Griffin, JN., Liu, KJ., Sempou, E. (2020) Editorial: Xenopus Models of Organogenesis and Disease. Frontiers in Physiology. doi: 10.3389/fphys.2020.00534

Harel, T.*, Griffin, JN.*, Arbogast, T.*, Monroe, T., Palombo, Marcella Martinelli, Marco Seri, Tommaso Pippucci, Orly Elpeleg, Nicholas Katsanis (2020). Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies. Human Molecular Genetics doi: 10.1093/hmg/ddaa073 (*Co-first author)

Alharatani, R., Ververi, A., Beleza-Meireles, A., Ji, W., Mis, E., Patterson, Q., Griffin, JN., Bhujel, N., Chang, C., Dixit, A., Konstantino, M., Healy, C., Hannan, S., Neo, N., Cash, A., Li, D., Bhoj, E., Zackai, E., Cleaver, R., Baralle, D., McEntagart, M., Newbury-Ecob, R., Scott, R., Hurst, J., Au, P., Hosey, MT., Khokha, M., Marciano, D., Lakhani, S., Liu, KJ (2020). Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome, Human Molecular Genetics, doi: 10.1093/hmg/ddaa050

Duncan, A., Robson, A., Khokha, M., and Griffin, JN. (2019) TMEM195, a heterotaxy candidate gene, regulates left-right patterning via Wnt signaling. Dev Biol doi: 10.1016/j.ydbio.2019.07.019.

Barrell, W., Griffin, JN, Harvey-Cox, J., Danovi, D., HipSci Consortium, Beales, P., Grigoriadis, A. and Liu, K. (2019) Induction of neural crest stem cells from Bardet-Biedl Syndrome patient derived hiPSCs. Frontiers in Molecular Neuroscience doi: 10.3389/fnmol.2019.00139.

Alharatani, R., Griffin, J. N., Liu, K.J., Expression of the small GTPase RAPGEF5 during mouse and human development (2019). Gene Expr Patterns. doi: 10.1016/j.gep.2019.119057

 Griffin, J. N, Sondalle, S., Robson, A., Mis, E., Baserga, Griffin, G., Deniz, E., S., Khokha. M. (2018). RPSA is required for rRNA processing and spleen development in Xenopus. Development doi: 10.1242/dev.166181

Kulkarni, S. S., Griffin, J. N., Date, P. P., Liem, K. F., Jr. And Khokha, M. K. (2018). WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation. Developmental Cell 46, 595-610 e593

Griffin, J.N., Del Viso, F., Duncan, A.R., Robson, A., Hwang, W., Kulkarni, S., Liu, K.J., Khokha, M.K., (2018). RAPGEF5 Regulates Nuclear Translocation of beta-Catenin. Developmental Cell 44, 248-260 e244.

Deniz, E., Jonas, S., Hooper, M., Griffin, J. N., Choma, M., Khokha, M. (2017). Analysis of Craniocardiac Malformations in Xenopus using OpticalCoherence Tomography. Scientific Reports 7, 42506; doi: 10.1038/srep42506

Robson, A., Owens, N. D., Baserga, S. J., Khokha, M. K. & Griffin, J. N.* (2016) Expression of ribosomopathy genes during Xenopus tropicalis embryogenesis. BMC Dev Biol 16, 38, doi:10.1186/s12861-016-0138-5. (* Author of correspondence)

 Griffin, J. N., Sondalle, S. B., del Viso, F., Baserga, S. J., Khokha, M. K. (2015) The Ribosome Biogenesis Factor Nol11 Is Required for Optimal rDNA Transcription and Craniofacial Development in Xenopus. PLoS Genetics 11(3): e1005018. doi:10.1371 (Faculty of 1000 recommended)

Compagnucci, C., Debiais, M., Coolen, M., Fish, J., Griffin, J. N., Bertocchini, F., Minoux, M., Rijli, FM., Borday-Birraux, V., Casane, D., Mazan, S., Depew, M. (2013). Pattern and Polarity in the Development and Evolution of the Gnathostome Jaw: Both Conservation and Heterotopy in the Branchial Arches of the Shark, Scyliorhinus canicula. Developmental Biology 1;374(1):185-97

Griffin J. N., Compagnucci, C., Hu, D., Fish, J., Klein, O., Marcucio. R., Depew, M. J., (2013). Fgf8 dosage determines midfacial integration and polarity within the nasal and optic capsules. Developmental Biology.1;374(1):185-97

Suture Neontology and Paleontology: The Bases for Where, When and How Boundaries between Bones Have Been Established and Have Evolved. Depew, M.; Compagnucci, C.; Griffin, J. Craniofacial Sutures. Development, Disease and Treatment, Rice DP (ed). Front Oral Biol. Basel, Karger, 2008, vol 12, pp 57-78


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