Baxter LL - Search Results

1

Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse.

Baxter LL, Moran TH, Richtsmeier JT, Troncoso J, Reeves RH. Baxter LL, et al. Hum Mol Genet. 2000 Jan 22;9(2):195-202. doi: 10.1093/hmg/9.2.195. Hum Mol Genet. 2000. PMID: 10607830

2

Integration of cytogenetic with recombinational and physical maps of mouse chromosome 16.

Moore CS, Lee JS, Birren B, Stetten G, Baxter LL, Reeves RH. Moore CS, et al. Among authors: baxter ll. Genomics. 1999 Jul 1;59(1):1-5. doi: 10.1006/geno.1999.5812. Genomics. 1999. PMID: 10395793 Free article.

3

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.

Richtsmeier JT, Baxter LL, Reeves RH. Richtsmeier JT, et al. Among authors: baxter ll. Dev Dyn. 2000 Feb;217(2):137-45. doi: 10.1002/(SICI)1097-0177(200002)217:2<137::AID-DVDY1>3.0.CO;2-N. Dev Dyn. 2000. PMID: 10706138 Free article.

4

Too much of a good thing: mechanisms of gene action in Down syndrome.

Reeves RH, Baxter LL, Richtsmeier JT. Reeves RH, et al. Among authors: baxter ll. Trends Genet. 2001 Feb;17(2):83-8. doi: 10.1016/s0168-9525(00)02172-7. Trends Genet. 2001. PMID: 11173117 Review.

5

Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.

Olson LE, Roper RJ, Baxter LL, Carlson EJ, Epstein CJ, Reeves RH. Olson LE, et al. Among authors: baxter ll. Dev Dyn. 2004 Jul;230(3):581-9. doi: 10.1002/dvdy.20079. Dev Dyn. 2004. PMID: 15188443 Free article.

6

Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice.

Roper RJ, Baxter LL, Saran NG, Klinedinst DK, Beachy PA, Reeves RH. Roper RJ, et al. Among authors: baxter ll. Proc Natl Acad Sci U S A. 2006 Jan 31;103(5):1452-6. doi: 10.1073/pnas.0510750103. Epub 2006 Jan 23. Proc Natl Acad Sci U S A. 2006. PMID: 16432181 Free PMC article.

7

A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy.

Matera I, Watkins-Chow DE, Loftus SK, Hou L, Incao A, Silver DL, Rivas C, Elliott EC, Baxter LL, Pavan WJ. Matera I, et al. Among authors: baxter ll. Hum Mol Genet. 2008 Jul 15;17(14):2118-31. doi: 10.1093/hmg/ddn110. Epub 2008 Apr 7. Hum Mol Genet. 2008. PMID: 18397875 Free PMC article.

8

Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann-Pick disease, type C1.

Fu R, Wassif CA, Yanjanin NM, Watkins-Chow DE, Baxter LL, Incao A, Liscum L, Sidhu R, Firnkes S, Graham M, Ory DS, Porter FD, Pavan WJ. Fu R, et al. Among authors: baxter ll. Hum Mol Genet. 2013 Sep 1;22(17):3508-23. doi: 10.1093/hmg/ddt206. Epub 2013 May 10. Hum Mol Genet. 2013. PMID: 23666527 Free PMC article. Clinical Trial.

9

Transcriptome of HPβCD-treated Niemann-Pick disease type C1 cells highlights GPNMB as a biomarker for therapeutics.

Rodriguez-Gil JL, Baxter LL, Watkins-Chow DE, Johnson NL, Davidson CD, Carlson SR, Incao AA; NISC Comparative Sequencing Program; Wallom KL, Farhat NY, Platt FM, Dale RK, Porter FD, Pavan WJ. Rodriguez-Gil JL, et al. Among authors: baxter ll. Hum Mol Genet. 2021 Nov 30;30(24):2456-2468. doi: 10.1093/hmg/ddab194. Hum Mol Genet. 2021. PMID: 34296265 Free PMC article.

10

Analysis of genotype effects and inter-individual variability in iPSC-derived trisomy 21 neural progenitor cells.

Lee SE, Baxter LL, Duran MI, Morris SD, Mosley IA, Fuentes KA, Pennings JLA, Guedj F, Bianchi DW. Lee SE, et al. Among authors: baxter ll. Hum Mol Genet. 2025 Jan 23;34(1):85-100. doi: 10.1093/hmg/ddae160. Hum Mol Genet. 2025. PMID: 39533854

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