HOX epimutations driven by maternal SMCHD1/LRIF1 haploinsufficiency trigger homeotic transformations in genetically wildtype offspring
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Title
HOX epimutations driven by maternal SMCHD1/LRIF1 haploinsufficiency trigger homeotic transformations in genetically wildtype offspring
Authors
Keywords
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Journal
Nature Communications
Volume 13, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2022-06-23
DOI
10.1038/s41467-022-31185-8
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Note: Only part of the references are listed.- AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia Syndrome
- (2021) Camille Laberthonnière et al. Biomedicines
- Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy
- (2020) Kohei Hamanaka et al. NEUROLOGY
- SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite
- (2019) Camille Dion et al. NUCLEIC ACIDS RESEARCH
- The maternal-to-zygotic transition revisited
- (2019) Nadine L. Vastenhouw et al. DEVELOPMENT
- Placeholder Nucleosomes Underlie Germline-to-Embryo DNA Methylation Reprogramming
- (2018) Patrick J. Murphy et al. CELL
- Novel key roles for Structural maintenance of chromosome flexible domain containing 1 (Smchd1) during preimplantation mouse development
- (2018) Uros Midic et al. MOLECULAR REPRODUCTION AND DEVELOPMENT
- Smchd1 regulates long-range chromatin interactions on the inactive X chromosome and at Hox clusters
- (2018) Natasha Jansz et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Intergenerational and transgenerational epigenetic inheritance in animals
- (2018) Marcos Francisco Perez et al. NATURE CELL BIOLOGY
- De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
- (2017) Christopher T Gordon et al. NATURE GENETICS
- SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome
- (2017) Natalie D Shaw et al. NATURE GENETICS
- The Epigenetic Regulator SMCHD1 in Development and Disease
- (2017) Natasha Jansz et al. TRENDS IN GENETICS
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- Independent Mechanisms Target SMCHD1 to Trimethylated Histone H3 Lysine 9-Modified Chromatin and the Inactive X Chromosome
- (2015) Nicholas J. Brideau et al. MOLECULAR AND CELLULAR BIOLOGY
- The Right Dorsal Habenula Limits Attraction to an Odor in Zebrafish
- (2014) Seetha Krishnan et al. CURRENT BIOLOGY
- Single-Cell RNA-Seq Reveals Dynamic, Random Monoallelic Gene Expression in Mammalian Cells
- (2014) Q. Deng et al. SCIENCE
- Reprogramming the Maternal Zebrafish Genome after Fertilization to Match the Paternal Methylation Pattern
- (2013) Magdalena E. Potok et al. CELL
- Sperm, but Not Oocyte, DNA Methylome Is Inherited by Zebrafish Early Embryos
- (2013) Lan Jiang et al. CELL
- Epigenetic Functions of Smchd1 Repress Gene Clusters on the Inactive X Chromosome and on Autosomes
- (2013) Anne-Valerie Gendrel et al. MOLECULAR AND CELLULAR BIOLOGY
- Single-cell RNA-Seq profiling of human preimplantation embryos and embryonic stem cells
- (2013) Liying Yan et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Human inactive X chromosome is compacted through a PRC2-independent SMCHD1-HBiX1 pathway
- (2013) Ryu-Suke Nozawa et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation
- (2013) Arne W Mould et al. Epigenetics & Chromatin
- Tactile stimulation reduces fear in fish
- (2013) Annett Schirmer et al. Frontiers in Behavioral Neuroscience
- Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes
- (2013) Slavé Petrovski et al. PLoS Genetics
- Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2
- (2012) Richard J L F Lemmers et al. NATURE GENETICS
- Trim28 Is Required for Epigenetic Stability During Mouse Oocyte to Embryo Transition
- (2012) D. M. Messerschmidt et al. SCIENCE
- Ribosome-Mediated Specificity in Hox mRNA Translation and Vertebrate Tissue Patterning
- (2011) Nadya Kondrashov et al. CELL
- miR-196 regulates axial patterning and pectoral appendage initiation
- (2011) Xinjun He et al. DEVELOPMENTAL BIOLOGY
- The Dynamic Architecture of Hox Gene Clusters
- (2011) D. Noordermeer et al. SCIENCE
- Chromatin signature of embryonic pluripotency is established during genome activation
- (2010) Nadine L. Vastenhouw et al. NATURE
- SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation
- (2008) Marnie E Blewitt et al. NATURE GENETICS
- MicroRNAs in the Hox network: an apparent link to posterior prevalence
- (2008) Soraya Yekta et al. NATURE REVIEWS GENETICS
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