S. Ticau

发表

Mechanism and Timing of Mcm2–7 Ring Closure During DNA Replication Origin Licensing

S. Bell, J. Gelles, Larry J. Friedman, 2017, Nature Structural &Molecular Biology.

Neurofilament Light Chain as a Biomarker of Hereditary Transthyretin-Mediated Amyloidosis

David John Adams, P. Nioi, M. Reilly, 2020, Neurology.

Transthyretin-stabilising mutation T119M is not associated with protection against vascular disease or death in the UK Biobank

G. Hinkle, P. Nioi, S. Ticau, 2020, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Transthyretin-stabilizing mutation T119M is not associated with protection against vascular disease or death in the UK Biobank

G. Hinkle, P. Nioi, S. Ticau, 2019, bioRxiv.

Plasma proteome analysis of patients with hereditary transthyretin-mediated (hATTR) amyloidosis establishes neurofilament light chain (NfL) as a biomarker of disease and treatment response

P. Nioi, M. Reilly, K. Fitzgerald, 2019 .

Widespread haploid-biased gene expression in mammalian spermatogenesis associated with frequent selective sweeps and evolutionary conflict

Robin C. Friedman, Kunal Bhutani, B. Fiske, 2019, bioRxiv.

Characterising a healthy adult with a rare HAO1 knockout to support a therapeutic strategy for primary hyperoxaluria

D. Lawlor, D. MacArthur, John Wright, 2020, eLife.

Deep phenotyping of a healthy human HAO1 knockout informs therapeutic development for primary hyperoxaluria type 1

D. MacArthur, John Wright, J. Lieske, 2019, bioRxiv.

Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity

J. Flannick, L. D. Ward, G. Hinkle, 2022, Nature Communications.

Widespread haploid-biased gene expression enables sperm-level natural selection

A. Villani, Robin C. Friedman, Kunal Bhutani, 2021, Science.

Viral E3 ubiquitin ligase-mediated degradation of a cellular E3: viral mimicry of a cellular phosphorylation mark targets the RNF8 FHA domain.

C. Lilley, M. Weitzman, J. Yates, 2012, Molecular cell.

Single-Molecule Studies of Origin Licensing Reveal Mechanisms Ensuring Bidirectional Helicase Loading

S. Bell, J. Gelles, S. Ticau, 2015, Cell.

Baculovirus AC102 Is a Nucleocapsid Protein That Is Crucial for Nuclear Actin Polymerization and Nucleocapsid Morphogenesis

G. Borgo, M. Welch, S. Ticau, 2018, Journal of Virology.

Association of the Transthyretin Variant V122I With Polyneuropathy Among Individuals of African Descent

T. Assimes, D. Rader, L. D. Ward, 2020, medRxiv.

The dynamics of eukaryotic replication initiation: origin specificity, licensing, and firing at the single-molecule level.

S. Bell, E. Greene, M. Warner, 2015, Molecular cell.

Single-molecule studies of eukaryotic helicase loading

S. Ticau, 2016 .

Treatment response and neurofilament light chain levels with long-term patisiran in hereditary transthyretin-mediated amyloidosis with polyneuropathy: 24-month results of an open-label extension study

P. Nioi, S. Ticau, M. Polydefkis, 2023, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Activin E is a TGFβ ligand that signals specifically through activin receptor-like kinase 7

A. Deaton, Chandramohan Kattamuri, S. Ticau, 2023, bioRxiv.

Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry

S. Damrauer, G. Hinkle, A. Deaton, 2021, Scientific Reports.