D. Iles

发表

Segregation of malignant hyperthermia, central core disease and chromosome 19 markers.

L. Bridges, A. Markham, R. Robinson, 1999, British journal of anaesthesia.

Segregation of malignant hyperthermia, central core disease and chromosome 19 markers.

L. Bridges, A. Markham, R. Robinson, 1999 .

Epigenetic allele silencing and variable penetrance of malignant hyperthermia susceptibility.

R. Robinson, D. Carpenter, M. Shaw, 2009, British journal of anaesthesia.

Investigation of a Family Following Fulminant Malignant Hyperthermia

H. T. ter Laak, R. Robinson, M. Snoeck, 2004, Journal of clinical neuromuscular disease.

Dinucleotide repeat polymorphism at the D19S191 locus.

B. Wieringa, J. Alleman, D. Iles, 1992, Nucleic acids research.

Analysis of a T-287C polymorphism in the tissue factor pathway inhibitor gene and identification of a repressor element in the promoter.

D. Iles, Ali Amini Nekoo, 2008, Thrombosis research.

Functional proteomics of BK potassium channels: defining the acute oxygen sensor.

C. Peers, D. Riccardi, P. Kemp, 2006, Novartis Foundation symposium.

Genetic variation in RYR1 and malignant hyperthermia phenotypes.

R. Robinson, D. Carpenter, M. Shaw, 2009, British journal of anaesthesia.

Implications of Recent Advances in the Understanding of Heritability for Neo-Darwinian Orthodoxy

David Miller, D. Iles, M. Brinkworth, 2012 .

The impact of maternal age on gene expression during the GV to MII transition in euploid human oocytes

E. Kanavakis, K. Pantos, G. Kokkali, 2021, Human reproduction.

siRNA knock-down of γ-glutamyl transpeptidase does not affect hypoxic K+ channel inhibition

C. Peers, P. Kemp, D. Iles, 2004 .

Refined genetic localization for central core disease.

F. Couch, J. Mulley, R. Gregg, 1993, American journal of human genetics.

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.

H. Willard, M. Phillips, B. Wieringa, 1990, American journal of human genetics.

Hemoxygenase-2 Is an Oxygen Sensor for a Calcium-Sensitive Potassium Channel

C. Peers, D. Riccardi, P. Kemp, 2004, Science.

Paternal DNA packaging in spermatozoa: more than the sum of its parts? DNA, histones, protamines and epigenetics.

David Miller, D. Iles, M. Brinkworth, 2010, Reproduction.

Endonuclease-sensitive regions of human spermatozoal chromatin are highly enriched in promoter and CTCF binding sequences.

S. Krawetz, A. Platts, David Miller, 2009, Genome research.

Multiple interacting gene products may influence susceptibility to malignant hyperthermia

R. Robinson, P. Hopkins, P. Halsall, 2000, Annals of human genetics.

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.

S. Scherer, L. Tsui, D. Weghuis, 1994, Human molecular genetics.

Evidence for genetic heterogeneity of malignant hyperthermia susceptibility.

T. Meitinger, A. Meindl, D. Schindelhauer, 1992, American journal of human genetics.

The testis as a conduit for genomic plasticity: an advanced interdisciplinary workshop.

D. Iles, M. Brinkworth, D. Miller, 2007, Biochemical Society transactions.

Key gene regulatory sequences with distinctive ontological signatures associate with differentially endonuclease-accessible mouse sperm chromatin.

David Miller, D. Iles, M. Brinkworth, 2011, Reproduction.

Can trophectoderm RNA analysis predict human blastocyst competency?

M. Tzetis, David Miller, H. Picton, 2019, Systems biology in reproductive medicine.

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.

B. Wieringa, R. Sengers, L. Heytens, 1992, Genomics.

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

A. Stewart, R. Robinson, P. Hopkins, 1997, American journal of human genetics.

Analysis of RYR1 Haplotype Profile in Patients with Malignant Hyperthermia

R. Robinson, D. Carpenter, M. Shaw, 2009, Annals of human genetics.

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

R. Tenconi, D. Smeets, M. Clementi, 1996, Human Genetics.

Characterization of the myotonic dystrophy region predicts multiple protein isoform–encoding mRNAs

C. Amemiya, G. Lennon, A. Carrano, 1992, Nature Genetics.

Potential sperm contributions to the murine zygote predicted by in silico analysis.

M. Tzetis, David Miller, D. Iles, 2017, Reproduction.

Genetic mapping of the β1- and γ-subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibility

A. Stewart, P. Hopkins, R. Sengers, 1993 .

Multipoint mapping of the central core disease locus.

C. Hübner, D. Maclennan, T. Grimm, 1993, Genomics.

A RYR1 mutation associated with recessive congenital myopathy and dominant malignant hyperthermia in Asian families

Azzam Ismail, R. Robinson, D. Carpenter, 2009, Muscle & nerve.

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

D. Weghuis, R. Sinke, M. Wakamori, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Oxygen sensing by human recombinant K+ channels: assessment of the use of stable cell lines.

C. Peers, P. Kemp, D. Iles, 2004, Methods in enzymology.

Nucleosomal chromatin in the mature sperm of Drosophila melanogaster

Abdul Hakim Elnfati, David Miller, D. Iles, 2015, Genomics data.

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.

D. Weghuis, B. Wieringa, D. Iles, 1993, Cytogenetics and cell genetics.

Properties of three COOH-terminal splice variants of a human cardiac L-type Ca2+-channel alpha1-subunit.

A. Schwartz, J. Mershon, U. Klöckner, 1997, The American journal of physiology.

In search of the acute oxygen sensor: functional proteomics and acute regulation of large-conductance, calcium-activated potassium channels by hemeoxygenase-2.

C. Peers, P. Kemp, D. Iles, 2006, Advances in experimental medicine and biology.