Search Results - "Monderer-Rothkoff G"

Author Correction: Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice.

Authors: Suliman-Lavie R Title B Cohen Y et al.

Source: Nature communications [Nat Commun] 2021 Jun 17; Vol. 12 (1), pp. 3874. Date of Electronic Publication: 2021 Jun 17.

Publication Type: Published Erratum

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE; PubMed not MEDLINE

CRISPR knockout screens reveal genes and pathways essential for neuronal differentiation and implicate PEDS1 in neurodevelopment.

Authors: Amelan A Collins SC Damseh NS et al.

Source: Nature neuroscience [Nat Neurosci] 2026 Mar; Vol. 29 (3), pp. 592-603. Date of Electronic Publication: 2026 Jan 05.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 9809671 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1726 (Electronic) Linking ISSN: 10976256 NLM ISO Abbreviation: Nat Neurosci Subsets: MEDLINE

Research on the potential mechanisms and therapeutic drug for the co-occurrence of major depressive disorder in castration-resistant prostate cancer.

Authors: Xu, Lei Zhang, Mingqiang Shi, Menghua et al.

Source: Scientific Reports. 10/23/2025, Vol. 15 Issue 1, p1-14. 14p.

POGZ targeted by LINC01355/miR-27b-3p retards thyroid cancer progression via interplaying with MAD2L2.

Authors: Lu, Jiancan Zhou, Xinglu Zhu, Hongling et al.

Source: 3 Biotech. 3/8/2025, Vol. 15 Issue 4, p1-15. 15p.

Analyses of Conditional Knockout Mice for Pogz , a Gene Responsible for Neurodevelopmental Disorders in Excitatory and Inhibitory Neurons in the Brain.

Authors: Hamada, Nanako Nishijo, Takuma Iwamoto, Ikuko et al.

Source: Cells (2073-4409). Mar2024, Vol. 13 Issue 6, p540. 16p.

Imputed expression of schizophrenia‐associated genes and cognitive measures in patients with schizophrenia.

Authors: Fabbri, Chiara Leggio, Gian Marco Drago, Filippo et al.

Source: Molecular Genetics & Genomic Medicine. Jun2022, Vol. 10 Issue 6, p1-8. 8p.

A novel AUTS2 Variant in a Patient with Global Developmental Delay and Intellectual Disability.

Authors: Shboul, Mohammad A. Darweesh, Reem F. El-Khateeb, Mohammad et al.

Source: Jordan Journal of Biological Sciences. Jun2024, Vol. 17 Issue 2, p217-222. 6p.

Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review.

Authors: GAULD, Christophe POISSON, Alice REVERSAT, Julie et al.

Source: BMC Psychiatry. 7/17/2021, Vol. 21 Issue 1, p1-11. 11p. 1 Color Photograph, 1 Diagram, 2 Charts.

Investigation of autism-related transcription factors underlying sex differences in the effects of bisphenol A on transcriptome profiles and synaptogenesis in the offspring hippocampus.

Authors: Thongkorn, Surangrat Kanlayaprasit, Songphon Kasitipradit, Kasidit et al.

Source: Biology of Sex Differences. 2/20/2023, Vol. 14 Issue 1, p1-27. 27p.

Critical Roles of Polycomb Repressive Complexes in Transcription and Cancer.

Authors: Dong, Guan-Jun Xu, Jia-Le Qi, Yu-Ruo et al.

Source: International Journal of Molecular Sciences. Sep2022, Vol. 23 Issue 17, p9574. 33p.

auts2 Features and Expression Are Highly Conserved during Evolution Despite Different Evolutionary Fates Following Whole Genome Duplication.

Authors: Merdrignac, Constance Clément, Antoine Emile Montfort, Jérôme et al.

Source: Cells (2073-4409). Sep2022, Vol. 11 Issue 17, p2694. 18p.

The Novel Protease Activities of JMJD5–JMJD6–JMJD7 and Arginine Methylation Activities of Arginine Methyltransferases Are Likely Coupled.

Authors: Liu, Haolin Wei, Pengcheng Zhang, Qianqian et al.

Source: Biomolecules (2218-273X). Mar2022, Vol. 12 Issue 3, p347. 21p.

Ancestry of the AUTS2 family–A novel group of polycomb-complex proteins involved in human neurological disease.

Authors: Sellers, Robert A. Robertson, David L. Tassabehji, May

Source: PLoS ONE. 12/11/2020, Vol. 15 Issue 12, p1-22. 22p.

Characteristics of allelic gene expression in human brain cells from single-cell RNA-seq data analysis.

Authors: Dejian Zhao Mingyan Lin Pedrosa, Erika et al.

Source: BMC Genomics. 11/10/2017, Vol. 18, p1-18. 18p. 1 Diagram, 1 Chart, 6 Graphs.

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

Source: Molecular Autism. 5/22/2017, Vol. 8, p1-17. 17p.

Association Study Identifying a New Susceptibility Gene (AUTS2) for Schizophrenia.

Authors: Bao Zhang Yue-Hong Xu Shu-Guang Wei et al.

Source: International Journal of Molecular Sciences. 2014, Vol. 15 Issue 11, p19406-19416. 11p. 1 Diagram, 3 Charts.

Nuwe bevindings oor die genetiese argitektuur van skisofrenie: Die bydrae van studies onder Afrikaners.

Alternate Title: Latest findings in the genetic architecture of schizophrenia: The contribution of genetic studies among Afrikaners.

Authors: Roos, Johannes L.¹ erna.fourie@up.ac.za

Source: Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie. 2014, Vol. 33 Issue 1, p1-9. 9p.

Structural Variation-Associated Expression Changes Are Paralleled by Chromatin Architecture Modifications.

Authors: Gheldof, Nele Witwicki, Robert M. Migliavacca, Eugenia et al.

Source: PLoS ONE. Nov2013, Vol. 8 Issue 11, p1-9. 9p.

Recent Advances in Target Characterization and Identification by Photoaffinity Probes.

Authors: Jitapa Sumranjit Sang J. Chung

Source: Molecules. Sep2013, Vol. 18 Issue 9, p10425-10451. 27p. 31 Diagrams.

Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.

Authors: Nagamani, Sandesh C S Erez, Ayelet Ben-Zeev, Bruria et al.

Source: European Journal of Human Genetics. Mar2013, Vol. 21 Issue 3, p343-346. 4p. 1 Diagram, 1 Chart.