1-anilino-8-naphthalenesulfonate has been researched along with Lipidoses in 30 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
Lipidoses: Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mixed hyperlipidemia, characterized by high levels of triglycerides and cholesterol, is a key risk factor leading to atherosclerosis and other cardiovascular diseases." | 1.91 | Novel application potential of cinaciguat in the treatment of mixed hyperlipidemia through targeting PTL/NPC1L1 and alleviating intestinal microbiota dysbiosis and metabolic disorders. ( Chen, P; Jia, A; Jiang, H; Liu, W; Sun, J; Xu, Q; Zhang, R, 2023) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 24 (80.00) | 18.7374 |
| 1990's | 2 (6.67) | 18.2507 |
| 2000's | 3 (10.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (3.33) | 2.80 |
| Authors | Studies |
|---|---|
| Jia, A | 1 |
| Jiang, H | 1 |
| Liu, W | 1 |
| Chen, P | 1 |
| Xu, Q | 1 |
| Zhang, R | 1 |
| Sun, J | 1 |
| Fischer, J | 1 |
| Lefèvre, C | 1 |
| Morava, E | 1 |
| Mussini, JM | 1 |
| Laforêt, P | 1 |
| Negre-Salvayre, A | 1 |
| Lathrop, M | 1 |
| Salvayre, R | 2 |
| Bruno, C | 1 |
| Bertini, E | 1 |
| Di Rocco, M | 1 |
| Cassandrini, D | 1 |
| Ruffa, G | 1 |
| De Toni, T | 1 |
| Seri, M | 1 |
| Spada, M | 1 |
| Li Volti, G | 1 |
| D'Amico, A | 1 |
| Trucco, F | 1 |
| Arca, M | 1 |
| Casali, C | 1 |
| Angelini, C | 1 |
| Dimauro, S | 1 |
| Minetti, C | 1 |
| Piva, E | 1 |
| Pajola, R | 1 |
| Binotto, G | 1 |
| Plebani, M | 1 |
| Leĭtes, FL | 1 |
| Golosovskaia, MA | 1 |
| Bruner, JM | 1 |
| Steiner, JM | 1 |
| Williams, DA | 1 |
| Van Alstine, WG | 1 |
| Blevins, W | 1 |
| vom Dahl, S | 1 |
| Harzer, K | 1 |
| Rolfs, A | 1 |
| Albrecht, B | 1 |
| Niederau, C | 1 |
| Vogt, C | 1 |
| van Weely, S | 1 |
| Aerts, J | 1 |
| Müller, G | 1 |
| Häussinger, D | 1 |
| Cortner, JA | 1 |
| Coates, PM | 1 |
| Swoboda, E | 1 |
| Schnatz, JD | 1 |
| Schaffner, T | 1 |
| Elner, VM | 1 |
| Bauer, M | 1 |
| Wissler, RW | 1 |
| Kelly, S | 1 |
| Bakhru-Kishore, R | 1 |
| von Bassewitz, DB | 1 |
| Roggenkamp, K | 1 |
| Strehl, H | 1 |
| Otto, H | 1 |
| Suzuki, Y | 1 |
| Kawai, S | 1 |
| Kobayashi, A | 1 |
| Ohbe, Y | 1 |
| Endo, H | 1 |
| Elleder, M | 1 |
| Douste-Blazy, L | 1 |
| Nègre, A | 1 |
| Maret, A | 1 |
| Kyriakides, EC | 1 |
| Paul, B | 1 |
| Balint, JA | 1 |
| Galton, DJ | 1 |
| Maggi, V | 1 |
| Gahan, PB | 1 |
| Khan, W | 1 |
| Kutty, KM | 1 |
| Rowden, G | 1 |
| Lake, BD | 2 |
| Fredrickson, DS | 2 |
| Sloan, HR | 2 |
| Ferrans, VJ | 1 |
| Demosky, SJ | 1 |
| Babushkina, LG | 1 |
| Burke, JA | 2 |
| Schubert, WK | 2 |
| Róiz, J | 1 |
| Young, EP | 1 |
| Patrick, AD | 1 |
| Wallis, K | 1 |
| Gross, M | 1 |
| Kohn, R | 1 |
| Zaidman, J | 1 |
| Joshi, UM | 1 |
| Kodavanti, PR | 1 |
| Coudert, B | 1 |
| Dwyer, TM | 1 |
| Mehendale, HM | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Prevalence and Mutation Rate of Lipa Gene in LIPIGEN Subjects With Clinical Diagnosis of FH[NCT03984149] | 1,000 participants (Anticipated) | Observational | 2017-09-01 | Recruiting | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
1 review available for 1-anilino-8-naphthalenesulfonate and Lipidoses
| Article | Year |
|---|---|
[The role of the lungs in fat metabolism and its disturbance in silicosis].
Topics: Aging; Animals; Cholesterol; Fatty Acids; Fibrin; Heparin; Humans; Hyperlipidemias; Lipase; Lipid Me | 1966 |
29 other studies available for 1-anilino-8-naphthalenesulfonate and Lipidoses
| Article | Year |
|---|---|
Novel application potential of cinaciguat in the treatment of mixed hyperlipidemia through targeting PTL/NPC1L1 and alleviating intestinal microbiota dysbiosis and metabolic disorders.
Topics: Cholesterol; Dysbiosis; Ezetimibe; Gastrointestinal Microbiome; Humans; Hyperlipidemias; Lipase; Lip | 2023 |
The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy.
Topics: Cells, Cultured; DNA Mutational Analysis; Female; Humans; Lipase; Lipidoses; Muscular Diseases; Muta | 2007 |
Clinical and genetic characterization of Chanarin-Dorfman syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adolescent; Adult; Child; Child, Preschool; DNA Mutati | 2008 |
Jordans' anomaly in a new neutral lipid storage disease.
Topics: Aged; Azo Compounds; Coloring Agents; Cytoplasm; Humans; Leukocytes; Lipase; Lipidoses; Lipids; Live | 2009 |
[Distribution of lipolytic enzymes in humans according to age].
Topics: Adolescent; Adrenal Glands; Adult; Aged; Aging; Blood Vessels; Bronchi; Child; Child, Preschool; Est | 1966 |
High feline trypsin-like immunoreactivity in a cat with pancreatitis and hepatic lipidosis.
Topics: Alanine Transaminase; Alkaline Phosphatase; Amylases; Animals; Antibodies; Bilirubin; Cat Diseases; | 1997 |
Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase -1 exon 8 splice junction mutation.
Topics: Adult; Anemia; Cholesterol Ester Storage Disease; Diagnosis, Differential; DNA, Recombinant; Exons; | 1999 |
Genetic variation of lysosomal acid lipase.
Topics: Cholesterol Esters; Electrophoresis; Female; Fibroblasts; Humans; Infant; Leukocytes; Lipase; Lipid | 1976 |
Acid lipase: a histochemical and biochemical study using triton X100-naphtyl palmitate micelles.
Topics: Animals; Colloids; Culture Techniques; Esterases; Haplorhini; Histocytochemistry; History, 18th Cent | 1978 |
Fluorimetric assay of acid lipase in human leukocytes.
Topics: Clinical Enzyme Tests; Fluorometry; Heterozygote; Humans; Leukocytes; Lipase; Lipidoses; Xanthomatos | 1979 |
[Wolman's disease].
Topics: Cholesterol Esters; Humans; Lipase; Lipidoses; Syndrome; Triglycerides; Xanthomatosis | 1978 |
Partial deficiency of acid lipase with storage of triglycerides and cholesterol esters in liver. Genetic variant of Wolman's disease?
Topics: Child; Cholesterol; Cholesterol Esters; Chromatography, Thin Layer; Fatty Liver; Humans; Lipase; Lip | 1976 |
So-called membranocystic lesion (MCL)--a new variant of ceroid type lipopigment.
Topics: Arteriosclerosis; Brain Diseases; Ceroid; Humans; Lipase; Lipidoses; Lipodystrophy; Sphingomyelin Ph | 1989 |
[Biotechnology and clinical biology].
Topics: Antibodies, Monoclonal; Apoproteins; Cholesterol; Clinical Enzyme Tests; Coronary Disease; Female; F | 1985 |
[Value of studying isoenzymes in hereditary lysosomal lipidoses. In particular beta-glucosidase (Gaucher's disease) and acid lipase (Wolman's disease and cholesterol ester storage disease)].
Topics: beta-Glucosidase; Gaucher Disease; Glucosidases; Humans; Isoenzymes; Lipase; Lipidoses | 1985 |
Lipid accumulation and acid lipase deficiency in fibroblasts from a family with Wolman's disease, and their apparent correction in vitro.
Topics: Adult; Cells, Cultured; Child; Cholesterol; Female; Fibroblasts; Humans; Lipase; Lipidoses; Male; Me | 1972 |
Hormonal control of lipolysis.
Topics: Adenylyl Cyclases; Adipose Tissue; Cyclic AMP; Enzyme Activation; Epinephrine; Fatty Acids; Humans; | 1974 |
Reinvestigation of the pathogenesis of familial xanthomatosis through conjoint cytochemical, ultrastructural, and biochemical studies.
Topics: Adrenal Glands; Diseases in Twins; Humans; Infant; Intestine, Small; Lipase; Lipid Metabolism; Lipid | 1972 |
When is a lipase not a lipase?
Topics: Esterases; Fatty Acids; Histocytochemistry; Hydrolases; Lipase; Lipidoses; Xanthomatosis | 1972 |
Cholesteryl ester storage disease: a most unusual manifestation of deficiency of two lysosomal enzyme activities.
Topics: Adolescent; Adult; Aorta; Arteriosclerosis; Autopsy; Carbon Isotopes; Child; Cholesterol; Coronary V | 1972 |
Is the histochemical demonstration of lipase activity possible?
Topics: Bile Acids and Salts; Esterases; Fatty Acids; Histocytochemistry; Lipase; Lipidoses; Lysosomes; Naph | 1972 |
Deficient activity of hepatic acid lipase in cholesterol ester storage disease.
Topics: Cholesterol; Colorimetry; Fatty Acids; Glycerol; Humans; Lipase; Lipid Metabolism, Inborn Errors; Li | 1972 |
Enzyme deficiency in cholesteryl ester storage idisease.
Topics: Adult; Aged; Aorta; Autopsy; Cholesterol; Chromatography, Thin Layer; Esterases; Esters; Gaucher Dis | 1972 |
Deficient activity of acid lipase in cholesterol-ester storage disease.
Topics: Cholesterol; Esters; Hepatomegaly; Humans; Lipase; Lipid Metabolism, Inborn Errors; Lipidoses; Liver | 1971 |
[Lipogenesis and lipolysis].
Topics: Body Weight; Epinephrine; Hormones; Humans; Lipase; Lipidoses; Obesity; Pituitary Gland; Triiodothyr | 1970 |
Deficiency of acid esterase activity in Wolman's disease.
Topics: Esterases; Esters; Fatty Acids; Female; Heterozygote; Humans; Hydrolases; Infant; Leukocytes; Lipase | 1970 |
A case of Wolman's disease.
Topics: Autopsy; Consanguinity; Humans; Infant, Newborn; Infant, Newborn, Diseases; Lipase; Lipidoses; Lipop | 1971 |
How much (or little) pancreas.
Topics: Humans; Intestinal Absorption; Lipase; Lipidoses; Pancreas; Pancreatectomy | 1968 |
Types of interaction of amphiphilic drugs with phospholipid vesicles.
Topics: Amiodarone; Anilino Naphthalenesulfonates; Binding Sites; Chloramphenicol; Chloroquine; Chlorpromazi | 1988 |