Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Elif Sibel Aslan"'
Autor:
Cansu Hemşinlioğlu, Elif Sibel Aslan, Cihan Tastan, Didem Çakırsoy, Raife Dilek Turan, Utku Seyis, Muhammer Elek, Gözde Sır Karakuş, Ömür Selin Günaydın, Selen Abanuz, Derya Dilek Kançağı, Bulut Yurtsever, Koray Yalçın, Murat Kasap, Ercüment Ovalı
Publikováno v:
Turkish Journal of Hematology, Vol 40, Iss 2, Pp 118-124 (2023)
Objective: Hemophilia A is an X-linked recessive bleeding disorder caused by a deficiency of plasma coagulation factor VIII (FVIII), and it accounts for about 80%-85% of all cases of hemophilia. Plasma-derived therapies or recombinant FVIII concentra
Externí odkaz:
https://doaj.org/article/c4d89b70bef242af9b222fa0e01cf281
Autor:
Elif Sibel Aslan, Hüseyin Aydın, Yusuf Kenan Tekin, Sami Keleş, Kenneth N. White, Nezih Hekim
Publikováno v:
Molecular Biology Reports. 50:2471-2478
Due to the growing evidence of the importance of iron status in immune responses, the biomarkers of iron metabolism are of interest in novel Coronavirus Disease 2019 (COVID-19). The present prospective study was carried out to compare iron status ind
Autor:
Cansu Hemşinlioğlu, Elif Sibel Aslan, Cihan Taştan, Didem Çakırsoy, Raife Dilek Turan, Utku Seyis, Muhammer Elek, Gözde Sir Karakuş, Ömur Selin Günaydın, Selen Abanuz, Derya Dilek Kançağı, Bulut Yurtsever, Koray Yalçın9, Murat Kasap, Ercüment Ovalı
Publikováno v:
Turkish Journal of Hematology.
Objective: Hemophilia A is an X-linked recessive bleeding disorder caused by a deficiency of plasma coagulation factor VIII (FVIII), and it accounts for about 80%-85% of all cases of hemophilia. Plasma-derived therapies or recombinant FVIII concentra
Autor:
Gülsen Meral, Elif Sibel Aslan
Publikováno v:
Moleküler Biyoloji ve Genetik ISBN: 9786258352481
After the completion of the human genome project in 2003, the use of Predictive, Preventive, Personalized, Participatory therapy has gained momentum in modern medicine and pharmacy, with the demonstration of genetic variations among humans. Genome st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1ea1f40d59af1374d4215d6a09b7ef7
https://doi.org/10.53478/tuba.978-625-8352-48-1.ch16
https://doi.org/10.53478/tuba.978-625-8352-48-1.ch16
Autor:
Safiye Gunes Sager, Ayberk Turkyilmaz, Hediye Pınar Gunbey, Elif Yuksel Karatoprak, Elif Sibel Aslan, Yasemin Akın
Background: Beck-Fahrner syndrome is caused by homozygous or heterozygous mutations in TET3 on chromosome 2p13. The general characteristics of this syndrome include behavioral abnormalities such as autistic features, attention-deficit hyperactivity d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c10af880260f6d3e4b56558921cc854
https://hdl.handle.net/20.500.12445/2841
https://hdl.handle.net/20.500.12445/2841
Publikováno v:
Croatian Medical Journal
Volume 61
Issue 5
Volume 61
Issue 5
Aim To assess kallikrein (KLK) expression in recurrent and non-recurrent prostate tumors and adjacent healthy prostate tissues. Methods The expression levels of 15 KLK genes in 34 recurrent and 36 non-recurrent prostate cancer samples and 19 adjacent
Publikováno v:
SSRN Electronic Journal.
Autor:
Huseyin Avni Solgun, Elif Sibel Aslan, Meryem Alagoz, Seyda Demirkol, Süreyya Bozkurt, Nasim Kherad, Alper Ozkılıc, Adnan Yuksel
X-lined intellectual disability (XLID), formerly known as X-lined mental retardation, is defined as genetically heterogeneous disorders with remarkable cognitive impairment and abnormal adaptive behaviour skills. This study demonstrates the Disc-larg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03f397ba349de72ac874390b5a812c98
https://doi.org/10.21203/rs.3.rs-692598/v1
https://doi.org/10.21203/rs.3.rs-692598/v1
Genetic manipulation of Escherichia coli influences the regulation of bacterial metabolism, which could be useful for the production of different targeted products. The RpoZ gene encodes for the omega subunit of the RNA polymerase (RNAP) and is invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fca16cd40686e3aac003f278a4c33a3
https://aperta.ulakbim.gov.tr/record/231836
https://aperta.ulakbim.gov.tr/record/231836
Publikováno v:
Turkish Journal of Biology
Volume: 44, Issue: 6 393-405
Volume: 44, Issue: 6 393-405
Hephaestin (Hp) is a trans-membrane protein, which plays a critical role in intestinal iron absorption. Hp was originally identified as the gene responsible for the phenotype of sex-linked anaemia in the sla mouse. The mutation in the sla protein cau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af598708ac70a2d1d9b21723f7b08df6
https://repository.londonmet.ac.uk/6227/1/Turkish-J-Biol_v44-393_2020_Soluble-hephaestin.pdf
https://repository.londonmet.ac.uk/6227/1/Turkish-J-Biol_v44-393_2020_Soluble-hephaestin.pdf