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Page 1
Prader-Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion.
Genes (Basel). 2020 Jan 25;11(2):128. doi: 10.3390/genes11020128.
Genes (Basel). 2020.
PMID: 31991769
Free PMC article.
Hypomorphism of Fto and Rpgrip1l causes obesity in mice.
Stratigopoulos G, Burnett LC, Rausch R, Gill R, Penn DB, Skowronski AA, LeDuc CA, Lanzano AJ, Zhang P, Storm DR, Egli D, Leibel RL.
Stratigopoulos G, et al. Among authors: burnett lc.
J Clin Invest. 2016 May 2;126(5):1897-910. doi: 10.1172/JCI85526. Epub 2016 Apr 11.
J Clin Invest. 2016.
PMID: 27064284
Free PMC article.
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Gel formation in protein amyloid aggregation: a physical mechanism for cytotoxicity.
Woodard D, Bell D, Tipton D, Durrance S, Burnett LC, Li B, Xu S.
Woodard D, et al. Among authors: burnett lc.
PLoS One. 2014 Apr 16;9(4):e94789. doi: 10.1371/journal.pone.0094789. eCollection 2014.
PLoS One. 2014.
PMID: 24740416
Free PMC article.
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Human oocytes reprogram adult somatic nuclei of a type 1 diabetic to diploid pluripotent stem cells.
Yamada M, Johannesson B, Sagi I, Burnett LC, Kort DH, Prosser RW, Paull D, Nestor MW, Freeby M, Greenberg E, Goland RS, Leibel RL, Solomon SL, Benvenisty N, Sauer MV, Egli D.
Yamada M, et al. Among authors: burnett lc.
Nature. 2014 Jun 26;510(7506):533-6. doi: 10.1038/nature13287. Epub 2014 Apr 28.
Nature. 2014.
PMID: 24776804
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Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes.
Burnett LC, Hubner G, LeDuc CA, Morabito MV, Carli JFM, Leibel RL.
Burnett LC, et al.
Hum Mol Genet. 2017 Dec 1;26(23):4606-4616. doi: 10.1093/hmg/ddx342.
Hum Mol Genet. 2017.
PMID: 28973544
Free PMC article.
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