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Michael L. Gonzales

Researcher at Fluidigm Corporation

Publications -  14
Citations -  2462

Michael L. Gonzales is an academic researcher from Fluidigm Corporation. The author has contributed to research in topics: MECP2 & Single-cell analysis. The author has an hindex of 11, co-authored 14 publications receiving 1930 citations. Previous affiliations of Michael L. Gonzales include University of California & Wisconsin Alumni Research Foundation.

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Single-cell chromatin accessibility reveals principles of regulatory variation

TL;DR: A robust method for mapping the accessible genome of individual cells by assay for transposase-accessible chromatin using sequencing (ATAC-seq) integrated into a programmable microfluidics platform is developed and single-cell analysis of DNA accessibility provides new insight into cellular variation of the ‘regulome’.
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A PtdIns4,5P2-regulated nuclear poly(A) polymerase controls expression of select mRNAs.

TL;DR: The data demonstrate a model by which phosphoinositide signalling works in tandem with complement pathways to regulate the activity of Star-PAP and the subsequent biosynthesis of its target mRNA and reveal a mechanism for the integration of nuclear phosphoinposide signals and a method for regulating gene expression.
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The role of MeCP2 in brain development and neurodevelopmental disorders.

TL;DR: The mutation types and inheritance patterns of the human disorders associated with MECP2 are compared and the current understanding of MeCP2 as a central epigenetic regulator of activity-dependent synaptic maturation is summarized.
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Phosphorylation of distinct sites in MeCP2 modifies cofactor associations and the dynamics of transcriptional regulation.

TL;DR: Phosphorylation is one of several factors that are important for interpreting the complexities of MeCP2 transcriptional modulation, including phosphorylation, acetylation, and ubiquitylation.
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MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation

TL;DR: The results suggest that, in addition to the established role of Me CP2 in transcriptional regulation of specific target genes, the global chromatin-binding function of MeCP2 is essential for activity-dependent global Chromatin dynamics during postnatal neuronal maturation.