Krisztina Fulop
Budapest, BU 1117, Hungary
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
Longitudinal Profiling of Plasma N-Glycomic Alterations in an STZ-Induced Mouse Model of Hyperglycemia.
Journal: International journal of molecular sciences
Published: January 23, 2026
Gram-Scale Synthesis of an Arylsulfonamide-Type Alkaline Phosphatase Inhibitor.
Journal: ChemMedChem
Published: September 23, 2025
Diabetes-induced vascular calcification is associated with low pyrophosphate and its oral supplementation prevents calcification in diabetic mice.
Journal: FEBS open bio
Published: May 08, 2025
Plasma Level of Pyrophosphate Is Low in Pseudoxanthoma Elasticum Owing to Mutations in the ABCC6 Gene, but It Does Not Correlate with ABCC6 Genotype.
Journal: Journal of clinical medicine
Published: November 04, 2022
Oral supplementation of inorganic pyrophosphate in pseudoxanthoma elasticum.
Journal: Experimental dermatology
Published: August 10, 2021
A New Zebrafish Model for Pseudoxanthoma Elasticum.
Journal: Frontiers in cell and developmental biology
Published: November 12, 2020
Creation of the first monoclonal antibody recognizing an extracellular epitope of hABCC6.
Journal: FEBS letters
Published: June 25, 2020
Pyrophosphate therapy prevents trauma-induced calcification in the mouse model of neurogenic heterotopic ossification.
Journal: Journal of cellular and molecular medicine
Published: April 21, 2020
Tissue-nonspecific alkaline phosphatase: a promising target for pseudoxanthoma elasticum therapy.
Journal: Annals of translational medicine
Published: January 05, 2018
The ABCC6 Transporter: A New Player in Biomineralization.
Journal: International journal of molecular sciences
Published: August 15, 2017
Analysis of pseudoxanthoma elasticum-causing missense mutants of ABCC6 in vivo; pharmacological correction of the mislocalized proteins.
Journal: The Journal of investigative dermatology
Published: July 22, 2013
Transcriptional regulation of the ABCC6 gene and the background of impaired function of missense disease-causing mutations.
Journal: Frontiers in genetics
Published: October 24, 2012
Last Updated: 09/26/2026