B
Billie M. Moats-Staats
Researcher at University of North Carolina at Chapel Hill
Publications - 44
Citations - 2326
Billie M. Moats-Staats is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Growth factor & Insulin-like growth factor. The author has an hindex of 24, co-authored 44 publications receiving 2260 citations.
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Journal ArticleDOI
Somatomedin-C/insulin-like growth factor-I and insulin-like growth factor-II mRNAs in rat fetal and adult tissues.
Pauline K. Lund,Billie M. Moats-Staats,Mary Hynes,James G. Simmons,M. Jansen,A J D'Ercole,J J Van Wyk +6 more
TL;DR: In this article, 32P-labeled complementary DNA probes encoding human and mouse Sm-C/IGF-I and human IGF-II were used in Northern blot hybridization to analyse rat SmC/I and insulin-like growth factor II mRNAs in poly(A+) RNAs from intestine, liver, lung, and brain of adults and fetal rats between day 14 and 17 of gestation.
Journal ArticleDOI
Nucleotide sequence analysis of a cDNA encoding human ubiquitin reveals that ubiquitin is synthesized as a precursor.
Pauline K. Lund,Billie M. Moats-Staats,James G. Simmons,Eileen C. Hoyt,A J D'Ercole,F Martin,J J Van Wyk +6 more
TL;DR: The finding that Ubiquitin is synthesized as a precursor raises the possibility that the precursor sequence may be important in compartmentalization of ubiquitin or ubiquitIn precursors.
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Gene expression of insulin-like growth factors (IGFs), the type 1 IGF receptor, and IGF-binding proteins in dexamethasone-induced fetal growth retardation.
TL;DR: Analysis of gene expression in 20-day gestation liver and lung of growth-retarded fetuses did not support a role for decreased IGF or IGF receptor expression in the etiology of DXM-mediated growth retardation, and suggested that increased expression of IGFBP-1, and possibly IGF BP-2, is involved in mediating the marked growth retardedation.
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Expression of insulin-like growth factor-i (igf-i) and igf-binding proteins during adipogenesis
TL;DR: The presence of a larger isoform of IGFBP-2 in a differentiation-dependent manner and a potentially novel IGFBP in response to IGF-I suggests that these IGFBPs may be important in modulating IGF- I action in adipogenesis.
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Treatment of childhood kaposiform hemangioendothelioma with sirolimus.
TL;DR: The experience with a 1‐year‐old female with a kaposiform hemangioendothelioma and Kasabach–Merritt phenomenon who had rapid and dramatic response to sirolimus (0.1 mg/kg/day) provides further rationale for clinical trials of siro Limus in the treatment of vascular lesions.