Justice MJ - Search Results

1

Aberrant lung lipids cause respiratory impairment in a Mecp2-deficient mouse model of Rett syndrome.

Vashi N, Ackerley C, Post M, Justice MJ. Vashi N, et al. Among authors: justice mj. Hum Mol Genet. 2021 Nov 1;30(22):2161-2176. doi: 10.1093/hmg/ddab182. Hum Mol Genet. 2021. PMID: 34230964 Free PMC article.

2

Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome.

Bi W, Ohyama T, Nakamura H, Yan J, Visvanathan J, Justice MJ, Lupski JR. Bi W, et al. Among authors: justice mj. Hum Mol Genet. 2005 Apr 15;14(8):983-95. doi: 10.1093/hmg/ddi085. Epub 2005 Mar 3. Hum Mol Genet. 2005. PMID: 15746153

3

A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.

Buchovecky CM, Turley SD, Brown HM, Kyle SM, McDonald JG, Liu B, Pieper AA, Huang W, Katz DM, Russell DW, Shendure J, Justice MJ. Buchovecky CM, et al. Among authors: justice mj. Nat Genet. 2013 Sep;45(9):1013-20. doi: 10.1038/ng.2714. Epub 2013 Jul 28. Nat Genet. 2013. PMID: 23892605 Free PMC article.

4

MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex.

Kyle SM, Saha PK, Brown HM, Chan LC, Justice MJ. Kyle SM, et al. Among authors: justice mj. Hum Mol Genet. 2016 Jul 15;25(14):3029-3041. doi: 10.1093/hmg/ddw156. Epub 2016 Jun 10. Hum Mol Genet. 2016. PMID: 27288453 Free PMC article.

5

Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.

Allemang-Grand R, Ellegood J, Spencer Noakes L, Ruston J, Justice M, Nieman BJ, Lerch JP. Allemang-Grand R, et al. Mol Autism. 2017 Jun 26;8:32. doi: 10.1186/s13229-017-0138-8. eCollection 2017. Mol Autism. 2017. PMID: 28670438 Free PMC article.

6

Rett syndrome: a neurological disorder with metabolic components.

Kyle SM, Vashi N, Justice MJ. Kyle SM, et al. Among authors: justice mj. Open Biol. 2018 Feb;8(2):170216. doi: 10.1098/rsob.170216. Open Biol. 2018. PMID: 29445033 Free PMC article. Review.

7

Treating Rett syndrome: from mouse models to human therapies.

Vashi N, Justice MJ. Vashi N, et al. Among authors: justice mj. Mamm Genome. 2019 Jun;30(5-6):90-110. doi: 10.1007/s00335-019-09793-5. Epub 2019 Feb 28. Mamm Genome. 2019. PMID: 30820643 Free PMC article. Review.

8

Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathology.

Enikanolaiye A, Ruston J, Zeng R, Taylor C, Schrock M, Buchovecky CM, Shendure J, Acar E, Justice MJ. Enikanolaiye A, et al. Among authors: justice mj. Genome Res. 2020 Apr;30(4):540-552. doi: 10.1101/gr.258400.119. Epub 2020 Apr 21. Genome Res. 2020. PMID: 32317254 Free PMC article.

9

Mouse ENU mutagenesis.

Justice MJ, Noveroske JK, Weber JS, Zheng B, Bradley A. Justice MJ, et al. Hum Mol Genet. 1999;8(10):1955-63. doi: 10.1093/hmg/8.10.1955. Hum Mol Genet. 1999. PMID: 10469849 Review.

10

Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome.

Yan J, Keener VW, Bi W, Walz K, Bradley A, Justice MJ, Lupski JR. Yan J, et al. Among authors: justice mj. Hum Mol Genet. 2004 Nov 1;13(21):2613-24. doi: 10.1093/hmg/ddh288. Epub 2004 Sep 30. Hum Mol Genet. 2004. PMID: 15459175

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

203 results

Search Page