Lidov HG - Search Results

1

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.

McNally EM, Passos-Bueno MR, Bönnemann CG, Vainzof M, de Sá Moreira E, Lidov HG, Othmane KB, Denton PH, Vance JM, Zatz M, Kunkel LM. McNally EM, et al. Among authors: lidov hg. Am J Hum Genet. 1996 Nov;59(5):1040-7. Am J Hum Genet. 1996. PMID: 8900232 Free PMC article.

2

Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy.

McNally EM, Duggan D, Gorospe JR, Bönnemann CG, Fanin M, Pegoraro E, Lidov HG, Noguchi S, Ozawa E, Finkel RS, Cruse RP, Angelini C, Kunkel LM, Hoffman EP. McNally EM, et al. Among authors: lidov hg. Hum Mol Genet. 1996 Nov;5(11):1841-7. doi: 10.1093/hmg/5.11.1841. Hum Mol Genet. 1996. PMID: 8923014

3

Caveolin-3 in muscular dystrophy.

McNally EM, de Sá Moreira E, Duggan DJ, Bönnemann CG, Lisanti MP, Lidov HG, Vainzof M, Passos-Bueno MR, Hoffman EP, Zatz M, Kunkel LM. McNally EM, et al. Among authors: lidov hg. Hum Mol Genet. 1998 May;7(5):871-7. doi: 10.1093/hmg/7.5.871. Hum Mol Genet. 1998. PMID: 9536092

4

Molecular organization of sarcoglycan complex in mouse myotubes in culture.

Chan YM, Bönnemann CG, Lidov HG, Kunkel LM. Chan YM, et al. Among authors: lidov hg. J Cell Biol. 1998 Dec 28;143(7):2033-44. doi: 10.1083/jcb.143.7.2033. J Cell Biol. 1998. PMID: 9864373 Free PMC article.

5

Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein.

Thompson TG, Chan YM, Hack AA, Brosius M, Rajala M, Lidov HG, McNally EM, Watkins S, Kunkel LM. Thompson TG, et al. Among authors: lidov hg. J Cell Biol. 2000 Jan 10;148(1):115-26. doi: 10.1083/jcb.148.1.115. J Cell Biol. 2000. PMID: 10629222 Free PMC article.

6

The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States.

Reddy HM, Cho KA, Lek M, Estrella E, Valkanas E, Jones MD, Mitsuhashi S, Darras BT, Amato AA, Lidov HG, Brownstein CA, Margulies DM, Yu TW, Salih MA, Kunkel LM, MacArthur DG, Kang PB. Reddy HM, et al. Among authors: lidov hg. J Hum Genet. 2017 Feb;62(2):243-252. doi: 10.1038/jhg.2016.116. Epub 2016 Oct 6. J Hum Genet. 2017. PMID: 27708273 Free PMC article.

7

Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile.

Bönnemann CG, Wong J, Jones KJ, Lidov HG, Feener CA, Shapiro F, Darras BT, Kunkel LM, North KN. Bönnemann CG, et al. Among authors: lidov hg. Neuromuscul Disord. 2002 Mar;12(3):273-80. doi: 10.1016/s0960-8966(01)00276-0. Neuromuscul Disord. 2002. PMID: 11801399

8

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: lidov hg. Neurology. 2006 Jul 11;67(1):167-9. doi: 10.1212/01.wnl.0000223600.78363.dd. Neurology. 2006. PMID: 16832103

9

Dp140: a novel 140 kDa CNS transcript from the dystrophin locus.

Lidov HG, Selig S, Kunkel LM. Lidov HG, et al. Hum Mol Genet. 1995 Mar;4(3):329-35. doi: 10.1093/hmg/4.3.329. Hum Mol Genet. 1995. PMID: 7795584

10

An alternative dystrophin transcript specific to peripheral nerve.

Byers TJ, Lidov HG, Kunkel LM. Byers TJ, et al. Among authors: lidov hg. Nat Genet. 1993 May;4(1):77-81. doi: 10.1038/ng0593-77. Nat Genet. 1993. PMID: 8513330

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