David Baltimore

TL;DR: This study provides a novel natural system to study autoimmune diabetes pathogenesis and reveals a previously unknown c-Rel–dependent mechanistic difference between chemically induced and spontaneous diabetogenesis, which is distinct from other T-cell–dependent autoimmune diseases such as arthritis and experimental autoimmune encephalomyelitis.

TL;DR: In light of recent human embryo editing developments, scientists and stakeholders from all nations should cooperate to take advantage of this historic opportunity for medicine and also basic human biology.

TL;DR: It is proposed that in the absence of plasmon waves in biological samples, these evanescent fields reflect the changes in EGFR kinase domain polarization upon ligand binding.

TL;DR: In this article, a method for determining lymphocyte distribution and trafficking in a mammal is described, where either a labelled ligand capable of interacting specifically with the lymphocytes of the mammal is administered to the mammal so that the labeled ligand interacts in vivo with the cells, resulting in labeled lymphocytes, or, the labeled l ligand is contacted with the cell in vitro so that it interacts with the leukocyte in vitro.