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Profil bibliographique

Bryan J. Matthews

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

40Publications signalées
1402Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

RNA Research and SplicingGenomics and Chromatin DynamicsMicroRNA in disease regulationRNA and protein synthesis mechanismsPeroxisome Proliferator-Activated Receptors

Les publications récentes

Accès ouvert 2026 preprint OpenAlex

Profiling and Targeting of Regulatory RNAs to Upregulate Gene Expression

Brynn N. Akerberg, Bryan J. Matthews, Yuting Liu, Cécile Mathieu et autres

Abstract Transcription of long noncoding RNAs (lncRNAs), including enhancer RNAs (eRNAs) and promoter-associated RNAs (paRNAs), collectively termed regulatory RNAs (regRNAs), is a hallmark of active gene expression, yet it remains unknown whether regRNAs can be targeted to selectively enhance transcription in cis …

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1 citation bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2024 erratum OpenAlex

Author Correction: Transcriptional characterization of iPSC-derived microglia as a model for therapeutic development in neurodegeneration

Gokul Ramaswami, Yeliz Yuva-Aydemir, Brynn N. Akerberg, Bryan J. Matthews et autres

“G.R. performed computational analyses and wrote the manuscript draft. Y.Y., B.A., B.M., J.W., and A.A.A. performed experiments. G.G., J.H., and Y.L. performed computational analyses. D.H., L.C.B., S.J.E., I.G., A.S., A.A.S., R.T.F., Y.L., and D.B. supervised the experiments and computational analyses. All authors …

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0 citations Scientific Reports
Accès ouvert 2024 article OpenAlex

Transcriptional characterization of iPSC-derived microglia as a model for therapeutic development in neurodegeneration

Gokul Ramaswami, Yeliz Yuva-Aydemir, Brynn N. Akerberg, Bryan J. Matthews et autres

Microglia are the resident immune cells in the brain that play a key role in driving neuroinflammation, a hallmark of neurodegenerative disorders. Inducible microglia-like cells have been developed as an in vitro platform for molecular and therapeutic hypothesis generation and testing. However, …

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14 citations Scientific Reports
Accès ouvert 2023 preprint OpenAlex

Transcriptional characterization of iPSC-derived microglia as a model for therapeutic development in neurodegeneration

Gokul Ramaswami, Yeliz Yuva-Aydemir, Brynn N. Akerberg, Bryan J. Matthews et autres

Abstract Background Microglia are the resident immune cells in the brain that play a key role in driving neuroinflammation, a hallmark of neurodegenerative disorders. Inducible microglia-like cells have been developed as an in vitro platform for molecular and therapeutic hypothesis generation and …

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3 citations bioRxiv (Cold Spring Harbor Laboratory)
2022 article OpenAlex

Progranulin upregulation by antisense oligonucleotides targeting regRNAs for treatment of FTD‐GRN

Yeliz Yuva Aydemir, Ali Al Abdullatif, Gokul Ramaswami, Gabriel Golczer et autres

Abstract Background Heterozygous mutations in progranulin (GRN) gene leading to progranulin protein (PGRN) haploinsufficieny are the major genetic cause of GRN‐related frontotemporal dementia (FTD‐GRN)1, 2 and 3. Decreased levels of PGRN disrupt lysosome homeostasis, cause aberrant microglia activation and neuronal cell death …

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0 citations Alzheimer s & Dementia
Accès ouvert 2021 article OpenAlex

Harnessing natural variation to identify cis regulators of sex-biased gene expression in a multi-strain mouse liver model

Bryan J. Matthews, Tisha Melia, David J. Waxman

Sex differences in gene expression are widespread in the liver, where many autosomal factors act in tandem with growth hormone signaling to regulate individual variability of sex differences in liver metabolism and disease. Here, we compare hepatic transcriptomic and epigenetic profiles of …

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13 citations PLoS Genetics
Accès ouvert 2021 preprint OpenAlex

Harnessing natural variation to identify cis regulators of sex-biased gene expression in a multi-strain mouse liver model

Bryan J. Matthews, David J. Waxman

Abstract Sex differences in gene expression are widespread in the liver, where a large number of autosomal factors act in tandem with growth hormone signaling to regulate individual variability of sex differences in liver metabolism and disease. Here, we compare hepatic transcriptomic …

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0 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2020 article OpenAlex

Impact of 3D genome organization, guided by cohesin and CTCF looping, on sex-biased chromatin interactions and gene expression in mouse liver

Bryan J. Matthews, David J. Waxman

Several thousand sex-differential distal enhancers have been identified in mouse liver; however, their links to sex-biased genes and the impact of any sex-differences in nuclear organization and chromatin interactions are unknown. To address these issues, we first characterized 1847 mouse liver genomic …

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36 citations Epigenetics & Chromatin
Accès ouvert 2020 preprint OpenAlex

Impact of 3-dimensional genome organization, guided by cohesin and CTCF looping, on sex-biased chromatin interactions and gene expression in mouse liver

Bryan J. Matthews, David J. Waxman

Abstract Background: Sex differences in the transcriptome and epigenome are widespread in mouse liver and are associated with sex-bias in liver disease. Several thousand sex-differential distal enhancers have been identified; however, their links to sex-biased genes and the impact of any sex-differences …

0 citations Research Square
Accès ouvert 2019 preprint OpenAlex

Impact of 3-dimensional genome organization, guided by cohesin and CTCF looping, on sex-biased chromatin interactions and gene expression in mouse liver

Bryan J. Matthews, David J. Waxman

Abstract Background Sex differences in the transcriptome and epigenome are widespread in mouse liver and are associated with sex-bias in liver disease. Several thousand sex-differential distal enhancers have been identified; however, their links to sex-biased genes and the impact of any sex-differences …

us (code pays fourni par la source)

1 citation bioRxiv (Cold Spring Harbor Laboratory)

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