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The Most Common VHL Point Mutation R167Q in Hereditary VHL ..:
Buart, Stéphanie
;
Terry, Stéphane
;
Diop, M'boyba, Khadija
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/cancers13153897. , 2021
Link:
https://hal.science/hal-03445289
RT Journal T1
The Most Common VHL Point Mutation R167Q in Hereditary VHL Disease Interferes with Cell Plasticity Regulation
UL https://suche.suub.uni-bremen.de/peid=base-ftinserm:oai:HAL:hal-03445289v1&Exemplar=1&LAN=DE A1 Buart, Stéphanie A1 Terry, Stéphane A1 Diop, M'boyba, Khadija A1 Dessen, Philippe A1 Couvé, Sophie A1 Abdou, Abdérémane A1 Adam, Julien A1 Thiery, Jérôme A1 Savagner, Pierre A1 Chouaib, Salem PB HAL CCSD; MDPI YR 2021 K1 ccRCCs K1 R167Q VHL mutation K1 hypoxia-related genes K1 temness-related genes K1 ccRCC patients survival K1 [SDV]Life Sciences [q-bio] K1 [SDV.CAN]Life Sciences [q-bio]/Cancer JF info:eu-repo/semantics/altIdentifier/doi/10.3390/cancers13153897 LK http://dx.doi.org/https://hal.science/hal-03445289 DO https://hal.science/hal-03445289 SF ELIB - SuUB Bremen
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