المؤلفون: Phan Q. Duy, Pasko Rakic, Seth L. Alper, William E. Butler, Christopher A. Walsh, Nenad Sestan, Daniel H. Geschwind, Sheng Chih Jin, Kristopher T. Kahle

المصدر: Neuron

مصطلحات موضوعية: Neural Stem Cells, General Neuroscience, Humans, Article, Cerebral Ventricles, Hydrocephalus

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed910eeb950c19b28a52dfae2ba1125
https://pubmed.ncbi.nlm.nih.gov/34990576

المؤلفون: Jungmin Choi, Seth L. Alper, James R. Knight, Alejandro Berenstein, Edward R. Smith, Christopher Castaldi, Ava Hunt, Carol Nelson-Williams, Michael L. DiLuna, Erin Loring, Kaya Bilguvar, Brian P. Walcott, Jinwei Zhang, Michelle Sorscher, August A Allocco, Kristopher T. Kahle, Mark W. Youngblood, Andrew T. Timberlake, Shrikant Mane, Murat Gunel, Jennifer Klein, Beverly Aagaard-Kienitz, Sheng Chih Jin, Charles C. Matouk, Jason K. Karimy, Richard P. Lifton, Alan Dardik, Francesc López-Giráldez, Eric M. Jackson, Georges Rodesch, Shozeb Haider, Xue Zeng, Charuta G. Furey, Jonathan Gaillard, Mariya Soban, Qiongshi Lu, Daniel Duran, Sierra B Conine, Joseph M. Zabramski, Weilai Dong, Christopher J Stapleton, Darren B. Orbach, Miikka Vikkula, Bogdan Yatsula, Irina Tikhonova, Masaki Komiyama, Andrew F. Ducruet

المساهمون: UCL - SSS/DDUV - Institut de Duve

المصدر: Neuron, Vol. 101, no.3, p. 429-443.e4 (2019)

مصطلحات موضوعية: Male, 0301 basic medicine, Proband, Receptor, EphB4, de novo mutations, Penetrance, Biology, medicine.disease_cause, whole exome sequencing, 03 medical and health sciences, 0302 clinical medicine, medicine, arterio-venous malformation, Humans, Ephrin, EPHB4, Vein, Gene, Exome sequencing, ephrin signaling, Genetics, Mutation, Membrane Glycoproteins, General Neuroscience, Metalloendopeptidases, Chromatin Assembly and Disassembly, pediatric neurosurgery, Pedigree, Chromatin, Vein of Galen malformation, chromatin modifier, 030104 developmental biology, medicine.anatomical_structure, Vein of Galen Malformations, Female, Ephrins, 030217 neurology & neurosurgery, Signal Transduction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43bfdf39cfad06b34d8257745d494dce
https://doi.org/10.1016/j.neuron.2018.11.041

المؤلفون: Charles C. Duncan, Shreyas Panchagnula, Carol Nelson-Williams, Charuta G. Furey, Richard P. Lifton, Kaya Bilguvar, Prince Antwi, Jason K. Karimy, Francesc López-Giráldez, August A Allocco, Gregory G. Heuer, Bulent Guclu, Shrikant M. Mane, Murat Gunel, Jonathan Gaillard, Bermans J. Iskandar, Yasar Bayri, Erin Loring, Xue Zeng, Edward R. Smith, William E. Butler, Phillip B. Storm, James R. Knight, Seth L. Alper, Christopher Castaldi, Kristopher T. Kahle, Daniel Duran, Andrew T. Timberlake, David D. Limbrick, Eric M. Jackson, Shozeb Haider, Sheng Chih Jin, Michael L.J. Apuzzo, Jungmin Choi, James M. Johnston, Benjamin C. Warf, Robert D. Bjornson, Michael L. DiLuna, Qiongshi Lu, Arjun Khanna, Yener Sahin, Tyrone DeSpenza, Irina Tikhonova, Jennifer Strahle, M. Shahid Mansuri

المساهمون: Acibadem University Dspace

المصدر: Neuron

مصطلحات موضوعية: Male, 0301 basic medicine, Biology, Article, Cohort Studies, Pathogenesis, 03 medical and health sciences, Cerebrospinal fluid, Neural Stem Cells, Exome Sequencing, medicine, Humans, Exome, Exome sequencing, General Neuroscience, Neurogenesis, Neural tube, medicine.disease, Neural stem cell, Pedigree, Patched-1 Receptor, 030104 developmental biology, medicine.anatomical_structure, PTCH1, Aqueductal stenosis, Mutation, Cancer research, Female, Hydrocephalus, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::184d068607110d72d9b261377af3d13e
https://doi.org/10.1016/j.neuron.2018.06.019