Zobrazeno 1 - 8
of 8
pro vyhledávání: '"MESH: Proteins / genetics"'
Autor:
Stephen P. Jackson, Mareike Herzog, Alejandra Bruna, Luca Pellegrini, Violeta Serra, Mark J. O'Connor, Zhongwu Lai, Chloé Lescale, Jacqueline J.L. Jacobs, Fengtang Yang, Jonathan Lam, Matylda Sczaniecka-Clift, Abigail Shea, Carlos Caldas, Matthias Ostermaier, Gabriel Balmus, Julia Coates, Wenming Wei, Inge de Krijger, Yaron Galanty, Mukerrem Demir, Ludovic Deriano, Petra Beli, Domenic Pilger, Harveer Dev, Rimma Belotserkovskaya, Alistair Martin, Beiyuan Fu, Ting-Wei Will Chiang, Qian Wu
Publikováno v:
Nature Cell Biology
Nature Cell Biology, 2018, 20 (8), pp.954-965. ⟨10.1038/s41556-018-0140-1⟩
Nature cell biology
Nature Cell Biology, Nature Publishing Group, 2018, 20 (8), pp.954-965. ⟨10.1038/s41556-018-0140-1⟩
Nature Cell Biology, 2018, 20 (8), pp.954-965. ⟨10.1038/s41556-018-0140-1⟩
Nature cell biology
Nature Cell Biology, Nature Publishing Group, 2018, 20 (8), pp.954-965. ⟨10.1038/s41556-018-0140-1⟩
International audience; BRCA1 deficiencies cause breast, ovarian, prostate and other cancers, and render tumours hypersensitive to poly(ADP-ribose) polymerase (PARP) inhibitors. To understand the resistance mechanisms, we conducted whole-genome CRISP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94c03882fb1aad0056e71d15c34e8ed4
https://www.repository.cam.ac.uk/handle/1810/282947
https://www.repository.cam.ac.uk/handle/1810/282947
Autor:
Vincent Caval, J Thalmensi, T Bestetti, E Pliquet, L Fiette, M Julithe, T. Huet, Anna Kostrzak, M Escande, Simon Wain-Hobson, Pierre Langlade-Demoyen
Publikováno v:
Gene Therapy
Gene Therapy, Nature Publishing Group, 2017, 24 (2), pp.74-83. ⟨10.1038/gt.2016.77⟩
Gene Therapy, 2017, 24 (2), pp.74-83. ⟨10.1038/gt.2016.77⟩
Gene Therapy, Nature Publishing Group, 2017, 24 (2), pp.74-83. ⟨10.1038/gt.2016.77⟩
Gene Therapy, 2017, 24 (2), pp.74-83. ⟨10.1038/gt.2016.77⟩
International audience; Human APOBEC3A (A3A) cytidine deaminase shows pro-apoptotic properties resulting from hypermutation of genomic DNA, induction of double-stranded DNA breaks (DSBs) and G1 cell cycle arrest. Given this, we evaluated the antitumo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8487b68fc1c4afe01c1197b742d10a6
https://hal-pasteur.archives-ouvertes.fr/pasteur-02545771
https://hal-pasteur.archives-ouvertes.fr/pasteur-02545771
Autor:
Anne Bergeron, Paul Guertin, Jean-Stéphane Varré, Samuel Blanquart, Amandine Perrin, Krister M. Swenson
Publikováno v:
BMC Genomics
BMC Genomics, BioMed Central, 2016, Proceedings of the 14th Annual Research in Computational Molecular Biology (RECOMB) Comparative Genomics Satellite Workshop: genomics, 17 (Suppl 10), pp.786. ⟨10.1186/s12864-016-3103-6⟩
BMC Genomics, Vol 17, Iss S10, Pp 157-164 (2016)
BMC Genomics, 2016, Proceedings of the 14th Annual Research in Computational Molecular Biology (RECOMB) Comparative Genomics Satellite Workshop: genomics, 17 (Suppl 10), pp.786. ⟨10.1186/s12864-016-3103-6⟩
BMC Genomics, BioMed Central, 2016, Proceedings of the 14th Annual Research in Computational Molecular Biology (RECOMB) Comparative Genomics Satellite Workshop: genomics, 17 (Suppl 10), pp.786. ⟨10.1186/s12864-016-3103-6⟩
BMC Genomics, Vol 17, Iss S10, Pp 157-164 (2016)
BMC Genomics, 2016, Proceedings of the 14th Annual Research in Computational Molecular Biology (RECOMB) Comparative Genomics Satellite Workshop: genomics, 17 (Suppl 10), pp.786. ⟨10.1186/s12864-016-3103-6⟩
International audience; Background: Transcriptome reconstruction, defined as the identification of all protein isoforms that may be expressed by a gene, is a notably difficult computational task. With real data, the best methods based on RNA-seq data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07ff4b687c4cc8ff1a3f89934888a731
https://hal.inria.fr/hal-01396410
https://hal.inria.fr/hal-01396410
Autor:
Patrick Weber, Mireille Nowakowski, Isabelle Miras, Mathieu Picardeau, William Shepard, Frederick Saul, Ahmed Haouz
Publikováno v:
Acta Crystallographica Section D: Biological Crystallography
Acta Crystallographica Section D: Biological Crystallography, International Union of Crystallography, 2015, 71 (6), pp.1351-1359. ⟨10.1107/S139900471500704X⟩
Acta crystallographica Section D : Structural biology [1993-...]
Acta crystallographica Section D : Structural biology [1993-..], 2015, 71 (6), pp.1351-1359. ⟨10.1107/S139900471500704X⟩
Acta Crystallographica Section D: Biological Crystallography, International Union of Crystallography, 2015, 71 (6), pp.1351-1359. ⟨10.1107/S139900471500704X⟩
Acta crystallographica Section D : Structural biology [1993-...]
Acta crystallographica Section D : Structural biology [1993-..], 2015, 71 (6), pp.1351-1359. ⟨10.1107/S139900471500704X⟩
Pathogenic Leptospira spp. are the agents of leptospirosis, an emerging zoonotic disease. Analyses of Leptospira genomes have shown that the pathogenic leptospires (but not the saprophytes) possess a large number of genes encoding proteins containing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::181ce67719d8c6537a6af49774b710ad
https://hal-pasteur.archives-ouvertes.fr/pasteur-02539010
https://hal-pasteur.archives-ouvertes.fr/pasteur-02539010
Publikováno v:
Journal of cell science, 127(Part 13), 2862-2872. Company of Biologists Ltd
Journal of Cell Science
Journal of Cell Science, 2014, 127 (13), pp.2862-2872. ⟨10.1242/jcs.144808⟩
Journal of Cell Science, Company of Biologists, 2014, 127 (13), pp.2862-2872. ⟨10.1242/jcs.144808⟩
Journal of Cell Science
Journal of Cell Science, 2014, 127 (13), pp.2862-2872. ⟨10.1242/jcs.144808⟩
Journal of Cell Science, Company of Biologists, 2014, 127 (13), pp.2862-2872. ⟨10.1242/jcs.144808⟩
International audience; Expression of the human dermokine gene (DMKN) leads to the production of four dermokine isoform families. The secreted α, β and γ isoforms have an epidermis-restricted expression pattern, with Dmkn β and γ being specifica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::076cfa563f3364839204565896569774
https://pure.amc.nl/en/publications/mice-deficient-for-the-epidermal-dermokine--and--isoforms-display-transient-cornification-defects(df4b76ca-0828-4b59-a52c-ae84d20f7a3e).html
https://pure.amc.nl/en/publications/mice-deficient-for-the-epidermal-dermokine--and--isoforms-display-transient-cornification-defects(df4b76ca-0828-4b59-a52c-ae84d20f7a3e).html
Autor:
Wassim Daher, Katia Cailliau, Jamal Khalife, Sylvain Fauquenoy, Gabrielle Oria, Stanislas Tomavo, Edith Browaeys
Publikováno v:
Eukaryotic Cell
Eukaryotic Cell, American Society for Microbiology, 2007, 6 (9), pp.1606-1617. ⟨10.1128/EC.00260-07⟩
Eukaryotic Cell, 2007, 6 (9), pp.1606-1617. ⟨10.1128/EC.00260-07⟩
Eukaryotic Cell, American Society for Microbiology, 2007, 6 (9), pp.1606-1617. ⟨10.1128/EC.00260-07⟩
Eukaryotic Cell, 2007, 6 (9), pp.1606-1617. ⟨10.1128/EC.00260-07⟩
We have characterized the Toxoplasma gondii protein phosphatase type 1 (TgPP1) and a potential regulatory binding protein belonging to the leucine-rich repeat protein family, designated TgLRR1. TgLRR1 is capable of binding to TgPP1 to inhibit its act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a000e7ce1199d023ad6163a30927aaad
https://hal.archives-ouvertes.fr/hal-00171738
https://hal.archives-ouvertes.fr/hal-00171738
Autor:
Bouchlaka, Chiraz, Abdelhak, Sonia, Amouri, Ahlem, Ben Abid, Hela, Hadiji, Sondes, Frikha, Mounir, Ben Othman, Tarek, Amri, Fethi, Ayadi, Hammadi, Hachicha, Mongia, Rebaï, Ahmed, Saad, Ali, Dellagi, Koussay, Group, Tunisian Fanconi Anemia Study
Publikováno v:
Journal of Human Genetics
Journal of Human Genetics, Nature Publishing Group, 2003, 48 (7), pp.352--361. ⟨10.1007/s10038-003-0037-z⟩
Journal of Human Genetics, Nature Publishing Group, 2003, 48 (7), pp.352--361. ⟨10.1007/s10038-003-0037-z⟩
International audience; Fanconi anemia (FA) is a rare autosomal recessive disease characterized by progressive pancytopenia, congenital malformations, and predisposition to acute myeloid leukemia. Fanconi anemia is genetically heterogeneous, with at
Autor:
Hai Song, Pascal Pineau, Jing Zhao, Pierre Tiollais, Cheng Liao, Hong-Yang Wang, Anne Dejean, Mujun Zhao, Agnès Marchio, Tsaiping Li
Publikováno v:
World Journal of Gastroenterology
World Journal of Gastroenterology, Baishideng Publishing Group Co. Limited, 2003, 9 (1), pp.89. ⟨10.3748/wjg.v9.i1.89⟩
World Journal of Gastroenterology, 2003, 9 (1), pp.89. ⟨10.3748/wjg.v9.i1.89⟩
World Journal of Gastroenterology, Baishideng Publishing Group Co. Limited, 2003, 9 (1), pp.89. ⟨10.3748/wjg.v9.i1.89⟩
World Journal of Gastroenterology, 2003, 9 (1), pp.89. ⟨10.3748/wjg.v9.i1.89⟩
International audience; Aim: To find the point mutations meaningful for inactivation of liver-related putative tumor suppressor gene (LPTS) gene, a human novel liver-related putative tumor suppressor gene and telomerase inhibitor in hepatocellular ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::235bc60ed9381326b8c359e0f5b5730d
https://hal-pasteur.archives-ouvertes.fr/pasteur-02870453
https://hal-pasteur.archives-ouvertes.fr/pasteur-02870453