Publications
Found 3 results
Filters: Author is A. Turkyılmaz [Clear All Filters]
“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
“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
“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. Scand. 82: 53-56.
PMid:12580840
Giaccardi A, Sardi R, Priora U, Vivalda M, et al. (1991). Trisomy 18 or Edwards' syndrome. A report of 4 clinical cases. Minerva Pediatr. 43: 343-349.
PMid:1870543
Goud MT, Al-Harassi SM, Al-Khalili SA, Al-Salmani KK, et al. (2005). Incidence of chromosome abnormalities in the Sultanate of Oman. Saudi Med. J. 26: 1951-1957.
PMid:16380780
Hamerton JL, Canning N, Ray M and Smith S (1975). A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. Clin. Genet. 8: 223-243.
http://dx.doi.org/10.1111/j.1399-0004.1975.tb01498.x
PMid:1183067
Hook EB and Hamerton JL (1977). The Frequency of Chromosome Abnormalities Detected in Consecutive Newborn Studies - Differences Between Studies - Results by Sex and by Severity of Phenotypic Involvement. In: Population Cytogenetics. Studies in Humans (Hook EB and Porter IH, eds.). Academic Press, New York, 63-79.
International Software Consulting Network (ISCN) (1995). An International System for Human Cytogenetic Nomenclature. Recommendations of the International Standing Committee on Human Cytogenetic Nomenclature (Mitelman F, ed.). S. Karger Publishers Inc., Basel.
Kim SS, Jung SC, Kim HJ, Moon HR, et al. (1999). Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases. J. Korean Med. Sci. 14: 373-376.
PMid:10485615 PMCid:3054395
Méhes K and Bajnoczky K (1981). Incidence of major chromosomal abnormalities. Clin. Genet. 19: 75-76.
http://dx.doi.org/10.1111/j.1399-0004.1981.tb00672.x
PMid:7460384
Milia A, Cardia S, Aste A, Santucci S, et al. (1984). Cytogenetic study on 282 patients with suspected chromosomal aberration. Eur. J. Obstet. Gynecol. Reprod. Biol. 18: 207-210.
http://dx.doi.org/10.1016/0028-2243(84)90118-7
Patil SR, Lubs HA, Brown J, Cohen M, et al. (1977). Incidence of major chromosome abnormalities in children. Cytogenet. Cell Genet. 18: 3102-3106.
http://dx.doi.org/10.1159/000130774
PMid:880833
Salamanca F and Armendares S (1974). C bands in human metaphase chromosomes treated by barium hydroxide. Ann. Genet. 17: 135-136.
PMid:4139928
Samonte RV, Conte RA, Ramesh KH and Verma RS (1996). Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9. Hum. Genet. 98: 576-580.
http://dx.doi.org/10.1007/s004390050262
PMid:8882878
Santos CB, Boy RT, Santos JM, Silva MPS, et al. (2000). Chromosomal investigations in patients with mental retardation and/or congenital malformations. Genet. Mol. Biol. 23: 703-707.
http://dx.doi.org/10.1590/S1415-47572000000400002
Seabright M (1971). A rapid banding technique for human chromosomes. Lancet 2: 971-972.
http://dx.doi.org/10.1016/S0140-6736(71)90287-X
Solak M, Fistik T, Eser B, Söylemez Z, et al. (2007). Cytogenetic Analyses in Medical Genetic Laboratory of Medical Biology Department in Afyonkarahisar Kocatepe University. Osmangazi J. Med. 29: 93-99.
Sumner AT (1972). A simple technique for demonstrating centromeric heterochromatin. Exp. Cell Res. 75: 304-306.
http://dx.doi.org/10.1016/0014-4827(72)90558-7
Taylor AI (1968). Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome. J. Med. Genet. 5: 227-252.
http://dx.doi.org/10.1136/jmg.5.3.227
PMid:5708029 PMCid:1468648
Tunç E, Demirhan O, Demir C and Tastemir D (2007). Cytogenetic study of recurrent miscarriages and their parents. Genetika 43: 545-552.
PMid:17555132
Verma RS and Dosik H (1980). Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases. Clin. Genet. 17: 305-308.
http://dx.doi.org/10.1111/j.1399-0004.1980.tb00154.x
PMid:7438487
Yuce H, Tekedereli I and Elyas H (2007). Cytogenetic results of recurrent spontaneous abortions in Turkey. Med. Sci. Monit. 13: CR286-CR289.
PMid:17534236