Cirakoglu B - Search Results

1

Gozu HI, Bircan R, Krohn K, Müller S, Vural S, Gezen C, Sargin H, Yavuzer D, Sargin M, Cirakoglu B, Paschke R. Gozu HI, et al. Among authors: cirakoglu b. Eur J Endocrinol. 2006 Oct;155(4):535-45. doi: 10.1530/eje.1.02253. Eur J Endocrinol. 2006. PMID: 16990652

2

Two novel mutations in the sixth transmembrane segment of the thyrotropin receptor gene causing hyperfunctioning thyroid nodules.

Gozu H, Avsar M, Bircan R, Claus M, Sahin S, Sezgin O, Deyneli O, Paschke R, Cirakoglu B, Akalin S. Gozu H, et al. Among authors: cirakoglu b. Thyroid. 2005 Apr;15(4):389-97. doi: 10.1089/thy.2005.15.389. Thyroid. 2005. PMID: 15876166

3

Mutations in the thyrotropin receptor signal transduction pathway in the hyperfunctioning thyroid nodules from multinodular goiters: a study in the Turkish population.

Gozu H, Avsar M, Bircan R, Sahin S, Deyneli O, Cirakoglu B, Akalin S. Gozu H, et al. Among authors: cirakoglu b. Endocr J. 2005 Oct;52(5):577-85. doi: 10.1507/endocrj.52.577. Endocr J. 2005. PMID: 16284436 Free article.

4

A new silent germline mutation of the TSH receptor: coexpression in a hyperthyroid family member with a second activating somatic mutation.

Gozu HI, Mueller S, Bircan R, Krohn K, Ekinci G, Yavuzer D, Sargin H, Sargin M, Ones T, Gezen C, Orbay E, Cirakoglu B, Paschke R. Gozu HI, et al. Among authors: cirakoglu b. Thyroid. 2008 May;18(5):499-508. doi: 10.1089/thy.2007.0335. Thyroid. 2008. PMID: 18466076

5

Does a Leu 512 Arg thyrotropin receptor mutation cause an autonomously functioning papillary carcinoma?

Gozu H, Avsar M, Bircan R, Sahin S, Ahiskanali R, Gulluoglu B, Deyneli O, Ones T, Narin Y, Akalin S, Cirakoglu B. Gozu H, et al. Among authors: cirakoglu b. Thyroid. 2004 Nov;14(11):975-80. doi: 10.1089/thy.2004.14.975. Thyroid. 2004. PMID: 15671779

6

A case of McCune-Albright syndrome associated with Gs alpha mutation in the bone tissue.

Sargin H, Gozu H, Bircan R, Sargin M, Avsar M, Ekinci G, Yayla A, Gulec I, Bozbuga M, Cirakoglu B, Tanakol R. Sargin H, et al. Among authors: cirakoglu b. Endocr J. 2006 Feb;53(1):35-44. doi: 10.1507/endocrj.53.35. Endocr J. 2006. PMID: 16543670 Free article.

7

Angiotensin converting enzyme gene polymorphism in Turkish asthmatic patients.

Eryüksel E, Ceyhan BB, Bircan R, Avşar M, Cirakoğlu B. Eryüksel E, et al. Among authors: cirakoglu b. J Asthma. 2009 May;46(4):335-8. doi: 10.1080/02770900802660972. J Asthma. 2009. PMID: 19484664

8

Regional distributions of beta-thalassemia mutations in Turkey.

Atalay EO, Cirakoğlu B, Dinçolç G, Atalay A, Kilinç Y, Aytekin H, Yüregir GT, Arpaci A, Bermek E, Aksoy M. Atalay EO, et al. Among authors: cirakoglu b. Int J Hematol. 1993 Jun;57(3):207-11. Int J Hematol. 1993. PMID: 8364184

9

Prenatal diagnosis of a beta-globin gene IVS 1nt/110 mutation in chorionic villus from a mosaic triple-X mother with high HbA2.

Atalay E, Cirakoğlu B, Erdoğan G, Bermek E, Aksoy M. Atalay E, et al. Among authors: cirakoglu b. Prenat Diagn. 1990 May;10(5):343-4. doi: 10.1002/pd.1970100511. Prenat Diagn. 1990. PMID: 2388885 No abstract available.

10

Beta-thalassemia in Iran: a high incidence of the nonsense codon 39 mutation on the island of Queshm.

Noori-Daloii MR, Moazami N, Farhangi S, Atalay A, Geren IN, Akar L, Atalay EO, Cirakoglu B, Bermek E. Noori-Daloii MR, et al. Among authors: cirakoglu b. Hemoglobin. 1994 Nov;18(6):449-53. doi: 10.3109/03630269409045779. Hemoglobin. 1994. PMID: 7713751 No abstract available.

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