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Translating multiscale research in rare disease.
Hooper KM, Justice MJ, Lek M, Liu KJ, Rauen KA. Hooper KM, et al. Among authors: liu kj. Dis Model Mech. 2024 Jun 1;17(6):dmm052009. doi: 10.1242/dmm.052009. Epub 2024 Jul 10. Dis Model Mech. 2024. PMID: 38982973 Free PMC article.
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome.
Alharatani R, Ververi A, Beleza-Meireles A, Ji W, Mis E, Patterson QT, Griffin JN, Bhujel N, Chang CA, Dixit A, Konstantino M, Healy C, Hannan S, Neo N, Cash A, Li D, Bhoj E, Zackai EH, Cleaver R, Baralle D, McEntagart M, Newbury-Ecob R, Scott R, Hurst JA, Au PYB, Hosey MT, Khokha M, Marciano DK, Lakhani SA, Liu KJ. Alharatani R, et al. Among authors: liu kj. Hum Mol Genet. 2020 Jul 21;29(11):1900-1921. doi: 10.1093/hmg/ddaa050. Hum Mol Genet. 2020. PMID: 32196547 Free PMC article.
Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes.
Tabler JM, Barrell WB, Szabo-Rogers HL, Healy C, Yeung Y, Perdiguero EG, Schulz C, Yannakoudakis BZ, Mesbahi A, Wlodarczyk B, Geissmann F, Finnell RH, Wallingford JB, Liu KJ. Tabler JM, et al. Among authors: liu kj. Dev Cell. 2013 Jun 24;25(6):623-35. doi: 10.1016/j.devcel.2013.05.021. Dev Cell. 2013. PMID: 23806618 Free PMC article.
Micrognathia in mouse models of ciliopathies.
Adel Al-Lami H, Barrell WB, Liu KJ. Adel Al-Lami H, et al. Among authors: liu kj. Biochem Soc Trans. 2016 Dec 15;44(6):1753-1759. doi: 10.1042/BST20160241. Biochem Soc Trans. 2016. PMID: 27913686 Review.
Animal models of craniofacial anomalies.
Liu KJ. Liu KJ. Dev Biol. 2016 Jul 15;415(2):169-170. doi: 10.1016/j.ydbio.2016.06.008. Dev Biol. 2016. PMID: 27321071 Free article. No abstract available.
610 results