Author

Katharine R. Maschhoff

Mayo ClinicORCID 0000-0002-8576-1145Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Mariah K NovakiD· 1 shared Qiuying LiuiD· 1 shared Rachel M. PepiniD· 1 shared Shaojie ZhangiD· 1 shared Wenqian HuiD· 1 shared Xiaoli Chen· 1 shared

Activity by Year

2022-2022 · peak 1/yr

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6 top collaborators · 15 mutual co-author links

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1 shared paperMolecular Biology

Mariah K NovakORCID

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1 paper

Recent·Most cited

Molecular BiologybioRxivPreprintApr 14, 2022

A congenital hydrocephalus causing mutation in Trim71 results in stem cell differentiation defects through inhibiting Lsd1 mRNA translation

Qiuying Liu, Mariah K Novak, Rachel M. Pepin…·Wenqian Hu

This study identifies a mutation in Trim71 that causes congenital hydrocephalus by impairing stem cell differentiation through repression of Lsd1 mRNA translation.

DOI 10.1101/2022.04.14.488304

mousebulk RNA-seq

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