Author

T. F. Uliasz

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 3 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:cell signaling & trafficking· 2 Research Focus:cell type annotation· 2 Assay:bulk RNA-seq· 1 Assay:imaging· 1 Assay:proteomics· 1 Organism:rat· 1

Frequent Co-Authors

K. M. Lowther· 3 shared L. A. Jaffe· 2 shared L. M. Mehlmann· 2 shared S.-P. Yee· 2 shared C. B. Bartels· 1 shared C. M. Owen· 1 shared H. Urlaub· 1 shared I. Silbern· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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3 shared papersCell Biology

K. M. Lowther

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Author profile →

4 papers

Recent·Most cited

Phosphatases modified by LH signaling in ovarian follicles: testing their role in regulating the NPR2 guanylyl cyclase

J. R. Egbert, I. Silbern, T. F. Uliasz, K. M. Lowther, S.-P. Yee, H. Urlaub, L. A. Jaffe

The paper identifies phosphatases rapidly modified by luteinizing hormone in ovarian follicles, revealing their role in regulating NPR2 guanylyl cyclase dephosphorylation.

bioRxiv · Jun 12, 2023Cell Biology

Testosterone use in female mice does not impair fertilizability of eggs: Implications for the fertility care of transgender males

C. B. Bartels, T. F. Uliasz, L. Lestz, L. M. Mehlmann

This study shows that testosterone treatment in female mice does not impair egg fertilizability, suggesting that transgender men may not need to stop testosterone before fertility treatments.

bioRxiv · Apr 9, 2020Physiology

Cellular heterogeneity of the LH receptor and its significance for cyclic GMP signaling in mouse preovulatory follicles

V. Baena, C. M. Owen, T. F. Uliasz, K. M. Lowther, S.-P. Yee, M. Terasaki, J. Egbert, L. A. Jaffe

This study investigates the cellular localization of LHR and NPR2 in mouse preovulatory follicles and suggests that LHR-expressing cells signal to neighboring cells to inactivate NPR2.

bioRxiv · Feb 6, 2020Cell Biology

SNAP23 is required for the maintenance of meiotic arrest and cortical granule exocytosis in mouse oocytes

L. M. Mehlmann, T. F. Uliasz, K. M. Lowther

This study identifies SNAP23 as essential for meiotic arrest and cortical granule exocytosis in mouse oocytes by disrupting gap junction communication and exocytic responses.

bioRxiv · May 20, 2019Cell Biology