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A study of cancer-related genes: Prevalence of polymorphic GSTT1 and GSTM1 deletions in Turkey

Karaca, Şefayet; Karaca, Mehmet; Kaymaz, Ayşe (2013)

The major burden of cancer in the general population is results from the complex interactions of multiple genetic and environmental factors over time. Population based studies support the involvement of GSTM1 and GSTT1 ...

Haplotypic similarity in immunogenes of Turkish population with Europeans and Central Asians

Karaca, Şefayet; Karaca, Mehmet; Civelek, Ersoy; Şekerel, Bülent Enis; Polimanti, Renato (Wiley-Blackwell, 2016)

Mutation analysis in biotinidase gene by denaturing high pressure liquid chromatography

Karaca, Mehmet; Özgül, Rıza Köksal; Güzel, A.; Kılıç, M.; Tokatlı, Ayşegül; Coskun, Turgay; Göksun, E.; Dursun, Ali; Sivri, Hatice Serap (SPRINGER, 2010)

Molecular characterisation of biotinidase gene mutations in Turkish patients; an update of the results

Karaca, Mehmet; Yucel, D.; Unal, O.; Guzel, A.; Tokatlı, Ayşegül; Coskun, Turgay; Dursun, Ali; Sivri, Hatice Serap (SPRINGER, 2012)

Molecular analysis of homocystinuria in Turkish patients

Karaca, Mehmet; Özgül, Rıza Köksal; Dündar, H.; Coşkun, Turgay; Tokatlı, Ayşegül; Sivri, Hatice Serap; Dursun, Ali (SPRINGER, 2010)

IDENTIFICATION OF MUTATIONS IN THE PCCA AND PCCB GENES CAUSING PROPIONIC ACIDEMIA IN TURKISH PATIENTS

Özgül, R. K.; Yücel, D.; Hismi, B.; Karaca, Mehmet; Sivri, H. S.; Coskun, T.; Tokatlı, A.; Dursun, A. (Springer, 2010)

Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiency

Kılıç, M.; ÖzgÜl, R. K.; Coşkun, T.; Yücel, D.; Karaca, Mehmet; Sivri, H. S.; Tokatlı, A.; Şahin, M.; Karagöz, T.; Dursun, A. (Springer, 2012)

Primary systemic carnitine deficiency (SCD) is an autosomal recessive disorder caused by defective cellular carnitine transport. Patients usually present with predominant metabolic or cardiac manifestations. SCD is caused ...

Mutation detection in Turkish patients with glutaric aciduria type I

Güzel, A.; Özgül, Rıza Köksal; Yücel, D.; Karaca, Mehmet; Kılıç, M.; Coşkun, Turgay; Tokatlı, Ayşegül; Sivri, Hatice Serap; Dursun, Ali (SPRINGER, 2010)

Mutation analysis in arsb gene in Turkish patients with mps type vı: high prevalence of L321P mutation

Özgül, Rıza Köksal; Karaca, Mehmet; Sivri, Hatice; Tokatlı, Ayşegül; Coşkun, Turgay; Dursun, Ali (SPRINGER, 2011)

Molecular and structural analysıs of six nonsense mutations in mut methylmalonic acidemia patients including two novel nonsense mutations

Dündar, H.; Özgül, Rıza Köksal; Ünal, O.; Karaca, Mehmet; Aydın, H., I; Tokatli, Ayşegül; Sivri, Hatice Serap; Coşkun, Turgay; Dursun, Ali (SPRINGER, 2010)