NIPBL+/- haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states.

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NIPBL+/- haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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NIPBL+/- haploinsufficiency re ...... luripotent and cardiac states.

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NIPBL+/- haploinsufficiency re ...... luripotent and cardiac states.

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NIPBL+/- haploinsufficiency re ...... luripotent and cardiac states.

@en

NIPBL+/- haploinsufficiency re ...... luripotent and cardiac states.

@nl

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NIPBL+/- haploinsufficiency re ...... luripotent and cardiac states.

@en

NIPBL+/- haploinsufficiency re ...... luripotent and cardiac states.

@nl

P1476

NIPBL+/- haploinsufficiency re ...... pluripotent and cardiac states

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P2093

Alyssa Gagne

http://www.w3.org/2001/XMLSchema#string

Deborah McEldrew

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Ian D Krantz

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Jason A Mills

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Jesus A Tintos-Hernandez

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Lanfranco Leo

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Maninder Kaur

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Pamela S Herrera

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Zhe Zhang

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P2860

Transcriptional dysregulation in NIPBL and cohesin mutant human cells

NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle

Pioneer transcription factors: establishing competence for gene expression

Mediator and cohesin connect gene expression and chromatin architecture

Genetics of congenital heart disease: the glass half empty

Genome-Wide Transcriptome and Binding Sites Analyses Identify Early FOX Expressions for Enhancing Cardiomyogenesis Efficiency of hESC Cultures.

Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome

Disorders of Transcriptional Regulation: An Emerging Category of Multiple Malformation Syndromes

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1056

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scholarly article

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10.1038/S41598-018-19173-9

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English

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Xilma R Ortiz-Gonzalez

Ramakrishnan Rajagopalan

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2018-01-18T00:00:00Z

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P698

29348408

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P921

transcriptome

haploinsufficiency

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5773608

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