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Page 1
Peroxisomal abnormalities and catalase deficiency in Hutchinson-Gilford Progeria Syndrome.
Mao X, Bharti P, Thaivalappil A, Cao K. Mao X, et al. Aging (Albany NY). 2020 Mar 18;12(6):5195-5208. doi: 10.18632/aging.102941. Epub 2020 Mar 18. Aging (Albany NY). 2020. PMID: 32186522 Free PMC article.
Our study presents the first characterization of peroxisomal function in HGPS and provides new insights into the cellular aspects of HGPS and the ongoing clinical trial....
Our study presents the first characterization of peroxisomal function in HGPS and provides new insights into the cellular aspects of HGPS an …
Reduced lifespan of mice lacking catalase correlates with altered lipid metabolism without oxidative damage or premature aging.
Pérez-Estrada JR, Hernández-García D, Leyva-Castro F, Ramos-León J, Cuevas-Benítez O, Díaz-Muñoz M, Castro-Obregón S, Ramírez-Solís R, García C, Covarrubias L. Pérez-Estrada JR, et al. Free Radic Biol Med. 2019 May 1;135:102-115. doi: 10.1016/j.freeradbiomed.2019.02.016. Epub 2019 Feb 25. Free Radic Biol Med. 2019. PMID: 30818059
Distribution of polymorphic traits in Mazandaranian and Guilanian in Iran.
Ohkura K, Miyashita T, Nakajima H, Matsumoto H, Matsutomo K, Rahabar S, Hedayat S. Ohkura K, et al. Hum Hered. 1984;34(1):27-39. doi: 10.1159/000153414. Hum Hered. 1984. PMID: 6234219
In 1972, over 2,000 blood specimens were obtained from two Iranian populations, Mazandaranians and Guilanians, who live on the southern coast of the Caspian Sea. All specimens were screened for hypocatalasemics and randomly selected samples were analyzed for several blood …
In 1972, over 2,000 blood specimens were obtained from two Iranian populations, Mazandaranians and Guilanians, who live on the southern coas …
Unstable mutants and molecular hybrids in enzyme deficiency conditions.
Aebi H, Wyss SR, Scherz B. Aebi H, et al. Acta Biol Med Ger. 1977;36(5-6):735-41. Acta Biol Med Ger. 1977. PMID: 602579
In heterozygous carriers of oligomeric enzyme defects, the formation of hybrid molecules is possible by random assembly of simultaneously synthetized normal and mutant subunits. ...
In heterozygous carriers of oligomeric enzyme defects, the formation of hybrid molecules is possible by random assembly of simultaneo …