Kristiina Makkonen
kristiina.makkonen@utu.fi |
- Altered skull and bone morphology in hyperthyroid knock-in mice with TSHR M453T and D633H mutations (2024)
- Endocrine Abstracts
- Decoding SLC26A7'S role in congenital hypothyroidism: delayed onset, very large goiters, and thyrotropin dependent basolateral expression (2024)
- Endocrine Abstracts
- Identification of a stat3 mutation, P.THR716MET in two cases of very early-onset autoimmune hypothyroidism (2024)
- Endocrine Abstracts
- Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model (2024)
- JCI Insight
- Screening for Mutations in Isolated Central Hypothyroidism Reveals a Novel Mutation in Insulin Receptor Substrate 4 (2021)
- Frontiers in Endocrinology
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