Page last updated: 2024-11-05

troglitazone and Fanconi Anemia

troglitazone has been researched along with Fanconi Anemia in 1 studies

Troglitazone: A chroman and thiazolidinedione derivative that acts as a PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS (PPAR) agonist. It was formerly used in the treatment of TYPE 2 DIABETES MELLITUS, but has been withdrawn due to hepatotoxicity.

Fanconi Anemia: Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Sertorio, M1
Du, W1
Amarachintha, S1
Wilson, A1
Pang, Q1

Other Studies

1 other study available for troglitazone and Fanconi Anemia

ArticleYear
InĀ Vivo RNAi Screen Unveils PPARĪ³ as a Regulator of Hematopoietic Stem Cell Homeostasis.
    Stem cell reports, 2017, 05-09, Volume: 8, Issue:5

    Topics: Animals; Benzamides; Cells, Cultured; Chromans; Fanconi Anemia; Fanconi Anemia Complementation Group

2017