Pietro Farinelli

3PUBLICATIONS
27CO-AUTHORS
Cell and nuclear divisionOptical technologyMolecular targets
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Publications (3)

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|Jan 31, 2020
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility.

Giulia Ascari, Frank Peelman, Pietro Farinelli

|Apr 24, 2019
A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa.

Virginie G Peter, Konstantinos Nikopoulos, Mathieu Quinodoz

|Dec 15, 2017
IFT20 modulates ciliary PDGFRα signaling by regulating the stability of Cbl E3 ubiquitin ligases.

Fabian Marc Schmid, Kenneth Bødtker Schou, Martin Juel Vilhelm

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Frequent Collaborators

2 joint publications

Carlo Rivolta

1 joint publications

Martin Juel Vilhelm

1 joint publications

Søren Tvorup Christensen

1 joint publications

Virginie G Peter

1 joint publications

Mathieu Quinodoz

1 joint publications

Andrea Superti-Furga

1 joint publications

Giulia Ascari

1 joint publications

Frank Peelman

1 joint publications

Toon Rosseel

1 joint publications

Nina Lambrechts

Frequent Collaborators

2 joint publications

Carlo Rivolta

1 joint publications

Martin Juel Vilhelm

1 joint publications

Søren Tvorup Christensen

1 joint publications

Virginie G Peter

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