Yazar "Okten, Gulsen" için listeleme
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Disruption of HDX gene in premature ovarian failure
Okten, Gulsen; Gunes, Sezgin; Onat, Onur Emre; Tukun, Ajlan; Ozcelik, Tayfun; Kocak, Idris (Taylor & Francis Inc, 2013)We present a case of a 19-year-old phenotypically normal girl with premature ovarian failure. Cytogenetic analysis using G banding and fluorescence in situ hybridization (FISH) from cultured peripheral blood lymphocytes ... -
The effect of mesenchymal stem cells and sildenafil on flap viability in perforator-based flaps for ischemia/reperfusion injury: An experimental study
Kelahmetoglu, Osman; Demir, Rukiye; Okten, Gulsen; Demir, Ahmet; Alpaslan Pinarli, Ferda; Diraman, Emine (Wiley, 2016)PurposeIn this study, we evaluated the individual and combined effects of mesenchymal stem cells (MSCs) and sildenafil citrate (SC) on the viability of pedicled perforator flaps in which ischemia/reperfusion injury developed ... -
An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion
Kara, Nurten; Okten, Gulsen; Gunes, Sezgin Ozgur; Saglam, Yaman; Tasdemir, Haydar Ali; Pinarli, Ferda Alparslan (Elsevier Science Bv, 2008)Ring chromosomes are rare chromosome disorders that arise usually de novo. Children with ring chromosome 6 have a wide range of intellectual functioning and congenital anomalies. We report an epileptic case of a 10-year-old ... -
Germ cell tumor showing partial trisomy 1 in a gonadectomized intersex child with monosomy X and double Y mosaicism
Ogur, Gonul; Pinarli, Faruk Guclu; Dagdemir, Ayhan; Artan, Sevilhan; Ariturk, Ender; Elli, Murat; Okten, Gulsen (Lippincott Williams & Wilkins, 2006)High incidence of germ cell tumors arising from dysgenetic gonads in patients with sexual chromosome abnormalities has been described, especially in patients with a Y chromosome bearing cell line. Here we report a 14-year-old ... -
Keratinocyte growth factor-2 and autologous serum potentiate the regenerative effect of mesenchymal stem cells in cornea damage in rats
Pinarli, Ferda Alpaslan; Okten, Gulsen; Beden, Umit; Fisgin, Tunc; Kefeli, Mehmet; Kara, Narten; Tomak, Leman (Ijo Press, 2014)AIM: To investigate the healing process after severe corneal epithelial damage in rats treated with mesenchymal stem cells (MSCs) cultured with or without keratinocyte growth factor (KGF -2) and autologous serum (AS) on ... -
De Novo Balanced (X;14) Translocation in a Patient with Recurrent Miscarriages: Case Report
Pinarli, Ferda Alpaslan; Okten, Gulsen; Ozcelik, Tayfun; Kara, Nurten; Gunes, Sezgin; Kocak, Idris (Ortadogu Ad Pres & Publ Co, 2011)We report a 23-year-old phenotypically normal female patient who had previously suffered from recurrent spontaneous abortion (RSA) who found to have an X;14 trans location and a Methylene- Tetrahdrofolate-Reductase (MTHFR) ... -
Trisomy Xq and Xp Deletion Phenotype in a Case with Primary Amenorrhea and Mosaic 45,X/46,X,der(X) Karyotype: Case Report
Kara, Nurten; Okten, Gulsen; Tural, Sengul; Artan, Sevilhan; Sezer, Ozlem; Kocak, Idris (Ortadogu Ad Pres & Publ Co, 2011)The samples of a 18-year-old girl who had a short stature and complaints of hair loss and amenorrhea were sent to our laboratory with a pre-diagnosis of primary amenorrhea. We tried to explain genotype-phenotype relationship ... -
Two Males with SRY-Positive 46,XX Testicular Disorder of Sex Development
Gunes, Sezgin; Asci, Ramazan; Okten, Gulsen; Atac, Fatih; Onat, Onur E.; Ogur, Gonul; Bagci, Hasan (Informa Healthcare, 2013)The 46,XX testicular disorder of sex development (46,XX testicular DSD) is a rare phenotype associated with disorder of the sex chromosomes. We describe the clinical, molecular, and cytogenetic findings of a 16- and a ... -
Two turner syndrome patients with the mosaic 45,X/46,X,i(Xq) karyotype: Case report
Gunes, Sezgin; Kara, Nurten; Surucu, Bulent; Okten, Gulsen; Yigit, Serbuelent; Sezer, Ozlem (Ortadogu Ad Pres & Publ Co, 2008)Turner's syndrome is one of the most common chromosomal aneuploidy disorders. Turner's syndrome occurs in 1 in 4000 live-born girls and approximately 5 to 10 percent of them have mosaic isochromosome 45,X/46,X,i(Xq). ...