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Shalin H. Naik on Muck Rack

Shalin H. Naik

Melbourne
As seen in: Nature, Cell Press, The Journal of Immunology
Scientist @WEHI_research, Host of thejabgab.com podcast, part-time singer of the #Inflammatones, co-host of #AskTheDoctor and #ABCCatalyst on @ABCTV.
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Articles

LoxCode in vivo barcoding reveals epiblast clonal fate bias to fetal organs

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By Tom Weber Verified, Christine Biben, Denise Miles, Stefan Glaser, Sara Tomei, Cheng-Yu Lin, Andrew J Kueh, Martin Pal, Stephen Zhang, Patrick P.L. Tam, Shalin H. Naik, Samir Taoudi
| Cell Press Verified
Keywords clonal barcoding epiblast phylogenetics pedigree lineage tracing Cre embryogenesis cell fate mathematical modeling Get full text access Log in, subscribe or purchase for full access. References 1. Lawson, K.A. ∙ Meneses, J.J. ∙ Pedersen, R.A. Clonal analysis of epiblast fate during germ layer formation in the mouse embryo Development. 1991; 113:891-911 2. Tam, P.P. ∙ Behringer, R.R. Mouse gastrulation: the formation of a mammalian body plan Mech. Dev. 1997; 68:3-25 3. Thomas, P.
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Experimental and spontaneous metastasis assays can result in divergence in clonal architecture - Communications Biology

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By Antonin Serrano, Tom Weber Verified, Jean Berthelet, Emmanuelle Charafe-Jauffret, Christophe Ginestier, John M. Mariadason, Shalin H. Naik
| Nature Verified
Abstract Intratumoural heterogeneity is associated with poor outcomes in breast cancer. To understand how malignant clones survive and grow in metastatic niches, in vivo models using cell lines and patient-derived xenografts (PDX) have become the gold standard.
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tDCs — a distinct subset with dual functional and developmental roles - Nature Immunology

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By Shalin H. Naik
| Nature Verified
Confusion exists as to whether transitional dendritic cells are a bone fide subset or just a transitional state, as the name indicates. New data are complicating matters further by showing some interesting heterogeneity in these cells. Dendritic cells (DCs) can be divided into at least three major subsets that are conserved between mice and humans: type 1 conventional DCs (cDC1s); type 2 cDCs (cDC2s); and plasmacytoid DCs (pDCs).
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