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UTX and UTY demonstrate histone demethylase-independent function in mouse embryonic development

PLoS genetics, 2012-09, Vol.8 (9), p.e1002964-e1002964

2012

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KDM6 demethylase independent loss of histone H3 lysine 27 trimethylation during early embryonic development

PLoS genetics, 2014-08, Vol.10 (8), p.e1004507-e1004507

2014

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UTX-guided neural crest function underlies craniofacial features of Kabuki syndrome

Proceedings of the National Academy of Sciences - PNAS, 2017-10, Vol.114 (43), p.E9046-E9055

2017

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Lipopolysaccharide-induced microglial activation and neuroprotection against experimental brain injury is independent of hematogenous TLR4

The Journal of neuroscience, 2012-08, Vol.32 (34), p.11706-11715

2012

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T Follicular Helper Cell-Dependent Clearance of a Persistent Virus Infection Requires T Cell Expression of the Histone Demethylase UTX

Immunity (Cambridge, Mass.), 2015-10, Vol.43 (4), p.703-714

2015

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Gemin Proteins Are Required for Efficient Assembly of Sm-Class Ribonucleoproteins

Proceedings of the National Academy of Sciences - PNAS, 2005-11, Vol.102 (48), p.17372-17377

2005

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UTX promotes CD8+ T cell-mediated antiviral defenses but reduces T cell durability

Cell reports (Cambridge), 2021-04, Vol.35 (2), p.108966-108966, Article 108966

2021

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Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle

The Journal of cell biology, 2007-03, Vol.176 (6), p.831-841

2007

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A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice

PLoS genetics, 2011-09, Vol.7 (9), p.e1002307-e1002307

2011

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The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology

Development (Cambridge), 2020-07, Vol.147 (21)

2020

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In vivo Kinetics of Cajal Body Components

The Journal of cell biology, 2004-03, Vol.164 (6), p.831-842

2004

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HNF1A recruits KDM6A to activate differentiated acinar cell programs that suppress pancreatic cancer

The EMBO journal, 2020-05, Vol.39 (9), p.e102808-n/a

2020

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BRD4 binds to active cranial neural crest enhancers to regulate RUNX2 activity during osteoblast differentiation

Development (Cambridge), 2024-01, Vol.151 (2)

2024

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Preconditioning paradigms and pathways in the brain

Cleveland Clinic journal of medicine, 2008-03, Vol.75 (Suppl 2), p.S77-S77

2008

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The histone demethylase Kdm6b regulates a mature gene expression program in differentiating cerebellar granule neurons

Molecular and cellular neuroscience, 2018-03, Vol.87, p.4-17

2018

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SETting up the genome: KMT2D and KDM6A genomic function in the Kabuki syndrome craniofacial developmental disorder

Birth defects research, 2023-12, Vol.115 (20), p.1885-1898

2023

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Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

Nature genetics, 1999-12, Vol.23 (4), p.413-419

1999

Volltextzugriff (PDF)

Pumping RNA: nuclear bodybuilding along the RNP pipeline

Current opinion in cell biology, 2006-06, Vol.18 (3), p.317-324

2006

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Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein

Genes & development, 2001-10, Vol.15 (20), p.2720-2729

2001

Volltextzugriff (PDF)

Gemin3 is an essential gene required for larval motor function and pupation in Drosophila

Molecular biology of the cell, 2009-01, Vol.20 (1), p.90-101

2009

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Coilin Methylation Regulates Nuclear Body Formation

Developmental cell, 2002-09, Vol.3 (3), p.329-337

2002

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Residual Cajal Bodies in Coilin Knockout Mice Fail to Recruit Sm snRNPs and SMN, the Spinal Muscular Atrophy Gene Product

The Journal of cell biology, 2001-07, Vol.154 (2), p.293-307

2001

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Control of Cajal body number is mediated by the coilin C-terminus

Journal of cell science, 2003-01, Vol.116 (Pt 2), p.303-312

2003

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C-terminal domain of coilin interacts with Sm proteins and U snRNPs

Chromosoma, 2005-08, Vol.114 (3), p.155-166

2005

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Col11a1 and col11a2 mRNA expression in the developing mouse Cochlea: Implications for the correlation of hearing loss phenotype with mutant type XI collagen genotype

Acta oto-laryngologica, 2004-03, Vol.124 (3), p.242-248

2004

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UTX and UTY demonstrate histone demethylase-independent function in mouse embryonic development

KDM6 demethylase independent loss of histone H3 lysine 27 trimethylation during early embryonic development

UTX-guided neural crest function underlies craniofacial features of Kabuki syndrome

Lipopolysaccharide-induced microglial activation and neuroprotection against experimental brain injury is independent of hematogenous TLR4

T Follicular Helper Cell-Dependent Clearance of a Persistent Virus Infection Requires T Cell Expression of the Histone Demethylase UTX

Gemin Proteins Are Required for Efficient Assembly of Sm-Class Ribonucleoproteins

UTX promotes CD8+ T cell-mediated antiviral defenses but reduces T cell durability

Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle

A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice

The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology

In vivo Kinetics of Cajal Body Components

HNF1A recruits KDM6A to activate differentiated acinar cell programs that suppress pancreatic cancer

BRD4 binds to active cranial neural crest enhancers to regulate RUNX2 activity during osteoblast differentiation

Preconditioning paradigms and pathways in the brain

The histone demethylase Kdm6b regulates a mature gene expression program in differentiating cerebellar granule neurons

SETting up the genome: KMT2D and KDM6A genomic function in the Kabuki syndrome craniofacial developmental disorder

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

Pumping RNA: nuclear bodybuilding along the RNP pipeline

Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein

Gemin3 is an essential gene required for larval motor function and pupation in Drosophila

Coilin Methylation Regulates Nuclear Body Formation

Residual Cajal Bodies in Coilin Knockout Mice Fail to Recruit Sm snRNPs and SMN, the Spinal Muscular Atrophy Gene Product

Control of Cajal body number is mediated by the coilin C-terminus

C-terminal domain of coilin interacts with Sm proteins and U snRNPs

Col11a1 and col11a2 mRNA expression in the developing mouse Cochlea: Implications for the correlation of hearing loss phenotype with mutant type XI collagen genotype

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