Search Results - "Alper, Ö. M."

Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens by Akin, Y., Demir, D., Görgişen, G., Lüleci, G., Alper, Ö. M., Watanabe, C. S., Sahiner, I. F., Usta, M. F.

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Consanguineous marriages in the province of Antalya, Turkey by Alper, Ö.M., Erengin, H., E Manguoğlu, A., Bilgen, T., Çetin, Z., Dedeoğlu, N., Lüleci, G.

“…To assess the trends in the frequency and the medical effects of consanguinity in the south coast of Turkish population using local and national data in the…”
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100 years of dental progress in the nation's Capital by Alper, M O

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Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens by Wu, Chien-Chih, Alper, Özgül M., Lu, Jyh-Feng, Wang, Song-Ping, Guo, Li, Chiang, Han-Sun, Wong, Lee-Jun C.

“…BACKGROUND: Clinically affected cystic fibrosis (CF) patients present a spectrum of genital phenotypes ranging from normal fertility to moderately impaired…”
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Detection of CFTR mutations using temporal temperature gradient gel electrophoresis by Wong, Lee-Jun C., Alper, Özgül M.

“…Cystic fibrosis (CF), caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, is one of the most common autosomal recessive…”
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Simultaneous suppression of epidermal growth factor receptor and c-erbB-2 reverses aneuploidy and malignant phenotype of a human ovarian carcinoma cell line by PACK, Svetlana D, ALPER, Özgül M, RIED, Thomas, SZALLASI, Zoltan, ALPER, Özge, STROMBERG, Kurt, AUGUSTUS, Meena, ÖZDEMIRLI, Metin, MIERMONT, Anne M, KLUS, Greg, RUSIN, Marek, SLACK, Rebecca, HACKER, Neville F

“…Coexpression of epidermal growth factor receptor (EGFR) and c-erbB-2 in 47-68% of ovarian cancer cells indicate their strong association with tumor formation…”
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The necessity of complete CFTR mutational analysis of an infertile couple before in vitro fertilization by Wong, Lee-Jun C, Alper, Ozgül M, Hsu, Evelyn, Woo, Marlyn S, Margetis, Monique F

“…To determine the genotype of a triplet resulted from an IVF procedure, with discordant cystic fibrosis (CF) phenotype. Molecular diagnosis of CF. Affected…”
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Two novel null mutations in a Taiwanese cystic fibrosis patient and a survey of East Asian CFTR mutations by Wong, Lee-Jun C., Alper, Özgül M., Wang, Bao-Tyan, Lee, Mei-Hui, Lo, Shin-Yu

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1154insTC is not a rare CFTR mutation by Alper, Özgül M., Hostetter, Galen, Cook, James, Tenenholz, Beverly, Hsu, Evelyn, Woo, Marlyn S., Wong, Lee-Jun C.

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Detection of novel CFTR mutations in Taiwanese cystic fibrosis patients by Alper, Ozgül M, Shu, San-Ging, Lee, Mei-Hui, Wang, Bao-Tyan, Lo, Shin-Yu, Lin, Keh-Liang, Chiu, Ya-Lan, Wong, Lee-Jun C

“…Cystic fibrosis (CF) in Asian populations is very rare. We performed molecular genetic analysis in 2 Taiwanese CF patients for detection of cystic fibrosis…”
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