Publications by authors named "Isabella Lin"

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Conservation and evolution of the programmed ribosomal frameshift in across the bacterial domain.
Cassidy R Prince, Isabella N Lin, Heather A Feaga

mBio· September 2025

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Conservation of sporulation genes and a transmembrane-containing Spo0B variant in .
Isabella N Lin, Cassidy R Prince, Heather A Feaga

bioRxiv· August 2025

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Conservation and evolution of the programmed ribosomal frameshift in across the bacterial domain.
Cassidy R Prince, Isabella N Lin, Heather A Feaga

bioRxiv· April 2025

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YebC2 resolves ribosome stalling and increases fitness of cells lacking EF-P and the ABCF ATPase YfmR.
Hye-Rim Hong, Cassidy R Prince, Letian Wu, Isabella N Lin, Katrina Callan

PLoS Genet· April 2025

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Increased frequency of clonal hematopoiesis of indeterminate potential in Bloom syndrome probands and carriers.
Isabella Lin, Angela Wei, Tsumugi A Gebo, Paul C Boutros, Maeve Flanagan

Haematologica· January 2025

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ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3.
Isabella Lin, Zain Awamleh, Mili Sinvhal, Andrew Wan, Leroy Bondhus

BMC Med Genomics· November 2024

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YebC2 resolves ribosome stalling at polyprolines independent of EF-P and the ABCF ATPase YfmR.
Hye-Rim Hong, Cassidy R Prince, Letian Wu, Isabella N Lin, Heather A Feaga

bioRxiv· October 2024

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Development of Highly Efficient Universal Primers and Their Application in Investigating the Prevalence and Genetic Diversity of in Wild Hares and Rabbits.
Liang Ma, Isabella Lin, Summer T Hunter, Barbara Blasi, Patrizia Danesi

J Fungi (Basel)· May 2024

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Increased Frequency of Clonal Hematopoiesis of Indeterminate Potential in Bloom Syndrome Probands and Carriers.
Isabella Lin, Angela Wei, Tsumugi A Gebo, P C Boutros, Maeve Flanagan

medRxiv· February 2024

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Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation.
Isabella Lin, Angela Wei, Zain Awamleh, Meghna Singh, Aileen Ning

JCI Insight· May 2023

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Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome.
Isabella Lin, Yalda Afshar, Jeffrey Goldstein, Jennifer Grossman, Wayne W Grody

Am J Med Genet A· October 2021

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Massively scaled-up testing for SARS-CoV-2 RNA via next-generation sequencing of pooled and barcoded nasal and saliva samples.
Joshua S Bloom, Laila Sathe, Chetan Munugala, Eric M Jones, Molly Gasperini, Isabella Lin, Jonathan Flint

Nat Biomed Eng· July 2021

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Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing.
Joshua S Bloom, Laila Sathe, Chetan Munugala, Eric M Jones, Molly Gasperini, Isabella Lin, Jonathan Flint

medRxiv· March 2021

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