Kunkel LM - Search Results

1

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.

Beggs AH, Neumann PE, Arahata K, Arikawa E, Nonaka I, Anderson MS, Kunkel LM. Beggs AH, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):623-7. doi: 10.1073/pnas.89.2.623. Proc Natl Acad Sci U S A. 1992. PMID: 1731332 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: kunkel lm. 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

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: kunkel lm. 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.

4

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24.

Ahn AH, Yoshida M, Anderson MS, Feener CA, Selig S, Hagiwara Y, Ozawa E, Kunkel LM. Ahn AH, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 1994 May 10;91(10):4446-50. doi: 10.1073/pnas.91.10.4446. Proc Natl Acad Sci U S A. 1994. PMID: 8183929 Free PMC article.

5

Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy.

Specht LA, Beggs AH, Korf B, Kunkel LM, Shapiro F. Specht LA, et al. Among authors: kunkel lm. Pediatr Neurol. 1992 Nov-Dec;8(6):432-6. doi: 10.1016/0887-8994(92)90004-i. Pediatr Neurol. 1992. PMID: 1476571

6

Additional dystrophin fragment in Becker muscular dystrophy may result from proteolytic cleavage at deletion junctions.

Beggs AH, Hoffman EP, Kunkel LM. Beggs AH, et al. Among authors: kunkel lm. Am J Med Genet. 1992 Oct 1;44(3):378-81. doi: 10.1002/ajmg.1320440322. Am J Med Genet. 1992. PMID: 1488990

7

ELISA quantitation of dystrophin for the diagnosis of Duchenne and Becker muscular dystrophies.

Byers TJ, Neumann PE, Beggs AH, Kunkel LM. Byers TJ, et al. Among authors: kunkel lm. Neurology. 1992 Mar;42(3 Pt 1):570-6. Neurology. 1992. PMID: 1549217

8

Improved diagnosis of Duchenne/Becker muscular dystrophy.

Beggs AH, Kunkel LM. Beggs AH, et al. Among authors: kunkel lm. J Clin Invest. 1990 Mar;85(3):613-9. doi: 10.1172/JCI114482. J Clin Invest. 1990. PMID: 1968908 Free PMC article. Review. No abstract available.

9

Dystrophin is transcribed in brain from a distant upstream promoter.

Boyce FM, Beggs AH, Feener C, Kunkel LM. Boyce FM, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 1991 Feb 15;88(4):1276-80. doi: 10.1073/pnas.88.4.1276. Proc Natl Acad Sci U S A. 1991. PMID: 1996328 Free PMC article.

10

Muscular dystrophy research: what have we learned and where do we go from here?

Boyce FM, Beggs AH, Kunkel LM. Boyce FM, et al. Among authors: kunkel lm. Res Publ Assoc Res Nerv Ment Dis. 1991;69:121-7. Res Publ Assoc Res Nerv Ment Dis. 1991. PMID: 2003155 Review. No abstract available.

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