Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ingrid Revet"'
Autor:
Ka Wing Fong, Kai Ming Chou, Ingrid Revet, Raymond A. Swanson, Angela M. Brennan-Minnella, Vladimir Bezrookove, Yih Wen Chen, James E. Cleaver, Junjie Chen
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, vol 111, iss 37
Cockayne syndrome (CS) is a human DNA repair-deficient disease that involves transcription coupled repair (TCR), in which three gene products, Cockayne syndrome A (CSA), Cockayne syndrome B (CSB), and ultraviolet stimulated scaffold protein A (UVSSA)
Publikováno v:
Annals of Clinical Biochemistry, 56(1), 179. SAGE Publications Ltd
Annals of Clinical Biochemistry
Annals of Clinical Biochemistry
The high-dose hook effect, or prozone effect, can lead to negative or falsely lowered plasma ferritin results. Here, cases of a 16-year-old boy and a 70-year-old woman with haemophagocytic lymphohystiocytosis with extremely high concentrations of pla
Autor:
Luzviminda Feeney, David Dankort, Tiffany K. Dong, Wade Wilson, Stephanie Bruguera, Dennis H. Oh, Ingrid Revet, James E. Cleaver
Publikováno v:
Proceedings of the National Academy of Sciences. 108:8663-8667
The phosphorylation of H2Ax on its S139 site, γH2Ax, is important during DNA double-strand repair and is considered necessary for assembly of repair complexes, but its functional role after other kinds of DNA damage is less clear. We have measured t
Publikováno v:
Proceedings of the National Academy of Sciences. 107:6870-6875
UV irradiation induces histone variant H2AX phosphorylated on serine 139 (gammaH2AX) foci and high levels of pan-nuclear gammaH2AX staining without foci, but the significance of this finding is still uncertain. We examined the formation of gammaH2AX
Autor:
Ingrid Revet, James E. Cleaver
Publikováno v:
Mechanisms of Ageing and Development. 129:492-497
Cancer, aging, and neurodegeneration are all associated with DNA damage and repair in complex fashions. Aging appears to be a cell and tissue-wide process linked to the insulin-dependent pathway in several DNA repair deficient disorders, especially i
Publikováno v:
Mechanisms of ageing and development. 134(5-6)
Cockayne syndrome is an autosomal recessive disease that covers a wide range of symptoms, from mild photosensitivity to severe neonatal lethal disorder. The pathology of Cockayne syndrome may be caused by several mechanisms such as a DNA repair defic
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 109(12)
Cockayne syndrome (CS) is a rare autosomal recessive neurodegenerative disease that is associated with mutations in either of two transcription-coupled DNA repair genes, CSA or CSB . Mice with a targeted mutation in the Csb gene (Cs-b m/m ) exhibit a
The DNA Damage-Binding Protein XPC Is a Frequent Target for Inactivation in Squamous Cell Carcinomas
Autor:
Pui-Yan Kwok, Katie Ridd, Lauren M. Richards, Luzviminda Feeney, Ingrid Revet, Dennis H. Oh, Sebastien de Feraudy, James E. Cleaver
XPC, the main damage-recognition protein responsible for nucleotide excision repair of UVB damage to DNA, is lost or mutated in xeroderma pigmentosum group C (XP-C), a rare inherited disease characterized by high incidence and early onset of non-mela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e30b5f15843a860ff3d9418421df34a
https://europepmc.org/articles/PMC2913339/
https://europepmc.org/articles/PMC2913339/
Autor:
Gerda Huizenga, Rogier Versteeg, Dirk Geerts, Ingrid Revet, Peter van Sluis, Jan Koster, Richard Volckmann
Publikováno v:
Cancer letters, 289(2), 195-207. Elsevier Ireland Ltd
Revet, I, Huizenga, G, Koster, J, Volckmann, R, van Sluis, P, Versteeg, R & Geerts, D 2010, ' MSX1 induces the Wnt pathway antagonist genes DKK1, DKK2, DKK3, and SFRP1 in neuroblastoma cells, but does not block Wnt3 and Wnt5A signalling to DVL3 ', Cancer Letters, vol. 289, no. 2, pp. 195-207 . https://doi.org/10.1016/j.canlet.2009.08.019
Cancer Letters, 289(2), 195-207. Elsevier Ireland Ltd
Revet, I, Huizenga, G, Koster, J, Volckmann, R, van Sluis, P, Versteeg, R & Geerts, D 2010, ' MSX1 induces the Wnt pathway antagonist genes DKK1, DKK2, DKK3, and SFRP1 in neuroblastoma cells, but does not block Wnt3 and Wnt5A signalling to DVL3 ', Cancer Letters, vol. 289, no. 2, pp. 195-207 . https://doi.org/10.1016/j.canlet.2009.08.019
Cancer Letters, 289(2), 195-207. Elsevier Ireland Ltd
Neuroblastoma is the most common extra-cranial solid childhood cancer; it arises from neural crest-derived cells of the sympathetic nervous system. The anomalous regulation of embryonic developmental pathways like Delta-Notch and Wnt has been implica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b904ff14cd258baa60572250d411dd7
https://pure.amc.nl/en/publications/msx1-induces-the-wnt-pathway-antagonist-genes-dkk1-dkk2-dkk3-and-sfrp1-in-neuroblastoma-cells-but-does-not-block-wnt3-and-wnt5a-signalling-to-dvl3(d31f595c-0f06-4165-83a5-7ebdff4e1e9c).html
https://pure.amc.nl/en/publications/msx1-induces-the-wnt-pathway-antagonist-genes-dkk1-dkk2-dkk3-and-sfrp1-in-neuroblastoma-cells-but-does-not-block-wnt3-and-wnt5a-signalling-to-dvl3(d31f595c-0f06-4165-83a5-7ebdff4e1e9c).html
Publikováno v:
Nature reviews. Genetics. 10(11)
Mutations in genes on the nucleotide excision repair pathway are associated with diseases, such as xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy, that involve skin cancer and developmental and neurological symptoms. These mutations