Zobrazeno 1 - 2
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pro vyhledávání: '"H. S. Karaman"'
Publikováno v:
Cytology and Genetics. 54:130-136
Proximal spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease caused by homozygous deletion in the seventh exon of the SMN1 gene. The aim of this work is to analyze the association of the allelic polymorphism of telomeric
Autor:
H S Karaman, O. G. Zabuga, Alexander Koliada, N. M. Koshel, Iryna Kozeretska, M V Inomistova, A. V. Pisaruk, Oleh V. Lushchak, Alexander Vaiserman, N M Khranovska, L. V. Mechova
Publikováno v:
Biogerontology. 20(2)
There is increasing evidence that stress during development can affect adult-life health status and longevity. In the present study, we examined life span (LS), fly weight, fecundity and expression levels of longevity-associated genes (Hsp70, InR, dS