Bu kısa süre içinde araştırmacılarımız tarafından altyapımız kullanılarak yapılan pek çok yayın mevcuttur. Bu sayfada araştırmacıların öne çıkmış yayınlarının bir özeti verilmektedir.

Bu makalelerin tam metnine erişmek için ilgili dergiye abone olmanız gerekebileceğini lütfen unutmayın.

Yayınlarınızda, sunumlarınızda ve posterlerinizde KUTTAM altyapısının kullanıldığının doğru bir şekilde ifade edilmesini önemsiyoruz. Ancak bu şekilde bilim topluluğu üzerindeki etkimizi gösterebilmemiz mümkündür. Böylelikle en yeni teknolojileri KUTTAM’a kazandırmak ve daha iyi hizmet sunmak için gerekli yeni kaynakları temin edebiliriz.

Önerilen ifade aşağıda bulunabilir;

“Bu çalışma, T.C. Cumhurbaşkanlığı Strateji ve Bütçe Başkanlığı tarafından desteklenen, Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)’nin hizmet ve altyapısı kullanılarak yürütülmüştür. Yazının içeriğinden tümüyle yazarlar sorumludur ve T.C. Cumhurbaşkanlığı Strateji ve Bütçe Başkanlığı’nın resmi görüşünü yansıtmamaktadır.”

ÖNE ÇIKAN MAKALELER

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Programmable Collective Behavior in Dynamically Self-Assembled Mobile Microrobotic Swarms Yigit, B.| Alapan, Y.| Sitti, M. 2019 Advanced Science
A new Luminex-based peptide assay to identify reactivity to baked, fermented, and whole milk Sackesen, C.| Suárez-Fariñas, M.| Silva, R.| Lin, J.| Schmidt, S.| Getts, R.| Gimenez, G.| Yilmaz, E.A.| Cavkaytar, O.| Buyuktiryaki, B.| Soyer, O.| Grishina, G.| Sampson, H.A. 2019 Allergy: European Journal of Allergy and Clinical Immunology
Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia Kariminejad, A.| Szenker-Ravi, E.| Lekszas, C.| Tajsharghi, H.| Moslemi, A.-R.| Naert, T.| Tran, H.T.| Ahangari, F.| Rajaei, M.| Nasseri, M.| Haaf, T.| Azad, A.| Superti-Furga, A.| Maroofian, R.| Ghaderi-Sohi, S.| Najmabadi, H.| Abbaszadegan, M.R.| Vleminckx, K.| Nikuei, P.| Reversade, B. 2019 American Journal of Human Genetics
CARM1 regulates senescence during airway epithelial cell injury in COPD pathogenesis Sarker, R.S.J.| Conlon, T.M.| Morrone, C.| Srivastava, B.| Konyalilar, N.| Verleden, S.E.| Bayram, H.| Fehrenbach, H.| Yildirim, A.Ö. 2019 American Journal of Physiology – Lung Cellular and Molecular Physiology
Error monitoring in decision-making and timing is disrupted in autism spectrum disorder Doenyas, C.| Mutluer, T.| Genç, E.| Balcı, F. 2019 Autism Research
Sclerosing bone dysplasias with hallmarks of dysosteosclerosis in four patients carrying mutations in SLC29A3 and TCIRG1 Howaldt, A.| Nampoothiri, S.| Quell, L.-M.| Ozden, A.| Fischer-Zirnsak, B.| Collet, C.| de Vernejoul, M.-C.| Doneray, H.| Kayserili, H.| Kornak, U. 2019 Bone
A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification Forouhideh, Y.| Müller, K.| Ruf, W.| Assi, M.| Şeker, T.| Tunca, C.| Knehr, A.| Strom, T.M.| Gorges, M.| Schradt, F.| Meitinger, T.| Ludolph, A.C.| Pinkhardt, E.H.| Başak, A.N.| Kassubek, J.| Uttner, I.| Weishaupt, J.H. 2019 Brain
Effects of methyl-beta-cyclodextrin on blood-brain barrier permeability in angiotensin II-induced hypertensive rats Atış, M.| Akcan, U.| Uğur Yılmaz, C.| Orhan, N.| Düzgün, P.| Deniz Ceylan, U.| Arıcan, N.| Karahüseyinoğlu, S.| Nur Şahin, G.| Ahıshalı, B.| Kaya, M. 2019 Brain Research
Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study Vural, S.| Gündoğdu, M.| Gökpınar İli, E.| Durmaz, C.D.| Vural, A.| Steinmüller-Magin, L.| Kleinhempel, A.| Holdt, L.M.| Ruzicka, T.| Giehl, K.A.| Ruhi, H.I.| Boyvat, A. 2019 British Journal of Dermatology
ARv7 Represses Tumor-Suppressor Genes in Castration-Resistant Prostate Cancer Cato, L.| de Tribolet-Hardy, J.| Lee, I.| Rottenberg, J.T.| Coleman, I.| Melchers, D.| Houtman, R.| Xiao, T.| Li, W.| Uo, T.| Sun, S.| Kuznik, N.C.| Göppert, B.| Ozgun, F.| van Royen, M.E.| Houtsmuller, A.B.| Vadhi, R.| Rao, P.K.| Li, L.| Balk, S.P.| Den, R.B.| Trock, B.J.| Karnes, R.J.| Jenkins, R.B.| Klein, E.A.| Davicioni, E.| Gruhl, F.J.| Long, H.W.| Liu, X.S.| Cato, A.C.B.| Lack, N.A.| Nelson, P.S.| Plymate, S.R.| Groner, A.C.| Brown, M. 2019 Cancer Cell
Identification of SERPINE1 as a regulator of glioblastoma cell dispersal with transcriptome profiling Seker, F.| Cingoz, A.| Sur-Erdem, İ.| Erguder, N.| Erkent, A.| Uyulur, F.| Selvan, M.E.| Gümüş, Z.H.| Gönen, M.| Bayraktar, H.| Wakimoto, H.| Bagci-Onder, T. 2019 Cancers
Spreading depolarization waves in neurological diseases: A short review about its pathophysiology and clinical relevance Taş, Y.C.| Solaroğlu, I.| Gürsoy-Özdemir, Y. 2019 Current Neuropharmacology
Image-Based Flow Cytometry and Angle-Resolved Light Scattering to Define the Sickling Process Goktas, P.| Sukharevsky, I.O.| Larkin, S.| Kuypers, F.A.| Yalcin, O.| Altintas, A. 2019 Cytometry Part A
Technology Advancements in Blood Coagulation Measurements for Point-of-Care Diagnostic Testing Mohammadi Aria, M.| Erten, A.| Yalcin, O. 2019 Frontiers in Bioengineering and Biotechnology
The glycosylation site of myelin oligodendrocyte glycoprotein affects autoantibody recognition in a large proportion of patients Fernandez, I.M.| MacRini, C.| Krumbholz, M.| Hensbergen, P.J.| Ederveen, A.L.H.| Winklmeier, S.| Vural, A.| Kurne, A.| Jenne, D.| Kamp, F.| Gerdes, L.A.| Hohlfeld, R.| Wuhrer, M.| Kümpfel, T.| Meinl, E. 2019 Frontiers in Immunology
Current Trends in Tolerance Induction in Cow’s Milk Allergy: From Passive to Proactive Strategies Sackesen, C.| Altintas, D.U.| Bingol, A.| Bingol, G.| Buyuktiryaki, B.| Demir, E.| Kansu, A.| Kuloglu, Z.| Tamay, Z.| Sekerel, B.E. 2019 Frontiers in Pediatrics
Increased hemoglobin oxygen affinity with 5-hydroxymethylfurfural supports cardiac function during severe hypoxia Lucas, A.| Ao-Ieong, E.S.Y.| Williams, A.T.| Jani, V.P.| Muller, C.R.| Yalcin, O.| Cabrales, P. 2019 Frontiers in Physiology
Luteal granulosa cells from natural cycles are more capable of maintaining their viability, steroidogenic activity and LH receptor expression than those of stimulated IVF cycles Bildik, G.| Akin, N.| Seyhan, A.| Esmaeilian, Y.| Yakin, K.| Keles, I.| Balaban, B.| Ata, B.| Urman, B.| Oktem, O. 2019 Human Reproduction
A novel adjustable locking plate (ALP) for segmental bone fracture treatment Subasi, O.| Oral, A.| Lazoglu, I. 2019 Injury
Utility of gonadotropin-releasing hormone agonists for fertility preservation: Lack of biologic basis and the need to prioritize proven methods Turan, V.| Bedoschi, G.| Rodriguez-Wallberg, K.| Sonmezer, M.| Silva Pacheco, F.| Oktem, O.| Taylor, H.| Oktay, K. 2019 Journal of Clinical Oncology
CPAP and health-related quality of life in adults with coronary artery disease and nonsleepy obstructive sleep apnea in the RICCADSA trial Wallström, S.| Balcan, B.| Thunström, E.| Wolf, A.| Peker, Y. 2019 Journal of Clinical Sleep Medicine
MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive c erebellar, o cular, cranio f acial and g enital features (COFG syndrome) Rad, A.| Altunoglu, U.| Miller, R.| Maroofian, R.| James, K.N.| Ça Layan, A.O.| Najafi, M.| Stanley, V.| Boustany, R.-M.| Ye Il, G.| Sahebzamani, A.| Ercan-Sencicek, G.| Saeidi, K.| Wu, K.| Bauer, P.| Bakey, Z.| Gleeson, J.G.| Hauser, N.| Gunel, M.| Kayserili, H.| Schmidts, M. 2019 Journal of Medical Genetics
Inter- and intra-tumoural heterogeneity in cancer-associated fibroblasts of human pancreatic ductal adenocarcinoma Neuzillet, C.| Tijeras-Raballand, A.| Ragulan, C.| Cros, J.| Patil, Y.| Martinet, M.| Erkan, M.| Kleeff, J.| Wilson, J.| Apte, M.| Tosolini, M.| Wilson, A.S.| Delvecchio, F.R.| Bousquet, C.| Paradis, V.| Hammel, P.| Sadanandam, A.| Kocher, H.M. 2019 Journal of Pathology
Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling Toksoy, G.| Durmus, H.| Aghayev, A.| Bagirova, G.| Sevinc Rustemoglu, B.| Basaran, S.| Avci, S.| Karaman, B.| Parman, Y.| Altunoglu, U.| Yapici, Z.| Tekturk, P.| Deymeer, F.| Topaloglu, H.| Kayserili, H.| Oflazer-Serdaroglu, P.| Uyguner, Z.O. 2019 Neuromuscular Disorders
High responders are not exempt from detrimental effects of prematurely rising progesterone levels in fresh embryo transfer cycles Oktem, O.| Yakin, K.| Oguz, S.Y.| Isiklar, A.| Balaban, B.| Urman, B. 2019 Reproductive BioMedicine Online
Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology Reichenstein, I.| Eitan, C.| Diaz-Garcia, S.| Haim, G.| Magen, I.| Siany, A.| Hoye, M.L.| Rivkin, N.| Olender, T.| Toth, B.| Ravid, R.| Mandelbaum, A.D.| Yanowski, E.| Liang, J.| Rymer, J.K.| Levy, R.| Beck, G.| Ainbinder, E.| Farhan, S.M.K.| Lennox, K.A.| Bode, N.M.| Behlke, M.A.| Möller, T.| Saxena, S.| Moreno, C.A.M.| Costaguta, G.| van Eijk, K.R.| Phatnani, H.| Al-Chalabi, A.| Başak, A.N.| van den Berg, L.H.| Hardiman, O.| Landers, J.E.| Mora, J.S.| Morrison, K.E.| Shaw, P.J.| Veldink, J.H.| Pfaff, S.L.| Yizhar, O.| Gross, C.| Brown, R.H.| Ravits, J.M.| Harms, M.B.| Miller, T.M.| Hornstein, E. 2019 Science Translational Medicine
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration Schaffer, A.E.| Breuss, M.W.| Caglayan, A.O.| Al-Sanaa, N.| Al-Abdulwahed, H.Y.| Kaymakçalan, H.| Yılmaz, C.| Zaki, M.S.| Rosti, R.O.| Copeland, B.| Baek, S.T.| Musaev, D.| Scott, E.C.| Ben-Omran, T.| Kariminejad, A.| Kayserili, H.| Mojahedi, F.| Kara, M.| Cai, N.| Silhavy, J.L.| Elsharif, S.| Fenercioglu, E.| Barshop, B.A.| Kara, B.| Wang, R.| Stanley, V.| James, K.N.| Nachnani, R.| Kalur, A.| Megahed, H.| Incecik, F.| Danda, S.| Alanay, Y.| Faqeih, E.| Melikishvili, G.| Mansour, L.| Miller, I.| Sukhudyan, B.| Chelly, J.| Dobyns, W.B.| Bilguvar, K.| Jamra, R.A.| Gunel, M.| Gleeson, J.G. 2018 Nature Genetics
Mutant KRAS-driven cancers depend on PTPN11/SHP2 phosphatase Ruess, D.A.| Heynen, G.J.| Ciecielski, K.J.| Ai, J.| Berninger, A.| Kabacaoglu, D.| Görgülü, K.| Dantes, Z.| Wörmann, S.M.| Diakopoulos, K.N.| Karpathaki, A.F.| Kowalska, M.| Kaya-Aksoy, E.| Song, L.| Van Der Laan, E.A.Z.| López-Alberca, M.P.| Nazaré, M.| Reichert, M.| Saur, D.| Erkan, M.M.| Hopt, U.T.| Sainz, B.| Birchmeier, W.| Schmid, R.M.| Lesina, M.| Algül, H. 2018 Nature Medicine
An approach to monitoring home-cage behavior in mice that facilitates data sharing Balzani, E.| Falappa, M.| Balci, F.| Tucci, V. 2018 Nature Protocols
Structural basis of RIP2 activation and signaling Gong, Q.| Long, Z.| Zhong, F.L.| Teo, D.E.T.| Jin, Y.| Yin, Z.| Boo, Z.Z.| Zhang, Y.| Zhang, J.| Yang, R.| Bhushan, S.| Reversade, B.| Li, Z.| Wu, B. 2018 Nature Communications
Dynamic landscape of pancreatic carcinogenesis reveals early molecular networks of malignancy Kong, B.| Bruns, P.| Behler, N.A.| Chang, L.| Schlitter, A.M.| Cao, J.| Gewies, A.| Ruland, J.| Fritzsche, S.| Valkovskaya, N.| Jian, Z.| Regel, I.| Raulefs, S.| Irmler, M.| Beckers, J.| Friess, H.| Erkan, M.| Mueller, N.S.| Roth, S.| Hackert, T.| Esposito, I.| Theis, F.J.| Kleeff, J.| Michalski, C.W. 2018 Gut
Plasma cell-free DNA methylation: A liquid biomarker of hepatic fibrosis Bergmann, C.| Distler, J.H.W.| Adalı, G.| Dayangaç, M.| Mann, D.A.| Zeybel, M.| Mann, J. 2018 Gut
Cholesterol metabolism promotes B-cell positioning during immune pathogenesis of chronic obstructive pulmonary disease Jia, J.| Conlon, T.M.| Sarker, R.S.J.| Taşdemir, D.| Smirnova, N.F.| Srivastava, B.| Verleden, S.E.| Güneş, G.| Wu, X.| Prehn, C.| Gao, J.| Heinzelmann, K.| Lintelmann, J.| Irmler, M.| Pfeiffer, S.| Schloter, M.| Zimmermann, R.| Hrabé de Angelis, M.| Beckers, J.| Adamski, J.| Bayram, H.| Eickelberg, O.| Yildirim, A.Ö. 2018 EMBO Molecular Medicine
Inadequate brain glycogen or sleep increases spreading depression susceptibility Kilic, K.| Karatas, H.| Dönmez-Demir, B.| Eren-Kocak, E.| Gursoy-Ozdemir, Y.| Can, A.| Petit, J.-M.| Magistretti, P.J.| Dalkara, T. 2018 Annals of Neurology
In vivo confocal microscopy detects bilateral changes of corneal immune cells and nerves in unilateral herpes zoster ophthalmicus Cavalcanti, B.M.| Cruzat, A.| Sahin, A.| Pavan-Langston, D.| Samayoa, E.| Hamrah, P. 2018 Ocular Surface
Influence of lipopolysaccharide on proinflammatory gene expression in human corneal, conjunctival and meibomian gland epithelial cells Chen, D.| Sahin, A.| Kam, W.R.| Liu, Y.| Darabad, R.R.| Sullivan, D.A. 2018 Ocular Surface
A homozygous loss-of-function camk2a mutation causes growth delay, frequent seizures and severe intellectual disability Chia, P.H.| Zhong, F.L.| Niwa, S.| Bonnard, C.| Utami, K.H.| Zeng, R.| Lee, H.| Eskin, A.| Nelson, S.F.| Xie, W.H.| Al-Tawalbeh, S.| El-Khateeb, M.| Shboul, M.| Pouladi, M.A.| Al-Raqad, M.| Reversade, B. 2018 eLife
Analysis of single amino acid variations in singlet hot spots of protein-protein interfaces Ozdemir, E.S.| Gursoy, A.| Keskin, O. 2018 Bioinformatics
C-Abl is not actıvated in DNA damage-induced and Tap63-mediated oocyte apoptosıs in human ovary Bildik, G.| Acılan, C.| Sahin, G.N.| Karahuseyinoglu, S.| Oktem, O. 2018 Cell Death and Disease
Endogenous c-Jun N-terminal kinase (JNK) activity marks the boundary between normal and malignant granulosa cells article Bildik, G.| Akin, N.| Senbabaoglu, F.| Esmalian, Y.| Sahin, G.N.| Urman, D.| Karahuseyinoglu, S.| Ince, U.| Palaoglu, E.| Taskiran, C.| Arvas, M.| Guzel, Y.| Yakin, K.| Oktem, O. 2018 Cell Death and Disease
Improving microcirculatory reperfusion reduces parenchymal oxygen radical formation and provides neuroprotection Taskiran-Sag, A.| Yemisci, M.| Gursoy-Ozdemir, Y.| Erdener, S.E.| Karatas, H.| Yuce, D.| Dalkara, T. 2018 Stroke
Autoantibodies against the node of ranvier in seropositive chronic inflammatory demyelinating polyneuropathy: Diagnostic, pathogenic, and therapeutic relevance Vural, A.| Doppler, K.| Meinl, E. 2018 Frontiers in Immunology
Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis Du, R.| Dinckan, N.| Song, X.| Coban-Akdemir, Z.| Jhangiani, S.N.| Guven, Y.| Aktoren, O.| Kayserili, H.| Petty, L.E.| Muzny, D.M.| Below, J.E.| Boerwinkle, E.| Wu, N.| Gibbs, R.A.| Posey, J.E.| Lupski, J.R.| Letra, A.| Uyguner, Z.O. 2018 Human Genetics
Cell death mechanisms in stroke and novel molecular and cellular treatment options Şekerdağ, E.| Solaroğlu, I.| Gürsoy-özdemir, Y. 2018 Current Neuropharmacology
Impact of the ST101 clone on fatality among patients with colistin-resistant Klebsiella pneumoniae infection Can, F.| Menekse, S.| Ispir, P.| Atac, N.| Albayrak, O.| Demir, T.| Karaaslan, D.C.| Karahan, S.N.| Kapmaz, M.| Azap, O.K.| Timurkaynak, F.| Yavuz, S.S.| Basaran, S.| Yoruk, F.| Azap, A.| Koculu, S.| Benzonana, N.| Lack, N.A.| Gönen, M.| Ergonul, O. 2018 Journal of Antimicrobial Chemotherapy
Features of asthma which provide meaningful insights for understanding the disease heterogeneity Deliu, M.| Yavuz, T.S.| Sperrin, M.| Belgrave, D.| Sahiner, U.M.| Sackesen, C.| Kalayci, O.| Custovic, A. 2018 Clinical and Experimental Allergy
Factors affecting food allergy-related quality of life from parents’ perception in Turkish children Yilmaz, E.A.| Cavkaytar, O.| Buyuktiryaki, B.| Soyer, O.| Sahiner, U.M.| Sekerel, B.E.| DunnGalvin, A.| Karabulut, E.| Sackesen, C. 2018 Allergy, Asthma and Immunology Research
Implications enzymatic degradation of the endothelial glycocalyx on the microvascular hemodynamics and the arteriolar red cell free layer of the rat cremaster muscle Yalcin, O.| Jani, V.P.| Johnson, P.C.| Cabrales, P. 2018 Frontiers in Physiology
Microembolism of single cortical arterioles can induce spreading depression and ischemic injury; a potential trigger for migraine and related MRI lesions Dönmez-Demir, B.| Yemisci, M.| Kılıç, K.| Gürsoy-Özdemir, Y.| Söylemezoğlu, F.| Moskowitz, M.| Dalkara, T. 2018 Brain Research
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development Gordon, C.T.| Xue, S.| Yigit, G.| Filali, H.| Chen, K.| Rosin, N.| Yoshiura, K.-I.| Oufadem, M.| Beck, T.J.| McGowan, R.| Magee, A.C.| Altmüller, J.| Dion, C.| Thiele, H.| Gurzau, A.D.| Nürnberg, P.| Meschede, D.| Mühlbauer, W.| Okamoto, N.| Varghese, V.| Irving, R.| Sigaudy, S.| Williams, D.| Ahmed, S.F.| Bonnard, C.| Kong, M.K.| Ratbi, I.| Fejjal, N.| Fikri, M.| Elalaoui, S.C.| Reigstad, H.| Bole-Feysot, C.| Nitschké, P.| Ragge, N.| Lévy, N.| Tunçbilek, G.| Teo, A.S.M.| Cunningham, M.L.| Sefiani, A.| Kayserili, H.| Murphy, J.M.| Chatdokmaiprai, C.| Hillmer, A.M.| Wattanasirichaigoon, D.| Lyonnet, S.| Magdinier, F.| Javed, A.| Blewitt, M.E.| Amiel, J.| Wollnik, B.| Reversade, B. 2017 Nature Genetics
Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing Lardelli, R.M.| Schaffer, A.E.| Eggens, V.R.C.| Zaki, M.S.| Grainger, S.| Sathe, S.| Van Nostrand, E.L.| Schlachetzki, Z.| Rosti, B.| Akizu, N.| Scott, E.| Silhavy, J.L.| Heckman, L.D.| Rosti, R.O.| Dikoglu, E.| Gregor, A.| Guemez-Gamboa, A.| Musaev, D.| Mande, R.| Widjaja, A.| Shaw, T.L.| Markmiller, S.| Marin-Valencia, I.| Davies, J.H.| De Meirleir, L.| Kayserili, H.| Altunoglu, U.| Freckmann, M.L.| Warwick, L.| Chitayat, D.| Blaser, S.| Ça Layan, A.O.| Bilguvar, K.| Per, H.| Fagerberg, C.| Christesen, H.T.| Kibaek, M.| Aldinger, K.A.| Manchester, D.| Matsumoto, N.| Muramatsu, K.| Saitsu, H.| Shiina, M.| Ogata, K.| Foulds, N.| Dobyns, W.B.| Chi, N.C.| Traver, D.| Spaccini, L.| Bova, S.M.| Gabriel, S.B.| Gunel, M.| Valente, E.M.| Nassogne, M.-C.| Bennett, E.J.| Yeo, G.W.| Baas, F.| Lykke-Andersen, J.| Gleeson, J.G. 2017 Nature Genetics
Induced-Pluripotent-Stem-Cell-Derived Primitive Macrophages Provide a Platform for Modeling Tissue-Resident Macrophage Differentiation and Function Takata, K.| Kozaki, T.| Lee, C.Z.W.| Thion, M.S.| Otsuka, M.| Lim, S.| Utami, K.H.| Fidan, K.| Park, D.S.| Malleret, B.| Chakarov, S.| See, P.| Low, D.| Low, G.| Garcia-Miralles, M.| Zeng, R.| Zhang, J.| Goh, C.C.| Gul, A.| Hubert, S.| Lee, B.| Chen, J.| Low, I.| Shadan, N.B.| Lum, J.| Wei, T.S.| Mok, E.| Kawanishi, S.| Kitamura, Y.| Larbi, A.| Poidinger, M.| Renia, L.| Ng, L.G.| Wolf, Y.| Jung, S.| Önder, T.| Newell, E.| Huber, T.| Ashihara, E.| Garel, S.| Pouladi, M.A.| Ginhoux, F. 2017 Immunity
Plasma DNA methylation: A potential biomarker for stratification of liver fibrosis in non-alcoholic fatty liver disease Hardy, T.| Zeybel, M.| Day, C.P.| Dipper, C.| Masson, S.| McPherson, S.| Henderson, E.| Tiniakos, D.| White, S.| French, J.| Mann, D.A.| Anstee, Q.M.| Mann, J. 2017 Gut
Co-clinical assessment of tumor cellularity in pancreatic cancer Heid, I.| Steiger, K.| Trajkovic-Arsic, M.| Settles, M.| Eßwein, M.R.| Erkan, M.| Kleeff, J.| Jäger, C.| Friess, H.| Haller, B.| Steingötter, A.| Schmid, R.M.| Schwaiger, M.| Rummeny, E.J.| Esposito, I.| Siveke, J.T.| Braren, R.F. 2017 Clinical Cancer Research
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita Xue, S.| Maluenda, J.| Marguet, F.| Shboul, M.| Quevarec, L.| Bonnard, C.| Ng, A.Y.J.| Tohari, S.| Tan, T.T.| Kong, M.K.| Monaghan, K.G.| Cho, M.T.| Siskind, C.E.| Sampson, J.B.| Rocha, C.T.| Alkazaleh, F.| Gonzales, M.| Rigonnot, L.| Whalen, S.| Gut, M.| Gut, I.| Bucourt, M.| Venkatesh, B.| Laquerrière, A.| Reversade, B.| Melki, J. 2017 American Journal of Human Genetics
CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays Windpassinger, C.| Piard, J.| Bonnard, C.| Alfadhel, M.| Lim, S.| Bisteau, X.| Blouin, S.| Ali, N.B.| Ng, A.Y.J.| Lu, H.| Tohari, S.| Talib, S.Z.A.| van Hul, N.| Caldez, M.J.| Van Maldergem, L.| Yigit, G.| Kayserili, H.| Youssef, S.A.| Coppola, V.| de Bruin, A.| Tessarollo, L.| Choi, H.| Rupp, V.| Roetzer, K.| Roschger, P.| Klaushofer, K.| Altmüller, J.| Roy, S.| Venkatesh, B.| Ganger, R.| Grill, F.| Ben Chehida, F.| Wollnik, B.| Altunoglu, U.| Al Kaissi, A.| Reversade, B.| Kaldis, P. 2017 American Journal of Human Genetics
A potential non-invasive glioblastoma treatment: Nose-to-brain delivery of farnesylthiosalicylic acid incorporated hybrid nanoparticles Sekerdag, E.| Lüle, S.| Bozdağ Pehlivan, S.| Öztürk, N.| Kara, A.| Kaffashi, A.| Vural, I.| Işıkay, I.| Yavuz, B.| Oguz, K.K.| Söylemezoğlu, F.| Gürsoy-Özdemir, Y.| Mut, M. 2017 Journal of Controlled Release
Behçet Disease serum is immunoreactive to neurofilament medium which share common epitopes to bacterial HSP-65, a putative trigger Lule, S.| Colpak, A.I.| Balci-Peynircioglu, B.| Gursoy-Ozdemir, Y.| Peker, S.| Kalyoncu, U.| Can, A.| Tekin, N.| Demiralp, D.| Dalkara, T. 2017 Journal of Autoimmunity
Epigenetic Reprogramming of Lineage-Committed Human Mammary Epithelial Cells Requires DNMT3A and Loss of DOT1L Breindel, J.L.| Skibinski, A.| Sedic, M.| Wronski-Campos, A.| Zhou, W.| Keller, P.J.| Mills, J.| Bradner, J.| Onder, T.| Kuperwasser, C. 2017 Stem Cell Reports
Homozygous mutation in NUP107 leads to microcephaly with steroid-resistant nephrotic condition similar to Galloway-Mowat syndrome Rosti, R.O.| Sotak, B.N.| Bielas, S.L.| Bhat, G.| Silhavy, J.L.| Aslanger, A.D.| Altunoglu, U.| Bilge, I.| Tasdemir, M.| Yzaguirrem, A.D.| Musaev, D.| Infante, S.| Thuong, W.| Marin-Valencia, I.| Nelson, S.F.| Kayserili, H.| Gleeson, J.G. 2017 Journal of Medical Genetics
A Proof-of-Concept for Epigenetic Therapy of Tissue Fibrosis: Inhibition of Liver Fibrosis Progression by 3-Deazaneplanocin A Zeybel, M.| Luli, S.| Sabater, L.| Hardy, T.| Oakley, F.| Leslie, J.| Page, A.| Moran Salvador, E.| Sharkey, V.| Tsukamoto, H.| Chu, D.C.K.| Singh, U.S.| Ponzoni, M.| Perri, P.| Di Paolo, D.| Mendivil, E.J.| Mann, J.| Mann, D.A. 2017 Molecular Therapy
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Ivacaftor and symptoms of extra-oesophageal reflux in patients with cystic fibrosis and G551D mutation Zeybel, G.L.| Pearson, J.P.| Krishnan, A.| Bourke, S.J.| Doe, S.| Anderson, A.| Faruqi, S.| Morice, A.H.| Jones, R.| McDonnell, M.| Zeybel, M.| Dettmar, P.W.| Brodlie, M.| Ward, C. 2017 Journal of Cystic Fibrosis
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