Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mehmet Bakırcıoğlu"'
Autor:
Victoria E. Clark, Murat Gunel, Jie Li, Ketu Mishra-Gorur, Geneive Carrión-Grant, Caner Çağlar, Mehmet Bakırcıoğlu, S. Bulent Omay, Koray Özduman, Akdes Serin Harmanci, Octavian Henegariu, E. Zeynep Erson-Omay, Lisa M. DeAngelis, Alexander O. Vortmeyer, Jennifer Moliterno, M. Necmettin Pamir, Joachim M. Baehring, Katsuhito Yasuno, Viviane Tabar, Mark W. Youngblood, Kaya Bilguvar
Publikováno v:
Genome Medicine
Background Glioblastoma multiforme (GBM) constitutes nearly half of all malignant brain tumors and has a median survival of 15 months. The standard treatment for these lesions includes maximal resection, radiotherapy, and chemotherapy; however, indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e2c6b217ede8f845ad7f24eb06c50a1
https://doi.org/10.1186/s13073-017-0401-9
https://doi.org/10.1186/s13073-017-0401-9
Autor:
Ketu Mishra-Gorur, S. Bulent Omay, Kaya Bilguvar, Alexander O. Vortmeyer, Akdes Serin Harmanci, Süleyman Coşkun, Jia Sun, Tanyeri Barak, Mehmet Bakırcıoğlu, Ahmet Okay Caglayan, Victoria E. Clark, Koray Özduman, Jie Li, M. Necmettin Pamir, Nikolaus Schultz, Anita Huttner, Nils Weinhold, Jennifer Moliterno Günel, Murat Gunel, Doğan Köse, Chris Sander, Katsuhito Yasuno, Yavuz Köksal, Burçin Baran, Jacob F Baranoski, E. Zeynep Erson-Omay, Caner Çağlar, Geneive Carrión-Grant
WOS: 000364783100007
PubMed: 25740784
Background. Malignant high-grade gliomas (HGGs), including the most aggressive form, glioblastoma multiforme, show significant clinical and genomic heterogeneity. Despite recent advances, the overall su
PubMed: 25740784
Background. Malignant high-grade gliomas (HGGs), including the most aggressive form, glioblastoma multiforme, show significant clinical and genomic heterogeneity. Despite recent advances, the overall su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d90624c511df9741dd5e005f8378622
https://avesis.deu.edu.tr/publication/details/52a7b7d2-6625-4e5c-94be-fd818db55416/oai
https://avesis.deu.edu.tr/publication/details/52a7b7d2-6625-4e5c-94be-fd818db55416/oai
Autor:
Wengi Han, Katsuhito Yasuno, Bulent Guclu, Ahmet Okay Caglayan, Murat Gunel, Barış Ekici, Phillip B. Murray, Beyhan Tüysüz, Yildirim Bayezit Sakalar, Hüseyin Çaksen, Hande Kaymakçalan, Senem Senturk, Mehmet Bakırcıoğlu, Nihat Demir, Kaya Bilguvar, Fesih Aktar, Ebru Guzel, Caner Çağlar, Oğuz Tuncer, Gozde Tugce Akgumus, Jacob F Baranoski, Nenad Sestan, Frank J. Minja, Berrin Aktekin, Aslan Guzel, Emine Z. Erson-Omay
BACKGROUND: Knobloch syndrome is a rare, autosomal recessive, developmental disorder characterized by stereotyped ocular abnormalities with or without occipital skull deformities (encephalocele, bone defects, and cutis aplasia). Although there is cle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f42d739dc56740eec78aa9cc986cd9c7
https://avesis.yyu.edu.tr/publication/details/37458afa-fdb6-45fd-b7ce-00b11a385eec/oai
https://avesis.yyu.edu.tr/publication/details/37458afa-fdb6-45fd-b7ce-00b11a385eec/oai
Autor:
Justin Cotney, M. Necmettin Pamir, Koray Özduman, Ahmet Okay Caglayan, Emre Ceyhun, Saliha Yilmaz, Leman Sencar, Eric C. Holland, Ryan Hebert, Geneive Carrión-Grant, Joseph M. Piepmeier, Yasar Bayri, Timucin Avsar, Ketu Mishra-Gorur, Jun Yin, Katsuhito Yasuno, Octavian Henegariu, Hanwen Bai, Jennifer Moliterno Günel, Joachim M. Baehring, Alexander O. Vortmeyer, Richard P. Lifton, Murat Gunel, Cameron Brennan, Victoria E. Clark, Matthew W. State, E. Zeynep Erson-Omay, Philip H. Gutin, Turker Kilic, Akdes Serin, Phillip B. Murray, Mehmet Bakırcıoğlu, S. Bulent Omay, Luis Kolb, Murim Choi, Baran Yılmaz, Bahattin Tanrıkulu, Jie Li, Shrikant Mane, John D. Overton, A. Fatih Atik, Hande Kaymakçalan, Kaya Bilguvar, James P. Noonan, Conor Grady
Publikováno v:
Science (New York, N.Y.), vol 339, iss 6123
Genetic Clues to Meningioma Meningiomas are the most common primary brain tumors in adults. Located within the layer of tissue covering the brain, these tumors are usually slow-growing and benign but can cause serious neurological complications. Abou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb0512ffe0748ecd16da8398274612f
https://hdl.handle.net/11424/244002
https://hdl.handle.net/11424/244002
Autor:
Kaya Bilguvar, Angeliki Louvi, Mehmet Bakırcıoğlu, Navneet K. Tyagi, Titus J. Boggon, Cigdem Ozkara, Michele H. Johnson, Ahmet Okay Caglayan, Arthur L. Horwich, Beyhan Tüysüz, Sreeganga S. Chandra, Richard P. Lifton, Ozdem Erturk, Shrikant Mane, Murat Karacorlu, Murat Gunel, Murim Choi, Alp Dinçer, Sakir Delil, Cengiz Yalcinkaya, Jacob F Baranoski
Ubiquitin C-terminal hydrolase-L1 (UCHL1), a neuron-specific de-ubiquitinating enzyme, is one of the most abundant proteins in the brain. We describe three siblings from a consanguineous union with a previously unreported early-onset progressive neur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6eab6e601551bd6f6cc8abd4ba623a2
https://doi.org/10.1073/pnas.1222732110
https://doi.org/10.1073/pnas.1222732110
Autor:
Eamonn Sheridan, Kaya Bilguvar, Murat Gunel, Susan Lindsay, James J. Cox, Saghira Malik, Ofélia P. Carvalho, Okay Caglayan, Caroline Gannon, Mehmet Bakırcıoğlu, Moira Crosier, Fanni Gergely, Alp Dinçer, Oliver Quarrell, C. Geoffrey Woods, G. Karbani, Saliha Yilmaz, Tanyeri Barak, Maryam Khurshid, Kelly Springell, Adeline K Nicholas, Steven Lisgo, Beyhan Tüysüz
We investigated three families whose offspring had extreme microcephaly at birth and profound mental retardation. Brain scans and postmortem data showed that affected individuals had brains less than 10\% of expected size (T (p.Ala29GlnfsX114) in a T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d6bdebf5cfd99f5ce124be258854baf
https://avesis.deu.edu.tr/publication/details/901aa39d-074e-4ffe-a6b9-657bee28d36e/oai
https://avesis.deu.edu.tr/publication/details/901aa39d-074e-4ffe-a6b9-657bee28d36e/oai
Autor:
Boris Krischek, Yusuke Nakamura, Shrikant Mane, Ynte M. Ruigrok, Juha Hernesniemi, Emilia I. Gaal, Siew-Kee Low, Aarno Palotie, François Cambien, Dietmar Krex, Gabriel J.E. Rinkel, Matthias Simon, Ali K. Ozturk, Georg Auburger, Philippe Bijlenga, Hitoshi Zembutsu, Richard P. Lifton, Ituro Inoue, Katsuhito Yasuno, Akira Hata, Kaya Bilguvar, Juha E. Jääskeläinen, Karl Lothard Schaller, Helmuth Steinmetz, Hidetoshi Kasuya, Mika Niemelä, Mehmet Bakırcıoğlu, Murat Gunel
Publikováno v:
Proceedings of the National Academy of Sciences, Vol. 108, No 49 (2011) pp. 19707-19712
The pathogenesis of intracranial aneurysm (IA) formation and rupture is complex, with significant contribution from genetic factors. We previously reported genome-wide association studies based on European discovery and Japanese replication cohorts o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0083e8132e33a3bcb74675ac6535dad
https://archive-ouverte.unige.ch/unige:78039
https://archive-ouverte.unige.ch/unige:78039
Autor:
Tanyeri Barak, Richard P. Lifton, Ying Zhu, Alp Dinçer, Hande Kaymakçalan, Ali K. Ozturk, Ergin Atalar, Katja Doerschner, Kaya Bilguvar, Murat Gunel, Cengiz Yalcinkaya, Tayfun Ozcelik, Katsuhito Yasuno, Shrikant Mane, Mehmet Bakırcıoğlu, Huseyin Boyaci, Nenad Sestan, Angeliki Louvi, Richard A. Bronen, Ahmet Okay Caglayan, Murim Choi, Kenneth Y. Kwan, Veysi Demirbilek, Beyhan Tüysüz, Serap Saygi, Saliha Yilmaz, William J Brunken
Publikováno v:
Nature Genetics
Cataloged from PDF version of article. The biological basis for regional and inter-species differences in cerebral cortical morphology is poorly understood. We focused on consanguineous Turkish families with a single affected member with complex bila
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b195428b17fbe90cfd02096177d9995
https://hdl.handle.net/11693/21906
https://hdl.handle.net/11693/21906
Autor:
Tanyeri Barak, Ying Zhu, Mehmet Bakırcıoğlu, Shrikant Mane, Richard P. Lifton, Hüseyin Per, Mehmet Necmettin Pamir, Nenad Sestan, Sarenur Gökben, Murat Gunel, Winson S. Ho, Sefer Kumandaş, Katsuhito Yasuno, Ali K. Ozturk, Matthew W. State, Dilek Yalnizoglu, Sanem Yilmaz, Michele H. Johnson, Beyhan Tüysüz, Angeliki Louvi, Richard A. Bronen, Stephen Sanders, Ahmet Okay Caglayan, Cengiz Yalcinkaya, Murim Choi, Burak Tatlı, Meral Topçu, Hande Kaymakçalan, Kenneth Y. Kwan, Meral Özmen, Kaya Bilguvar, Alp Dinçer, Naci Kocer
Publikováno v:
Nature, vol 467, iss 7312
WOS: 000281616300034
PubMed ID: 20729831
The development of the human cerebral cortex is an orchestrated process involving the generation of neural progenitors in the periventricular germinal zones, cell proliferation characterized by symme
PubMed ID: 20729831
The development of the human cerebral cortex is an orchestrated process involving the generation of neural progenitors in the periventricular germinal zones, cell proliferation characterized by symme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4462755dd94fefa4008ed2b337258a4
https://avesis.deu.edu.tr/publication/details/b46afe24-0a93-4e5e-9690-6ba68814d1ad/oai
https://avesis.deu.edu.tr/publication/details/b46afe24-0a93-4e5e-9690-6ba68814d1ad/oai