Hoffman EP - Search Results

1

Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding.

Rudolph JA, Spier SJ, Byrns G, Rojas CV, Bernoco D, Hoffman EP. Rudolph JA, et al. Among authors: hoffman ep. Nat Genet. 1992 Oct;2(2):144-7. doi: 10.1038/ng1092-144. Nat Genet. 1992. PMID: 1338908

2

Sequence and genomic structure of the human adult skeletal muscle sodium channel alpha subunit gene on 17q.

Wang JZ, Rojas CV, Zhou JH, Schwartz LS, Nicholas H, Hoffman EP. Wang JZ, et al. Among authors: hoffman ep. Biochem Biophys Res Commun. 1992 Jan 31;182(2):794-801. doi: 10.1016/0006-291x(92)91802-w. Biochem Biophys Res Commun. 1992. PMID: 1310396

3

Linkage of hyperkalaemic periodic paralysis in quarter horses to the horse adult skeletal muscle sodium channel gene.

Rudolph JA, Spier SJ, Byrns G, Hoffman EP. Rudolph JA, et al. Among authors: hoffman ep. Anim Genet. 1992;23(3):241-50. doi: 10.1111/j.1365-2052.1992.tb00136.x. Anim Genet. 1992. PMID: 1323940

4

The genomic structure of the human skeletal muscle sodium channel gene.

McClatchey AI, Lin CS, Wang J, Hoffman EP, Rojas C, Gusella JF. McClatchey AI, et al. Among authors: hoffman ep. Hum Mol Genet. 1992 Oct;1(7):521-7. doi: 10.1093/hmg/1.7.521. Hum Mol Genet. 1992. PMID: 1339144

5

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis.

Rojas CV, Wang JZ, Schwartz LS, Hoffman EP, Powell BR, Brown RH Jr. Rojas CV, et al. Among authors: hoffman ep. Nature. 1991 Dec 5;354(6352):387-9. doi: 10.1038/354387a0. Nature. 1991. PMID: 1659668

6

Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

Koch MC, Ricker K, Otto M, Grimm T, Bender K, Zoll B, Harper PS, Lehmann-Horn F, Rüdel R, Hoffman EP. Koch MC, et al. Among authors: hoffman ep. Hum Genet. 1991 Nov;88(1):71-4. doi: 10.1007/BF00204932. Hum Genet. 1991. PMID: 1660029

7

Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17.

Koch MC, Ricker K, Otto M, Grimm T, Hoffman EP, Rüdel R, Bender K, Zoll B, Harper PS, Lehmann-Horn F. Koch MC, et al. Among authors: hoffman ep. J Med Genet. 1991 Sep;28(9):583-6. doi: 10.1136/jmg.28.9.583. J Med Genet. 1991. PMID: 1683408 Free PMC article.

8

Recent advances in dystrophin research.

Rojas CV, Hoffman EP. Rojas CV, et al. Among authors: hoffman ep. Curr Opin Neurobiol. 1991 Oct;1(3):420-9. doi: 10.1016/0959-4388(91)90064-e. Curr Opin Neurobiol. 1991. PMID: 1821686 Review.

9

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.

Fontaine B, Khurana TS, Hoffman EP, Bruns GA, Haines JL, Trofatter JA, Hanson MP, Rich J, McFarlane H, Yasek DM, et al. Fontaine B, et al. Among authors: hoffman ep. Science. 1990 Nov 16;250(4983):1000-2. doi: 10.1126/science.2173143. Science. 1990. PMID: 2173143

10

Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation.

Wang J, Pegoraro E, Menegazzo E, Gennarelli M, Hoop RC, Angelini C, Hoffman EP. Wang J, et al. Among authors: hoffman ep. Hum Mol Genet. 1995 Apr;4(4):599-606. doi: 10.1093/hmg/4.4.599. Hum Mol Genet. 1995. PMID: 7543316

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