Sylvia Bahring
Berlin, BE, Germany
Last Updated: 09/26/2026
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Found 13 publications
ADAM19 cleaves the PTH receptor and associates with brachydactyly type E.
Journal: Life science alliance
Published: September 27, 2023
Mutant phosphodiesterase 3A protects the kidney from hypertension-induced damage.
Journal: Kidney international
Published: February 14, 2023
Mutant Phosphodiesterase 3A Protects From Hypertension-Induced Cardiac Damage.
Journal: Circulation
Published: October 19, 2022
Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: March 05, 2020
Reorganization of inter-chromosomal interactions in the 2q37-deletion syndrome.
Journal: The EMBO journal
Published: December 06, 2016
Gene silencing and a novel monoallelic expression pattern in distinct CD177 neutrophil subsets.
Journal: The Journal of experimental medicine
Published: July 13, 2016
From phenotype to genotype: a glimpse behind the scenes of an unending story
Journal: Deutsche medizinische Wochenschrift (1946)
Published: December 18, 2015
Clinical effects of phosphodiesterase 3A mutations in inherited hypertension with brachydactyly.
Journal: Hypertension (Dallas, Tex. : 1979)
Published: June 13, 2015
PDE3A mutations cause autosomal dominant hypertension with brachydactyly.
Journal: Nature genetics
Published: August 18, 2014
Long non-coding RNA in health and disease.
Journal: Journal of molecular medicine (Berlin, Germany)
Published: November 25, 2013
Last Updated: 09/26/2026