Daniel Liedtke

Wuerzburg, BY, Germany

Last Updated: 09/26/2026

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Found 25 publications

FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.

FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.

Journal: medRxiv : the preprint server for health sciences

Published: April 10, 2026

AI-assisted phenotyping in a zebrafish hypophosphatasia model enables early and precise detection of skeletal alterations.

AI-assisted phenotyping in a zebrafish hypophosphatasia model enables early and precise detection of skeletal alterations.

Journal: Scientific reports

Published: May 23, 2025

Establishment of human periodontal ligament cell lines with ALPL mutations to mimic dental aspects of hypophosphatasia.

Establishment of human periodontal ligament cell lines with ALPL mutations to mimic dental aspects of hypophosphatasia.

Journal: Frontiers in cell and developmental biology

Published: February 07, 2025

Live-cell imaging reveals decreased cAMP in a PFE-associated c.1050-3C>G PTH1R cell model.

Live-cell imaging reveals decreased cAMP in a PFE-associated c.1050-3C>G PTH1R cell model.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: January 28, 2025

Machine learning predictions of unplanned readmissions using electronic medical records: Predictor importance across medical and surgical patient populations.

Machine learning predictions of unplanned readmissions using electronic medical records: Predictor importance across medical and surgical patient populations.

Journal: PloS one

Published: January 07, 2025

Understanding disorders of the human nervous system: How fish models reveal disease mechanisms from single molecules to behavior (part 2).

Understanding disorders of the human nervous system: How fish models reveal disease mechanisms from single molecules to behavior (part 2).

Journal: Development, growth & differentiation

Published: November 27, 2024

Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome.

Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome.

Journal: Human genomics

Published: January 26, 2024

Understanding disorders of the human nervous system: How fish models reveal disease mechanisms from single molecules to behavior (part 1).

Understanding disorders of the human nervous system: How fish models reveal disease mechanisms from single molecules to behavior (part 1).

Journal: Development, growth & differentiation

Published: October 02, 2023

Microarray expression profiling of fndc3a zebrafish mutants.

Microarray expression profiling of fndc3a zebrafish mutants.

Journal: microPublication biology

Published: August 19, 2022

Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish.

Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish.

Journal: International journal of molecular sciences

Published: July 26, 2022

Intrasexual cuticular hydrocarbon dimorphism in a wasp sheds light on hydrocarbon biosynthesis genes in Hymenoptera.

Intrasexual cuticular hydrocarbon dimorphism in a wasp sheds light on hydrocarbon biosynthesis genes in Hymenoptera.

Journal: Communications biology

Published: January 28, 2022

Zebrafish Embryos and Larvae as Alternative Animal Models for Toxicity Testing.

Zebrafish Embryos and Larvae as Alternative Animal Models for Toxicity Testing.

Journal: International journal of molecular sciences

Published: November 14, 2021

Showing 1-12 of 25

Last Updated: 09/26/2026