Rezultati pretrage - Shereen G. Ghosh
- Prikaz rezultata 1 – 4 od 4
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1
Pathogenic ARH3 mutations result in ADP-ribose chromatin scars during DNA strand break repair od Hana Hanzlíková, Evgeniia Prokhorova, Kateřina Krejčíková, Zuzana Cihlářová, Ilona Kalasová, Jan Kubovčiak, Jana Šáchová, Richard Hailstone, Jan Bražina, Shereen G. Ghosh, Sebahattin Çırak, Joseph G. Gleeson, Ivan Ahel, Keith W. Caldecott
Izdano 2020Artigo -
2
Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly od Lu Wang, Zhen Li, David Sievert, Desirée E.C. Smith, Marisa I. Mendes, Dillon Y. Chen, Valentina Stanley, Shereen G. Ghosh, Yulu Wang, Majdi Kara, Ayça Dilruba Aslanger, Rasim Özgür Rosti, Henry Houlden, Gajja S. Salomons, Joseph G. Gleeson
Izdano 2020Artigo -
3
Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism od Wendy Wenderski, Lu Wang, A. Krokhotin, Jessica J. Walsh, Hongjie Li, Hirotaka Shoji, Shereen G. Ghosh, Renee D. George, Erik L. Miller, Laura Elias, Mark A. Gillespie, Esther Son, Brett T. Staahl, Seung Tae Baek, Valentina Stanley, Cynthia Moncada-Reid, Zohar Shipony, Sara B. Linker, Maria C. Marchetto, Fred H. Gage, Dillon Chen, Tipu Sultan, Maha S. Zaki, Jeffrey A. Ranish, Tsuyoshi Miyakawa, Liqun Luo, Robert C. Malenka, Robert H. Crabtree, Joseph G. Gleeson
Izdano 2020Artigo -
4
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome od Shereen G. Ghosh, Kerstin Becker, He Huang, Tracy Dixon‐Salazar, Guoliang Chai, Vincenzo Salpietro, Lihadh Al‐Gazali, Quinten Waisfisz, Haicui Wang, Keith K. Vaux, Valentina Stanley, Andreea Manole, Uğur Akpulat, Marjan M. Weiss, Stéphanie Efthymiou, Michael G. Hanna, Carlo Minetti, Pasquale Striano, Livia Pisciotta, Elisa De Grandis, Janine Altmüller, Lisa Weixler, Peter Nürnberg, Hölger Thiele, Uluç Yiş, Tuncay Derya Okur, Ayşe Polat, Nafise Amiri, Mohammad Doosti, Ehsan Ghayoor Karimani, Mehran Beiraghi Toosi, Gabriel Haddad, Mert Karakaya, Brunhilde Wirth, Johanna M. van Hagen, Nicole I. Wolf, Reza Maroofian, Henry Houlden, Sebahattin Çırak, Joseph G. Gleeson
Izdano 2018Artigo
Alati za pretragu:
Povezani predmeti
Biology
Gene
Genetics
Cell biology
Chromatin
Mutation
Neuroscience
Acetylation
Ataxia
Cell culture
Cell growth
DNA
DNA damage
DNA repair
Degenerative Disorder
Disease
Epilepsy
FOSB
Frameshift mutation
Gene expression
HEK 293 cells
Histone
Internal medicine
MECP2
Medicine
Messenger RNA
Microcephaly
Molecular biology
Organoid
Phenotype