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2013
S. Simsek, Tekes, S., Oral, D., Turkyılmaz, A., Isik, B., Isik, M. R., and Akkoc, H., The insertion/deletion polymorphism in the ACE gene and chronic obstructive pulmonary disease, vol. 12, pp. 1392-1398, 2013.
Ahsan A, Ram R, Baig MA and Pasha MA (2004). ACE I allele and eNOS G allele crosstalk may have a role in chronic obstructive pulmonary disease. Clin. Biochem. 37: 1037-1040. http://dx.doi.org/10.1016/j.clinbiochem.2004.05.026 PMid:15498534   Bayram B, Kilicci C, Onlu H, Ozkurt M, et al. (2011). Association of angiotensin converting enzyme (ACE) gene I/D polymorphism and polycystic ovary syndrome (PCOS). Gene 489: 86-88. http://dx.doi.org/10.1016/j.gene.2011.08.012 PMid:21939743   Berdeli A and Cam FS (2009). Prevalence of the angiotensin I converting enzyme gene insertion/deletion polymorphism in a healthy Turkish population. Biochem. Genet. 47: 412-420. http://dx.doi.org/10.1007/s10528-009-9240-8 PMid:19390959   Borzyszkowska J, Stanislawska-Sachadyn A, Wirtwein M, Sobiczewski W, et al. (2012). Angiotensin converting enzyme gene polymorphism is associated with severity of coronary artery disease in men with high total cholesterol levels. J. Appl. Genet. 53: 175-182. http://dx.doi.org/10.1007/s13353-012-0083-3 PMid:22307319 PMCid:3334489   Brice EA, Friedlander W, Bateman ED and Kirsch RE (1995). Serum angiotensin-converting enzyme activity, concentration, and specific activity in granulomatous interstitial lung disease, tuberculosis, and COPD. Chest 107: 706-710. http://dx.doi.org/10.1378/chest.107.3.706 PMid:7874941   Busquets X, MacFarlane NG, Heine-Suner D, Morla M, et al. (2007). Angiotensin-converting-enzyme gene polymorphisms, smoking and chronic obstructive pulmonary disease. Int. J. Chron. Obstruct. Pulmon. Dis. 2: 329-334. PMid:18229571 PMCid:2695206   Domingues-Montanari S, Fernandez-Cadenas I, del Rio-Espinola A, Mendioroz M, et al. (2010). The I/D polymorphism of the ACE1 gene is not associated with ischaemic stroke in Spanish individuals. Eur. J. Neurol. 17: 1390-1392. PMid:20402757   Gurkan A, Emingil G, Saygan BH, Atilla G, et al. (2009). Angiotensin-converting enzyme (ACE), angiotensinogen (AGT), and angiotensin II type 1 receptor (AT1R) gene polymorphisms in generalized aggressive periodontitis. Arch. Oral Biol. 54: 337-344. http://dx.doi.org/10.1016/j.archoralbio.2008.12.005 PMid:19162259   Harry RG, Herman-Jan P, Ann Emil MWJS, Nicholas SH, et al. (2004). ACE gene polymorphism in COPD. Am. J. Respir. Crit. Care Med. 170: 572-573.   Hocher B, Schlemm L, Haumann H, Jian L, et al. (2011). Offspring sex determines the impact of the maternal ACE I/D polymorphism on maternal glycaemic control during the last weeks of pregnancy. J. Renin-Angiotensin-Aldosterone Syst. 12: 254-261. http://dx.doi.org/10.1177/1470320310387843 PMid:21393357   Hopkinson NS, Nickol AH, Payne J, Hawe E, et al. (2004). Angiotensin converting enzyme genotype and strength in chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med. 170: 395-399. http://dx.doi.org/10.1164/rccm.200304-578OC PMid:15117739   Indrajaya T (2011). The role of ACE gene polymorphism on pathogenesis of ischemic stroke. Acta Med. Indones. 43: 152-157. PMid:21979279   Kanazawa H, Okamoto T, Hirata K and Yoshikawa J (2000). Deletion polymorphisms in the angiotensin converting enzyme gene are associated with pulmonary hypertension evoked by exercise challenge in patients with chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med. 162: 1235-1238. http://dx.doi.org/10.1164/ajrccm.162.4.9909120 PMid:11029323   Kanazawa H, Otsuka T, Hirata K and Yoshikawa J (2002). Association between the angiotensin-converting enzyme gene polymorphisms and tissue oxygenation during exercise in patients with COPD. Chest 121: 697-701. http://dx.doi.org/10.1378/chest.121.3.697 PMid:11888948   Lee J, Nordestgaard BG and Dahl M (2009). Elevated ACE activity is not associated with asthma, COPD, and COPD co-morbidity. Respir. Med. 103: 1286-1292. http://dx.doi.org/10.1016/j.rmed.2009.04.003 PMid:19423314   MacNee W (2005). Pulmonary and systemic oxidant/antioxidant imbalance in chronic obstructive pulmonary disease. Proc. Am. Thorac. Soc. 2: 50-60. http://dx.doi.org/10.1513/pats.200411-056SF PMid:16113469   Mak JC (2008). Pathogenesis of COPD. Part II. Oxidative-antioxidative imbalance. Int. J. Tuberc. Lung Dis. 12: 368-374. PMid:18371260   Marc D, Janssens W and Miravitles M (2012). Chronic obstructive pulmonary disease. Semin. Lancet. 379: 1341-1351. http://dx.doi.org/10.1016/S0140-6736(11)60968-9   Miller MR, Crapo R, Hankinson J, Brusasco V, et al. (2005a). General considerations for lung function testing. Eur. Respir. J. 26: 153-161. http://dx.doi.org/10.1183/09031936.05.00034505 PMid:15994402   Miller MR, Hankinson J, Brusasco V, Burgos F, et al. (2005b). Standardisation of spirometry. Eur. Respir. J. 26: 319-338. http://dx.doi.org/10.1183/09031936.05.00034805 PMid:16055882   Namazi S, Monabati A, Ardeshir-Rouhani-Fard S and Azarpira N (2010). Association of angiotensin I converting enzyme (insertion/deletion) and angiotensin II type 1 receptor (A1166C) polymorphisms with breast cancer prognostic factors in Iranian population. Mol. Carcinog. 49: 1022-1030. http://dx.doi.org/10.1002/mc.20685 PMid:20945417   Pabst S, Theis B, Gillissen A, Lennarz M, et al. (2009). Angiotensin-converting enzyme I/D polymorphism in chronic obstructive pulmonary disease. Eur. J. Med. Res. 4 (Suppl 14): 177-181.   Rigat B, Hubert C, Corvol P and Soubrier F (1992). PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1). Nucleic Acids Res. 20: 1433. http://dx.doi.org/10.1093/nar/20.6.1433-a PMid:1313972 PMCid:312213   Selahaddin T, Birgul I, Tekin Y and Selda S (2010). Chronic Obstructive Pulmonary Disease and Paraoxonase-1 192 and 55 Gene Polymorphisms. Biotechnol. Biotechnol. 24: 1644-1647. http://dx.doi.org/10.2478/V10133-010-0019-1   Tkacova R, Joppa P, Stancak B, Salagovic J, et al. (2005). The link between angiotensin-converting enzyme genotype and pulmonary artery pressure in patients with COPD. Wien. Klin. Wochenschr. 117: 210-214. http://dx.doi.org/10.1007/s00508-005-0333-z PMid:15875760   Ucar G, Yildirim Z, Ataol E, Erdogan Y, et al. (1997). Serum angiotensin converting enzyme activity in pulmonary diseases: correlation with lung function parameters. Life Sci. 61: 1075-1082. http://dx.doi.org/10.1016/S0024-3205(97)00616-4   Ueda S, Heeley RP, Lees KR, Elliott HL, et al. (1996). Mistyping of the human angiotensin-converting enzyme gene polymorphism: frequency, causes and possible methods to avoid errors in typing. J. Mol. Endocrinol. 17: 27-30. http://dx.doi.org/10.1677/jme.0.0170027 PMid:8863184   Yakut T, Karkucak M, Ursavas A, Gulten T, et al. (2010). Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients. Genet. Mol. Res. 9: 734-738. http://dx.doi.org/10.4238/vol9-2gmr755 PMid:20449805   Yaren A, Turgut S, Kursunluoglu R, Oztop I, et al. (2006). Association between the polymorphism of the angiotensin-converting enzyme gene and tumor size of breast cancer in premenopausal patients. Tohoku J. Exp. Med. 210: 109- 116. http://dx.doi.org/10.1620/tjem.210.109 PMid:17023764   Yaren A, Turgut S, Kursunluoglu R, Oztop I, et al. (2007). Insertion/deletion polymorphism of the angiotensin I-converting enzyme gene in patients with breast cancer and effects on prognostic factors. J. Investig. Med. 55: 255-261. http://dx.doi.org/10.2310/6650.2007.00006 PMid:17850737   Zhang X, Wang C, Dai H, Lin Y, et al. (2008). Association between angiotensin-converting enzyme gene polymorphisms and exercise performance in patients with COPD. Respirology 13: 683-688. http://dx.doi.org/10.1111/j.1440-1843.2008.01325.x PMid:18713090   Zhang Y, He J, Deng Y, Zhang J, et al. (2011). The insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme gene and cancer risk: a meta-analysis. BMC Med. Genet. 12: 159. http://dx.doi.org/10.1186/1471-2350-12-159 PMid:22151803 PMCid:3254074
2012
H. Akbas, İsi, H., İsi, H., Oral, D., Turkyılmaz, A., Kalkanlı-Taş, S., Simsek, S., Balkan, M., Sakar, M. N., Fidanboy, M., Alp, M. N., and Budak, T., Chromosome heteromorphisms are more frequent in couples with recurrent abortions, vol. 11, pp. 3847-3851, 2012.
Blumberg BD, Shulkin JD, Rotter JI, Mohandas T, et al. (1982). Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion. Am. J. Hum. Genet. 34: 948-960. PMid:7180849 PMCid:1685697   Brothman AR, Schneider NR, Saikevych I, Cooley LD, et al. (2006). Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years. Arch. Pathol. Lab. Med. 130: 947-949. PMid:16831047   Caglayan AO, Ozyazgan I, Demiryilmaz F and Ozgun MT (2010). Are heterochromatin polymorphisms associated with recurrent miscarriage? J. Obstet. Gynaecol. Res. 36: 774-776. http://dx.doi.org/10.1111/j.1447-0756.2010.01207.x PMid:20666944   Codina-Pascual M, Navarro J, Oliver-Bonet M, Kraus J, et al. (2006). Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes. Hum. Reprod. 21: 1490-1497. http://dx.doi.org/10.1093/humrep/del028 PMid:16484310   De la Fuente-Cortés BE, Cerda-Flores RM, Davila-Rodriguez MI, Garcia-Vielma C, et al. (2009). Chromosomal abnormalities and polymorphic variants in couples with repeated miscarriage in Mexico. Reprod. Biomed. Online 18: 543-548. http://dx.doi.org/10.1016/S1472-6483(10)60132-0   de Braekleer M and Dao TN (1990). Cytogenetic studies in couples experiencing repeated pregnancy losses. Hum. Reprod. 5: 519-528.   Düzcan F, Atmaca M, Cetin GO and Bagci H (2003). Cytogenetic studies in patients with reproductive failure. Acta Obstet. Gynecol. Scand. 82: 53-56. PMid:12580840   Eiben B, Leipoldt M, Rammelsberg O, Krause W, et al. (1987). High incidence of minor chromosomal variants in teratozoospermic males. Andrologia 19: 684-687. http://dx.doi.org/10.1111/j.1439-0272.1987.tb01929.x PMid:3434859   Karpen G and Kndow S (1998). Meiosis: Chromosome Bhaviour and Spindle Dynamics. In: Froniiers in Biology (Endow S and Glover D, eds.). Oxford University Press, Oxford. 203-247.   Madon PF, Athalye AS and Parikh FR (2005). Polymorphic variants on chromosomes probably play a significant role in infertility. Reprod. Biomed. Online 11: 726-732. http://dx.doi.org/10.1016/S1472-6483(10)61691-4   Makino T, Tabuchi T, Nakada K, Iwasaki K, et al. (1990). Chromosomal analysis in Japanese couples with repeated spontaneous abortions. Int. J. Fertil. 35: 266-270. PMid:1980661   Mau UA, Backert IT, Kaiser P and Kiesel L (1997). Chromosomal findings in 150 couples referred for genetic counselling prior to intracytoplasmic sperm injection. Hum. Reprod. 12: 930-937. http://dx.doi.org/10.1093/humrep/12.5.930 PMid:9194642   Nakamura Y, Kitamura M, Nishimura K, Koga M, et al. (2001). Chromosomal variants among 1790 infertile men. Int. J. Urol. 8: 49-52. http://dx.doi.org/10.1046/j.1442-2042.2001.00242.x PMid:11240825   Penna-Videau S, Araujo H, Ballesta F, Ballesca JL, et al. (2001). Chromosomal abnormalities and polymorphisms in infertile men. Arch. Androl. 46: 205-210. http://dx.doi.org/10.1080/01485010151096504 PMid:11339646   Sahin FI, Yilmaz Z, Yuregir OO, Bulakbasi T, et al. (2008). Chromosome heteromorphisms: an impact on infertility. J. Assist. Reprod. Genet. 25: 191-195. http://dx.doi.org/10.1007/s10815-008-9216-3 PMid:18461436 PMCid:2582066   Verma R and Babu A (1989). Human Chromosomes Manual of Basic Techniques. Pergamon Press, New York.   Wyandt HE and Tonk VS (2004). Atlas of Human Chromosome Heteromorphisms. Kluwer, Dordrecht.   Yakin K, Balaban B and Urman B (2005). Is there a possible correlation between chromosomal variants and spermatogenesis? Int. J. Urol. 12: 984-989. http://dx.doi.org/10.1111/j.1442-2042.2005.01185.x PMid:16351655
2010
M. Balkan, Akbas, H., İsi, H., İsi, H., Oral, D., Turkyılmaz, A., Kalkanli, S., Simsek, S., Fidanboy, M., Alp, M. N., Gedik, A., and Budak, T., Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey, vol. 9, pp. 1094-1103, 2010.
Akgül M, Ozkinay F, Ercal D, Cogulu O, et al. (2009). Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: report and review. J. Assist. Reprod. Genet. 26: 119-122. http://dx.doi.org/10.1007/s10815-009-9296-8 PMid:19184395 PMCid:2654936   Al Husain M and Zaki OK (1999). A survey of 1,000 cases referred for cytogenetic study to King Khalid University Hospital, Saudi Arabia. Hum. Hered. 49: 208-214. http://dx.doi.org/10.1159/000022877 PMid:10436383   Amudha S, Aruna N and Rajangam S (2005). Consanguinity and chromosomal abnormality. Indian J. Hum. Genet. 11: 108-110. http://dx.doi.org/10.4103/0971-6866.16812   Awwad R, Veach PM, Bartels DM and LeRoy BS (2008). Culture and acculturation influences on Palestinian perceptions of prenatal genetic counseling. J. Genet. Couns. 17: 101-116. http://dx.doi.org/10.1007/s10897-007-9131-2 PMid:17963027   Balkan M, Tekes S and Gedik A (2008). Cytogenetic and Y chromosome microdeletion screening studies in infertile males with oligozoospermia and azoospermia in Southeast Turkey. J. Assist. Reprod. Genet. 25: 559-565. http://dx.doi.org/10.1007/s10815-008-9272-8 PMid:18953646 PMCid:2593766   Butler MG and Hamill T (1995). Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992. South Med. J. 88: 309-314. http://dx.doi.org/10.1097/00007611-199503000-00012 PMid:7886528   Chandley AC (1990). Infertility and Recurrent Abortions. In: Principles and Practice of Medical Genetics (Emery A and Rimoin D, eds.). Chapter 21. Churchill Livingstone, New York, 313-319.   Duarte AC, Cunha E, Roth JM, Ferreira FL, et al. (2004). Cytogenetics of genetic counseling patients in Pelotas, Rio Grande do Sul, Brazil. Genet. Mol. Res. 3: 303-308. PMid:15614723   Düzcan F, Atmaca M, Cetin GO and Bagci H (2003). Cytogenetic studies in patients with reproductive failure. Acta Obstet. Gynecol. 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