Insa Buers

Muenster, NW 48149, Germany

Last Updated: 09/26/2026

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Found 19 publications

Improved Reversion of Calcifications in Porcine Aortic Heart Valves Using Elastin-Targeted Nanoparticles.

Improved Reversion of Calcifications in Porcine Aortic Heart Valves Using Elastin-Targeted Nanoparticles.

Journal: International journal of molecular sciences

Published: September 29, 2023

CRLF1 and CLCF1 in Development, Health and Disease.

CRLF1 and CLCF1 in Development, Health and Disease.

Journal: International journal of molecular sciences

Published: December 30, 2021

Hereditary Disorders of Cardiovascular Calcification.

Hereditary Disorders of Cardiovascular Calcification.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: November 12, 2020

Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line.

Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line.

Journal: Stem cell research

Published: April 20, 2020

Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual.

Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual.

Journal: Stem cell research

Published: March 03, 2020

Crisponi/cold-induced sweating syndrome: Differential diagnosis, pathogenesis and treatment concepts.

Crisponi/cold-induced sweating syndrome: Differential diagnosis, pathogenesis and treatment concepts.

Journal: Clinical genetics

Published: June 20, 2019

Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses.

Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses.

Journal: Clinical genetics

Published: December 18, 2018

ENPP1-Fc prevents neointima formation in generalized arterial calcification of infancy through the generation of AMP.

ENPP1-Fc prevents neointima formation in generalized arterial calcification of infancy through the generation of AMP.

Journal: Experimental & molecular medicine

Published: May 08, 2018

Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.

Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.

Journal: American journal of human genetics

Published: April 07, 2018

MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum.

MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum.

Journal: Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research

Published: May 06, 2017

Mutations in CRLF1 cause familial achalasia.

Mutations in CRLF1 cause familial achalasia.

Journal: Clinical genetics

Published: September 30, 2016

Effects of Different Variants in the ENPP1 Gene on the Functional Properties of Ectonucleotide Pyrophosphatase/Phosphodiesterase Family Member 1.

Effects of Different Variants in the ENPP1 Gene on the Functional Properties of Ectonucleotide Pyrophosphatase/Phosphodiesterase Family Member 1.

Journal: Human mutation

Published: April 28, 2016

Showing 1-12 of 19

Last Updated: 09/26/2026