Yayınlar

A Novel Mutation of ATP7B Gene in a Case of Wilson Disease

Çiğdem Yüce Kahraman, Ali İşlek, Abdulgani Tatar, Ozlem Ozdemir, Adil Mardinglu, Hasan Türkez

• WoS Q3
• Scopus Q2
• WoS 3 atıf

The Assessment of Selected miRNA Profile in Familial Mediterranean Fever

Çiğdem Yüce Kahraman, Mehmet Ertugrul Egin, Abdulgani Tatar, Hasan Türkez, Adil Mardinoglu

• WoS Q3
• Scopus Q2
• WoS 6 atıf

Mitochondrial DNA copy number may be associated with attention deficit/hyperactivity disorder severity in treatment: a one-year follow-up study

Hakan Ogutlu, İbrahim Selçuk ESİN, Haktan Bagis Erdem, Abdulgani Tatar, Onur Burak Dursun

• WoS Q3
• Scopus Q2
• WoS 8 atıf

Glycyl-L-Prolyl-L-Glutamate Pseudotripeptides for Treatment of Alzheimer's Disease

Hasan Türkez, Ivana Cacciatore, Lisa Marinelli, Erika Fornasari, Mehmet Enes Aslan, Kenan Cadirci, Çiğdem Yüce Kahraman, Ozge Caglar, Abdulgani Tatar, Giuseppe Di Biase, Ahmet Hacımüftüoğlu, Antonio Di Stefano ve 1 yazar daha

• WoS Q2
• Scopus Q2
• WoS 12 atıf

Is there an association between nasal polyposis and adamts genes expressions?

Çiğdem Yüce Kahraman, Arzu Tatar, Muzaffer Keles, Zeynep Ipek Ocak, Abdulgani Tatar

• Scopus Q2
• WoS 1 atıf
• PlumX

GEBELİKTE HEREDİTER KANSER VE GENETİK KONULAR

Çiğdem Yüce Kahraman

Myeloid Malignitesi Olan Hastalarda NGS Temelli Panel Test Kullanımı ve Sonuçları

Çiğdem Yüce Kahraman, Abdulgani Tatar

Analysis of polyposis and hereditary colorectal cancer related genes by targeted next generation sequencing

Pelin Ercoşkun, Çiğdem Yüce Kahraman, Abdulgani Tatar, Neslihan Cinkara, Ömer Yakar, Kübra Adanur

A Novel NPR2 Mutation in Two Turkish Siblings with Acromesomelic Dysplasia Maroteaux Type

Neslihan Cinkara, Abdulgani Tatar, Çiğdem Yüce Kahraman, Pelin Ercoşkun, Ömer Yakar, Kübra Adanur

Expression profiling and pathway analysis of iron oxide nanoparticles toxicity on human lung alveolar epithelial cell line using microarray analysis,

Hasan Türkez, MEHMET ENES ARSLAN, Erdal Sönmez, Abdulgani Tatar, Fatime Geyikoğlu, METİN AÇIKYILDIZ

• PlumX

A novel mutation of infantile epileptic encephalopathy type 9; a rare genetic disorder with an interesting inheritance pattern

Çiğdem Yüce Kahraman

A case of myhre syndrome with a very rare finding: Severe constipation

Neslihan Cinkara, Abdulgani Tatar

MITOCHONDRIAL DNA COPY NUMBER IS ASSOCIATED WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER

Hakan Ogutlu, İbrahim Selçuk ESİN, Haktan Bagis Erdem, Abdulgani Tatar, Onur Burak Dursun

• WoS Q4
• Scopus Q3
• WoS 24 atıf

Clinical results and importance of next-generation sequencing (NGS) in detecting targeted mutations in the treatment of metastatic Lung Cancer: Single center initial results

Cem Mirili, Çiğdem Yüce Kahraman, Ali Yılmaz, Mehmet Bilici, Salim Başol Tekin, Abdulgani Tatar, Ömer Yakar, Pelin Ercoşkun

• PlumX

Nutrigenomik, Nutrigenetik ve Kronik Hastalıklar

Çiğdem Yüce Kahraman

Farklı Nano-Kalsiyum Fosfat Nanopartiküllerin Sentezi ve In Vitro Toksisite Değerlendirmesi

Hasan Türkez, FERAY BAKAN, BAŞAK TOĞAR, MEHMET ENES ARSLAN, Abdulgani Tatar, Ivana CACCIATORE, Kenan ÇADIRCI, Antonio DI STEFANO, Adil MARDİNOĞLU

Farklı Nano-Kalsiyum Fosfat Nanopartiküllerin Sentezi ve Ġ n V tro Toksisite Değerlendirmesi

Hasan Türkez, Feray Bakan, Başak Toğar, Mehmet Enes Arslan, Abdulgani Tatar, Ivana Cacciatore, Ahmet Hacımüftüoğlu, Kenan Çadırcı, Antonıo Dı Stefano, Adil Mardinoğlu

Stuve-Wiedemann syndrome: a case report without osteorosis

Zerrin Orbak, Çiğdem Yüce Kahraman, Recep Orbak, Ayşe Özden, Abdulgani Tatar

• PlumX

Stuve-Wiedemann syndrome: a case report without osteorosis

Zerrin Orbak, Çiğdem Yüce Kahraman, Recep Orbak, Ayşe ÖZDEN, Abdulgani Tatar

• WoS Q2
• Scopus Q1

(R)-α-LIPOYL-GLY-L-PRO-L-GLU DIMETHYL ESTER MODULATES β-AMYLOID 1-42 INDUCED CYTOTOXIC, OXIDATIVE AND INFLAMMATORY RESPONSES IN CULTURED NEUROBLASTOMA N2A CELLS

Hasan Türkez, MEHMET ENES ARSLAN, IVANA CACCİATORE, Abdulgani Tatar, Ahmet Hacımüftüoğlu, BÜNYAMİN ÖZGERİŞ, TUBA ÖZNÜLÜER, YUSUF AKBABA, Yücel Kadıoğlu, MEVLÜT SAİT KELEŞ, MUHAMMET ÇALIK, ÖZLEM ÖZDEMİR TOZLU ve 2 yazar daha