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Holly A. Ingraham

Researcher at University of California, San Francisco

Publications -  112
Citations -  14551

Holly A. Ingraham is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Receptor & Steroidogenic factor 1. The author has an hindex of 56, co-authored 107 publications receiving 13705 citations. Previous affiliations of Holly A. Ingraham include Howard Hughes Medical Institute & Boston University.

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A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotype.

TL;DR: The structure of Pit-1 and its recognition elements suggests that metazoan tissue phenotype is controlled by a family of transcription factors that bind to related cis-active elements and contain several highly conserved domains.
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Expression of a large family of POU-domain regulatory genes in mammalian brain development.

TL;DR: The identification of multiple new members of a large family of POU-domain genes expressed in adult brain are reported, and it is documented that all the known mammalian Pou- domain genes, including Pit-1 and Oct-2, are expressed widely in the developing nervous system.
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Anti-Müllerian Hormone Inhibits Initiation of Primordial Follicle Growth in the Mouse Ovary

TL;DR: It is suggested that AMH inhibits initia- tion of primordial follicle growth and therefore functions as an inhibitory growth factor in the ovary during these early stages of folliculogenesis.
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The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products

TL;DR: The POU domain is a novel bipartite DNA-binding structure in which the POU homoeo and POU-specific regions form two subdomains that are both required for DNA binding but are held together by a flexible linker.
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Developmental expression of mouse steroidogenic factor-1, an essential regulator of the steroid hydroxylases.

TL;DR: Analysis of the developmental profile of steroidogenic factor-1 (SF-1), a nuclear receptor that regulates the steroid hydroxylases, suggests that SF-1 plays a role in gonadal development distinct from regulating the steroidogenic enzymes.