نتایج جستجو برای: all trans retinoic acid

تعداد نتایج: 2555880  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1995
P S Bernstein S Y Choi Y C Ho R R Rando

Retinoid-binding proteins are essential mediators of vitamin A function in vertebrate organisms. They solubilize and stabilize retinoids, and they direct the intercellular and intracellular trafficking, transport, and metabolic function of vitamin A compounds in vision and in growth and development. Although many soluble retinoid-binding proteins and receptors have been purified and extensively...

Journal: :The Journal of clinical investigation 1985
H Oikarinen A I Oikarinen E M Tan R P Abergel C A Meeker M L Chu D J Prockop J Uitto

Recent clinical observations have suggested that retinoids, which are in frequent use in dermatology, can affect the connective tissue metabolism in skin and other tissues. In this study, we examined the effects of several retinoids on the metabolism of collagen by human skin fibroblasts in culture. Incubation of cultured fibroblasts with all-trans-retinoic acid or 13-cis-retinoic acid, in 10(-...

Journal: :Environmental toxicology and chemistry 2004
Patrick K Schoff Gerald T Ankley

Methoprene (isopropyl (2E,4E)-11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate) is an insect juvenile hormone agonist that blocks metamorphosis in some insects. Recent evidence suggests that a metabolite, methoprene acid, activates vertebrate retinoid X receptors (RXRs), and may interfere with retinoic acid-regulated developmental processes. Methoprene, methoxy-methoprene acid, and two major brea...

2012
Yifei Zhong Yingwei Wu Ruijie Liu Yueyi Deng Sandeep Mallipattu Paul Klotman Peter Chuang John Cijiang He

Retinoic acid decreases proteinuria and glomerulosclerosis in several animal models of kidney disease by protecting podocytes from injury. Our recent in vitro studies suggest that all-trans retinoic acid induces podocyte differentiation by activating the retinoic acid receptor-α (RARα)/cAMP/PKA/CREB pathway. When used in combination with all-trans retinoic acid, an inhibitor of phosphodiesteras...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2005
Michinaga Matsumoto Hirokazu Yokoyama Hidekazu Suzuki Haruko Shiraishi-Yokoyama Toshifumi Hibi

Alcohol dehydrogenase (ADH) participates in the formation of retinoic acid from retinol in various organs including the gastric mucosa. However, its clinical significance still remains to be clarified. In this study, we identified the ADH isoforms responsible for the retinoic acid formation among various ADH isoforms and examined associations among the ADH activities, the retinoic acid formatio...

Journal: :Blood 1990
C Chomienne P Ballerini N Balitrand M T Daniel P Fenaux S Castaigne L Degos

All-trans retinoic acid induces leukemic cells from patients with acute promyelocytic leukemia (M3) to differentiate in vitro to mature granulocytes which express the CD15 antigen and are capable of respiratory burst function. Of 35 M3 samples, only one failed to respond. In eight cases, we compared the efficacy of two naturally occurring isomers of retinoic acid, all-trans RA and 13-cis RA. Bo...

2003
Masahiro Kizaki Yasuo Ikeda Ryuji Tanosaki Hideaki Nakajima Minoru Morikawa Akiko Sakashita Phillip Koeffler

Retinoic acid modulates proliferation and differentiation of a wide variety of normal and leukemic cells through two distinct families of transcriptional factors: the retinoic acid receptors (RARs) and the retinoid X receptors (RXRs). A stereoisomer of retinoic acid, 9-cis-retinoic acid, is a highaffinity ligand for RXR and binds efficiently to RAR. In contrast, all-trans-retinoic acid interact...

Journal: :E3S web of conferences 2022

All-trans retinoic acid (10) was synthesized by β-ionone (5) through knoevenagel condensation, reduction and hydrolysis reaction. Then, hydroxyl-pinacolone retinoate (11) prepared the esterification with 1-hydroxy- 3, 3-dimethylbutan-2-ketone. This route not only reduces synthesis steps but also helps to increase yield. The structure of product characterized 1 H NMR 13 C NMR.

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