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Papers authored by Tukun A

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Effects of genomic imbalances on telomerase activity in gastric cancer: clues to telomerase regulation.

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Gümüş-Akay G, Elhan AH, Unal AE, Demirkazik A, Sunguroğlu A, and Tükün A

Oncology research 17(10):455-62, 2009 - Who cited this? | PubMed ID: 19725225 | Fulltext

Effects of Imatinib Mesylate on Renin-Angiotensin System (RAS) Activity During the Clinical Course of Chronic Myeloid Leukaemia.

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Sayitoglu M, Haznedaroğlu IC, Hatirnaz O, Erbilgin Y, Aksu S, Koca E, Adiguzel C, Bayik M, Akalin I, Gülbas Z, Akay M, Unal A, Kaynar L, Ovali E, Yilmaz M, Yenerel M,

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The Journal of international medical research 37(4):1018-28, 2009 - Who cited this? | PubMed ID: 19761684 | Fulltext

Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey.

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Sadeghi F, Yurur-Kutlay N, Berberoglu M, Cetinkaya E, Aycan Z, Kara C, Ilgin Ruhi H, Ocal G, Siklar Z, Elhan A, and Tukun A

Journal of pediatric endocrinology & metabolism : JPEM 21(8):781-7, 2008 Aug - Who cited this? | PubMed ID: 18825878 | Fulltext

Novel chromosomal translocations in multiple myeloma: t(13;16)(q14;q24) and t(1;15)(q10;q26).

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Akalin I, Kutlay NY, Ilhan O, and Tukun A

International journal of laboratory hematology 29(3):215-20, 2007 Jun - Who cited this? | PubMed ID: 17474900 | Fulltext

Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum.

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Siklar Z, Berberoğlu M, Adiyaman P, Salih M, Tükün A, Cetinkaya E, Aycan Z, Evliyaoğlu O, Ergur AT, and Oçal G

Pediatric endocrinology reviews : PER 4(3):210-7, 2007 Mar - Who cited this? | PubMed ID: 17551482 | Fulltext

Biology of stem cells in human umbilical cord stroma: in situ and in vitro surveys.

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Karahuseyinoglu S, Cinar O, Kilic E, Kara F, Akay GG, Demiralp DO, Tukun A, Uckan D, and Can A

Stem cells (Dayton, Ohio) 25(2):319-31, 2007 Feb - Who cited this? | PubMed ID: 17053211 | Fulltext

Telomerase activity could be used as a marker for neoplastic transformation in gastric adenocarcinoma: but it does not have a prognostic significance.

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Gümüş-Akay G, Unal AE, Bayar S, Karadayi K, Elhan AH, Sunguroĝlu A, and Tükün A

Genetics and molecular research : GMR 6(1):41-9, 2007 - Who cited this? | PubMed ID: 17469053 | Fulltext

TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy.

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Cabuk F, Karabulut HG, Tuncali T, Karademir S, Bozdayi M, and Tükün A

The Turkish journal of pediatrics 49(1):61-8, 2007 - Who cited this? | PubMed ID: 17479646 | Fulltext

ACE gene deletion/deletion polymorphism may be a protective factor for respiratory distress in preterm infants.

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Sivasli E, Yurdakök M, Babaoğlu E, Karabulut H, Yiğit S, Babaoğlu M, Tekinalp G, and Tükün A

The Turkish journal of pediatrics 49(1):69-74, 2007 - Who cited this? | PubMed ID: 17479647 | Fulltext

Does telomere length affect blood pressure?.

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Aydos SE and Tükün A

Advances in therapy 24(2):269-72, 2007 - Who cited this? | PubMed ID: 17565916 | Fulltext

Infertility in a man with oligoasthenoteratozoospermia associated with nonrobertsonian translocation t(9;15)(p10;q10).

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Aydos SE and Tükün A

Fertility and sterility 86(4):1001.e7-9, 2006 Oct - Who cited this? | PubMed ID: 17027368 | Fulltext

Translocation (13;17)(q14;q25) as a novel chromosomal abnormality in acute myeloid leukemia-M4.

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Turhan N, Yürür-Kutlay N, Topcuoglu P, Sayki M, Yüksel M, Gürman G, and Tükün A

Leukemia research 30(7):903-5, 2006 Jul - Who cited this? | PubMed ID: 16469377 | Fulltext

del5p/dup5q in a 'cri du chat' patient without parental chromosomal rearrangement.

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Akalin I, Yararbas K, Akgul N, Babaoglu E, Akay GG, Dyer S, Kutlay NY, Ruhi HI, Kog G, and Tukun A

American journal of medical genetics. Part A 140(9):1016-20, 2006 May 1 - Who cited this? | PubMed ID: 16619202 | Fulltext

Is telomere length one of the determinants of reproductive life span?.

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Aydos SE, Elhan AH, and Tükün A

Archives of gynecology and obstetrics 272(2):113-6, 2005 Jul - Who cited this? | PubMed ID: 15868185 | Fulltext

The role of genetic counseling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey.

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Ilgin-Ruhi H, Yürür-Kutlay N, Tükün A, and Bökesoy I

European journal of medical genetics 48(1):13-9, 2005 - Who cited this? | PubMed ID: 15953401 | Fulltext

A novel Fryns "Anophthalmia-plus" syndrome associated with primary hypothyroidism.

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Akalin I, Senses DA, Ilgin-Ruhi H, Misirlioğlu E, Yalçiner M, Cetinkaya E, Fryns JP, and Tükün A

Genetic counseling (Geneva, Switzerland) 16(2):145-8, 2005 - Who cited this? | PubMed ID: 16080293 | Fulltext

Recipient-derived hepatocytes in sex-mismatched liver allografts after liver transplantation: early versus late transplant biopsies.

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Idilman R, Erden E, Kuzu I, Ersoz S, Karasu Z, Karayalcin K, Yuce G, Tokat Y, Sahin Y, Tukun A, Akarca US, and Karayalcin S

Transplantation 78(11):1647-52, 2004 Dec 15 - Who cited this? | PubMed ID: 15591954 | Fulltext

Toxic hepatitis in a case of Angelman syndrome associated with Lennox-Gastaut syndrome.

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Deda G, Caksen H, Kansu A, Girgin N, Suskan E, Uysal S, and Tükün A

Genetic counseling (Geneva, Switzerland) 15(3):357-61, 2004 - Who cited this? | PubMed ID: 15517829 | Fulltext

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter-->q22:).

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Aydos S, Tükün A, and Bökesoy I

Archives of gynecology and obstetrics 267(3):173-4, 2003 Jan - Who cited this? | PubMed ID: 12552332 | Fulltext

Common fragile sites associated with the breakpoints of chromosomal aberrations in hematologic neoplasms.

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Gümüş G, Sunguroğlu A, Tükün A, Sayin DB, and Bökesoy I

Cancer genetics and cytogenetics 133(2):168-71, 2002 Mar - Who cited this? | PubMed ID: 11943347 | Fulltext

A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21.

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Ilgin Ruhi H, Tükün A, Karabulut H, Bayazit P, and Bökesoy I

Clinical genetics 59(5):368-70, 2001 May - Who cited this? | PubMed ID: 11359472 | Fulltext

Mental retardation with rare fragile site expressed at 2q11.

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Tükün A, Renda Y, Topçu M, Tuncali T, and Bökesoy I

Brain & development 22(8):498-500, 2000 Dec - Who cited this? | PubMed ID: 11111064 | Fulltext

Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.

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Toydemir PB, Elhan AH, Tükün A, Toydemir R, Gürler A, Tüzüner A, and Bökesoy I

The Journal of rheumatology 27(12):2849-54, 2000 Dec - Who cited this? | PubMed ID: 11128675 | Fulltext

Molecular alterations in the TP53 gene of peripheral blood cells of patients with chronic myeloid leukemia.

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Peller S, Yona R, Kopilova Y, Prokocimer M, Goldfinger N, Uysal A, Karabulut HG, Tukun A, Bokesoy I, Tuncman G, and Rotter V

Genes, chromosomes & cancer 21(1):2-7, 1998 Jan - Who cited this? | PubMed ID: 9443036 | Fulltext

A case of Prader Willi syndrome with del 15 (q11-->q13).

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Tunçman G, Tükün A, Yalaz K, and Bökesoy I

The Turkish journal of pediatrics 35(4):333-6, 1993 - Who cited this? | PubMed ID: 8160287 | Fulltext

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