Iles DE - Search Results

1

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

2

High-resolution physical mapping of four microsatellite repeat markers near the RYR1 locus on chromosome 19q13.1 and apparent exclusion of the MHS locus from this region in two malignant hyperthermia susceptible families.

Iles DE, Segers B, Heytens L, Sengers RC, Wieringa B. Iles DE, et al. Genomics. 1992 Nov;14(3):749-54. doi: 10.1016/s0888-7543(05)80179-x. Genomics. 1992. PMID: 1427902

3

Refined localization of the alpha 1-subunit of the skeletal muscle L-type voltage-dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization.

Iles DE, Segers B, Olde Weghuis D, Suijkerbuijk R, Mikala G, Schwartz A, Wieringa B. Iles DE, et al. Genomics. 1994 Feb;19(3):561-3. doi: 10.1006/geno.1994.1106. Genomics. 1994. PMID: 8188298

4

Cloning, chromosomal localization, and functional expression of the alpha 1 subunit of the L-type voltage-dependent calcium channel from normal human heart.

Schultz D, Mikala G, Yatani A, Engle DB, Iles DE, Segers B, Sinke RJ, Weghuis DO, Klöckner U, Wakamori M, et al. Schultz D, et al. Among authors: iles de. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6228-32. doi: 10.1073/pnas.90.13.6228. Proc Natl Acad Sci U S A. 1993. PMID: 8392192 Free PMC article.

5

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

6

Dinucleotide repeat polymorphism at the D19S191 locus.

Iles DE, Segers B, de Jong P, Alleman J, Wieringa B. Iles DE, et al. Among authors: de jong p. Nucleic Acids Res. 1992 Mar 11;20(5):1170. Nucleic Acids Res. 1992. PMID: 1549505 Free PMC article. No abstract available.

7

Trinucleotide repeat polymorphism at the D19S190 locus.

Iles DE, Segers B, de Jong P, Alleman J, Wieringa B. Iles DE, et al. Among authors: de jong p. Nucleic Acids Res. 1992 Mar 11;20(5):1170. Nucleic Acids Res. 1992. PMID: 1549506 Free PMC article. No abstract available.

8

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

9

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.

10

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.

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