Carey N - Search Results

1

Is myotonic dystrophy a single-gene disorder?

Johnson KJ, Boucher Ca, King SK, Winchester CL, Bailey ME, Hamilton GM, Carey N. Johnson KJ, et al. Among authors: carey n. Biochem Soc Trans. 1996 May;24(2):510-3. doi: 10.1042/bst0240510. Biochem Soc Trans. 1996. PMID: 8736794 Review. No abstract available.

2

A 3.7kb fragment from the myotonic dystrophy protein kinase promoter directs neural-specific expression in vivo.

King SK, Wells DJ, Wells KE, Carey N, Johnson KJ. King SK, et al. Among authors: carey n. Biochem Soc Trans. 1996 May;24(2):283S. doi: 10.1042/bst024283s. Biochem Soc Trans. 1996. PMID: 8736941 No abstract available.

3

Cloning of the human SIX1 gene and its assignment to chromosome 14.

Boucher CA, Carey N, Edwards YH, Siciliano MJ, Johnson KJ. Boucher CA, et al. Among authors: carey n. Genomics. 1996 Apr 1;33(1):140-2. doi: 10.1006/geno.1996.0172. Genomics. 1996. PMID: 8617500

4

Over expression of the murine myotonic dystrophy protein kinase in the mouse myogenic C2C12 cell line leads to inhibition of terminal differentiation.

Okoli G, Carey N, Johnson KJ, Watt DJ. Okoli G, et al. Among authors: carey n. Biochem Biophys Res Commun. 1998 May 29;246(3):905-11. doi: 10.1006/bbrc.1998.8723. Biochem Biophys Res Commun. 1998. PMID: 9618310

5

A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat.

Boucher CA, King SK, Carey N, Krahe R, Winchester CL, Rahman S, Creavin T, Meghji P, Bailey ME, Chartier FL, et al. Boucher CA, et al. Among authors: carey n. Hum Mol Genet. 1995 Oct;4(10):1919-25. doi: 10.1093/hmg/4.10.1919. Hum Mol Genet. 1995. PMID: 8595416

6

Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period.

Martorell L, Martinez JM, Carey N, Johnson K, Baiget M. Martorell L, et al. Among authors: carey n. J Med Genet. 1995 Aug;32(8):593-6. doi: 10.1136/jmg.32.8.593. J Med Genet. 1995. PMID: 7473648 Free PMC article.

7

Direct molecular analysis of myotonic dystrophy in the German population: important considerations in genetic counselling.

Meiner A, Wolf C, Carey N, Okitsu A, Johnson K, Shelbourne P, Kunath B, Sauermann W, Thiele H, Kupferling P, et al. Meiner A, et al. Among authors: carey n. J Med Genet. 1995 Aug;32(8):645-9. doi: 10.1136/jmg.32.8.645. J Med Genet. 1995. PMID: 7473660 Free PMC article.

8

Myotonic disorders and periodic paralysis.

Carey N, Johnson KJ. Carey N, et al. Baillieres Clin Neurol. 1994 Aug;3(2):387-405. Baillieres Clin Neurol. 1994. PMID: 7952854 Review.

9

Meiotic drive at the myotonic dystrophy locus?

Carey N, Johnson K, Nokelainen P, Peltonen L, Savontaus ML, Juvonen V, Anvret M, Grandell U, Chotai K, Robertson E, et al. Carey N, et al. Nat Genet. 1994 Feb;6(2):117-8. doi: 10.1038/ng0294-117. Nat Genet. 1994. PMID: 8162064 No abstract available.

10

Decreased DMPK transcript levels in myotonic dystrophy 1 type IIA muscle fibers.

Eriksson M, Hedberg B, Carey N, Ansved T. Eriksson M, et al. Among authors: carey n. Biochem Biophys Res Commun. 2001 Sep 7;286(5):1177-82. doi: 10.1006/bbrc.2001.5516. Biochem Biophys Res Commun. 2001. PMID: 11527424

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