Ilona Zvetkova
Cambridge, ENG CB20QQ, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
Germline variants in UHRF1 are associated with multilocus imprinting disturbance in humans and mice.
Germline variants in UHRF1 are associated with multilocus imprinting disturbance in humans and mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: August 18, 2025
The gastrointestinal tract is a major source of the acute metformin-stimulated rise in GDF15.
Journal: Scientific reports
Published: November 23, 2023
Overexpression of Igf2-derived Mir483 inhibits Igf1 expression and leads to developmental growth restriction and metabolic dysfunction in mice.
Journal: Cell reports
Published: January 10, 2023
Combined genetic deletion of GDF15 and FGF21 has modest effects on body weight, hepatic steatosis and insulin resistance in high fat fed mice.
Journal: Molecular metabolism
Published: June 18, 2022
Murine neuronatin deficiency is associated with a hypervariable food intake and bimodal obesity.
Journal: Scientific reports
Published: May 15, 2021
Mesenchyme-derived IGF2 is a major paracrine regulator of pancreatic growth and function.
Journal: PLoS genetics
Published: April 29, 2020
Truncation of Pik3r1 causes severe insulin resistance uncoupled from obesity and dyslipidaemia by increased energy expenditure.
Journal: Molecular metabolism
Published: February 06, 2020
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.
Journal: JCI insight
Published: January 04, 2018
Trim28 Haploinsufficiency Triggers Bi-stable Epigenetic Obesity.
Journal: Cell
Published: July 30, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026