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G protein-coupled receptor (GPCR) gene variants and human genetic disease.
Thompson MD, Percy ME, Cole DEC, Bichet DG, Hauser AS, Gorvin CM. Thompson MD, et al. Among authors: cole dec. Crit Rev Clin Lab Sci. 2024 Mar 18:1-30. doi: 10.1080/10408363.2023.2286606. Online ahead of print. Crit Rev Clin Lab Sci. 2024. PMID: 38497103 Review.
Genetic variants in the vitamin D pathway and their association with vitamin D metabolite levels: Detailed studies of an inner-city pediatric population suggest a modest but significant effect in early childhood.
Fu L, Wong BYL, Li Z, Horst RL, Williams R, Lee B, Miller J, Carpenter TO, Cole DEC. Fu L, et al. Among authors: cole dec. J Steroid Biochem Mol Biol. 2023 Oct;233:106369. doi: 10.1016/j.jsbmb.2023.106369. Epub 2023 Jul 23. J Steroid Biochem Mol Biol. 2023. PMID: 37490983
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders.
Canaff L, Guarnieri V, Kim Y, Wong BYL, Nolin-Lapalme A, Cole DEC, Minisola S, Eller-Vainicher C, Cetani F, Repaci A, Turchetti D, Corbetta S, Scillitani A, Goltzman D. Canaff L, et al. Among authors: cole dec. Eur J Endocrinol. 2022 Feb 4;186(3):351-366. doi: 10.1530/EJE-21-0433. Eur J Endocrinol. 2022. PMID: 35038313 Free PMC article.
Parathyroid carcinoma.
Salcuni AS, Cetani F, Guarnieri V, Nicastro V, Romagnoli E, de Martino D, Scillitani A, Cole DEC. Salcuni AS, et al. Among authors: cole dec. Best Pract Res Clin Endocrinol Metab. 2018 Dec;32(6):877-889. doi: 10.1016/j.beem.2018.11.002. Epub 2018 Dec 1. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30551989 Review.
Stage Dependence, Cell-Origin Independence, and Prognostic Capacity of Serum Glycan Fucosylation, β1-4 Branching, β1-6 Branching, and α2-6 Sialylation in Cancer.
Ferdosi S, Rehder DS, Maranian P, Castle EP, Ho TH, Pass HI, Cramer DW, Anderson KS, Fu L, Cole DEC, Le T, Wu X, Borges CR. Ferdosi S, et al. Among authors: cole dec. J Proteome Res. 2018 Jan 5;17(1):543-558. doi: 10.1021/acs.jproteome.7b00672. Epub 2017 Nov 21. J Proteome Res. 2018. PMID: 29129073 Free PMC article.
MEN1 gene mutation with parathyroid carcinoma: first report of a familial case.
Cinque L, Sparaneo A, Salcuni AS, de Martino D, Battista C, Logoluso F, Palumbo O, Cocchi R, Maiello E, Graziano P, Hendy GN, Cole DEC, Scillitani A, Guarnieri V. Cinque L, et al. Among authors: cole dec. Endocr Connect. 2017 Nov;6(8):886-891. doi: 10.1530/EC-17-0207. Epub 2017 Nov 2. Endocr Connect. 2017. PMID: 29097378 Free PMC article.
141 results