Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Joelle El Hajjar"'
Autor:
Nadeem Murtaza, Annie A. Cheng, Chad O. Brown, Durga Praveen Meka, Shuai Hong, Jarryll A. Uy, Joelle El-Hajjar, Neta Pipko, Brianna K. Unda, Birgit Schwanke, Sansi Xing, Bhooma Thiruvahindrapuram, Worrawat Engchuan, Brett Trost, Eric Deneault, Froylan Calderon de Anda, Bradley W. Doble, James Ellis, Evdokia Anagnostou, Gary D. Bader, Stephen W. Scherer, Yu Lu, Karun K. Singh
Publikováno v:
Cell reports. 41(8)
There are hundreds of risk genes associated with autism spectrum disorder (ASD), but signaling networks at the protein level remain unexplored. We use neuron-specific proximity-labeling proteomics (BioID2) to identify protein-protein interaction (PPI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08648b7654c1d3d609e43931091d58ee
https://pubmed.ncbi.nlm.nih.gov/36417873
https://pubmed.ncbi.nlm.nih.gov/36417873
Autor:
Nadeem Murtaza, Annie A. Cheng, Chad O. Brown, Durga Praveen Meka, Shuai Hong, Jarryll A. Uy, Joelle El-Hajjar, Neta Pipko, Brianna K. Unda, Birgit Schwanke, Sansi Xing, Bhooma Thiruvahindrapuram, Worrawat Engchuan, Brett Trost, Eric Deneault, Froylan Calderon de Anda, Bradley W. Doble, James Ellis, Evdokia Anagnostou, Gary D. Bader, Stephen W. Scherer, Yu Lu, Karun K. Singh
Manuscript summaryThere are hundreds of risk genes associated with autism spectrum disorder (ASD), but signaling networks at the protein level remain unexplored. We use neuron-specific proximity-labeling proteomics (BioID) to identify protein-protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0314bce6a113bb81a7d66ef76e3b58f0
https://doi.org/10.1101/2022.01.17.476220
https://doi.org/10.1101/2022.01.17.476220
Autor:
Alina Piekna, Michael W. Salter, Eric Deneault, Stephen W. Scherer, Peter Pasceri, Wei Wei, Tadeo Thompson, James Ellis, P. Joel Ross, Fraser P. McCready, Deivid C. Rodrigues, Kirill Zaslavsky, Wen-Bo Zhang, Melody Zhao, Joelle El Hajjar, Caitlin Loo, Zhuozhi Wang, Marat Mufteev, Shahryar Khattak, Asli Romm
Publikováno v:
Nature neuroscience
Heterozygous loss-of-function mutations in SHANK2 are associated with autism spectrum disorder (ASD). We generated cortical neurons from induced pluripotent stem cells (iPSC) derived from neurotypic and ASD-affected donors. We developed Sparse cocult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f0776292618444005f36b2530015f2e
https://doi.org/10.1038/s41593-019-0365-8
https://doi.org/10.1038/s41593-019-0365-8