Ozer A - Search Results

1

The molecular basis of beta-thalassemia in Turkey.

Başak AN, Ozçelik H, Ozer A, Tolun A, Aksoy M, Ağaoğlu L, Ridolfi F, Ulukutlu L, Akar N, Gürgey A, et al. Başak AN, et al. Among authors: ozer a. Hum Genet. 1992 May;89(3):315-8. doi: 10.1007/BF00220549. Hum Genet. 1992. PMID: 1351036

2

A novel frameshift mutation: deletion of C in codons 74/75 of the beta-globin gene causes beta zero-thalassemia in a Turkish patient.

Başak AN, Ozer A, Ozçelik H, Kirdar B, Gürgey A. Başak AN, et al. Among authors: ozer a. Hemoglobin. 1992;16(4):309-12. doi: 10.3109/03630269208998874. Hemoglobin. 1992. PMID: 1517110 No abstract available.

3

A novel 13 Bp deletion in the 3'UTR of the beta-globin gene causes beta-thalassemia in a Turkish patient.

Başak AN, Ozer A, Kirdar B, Akar N. Başak AN, et al. Among authors: ozer a. Hemoglobin. 1993 Dec;17(6):551-5. doi: 10.3109/03630269309043496. Hemoglobin. 1993. PMID: 8144356 No abstract available.

4

Prenatal diagnosis of beta-thalassaemia and sickle cell anaemia in Turkey.

Tüzmen S, Tadmouri GO, Ozer A, Baig SM, Ozçelik H, Başaran S, Başak AN. Tüzmen S, et al. Among authors: ozer a. Prenat Diagn. 1996 Mar;16(3):252-8. doi: 10.1002/(SICI)1097-0223(199603)16:3<252::AID-PD839>3.0.CO;2-W. Prenat Diagn. 1996. PMID: 8710780

5

Molecular and population genetic analyses of beta-thalassemia in Turkey.

Tadmouri GO, Tüzmen S, Ozçelik H, Ozer A, Baig SM, Senga EB, Başak AN. Tadmouri GO, et al. Among authors: ozer a. Am J Hematol. 1998 Mar;57(3):215-20. doi: 10.1002/(sici)1096-8652(199803)57:3<215::aid-ajh6>3.0.co;2-y. Am J Hematol. 1998. PMID: 9495372 Free article.

6

Impact of glucocorticoid receptor gene (NR3C1) polymorphisms in Turkish patients with metabolic syndrome.

Kaya Z, Caglayan S, Akkiprik M, Aral C, Ozisik G, Ozata M, Ozer A. Kaya Z, et al. Among authors: ozer a. J Endocrinol Invest. 2016 May;39(5):557-66. doi: 10.1007/s40618-015-0409-1. Epub 2015 Nov 23. J Endocrinol Invest. 2016. PMID: 26596278

7

A novel approach for rapid screening of mitochondrial D310 polymorphism.

Aral C, Kaya H, Ataizi-Celikel C, Akkiprik M, Sonmez O, Gulluoglu BM, Ozer A. Aral C, et al. Among authors: ozer a. BMC Cancer. 2006 Jan 24;6:21. doi: 10.1186/1471-2407-6-21. BMC Cancer. 2006. PMID: 16433919 Free PMC article.

8

Analysis of p53 gene polymorphisms and protein over-expression in patients with breast cancer.

Akkiprik M, Sonmez O, Gulluoglu BM, Caglar HB, Kaya H, Demirkalem P, Abacioglu U, Sengoz M, Sav A, Ozer A. Akkiprik M, et al. Among authors: ozer a. Pathol Oncol Res. 2009 Sep;15(3):359-68. doi: 10.1007/s12253-008-9129-6. Pathol Oncol Res. 2009. PMID: 19048399 Free article.

9

Detection of PIK3CA gene mutations with HRM analysis and association with IGFBP-5 expression levels in breast cancer.

Dirican E, Kaya Z, Gullu G, Peker I, Ozmen T, Gulluoglu BM, Kaya H, Ozer A, Akkiprik M. Dirican E, et al. Among authors: ozer a. Asian Pac J Cancer Prev. 2014;15(21):9327-33. doi: 10.7314/apjcp.2014.15.21.9327. Asian Pac J Cancer Prev. 2014. PMID: 25422220 Free article.

10

Investigation of relationship of the mitochondrial DNA 16189 T>C polymorphism with metabolic syndrome and its associated clinical parameters in Turkish patients.

Aral C, Akkiprik M, Caglayan S, Atabey Z, Ozişik G, Bekiroglu N, Ozer A. Aral C, et al. Among authors: ozer a. Hormones (Athens). 2011 Oct-Dec;10(4):298-303. doi: 10.14310/horm.2002.1321. Hormones (Athens). 2011. PMID: 22281886 Free article.

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