| Year |
Citation |
Score |
| 2016 |
Zhang S, Pondarre C, Pennarun G, Labussiere-Wallet H, Vera G, France B, Chansel M, Rouvet I, Revy P, Lopez B, Soulier J, Bertrand P, Callebaut I, de Villartay JP. A nonsense mutation in the DNA repair factor Hebo causes mild bone marrow failure and microcephaly. The Journal of Experimental Medicine. PMID 27185855 DOI: 10.1084/Jem.20151183 |
0.398 |
|
| 2013 |
Grabarz A, Guirouilh-Barbat J, Barascu A, Pennarun G, Genet D, Rass E, Germann SM, Bertrand P, Hickson ID, Lopez BS. 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. PMID 24095737 DOI: 10.1016/J.Celrep.2013.08.034 |
0.319 |
|
| 2012 |
Barascu A, Le Chalony C, Pennarun G, Genet D, Zaarour N, Bertrand P. Oxydative stress alters nuclear shape through lamins dysregulation: a route to senescence. Nucleus (Austin, Tex.). 3: 411-7. PMID 22895091 DOI: 10.4161/Nucl.21674 |
0.326 |
|
| 2012 |
Barascu A, Le Chalony C, Pennarun G, Genet D, Imam N, Lopez B, Bertrand P. Oxidative stress induces an ATM-independent senescence pathway through p38 MAPK-mediated lamin B1 accumulation. The Embo Journal. 31: 1080-94. PMID 22246186 DOI: 10.1038/Emboj.2011.492 |
0.332 |
|
| 2011 |
Laulier C, Barascu A, Guirouilh-Barbat J, Pennarun G, Le Chalony C, Chevalier F, Palierne G, Bertrand P, Verbavatz JM, Lopez BS. Bcl-2 inhibits nuclear homologous recombination by localizing BRCA1 to the endomembranes. Cancer Research. 71: 3590-602. PMID 21444675 DOI: 10.1158/0008-5472.Can-10-3119 |
0.325 |
|
| 2006 |
Zariwala MA, Leigh MW, Ceppa F, Kennedy MP, Noone PG, Carson JL, Hazucha MJ, Lori A, Horvath J, Olbrich H, Loges NT, Bridoux AM, Pennarun G, Duriez B, Escudier E, et al. 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. PMID 16858015 DOI: 10.1164/Rccm.200603-370Oc |
0.515 |
|
| 2005 |
Pennarun G, Granotier C, Gauthier LR, Gomez D, Hoffschir F, Mandine E, Riou JF, Mergny JL, Mailliet P, Boussin FD. 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. PMID 15735722 DOI: 10.1038/Sj.Onc.1208468 |
0.306 |
|
| 2005 |
Delgado JP, Parouchev A, Allain JE, Pennarun G, Gauthier LR, Dutrillaux AM, Dutrillaux B, Di Santo J, Capron F, Boussin FD, Weber A. Long-term controlled immortalization of a primate hepatic progenitor cell line after Simian virus 40 T-Antigen gene transfer. Oncogene. 24: 541-51. PMID 15608689 DOI: 10.1038/Sj.Onc.1208089 |
0.318 |
|
| 2002 |
Pennarun G, Bridoux AM, Escudier E, Dastot-Le Moal F, Cacheux V, Amselem S, Duriez B. 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. PMID 11867345 DOI: 10.1165/Ajrcmb.26.3.4738 |
0.581 |
|
| 2000 |
Pennarun G, Chapelin C, Escudier E, Bridoux AM, Dastot F, Cacheux V, Goossens M, Amselem S, Duriez B. 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. PMID 11153919 DOI: 10.1007/S004390000427 |
0.578 |
|
| 1999 |
Pennarun G, Escudier E, Chapelin C, Bridoux AM, Cacheux V, Roger G, Clément A, Goossens M, Amselem S, Duriez B. Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia. American Journal of Human Genetics. 65: 1508-19. PMID 10577904 DOI: 10.1086/302683 |
0.595 |
|
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