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Researcher
Nina Lambrechts
Profile
Projects
Publications
Activities
Awards & Distinctions
5
Results
2022
Identification and purification of human T cell precursors
Inge Van de Walle
Nina Lambrechts
Anaïs Derveeuw
Marieke Lavaert
Juliette Roels
Tom Taghon
Bookchapter
in
T-cell development : methods and protocols
2022
In vitro model systems to study human T cell development
Nina Lambrechts
Kai Ling Liang
Imke Velghe
Steven Strubbe
Anne-Catherine Dolens
Tom Taghon
Bookchapter
in
T-cell development : methods and protocols
2022
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
Toon Rosseel
Nina Lambrechts
Kirsten A. Wunderlich
Matias Wagner
Konstantinos Nikopoulos
Pernille Martens
Irina Balikova
et al.
A1
Journal Article
in
HUMAN MUTATION
2020
2019
Expansion of the role and functional characterization of a missense variant in CEP78 associated with cone-rod dystrophy and hearing loss
Giulia Ascari
Frank Peelman
Pietro Farinelli
Toon Rosseel
Nina Lambrechts
Irina Balikova
Lara Derycke
Gabriële Holtappels
Olga Krysko
Thalia Van Laethem
et al.
C3
Conference
2019
Expansion of the role and functional characterization of a missense variant in CEP78 associated with cone-rod dystrophy and hearing loss
Giulia Ascari
Frank Peelman
Nina Lambrechts
Thalia Van Laethem
Toon Rosseel
Pietro Farinelli
David Creytens
Irina Balikova
Jan Gerris
Claus Bachert
et al.
C3
Conference
2019