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Author/Creator Stracker, Travis H

1. Centrosome defects cause microcephaly by activating the 53BP1‐USP28‐TP53 mitotic surveillance pathway. (23rd November 2020)

Authors:
Phan, Thao P; Maryniak, Aubrey L; Boatwright, Christina A; Lee, Junsu; Atkins, Alisa; Tijhuis, Andrea; Spierings, Diana CJ; Bazzi, Hisham; Foijer, Floris; Jordan, Philip W; Stracker, Travis H; Holland, Andrew J
Journal:
EMBO journal
Issue:
Volume 40:Number 1(2021)
Page Start:
n/a
Record Type:
Journal Article
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2. Functional analysis of TLK2 variants and their proximal interactomes implicates impaired kinase activity and chromatin maintenance defects in their pathogenesis. Issue 2 (15th December 2020)

Authors:
Pavinato, Lisa; Villamor-Payà, Marina; Sanchiz-Calvo, Maria; Andreoli, Cristina; Gay, Marina; Vilaseca, Marta; Arauz-Garofalo, Gianluca; Ciolfi, Andrea; Bruselles, Alessandro; Pippucci, Tommaso; Prota, Valentina; Carli, Diana; Giorgio, Elisa; Radio, Francesca Clementina; Antona, Vincenzo; Giuffrè...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 2(2022)
Page Start:
170
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. GEMC1 is a critical regulator of multiciliated cell differentiation. (1st March 2016)

Authors:
Terré, Berta; Piergiovanni, Gabriele; Segura‐Bayona, Sandra; Gil‐Gómez, Gabriel; Youssef, Sameh A; Attolini, Camille Stephan‐Otto; Wilsch‐Bräuninger, Michaela; Jung, Carole; Rojas, Ana M; Marjanović, Marko; Knobel, Philip A; Palenzuela, Lluís; López‐Rovira, Teresa; Forrow, Stephen; Huttner, Wiela...
Journal:
EMBO journal
Issue:
Volume 35:Number 9(2016)
Page Start:
942
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗