Zobrazeno 1 - 10
of 14
pro vyhledávání: '"M Selman, Yildirim"'
Autor:
Sema Soysal, Ebru Tuncez, Ayse Gul Zamani, M. Selman Yildirim, Rengin Karataylı, Aynur Acar, Kazım Gezginç, Fikriye Karanfil
Publikováno v:
Turkish Journal of Obstetrics and Gynecology
Turkish Journal of Obstetrics and Gynecology, Vol 14, Iss 3, Pp 151-155 (2017)
Turkish Journal of Obstetrics and Gynecology, Vol 14, Iss 3, Pp 151-155 (2017)
Amaç: Bu çalışmanın amacı, polikistik over sendromlu (PKOS) kadınların eksfoliyatif servikal hücrelerinde ve periferik kan lenfositlerinde mikronükleus (MN) frekanslarını belirlemektir. Gereç ve Yöntemler: PKOS'li 15 hasta ve 11 sağlı
Publikováno v:
Molecular Genetics and Metabolism. 132:S120
Autor:
Neslihan Iyit, M. Selman Yildirim, Banu Ozturk, Berker Bakbak, Sansal Gedik, Saban Gonul, Ayse Gul Zamani
Publikováno v:
Current Eye Research. 41:862-866
Genetic factors are known to influence the response to anti-vascular endothelial growth factor (VEGF) treatment in exudative age-related macular degeneration (AMD). The current study was conducted to investigate the association of Apolipoprotein E (A
Autor:
Oguz Cilingir, Kayhan Öztürk, M. Hamza Muslumanoglu, Bedri Özer, M. Selman Yildirim, Hasan Acar, Tülin Çora
Publikováno v:
Cancer Genetics and Cytogenetics. 169:89-93
The purpose of the present study was to investigate GSTM1 and GSTT1 genotypes by using multiplex polymerase chain reaction (PCR) in patients with laryngeal squamous cell carcinoma (LSCC). The genotypes of 110 patients with LSCC and of 197 healthy sub
Publikováno v:
Acta Oto-Laryngologica. 124:924-928
To determine the micronucleus (MN) frequency of acquired cholesteatoma tissue using an MN assay.Eighteen patients were diagnosed as having chronic otitis media with acquired cholesteatoma and were divided into primary and secondary acquired cholestea
Publikováno v:
Molecular Reproduction and Development. 63:232-236
Meiotic segregation patterns of carriers of Robertsonian translocations (RT) are important for assessing the risk of unbalanced forms. We investigated the ratio of sperm with t(21;21) to sperm with nullisomy for chromosome 21; the segregation of the
Publikováno v:
Clinical & Laboratory Haematology. 23:255-258
We present a rare case of a paediatric myelodysplastic syndrome (MDS) with congenital anomalies (frontal bossing and premature closure of anterior fontanelle). The case showed the clinical and biological features of a refractory anaemia excess blasts
Autor:
Ayse Gul Zamani, Ebru Tuncez, Gul Durakbasi-Dursun, M. Selman Yildirim, Serdar Ceylaner, Aynur Acar
Publikováno v:
American journal of medical genetics. Part A. (5)
Here, we report on a family with pericentric inversion of chromosome 18 [inv(18)(p11.2q21)] and two recombinants with a duplication of q21 qter and a deletion of p11.2 pter regions in a four-generation family. This chromosomal abnormality was inherit
Publikováno v:
American journal of medical genetics. Part A. (3)
Trisomy 13, or Patau syndrome is a rare chromosomal disorder characterized by a triad of cleft lip and palate, postaxial polydactyly and microcephaly. Complete, partial, or mosaic forms of the disorder can occur. Mosaic trisomy 13 is very rare, it oc
Publikováno v:
The Turkish journal of pediatrics. 52(1)
The present case report describes the oral features of tetraploid/diploid mosaicism. An 11-year-old boy with severe periodontal destruction is presented in this report. He was examined clinically, radiologically, immunologically, and genetically. Sig