Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Duzcan F"'
Intracytoplasmic sperm injection (ICSI) is a widespread and powerful method enabling men with low sperm quantity and quality to become fathers. However, compared with naturally conceived children, there are increased risks of problems, such as congen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1322b3f6eb250d12a91fa68e515f6b3c
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/24314
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/24314
Autor:
Kucuktasci, K, Semiz, S, Balci, YI, Ozsari, T, Gurses, D, Onem, G, Sacar, M, Duzcan, F, Yuksel, D, Semiz, E
Wolfram syndrome-1 is a rare and severe autosomal recessive neurodegenerative disease characterized by diabetes mellitus (DM), optic atrophy, diabetes insipidus, and deafness. Poorly controlled type 1 DM increases the risk for thrombosis. However, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::cab25d6713fa186f92f72090eff2ad86
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22938
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/22938
Autor:
Ergin, H, Ozdemir, OMA, Karaca, A, Sen Turk, N, Duzcan, F, Ergin, S, Kazanci, E, Vergin, C, Erbay, A
Congenital leukemia is a rare disease. The majority of cases of this disease are acute myelogenous leukemia (AML). Congenital acute lymphoblastic leukemia (ALL) is rare and most often is of B cell lineage. Rarely, some cases have been designated biph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::d20160e3e81931ac3b7496db5de12bf0
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/14829
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/14829
Excision Repair Cross-Complementing Group 1 (ERCC1) is an important DNA repair gene, playing critical role in nucleotide excision repair pathway and having a significant influence on genomic instability. Some studies support that ERCCI might be a pot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::89af9038a268e6b9d33c8ef8112a399b
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/14065
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/14065
Our aim was to investigate the expression of apoptosis-associated proteins (bcl-2, bcl-xl, bax, bak, bid), apoptotic index (AI) and proliferation index (PI) in germinal center B-cell-like immunophenotypic profile (GCB) and non-GCB of diffuse large B-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1cedc2129a5b245b23af9165beb10699
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13466
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13466
The generation of urothelial carcinoma is caused by the accumulation of various molecular changes, as in most malignancies. There are conflicting data about the status of HER-2/neu oncogene in urothelial carcinomas. The aim of this study was to deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::bbbf4789a2ef91aba1d43b59049bd7ba
Autor:
Semerci, CN, Satiroglu-Tufan, NL, Turan, S, Bereket, A, Tuysuz, B, Yilmaz, E, Kayserili, H, Karaman, B, Semiz, S, Duzcan, F, Bagci, H
A 45,X karyotype is one of the common chromosomal abnormalities characterized by short stature, lack of development of secondary sexual characteristics, webbed neck and cubitus valgus. This phenotype was described by Turner in 1938 and was called Tur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::6de3256f065f8257f31ca45ffb95880e
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/19013
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/19013
Autor:
Chang, BS, Duzcan, F, Kim, S, Cinbis, M, Aggarwal, A, Apse, KA, Ozde, O, Atmaca, M, Zencir, S, Bagci, H, Walsh, CA, TISM
Reelin is an extracellular matrix-associated protein important in the regulation of neuronal migration during cerebral cortical development. Point mutations in the RELN gene have been shown to cause an autosomal recessive human brain malformation ter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::b6df26a4306e95ac6b784d5afc7f32a2
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/19039
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/19039
Malformations of the lower limbs are rare and heterogeneous anomalies. Some congenital anomalies involving face, gastrointestinal system, skeletal system, urogenital system, heart, lung and diaphragma associated with lower limb malformations have bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::560badbc0285855cd6dc4fd5e9743387
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/18573
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/18573