Search Results - "Ocak, Z"

Association of recurrent pregnancy loss with chromosomal abnormalities and hereditary thrombophilias by Ocak, Z, Özlü, T, Ozyurt, O

“…Background: Recurrent pregnancy loss (RPL) which is generally known as >3 consecutive pregnancy losses before 20 weeks' gestation is seen in 0.5-2% of women…”
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Walker–Warburg syndrome with persistent hyperplastic primary vitreous detected by prenatal ultrasonography by Yazicioǧlu, H. F., Ocak, Z.

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Energy utilization, environmental pollution and renewable energy sources in Turkey by Ocak, M., Ocak, Z., Bilgen, S., Keleş, S., Kaygusuz, K.

“…In this study, energy utilization and its major environmental impacts are discussed from the standpoint of sustainable development, including anticipated…”
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Polymorphisms of toll-like receptors 2, 3 and 4 in patients that do and do not enter labour spontaneously at term by Ozlü, T., Ocak, Z., Simavli, S. A., Karatas, A.

“…Abstract To assess the association of polymorphisms of toll-like receptors (TLRs) 2, 3 and 4 with the delay in onset of labour at term pregnancies, patients…”
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Effect of hypericin on the ADAMTS-9 and ADAMTS-8 gene expression in MCF7 breast cancer cells by Ocak, Z, Acar, M, Gunduz, E, Gunduz, M, Demircan, K, Uyeturk, U, Ozlü, T

“…To investigate the effects of hypericin which is obtained from the plant Hypericum perforatum on the expression and the regulation of ADAMTS8 and ADAMTS9 genes…”
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Location of Municipal Centers for New Counties within the Istanbul Metropolitan Municipality by Tüzün Aksu, D, Ocak, Z

“…AbstractIn this case study, a methodology to determine the locations of municipal centers for eight newly established counties within the Istanbul Metropolitan…”
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Molecular cytogenetic characterization of a case of primary amenorrhea with intrachromosomal triplication of the X chromosome q arm by Ocak, Z, Surucu, R

“…This is a unique case of intrachromosomal triplication of the X chromosome q arm detected with cytogenetic and spectral karyotyping in a 21-year-old woman with…”
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Anal atresia, abnormal genitalia, and absent thumb: congenital malformations associated with mosaic ring chromosome 13 by Ocak, Z, Ozlu, T, Vural, M

“…Because of the deletion of a segment of the chromosome during the formation of a ring, several clinical findings may be associated with ring chromosomes. Ring…”
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Prenatal detection of Pai syndrome without cleft lip and palate: a case report by Ocak, Z, Yazicioglu, H F, Aygun, M, Ilter, M K I, Ozlu, T

“…Pai syndrome is a rarely encountered disease characterized by findings of median cleft lip, facial skin polyps, nasal mucosal polyps and midline central…”
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Frequency of Y chromosome microdeletions and chromosomal abnormalities in infertile Turkish men by Dinçer, M, Karahasanoglu, A, Uzun Çilingir, I, Ozdemir, M Eriç, Ocak, Z, Karahuseyinoglu, S, Yucel, O

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Association of Toll-like receptors 2, 3, and 4 genes polymorphisms with periapical pathosis risk by Özan, Ü, Ocak, Z, Özan, F, Oktay, E-A, Toptaş, O, Şahman, H, Yikilgan, I, Oruçoğlu, H, Er, K

“…The aim of this study was to investigate the role of gene variations of Toll-like receptors (TLR) 2, 3, and 4 on genetic susceptibility to periapical pathosis…”
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Swallowed amniotic band presenting as a cystic mass of the fetal nasal cavity by Boulet, S., Dusonchet, P., Berthier, D., André, D. M., Barbier, C., Schaal, J. P., Jouk, P. S.

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Synthesis and non-aqueous medium titrations of some new 4-benzylidenamino-4,5-dihydro-1H-1,2,4-triazol-5-one derivatives by Yüksek, Haydar, Uçüncü, Osman, Alkan, Muzaffer, Ocak, Zafer, Bahçeci, Sule

“…The synthesis of 3-alkyl(aryl)-4-(3-ethoxy-4-hydroxybenzylidenamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones 3 from the reactions of…”
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Synthesis and Potentiometric Titrations of Some New 4-(Benzylideneamino)-4,5-dihydro-1H-1,2,4-triazol-5-one Derivatives in Non-Aqueous Media by Bahçeci, Şule, Yüksek, Haydar, Ocak, Zafer, Azakli, Ibrahim, Alkan, Muzaffer, Özdemir, Mustafa

“…The synthesis of 3-alkyl(aryl)-4-[4-(dimethylamino)benzylideneamino]-4,5-dihydro-1 H -1,2,4-triazol-5-ones ( 3 ) from the reactions of…”
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Walker-Warburg syndrome with persistent hyperplastic primary vitreous detected by prenatal ultrasonography by Yazicioglu, H F, Ocak, Z

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