Zhang L - Search Results

1

Leveraging the Mendelian disorders of the epigenetic machinery to systematically map functional epigenetic variation.

Luperchio TR, Boukas L, Zhang L, Pilarowski G, Jiang J, Kalinousky A, Hansen KD, Bjornsson HT. Luperchio TR, et al. Among authors: zhang l. Elife. 2021 Aug 31;10:e65884. doi: 10.7554/eLife.65884. Elife. 2021. PMID: 34463256 Free PMC article.

2

Histone deacetylase inhibition rescues structural and functional brain deficits in a mouse model of Kabuki syndrome.

Bjornsson HT, Benjamin JS, Zhang L, Weissman J, Gerber EE, Chen YC, Vaurio RG, Potter MC, Hansen KD, Dietz HC. Bjornsson HT, et al. Among authors: zhang l. Sci Transl Med. 2014 Oct 1;6(256):256ra135. doi: 10.1126/scitranslmed.3009278. Sci Transl Med. 2014. PMID: 25273096 Free PMC article.

3

A ketogenic diet rescues hippocampal memory defects in a mouse model of Kabuki syndrome.

Benjamin JS, Pilarowski GO, Carosso GA, Zhang L, Huso DL, Goff LA, Vernon HJ, Hansen KD, Bjornsson HT. Benjamin JS, et al. Among authors: zhang l. Proc Natl Acad Sci U S A. 2017 Jan 3;114(1):125-130. doi: 10.1073/pnas.1611431114. Epub 2016 Dec 20. Proc Natl Acad Sci U S A. 2017. PMID: 27999180 Free PMC article.

4

Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities.

Sobreira N, Brucato M, Zhang L, Ladd-Acosta C, Ongaco C, Romm J, Doheny KF, Mingroni-Netto RC, Bertola D, Kim CA, Perez AB, Melaragno MI, Valle D, Meloni VA, Bjornsson HT. Sobreira N, et al. Among authors: zhang l. Eur J Hum Genet. 2017 Dec;25(12):1335-1344. doi: 10.1038/s41431-017-0023-0. Epub 2017 Nov 7. Eur J Hum Genet. 2017. PMID: 29255178 Free PMC article.

5

Precocious neuronal differentiation and disrupted oxygen responses in Kabuki syndrome.

Carosso GA, Boukas L, Augustin JJ, Nguyen HN, Winer BL, Cannon GH, Robertson JD, Zhang L, Hansen KD, Goff LA, Bjornsson HT. Carosso GA, et al. Among authors: zhang l. JCI Insight. 2019 Oct 17;4(20):e129375. doi: 10.1172/jci.insight.129375. JCI Insight. 2019. PMID: 31465303 Free PMC article.

6

Abnormal Peyer patch development and B-cell gut homing drive IgA deficiency in Kabuki syndrome.

Pilarowski GO, Cazares T, Zhang L, Benjamin JS, Liu K, Jagannathan S, Mousa N, Kasten J, Barski A, Lindsley AW, Bjornsson HT. Pilarowski GO, et al. Among authors: zhang l. J Allergy Clin Immunol. 2020 Mar;145(3):982-992. doi: 10.1016/j.jaci.2019.11.034. Epub 2019 Dec 6. J Allergy Clin Immunol. 2020. PMID: 31816409

7

Inhibition of KDM1A activity restores adult neurogenesis and improves hippocampal memory in a mouse model of Kabuki syndrome.

Zhang L, Pilarowski G, Pich EM, Nakatani A, Dunlop J, Baba R, Matsuda S, Daini M, Hattori Y, Matsumoto S, Ito M, Kimura H, Bjornsson HT. Zhang L, et al. Mol Ther Methods Clin Dev. 2021 Feb 18;20:779-791. doi: 10.1016/j.omtm.2021.02.011. eCollection 2021 Mar 12. Mol Ther Methods Clin Dev. 2021. PMID: 33738331 Free PMC article.

8

Kabuki syndrome stem cell models reveal locus specificity of histone methyltransferase 2D (KMT2D/MLL4).

Jefri M, Zhang X, Stumpf PS, Zhang L, Peng H, Hettige N, Theroux JF, Aouabed Z, Wilson K, Deshmukh S, Antonyan L, Ni A, Alsuwaidi S, Zhang Y, Jabado N, Garcia BA, Schuppert A, Bjornsson HT, Ernst C. Jefri M, et al. Among authors: zhang l, zhang x, zhang y. Hum Mol Genet. 2022 Oct 28;31(21):3715-3728. doi: 10.1093/hmg/ddac121. Hum Mol Genet. 2022. PMID: 35640156 Free PMC article.

9

SMYD5 is a novel epigenetic gatekeeper of the mild hypothermia response.

Rafnsdottir S, Jang K, Halldorsdottir ST, Tomasdottir A, Vinod M, Möller K, Reynisdottir T, Atladottir LH, Allison KE, He J, Zhang L, Northington FJ, Chavez-Valdez R, Anderson KJ, Bjornsson HT. Rafnsdottir S, et al. Among authors: zhang l. bioRxiv [Preprint]. 2023 Jun 9:2023.05.11.540170. doi: 10.1101/2023.05.11.540170. bioRxiv. 2023. PMID: 37333301 Free PMC article. Preprint.

10

KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans.

Kalinousky AJ, Luperchio TR, Schrode KM, Harris JR, Zhang L, DeLeon VB, Fahrner JA, Lauer AM, Bjornsson HT. Kalinousky AJ, et al. Among authors: zhang l. Genes (Basel). 2023 Dec 28;15(1):48. doi: 10.3390/genes15010048. Genes (Basel). 2023. PMID: 38254937 Free PMC article.

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