Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

A novel homozygous RIPK4 variant in a family with severe Bartsocas-Papas syndrome

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.185, no.6, pp.1691-1699, 2021 (Journal Indexed in SCI) identifier identifier identifier

RIPK4 suppresses the TGF-beta 1 signaling pathway in HaCaT cells

CELL BIOLOGY INTERNATIONAL, vol.44, no.3, pp.848-860, 2020 (Journal Indexed in SCI) identifier identifier identifier

A role for the TGF beta-Par6 polarity pathway in breast cancer progression

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, vol.106, no.33, pp.14028-14033, 2009 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

Foxh1 is essential for development of the anterior heart field

DEVELOPMENTAL CELL, vol.7, no.3, pp.331-345, 2004 (Journal Indexed in SCI) identifier identifier identifier

Articles Published in Other Journals

Knock-Out of Receptor Interacting Serine/Threonine Kinase 4 (RIPK4) Induces De-Differentiation process in Keratinocytes

Fırat Üniversitesi Sağlık Bilimleri Tıp Dergisi, vol.34, no.2, pp.117-122, 2020 (National Refreed University Journal)

Refereed Congress / Symposium Publications in Proceedings

The wound healing basics, innovations and models

Euroasian Congress on Molecular Biotechnology (ECOMB 2019), 19 - 21 September 2019

The Investigation of Cytotoxic Effects of Ethanol and Water-Soluble Propolis Extracts on VERO cells

6th International Muğla Beekeping and Honey Congress, Muğla, Turkey, 15 - 19 October 2018, pp.569-570

Otizm spektrum bozukluklarının etiyolojisinde kromozomal anomaliler

XIII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Aydın, Turkey, 27 - 30 October 2013, pp.338

Sendromik Mental Retardasyonlu Bir Ailede de novo PQBP1 Mutasyonu

XIII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Aydın, Turkey, 27 - 30 October 2013, pp.112

Smurf’ler ve Sitokinez

XIII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Aydın, Turkey, 27 - 30 October 2013, pp.119-120

Otizm Spektrum Bozuklukların Etiyolojisinde Kromozomal Anomaliler

XIII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Aydın, Turkey, 27 - 30 October 2013, pp.338

Books & Book Chapters

Genomik DNA'nın Replikasyonu, Korunması ve Yeniden Düzenlenmesi

in: Hücre Moleküler Yaklaşım, Atabey N., Kalay E., Sakızlı M., Editor, İzmir Tıp Kitapevi Yayınları, İzmir, pp.217, 2016