
Brain-derived neurotrophic factor
BDNF was isolated from pig brain tissue in 1982 by Yves-Alain Barde and Hans Thoenen, identifying it as a distinct protein.
Three pounds of tissue, and the slow business of mapping it.

BDNF was isolated from pig brain tissue in 1982 by Yves-Alain Barde and Hans Thoenen, identifying it as a distinct protein.







Ehrlich’s intravenous dye experiments revealed selective absence of brain staining — but he misinterpreted it as passive under-uptake. His student Goldmann’s 1913 intracerebrospinal injection proved compartmentalization. The barrier was attributed to blood vessels, not a membrane. Ehrlich never believed in it. The term came later, from Lina Stern.









Camillo Golgi discovered the Golgi apparatus in 1898 using osmium dichromate staining on barn owl Purkinje cells. He named it 'apparato reticolare interno' and asserted it was a real, unique cellular component. Initial scepticism held that it was an optical illusion. The finding was not firmly established until electron microscopy emerged ~50 years later. It revealed a new intracellular structure but gave no insight into its function, mechanism, or universality.




Baddeley and Hitch’s 1974 model reframed working memory as a set of interacting, domain-specific components — not a single bottleneck. Dual-task interference, the word length effect, and amnesic patient profiles provide direct empirical support. Later additions (episodic buffer in 2000, renamed awareness buffer in 2026) extend but do not overturn the core claim of fractionation. It remains indispensable — not because it is complete, but because it is falsifiable, componential, and repeatedly predictive.