E-LIB Suche - Ergebnisse für: Beleggia, Filippo

1

An inducible Cd79b mutation confers ibrutinib sensitivity i..:

Flümann, Ruth ; Hansen, Julia ; Meinel, Jörn...
Blood Advances. 8 (2024) 5 - p. 1063-1074 , 2024

Link: https://doi.org/10.1182/..

2

wnt10a is required for zebrafish median fin fold maintenanc..:

Benard, Erica L. ; Küçükaylak, Ismail ; Hatzold, Julia...
Developmental Dynamics. , 2023

Link: https://doi.org/10.1002/..

3

Distinct Genetically Determined Origins of Myd88/BCL2-Drive..:

Flümann, Ruth ; Hansen, Julia ; Pelzer, Benedikt W....
Blood Cancer Discovery. 4 (2022) 1 - p. 78-97 , 2022

Link: https://doi.org/10.1158/..

4

Ferroptosis response segregates small cell lung cancer (SCL..:

Bebber, Christina M. ; Thomas, Emily S. ; Stroh, Jenny...
Nature Communications. 12 (2021) 1 - p. , 2021

Link: https://doi.org/10.1038/..

5

Human RAD50 deficiency: Confirmation of a distinctive pheno..:

Ragamin, Aviël ; Yigit, Gökhan ; Bousset, Kristine...
American Journal of Medical Genetics Part A. 182 (2020) 6 - p. 1378-1386 , 2020

Link: https://doi.org/10.1002/..

6

UBQLN4 Represses Homologous Recombination and Is Overexpres..:

Jachimowicz, Ron D. ; Beleggia, Filippo ; Isensee, Jörg...
Cell. 176 (2019) 3 - p. 505-519.e22 , 2019

Link: https://doi.org/10.1016/..

7

The Cdkn1aSUPER Mouse as a Tool to Study p53-Mediated Tumor..:

Torgovnick, Alessandro ; Heger, Jan Michel ; Liaki, Vasiliki...
Cell Reports. 25 (2018) 4 - p. 1027-1039.e6 , 2018

Link: https://doi.org/10.1016/..

8

Targeting a non-oncogene addiction to the ATR/CHK1 axis for..:

Doerr, Fabian ; George, Julie ; Schmitt, Anna...
Scientific Reports. 7 (2017) 1 - p. , 2017

Link: https://doi.org/10.1038/..

9

Heterozygous HNRNPU variants cause early onset epilepsy and..:

Bramswig, Nuria C. ; Lüdecke, Hermann-Josef ; Hamdan, Fadi F....
Human Genetics. 136 (2017) 7 - p. 821-834 , 2017

Link: https://doi.org/10.1007/..

10

Two mouse models reveal an actionable PARP1 dependence in a..:

Knittel, Gero ; Rehkämper, Tim ; Korovkina, Darya...
Nature Communications. 8 (2017) 1 - p. , 2017

Link: https://doi.org/10.1038/..

11

New gain-of-function mutation shows CACNA1D as recurrently ..:

Pinggera, Alexandra ; Mackenroth, Luisa ; Rump, Andreas...
Human Molecular Genetics. 26 (2017) 15 - p. 2923-2932 , 2017

Link: https://doi.org/10.1093/..

12

Tumor suppression in basal keratinocytes via dual non-cell-..:

Hatzold, Julia ; Beleggia, Filippo ; Herzig, Hannah...
eLife. 5 (2016) - p. , 2016

Link: https://doi.org/10.7554/..

13

Smith–Kingsmore syndrome: A third family with the MTOR muta..:

Moosa, Shahida ; Böhrer‐Rabel, Helena ; Altmüller, Janine...
American Journal of Medical Genetics Part A. 173 (2016) 1 - p. 264-267 , 2016

Link: https://doi.org/10.1002/..

14

An unusual presentation of Kabuki syndrome with orbital cys..:

Bögershausen, Nina ; Altunoglu, Umut ; Beleggia, Filippo...
American Journal of Medical Genetics Part A. 170 (2016) 12 - p. 3282-3288 , 2016

Link: https://doi.org/10.1002/..

15

Papillon–Lefèvre syndrome: report of six patients and ident..:

Tekin, Burak ; Yucelten, Deniz ; Beleggia, Filippo..
International Journal of Dermatology. 55 (2016) 8 - p. 898-902 , 2016

Link: https://doi.org/10.1111/..