Zobrazeno 1 - 10
of 288
pro vyhledávání: '"Emin, Karaca"'
Autor:
Gizem Kok Kilic, Erhan Pariltay, Emin Karaca, Burak Durmaz, Huseyin Ekici, Metehan Imamoglu, Firat Okmen, Haluk Akin, Ozgur Cogulu
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 1, Pp 122-126 (2022)
Objective: Tetrasomy 9p is a rare fetal condition. Cases are usually mosaic. Here, we present a non-mosaic tetrasomy 9p case with cytogenetic analysis, fluorescence in situ hybridization, microarray data, ultrasound findings, and phenotypic presentat
Externí odkaz:
https://doaj.org/article/7e0b6c8167b34c64b5ec7fcc4b839b03
Autor:
Emin Karaca, Ayça Aykut, Biray Ertürk, Burak Durmaz, Ahmet Güler, Barış Büke, Ahmet Özgür Yeniel, Ahmet Mete Ergenoğlu, Ferda Özkınay, Mehmet Özeren, Mert Kazandı, Fuat Akercan, Sermet Sağol, Cumhur Gündüz, Özgür Çoğulu
Publikováno v:
Balkan Medical Journal, Vol 35, Iss 2, Pp 163-166 (2018)
Background: Down syndrome, which is the most common human chromosomal anomaly that can affect people of any race and age, can be diagnosed prenatally in most cases. Prenatal diagnosis via culture method is time-consuming; thus, genetic analysis has t
Externí odkaz:
https://doaj.org/article/4456d579588345c4992475c753234e0f
Autor:
Ebru Canda, Melis Köse, Havva Yazıcı, Esra Er, Cenk Eraslan, Ferda Özkınay, Mahmut Çoker, Sema Kalkan Uçar, Sara Habif, Emin Karaca, Hüseyin Onay
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 1, Pp 39-43 (2018)
Aim:L-2-hydroxyglutaric aciduria (L2HGA) is a rare autosomal recessive encephalopathy caused by mutations in the L-2-hydroxyglutarate dehydrogenase gene.Materials and Methods:Here we discuss the clinical and molecular characteristics in patients with
Externí odkaz:
https://doaj.org/article/f28b0eb585b54012802d2b794144d65e
Autor:
Mehmet Karakuş, Abed Nasereddin, Hüseyin Onay, Emin Karaca, Ahmet Özkeklikçi, Charles L Jaffe, Katrin Kuhls, Ahmet Özbilgin, Hatice Ertabaklar, Samiye Demir, Yusuf Özbel, Seray Töz
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 11, Iss 4, p e0005538 (2017)
Turkey is located in an important geographical location, in terms of the epidemiology of vector-borne diseases, linking Asia and Europe. Cutaneous leishmaniasis (CL) is one of the endemic diseases in a Turkey and according to the Ministry Health of T
Externí odkaz:
https://doaj.org/article/279601549fe34cf9bb3e811088ddee3a
Autor:
Lamiya Mardan, Ozgur Cogulu, Erhan Pariltay, Burak Durmaz, Yasemin Karaca, Ayca Aykut, Asude Durmaz, Haluk Akin, Emin Karaca
Publikováno v:
Reproductive Biology. 20:42-47
Although the polymorphic heterochromatin regions of chromosomes (heteromorphisms) have been extensively studied for their phenotypic effects on humans, co-occurrences of chromosome 1, 9, 16 and Y heteromorphisms and of acrocentric variants have never
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b76e2c9d3d0e9ad734dc6fa6190232c3
https://doi.org/10.1016/j.repbio.2019.12.006
https://doi.org/10.1016/j.repbio.2019.12.006
Autor:
Burak Durmaz, Ugur Yilmaz, Bakiye Goker Bagca, Sunde Yilmaz Susluer, Hüsniye Kayalar, Erhan Pariltay, Cumhur Gündüz, Emin Karaca, Asude Durmaz, Ozgur Cogulu, Ayca Aykut, Cigir Biray Avci
Background: Grade IV gliomas are classified as glioblastoma (GBM), which is the most malignant brain cancer type. Various genetic and epigenetic mechanisms play a role in the initiation and progression of GBM. MicroRNAs (miRNAs) are small, non-coding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::369f067fbe76e67db11bd924f2b227d3
https://hdl.handle.net/11454/78176
https://hdl.handle.net/11454/78176
Autor:
Ezgi, Aksoy, Ozgur, Cogulu, Erhan, Pariltay, Samim, Ozen, Aysun, Ata, Emin, Karaca, Sukran, Darcan
Objectives Turner syndrome (TS) is one of the most common chromosomal abnormalities with an incidence of approximately one in 2,500 live births. Short stature and primary ovarian insufficiency are two most important characteristic findings of TS. Tur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0987bbc26c06539511b47f8399ed0d2
https://hdl.handle.net/11454/77982
https://hdl.handle.net/11454/77982
Autor:
Eren Arslan Davulcu, Mert Pekerbas, Emin Karaca, Burak Durmaz, Nazan Özsan, Haluk Akın, Güray Saydam
Chronic myeloid leukemia (CML) is a common hematological malignancy originating from bone marrow stem cells. Chromosomal abnormalities can be seen in almost all cases, the most known anomaly being Philadelphia (Ph) chromosome, a derivative chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d04cc5fea742ad6b61a2305e35571c7
https://hdl.handle.net/11454/76443
https://hdl.handle.net/11454/76443
Autor:
Nur Selvi, Buket Kosova, Mine Hekimgil, Cumhur Gündüz, Burçin Tezcanlı Kaymaz, Emin Karaca, Güray Saydam, Murat Tombuloğlu, Filiz Büyükkeçeci, Seçkin Çağırgan, Yeşim Ertan, Nejat Topçuoğlu
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 2, Pp 126-134 (2012)
OBJECTIVE: Follicular lymphoma (FL) is one of the most common lymphomas, and is characterized by t(14;18) (q32;q21) in more than 80% of patients. The aim of this study was to determine the rate of t(14;18) positivity based on the detection of mbr or
Externí odkaz:
https://doaj.org/article/b4facb6808064c92bc182c01025a0586
Publikováno v:
Turkish Journal of Hematology, Vol 27, Iss 04, Pp 299-302 (2010)
We report herein a very rare case of acute lymphoblastic leukemia having a chromosomal constitution of 48,XY,+X,+5,t(9;22)(q34;q11) in the bone marrow. A patient with additional chromosomes X and 5 with a Philadelphia chromosome has not been reported
Externí odkaz:
https://doaj.org/article/7347e378128840fea97171dcd325f68e