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phenylmethylsulfonyl fluoride and Thalassemias

phenylmethylsulfonyl fluoride has been researched along with Thalassemias in 1 studies

Phenylmethylsulfonyl Fluoride: An enzyme inhibitor that inactivates IRC-50 arvin, subtilisin, and the fatty acid synthetase complex.
phenylmethanesulfonyl fluoride : An acyl fluoride with phenylmethanesulfonyl as the acyl group.

Research Excerpts

ExcerptRelevanceReference
"beta-Thalassemia is an inherited human disorder which is characterized by a deficient production of hemoglobin beta chains and an attendant accumulation of structurally normal alpha chains in the erythropoietic cells."1.27ATP-dependent proteolysis of hemoglobin alpha chains in beta-thalassemic hemolysates is ubiquitin-dependent. ( Shaeffer, JR, 1988)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Shaeffer, JR1

Other Studies

1 other study available for phenylmethylsulfonyl fluoride and Thalassemias

ArticleYear
ATP-dependent proteolysis of hemoglobin alpha chains in beta-thalassemic hemolysates is ubiquitin-dependent.
    The Journal of biological chemistry, 1988, Sep-25, Volume: 263, Issue:27

    Topics: Adenosine Triphosphate; Antibodies; Cell-Free System; Ethylmaleimide; Globins; Hemoglobins; Humans;

1988