@PeterDiamandis@DrWoappi This idea of funding just projects that are basically completed (because they value tones of preliminary data) defeats the purpose of innovation.
Endogenous Osteocyte-Osteoclast Signaling Enables Growth Factor-Free Bone Remodeling, Drug Response, and Cancer Invasion in a Nanoscale Calcified Bone-on-a-Chip Model
https://t.co/0CrwSwfQFm
#biorxiv_bioE
Cancer stem cells produce large oncosomes that deliver IL-33 specifically to niche macrophage precursors, promoting the differentiation of these cells into an immune-suppressive phenotype @ImmunityCP
https://t.co/OTGj06wC9a
Macrophages are terrible at migrating. In contrast, their precursor cells - monocytes - are highly motile.
Monocytes exploit interleukin 6 (IL-6) secreted by cancer cells and themselves to migrate fast and promote cancer cell proliferation.
More here: https://t.co/r2uyQ2I6pB
AADOCR strongly opposes the proposal to consolidate the existing 27 institutes and centers (ICs) of the @NIH into 15 newly renamed ICs. Read the statement:
https://t.co/McvCgXQuJu
Almost half of those living on our planet today are living in poverty.
In his latest Offline, Richard Horton calls for poverty reduction to be back at the centre of attention in the global health community.
Read this and more in our latest issue: https://t.co/v0Bi6l0QxM
Apply by May 10th to be part of Cohort 5 of the AADOCR MIND the Future Program! The program offers educational activities and interactive opportunities between mentors and mentees to support the development of a diverse cadre of DOC researchers.
https://t.co/uKyEVkbFm3
Apply to the MIND the Future Program! Be part of a network of mentors and mentees dedicated to supporting a diverse pool of young investigators in developing their careers in DOC research.
Apply by Friday, May 10th! #oralhealth#dentalresearch
https://t.co/zwcY9v2UCe
Bacteria in metastatic cancer tissue, mostly anaerobic and affected by anatomic site, predicts responsiveness to immunotherapy
https://t.co/rm8vqcMfy2 @CellCellPress
Immune checkpoint blockade plus a vaccine including self-amplifying mRNA-encoded neoantigens derived from common oncogenic driver mutations was safe and elicited neoantigen-specific T cell responses in patients with advanced solid tumors #CancerVaccine
https://t.co/CsqDQ381Zo