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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 3 |
2022 | 1 |
2023 | 2 |
2024 | 0 |
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6 results
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Page 1
A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels.
Genes Dev. 2023 Oct 1;37(19-20):883-900. doi: 10.1101/gad.350733.123. Epub 2023 Oct 27.
Genes Dev. 2023.
PMID: 37890975
Free PMC article.
Disruption of MeCP2-TCF20 complex underlies distinct neurodevelopmental disorders.
Zhou J, Hamdan H, Yalamanchili HK, Pang K, Pohodich AE, Lopez J, Shao Y, Oses-Prieto JA, Li L, Kim W, Durham MA, Bajikar SS, Palmer DJ, Ng P, Thompson ML, Bebin EM, Müller AJ, Kuechler A, Kampmeier A, Haack TB, Burlingame AL, Liu Z, Rasband MN, Zoghbi HY.
Zhou J, et al.
Proc Natl Acad Sci U S A. 2022 Jan 25;119(4):e2119078119. doi: 10.1073/pnas.2119078119.
Proc Natl Acad Sci U S A. 2022.
PMID: 35074918
Free PMC article.
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MeCP2 regulates Gdf11, a dosage-sensitive gene critical for neurological function.
Bajikar SS, Anderson AG, Zhou J, Durham MA, Trostle AJ, Wan YW, Liu Z, Zoghbi HY.
Bajikar SS, et al.
Elife. 2023 Feb 27;12:e83806. doi: 10.7554/eLife.83806.
Elife. 2023.
PMID: 36848184
Free PMC article.
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Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.
Ravenscroft TA, Phillips JB, Fieg E, Bajikar SS, Peirce J, Wegner J, Luna AA, Fox EJ, Yan YL, Rosenfeld JA, Zirin J, Kanca O; Undiagnosed Diseases Network; Benke PJ, Cameron ES, Strehlow V, Platzer K, Jamra RA, Klöckner C, Osmond M, Licata T, Rojas S, Dyment D, Chong JSC, Lincoln S, Stoler JM, Postlethwait JH, Wangler MF, Yamamoto S, Krier J, Westerfield M, Bellen HJ.
Ravenscroft TA, et al.
Genet Med. 2021 Oct;23(10):1889-1900. doi: 10.1038/s41436-021-01216-8. Epub 2021 Jun 10.
Genet Med. 2021.
PMID: 34113007
Free PMC article.
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Antisense oligonucleotide therapy in a humanized mouse model of MECP2 duplication syndrome.
Shao Y, Sztainberg Y, Wang Q, Bajikar SS, Trostle AJ, Wan YW, Jafar-Nejad P, Rigo F, Liu Z, Tang J, Zoghbi HY.
Shao Y, et al.
Sci Transl Med. 2021 Mar 3;13(583):eaaz7785. doi: 10.1126/scitranslmed.aaz7785.
Sci Transl Med. 2021.
PMID: 33658357
Free PMC article.
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Identification and characterization of conserved noncoding cis-regulatory elements that impact Mecp2 expression and neurological functions.
Shao Y, Bajikar SS, Tirumala HP, Gutierrez MC, Wythe JD, Zoghbi HY.
Shao Y, et al.
Genes Dev. 2021 Apr 1;35(7-8):489-494. doi: 10.1101/gad.345397.120. Epub 2021 Mar 18.
Genes Dev. 2021.
PMID: 33737384
Free PMC article.
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