Boggs BA - Search Results

1

Immunofluorescent studies of human chromosomes with antibodies against phosphorylated H1 histone.

Boggs BA, Allis CD, Chinault AC. Boggs BA, et al. Chromosoma. 2000 Mar;108(8):485-90. doi: 10.1007/s004120050400. Chromosoma. 2000. PMID: 10794570

2

Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes.

Boggs BA, Cheung P, Heard E, Spector DL, Chinault AC, Allis CD. Boggs BA, et al. Nat Genet. 2002 Jan;30(1):73-6. doi: 10.1038/ng787. Epub 2001 Dec 10. Nat Genet. 2002. PMID: 11740495

3

Reduced levels of histone H3 acetylation on the inactive X chromosome in human females.

Boggs BA, Connors B, Sobel RE, Chinault AC, Allis CD. Boggs BA, et al. Chromosoma. 1996 Dec;105(5):303-9. doi: 10.1007/BF02524648. Chromosoma. 1996. PMID: 8939823

4

Analysis of replication timing properties of human X-chromosomal loci by fluorescence in situ hybridization.

Boggs BA, Chinault AC. Boggs BA, et al. Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6083-7. doi: 10.1073/pnas.91.13.6083. Proc Natl Acad Sci U S A. 1994. PMID: 8016119 Free PMC article.

5

Analysis of DNA replication by fluorescence in situ hybridization.

Boggs BA, Chinault AC. Boggs BA, et al. Methods. 1997 Nov;13(3):259-70. doi: 10.1006/meth.1997.0525. Methods. 1997. PMID: 9441852 Review.

6

Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.

del Gaudio D, Yang Y, Boggs BA, Schmitt ES, Lee JA, Sahoo T, Pham HT, Wiszniewska J, Chinault AC, Beaudet AL, Eng CM. del Gaudio D, et al. Among authors: boggs ba. Hum Mutat. 2008 Sep;29(9):1100-7. doi: 10.1002/humu.20841. Hum Mutat. 2008. PMID: 18752307

7

20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.

Lalani SR, Thakuria JV, Cox GF, Wang X, Bi W, Bray MS, Shaw C, Cheung SW, Chinault AC, Boggs BA, Ou Z, Brundage EK, Lupski JR, Gentile J, Waisbren S, Pursley A, Ma L, Khajavi M, Zapata G, Friedman R, Kim JJ, Towbin JA, Stankiewicz P, Schnittger S, Hansmann I, Ai T, Sood S, Wehrens XH, Martin JF, Belmont JW, Potocki L. Lalani SR, et al. Among authors: boggs ba. J Med Genet. 2009 Mar;46(3):168-75. doi: 10.1136/jmg.2008.061002. Epub 2008 Sep 23. J Med Genet. 2009. PMID: 18812404 Free PMC article.

8

Determination of clonality in acute nonlymphocytic leukemia by restriction fragment length polymorphism and methylation analysis.

Yoffe G, Spitzer G, Boggs BA, McCredie KB, Stass SA, Chinault AC. Yoffe G, et al. Among authors: boggs ba. Leukemia. 1987 Mar;1(3):226-30. Leukemia. 1987. PMID: 2889856

9

New mutation and prenatal diagnosis in ornithine transcarbamylase deficiency.

Nussbaum RL, Boggs BA, Beaudet AL, Doyle S, Potter JL, O'Brien WE. Nussbaum RL, et al. Among authors: boggs ba. Am J Hum Genet. 1986 Feb;38(2):149-58. Am J Hum Genet. 1986. PMID: 3004207 Free PMC article.

10

MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development.

Lalani SR, Ware SM, Wang X, Zapata G, Tian Q, Franco LM, Jiang Z, Bucasas K, Scott DA, Campeau PM, Hanchard N, Umaña L, Cast A, Patel A, Cheung SW, McBride KL, Bray M, Craig Chinault A, Boggs BA, Huang M, Baker MR, Hamilton S, Towbin J, Jefferies JL, Fernbach SD, Potocki L, Belmont JW. Lalani SR, et al. Among authors: boggs ba. Hum Mol Genet. 2013 Nov 1;22(21):4339-48. doi: 10.1093/hmg/ddt283. Epub 2013 Jun 16. Hum Mol Genet. 2013. PMID: 23773997 Free PMC article.

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