Weinholtz CA, Zhou L, Muraleedharan Saraswathy V, Xu Y, Klatt Shaw D, McAdow R, Park D, Shin J, Solnica-Krezel L, Johnson AN, Mokalled MH (2026). Transient activation of potent progenitor cells is required for spinal cord regeneration. biorxiv. https://pubmed.ncbi.nlm.nih.gov/41924399/

Klatt Shaw D, Zhou L, Muraleedharan Saraswathy V, McAdow R, Park D, Johnson AN, and Mokalled MH. (2026). Elevated phagocytic capacity directs innate spinal cord repair. Cell Reports. https://pubmed.ncbi.nlm.nih.gov/42247297/

Zhou L, McAdow R, Yamada H, Burris B, Klatt Shaw D, Oonk K, Poss KD, and Mokalled MH. (2023). Progenitor derived glia are required for spinal cord regeneration in zebrafish. Development. https://pubmed.ncbi.nlm.nih.gov/37213080/

Klatt Shaw D and Mokalled MH. (2021). Efficient CRISPR/Cas9 mutagenesis for neurobehavioral screening in adult zebrafish. G3 (Genes, Genomes, Genetics). https://pubmed.ncbi.nlm.nih.gov/33742663/

Klatt Shaw D*, Saraswathy V*, Zhou L*, McAdow R, Burris B, Li T, Morris S, Dietmann S, Zhang B, and Mokalled MH. (2021). Localized EMT reprograms glial progenitors to promote spinal cord repair. Developmental Cell. https://pubmed.ncbi.nlm.nih.gov/33609461/

Wike C, Guo Y, Tan M, Nakamura R, Klatt Shaw D, Durand NC, Aiden EL, Vaquerizas J, Grunwald DJ, Takeda H, Cairns BR. (2021).Chromatin architecture transitions from zebrafish sperm through early embryogenesis. Genome Research. https://pubmed.ncbi.nlm.nih.gov/34006569/

Arveseth CD, Happ JT, Hedeen DS, Zhu J, Capener JL, Klatt Shaw D, Deshpande I, Liang J, Xu J, Stubben SL, Nelson IB, Walker MF, Krogan NJ, Grunwald DJ, Huttenhain R, Manglik A, and Myers BR.(2021). Smoothened Transduces Hedgehog Signals via Activity-Dependent Sequestration of PKA Catalytic Subunits. PLoS Biology. https://pubmed.ncbi.nlm.nih.gov/33886552/

Chagovetz AA, Ritchie E, Klatt Shaw D, Hoshijima K, and Grunwald DJ. (2020). Ryanodine Receptor isotype interactions contribute to muscle fiber type function and development. Disease Models and Mechanisms. https://pmc.ncbi.nlm.nih.gov/articles/PMC6906632/ Selected as Disease Models and Mechanisms Editor’s Choice

Hoshijima K, Jurynec M*, Klatt Shaw D*, Jacobi AM, Behlke MA, and Grunwald DJ. (2019). Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish. Developmental Cell. https://pubmed.ncbi.nlm.nih.gov/31708433/ Highlighted on Faculty of 1000

Klatt Shaw D*, Gunther D*, Jurynec M, Chagovetz AA, Ritchie E, and Grunwald DJ. (2018). Intracellular calcium mobilization is required for Sonic hedgehog signaling. Developmental Cell. https://pubmed.ncbi.nlm.nih.gov/29754802/ Highlighted on Faculty of 1000 and Selected as Best of Developmental Cell 2018