Krzysztof Jagla

7PUBLICATIONS
10CO-AUTHORS
Medical devicesEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesMechanobiologyRegenerative medicine (incl. stem cells)
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Publications (7)

|May 13, 2026
Drosophila ryanodine receptor gene triggers functional and developmental muscle properties and could be used to assess the impact of human RYR1 mutations.

|Feb 28, 2023
Deregulations of miR-1 and its target Multiplexin promote dilated cardiomyopathy associated with myotonic dystrophy type 1.

Anissa Souidi, Masayuki Nakamori, Monika Zmojdzian

|Apr 16, 2021
The relationship between muscle stem cells and motor neurons.

Monika Zmojdzian, Krzysztof Jagla

|Feb 01, 2020
Drosophila adult muscle precursor cells contribute to motor axon pathfinding and proper innervation of embryonic muscles.

Guillaume Lavergne, Monika Zmojdzian, Jean Philippe Da Ponte

|Dec 13, 2019
Straightjacket/α2δ3 deregulation is associated with cardiac conduction defects in myotonic dystrophy type 1.

Emilie Auxerre-Plantié, Masayuki Nakamori, Yoan Renaud

|May 03, 2018
Bruno-3 regulates sarcomere component expression and contributes to muscle phenotypes of myotonic dystrophy type 1.

Lucie Picchio, Vincent Legagneux, Stephane Deschamps

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Frequent Collaborators

4 joint publications

Monika Zmojdzian

3 joint publications

Teresa Jagla

1 joint publications

Lucie Picchio

1 joint publications

Vincent Legagneux