Beggs AH - Search Results

1

Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes.

Bennett RR, Schneider HE, Estrella E, Burgess S, Cheng AS, Barrett C, Lip V, Lai PS, Shen Y, Wu BL, Darras BT, Beggs AH, Kunkel LM. Bennett RR, et al. Among authors: beggs ah. BMC Genet. 2009 Oct 18;10:66. doi: 10.1186/1471-2156-10-66. BMC Genet. 2009. PMID: 19835634 Free PMC article.

2

Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle.

Haslett JN, Sanoudou D, Kho AT, Bennett RR, Greenberg SA, Kohane IS, Beggs AH, Kunkel LM. Haslett JN, et al. Among authors: beggs ah. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):15000-5. doi: 10.1073/pnas.192571199. Epub 2002 Nov 1. Proc Natl Acad Sci U S A. 2002. PMID: 12415109 Free PMC article.

3

Gene expression profiling of Duchenne muscular dystrophy skeletal muscle.

Haslett JN, Sanoudou D, Kho AT, Han M, Bennett RR, Kohane IS, Beggs AH, Kunkel LM. Haslett JN, et al. Among authors: beggs ah. Neurogenetics. 2003 Aug;4(4):163-71. doi: 10.1007/s10048-003-0148-x. Epub 2003 Apr 16. Neurogenetics. 2003. PMID: 12698323

4

The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies.

Gupta V, Kawahara G, Gundry SR, Chen AT, Lencer WI, Zhou Y, Zon LI, Kunkel LM, Beggs AH. Gupta V, et al. Among authors: beggs ah. Hum Mol Genet. 2011 May 1;20(9):1712-25. doi: 10.1093/hmg/ddr047. Epub 2011 Feb 4. Hum Mol Genet. 2011. PMID: 21296866 Free PMC article.

5

Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores.

Boyden SE, Mahoney LJ, Kawahara G, Myers JA, Mitsuhashi S, Estrella EA, Duncan AR, Dey F, DeChene ET, Blasko-Goehringer JM, Bönnemann CG, Darras BT, Mendell JR, Lidov HG, Nishino I, Beggs AH, Kunkel LM, Kang PB. Boyden SE, et al. Among authors: beggs ah. Neurogenetics. 2012 May;13(2):115-24. doi: 10.1007/s10048-012-0315-z. Epub 2012 Feb 28. Neurogenetics. 2012. PMID: 22371254 Free PMC article.

6

Distinctive patterns of microRNA expression in primary muscular disorders.

Eisenberg I, Eran A, Nishino I, Moggio M, Lamperti C, Amato AA, Lidov HG, Kang PB, North KN, Mitrani-Rosenbaum S, Flanigan KM, Neely LA, Whitney D, Beggs AH, Kohane IS, Kunkel LM. Eisenberg I, et al. Among authors: beggs ah. Proc Natl Acad Sci U S A. 2007 Oct 23;104(43):17016-21. doi: 10.1073/pnas.0708115104. Epub 2007 Oct 17. Proc Natl Acad Sci U S A. 2007. PMID: 17942673 Free PMC article.

7

α-Actinin-2 deficiency results in sarcomeric defects in zebrafish that cannot be rescued by α-actinin-3 revealing functional differences between sarcomeric isoforms.

Gupta V, Discenza M, Guyon JR, Kunkel LM, Beggs AH. Gupta V, et al. Among authors: beggs ah. FASEB J. 2012 May;26(5):1892-908. doi: 10.1096/fj.11-194548. Epub 2012 Jan 17. FASEB J. 2012. PMID: 22253474 Free PMC article.

8

Reproducibility of gene expression across generations of Affymetrix microarrays.

Nimgaonkar A, Sanoudou D, Butte AJ, Haslett JN, Kunkel LM, Beggs AH, Kohane IS. Nimgaonkar A, et al. Among authors: beggs ah. BMC Bioinformatics. 2003 Jun 25;4:27. doi: 10.1186/1471-2105-4-27. Epub 2003 Jun 25. BMC Bioinformatics. 2003. PMID: 12823866 Free PMC article.

9

Transcriptional profile of postmortem skeletal muscle.

Sanoudou D, Kang PB, Haslett JN, Han M, Kunkel LM, Beggs AH. Sanoudou D, et al. Among authors: beggs ah. Physiol Genomics. 2004 Jan 15;16(2):222-8. doi: 10.1152/physiolgenomics.00137.2003. Physiol Genomics. 2004. PMID: 14625377

10

Molecular classification of nemaline myopathies: "nontyping" specimens exhibit unique patterns of gene expression.

Sanoudou D, Frieden LA, Haslett JN, Kho AT, Greenberg SA, Kohane IS, Kunkel LM, Beggs AH. Sanoudou D, et al. Among authors: beggs ah. Neurobiol Dis. 2004 Apr;15(3):590-600. doi: 10.1016/j.nbd.2003.12.013. Neurobiol Dis. 2004. PMID: 15056467

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