Gaëlle Pennarun
Affiliations: | Université Paris-Est Créteil Val de Marne (UPEC) |
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"Gaëlle Pennarun"Parents
Sign in to add mentorSerge Amselem | grad student | 2002 | Université Paris-Est Créteil Val de Marne (UPEC) | |
(Etude des bases moléculaires des dyskinésies ciliaires primitives) |
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Publications
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Zhang S, Pondarre C, Pennarun G, et al. (2016) A nonsense mutation in the DNA repair factor Hebo causes mild bone marrow failure and microcephaly. The Journal of Experimental Medicine |
Grabarz A, Guirouilh-Barbat J, Barascu A, et al. (2013) A role for BLM in double-strand break repair pathway choice: prevention of CtIP/Mre11-mediated alternative nonhomologous end-joining. Cell Reports. 5: 21-8 |
Barascu A, Le Chalony C, Pennarun G, et al. (2012) Oxydative stress alters nuclear shape through lamins dysregulation: a route to senescence. Nucleus (Austin, Tex.). 3: 411-7 |
Barascu A, Le Chalony C, Pennarun G, et al. (2012) Oxidative stress induces an ATM-independent senescence pathway through p38 MAPK-mediated lamin B1 accumulation. The Embo Journal. 31: 1080-94 |
Laulier C, Barascu A, Guirouilh-Barbat J, et al. (2011) Bcl-2 inhibits nuclear homologous recombination by localizing BRCA1 to the endomembranes. Cancer Research. 71: 3590-602 |
Zariwala MA, Leigh MW, Ceppa F, et al. (2006) Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation. American Journal of Respiratory and Critical Care Medicine. 174: 858-66 |
Pennarun G, Granotier C, Gauthier LR, et al. (2005) Apoptosis related to telomere instability and cell cycle alterations in human glioma cells treated by new highly selective G-quadruplex ligands. Oncogene. 24: 2917-28 |
Delgado JP, Parouchev A, Allain JE, et al. (2005) Long-term controlled immortalization of a primate hepatic progenitor cell line after Simian virus 40 T-Antigen gene transfer. Oncogene. 24: 541-51 |
Pennarun G, Bridoux AM, Escudier E, et al. (2002) Isolation and expression of the human hPF20 gene orthologous to Chlamydomonas PF20: evaluation as a candidate for axonemal defects of respiratory cilia and sperm flagella. American Journal of Respiratory Cell and Molecular Biology. 26: 362-70 |
Pennarun G, Chapelin C, Escudier E, et al. (2000) The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia. Human Genetics. 107: 642-9 |