1910 Genetics

In 1910, James Herrick published a report describing sickle-shaped red blood cells in a 20-year-old African-American student. Almost 45 years later, scientists discovered a mutation in hemoglobin that causes this “mysterious disease,” making sickle cell anemia the first genetic disease known to man.
At 1910 Genetics, we first establish an understanding of the molecular basis of disease to the granularity at which the world understands sickle cell anemia. This understanding centers biology as our North Star, and drives our integration of artificial intelligence (AI), computation and biological automation to accelerate the design of small molecule and protein therapeutics.

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