Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Bahareh Haddad"'
Autor:
Bahareh Haddad Derafshi, Tamas Danko, Soham Chanda, Pedro J. Batista, Ulrike Litzenburger, Qian Yi Lee, Yi Han Ng, Anu Sebin, Howard Y. Chang, Thomas C. Südhof, Marius Wernig
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-28 (2022)
Abstract The chromodomain helicase DNA-binding protein CHD8 is the most frequently mutated gene in autism spectrum disorder. Despite its prominent disease involvement, little is known about its molecular function in the human brain. CHD8 is a chromat
Externí odkaz:
https://doaj.org/article/f6144c8eb12747dd9d2726213f094bb0
Akademický článek
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Autor:
Pedro J. Batista, Bahareh Haddad Derafshi, Tamas Danko, Marius Wernig, Thomas C. Südhof, Yi Han Ng, Ulrike Litzenburger, Anu Sebin, Soham Chanda, Howard Y. Chang, Qian Yi Lee
Publikováno v:
Scientific Reports. 12
The chromodomain helicase DNA-binding protein CHD8 is among the most frequently found de-novo mutations in autism (1–3). Unlike most other autism-risk genes, CHD8 mutations appear to be fully penetrant (4). Despite its prominent disease involvement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::703eeb418f2cef61d6ebc2d0c8772255
https://doi.org/10.1038/s41598-022-23614-x
https://doi.org/10.1038/s41598-022-23614-x
Autor:
Bahareh Haddad, Alex Rialdi, Ernesto Guccione, Jessica Sook Yuin Ho, Kimaada Allette, Natasha Moshkina, Minji Byun, Jian Jin, Adolfo García-Sastre, Sweta Ravisankar, Nevan J. Krogan, Randy A. Albrecht, Dalila Pinto, Rab K. Prinjha, Terrence M. Tumpey, Vittorio Sebastiano, Nacho Mena, Judd F. Hultquist, Alexander Tarakhovsky, Massimo Squatrito, Vyacheslav Yurchenko, Nan Zhao, Diana Low, Juan Ayllon, Ivan Marazzi, Yixuan Ma, Melissa Smith, Romain Fenouil, David Jimenez-Morales, Harm van Bakel, Benjamin Greenbaum, Maria Teresa Sánchez-Aparicio, Robert Sebra
Publikováno v:
Nature Structural & Molecular Biology. 25:885-893
Viral infection perturbs host cells and can be used to uncover regulatory mechanisms controlling cellular responses and susceptibility to infections. Using cell biological, biochemical, and genetic tools, we reveal that influenza A virus (IAV) infect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::052ce431bd6d3be6be6fe4aecf25355c
https://doi.org/10.1038/s41594-018-0124-7
https://doi.org/10.1038/s41594-018-0124-7
Autor:
Donna M. Bouley, Howard Y. Chang, Bahareh Haddad, Ryan A. Flynn, Pedro J. Batista, Kaveh Daneshvar, Jiajing Zhang, Lingjie Li, Ava C. Carter, Alan C. Mullen, Benoit Molinie, Yi Xing, Jinkai Wang, Cosmas Giallourakis, Kok-Seong Lim, Marius Wernig, Ernesto Lujan, Kun Qu, Chan Zhou, Peter C. Dedon
Publikováno v:
Cell Stem Cell. 15(6):707-719
Summary N6-methyl-adenosine (m 6 A) is the most abundant modification on messenger RNAs and is linked to human diseases, but its functions in mammalian development are poorly understood. Here we reveal the evolutionary conservation and function of m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::996df755895b2d27da239c75443fa52d
Autor:
Vittorio, Sebastiano, Hanson Hui, Zhen, Bahareh, Haddad, Bahareh Haddad, Derafshi, Elizaveta, Bashkirova, Sandra P, Melo, Pei, Wang, Thomas L, Leung, Zurab, Siprashvili, Andrea, Tichy, Jiang, Li, Mohammed, Ameen, John, Hawkins, Susie, Lee, Lingjie, Li, Aaron, Schwertschkow, Gerhard, Bauer, Leszek, Lisowski, Mark A, Kay, Seung K, Kim, Alfred T, Lane, Marius, Wernig, Anthony E, Oro
Publikováno v:
Science Translational Medicine. 6
Patients with recessive dystrophic epidermolysis bullosa (RDEB) lack functional type VII collagen owing to mutations in the gene COL7A1 and suffer severe blistering and chronic wounds that ultimately lead to infection and development of lethal squamo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::164b5a830e2ae0bb7e90a0ee2ad68ee2
https://doi.org/10.1126/scitranslmed.3009540
https://doi.org/10.1126/scitranslmed.3009540
Autor:
Sandra P. Melo, Hanson H. Zhen, Alfred T. Lane, Mohamed Ameen, Gerhard Bauer, Jiang Li, Pei Wang, T. L. Leung, Vittorio Sebastiano, Anthony E. Oro, Mark A. Kay, Bahareh Haddad, Aaron H. Schwertschkow, John S. Hawkins, Marius Wernig, Lingjie Li, Leszek Lisowski, Zurab Siprashvili, Seung K. Kim, S. Lee, Elizaveta Bashkirova, Andrea L. Tichy
Publikováno v:
Science Translational Medicine. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::179bf0114fa1863c867aae08c60cb351
https://doi.org/10.1126/scitranslmed.aaa4871
https://doi.org/10.1126/scitranslmed.aaa4871
Autor:
J. Keith Joung, Steven E. Artandi, Luis F.Z. Batista, Morgan L. Maeder, Cyd Khayter, Mathew J. Goodwin, John S. Hawkins, Cherie L. Ramirez, James Angstman, Vittorio Sebastiano, Marius Wernig, Bahareh Haddad, Dana T. Yeo
The combination of induced pluripotent stem cell (iPSC) technology and targeted gene modification by homologous recombination (HR) represents a promising new approach to generate genetically corrected, patient-derived cells that could be used for aut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74ef4dd09eb0f4e135c4a785929ac677
https://europepmc.org/articles/PMC3285772/
https://europepmc.org/articles/PMC3285772/
Akademický článek
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