FOXE1 susceptibility polymorphisms and functional characterization of rare DUOX2 variants provide new insights into congenital hypothyroidism with thyroid dysgenesis.

Brust ES, Caso GF, de Sá Suetsugu RC, de Oliveira PR, Lambiasi GTM, de Oliveira Cerqueira TL, Amorim T, Medeiros-Neto G, Friguglietti CU, Deprá I, Iessi MRG, Nogueira CR, Padua LMS, Sgarbi JA, Koyama FC, Camargo AA, Santos FFD, Rego FORD, Galante PAF, Silva KSFE, Ramos HE, de Rubio IGS

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DOI: 10.1016/j.mce.2026.112923
Published: 2026 Sep 23
Container: Molecular and cellular endocrinology
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1016/j.mce.2026.112923,
  title = {FOXE1 susceptibility polymorphisms and functional characterization of rare DUOX2 variants provide new insights into congenital hypothyroidism with thyroid dysgenesis.},
  author = {Brust ES and Caso GF and de Sá Suetsugu RC and de Oliveira PR and Lambiasi GTM and de Oliveira Cerqueira TL and Amorim T and Medeiros-Neto G and Friguglietti CU and Deprá I and Iessi MRG and Nogueira CR and Padua LMS and Sgarbi JA and Koyama FC and Camargo AA and Santos FFD and Rego FORD and Galante PAF and Silva KSFE and Ramos HE and de Rubio IGS},
  year = {2026},
  journal = {Molecular and cellular endocrinology},
  doi = {10.1016/j.mce.2026.112923},
  url = {https://doi.org/10.1016/j.mce.2026.112923}
}

RIS

TY  - JOUR
TI  - FOXE1 susceptibility polymorphisms and functional characterization of rare DUOX2 variants provide new insights into congenital hypothyroidism with thyroid dysgenesis.
AU  - Brust ES
AU  - Caso GF
AU  - de Sá Suetsugu RC
AU  - de Oliveira PR
AU  - Lambiasi GTM
AU  - de Oliveira Cerqueira TL
AU  - Amorim T
AU  - Medeiros-Neto G
AU  - Friguglietti CU
AU  - Deprá I
AU  - Iessi MRG
AU  - Nogueira CR
AU  - Padua LMS
AU  - Sgarbi JA
AU  - Koyama FC
AU  - Camargo AA
AU  - Santos FFD
AU  - Rego FORD
AU  - Galante PAF
AU  - Silva KSFE
AU  - Ramos HE
AU  - de Rubio IGS
PY  - 2026
JO  - Molecular and cellular endocrinology
DO  - 10.1016/j.mce.2026.112923
UR  - https://doi.org/10.1016/j.mce.2026.112923
ER  -

APA

ES, B., GF, C., RC, D. S. S., PR, D. O., GTM, L., TL, D. O. C., T, A., G, M., CU, F., I, D., MRG, I., CR, N., LMS, P., JA, S., FC, K., AA, C., FFD, S., FORD, R., PAF, G., KSFE, S., HE, R., & IGS, D. R. (2026). FOXE1 susceptibility polymorphisms and functional characterization of rare DUOX2 variants provide new insights into congenital hypothyroidism with thyroid dysgenesis.. Molecular and cellular endocrinology. https://doi.org/10.1016/j.mce.2026.112923

Source records

pubmed · retrieved 2026-09-25T03:53:53.974Z