Search Results - "Learned, Marc R."
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1
Non-cell-autonomous activation of IL-6/STAT3 signaling mediates FGF19-driven hepatocarcinogenesis
Published in Nature communications (16-05-2017)“…Hepatocellular carcinoma (HCC), a primary malignancy of the liver, is the second leading cause of cancer mortality worldwide. Fibroblast Growth Factor 19 (…”
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2
FGF19 Analog as a Surgical Factor Mimetic That Contributes to Metabolic Effects Beyond Glucose Homeostasis
Published in Diabetes (New York, N.Y.) (01-06-2019)“…Bariatric surgery has proven to be the most effective treatment for controlling hyperglycemia in severely obese patients with diabetes. We show that fibroblast…”
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3
Therapeutic FGF19 promotes HDL biogenesis and transhepatic cholesterol efflux to prevent atherosclerosis[S]
Published in Journal of lipid research (01-03-2019)“…Fibroblast growth factor (FGF)19, an endocrine hormone produced in the gut, acts in the liver to control bile acid synthesis. NGM282, an engineered FGF19…”
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4
Separating Tumorigenicity from Bile Acid Regulatory Activity for Endocrine Hormone FGF19
Published in Cancer research (Chicago, Ill.) (15-06-2014)“…Hepatocellular carcinoma (HCC), one of the leading causes of cancer-related death, develops from premalignant lesions in chronically damaged livers. Although…”
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5
Mouse species-specific control of hepatocarcinogenesis and metabolism by FGF19/FGF15
Published in Journal of hepatology (01-06-2017)“…Graphical abstract…”
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6
A nontumorigenic variant of FGF19 treats cholestatic liver diseases
Published in Science translational medicine (30-07-2014)“…Hepatic accumulation of bile acids is central to the pathogenesis of cholestatic liver diseases. Endocrine hormone fibroblast growth factor 19 (FGF19) may…”
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7
Engineered FGF19 eliminates bile acid toxicity and lipotoxicity leading to resolution of steatohepatitis and fibrosis in mice
Published in Hepatology communications (01-12-2017)“…Nonalcoholic fatty liver disease (NAFLD) is an increasingly prevalent chronic liver disease for which no approved therapies are available. Despite intensive…”
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8
T0070907, a Selective Ligand for Peroxisome Proliferator-activated Receptor γ, Functions as an Antagonist of Biochemical and Cellular Activities
Published in The Journal of biological chemistry (31-05-2002)“…The nuclear hormone receptor peroxisome proliferator-activated receptor γ (PPARγ (NR1C3)) plays a central role in adipogenesis and is the molecular target for…”
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9
Engineered fibroblast growth factor 19 reduces liver injury and resolves sclerosing cholangitis in Mdr2‐deficient mice
Published in Hepatology (Baltimore, Md.) (01-03-2016)“…Defects in multidrug resistance 3 gene (MDR3), which encodes the canalicular phospholipid flippase, cause a wide spectrum of cholangiopathy phenotypes in…”
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10
INT131: A Selective Modulator of PPARγ
Published in Journal of molecular biology (13-03-2009)“…The nuclear hormone receptor peroxisome proliferator-activated receptor γ (PPARγ; NR1C3) plays a central role in adipogenesis and is the molecular target of…”
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11
T2384, a Novel Antidiabetic Agent with Unique Peroxisome Proliferator-activated Receptor γ Binding Properties
Published in The Journal of biological chemistry (04-04-2008)“…The nuclear hormone receptor peroxisome proliferator-activated receptor γ (PPARγ) plays central roles in adipogenesis and glucose homeostasis and is the…”
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12
Discovery of INT131: A selective PPARγ modulator that enhances insulin sensitivity
Published in Bioorganic & medicinal chemistry (15-02-2013)“…PPARγ is a member of the nuclear hormone receptor family and plays a key role in the regulation of glucose homeostasis. This Letter describes the discovery of…”
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13
Identification of a Nuclear Receptor for Bile Acids
Published in Science (American Association for the Advancement of Science) (21-05-1999)“…Bile acids are essential for the solubilization and transport of dietary lipids and are the major products of cholesterol catabolism. Results presented here…”
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14
Functional Cooperativity between Transcription Factors UBF1 and SL1 Mediates Human Ribosomal RNA Synthesis
Published in Science (American Association for the Advancement of Science) (02-09-1988)“…The human ribosomal RNA promoter contains two distinct control elements (UCE and core) both of which are recognized by the sequence-specific DNA binding…”
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15
Novel antineoplastic agents with efficacy against multidrug resistant tumor cells
Published in Bioorganic & medicinal chemistry letters (06-10-1998)“…A novel series of pentafluorobenzenesulfonamides has been shown to inhibit the growth of a variety of human tumor cell lines. Among the cell types against…”
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16
Light modulates the spatial patterns of 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase gene expression in Arabidopsis thaliana
Published in The Plant journal : for cell and molecular biology (01-03-1997)“…Summary Although the coordinated biosynthesis of isoprenoid compounds is thought to be essential to the normal processes of plant growth and development, the…”
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17
Co‐expression of native and introduced genes reveals cryptic regulation of HMG CoA reductase expression in Arabidopsis
Published in The Plant journal : for cell and molecular biology (01-05-1995)“…In eukaryotes, all isoprenoid compounds share a common precursor, mevalonic acid, whose synthesis is catalyzed by the enzyme 3‐hydroxy‐3‐methylglutaryl…”
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18
Discovery of INT131: A selective PPAR[gamma] modulator that enhances insulin sensitivity
Published in Bioorganic & medicinal chemistry (15-02-2013)“…PPAR[gamma] is a member of the nuclear hormone receptor family and plays a key role in the regulation of glucose homeostasis. This Letter describes the…”
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19
T2384, a Novel Antidiabetic Agent with Unique Peroxisome Proliferator-activated Receptor γ Binding Properties
Published in The Journal of biological chemistry (04-04-2008)“…The nuclear hormone receptor peroxisome proliferator-activated receptor γ (PPARγ) plays central roles in adipogenesis and glucose homeostasis and is the…”
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Journal Article -
20
Novel halogenated sulfonamides inhibit the growth of multidrug resistant MCF-7/ADR cancer cells
Published in Bioorganic & medicinal chemistry letters (05-07-1999)“…In this report, we describe the synthesis of halogenated benzenesulfonamide compounds and their ability to inhibit the growth of HeLa, MCF-7 and MCF-7/ADR…”
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