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iPSC-derived β cells model diabetes due to glucokinase deficiency.
Hua H, Shang L, Martinez H, Freeby M, Gallagher MP, Ludwig T, Deng L, Greenberg E, LeDuc C, Chung WK, Goland R, Leibel RL, Egli D. Hua H, et al. Among authors: shang l. J Clin Invest. 2017 Mar 1;127(3):1115. doi: 10.1172/JCI92775. Epub 2017 Jan 17. J Clin Invest. 2017. PMID: 28094769 Free PMC article. No abstract available.
iPSC-derived β cells model diabetes due to glucokinase deficiency.
Hua H, Shang L, Martinez H, Freeby M, Gallagher MP, Ludwig T, Deng L, Greenberg E, Leduc C, Chung WK, Goland R, Leibel RL, Egli D. Hua H, et al. Among authors: shang l. J Clin Invest. 2013 Jul;123(7):3146-53. doi: 10.1172/JCI67638. Epub 2013 Jun 17. J Clin Invest. 2013. Retraction in: J Clin Invest. 2017 Mar 1;127(3):1115. doi: 10.1172/JCI92775 PMID: 23778137 Free PMC article. Retracted.
Bardet-Biedl syndrome proteins regulate intracellular signaling and neuronal function in patient-specific iPSC-derived neurons.
Wang L, Liu Y, Stratigopoulos G, Panigrahi S, Sui L, Zhang Y, Leduc CA, Glover HJ, De Rosa MC, Burnett LC, Williams DJ, Shang L, Goland R, Tsang SH, Wardlaw S, Egli D, Zheng D, Doege CA, Leibel RL. Wang L, et al. Among authors: shang l. J Clin Invest. 2021 Apr 15;131(8):e146287. doi: 10.1172/JCI146287. J Clin Invest. 2021. PMID: 33630762 Free PMC article.
Congenital diaphragmatic hernias: from genes to mechanisms to therapies.
Kardon G, Ackerman KG, McCulley DJ, Shen Y, Wynn J, Shang L, Bogenschutz E, Sun X, Chung WK. Kardon G, et al. Among authors: shang l. Dis Model Mech. 2017 Aug 1;10(8):955-970. doi: 10.1242/dmm.028365. Dis Model Mech. 2017. PMID: 28768736 Free PMC article. Review.
Mutations in ARID2 are associated with intellectual disabilities.
Shang L, Cho MT, Retterer K, Folk L, Humberson J, Rohena L, Sidhu A, Saliganan S, Iglesias A, Vitazka P, Juusola J, O'Donnell-Luria AH, Shen Y, Chung WK. Shang L, et al. Neurogenetics. 2015 Oct;16(4):307-14. doi: 10.1007/s10048-015-0454-0. Epub 2015 Aug 4. Neurogenetics. 2015. PMID: 26238514
De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism.
Shang L, Henderson LB, Cho MT, Petrey DS, Fong CT, Haude KM, Shur N, Lundberg J, Hauser N, Carmichael J, Innis J, Schuette J, Wu YW, Asaikar S, Pearson M, Folk L, Retterer K, Monaghan KG, Chung WK. Shang L, et al. Neurogenetics. 2016 Jan;17(1):43-9. doi: 10.1007/s10048-015-0466-9. Epub 2015 Nov 17. Neurogenetics. 2016. PMID: 26576547 Free PMC article.
2,195 results