Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jean-Louis Fournier"'
Publikováno v:
Cybergeo (2012)
Externí odkaz:
https://doaj.org/article/dab788c93d6745debdf270f09dafec8c
Autor:
Jean-Louis Fournier
Muchas personas sienten cierta aversión a la aritmética, pues sus encuentros con esa disciplina nunca fueron un placer sino más bien una tortura. Para remediarlo, Jean-Louis Fournier te propone una insólita terapia de cálculos elementales y humo
Autor:
B. Leroy, Thierry Soussi, Jitka Malčíková, Rosa Ana Risques, Jean Louis Fournier, Tuomas Tikkanen
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2018, 39 (7), pp.925-933. ⟨10.1002/humu.23543⟩
Human Mutation, Wiley, 2018, 39 (7), pp.925-933. ⟨10.1002/humu.23543⟩
International audience; Accurate annotation of genomic variants in human diseases is essential to allow personalized medicine. Assessment of somatic and germline TP53 alterations has now reached the clinic and is required in several circumstances suc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee9a361d79e04ceb9d117ccef0414234
https://hal.sorbonne-universite.fr/hal-02318087
https://hal.sorbonne-universite.fr/hal-02318087
Autor:
Jean-Louis Fournier
Un padre scrittore. Un padre solo, vedovo, anziano. Una figlia che a trent'anni decide di uscire dal mondo, ritirarsi in un luogo remoto per darsi a una vita religiosa fatta di preghiera e di meditazione. Per la figlia quella ricerca di Dio è la con
Autor:
Jean-Louis Fournier
Publikováno v:
Quand j'étais petit, on m'a retiré de ma famille
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7c1558bf8c946b49edeaf086134a01b
https://doi.org/10.3917/ehesp.cadou.2015.01.0008
https://doi.org/10.3917/ehesp.cadou.2015.01.0008
Autor:
Gilberto Fronza, B. Leroy, Chikashi Ishioka, Thierry Soussi, Jean Louis Fournier, Alberto Inga, Paola Monti
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2013, 41 (D1), pp.D962-D969. ⟨10.1093/nar/gks1033⟩
Nucleic Acids Research, 2013, 41 (D1), pp.D962-D969. ⟨10.1093/nar/gks1033⟩
Nucleic Acids Research, Oxford University Press, 2013, 41 (D1), pp.D962-D969. ⟨10.1093/nar/gks1033⟩
Nucleic Acids Research, 2013, 41 (D1), pp.D962-D969. ⟨10.1093/nar/gks1033⟩
International audience; A novel resource centre for TP53 mutations and mutants has been developed (http://p53.fr). TP53 gene dysfunction can be found in the majority of human cancer types. The potential use of TP53 mutation as a biomarker for clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0152b9794752515f8592d995bb915a31
https://hal.sorbonne-universite.fr/hal-01590745/document
https://hal.sorbonne-universite.fr/hal-01590745/document
Autor:
Jean Michel Rubio-Nevado, Jean Louis Fournier, Linn Hjortsberg, Dalil Hamroun, Thierry Soussi, Christophe Béroud
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2010, 31 (9), pp.1020-1025. ⟨10.1002/humu.21313⟩
Human Mutation, 2010, 31 (9), pp.1020-1025. ⟨10.1002/humu.21313⟩
Human Mutation, Wiley, 2010, 31 (9), pp.1020-1025. ⟨10.1002/humu.21313⟩
Human Mutation, 2010, 31 (9), pp.1020-1025. ⟨10.1002/humu.21313⟩
International audience; Analysis of the literature reporting p53 mutations shows that 8% of report display typographical mistakes with a notable increase in recent years. These errors are sometimes isolated, but in some cases, they concern several or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa74032e1edcdce3e7b533b9f8a75446
https://hal-amu.archives-ouvertes.fr/hal-01681836
https://hal-amu.archives-ouvertes.fr/hal-01681836