Iles DE - Search Results

1

Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involved.

Mammi I, Iles DE, Smeets D, Clementi M, Tenconi R. Mammi I, et al. Among authors: iles de. Hum Genet. 1996 Sep;98(3):317-20. doi: 10.1007/s004390050214. Hum Genet. 1996. PMID: 8707301 Free article.

2

Localization of the gene encoding the alpha 2/delta-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families.

Iles DE, Lehmann-Horn F, Scherer SW, Tsui LC, Olde Weghuis D, Suijkerbuijk RF, Heytens L, Mikala G, Schwartz A, Ellis FR, et al. Iles DE, et al. Hum Mol Genet. 1994 Jun;3(6):969-75. doi: 10.1093/hmg/3.6.969. Hum Mol Genet. 1994. PMID: 7951247

3

Genetic mapping of the beta 1- and gamma-subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibility.

Iles DE, Segers B, Sengers RC, Monsieurs K, Heytens L, Halsall PJ, Hopkins PM, Ellis FR, Hall-Curran JL, Stewart AD, et al. Iles DE, et al. Hum Mol Genet. 1993 Jul;2(7):863-8. doi: 10.1093/hmg/2.7.863. Hum Mol Genet. 1993. PMID: 8395940

4

Evidence for genetic heterogeneity of malignant hyperthermia susceptibility.

Deufel T, Golla A, Iles D, Meindl A, Meitinger T, Schindelhauer D, DeVries A, Pongratz D, MacLennan DH, Johnson KJ, et al. Deufel T, et al. Am J Hum Genet. 1992 Jun;50(6):1151-61. Am J Hum Genet. 1992. PMID: 1598899 Free PMC article.

5

The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree.

Adeokun AM, West SP, Ellis FR, Halsall PJ, Hopkins PM, Foroughmand AM, Iles DE, Robinson RL, Stewart AD, Curran JL. Adeokun AM, et al. Among authors: iles de. Am J Hum Genet. 1997 Apr;60(4):833-41. Am J Hum Genet. 1997. PMID: 9106529 Free PMC article.

6

Multiple interacting gene products may influence susceptibility to malignant hyperthermia.

Robinson RL, Curran JL, Ellis FR, Halsall PJ, Hall WJ, Hopkins PM, Iles DE, West SP, Shaw MA. Robinson RL, et al. Among authors: iles de. Ann Hum Genet. 2000 Jul;64(Pt 4):307-20. doi: 10.1017/S0003480000008186. Ann Hum Genet. 2000. PMID: 11415515

7

Refined genetic localization for central core disease.

Mulley JC, Kozman HM, Phillips HA, Gedeon AK, McCure JA, Iles DE, Gregg RG, Hogan K, Couch FJ, MacLennan DH, et al. Mulley JC, et al. Among authors: iles de. Am J Hum Genet. 1993 Feb;52(2):398-405. Am J Hum Genet. 1993. PMID: 8430700 Free PMC article.

8

The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.

MacKenzie AE, Korneluk RG, Zorzato F, Fujii J, Phillips M, Iles D, Wieringa B, Leblond S, Bailly J, Willard HF, et al. MacKenzie AE, et al. Am J Hum Genet. 1990 Jun;46(6):1082-9. Am J Hum Genet. 1990. PMID: 1971150 Free PMC article.

9

Localization of the gamma-subunit of the skeletal muscle L-type voltage-dependent calcium channel gene (CACNLG) to human chromosome band 17q24 by in situ hybridization and identification of a polymorphic repetitive DNA sequence at the gene locus.

Iles DE, Segers B, Weghuis DO, Suikerbuijk R, Wieringa B. Iles DE, et al. Cytogenet Cell Genet. 1993;64(3-4):227-30. doi: 10.1159/000133583. Cytogenet Cell Genet. 1993. PMID: 8404045

10

Analysis of RYR1 haplotype profile in patients with malignant hyperthermia.

Carpenter D, Morris A, Robinson RL, Booms P, Iles D, Halsall PJ, Steele D, Hopkins PM, Shaw MA. Carpenter D, et al. Ann Hum Genet. 2009 Jan;73(1):10-8. doi: 10.1111/j.1469-1809.2008.00482.x. Epub 2008 Oct 15. Ann Hum Genet. 2009. PMID: 18945287

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