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Mary M. Lee

Researcher at Thomas Jefferson University

Publications -  117
Citations -  5161

Mary M. Lee is an academic researcher from Thomas Jefferson University. The author has contributed to research in topics: Environmental exposure & Leydig cell. The author has an hindex of 38, co-authored 111 publications receiving 4747 citations. Previous affiliations of Mary M. Lee include Harvard University & Cornell University.

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Mullerian inhibiting substance in humans: normal levels from infancy to adulthood

TL;DR: Data reveal an easily discernible sexually dimorphic pattern of expression of MIS and confirm that MIS can be used as a testis-specific marker during infancy and early childhood and facilitate the use of MIS in the management of gonadal disorders.
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Mullerian Inhibiting Substance: A Gonadal Hormone with Multiple Functions

TL;DR: The current understanding of the biology and multiple functions of MIS including its activation, regulation, and mechanism of action are summarized and areas of interest in ongoing research are discussed.
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Augmented growth hormone (GH) secretory burst frequency and amplitude mediate enhanced GH secretion during a two-day fast in normal men.

TL;DR: The present data suggest that starvation-induced enhancement of GH secretion is mediated by an increased frequency of GHRH release, and longer and more pronounced periods of somatostatin withdrawal.
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Measurements of Serum Müllerian Inhibiting Substance in the Evaluation of Children with Nonpalpable Gonads

TL;DR: Measurements of serum mullerian inhibiting substance can be used to determine testicular status in prepubertal children with nonpalpable gonads, thus differentiating anorchia from undescended testes in boys with bilateral cryptorchidism and serving as a measure of testicular integrity in children with intersexual anomalies.
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Alterations in the Pulsatile Mode of Growth Hormone Release in Men and Women with Insulin-Dependent Diabetes Mellitus

TL;DR: The altered frequency of GH pulses together with enhanced interpulse GH concentrations and an amplified circadian GH rhythm are compatible with hypothalamic dysfunction associated with dysregulation of somatostatin and/or GHRH secretion.