2017 Publications

PMID | 28265587

Deciphering cell-cell communication in the developing mammalian brain. Yuzwa SA, Miller FD. Neurogenesis (Austin). 2017 Feb 6;4(1):e1286425

PMID | 27899382

A Metastatic Mouse Model Identifies Genes That Regulate Neuroblastoma Metastasis. Seong BK, Fathers KE, Hallett R, Yung CK, Stein LD, Mouaaz S, Kee L, Hawkins CE, Irwin MS, Kaplan DR. Cancer Res. 2017 Feb 1;77(3):696-706. doi: 10.1158/0008-5472.CAN-16-1502. Epub 2016 Nov 29

PMID | 28472653

Migrating Interneurons Secrete Fractalkine to Promote Oligodendrocyte Formation in the Developing Mammalian Brain. Voronova A, Yuzwa SA, Wang BS, Zahr S, Syal C, Wang J, Kaplan DRMiller FD. Neuron. 2017 May 3;94(3):500-516

PMID | 201705085

A neuroprotective agent that inactivates prodegenerative TrkA and preserves mitochondria. Feinberg K., Kolaj A., Rubin L., Miller F.D., and Kaplan D.R. (2017) J. Cell Biol. 216:3655-3675.

PMID | 29284841

Developmental Emergence of Adult Neural Stem Cells as Revealed by Single-Cell Transcriptional Profiling. Yuzwa SA, Borrett MJ, Innes BT, Voronova A, Ketela T, Kaplan DR, Bader GD, Miller FD. Cell Rep. 2017 Dec 26;21(13):3970-3986

Other Publications

PMID | 28696690

A Kinome-Wide Selective Radiolabeled TrkB/C Inhibitor for in Vitro and in Vivo Neuroimaging: Synthesis, Preclinical Evaluation, and First-in-Human. Bernard-Gauthier V, Bailey JJ, Mossine AV, Lindner S, Vomacka L, Aliaga A, Shao X, Quesada CA, Sherman P, Mahringer A, Kostikov A, Grand’Maison M, Rosa-Neto P, Soucy JP, Thiel A, Kaplan DR, Fricker G, Wängler B, Bartenstein P, Schirrmacher R, Scott PJH. J Med Chem. 2017 Aug 24;60(16):6897-6910

PMID | 28766011

RNAi screen identifies essential regulators of human brain metastasis-initiating cells. Singh M, Venugopal C, Tokar T, Brown KR, McFarlane N, Bakhshinyan D, Vijayakumar T, Manoranjan B, Mahendram S, Vora P, Qazi M, Dhillon M, Tong A, Durrer K, Murty N, Hallet R, Hassell JA, Kaplan DR, Cutz JC, Jurisica I, Moffat J, Singh SK. Acta Neuropathol. 2017 Dec;134(6):923-940

PMID | 28453519

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation. Ravindran E, Hu H, Yuzwa SA, Hernandez-Miranda LR, Kraemer N, Ninnemann O, Musante L, Boltshauser E, Schindler D, Hübner A, Reinecker HC, Ropers HH, Birchmeier C, Miller FD, Wienker TF, Hübner C, Kaindl AM. PLoS Genet. 2017 Apr 28;13(4):e1006746