نتایج جستجو برای: 22 dehydrocholesterol

تعداد نتایج: 212275  

Journal: :The Journal of Cell Biology 1969
Scott E. Dietert Terence J. Scallen

Triparanol and 20,25-diazacholesterol inhibit cholesterol biosynthesis and result in the accumulation of desmosterol. AY-9944, another inhibitor, produces an accumulation of 7-dehydrocholesterol. Adult male C3H mice receive one of these drugs intraperitoneally. Livers, adrenal glands, and testes from each drug group are excised, and portions of each are analyzed by a modified Liebermann-Burchar...

Journal: :Journal of lipid research 2010
Zeljka Korade Libin Xu Richard Shelton Ned A Porter

Smith-Lemli-Opitz syndrome (SLOS) is a metabolic and developmental disorder caused by mutations in the gene encoding the enzyme 7-dehydrocholesterol reductase (Dhcr7). This reductase catalyzes the last step in cholesterol biosynthesis, and levels of 7-dehydrocholesterol (7-DHC), the substrate for this enzyme, are elevated in SLOS patients as a result of this defect. Our group has previously sho...

2012
Stephanie Seneff

7-dehydrocholesterol 7-Dehydrocholesterol is a cholesterol precursor, and is converted to vitamin D3 in the skin, therefore functioning as provitamin-D3. It is converted to vitamin D3 in the presence of UV rays from the sun. —————————————————————————————————————————— Acidosis Acidosis is an increased acidity in the blood and other body tissue (i.e., an increased hydrogen ion concentration). ———...

Journal: :Journal of lipid research 2004
Irina Serbanescu Mary Ann Ryan Ruchika Shukla Miguel A Cortez O Carter Snead Stephen C Cunnane

AY-9944 (AY) exacerbates chronic recurrent seizures in rats that are analogous to atypical absence epilepsy in humans. The mechanism by which AY affects the slow spike-and-wave discharges associated with these seizures is not known, but is thought to involve inhibition of cholesterol synthesis. We tested the hypothesis that seizures seen with AY are due to significant reduction in brain cholest...

2003
J. SCALLEN

Triparanol and 20,25-diazacholesterol inhibit cholesterol biosynthesis and result in the accumulation of desmosterol. AY-9944, another inhibitor, produces an accumulation of 7-dehydrocholesterol. Adult male C3H mice receive one of these drugs intraperitoneally. Livers, adrenal glands, and testes from each drug group are excised, and portions of each are analyzed by a modified Liebermann-Burchar...

2003
J. SCALLEN

Triparanol and 20,25-diazacholesterol inhibit cholesterol biosynthesis and result in the accumulation of desmosterol. AY-9944, another inhibitor, produces an accumulation of 7-dehydrocholesterol. Adult male C3H mice receive one of these drugs intraperitoneally. Livers, adrenal glands, and testes from each drug group are excised, and portions of each are analyzed by a modified Liebermann-Burchar...

2012
Enzo Emanuele Marco Bertona Karmela Altabas Velimir Altabas Giuseppe Alessandrini

PURPOSE Acne vulgaris is a skin disorder of the sebaceous follicles, involving hyperkeratinization and perifollicular inflammation. Aberrant extracellular matrix remodeling due to matrix metalloproteinases (MMPs) has been associated with the presence of acne conditions. Given the complex pathophysiology of acne, novel topical therapies should include combination products that target multiple pa...

Journal: :Journal of lipid research 2002
Françoise Chevy Françoise Illien Claude Wolf Charles Roux

Triparanol, an inhibitor of desmosterol Delta24 reductase, produces a high rate of limb malformations in rat fetuses exposed at gestational day 10 (gd 10) to a single oral dose (150-200 mg/kg) given to the pregnant dam. AY9944, another efficient distal inhibitor of cholesterol biosynthesis that blocks dehydrocholesterol Delta7 reductase, produces a similar degree of cholesterol depletion but fe...

2014
Lee Ying Xavier Matabosch Montserrat Serra Berna Watson Cedric Shackleton Gordon Watson

Smith-Lemli-Opitz syndrome (SLOS) is an inborn error of cholesterol synthesis resulting from a defect in 7-dehydrocholesterol reductase (DHCR7), the enzyme that produces cholesterol from its immediate precursor 7-dehydrocholesterol. Current therapy employing dietary cholesterol is inadequate. As SLOS is caused by a defect in a single gene, restoring enzyme functionality through gene therapy may...

Journal: :American journal of medical genetics. Part A 2006
Darryn M Sikora Kersti Pettit-Kekel Jennifer Penfield Louise S Merkens Robert D Steiner

Smith-Lemli-Opitz syndrome (SLOS) is an autosomal recessive condition caused by a defect in cholesterol synthesis. Affected children often have malformations and mental retardation. Autistic behaviors also are evident. The purpose of the present study was to determine the prevalence of autism spectrum disorders (ASDs) in children with SLOS. Fourteen children, 3-16 years old, were evaluated usin...

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