Jenny Lai

发表

Persistent DNA damage associated with ATM kinase deficiency promotes microglial dysfunction

E. Lee, Michael A. Lodato, Ailsa M. Jeffries, 2022, Nucleic acids research.

Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers

Sakae Tanaka, H. Nakauchi, D. Rowe, 2020, Regenerative therapy.

Prevalence and mechanisms of somatic deletions in single human neurons during normal aging and in DNA repair disorders

E. Lee, Michael A. Lodato, Junho Kim, 2022, Nature Communications.

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

R. Pfundt, A. Hamosh, M. Broly, 2020, Genetics in Medicine.

Single-nucleus transcriptomic analyses reveal microglial activation underlying cerebellar degeneration in Ataxia Telangiectasia

E. Lee, T. Yu, T. Chittenden, 2021 .

Flanking nucleotide specificity for DNA mismatch repair-deficient frameshifts within activin receptor 2 (ACVR2).

J. Carethers, Heekyung Chung, Joy Chaudhry, 2012, Mutation research.

Flanking Sequence Specificity Determines Coding Microsatellite Heteroduplex and Mutation Rates with Defective DNA Mismatch Repair (MMR)

J. Carethers, Heekyung Chung, B. Cabrera, 2010, Oncogene.

ATM-deficiency-induced microglial activation promotes neurodegeneration in ataxia-telangiectasia

E. Lee, T. Yu, T. Chittenden, 2021, bioRxiv.