine-tuning of alternative splicing.

Concepcion D, Flores-García L, Hamilton BA. Concepcion D, et al. Among authors: hamilton ba. PLoS Genet. 2009 May;5(5):e1000484. doi: 10.1371/journal.pgen.1000484. Epub 2009 May 15. PLoS Genet. 2009. PMID: 19436707 Free PMC article.

5

Modifier genes for mouse phosphatidylinositol transfer protein α (vibrator) that bypass juvenile lethality.

Concepcion D, Johannes F, Lo YH, Yao J, Fong J, Hamilton BA. Concepcion D, et al. Among authors: hamilton ba. Genetics. 2011 Apr;187(4):1185-91. doi: 10.1534/genetics.110.125906. Epub 2011 Feb 14. Genetics. 2011. PMID: 21321132 Free PMC article.

6

Nxf1 natural variant E610G is a semi-dominant suppressor of IAP-induced RNA processing defects.

Concepcion D, Ross KD, Hutt KR, Yeo GW, Hamilton BA. Concepcion D, et al. Among authors: hamilton ba. PLoS Genet. 2015 Apr 2;11(4):e1005123. doi: 10.1371/journal.pgen.1005123. eCollection 2015 Apr. PLoS Genet. 2015. PMID: 25835743 Free PMC article.

7

An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension.

Wen G, Wessel J, Zhou W, Ehret GB, Rao F, Stridsberg M, Mahata SK, Gent PM, Das M, Cooper RS, Chakravarti A, Zhou H, Schork NJ, O'connor DT, Hamilton BA. Wen G, et al. Among authors: hamilton ba. Hum Mol Genet. 2007 Jul 15;16(14):1752-64. doi: 10.1093/hmg/ddm123. Epub 2007 Jun 21. Hum Mol Genet. 2007. PMID: 17584765 Free PMC article.

8

ZNF423 patient variants, truncations, and in-frame deletions in mice define an allele-dependent range of midline brain abnormalities.

Deshpande O, Lara RZ, Zhang OR, Concepcion D, Hamilton BA. Deshpande O, et al. Among authors: hamilton ba. PLoS Genet. 2020 Sep 14;16(9):e1009017. doi: 10.1371/journal.pgen.1009017. eCollection 2020 Sep. PLoS Genet. 2020. PMID: 32925911 Free PMC article.

9

Zfp423 controls proliferation and differentiation of neural precursors in cerebellar vermis formation.

Alcaraz WA, Gold DA, Raponi E, Gent PM, Concepcion D, Hamilton BA. Alcaraz WA, et al. Among authors: hamilton ba. Proc Natl Acad Sci U S A. 2006 Dec 19;103(51):19424-9. doi: 10.1073/pnas.0609184103. Epub 2006 Dec 6. Proc Natl Acad Sci U S A. 2006. PMID: 17151198 Free PMC article.

10

Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension.

Rao F, Wen G, Gayen JR, Das M, Vaingankar SM, Rana BK, Mahata M, Kennedy BP, Salem RM, Stridsberg M, Abel K, Smith DW, Eskin E, Schork NJ, Hamilton BA, Ziegler MG, Mahata SK, O'Connor DT. Rao F, et al. Among authors: hamilton ba. Circulation. 2007 May 1;115(17):2271-81. doi: 10.1161/CIRCULATIONAHA.106.628859. Epub 2007 Apr 16. Circulation. 2007. PMID: 17438154

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