SomatiCA: Identifying, Characterizing and Quantifying Somatic Copy Number Aberrations from Cancer Genome Sequencing Data

le Chen, Mengjie, Gunel, Murat, Zhao, Hongyu
Foilsithe 2013

Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration

le Louvi, Angeliki, Nishimura, Sayoko, Günel, Murat
Foilsithe 2014

Extraction of Fronto-orbital Shower Hook through Transcranial Orbitotomy

le Elia, Maxwell D., Gunel, Murat, Servat, Juan J., Levin, Flora
Foilsithe 2014

Complications from cervical intra‐arterial heroin injection

le DiLuna, Michael L, Bydon, Mohamad, Gunel, Murat, Johnson, Michele H
Foilsithe 2007

Complications from cervical intra-arterial heroin injection

le DiLuna, Michael L, Bydon, Mohamad, Gunel, Murat, Johnson, Michele H
Foilsithe 2009

Apoptotic functions of PDCD10, the gene mutated in Cerebral Cavernous Malformation 3

le Chen, Leiling, Tanriover, Gamze, Yano, Hiroko, Friedlander, Robert, Louvi, Angeliki, Gunel, Murat
Foilsithe 2009

Functional Synergy between Cholecystokinin Receptors CCKAR and CCKBR in Mammalian Brain Development

le Nishimura, Sayoko, Bilgüvar, Kaya, Ishigame, Keiko, Sestan, Nenad, Günel, Murat, Louvi, Angeliki
Foilsithe in PLoS One (2015)

Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathology

le Louvi, Angeliki, Chen, Leiling, Two, Aimee M., Zhang, Haifeng, Min, Wang, Günel, Murat
Foilsithe 2011

A Quantitative Assessment of Pre-Operative MRI Reports in Glioma Patients: Report Metrics and IDH Prediction Ability

le Cao, Hang, Erson-Omay, E. Zeynep, Günel, Murat, Moliterno, Jennifer, Fulbright, Robert K.
Foilsithe in Front Oncol (2021)

The AHNAKs are a class of giant propeller-like proteins that associate with calcium channel proteins of cardiomyocytes and other cells

le Komuro, Akihiko, Masuda, Yutaka, Kobayashi, Koichi, Babbitt, Roger, Gunel, Murat, Flavell, Richard A., Marchesi, Vincent T.
Foilsithe 2004

Cerebral cavernous malformation gene CCM3 is critical for vascular development by regulating VEGFR2 signaling

le He, Yun, Zhang, Haifeng, Yu, Luyang, Gunel, Murat, Boggon, Titus J., Chen, Hong, Min, Wang
Foilsithe 2010

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

le Emre Onat, Onur, Gulsuner, Suleyman, Bilguvar, Kaya, Nazli Basak, Ayse, Topaloglu, Haluk, Tan, Meliha, Tan, Uner, Gunel, Murat, Ozcelik, Tayfun
Foilsithe 2013

Combined HMG-COA reductase and prenylation inhibition in treatment of CCM

le Nishimura, Sayoko, Mishra-Gorur, Ketu, Park, JinSeok, Surovtseva, Yulia V., Sebti, Said M., Levchenko, Andre, Louvi, Angeliki, Gunel, Murat
Foilsithe in Proc Natl Acad Sci U S A (2017)

KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein

le Gunel, Murat, Laurans, Maxwell S. H., Shin, Dana, DiLuna, Michael L., Voorhees, Jennifer, Choate, Keith, Nelson-Williams, Carol, Lifton, Richard P.
Foilsithe 2002

A congenital disorder of deglycosylation: Biochemical characterization of N-glycanase 1 deficiency in patient fibroblasts

le He, Ping, Grotzke, Jeff E, Ng, Bobby G, Gunel, Murat, Jafar-Nejad, Hamed, Cresswell, Peter, Enns, Gregory M, Freeze, Hudson H
Foilsithe in Glycobiology (2015)

COL4A1 Mutation in Preterm Intraventricular Hemorrhage

le Bilguvar, Kaya, DiLuna, Michael L., Bizzarro, Matthew J., Bayri, Yasar, Schneider, Karen C., Lifton, Richard P., Gunel, Murat, Ment, Laura R.
Foilsithe 2009

Augmentor α and β (FAM150) are ligands of the receptor tyrosine kinases ALK and LTK: Hierarchy and specificity of ligand–receptor interactions

le Reshetnyak, Andrey V., Murray, Phillip B., Shi, Xiarong, Mo, Elizabeth S., Mohanty, Jyotidarsini, Tome, Francisco, Bai, Hanwen, Gunel, Murat, Lax, Irit, Schlessinger, Joseph
Foilsithe in Proc Natl Acad Sci U S A (2015)

9p24 triplication in syndromic hydrocephalus with diffuse villous hyperplasia of the choroid plexus

le Furey, Charuta, Antwi, Prince, Duran, Daniel, Timberlake, Andrew T., Nelson-Williams, Carol, Matouk, Charles C., DiLuna, Michael L., Günel, Murat, Kahle, Kristopher T.
Foilsithe in Cold Spring Harb Mol Case Stud (2018)

Recurrent Recessive Mutation in DGUOK Causes Idiopathic Non-Cirrhotic Portal Hypertension

le Vilarinho, Sílvia, Sari, Sinan, Yilmaz, Güldal, Stiegler, Amy L., Boggon, Titus J., Jain, Dhanpat, Akyol, Gulen, Dalgic, Buket, Günel, Murat, Lifton, Richard P.
Foilsithe in Hepatology (2016)

Exome Analysis of the Evolutionary Path of Hepatocellular Adenoma-Carcinoma Transition, Vascular Invasion and Brain Dissemination

le Vilarinho, Sílvia, Erson-Omay, Zeynep, Mitchell-Richards, Kisha, Cha, Charles, Nelson-Williams, Carol, Harmancı, Akdes Serin, Yasuno, Katsuhito, Günel, Murat, Taddei, Tamar H.
Foilsithe in J Hepatol (2017)