Diagnosis of human prion disease. Safar JG, Geschwind MD, Deering C, Didorenko S, Sattavat M, Sanchez H, Serban A, Vey M, Baron H, Giles K, Miller BL, Dearmond SJ, Prusiner SB Proceedings of the National Academy of Sciences of the United States of America
Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness. Geschwind DH, Miller BL, DeCarli C, Carmelli D Proceedings of the National Academy of Sciences of the United States of America
Specificity in transforming growth factor beta-induced transcription of the plasminogen activator inhibitor-1 gene: interactions of promoter DNA, transcription factor muE3, and Smad proteins. Hua X, Miller ZA, Wu G, Shi Y, Lodish HF Proceedings of the National Academy of Sciences of the United States of America
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. Clark LN, Poorkaj P, Wszolek Z, Geschwind DH, Nasreddine ZS, Miller B, Li D, Payami H, Awert F, Markopoulou K, Andreadis A, D'Souza I, Lee VM, Reed L, Trojanowski JQ, Zhukareva V, Bird T, Schellenberg G, Wilhelmsen KC Proceedings of the National Academy of Sciences of the United States of America
Evidence for myosin motors on organelles in squid axoplasm. Bearer EL, DeGiorgis JA, Bodner RA, Kao AW, Reese TS Proceedings of the National Academy of Sciences of the United States of America
Expression of nerve growth factor in vivo from a defective herpes simplex virus 1 vector prevents effects of axotomy on sympathetic ganglia. Federoff HJ, Geschwind MD, Geller AI, Kessler JA Proceedings of the National Academy of Sciences of the United States of America
