Mesenchyme-specific loss of Dot1L histone methyltransferase leads to skeletal dysplasia phenotype in mice - Concepedia

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Mesenchyme-specific loss of Dot1L histone methyltransferase leads to skeletal dysplasia phenotype in mice

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11

Citations

66

References

2020

Year

Pearl A. Sutter, Sangita Karki, Ilan Crawley, Vijender Singh, Kathrin M. Bernt, David W. Rowe, Stephen J. Crocker, Dashzeveg Bayarsaihan, Rosa M. Guzzo

Histone ModificationsChromatinDevelopmental BiologyBone Morphogenic ProteinChromatin RemodelingEpigenetic ChangeGeneticsDot1l Histone MethyltransferaseEpigenomicsDysplasia PhenotypeGene ExpressionMedicineCell BiologyEpigeneticsMesenchyme-specific Loss

References

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