Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: PDIA3[original query] |
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Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients. Gene 2015 Jul 566 (2): 158-65. Gonzalez-Perez Paloma, Woehlbier Ute, Chian Ru-Ju, Sapp Peter, Rouleau Guy A, Leblond Claire S, Daoud Hussein, Dion Patrick A, Landers John E, Hetz Claudio, Brown Robert |
Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
The vitamin D receptor Taq I polymorphism is associated with reduced VDR and increased PDIA3 protein levels in human intestinal fibroblasts. The Journal of steroid biochemistry and molecular biology 2020 6 202 105720. Gisbert-Ferrándiz Laura, Cosin-Roger Jesus, Hernández Carlos, Macias-Ceja Dulce C, Ortiz-Masiá Dolores, Salvador Pedro, Wildenberg M E, Esplugues Juan V, Alós Rafael, Navarro Francisco, Calatayud Sara, Barrachina María |
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- Page last updated:Apr 22, 2024
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