Resultados da pesquisa - Gunel, Murat

SomatiCA: Identifying, Characterizing and Quantifying Somatic Copy Number Aberrations from Cancer Genome Sequencing Data Por Chen, Mengjie, Gunel, Murat, Zhao, Hongyu

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Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration Por Louvi, Angeliki, Nishimura, Sayoko, Günel, Murat

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Extraction of Fronto-orbital Shower Hook through Transcranial Orbitotomy Por Elia, Maxwell D., Gunel, Murat, Servat, Juan J., Levin, Flora

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Complications from cervical intra‐arterial heroin injection Por DiLuna, Michael L, Bydon, Mohamad, Gunel, Murat, Johnson, Michele H

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Complications from cervical intra-arterial heroin injection Por DiLuna, Michael L, Bydon, Mohamad, Gunel, Murat, Johnson, Michele H

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Apoptotic functions of PDCD10, the gene mutated in Cerebral Cavernous Malformation 3 Por Chen, Leiling, Tanriover, Gamze, Yano, Hiroko, Friedlander, Robert, Louvi, Angeliki, Gunel, Murat

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Functional Synergy between Cholecystokinin Receptors CCKAR and CCKBR in Mammalian Brain Development Por Nishimura, Sayoko, Bilgüvar, Kaya, Ishigame, Keiko, Sestan, Nenad, Günel, Murat, Louvi, Angeliki

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Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathology Por Louvi, Angeliki, Chen, Leiling, Two, Aimee M., Zhang, Haifeng, Min, Wang, Günel, Murat

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A Quantitative Assessment of Pre-Operative MRI Reports in Glioma Patients: Report Metrics and IDH Prediction Ability Por Cao, Hang, Erson-Omay, E. Zeynep, Günel, Murat, Moliterno, Jennifer, Fulbright, Robert K.

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Cerebral cavernous malformation gene CCM3 is critical for vascular development by regulating VEGFR2 signaling Por He, Yun, Zhang, Haifeng, Yu, Luyang, Gunel, Murat, Boggon, Titus J., Chen, Hong, Min, Wang

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The AHNAKs are a class of giant propeller-like proteins that associate with calcium channel proteins of cardiomyocytes and other cells Por Komuro, Akihiko, Masuda, Yutaka, Kobayashi, Koichi, Babbitt, Roger, Gunel, Murat, Flavell, Richard A., Marchesi, Vincent T.

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Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion Por Emre Onat, Onur, Gulsuner, Suleyman, Bilguvar, Kaya, Nazli Basak, Ayse, Topaloglu, Haluk, Tan, Meliha, Tan, Uner, Gunel, Murat, Ozcelik, Tayfun

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Combined HMG-COA reductase and prenylation inhibition in treatment of CCM Por Nishimura, Sayoko, Mishra-Gorur, Ketu, Park, JinSeok, Surovtseva, Yulia V., Sebti, Said M., Levchenko, Andre, Louvi, Angeliki, Gunel, Murat

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KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein Por Gunel, Murat, Laurans, Maxwell S. H., Shin, Dana, DiLuna, Michael L., Voorhees, Jennifer, Choate, Keith, Nelson-Williams, Carol, Lifton, Richard P.

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A congenital disorder of deglycosylation: Biochemical characterization of N-glycanase 1 deficiency in patient fibroblasts Por He, Ping, Grotzke, Jeff E, Ng, Bobby G, Gunel, Murat, Jafar-Nejad, Hamed, Cresswell, Peter, Enns, Gregory M, Freeze, Hudson H

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COL4A1 Mutation in Preterm Intraventricular Hemorrhage Por Bilguvar, Kaya, DiLuna, Michael L., Bizzarro, Matthew J., Bayri, Yasar, Schneider, Karen C., Lifton, Richard P., Gunel, Murat, Ment, Laura R.

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9p24 triplication in syndromic hydrocephalus with diffuse villous hyperplasia of the choroid plexus Por Furey, Charuta, Antwi, Prince, Duran, Daniel, Timberlake, Andrew T., Nelson-Williams, Carol, Matouk, Charles C., DiLuna, Michael L., Günel, Murat, Kahle, Kristopher T.

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Recurrent Recessive Mutation in DGUOK Causes Idiopathic Non-Cirrhotic Portal Hypertension Por Vilarinho, Sílvia, Sari, Sinan, Yilmaz, Güldal, Stiegler, Amy L., Boggon, Titus J., Jain, Dhanpat, Akyol, Gulen, Dalgic, Buket, Günel, Murat, Lifton, Richard P.

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Exome Analysis of the Evolutionary Path of Hepatocellular Adenoma-Carcinoma Transition, Vascular Invasion and Brain Dissemination Por Vilarinho, Sílvia, Erson-Omay, Zeynep, Mitchell-Richards, Kisha, Cha, Charles, Nelson-Williams, Carol, Harmancı, Akdes Serin, Yasuno, Katsuhito, Günel, Murat, Taddei, Tamar H.

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NCOG-50. CLINICAL AND GENOMIC FACTORS ASSOCIATED WITH SEIZURES IN MENINGIOMAS Por Gupte, Trisha, Jin, Lan, Li, Chang, Yalcin, Kanat, Youngblood, Mark, Miyagishima, Danielle, Mishra, Ketu, Fulbright, Robert, Erson-omay, Zeynep, Gunel, Murat, Moliterno, Jennifer

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