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1-anilino-8-naphthalenesulfonate and Lipodystrophy

1-anilino-8-naphthalenesulfonate has been researched along with Lipodystrophy in 6 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.

Lipodystrophy: A collection of heterogenous conditions resulting from defective LIPID METABOLISM and characterized by ADIPOSE TISSUE atrophy. Often there is redistribution of body fat resulting in peripheral fat wasting and central adiposity. They include generalized, localized, congenital, and acquired lipodystrophy.

Research Excerpts

ExcerptRelevanceReference
"Ritonavir-treated cells had increased FA efflux, uptake, and incorporation into TAG (all P < 0."1.36Long-term ritonavir exposure increases fatty acid and glycerol recycling in 3T3-L1 adipocytes as compensatory mechanisms for increased triacylglycerol hydrolysis. ( Adler-Wailes, DC; Guiney, EL; Wolins, NE; Yanovski, JA, 2010)
"Lipoatrophic panniculitis describes the panniculitides in which atrophy is a feature."1.31Lipoatrophic panniculitis and chromosome 10 abnormality. ( Harper, JI; Hoeger, P; Malone, M; Martinez, A; Palmer, R, 2000)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's1 (16.67)18.2507
2000's2 (33.33)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Adler-Wailes, DC1
Guiney, EL1
Wolins, NE1
Yanovski, JA1
Gandotra, S1
Lim, K1
Girousse, A1
Saudek, V1
O'Rahilly, S1
Savage, DB1
vom Dahl, S1
Harzer, K1
Rolfs, A1
Albrecht, B1
Niederau, C1
Vogt, C1
van Weely, S1
Aerts, J1
Müller, G1
Häussinger, D1
Martinez, A1
Malone, M1
Hoeger, P1
Palmer, R1
Harper, JI1
Paglione, AM1
Ferrari, N1
Berg, G1
Frechtel, G1
Taverna, M1
Fasulo, V1
Lopez, GI1
Gomez, RM1
Bruno, O1
Ruiz, M1
Wikinski, RL1
Elleder, M1

Other Studies

6 other studies available for 1-anilino-8-naphthalenesulfonate and Lipodystrophy

ArticleYear
Long-term ritonavir exposure increases fatty acid and glycerol recycling in 3T3-L1 adipocytes as compensatory mechanisms for increased triacylglycerol hydrolysis.
    Endocrinology, 2010, Volume: 151, Issue:5

    Topics: 3T3-L1 Cells; Adipocytes; Adrenergic beta-Agonists; Animals; Enzyme Inhibitors; Fatty Acids; Gene Ex

2010
Human frame shift mutations affecting the carboxyl terminus of perilipin increase lipolysis by failing to sequester the adipose triglyceride lipase (ATGL) coactivator AB-hydrolase-containing 5 (ABHD5).
    The Journal of biological chemistry, 2011, Oct-07, Volume: 286, Issue:40

    Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; 3T3-L1 Cells; Adipose Tissue; Animals; Carrier Protein

2011
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.
    Journal of hepatology, 1999, Volume: 31, Issue:4

    Topics: Adult; Anemia; Cholesterol Ester Storage Disease; Diagnosis, Differential; DNA, Recombinant; Exons;

1999
Lipoatrophic panniculitis and chromosome 10 abnormality.
    The British journal of dermatology, 2000, Volume: 142, Issue:5

    Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 10; Female;

2000
[Acquired partial lipodystrophy. Insulin resistance, hepatic lipase activity and small and dense LDL particles].
    Medicina, 2001, Volume: 61, Issue:1

    Topics: Female; Humans; Insulin Resistance; Lipase; Lipid Metabolism; Lipodystrophy; Lipoprotein Lipase; Lip

2001
So-called membranocystic lesion (MCL)--a new variant of ceroid type lipopigment.
    Advances in experimental medicine and biology, 1989, Volume: 266

    Topics: Arteriosclerosis; Brain Diseases; Ceroid; Humans; Lipase; Lipidoses; Lipodystrophy; Sphingomyelin Ph

1989