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Items: 13

1.
Protooncogenic Role of ARHGAP11A and ARHGAP11B in Invasive Ductal Carcinoma: Two Promising Breast Cancer Biomarkers
Y. Naeimzadeh, S. Ilbeigi, H. Dastsooz, M. Rafiee Monjezi, Y. Mansoori, S. M. B. Tabei
Biomed Res Int. 2023; 2023: 8236853. Published online 2023 Nov 23. doi: 10.1155/2023/8236853
PMCID:
PMC10689071
AbstractArticlePDF–2.8M
2.
Human‐specific ARHGAP11B ensures human‐like basal progenitor levels in hominid cerebral organoids
Jan Fischer, Eduardo Fernández Ortuño, Fabio Marsoner, Annasara Artioli, Jula Peters, Takashi Namba, Christina Eugster Oegema, Wieland B. Huttner, Julia Ladewig, Michael Heide
EMBO Rep. 2022 Nov; 23(11): e54728. Published online 2022 Sep 13. doi: 10.15252/embr.202254728
PMCID:
PMC9646322
AbstractArticlePDF–4.7M
3.
Histone deacetylase inhibitors inhibit cervical cancer growth through Parkin acetylation-mediated mitophagy
Xin Sun, Yuhan Shu, Guiqin Ye, Caixia Wu, Mengting Xu, Ruilan Gao, Dongsheng Huang, Jianbin Zhang
Acta Pharm Sin B. 2022 Feb; 12(2): 838–852. Published online 2021 Jul 21. doi: 10.1016/j.apsb.2021.07.003
PMCID:
PMC8897022
AbstractArticlePDF–3.0M
4.
Expression of human‐specific ARHGAP11B in mice leads to neocortex expansion and increased memory flexibility
Lei Xing, Agnieszka Kubik‐Zahorodna, Takashi Namba, Anneline Pinson, Marta Florio, Jan Prochazka, Mihail Sarov, Radislav Sedlacek, Wieland B Huttner
EMBO J. 2021 Jul 1; 40(13): e107093. Published online 2021 May 3. doi: 10.15252/embj.2020107093
PMCID:
PMC8246068
AbstractArticlePDF–1.5M
5.
The midbody interactome reveals unexpected roles for PP1 phosphatases in cytokinesis
Luisa Capalbo, Zuni I. Bassi, Marco Geymonat, Sofia Todesca, Liviu Copoiu, Anton J. Enright, Giuliano Callaini, Maria Giovanna Riparbelli, Lu Yu, Jyoti S. Choudhary, Enrico Ferrero, Sally Wheatley, Max E. Douglas, Masanori Mishima, Pier Paolo D’Avino
Nat Commun. 2019; 10: 4513. Published online 2019 Oct 4. doi: 10.1038/s41467-019-12507-9
PMCID:
PMC6778137
AbstractArticlePDF–7.8M
6.
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
Nirmal Vadgama, Alan Pittman, Michael Simpson, Niranjanan Nirmalananthan, Robin Murray, Takeo Yoshikawa, Peter De Rijk, Elliott Rees, George Kirov, Deborah Hughes, Tomas Fitzgerald, Mark Kristiansen, Kerra Pearce, Eliza Cerveira, Qihui Zhu, Chengsheng Zhang, Charles Lee, John Hardy, Jamal Nasir
Eur J Hum Genet. 2019 Jul; 27(7): 1121–1133. Published online 2019 Mar 18. doi: 10.1038/s41431-019-0376-7
PMCID:
PMC6777616
AbstractArticlePDF–1.0M
7.
Human-specific ARHGAP11B induces hallmarks of neocortical expansion in developing ferret neocortex
Nereo Kalebic, Carlotta Gilardi, Mareike Albert, Takashi Namba, Katherine R Long, Milos Kostic, Barbara Langen, Wieland B Huttner
eLife. 2018; 7: e41241. Published online 2018 Nov 28. doi: 10.7554/eLife.41241
PMCID:
PMC6303107
AbstractArticlePDF–7.1M
8.
Transcriptional fates of human-specific segmental duplications in brain
Max L. Dougherty, Jason G. Underwood, Bradley J. Nelson, Elizabeth Tseng, Katherine M. Munson, Osnat Penn, Tomasz J. Nowakowski, Alex A. Pollen, Evan E. Eichler
Genome Res. 2018 Oct; 28(10): 1566–1576. doi: 10.1101/gr.237610.118
PMCID:
PMC6169893
AbstractArticlePDF–2.3M
9.
VIRMA mediates preferential m6A mRNA methylation in 3′UTR and near stop codon and associates with alternative polyadenylation
Yanan Yue, Jun Liu, Xiaolong Cui, Jie Cao, Guanzheng Luo, Zezhou Zhang, Tao Cheng, Minsong Gao, Xiao Shu, Honghui Ma, Fengqin Wang, Xinxia Wang, Bin Shen, Yizhen Wang, Xinhua Feng, Chuan He, Jianzhao Liu
Cell Discov. 2018; 4: 10. Published online 2018 Feb 27. doi: 10.1038/s41421-018-0019-0
PMCID:
PMC5826926
AbstractArticlePDF–2.3M
10.
A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
Marta Florio, Takashi Namba, Svante Pääbo, Michael Hiller, Wieland B. Huttner
Sci Adv. 2016 Dec; 2(12): e1601941. Published online 2016 Dec 7. doi: 10.1126/sciadv.1601941
PMCID:
PMC5142801
AbstractArticlePDF–498K
11.
A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy
Doug Speed, Clive Hoggart, Slave Petrovski, Ioanna Tachmazidou, Alison Coffey, Andrea Jorgensen, Hariklia Eleftherohorinou, Maria De Iorio, Marian Todaro, Tisham De, David Smith, Philip E. Smith, Margaret Jackson, Paul Cooper, Mark Kellett, Stephen Howell, Mark Newton, Raju Yerra, Meng Tan, Chris French, Markus Reuber, Graeme E. Sills, David Chadwick, Munir Pirmohamed, David Bentley, Ingrid Scheffer, Samuel Berkovic, David Balding, Aarno Palotie, Anthony Marson, Terence J. O'Brien, Michael R. Johnson
Hum Mol Genet. 2014 Jan 1; 23(1): 247–258. Published online 2013 Aug 19. doi: 10.1093/hmg/ddt403
PMCID:
PMC3857947
AbstractArticlePDF–645K
12.
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Claire S. Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Rastam, Henrik Anckarsäter, Gudrun Nygren, I. Carina Gillberg, Jonas Melke, Roberto Toro, Beatrice Regnault, Fabien Fauchereau, Oriane Mercati, Nathalie Lemière, David Skuse, Martin Poot, Richard Holt, Anthony P. Monaco, Irma Järvelä, Katri Kantojärvi, Raija Vanhala, Sarah Curran, David A. Collier, Patrick Bolton, Andreas Chiocchetti, Sabine M. Klauck, Fritz Poustka, Christine M. Freitag, Regina Waltes, Marnie Kopp, Eftichia Duketis, Elena Bacchelli, Fiorella Minopoli, Liliana Ruta, Agatino Battaglia, Luigi Mazzone, Elena Maestrini, Ana F. Sequeira, Barbara Oliveira, Astrid Vicente, Guiomar Oliveira, Dalila Pinto, Stephen W. Scherer, Diana Zelenika, Marc Delepine, Mark Lathrop, Dominique Bonneau, Vincent Guinchat, Françoise Devillard, Brigitte Assouline, Marie-Christine Mouren, Marion Leboyer, Christopher Gillberg, Tobias M. Boeckers, Thomas Bourgeron
PLoS Genet. 2012 Feb; 8(2): e1002521. Published online 2012 Feb 9. doi: 10.1371/journal.pgen.1002521
PMCID:
PMC3276563
AbstractArticlePDF–1.0M
13.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K

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