Publications by authors named "J-B Briere"

Background Brain metastases are manually identified during stereotactic radiosurgery (SRS) treatment planning, which is time consuming and potentially challenging. Purpose To develop and investigate deep learning (DL) methods for detecting brain metastasis with MRI to aid in treatment planning for SRS. Materials and Methods In this retrospective study, contrast material-enhanced three-dimensional T1-weighted gradient-echo MRI scans from patients who underwent gamma knife SRS from January 2011 to August 2018 were analyzed.

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Despite decades of research, efforts to directly target KRAS have been challenging. MRTX849 was identified as a potent, selective, and covalent KRAS inhibitor that exhibits favorable drug-like properties, selectively modifies mutant cysteine 12 in GDP-bound KRAS, and inhibits KRAS-dependent signaling. MRTX849 demonstrated pronounced tumor regression in 17 of 26 (65%) KRAS-positive cell line- and patient-derived xenograft models from multiple tumor types, and objective responses have been observed in patients with KRAS-positive lung and colon adenocarcinomas.

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Aim: To evaluate antithrombotic treatment patterns in patients in Italy with nonvalvular atrial fibrillation (NVAF) before and after direct oral anticoagulants (DOACs) were approved.

Methods: This analysis included patients with a discharge diagnosis of NVAF in 2010 and 2014, which constituted the pre- and post-DOACs populations, respectively.

Results: Approximately 90% of patients were eligible for oral anticoagulant (OAC) therapy.

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Article Synopsis
  • Ca(2+)-dependent protein kinases (CPKs) in Arabidopsis thaliana comprise a family of 34 genes, which can be categorized based on their calcium dependence into strictly dependent, Ca(2+)-stimulated, and essentially calcium-insensitive types.
  • The study focuses on CPK13, a calcium-insensitive CPK expressed in guard cells, which appears to inhibit light-induced stomatal opening when overexpressed.
  • Research shows that CPK13 specifically phosphorylates and inhibits the K(+) channels KAT2 and KAT1, suggesting it plays a role in reducing stomatal aperture by interacting with these channels in guard cells.
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