Search Results - "Şener, Elif Funda"

Targeting LC3 and Beclin-1 autophagy genes suppresses proliferation, survival, migration and invasion by inhibition of Cyclin-D1 and uPAR/Integrin β1/ Src signaling in triple negative breast cancer cells by Hamurcu, Zuhal, Delibaşı, Nesrin, Geçene, Seda, Şener, Elif Funda, Dönmez-Altuntaş, Hamiyet, Özkul, Yusuf, Canatan, Halit, Ozpolat, Bulent

“…Autophagy is a catabolic process for degrading dysfunctional proteins and organelles, and closely associated with cancer cell survival under therapeutic,…”
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Investigation of Interleukin 1 Alpha Gene Promoter Polymorphism in Hemodialysis Patients with Arteriovenous Fistula Thrombosis by Emirogulları, Omer Naci, Tuncay, Aydin, Sener, Elif Funda, Taheri, Serpil, Unal, Aydin, Ozkul, Yusuf

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FOXM1 plays a role in autophagy by transcriptionally regulating Beclin-1 and LC3 genes in human triple-negative breast cancer cells by Hamurcu, Zuhal, Delibaşı, Nesrin, Nalbantoglu, Ufuk, Sener, Elif Funda, Nurdinov, Nursultan, Tascı, Bayram, Taheri, Serpil, Özkul, Yusuf, Donmez-Altuntas, Hamiyet, Canatan, Halit, Ozpolat, Bulent

“…Triple-negative breast cancer (TNBC) is associated with poor prognosis owing to its aggressive and heterogeneous nature, and the lack of therapeutic targets…”
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Variants in TNF and NOS3 (eNOS) genes associated with sepsis in adult patients by Özkan, Mustafa, Günay, Nurullah, Sener, Elif Funda, Karcıoglu, Özgür, Tahtasakal, Reyhan, Dal, Fatma, Günay, Nahide Ekici, Demiryürek, Abdullah Tuncay

“…Background Sepsis is a life‐threatening condition caused by a dysregulated host response to infections and is a leading cause of death in hospitalized…”
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Autism-Related Cc2d1a Heterozygous Mice: Increased Levels of miRNAs Retained in DNA/RNA Hybrid Profiles (R-Loop) by Sener, Elif Funda, Dana, Halime, Tahtasakal, Reyhan, Taheri, Serpil, Rassoulzadegan, Minoo

“…Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a highly variable expression of phenotypes (restricted interest or activity and…”
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Altered Global mRNA Expressions of Pain and Aggression Related Genes in the Blood of Children with Autism Spectrum Disorders by Sener, Elif Funda, Taheri, Serpil, Sahin, Mustafa Caglar, Bayramov, Keziban Korkmaz, Marasli, Mert Kahraman, Zararsiz, Gokmen, Mehmetbeyoglu, Ecmel, Oztop, Didem Behice, Canpolat, Mehmet, Canatan, Halit, Ozkul, Yusuf

“…Autism spectrum disorder (ASD) is characterized by repetitive stereotypic behaviors, restricted interests, social withdrawal, and communication deficits…”
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Role of Glutamate Receptor-related Biomarkers in the Etiopathogenesis of ADHD by Ulu, Ebru, Demirci, Esra, Sener, Elif Funda, Özmen, Sevgi, Gul, Melike Kevser, Tahtasakal, Reyhan, Dal, Fatma

“…: Pathways associated with glutamate receptors are known to play a role in the pathophysiology of attention-deficit hyperactivity disorder (ADHD). However,…”
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Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology by Sener, Elif Funda, Canatan, Halit, Ozkul, Yusuf

“…Autism spectrum disorders (ASD) is characterized by three core symptoms with impaired reciprocal social interaction and communication, a pattern of repetitive…”
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Trans Species RNA Activity: Sperm RNA of the Father of an Autistic Child Programs Glial Cells and Behavioral Disorders in Mice by Yilmaz Sukranli, Zeynep, Korkmaz Bayram, Keziban, Mehmetbeyoglu, Ecmel, Doganyigit, Zuleyha, Beyaz, Feyzullah, Sener, Elif Funda, Taheri, Serpil, Ozkul, Yusuf, Rassoulzadegan, Minoo

“…Recently, we described the alteration of six miRNAs in the serum of autistic children, their fathers, mothers, siblings, and in the sperm of autistic mouse…”
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A role of the endothelial nitric oxide system in acute renal colic caused by ureteral stone by Bulbul, Emre, Sener, Elif Funda, Gunay, Nahide Ekici, Taslidere, Bahadir, Taslidere, Elif, Koyuncu, Serhat, Gunay, Nurullah

“…Endothelial nitric oxide synthase gene polymorphisms play a role in some pathophysiological processes. In this study, the possible effects of endothelial…”
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Blood mRNA Expression Profiles of Autophagy, Apoptosis, and Hypoxia Markers on Blood Cardioplegia and Custodiol Cardioplegia Groups by Elcik, Deniz, Tuncay, Aydın, Sener, Elif Funda, Taheri, Serpil, Tahtasakal, Reyhan, Mehmetbeyoğlu, Ecmel, Gunes, Isın, Emirogullari, Omer Naci

“…Blood cardioplegia (BC) and Custodiol cardioplegia (CC) have been used for a long time in open heart surgery and are highly effective solutions. The most…”
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MTHFR Gene C677T Polymorphism in Autism Spectrum Disorders by Sener, Elif Funda, Oztop, Didem Behice, Ozkul, Yusuf

“…Aim. Autism is a subgroup of autism spectrum disorders, classified as a heterogeneous neurodevelopmental disorder and symptoms occur in the first three years…”
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Association of OSR‐1 With Vascular Dysfunction and Hypertension in Polycystic Kidney Disease by Kocyigit, Ismail, Taheri, Serpil, Eroglu, Eray, Zararsiz, Gokmen, Sener, Elif Funda, Uzun, Ilknur, Imamoglu, Hakan, Mehmetbeyoglu, Ecmel, Unal, Aydin, Korkmaz, Keziban, Sipahioglu, Murat Hayri, Oymak, Oktay, Tokgoz, Bulent

“…Autosomal‐dominant polycystic kidney disease (ADPKD) is associated with oxidative stress and hypertension development before renal function decline and…”
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Serum micro-rna profiles in patients with autosomal dominant polycystic kidney disease according to hypertension and renal function by Kocyigit, Ismail, Taheri, Serpil, Sener, Elif Funda, Eroglu, Eray, Ozturk, Fahir, Unal, Aydin, Korkmaz, Kezban, Zararsiz, Gokmen, Sipahioglu, Murat Hayri, Ozkul, Yusuf, Tokgoz, Bulent, Oymak, Oktay, Ecder, Tevfik, Axelsson, Jonas

“…Autosomal dominant polycystic kidney disease (ADPKD) is a common hereditary disorder with unclear disease mechanism. Currently, overt hypertension and…”
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Systemic Succinate, Hypoxia-Inducible Factor-1 Alpha, and IL-1β Gene Expression in Autosomal Dominant Polycystic Kidney Disease with and without Hypertension by Kocyigit, Ismail, Taheri, Serpil, Eroglu, Eray, Sener, Elif Funda, Zararsız, Gokmen, Uzun, Ilknur, Tufan, Esra, Mehmetbeyoglu, Ecmel, Korkmaz Bayramov, Kezban, Sipahioglu, Murat Hayri, Ozkul, Yusuf, Tokgoz, Bulent, Oymak, Oktay, Axelsson, Jonas

“…Background and Objectives: Cyst pressure induces renin-angiotensin-aldosterone system activation and kidney hypoxia in autosomal dominant polycystic kidney…”
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Role of circulating microRNAs in acute appendicitis by Seyhan, Avni Uygar, Şener, Elif Funda, Bol, Oğuzhan, Taheri, Serpil, Topaloglu, Tugba, Tufan, Esra, Tahtasakal, Reyhan, Ekici Günay, Nahide, Karabulut, Hatice, Günay, Nurullah

“…Acute appendicitis (AA) is a momentous, emergency, surgical pathology that has still been investigated for both etiopathogenetic unknowns and challenges in…”
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Investigation of the promoter polymorphisms of the growth hormone (GH1), growth hormone receptor (GHR), insulin-like growth factor (IGF-I), and prolactin (PRL) genes and the correlation between gene expression and milk yields in Holstein cattle raised in Central Anatolia by ARSLAN, Korhan, TAHERİ, Serpil, ŞENER, Elif Funda, AKYÜZ, Bilal, AKÇAY, Aytaç, ÖZKUL, Yusuf, İŞCAN, Kaan Muhsin

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Toll-Like Receptors in the Progression of Autosomal Dominant Polycystic Kidney Disease by Kocyigit, Ismail, Sener, Elif Funda, Taheri, Serpil, Eroglu, Eray, Ozturk, Fahir, Unal, Aydin, Zararsiz, Gokmen, Uzun, Ilknur, Imamoglu, Hakan, Sipahioglu, Murat Hayri, Tokgoz, Bulent, Oymak, Oktay, Ecder, Tevfik

“…Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary cause of chronic kidney disease. The intriguing role of innate immune system…”
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Expression Profiles Of PTEN And POGZ Genes In Patients With Autism by TEZCAN, Tuğba, ŞENER, Elif Funda, DEMİRCİ, Esra, ŞAHİN, Nilfer, HAMURCU, Zuhal, ÖZTOP, Didem

“…Aim: Autism spectrum disorder (ASD), a group of heterogeneous neurodevelopmental disorders, is characterized by complex behavioral phenotypes. Despite…”
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The relationship of learning and memory disfunction with NEURL1 and RGS14 genes in patients with autism spectrum disorders by ECIROGLU, Hamiyet, ŞENER, Elif Funda, ÖZTOP, Didem Behice, ÖZMEN, Sevgi, KAAN, Dilek, ÖZKUL, Yusuf

“…Aim: We aimed to evaluate the relationship between learning-memory difficulties and NEURL1 and RGS14 genes in patients with autism spectrum disorders…”
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