Daniel Liedtke

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Universitätsklinikum Essen Institut für Humangenetik

Germany

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Establishment of different cell culture and zebrafish models as a basis for the identification of new potential therapies for the hereditary disease hypophosphatasia

Open Date: 2017-01-01

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Articles (10)

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2025

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2025

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2025

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2025

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2025

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2025

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2024

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2024

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2024

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2023

Collaborators (2)

Felix Boschann

GERMANY

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Caroline Lekszas

GERMANY

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Daniel Liedtke

Research Interests

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Recent Grants

Articles (10)

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

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) preface

Establishment of human periodontal ligament cell lines with <i>ALPL</i> mutations to mimic dental aspects of hypophosphatasia

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

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 <i>MSGN1</i>, 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

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

Collaborators (2)

Felix Boschann

Caroline Lekszas

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