Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Xpa gene"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Michal Hammel, Norie Sugitani, Daniel J. Rosenberg, Kateryna V Le Meur, Agnieszka M. Topolska-Woś, Orlando D. Schärer, Remy Le Meur, Hyunsuk Kim, Jung-Eun Yeo, Walter J. Chazin, John J Cordoba
Publikováno v:
Nucleic acids research, vol 48, iss 4
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2020, 48 (4), pp.2173-2188. ⟨10.1093/nar/gkz1231⟩
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2020, 48 (4), pp.2173-2188. ⟨10.1093/nar/gkz1231⟩
The XPA protein functions together with the single-stranded DNA (ssDNA) binding protein RPA as the central scaffold to ensure proper positioning of repair factors in multi-protein nucleotide excision repair (NER) machinery. We previously determined t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28e16d90031468ce11a44073363fb9b9
https://escholarship.org/uc/item/80p224cp
https://escholarship.org/uc/item/80p224cp
Publikováno v:
Journal of Cancer
Neuroblastoma is a malignant tumor arising from the developing sympathetic nervous system, which mainly affects children. Variations in XPA gene have been shown to confer cancer susceptibility. However, no investigation has been reported regarding th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0722767be630b0f060e787d8c9a37d93
http://europepmc.org/articles/PMC6072815
http://europepmc.org/articles/PMC6072815
Publikováno v:
Practical Neurology. 18:489-491
Xeroderma pigmentosum is a group of rare autosomal recessive disorders characterised by skin sensitivity to ultraviolet light, a higher frequency of skin cancers, and abnormal skin pigmentation.1 Several neurological symptoms are described in xeroder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::473763cdc19e44b1e4b116907e7484c3
https://doi.org/10.1136/practneurol-2018-001888
https://doi.org/10.1136/practneurol-2018-001888
Publikováno v:
Journal of Genetic Medicine. 13:20-25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b44c176d96caafd3344fb02b186a4380
https://doi.org/10.5734/jgm.2016.13.1.20
https://doi.org/10.5734/jgm.2016.13.1.20
Publikováno v:
Oxford
Nucleic Acids Research
Nucleic Acids Research
The Freiburg RNA tools web server integrates three tools for the advanced analysis of RNA in a common web-based user interface. The tools IntaRNA, ExpaRNA and LocARNA support the prediction of RNA–RNA interaction, exact RNA matching and alignment o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::320314e8213be196c9ee69bbff140d4c
https://doi.org/10.1093/nar/gkq316
https://doi.org/10.1093/nar/gkq316
Autor:
Rafael Malagoli Rocha, Silvia Regina Rogatto, Amanda F. Nóbrega, Maria Isabel Achatz, Karina Miranda Santiago
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 16, Iss 4, Pp 8988-8996 (2015)
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
International Journal of Molecular Sciences, Vol 16, Iss 4, Pp 8988-8996 (2015)
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2022-04-29T08:45:01Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-04-01 Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder characterized by DNA repair defects that cause photophobia, sunlight-induce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d48acde7c03c3b1ae60239c63bf8046e
https://pubmed.ncbi.nlm.nih.gov/25913378
https://pubmed.ncbi.nlm.nih.gov/25913378
Publikováno v:
Gene. 576:379-380
• We performed mutational analysis of Xeroderma pigmentosum associated genes in an 8-year female patient.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::617be9c67956c9a9bc47c68b66943cdc
https://doi.org/10.1016/j.gene.2015.08.039
https://doi.org/10.1016/j.gene.2015.08.039
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on XPA (xeroderma pigmentosum, complementation group A), with data on DNA, on the protein encoded, and where the gene is implicated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::509bd68f70f2d8e4d0f1bcbd0f0523aa
https://doi.org/10.4267/2042/37722
https://doi.org/10.4267/2042/37722