Zobrazeno 1 - 10
of 10
pro vyhledávání: '"MESH: DNA Mismatch Repair"'
Autor:
Jary, Marine, Liu, Wen-Wei, Yan, Dongyao, Bai, Isaac, Muranyi, Andrea, Colle, Elise, Brocheriou, Isabelle, Turpin, Anthony, Radosevic-Robin, Nina, Bourgoin, Pierre, Penault-Llorca, Frédérique, Cohen, Romain, Vernerey, Dewi, André, Thierry, Borg, Christophe, Shanmugam, Kandavel, Svrcek, Magali, Liu, Wen‐wei
Publikováno v:
Molecular Oncology
Molecular Oncology, 2021, ⟨10.1002/1878-0261.13173⟩
Molecular Oncology, Elsevier, 2022, 16 (11), pp.2260-2273. ⟨10.1002/1878-0261.13173⟩
Molecular Oncology, 2022, 16 (11), pp.2260-2273. ⟨10.1002/1878-0261.13173⟩
Molecular Oncology, Elsevier, 2021, ⟨10.1002/1878-0261.13173⟩
Molecular Oncology, 2021, ⟨10.1002/1878-0261.13173⟩
Molecular Oncology, Elsevier, 2022, 16 (11), pp.2260-2273. ⟨10.1002/1878-0261.13173⟩
Molecular Oncology, 2022, 16 (11), pp.2260-2273. ⟨10.1002/1878-0261.13173⟩
Molecular Oncology, Elsevier, 2021, ⟨10.1002/1878-0261.13173⟩
International audience; In the era of immune checkpoint inhibitors, understanding the metastatic microenvironment of proficient mismatch repair/microsatellite stable (pMMR/MSS) colorectal cancer (CRC) is of paramount importance to both prognosticatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f5622219813877e6f35c8bc4a090e8e
https://doi.org/10.1002/1878-0261.13173
https://doi.org/10.1002/1878-0261.13173
Autor:
Richard, Guy-Franck
Publikováno v:
Cells
Cells, Vol 10, Iss 1019, p 1019 (2021)
Cells, 2021, 10 (5), pp.1019. ⟨10.3390/cells10051019⟩
Cells, Vol 10, Iss 1019, p 1019 (2021)
Cells, 2021, 10 (5), pp.1019. ⟨10.3390/cells10051019⟩
International audience; Trinucleotide repeats are a peculiar class of microsatellites whose expansions are responsible for approximately 30 human neurological or developmental disorders. The molecular mechanisms responsible for these expansions in hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::245caabfd37048d6e53d572e428a4618
https://pubmed.ncbi.nlm.nih.gov/33925919
https://pubmed.ncbi.nlm.nih.gov/33925919
Autor:
Guy-Franck Richard, Lucie Poggi
Publikováno v:
Microbiology and Molecular Biology Reviews
Microbiology and Molecular Biology Reviews, 2020, 85 (1), pp.e00110-20. ⟨10.1128/MMBR.00110-20⟩
Microbiology and Molecular Biology Reviews, 2020, 85 (1), pp.e00110-20. ⟨10.1128/MMBR.00110-20⟩
International audience; Duplex DNA naturally folds into a right-handed double helix in physiological conditions. Some sequences of unusual base composition may nevertheless form alternative structures, as was shown for many repeated sequences in vitr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5c6b4279e0c954122f3d9cd694fe5ff
https://doi.org/10.1128/mmbr.00110-20
https://doi.org/10.1128/mmbr.00110-20
Autor:
M Mahmoudi, Samir Boubaker, Amira Jaballah-Gabteni, Haifa Tounsi, Mousaddak Azzouz, Hamza Dallali, Hamza Yaiche, Sahar Elouej, Maria Kabbage, Ines Ben Ayed, Lamine Hamzaoui, Mouna Medhioub, Sonia Abdelhak, Afifa Maaloul, Yosr Hamdi, Nadia Ben Jemii, Najla Mezghani
Publikováno v:
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-13 (2019)
Journal of Translational Medicine
Journal of Translational Medicine, BioMed Central, 2019, 17 (1), pp.212. ⟨10.1186/s12967-019-1961-9⟩
Journal of Translational Medicine
Journal of Translational Medicine, BioMed Central, 2019, 17 (1), pp.212. ⟨10.1186/s12967-019-1961-9⟩
Background Lynch syndrome (LS) is a highly penetrant inherited cancer predisposition syndrome, characterized by autosomal dominant inheritance and germline mutations in DNA mismatch repair genes. Despite several genetic variations that have been iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3714aec0aaa66ec377220ed5bbeb7de9
https://doi.org/10.1186/s12967-019-1961-9
https://doi.org/10.1186/s12967-019-1961-9
Autor:
Alba Guarné, Jean-Baptiste Charbonnier
Publikováno v:
Progress in Biophysics and Molecular Biology
Progress in Biophysics and Molecular Biology, 2015, 117 (2-3), pp.149-56. ⟨10.1016/j.pbiomolbio.2015.02.002⟩
Progress in Biophysics and Molecular Biology, Elsevier, 2015, 117 (2-3), pp.149-56. 〈10.1016/j.pbiomolbio.2015.02.002〉
Progress in Biophysics and Molecular Biology, Elsevier, 2015, 117 (2-3), pp.149-56. ⟨10.1016/j.pbiomolbio.2015.02.002⟩
Progress in Biophysics and Molecular Biology, 2015, 117 (2-3), pp.149-56. ⟨10.1016/j.pbiomolbio.2015.02.002⟩
Progress in Biophysics and Molecular Biology, Elsevier, 2015, 117 (2-3), pp.149-56. 〈10.1016/j.pbiomolbio.2015.02.002〉
Progress in Biophysics and Molecular Biology, Elsevier, 2015, 117 (2-3), pp.149-56. ⟨10.1016/j.pbiomolbio.2015.02.002⟩
International audience; DNA mismatch repair (MMR) is a conserved pathway that safeguards genome integrity by correcting replication errors. The coordinated actions of two proteins (MutS and MutL) initiate the mismatch repair response and defects in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44b16cd30743bab943309cf40ab81b13
https://hal.science/hal-01430063
https://hal.science/hal-01430063
Autor:
Frédéric Bibeau, L. Roca, Evelyne Crapez, Hélène de Forges, Julie Courraud, Marc Ychou, Jacqueline Duffour, Florence Boissière-Michot, Audrey Combes, Pierre Senesse
Publikováno v:
Journal of Genetic Counseling
Journal of Genetic Counseling, Springer Verlag, 2016, 25 (3), pp.432-442. ⟨10.1007/s10897-015-9888-7⟩
Journal of Genetic Counseling, Springer Verlag, 2016, 25 (3), pp.432-442. ⟨10.1007/s10897-015-9888-7⟩
International audience; Reproductive techniques such as prenatal diagnosis (PND) or preimplantation genetic diagnosis (PGD), although debated, are legally forbidden in France in case of Lynch syndrome. The preference of mutation carriers about their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e3858ac161d8a5e606b59761b793b40
https://hal.umontpellier.fr/hal-02295670
https://hal.umontpellier.fr/hal-02295670
Publikováno v:
Journal of Experimental Medicine
Journal of Experimental Medicine, Rockefeller University Press, 2007, 204 (1), pp.17-23. ⟨10.1084/jem.20062131⟩
Journal of Experimental Medicine, 2007, 204 (1), pp.17-23. ⟨10.1084/jem.20062131⟩
The Journal of Experimental Medecine
The Journal of Experimental Medecine, The Rockefeller University Press, 2007, 204 (1), pp.17-23. 〈10.1084/jem.20062131〉
The Journal of Experimental Medicine
Journal of Experimental Medicine, Rockefeller University Press, 2007, 204 (1), pp.17-23. ⟨10.1084/jem.20062131⟩
Journal of Experimental Medicine, 2007, 204 (1), pp.17-23. ⟨10.1084/jem.20062131⟩
The Journal of Experimental Medecine
The Journal of Experimental Medecine, The Rockefeller University Press, 2007, 204 (1), pp.17-23. 〈10.1084/jem.20062131〉
The Journal of Experimental Medicine
International audience; Mutations at A/T bases within immunoglobulin genes have been shown to be generated by a repair pathway involving the DNA-binding moiety of the mismatch repair complex constituted by the MSH2-MSH6 proteins, together with DNA po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16bc73de6ce77970f0485f5196b8dc71
https://doi.org/10.1084/jem.20062131
https://doi.org/10.1084/jem.20062131
Autor:
Zeynep Baharoglu, Didier Mazel
Publikováno v:
Research in Microbiology
Research in Microbiology, Elsevier, 2014, 165 (6), pp.476-80. ⟨10.1016/j.resmic.2014.05.039⟩
Research in Microbiology, 2014, 165 (6), pp.476-80. ⟨10.1016/j.resmic.2014.05.039⟩
Research in Microbiology, Elsevier, 2014, 165 (6), pp.476-80. ⟨10.1016/j.resmic.2014.05.039⟩
Research in Microbiology, 2014, 165 (6), pp.476-80. ⟨10.1016/j.resmic.2014.05.039⟩
International audience; Low concentrations of aminoglycosides induce the SOS response in Vibrio cholerae but not in Escherichia coli. In order to determine whether a specific factor present in E. coli prevents this induction, we developed a genetic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7294577f9b63d62b3f0e0b33c3fc43d
https://hal-pasteur.archives-ouvertes.fr/pasteur-01423361
https://hal-pasteur.archives-ouvertes.fr/pasteur-01423361
Autor:
Pierre Vabres, Emilie Bouvignies, Gaëlle Bougeard, Mario Tosi, Stéphanie Baert-Desurmont, Julie Tinat, David Malka, Brigitte Bressac-de Paillerets, Frédéric Huet, Laurence Olivier-Faivre, Caroline Chapusot, Cosette Martin, G. Couillault, Stéphanie Vasseur, Thierry Frebourg, Florence Le Pessot
Publikováno v:
Familial Cancer
Familial Cancer, Springer Verlag (Germany), 2014, 13 (1), pp.131-135. ⟨10.1007/s10689-013-9676-1⟩
Familial Cancer, Springer Verlag (Germany), 2014, 13 (1), pp.131-135. ⟨10.1007/s10689-013-9676-1⟩
International audience; Constitutional mismatch repair-deficiency, due to biallelic mutations of MMR genes, results in a tumour spectrum characterized by leukaemias, lymphomas, brain tumours and adenocarcinomas of the gastro-intestinal tract, occurri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::459320af0e16285cc79b6db05da0a690
https://hal.archives-ouvertes.fr/hal-03106912
https://hal.archives-ouvertes.fr/hal-03106912
Autor:
Anne Jolivet-Gougeon, Claude-James Soussy, Sandrine Le Gall-David, Hervé Le Bars, Bernard Lobel, Peter Tenke, Latifa Bousarghin, Martine Bonnaure-Mallet, Francois Guille, Béla Kovács
Publikováno v:
Journal of Medical Microbiology
Journal of Medical Microbiology, Society for General Microbiology, 2011, 60 (Pt 5), pp.563-73. ⟨10.1099/jmm.0.024083-0⟩
Journal of Medical Microbiology, 2011, 60 (Pt 5), pp.563-73. ⟨10.1099/jmm.0.024083-0⟩
Journal of Medical Microbiology, Society for General Microbiology, 2011, 60 (Pt 5), pp.563-73. ⟨10.1099/jmm.0.024083-0⟩
Journal of Medical Microbiology, 2011, 60 (Pt 5), pp.563-73. ⟨10.1099/jmm.0.024083-0⟩
International audience; Heritable hypermutation in bacteria is mainly due to alterations in the methyl-directed mismatch repair (MMR) system. MMR-deficient strains have been described from several bacterial species, and all of the strains exhibit inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26f81bcb50414158b3e262f8bcc3fcaf
https://pubmed.ncbi.nlm.nih.gov/21349992
https://pubmed.ncbi.nlm.nih.gov/21349992