Yalan Hu — Amsterdam UMC research portal

Research activity per year

Research interests

congenital central hypothyroidism

specialisation

endocrinology

4 Article
1 Review article

Analysis of genes differentially expressed in the cortex of mice with the Tbl1xr1 Y446C/Y446C variant.
Hu, Y., Lauffer, P., Jongejan, A., Falize, K., Bruinstroop, E., van Trotsenburg, P., Fliers, E., Hennekam, R. C. & Boelen, A., 15 Nov 2024, In: Gene. 927, p. 148707 148707.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
Mutant Tbl1x male mice have a short life span and do not breed: unexpected findings
Hu, Y., Codner, G. F., Stewart, M., la Fleur, S. E., van Trotsenburg, P. A. S., Fliers, E., Hennekam, R. C. & Boelen, A., 1 Jul 2024, In: Journal of molecular endocrinology. 73, 1, e230116.
Research output: Contribution to journal › Article › Academic › peer-review
The role of transducin β-like 1 X-linked receptor 1 (TBL1XR1) in thyroid hormone metabolism and action in mice
Hu, Y., Falize, K., van Trotsenburg, A. S. P., Hennekam, R., Fliers, E., Bruinstroop, E. & Boelen, A., 2023, In: European thyroid journal. 12, 5, e230077.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

1 Citation (Scopus)
The role of WD40 repeat-containing proteins in endocrine (dys)function
Hu, Y., Bruinstroop, E., Hollenberg, A. N., Fliers, E. & Boelen, A., 1 Jul 2023, In: Journal of molecular endocrinology. 71, 1, e220217.
Research output: Contribution to journal › Review article › Academic › peer-review

Open Access

2 Citations (Scopus)
An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation
Hu, Y., Lauffer, P., Stewart, M., Codner, G., Mayerl, S., Heuer, H., Ng, L., Forrest, D., van Trotsenburg, P., Jongejan, A., Fliers, E., Hennekam, R. & Boelen, A., 25 Aug 2022, In: Human Molecular Genetics. 31, 17, p. 2951-2963 13 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

6 Citations (Scopus)