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Akademický článek
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Autor:
Jake D'Addiego, Nazif Elaldi, Nadina Wand, Karen Osman, Binnur Koksal Bagci, Emma Kennedy, Ayse Nur Pektas, Eilish Hart, Gillian Slack, Roger Hewson
Publikováno v:
Journal of Medical Virology. 95
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae0f5cdcdb194bb082a2613c2c616622
https://doi.org/10.1002/jmv.28548
https://doi.org/10.1002/jmv.28548
Autor:
Jake D'Addiego, Sonal Shah, Ayşe Nur Pektaş, Bi̇nnur Köksal Bağci, Murtaza Öz, Sasha Sebastianelli, Nazif Elaldı, David J Allen, Roger Hewson
Publikováno v:
Virus Research, Vol 350, Iss , Pp 199464- (2024)
Crimean-Congo haemorrhagic fever (CCHF) is the most prevalent human tick-borne viral disease, with a reported case fatality rate of 30 % or higher. The virus contains a tri-segmented, negative-sense RNA genome consisting of the small (S), medium (M)
Externí odkaz:
https://doaj.org/article/a55ee49ef89645f682a39966e56229d1
Autor:
Selma Cetinkaya, Ilhan Sezgin, Zekeriya Öztemur, Haldun Sümer, Dilara İçağasıoğlu, Ferhan Candan, Atilla Uslu, Şenol Çitli, Mansur Kayataş, Binnur Koksal, Fazilet Yildiz, Sulhattin Arslan, Hande Küçük Kurtulgan, Öztürk Özdemir
Publikováno v:
Molecular Biology Reports. 38:3195-3200
WOS: 000290102100044
PubMed ID: 20165923
The Familial Mediterranean Fever (FMF) shows an autosomal recessive pattern of inheritance and affects certain ethnic groups. Disease is caused by mutations in MEFV gene and more than 180 mutations h
PubMed ID: 20165923
The Familial Mediterranean Fever (FMF) shows an autosomal recessive pattern of inheritance and affects certain ethnic groups. Disease is caused by mutations in MEFV gene and more than 180 mutations h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2ef5f792d716bc8f4b56026e46769ac
https://doi.org/10.1007/s11033-010-9991-7
https://doi.org/10.1007/s11033-010-9991-7
Autor:
Fazilet Yildiz, Eylem Gul, Esin Yildiz, Binnur Koksal, Gökhan Gökçe, Semih Ayan, Öztürk Özdemir
Publikováno v:
Health. :850-856
In a total of 83 UN specimens were investigated for proto-oncogene mutations, tumor supressor genes promoter methylation status and c-myc and Ki-67 expression. Point mutations in c-myc were detected in cases with high grade and proliferation index. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2b73b2163aa317244817fbbc126f77c
https://doi.org/10.4236/health.2010.28128
https://doi.org/10.4236/health.2010.28128
Autor:
Musa Sari, Ferhan Candan, Öztürk Özdemir, Binnur Koksal, Mursit Acemoglu, Naim Nur, Nadir Koçak, Filiz Ozen
Publikováno v:
Biologia. 64:388-393
WOS: 000263540800026
Familial Mediterranean fever (FMF) is the most frequent hereditary inflammatory disease characterized by self-limited recurrent attacks of fever and serositis. The aim of the current study is to determine the frequency of th
Familial Mediterranean fever (FMF) is the most frequent hereditary inflammatory disease characterized by self-limited recurrent attacks of fever and serositis. The aim of the current study is to determine the frequency of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a69c4de0907bc01aaa82c2ed9f4a58f
https://doi.org/10.2478/s11756-009-0047-1
https://doi.org/10.2478/s11756-009-0047-1
Autor:
Öztürk Özdemir, Ferhan Candan, Malik Ejder Yildirim, Hande Küçük Kurtulgan, Fatma Silan, Mansur Kayataş, Mine Urfali, Binnur Koksal, Selma Cetinkaya
Publikováno v:
Renal failure. 37(2)
WOS: 000350554300021
PubMed ID: 25394530
Background and aim: There is an increased mortality risk in long-term hemodialysis patients of renal failure due to the chronic inflammation. The relationship between the chronic renal failure (CRF)
PubMed ID: 25394530
Background and aim: There is an increased mortality risk in long-term hemodialysis patients of renal failure due to the chronic inflammation. The relationship between the chronic renal failure (CRF)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f36269e84970f9f55c3613dbf2ee1b3b
https://pubmed.ncbi.nlm.nih.gov/25394530
https://pubmed.ncbi.nlm.nih.gov/25394530
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6f3d8731b2860d07b31592ff85a8578
https://doi.org/10.1530/endoabs.32.p379
https://doi.org/10.1530/endoabs.32.p379
WOS: 000328273000092
PubMed ID: 24175847
In the current study we aimed to show the common YMDD motif mutations in viral polymerase gene in chronic hepatitis B patients during lamivudine and adefovir therapy. Forty-one serum samples obtained
PubMed ID: 24175847
In the current study we aimed to show the common YMDD motif mutations in viral polymerase gene in chronic hepatitis B patients during lamivudine and adefovir therapy. Forty-one serum samples obtained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::873caa56ed2e96e1dcf76f0ac7587539
https://hdl.handle.net/20.500.12418/8839
https://hdl.handle.net/20.500.12418/8839
