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Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons

Human molecular genetics, 2018-02, Vol.27 (3), p.505-515

2018

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Monosomy X in isogenic human iPSC-derived trophoblast model impacts expression modules preserved in human placenta

Proceedings of the National Academy of Sciences - PNAS, 2022-10, Vol.119 (40), p.e2211073119-e2211073119

2022

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Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neurons

Human molecular genetics, 2020-11, Vol.29 (19), p.3285-3295

2020

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A dynamic in vitro model of Down syndrome neurogenesis with trisomy 21 gene dosage correction

Science advances, 2024-06, Vol.10 (23), p.eadj0385

2024

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Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1

Molecular autism, 2014-08, Vol.5 (1), p.44-44, Article 44

2014

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Neuronal Expression of p53 Dominant-Negative Proteins in Adult Drosophila melanogaster Extends Life Span

Current biology, 2005-11, Vol.15 (22), p.2063-2068

2005

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Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn

Nucleic acids research, 2004, Vol.32 (11), p.3480

2004

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The Human Magel2 Gene and Its Mouse Homologue Are Paternally Expressed and Mapped to the Prader-Willi Region

Human molecular genetics, 1999-12, Vol.8 (13), p.2497-2505

1999

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Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion

Human molecular genetics, 2014-05, Vol.23 (9), p.2364-2373

2014

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Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells

Methods in molecular biology (Clifton, N.J.), 2016, Vol.1353, p.45

2016

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Epigenetic activation of the 5-hydroxytryptamine (serotonin) receptor 2C in embryonal carcinoma cells is DNA replication-dependent

Experimental cell research, 2004-08, Vol.298 (1), p.262-267

2004

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Abstract 3938: Massively parallel sequencing of formalin-fixed, paraffin-embedded tissue

Cancer research (Chicago, Ill.), 2011-04, Vol.71 (8_Supplement), p.3938-3938

2011

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Prader-Willi syndrome, Snord115, and Htr2c editing

Neurogenetics, 2010-02, Vol.11 (1), p.143-144

2010

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Prader–Willi syndrome, Snord115, and Htr2c editing

Neurogenetics, 2010-02, Vol.11 (1), p.143-144

2010

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Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans

Nucleic acids research, 2005-01, Vol.33 (13), p.3976

2005

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Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons

Monosomy X in isogenic human iPSC-derived trophoblast model impacts expression modules preserved in human placenta

Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neurons

A dynamic in vitro model of Down syndrome neurogenesis with trisomy 21 gene dosage correction

Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1

Neuronal Expression of p53 Dominant-Negative Proteins in Adult Drosophila melanogaster Extends Life Span

Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn

The Human Magel2 Gene and Its Mouse Homologue Are Paternally Expressed and Mapped to the Prader-Willi Region

Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion

Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells

Epigenetic activation of the 5-hydroxytryptamine (serotonin) receptor 2C in embryonal carcinoma cells is DNA replication-dependent

Abstract 3938: Massively parallel sequencing of formalin-fixed, paraffin-embedded tissue

Prader-Willi syndrome, Snord115, and Htr2c editing

Prader–Willi syndrome, Snord115, and Htr2c editing

Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans

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