Sarah E Whitehead

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Deletion or mutation of the SMN1 (survival of motor neurons) gene causes the common, fatal neuromuscular disease spinal muscular atrophy. The SMN protein is important in small nuclear ribonucleoprotein (snRNP) assembly and interacts with snRNP proteins via arginine/glycine-rich domains. Recently, SMN was also found to interact with core protein components(More)
The cytochrome P450 2F (CYP2F) subfamily genes are currently known only from cDNA sequences in human, mouse, rat and goat. Compared to other divisions of the CYP2 gene family, the CYP2F subfamily is unusual in having few genes per species and in being selectively expressed in lung tissues. Sequencing genomic DNAs from human and gorilla has allowed us to(More)
In a time of financial constraints, Harvard Medical School's Countway Library has found a way to acquire additional funding to expand its services while integrating librarians further into the medical school organization. This paper describes the contractual arrangement between the library and a medical school department and shows how a professional(More)
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