Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Uğur Akpulat"'
Autor:
Kouadio Ibrahime Sinan, Uğur Akpulat, Afaf A. Aldahish, Yasemin Celik Altunoglu, Mehmet Cengiz Baloğlu, Dimitrina Zheleva-Dimitrova, Reneta Gevrenova, Devina Lobine, Mohamad Fawzi Mahomoodally, Ouattara Katinan Etienne, Gokhan Zengin, Shafi Mahmud, Raffaele Capasso
Publikováno v:
Antioxidants, Vol 10, Iss 12, p 2003 (2021)
Boerhavia diffusa is a great tropical plant and is widely used for various traditional purposes. In the present study, we examined the influence of solvents (dichloromethane, ethyl acetate, methanol and infusion (water)) on chemical composition and b
Externí odkaz:
https://doaj.org/article/dce6d9ef817343ee89dbaddbfdf70664
Publikováno v:
Physiological genomics. 48(6)
The pathological endpoint of congenital and senile myopathies is chronic muscle degeneration characterized by the atrophy of contractile elements, accompanied by fibrosis and fatty infiltration of the interstitium. Tenotomy is the release of preload
Publikováno v:
Gene. 553(2)
The transcriptional events and pathways responsible for the acquisition of the myogenic phenotype during regeneration and myogenesis have been studied extensively. The modulators that shape the extracellular matrix in health and disease, however, are
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 383(5)
Hydrogen sulfide (H2S) is an endogenous gas which has potent relaxant effect in vascular and nonvascular smooth muscles. In the present study, we have investigated how streptozotocin (STZ)-induced diabetes affected the relaxant effect of H2S in rat i
Autor:
Berna Binnur Akdede, Arzu Dalmiş, Çiğdem Eresen, Sefa Kızıldağ, Uğur Akpulat, Haluk Arkar, Yildiz Akvardar, Köksal Alptekin, Şebnem Yildirimcan
Objective: Focusing on dopaminergic system, which is regarded to be responsible for alcohol dependence in many studies on animals and human beings, it is aimed to investigate TaqI A and B allel polymorphisms of Dopamine 2 receptor and personality cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b107571fc80415073ad11e528695ed7a
https://avesis.deu.edu.tr/publication/details/b5e5097f-73c6-4799-ab03-c8bdb6e842ca/oai
https://avesis.deu.edu.tr/publication/details/b5e5097f-73c6-4799-ab03-c8bdb6e842ca/oai
Autor:
Ugur Akpulat, Haicui Wang, Kerstin Becker, Adriana Contreras, Terence A. Partridge, James S. Novak, Sebahattin Cirak
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 13, Iss , Pp 534-542 (2018)
Duchenne muscular dystrophy is a fatal muscle disease, caused by mutations in DMD, leading to loss of dystrophin expression. Phosphorodiamidate morpholino splice-switching oligonucleotides (PMO-SSOs) have been used to elicit the restoration of a part
Externí odkaz:
https://doaj.org/article/4a0a9be8197348849a6261c46ded45ab