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Wnt/-catenin signaling in midbrain dopaminergic neuron specification and neurogenesis
Peptides and the blood-brain barrier
The Biology of Wool and Hair 1988:5167
Mutations in the lipoyltransferase LIPT1 gene cause a fatal disease associated with a specific lipoylation defect of the 2-ketoacid dehydrogenase complexes
Efforts to supplement T4 and T3 in critically ill patients do not improve outcomes and may be detrimental
76 Rossi J 3rd, Nordholm AF, Carpenter RL, Ritchie GD, Malcomb W
