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yu yuan tan
(3 results)?
Pioneer factor ASCL1 cooperates with the mSWI/SNF complex at distal regulatory elements to regulate human neural differentiation.
Genes Dev. 2023 Mar 1;37(5-6):218-242. doi: 10.1101/gad.350269.122. Epub 2023 Mar 17.
Genes Dev. 2023.
PMID: 36931659
Free PMC article.
RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis.
Wong S, Tan YX, Loh AYT, Tan KY, Lee H, Aziz Z, Nelson SF, Özkan E, Kayserili H, Escande-Beillard N, Reversade B.
Wong S, et al. Among authors: tan yx.
EMBO Mol Med. 2023 May 8;15(5):e17078. doi: 10.15252/emmm.202217078. Epub 2023 Apr 17.
EMBO Mol Med. 2023.
PMID: 37066513
Free PMC article.
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Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica.
Kariminejad A, Afroozan F, Bozorgmehr B, Ghanadan A, Akbaroghli S, Khorram Khorshid HR, Mojahedi F, Setoodeh A, Loh A, Tan YX, Escande-Beillard N, Malfait F, Reversade B, Gardeitchik T, Morava E.
Kariminejad A, et al. Among authors: tan yx.
Int J Mol Sci. 2017 Mar 15;18(3):635. doi: 10.3390/ijms18030635.
Int J Mol Sci. 2017.
PMID: 28294978
Free PMC article.
Review.
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Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa.
Fischer-Zirnsak B, Escande-Beillard N, Ganesh J, Tan YX, Al Bughaili M, Lin AE, Sahai I, Bahena P, Reichert SL, Loh A, Wright GD, Liu J, Rahikkala E, Pivnick EK, Choudhri AF, Krüger U, Zemojtel T, van Ravenswaaij-Arts C, Mostafavi R, Stolte-Dijkstra I, Symoens S, Pajunen L, Al-Gazali L, Meierhofer D, Robinson PN, Mundlos S, Villarroel CE, Byers P, Masri A, Robertson SP, Schwarze U, Callewaert B, Reversade B, Kornak U.
Fischer-Zirnsak B, et al. Among authors: tan yx.
Am J Hum Genet. 2015 Sep 3;97(3):483-92. doi: 10.1016/j.ajhg.2015.08.001. Epub 2015 Aug 27.
Am J Hum Genet. 2015.
PMID: 26320891
Free PMC article.
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