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Methods in Molecular Biology (Clifton, N.J.)|September 17, 2017
Identification of Genetic Disorders Causing Disruption of Selenoprotein BiosynthesisErik Schoenmakers, Krishna Chatterjee
International Journal of Molecular Sciences|December 10, 2021
Human Genetic Disorders Resulting in Systemic Selenoprotein DeficiencyErik Schoenmakers, Krishna Chatterjee
Antioxidants & Redox Signaling|April 17, 2020
Human Disorders Affecting the Selenocysteine Incorporation Pathway Cause Systemic Selenoprotein DeficiencyErik Schoenmakers, Krishna Chatterjee
Genomics|November 13, 2003
Controlled transgene dosage and PAC-mediated transgenesis in mice using a chromosomal vectorThierry Voet, Erik Schoenmakers, Sebastien Carpentier, et al.
The Biochemical Journal|December 18, 2001
Comparative analysis of the influence of the high-mobility group box 1 protein on DNA binding and transcriptional activation by the androgen, glucocorticoid, progesterone and mineralocorticoid receptorsGuy Verrijdt, Annemie Haelens, Erik Schoenmakers, et al.
BMJ Case Reports|May 19, 2012
Resistance to thyroid hormone--an incidental findingDonna Chantler, Carla Moran, Erik Schoenmakers, et al.
Clinical Endocrinology|August 23, 2022
Genetic disorders of thyroid development, hormone biosynthesis and signallingCarla Moran, Nadia Schoenmakers, W Edward Visser, et al.
Clinical Endocrinology|December 31, 2015
Nephrogenic syndrome of inappropriate antidiuresis secondary to an activating mutation in the arginine vasopressin receptor AVPR2Andrew S Powlson, Benjamin G Challis, David J Halsall, et al.
Thyroid : Official Journal of the American Thyroid Association|November 22, 2021
Brief Report: A Novel Sodium/Iodide Symporter Mutation, S356F, Causing Congenital HypothyroidismHarsh Durgia, Adeline K Nicholas, Erik Schoenmakers, et al.
The Journal of Clinical Endocrinology and Metabolism|May 21, 2010
Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidismMireille Castanet, Uma Mallya, Maura Agostini, et al.
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