Suchergebnisse - "Löf, Christoffer"

PubPharm (40)

1

Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model

enthalten in: JCI insight | 2024

von Makkonen, K. | Jännäri, M. | Crisóstomo, L. | +22

2

The variant rs77559646 associated with aggressive prostate cancer disrupts ANO7 mRNA splicing and protein expression

enthalten in: Human molecular genetics | 2022

von Wahlström, G. | Heron, S. | Knuuttila, M. | +9

3

Congenital Hypothyroidism and Hyperthyroidism Alters Adrenal Gene Expression, Development, and Function

enthalten in: Thyroid : official journal of the American Thyroid Association | 2022

von Patyra, K. | Löf, C. | Jaeschke, H. | +19

4

Stromal interaction molecule 1 (STIM1) knock down attenuates invasion and proliferation and enhances the expression of thyroid-specific proteins in human follicular thyroid cancer cells

enthalten in: Cellular and molecular life sciences : CMLS | 2021

von Asghar, M. | Lassila, T. | Paatero, I. | +8

5

Stromal interaction molecule 1 (STIM1) knock down attenuates invasion and proliferation and enhances the expression of thyroid-specific proteins in human follicular thyroid cancer cells

enthalten in: Cellular and molecular life sciences | 2021

von Asghar, M. | Lassila, T. | Paatero, I. | +8

6

Stromal interaction molecule 1 (STIM1) knock down attenuates invasion and proliferation and enhances the expression of thyroid-specific proteins in human follicular thyroid cancer cells

enthalten in: Cellular and molecular life sciences | 2021

von Asghar, M. | Lassila, T. | Paatero, I. | +8

7

Stromal Interaction Molecule 1 (STIM1) Knock-down Attenuates Migration and Proliferation and Enhances the Expression of Thyroid Specific Proteins in Human Follicular Thyroid Cancer Cells.

enthalten in: ResearchSquare.com | 2021

von Asghar, M. | Lassila, T. | Paatero, I. | +8

8

Hyperthyroidism and Papillary Thyroid Carcinoma in Thyrotropin Receptor D633H Mutant Mice

enthalten in: Thyroid : official journal of the American Thyroid Association | 2018

von Jaeschke, H. | Undeutsch, H. | Patyra, K. | +10

9

Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism

enthalten in: JCI insight | 2018

von Cangul, H. | Liao, X. | Schoenmakers, E. | +25

10

Partial thyrocyte-specific Gαs deficiency leads to rapid-onset hypothyroidism, hyperplasia, and papillary thyroid carcinoma-like lesions in mice

enthalten in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2018

von Patyra, K. | Jaeschke, H. | Löf, C. | +11