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Kermasson, Laëtitia
63
results:
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Online (63)
Mediatypes
Articles (Online) (14)
OpenAccess-fulltext (49)
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1
Characterization of novel mutations in the TEL-patch domain..:
Bertrand, Alexis
;
Ba, Ibrahima
;
Kermasson, Laëtitia
...
Human Molecular Genetics. , 2024
Link:
https://doi.org/10.1093/..
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2
DCLRE1B/Apollo germline mutations associated with renal cel..:
Bories, Charlie
;
Lejour, Thomas
;
Adolphe, Florine
...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870 (2024) 4 - p. 167107 , 2024
Link:
https://doi.org/10.1016/..
?
3
Publisher Correction: Somatic genetic rescue of a germline ..:
Tan, Shengjiang
;
Kermasson, Laëtitia
;
Hilcenko, Christine
...
Nature Communications. 13 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
4
Inherited human Apollo deficiency causes severe bone marrow..:
Kermasson, Laëtitia
;
Churikov, Dmitri
;
Awad, Aya
...
Blood. 139 (2022) 16 - p. 2427-2440 , 2022
Link:
https://doi.org/10.1182/..
?
5
Somatic genetic rescue of a germline ribosome assembly defe..:
Tan, Shengjiang
;
Kermasson, Laëtitia
;
Hilcenko, Christine
...
Nature Communications. 12 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
6
A Disease-Causing Single Amino Acid Deletion in the Coiled-..:
Chansel-Da Cruz, Marie
;
Hohl, Marcel
;
Ceppi, Ilaria
...
Cell Reports. 33 (2020) 13 - p. 108559 , 2020
Link:
https://doi.org/10.1016/..
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7
NHP2 deficiency impairs rRNA biogenesis and causes pulmonar..:
Revy, Patrick
;
Kannengiesser, Caroline
;
Callebaut, Isabelle
...
Human Molecular Genetics. 29 (2020) 6 - p. 907-922 , 2020
Link:
https://doi.org/10.1093/..
?
8
Impaired telomere integrity and rRNA biogenesis in PARN‐def..:
Benyelles, Maname
;
Episkopou, Harikleia
;
O'Donohue, Marie‐Françoise
...
EMBO Molecular Medicine. 11 (2019) 7 - p. , 2019
Link:
https://doi.org/10.15252..
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9
Sonic Hedgehog Is a Remotely Produced Cue that Controls Axo..:
Peng, Jimmy
;
Fabre, Pierre J.
;
Dolique, Tiphaine
...
Neuron. 97 (2018) 2 - p. 326-340.e4 , 2018
Link:
https://doi.org/10.1016/..
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10
PAXX and Xlf interplay revealed by impaired CNS development..:
Abramowski, Vincent
;
Etienne, Olivier
;
Elsaid, Ramy
...
Cell Death & Differentiation. 25 (2017) 2 - p. 444-452 , 2017
Link:
https://doi.org/10.1038/..
?
11
Mutations of the RTEL1 Helicase in a Hoyeraal-Hreidarsson S..:
Jullien, Laurent
;
Kannengiesser, Caroline
;
Kermasson, Laetitia
...
Human Mutation. 37 (2016) 5 - p. 469-472 , 2016
Link:
https://doi.org/10.1002/..
?
12
Characterization of an A-kinase anchoring protein-like sugg..:
Bandje, Kossiwa
;
Naissant, Bernina
;
Bigey, Pascal
...
Malaria Journal. 15 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1186/..
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13
Extended clinical and genetic spectrum associated with bial..:
Touzot, Fabien
;
Kermasson, Laetitia
;
Jullien, Laurent
...
Blood Advances. 1 (2016) 1 - p. 36-46 , 2016
Link:
https://doi.org/10.1182/..
?
14
An in vivo genetic reversion highlights the crucial role of..:
Le Guen, Tangui
;
Touzot, Fabien
;
André-Schmutz, Isabelle
...
Journal of Allergy and Clinical Immunology. 136 (2015) 6 - p. 1619-1626.e5 , 2015
Link:
https://doi.org/10.1016/..
?
15
Inherited human Apollo deficiency causes severe bone marrow..:
Kermasson, Laëtitia
;
Churikov, Dmitri
;
Awad, Aya
...
info:eu-repo/semantics/altIdentifier/doi/10.1182/blood.2021010791. , 2022
Link:
https://hal.science/hal-..
1-15