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Sehime G. Temel

Uludağ University

50

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Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia.

2021 Applied Immunohistochemistry & Molecular Morphology
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Sıçan Beyninde Vanilloid Resptör Altgrup Tip-1’in Gonodotropin Salgılayan Hormon Nöronlarında Ifade Edilmesi

2021
- Sehime G. Temel
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Psychomotor Delay in a Child with FGFR3 G380R Pathogenic Mutation Causing Achondroplasia

2021
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RAB25 confers resistance to chemotherapy by altering mitochondrial apoptosis signaling in ovarian cancer cells.

2020 Apoptosis
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CC2D1A AS A NOVEL CILIOPATHY GENE

2020
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Functional coding/non-coding variants in EGFR, ROS1 and ALK genes and their role in liquid biopsy as a personalized therapy.

2020 Critical Reviews in Oncology Hematology
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Biallelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility

2020 American Journal of Human Genetics
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The use of ACE INDEL polymorphism as a biomarker of coronary artery disease (CAD) in humans with Mediterranean-style diet

2019 International Journal of Biological Macromolecules
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Investigation of KCNQ1 polymorphisms as biomarkers for cardiovascular diseases in the Turkish Cypriots for establishing preventative medical measures

2019 International Journal of Biological Macromolecules
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Strong association between VDR FokI (rs2228570) gene variant and serum vitamin D levels in Turkish Cypriots

2019 Molecular Biology Reports
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