Researcher
Daniel Duran
University of Mississippi Medical Center
Statistics
27 papers found
All papers authored by Daniel Duran
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Kedous Y. Mekbib ,
Martijn A. van der Ent,
Garrett Allington ,
Andrew Prendergast,
Jocelyn E. Chau ,
Hannah Smith,
John Shohfi,
Jack Ocken,
Daniel Duran ,
Charuta G. Furey,
Le Thi Hao,
Phan Q. Duy,
Benjamin C. Reeves ,
Junhui Zhang
and 51 other authors
Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations
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Danielle F. Miyagishima,
Lan Jin,
Trisha Gupte,
Chang Li,
Daniel Duran ,
Julio D. Montejo,
Amy Zhao,
Amar Sheth,
Evgeniya Tyrtova,
Koray Özduman,
Francesco Iacoangeli,
Matthieu Peyre,
Julien Boetto,
Matthew Pease
and 10 other authors
Associations of Meningioma Molecular Subgroup and Tumor Recurrence
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Mohammad Iqbal H. Bhuiyan ,
Ting Zhang,
Jason K. Karimy,
Zhijuan Wu ,
Victoria M. Fiesler,
Jingfang Zhang,
Huachen Huang,
Md Nabiul Hasan,
Anna E. Skrzypiec,
Mariusz Mucha,
Daniel Duran ,
Wei Huang,
Robert Pawlak,
Lesley M. Foley
and 9 other authors
Modulation of brain cation-Cl− cotransport via the SPAK kinase inhibitor ZT-1a
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Julio D. Montejo,
Chang Li,
Sacit Bulent Omay,
Koray Özduman,
Amar H. Sheth,
Amy Y. Zhao,
Evgeniya Tyrtova,
Danielle F. Miyagishima,
Elena I. Fomchenko,
Christopher S. Hong,
Victoria E. Clark,
Maximilien Riche,
Matthieu Peyre
and 26 other authors
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Xue Zeng,
Sheng Chih Jin,
Jungmin Choi,
Carol Nelson-Williams,
Bogdan Yatsula,
Jonathan Gaillard,
Charuta Gavankar Furey,
Qiongshi Lu,
Andrew T. Timberlake,
Weilai Dong,
Michelle A. Sorscher,
Erin Loring,
Jennifer Klein,
August Allocco
and 32 other authors
Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation
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Shreyas Panchagnula,
August Allocco,
Jason K. Karimy,
Arjun Khanna,
Jonathan R. Gaillard,
Tyrone DeSpenza
and 30 other authors
De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus
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Sheng Chih Jin,
Weilai Dong,
E. Zeynep Erson-Omay,
Prince Antwi,
August Allocco,
Jonathan R. Gaillard,
Anita Huttner,
Murat Gunel,
Michael L. DiLuna,
Kristopher T. Kahle
De novo MYH9 mutation in congenital scalp hemangioma
Download from molecularcasestudies.cshlp.org
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Andrew T. Timberlake,
Carol Nelson-Williams,
Charles C. Matouk,
Michael L. DiLuna,
Murat Günel,
Kristopher T. Kahle
9p24 triplication in syndromic hydrocephalus with diffuse villous hyperplasia of the choroid plexus
Download from molecularcasestudies.cshlp.org
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Philipp Karschnia,
Jonathan R. Gaillard,
Jason K. Karimy,
Mark W. Youngblood,
Michael L. DiLuna,
Charles C. Matouk,
Beverly Aagaard-Kienitz,
Edward R. Smith,
Darren B. Orbach,
Georges Rodesch,
Alejandro Berenstein,
Murat Gunel,
Kristopher T. Kahle
Human genetics and molecular mechanisms of vein of Galen malformation
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Robert D. Messina,
Lauren A. Beslow,
Julio D. Montejo,
Jason K. Karimy,
Charuta Gavankar Furey,
Alison D. Sheridan,
Gordon Sze,
Yanki Yarman,
Michael L. DiLuna,
Kristopher T. Kahle
Malignant Cerebellar Edema Subsequent to Accidental Prescription Opioid Intoxication in Children
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Jesse A. Stokum,
Charuta Gavankar Furey,
Xu Zhou ,
M. Shahid Mansuri,
Julio Montejo,
Alberto Vera,
Michael L. DiLuna,
Eric Delpire,
Seth L. Alper,
Murat Gunel
and 4 other authors
Download from ore.exeter.ac.uk
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Richard A. Young ,
Youngblood Mw,
Victoria E. Clark,
Clark Ve,
Süleyman Coşkun,
Octavian Henegariu,
E. Zeynep Erson-Omay,
Daniel Duran ,
Leon D. Kaulen,
Tong Ihn Lee
and 20 other authors
Integrated genomic analyses of de novo pathways underlying atypical meningiomas
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