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Cell Chemical Biology|November 23, 2021
PALP: A rapid imaging technique for stratifying ferroptosis sensitivity in normal and tumor tissues in situFengxiang Wang, Emily T Graham, Nathchar Naowarojna, et al.Experimental Biology and Medicine (Maywood, N.J.)|September 2, 2025
Natural killer cell subpopulations in the peripheral blood of single ventricle/hypoplastic left heart syndrome patients via single-cell RNA sequencingHui-Qi Qu, Kushagra Goel, Kayleigh Ostberg, et al.Biomaterials|March 25, 2011
The effect of CD47 modified polymer surfaces on inflammatory cell attachment and activationStanley J Stachelek, Matthew J Finley, Ivan S Alferiev, et al.Cell|November 26, 2024
ACSL4 and polyunsaturated lipids support metastatic extravasation and colonizationYuqi Wang, Mangze Hu, Jian Cao, et al.BMC Musculoskeletal Disorders|November 11, 2016
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing studyChristopher J Cardinale, Dong Li, Lifeng Tian, et al.Human Genomics|November 13, 2015
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligamentsYichuan Liu, Yun Li, Michael E March, et al.Ophthalmic Genetics|February 20, 2014
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital AmaurosisYiran Guo, Ivan Prokudin, Cong Yu, et al.Journal of Immunology (Baltimore, Md. : 1950)|July 19, 2015
Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food AllergyJin Li, Irene Fung, Joseph T Glessner, et al.The Journal of Allergy and Clinical Immunology|April 19, 2011
Genome-wide association identifies diverse causes of common variable immunodeficiencyJordan S Orange, Joseph T Glessner, Elena Resnick, et al.Plos One|February 6, 2013
Copy number variations in alternative splicing gene networks impact lifespanJoseph T Glessner, Albert Vernon Smith, Saarene Panossian, et al.Pageof 7