Results 121 to 130 of about 2,125,818 (314)

Heterozygous loss‐of‐function alleles associate the conserved 3′‐5′ exoribonuclease EXOSC10 with hypersensitivity to the anticancer drug 5‐fluorouracil

open access: yesMolecular Oncology, EarlyView.
EXOSC10, an essential nuclear RNA exosome‐associated 3′‐5′ exoribonuclease, is inhibited by the anticancer drug 5‐fluorouracil (5‐FU), and EXOSC10 depletion increases 5‐FU sensitivity. The colon‐cancer variant EXOSC10S402T, located in a proteolysis motif, is stable and nuclear but nonfunctional in vivo.
Radhika Sain   +10 more
wiley   +1 more source

PHOSPHATIC DIABETES. [PDF]

open access: yesThe Lancet, 1887
n ...
openaire   +1 more source

Glassy carbon electrode modified with hybrid films containing inorganic molybdate anions trapped in organic matrices of chitosan and ionic liquid for the amperometric sensing of phosphate at neutral pH

open access: yes, 2011
This work reports an amperometric method for phosphate analysis based on the use of a surface modified glassy carbon electrode (GC). In one configuration of the electrode the surface is modified with ammonium heptamolybdate incorporated in chitosan ...
Singh, P.   +5 more
core  

Interpreting the effects of DNA polymerase variants at the structural level

open access: yesMolecular Oncology, EarlyView.
Using MAVISp and molecular dynamics simulations, we analyzed over 60 000 missense variants in POLE and POLD1 from ClinVar, COSMIC, cBioPortal, and saturation mutagenesis. Identified mechanistic indicators, including stability, binding, and long‐range, enable structural interpretation, providing ACMG‐like evidence for possible reclassification of VUS ...
Matteo Arnaudi   +7 more
wiley   +1 more source

Jhamarkotra phosphate ore processing plant

open access: yes, 2009
: Low grade phosphate ore of Jhamarkotra that analyzes 16.5% P~2~O~5~ is upgraded to 34% P~2~O~5~ by a two stage flotation process after size reducing the ore to 90% passing through 200mesh using conventional equipment such as jaw and cone crushers ...
Sekhar Dmr, C.L Jain
core   +1 more source

Proteasome inhibitor, ixazomib prevents topoisomerase‐I degradation and reverses irinotecan resistance in colorectal cancer

open access: yesMolecular Oncology, EarlyView.
Ixazomib inhibits proteasome‐mediated degradation of topoisomerase I induced by irinotecan, thereby restoring drug sensitivity and promoting tumor cell death in colorectal cancer. Irinotecan, a topoisomerase I (topoI) inhibitor, is widely used for colorectal cancer, but resistance remains a major clinical challenge.
Yuho Ebata   +10 more
wiley   +1 more source

Global dataset on phosphate mining and beneficiation

open access: yes
<p>The dataset covers worldwide production of phosphate rock (PR) at the level of phosphate mining and beneficiation complex. The objective is to gather complex-specific data on the P content of mined and beneficiated resource and on the recovery ...
Anna Shchiptsova
core   +2 more sources

Sodium Benzoate as Promoter in the Soap Flotation of Phosphate Minerals

open access: yes, 2011
In the present study we show that sodium benzoate substantially improves the efficiency of Soap LDO collector in the flotation of phosphate minerals. ...
Mihir DM   +2 more
core  

Stimulator of interferon genes agonist augmented antitumor immunity of osimertinib in Egfr‐mutated lung cancer

open access: yesMolecular Oncology, EarlyView.
Combining osimertinib with the STING agonist ADU‐S100 activates innate and adaptive immunity to overcome the non‐inflamed microenvironment of Egfr‐mutant lung cancer. This combination increases NK and CD8+ T‐cell infiltration, associated with activation of the STING‐IRF3 pathway and local immunogenic cell death.
Jun Nishimura   +19 more
wiley   +1 more source

Loss of IGF‐1R impairs DNA‐PKcs recruitment to chromatin leading to defective end‐joining

open access: yesMolecular Oncology, EarlyView.
IGF‐1R promotes radioresistance by facilitating DNA‐PKcs recruitment to chromatin, enabling non‐homologous end‐joining (NHEJ) repair of double‐strand breaks. Inhibition or loss of IGF‐1R disrupts this recruitment to damage sites, driving compensatory reliance on microhomology‐mediated end‐joining (MMEJ) repair.
Matthew O. Ellis   +3 more
wiley   +1 more source

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