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Andrew H. Miller
Publications - 5
Citations - 59
Andrew H. Miller is an academic researcher. The author has contributed to research in topics: Joint-stock company & Counterfactual thinking. The author has an hindex of 3, co-authored 4 publications receiving 57 citations.
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Subjectivity LTD: The Discourse of Liability in the Joint Stock Companies Act of 1856 and Gaskell's Cranford
TL;DR: The Joint Stock Companies Act of 1856 as discussed by the authors distinguished sharply between private and public identities, as one contemporary commentator wrote, the investor in a company "and his family" no longer need fear being "stripped of every earthly thing which they possess, even to their very beds".
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"A Case of Metaphysics": Counterfactuals, Realism, Great Expectations
TL;DR: In this article, optative or counterfactual self-understanding both in general and as it shapes the narrative structure, moral psychology, and emotional logic of Charles Dickens's Great Expectations is discussed.
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Bruising, Laceration, and Lifelong Maiming; Or, How We Encourage Research
TL;DR: In this paper, a conceptual structure within which to read George Eliot's Impressions of Theophrastus Such is provided, which is based on what, following Stanley Cavell, I call Eliot's moral perfectionism.
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Spenser's Shameful Shepheardes Calender
TL;DR: The authors argue that the shame of stylistic primitivism is central to Edmund Spenser's Shepheardes Calender, which explores the tension between an affiliation with England's linguistic past as a means for shaming the present and as a shameful attachment to a superseded moment in style's evolutionary history.
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IGF2BP2 Promotes Cancer Progression by Degrading the RNA Transcript Encoding a v‐ATPase Subunit
Fang Wang,Arash Latifkar,James Mullmann,Elena Panizza,Irma Fernandez,Lu Ling,Andrew H. Miller,Claudia Fischbach,Robert Weiss,Hening Lin,Richard A. Cerione,Marc A. Antonyak +11 more
TL;DR: A previously unrecognized role for IGF2BP2 is described in mediating the degradation of an mRNA transcript essential for lysosomal function and how its sirtuin‐regulated acetylation state can have significant biological and disease consequences is highlighted.