Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Murat Büyükdoğan"'
Publikováno v:
Thalassemia Reports, Vol 8, Iss 2 (2018)
The mutation detection of β thalassemia is absolutely necessary for molecular diagnosis, as well as any genetic epidemiological study. The β globin gene has 3 exons and 2 introns, involved in β-thalassemic pathogenesis. The study aim of the study
Externí odkaz:
https://doaj.org/article/b1ca060f861c4252bf2f0dbee52d01b4
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 2, Pp 135-136 (2020)
Externí odkaz:
https://doaj.org/article/6c7cecdc52c64d4cabca5d4ca93d4d92
Publikováno v:
Turkish Journal of Hematology, Vol 35, Iss 1, Pp 79-80 (2018)
Externí odkaz:
https://doaj.org/article/e33ade50b8b54ee6a0e6da1f67d699ee
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 4, Pp 360-361 (2017)
Externí odkaz:
https://doaj.org/article/a45f57eb09cb4fd6bc04cba2698dd768
Publikováno v:
Mol Syndromol
Mucopolysaccharidosis (MPS) type VI, also known as Maroteaux-Lamy syndrome, is a lysosomal storage disorder, characterized by the deficiency of the arylsulfatase B enzyme. The clinical phenotype and severity of the illness varies according to the res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc2d2e87975c5334442c6aa1fd28e90b
https://doi.org/10.1159/000502597
https://doi.org/10.1159/000502597
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 37, Iss 2, Pp 135-136 (2020)
Turkish Journal of Hematology, Vol 37, Iss 2, Pp 135-136 (2020)
WOS: 000531086600014 The β-thalassemias are a group of hereditary disorders with autosomal recessive inheritance characterized by the presence of defective synthesis of the β-globin chain, an integral component of the hemoglobin molecule, resulting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80048d10f9ee93c9e898e4bd1dbed166
https://hdl.handle.net/20.500.12713/474
https://hdl.handle.net/20.500.12713/474
Publikováno v:
Thalassemia Reports, Vol 8, Iss 2 (2018)
Thalassemia Reports; Volume 8; Issue 2; Pages: 7286
Thalassemia Reports; Volume 8; Issue 2; Pages: 7286
The mutation detection of β thalassemia is absolutely necessary for molecular diagnosis, as well as any genetic epidemiological study. The β globin gene has 3 exons and 2 introns, involved in β-thalassemic pathogenesis. The study aim of the study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d664cbef5e093b42dcdd879a7b3e28a
https://www.pagepressjournals.org/index.php/thal/article/view/7286
https://www.pagepressjournals.org/index.php/thal/article/view/7286
Publikováno v:
Journal of Cytology, Vol 35, Iss 4, Pp 252-254 (2018)
Journal of Cytology
Journal of Cytology
Background: Human papilloma virus (HPV) infection is the major etiologic agent of cervical carcinoma. The aim of this study was to determine the prevalence of HPV infection and genotype distribution in cervical swabs from 2,234 Turkish and 357 Albani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5ceeab31934d868367866ebb43dd3ef
http://www.jcytol.org/article.asp?issn=0970-9371
http://www.jcytol.org/article.asp?issn=0970-9371
Autor:
Kezban Nur Pilanci, Alper Toker, Pinar Firat, Kamuran Ibis, Murat Büyükdoğan, Dilek Yilmazbayhan, Sezer Saglam, Berker Özkan, Rian Disci, Veysel Sabri Hancer, Esra Kaytan Saglam
Background: To assess the prognostic importance of carbonic anhydrase IX (CA IX), a hypoxic biomarker, after neoadjuvant treatment in Stage III non-small cell lung cancer (NSCLC) patients. Methods: Tissue CA IX expression was examined after surgical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::954809fae317015638177c84e6d70bfa
https://hdl.handle.net/20.500.12713/749
https://hdl.handle.net/20.500.12713/749
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 34, Iss 4, Pp 360-361 (2017)
Turkish Journal of Hematology, Vol 34, Iss 4, Pp 360-361 (2017)
WOS: 000418383400018
PubMed: 28747287
…
PubMed: 28747287
…
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4596b2e0827dace81d231820b7580926
https://hdl.handle.net/20.500.12395/35625
https://hdl.handle.net/20.500.12395/35625