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Alexandria Blackburn - Publications

Affiliations: 
2017- Pediatrics McGovern Medical School - UT 
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4 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Hong JY, Zapata J, Blackburn A, Baumert R, Bae SM, Ji H, Nam HJ, Miller RK, McCrea PD. A catenin of the plakophilin-subfamily, Pkp3, responds to canonical-Wnt pathway components and signals. Biochemical and Biophysical Research Communications. 563: 31-39. PMID 34058472 DOI: 10.1016/j.bbrc.2021.05.043  0.497
2019 Blackburn ATM, Bekheirnia N, Uma VC, Corkins ME, Xu Y, Rosenfeld JA, Bainbridge MN, Yang Y, Liu P, Madan-Khetarpal S, Delgado MR, Hudgins L, Krantz I, Rodriguez-Buritica D, Wheeler PG, et al. Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31857706 DOI: 10.1038/s41436-019-0732-6  0.577
2019 Blackburn ATM, Bekheirnia N, Uma VC, Corkins ME, Xu Y, Rosenfeld JA, Bainbridge MN, Yang Y, Liu P, Madan-Khetarpal S, Delgado MR, Hudgins L, Krantz I, Rodriguez-Buritica D, Wheeler PG, et al. DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31263215 DOI: 10.1038/S41436-019-0576-0  0.578
2019 Blackburn ATM, Miller RK. Modeling congenital kidney diseases in . Disease Models & Mechanisms. 12. PMID 30967415 DOI: 10.1242/Dmm.038604  0.518
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