PMC Links for GEO Profiles (Select 80123987) - PMC

Select item 106890711.

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

Select item 96463222.

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

Abstract Article PDF–4.7M

Select item 88970223.

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

Abstract Article PDF–3.0M

Select item 82460684.

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

Abstract Article PDF–1.5M

Select item 67781375.

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

Abstract Article PDF–7.8M

Select item 67776166.

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

Abstract Article PDF–1.0M

Select item 63031077.

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

Abstract Article PDF–7.1M

Select item 61698938.

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

Abstract Article PDF–2.3M

Select item 58269269.

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

Abstract Article PDF–2.3M

Select item 514280110.

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

Abstract Article PDF–498K

Select item 484160711.

High-throughput analyses of hnRNP H1 dissects its multi-functional aspect

Philip J. Uren, Emad Bahrami-Samani, Patricia Rosa de Araujo, Christine Vogel, Mei Qiao, Suzanne C. Burns, Andrew D. Smith, Luiz O. F. Penalva

RNA Biol. 2016 Apr; 13(4): 400–411. Published online 2016 Jan 13. doi: 10.1080/15476286.2015.1138030

PMCID:: PMC4841607

Abstract Article PDF–1.6M

Select item 385794712.

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

Abstract Article PDF–645K

Select item 327656313.

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

Abstract Article PDF–1.0M

Select item 13924114.

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

Abstract Article PDF–118K

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