ZFIN ID: ZDB-LAB-170531-1
Engle Lab
PI/Director: Engle, Elizabeth
Contact Person: Chan, Wai-Man
Email: wchan@enders.tch.harvard.edu
URL:
Address: Boston Children's Hospital Neurology / Engle Lab, CLS14075, BCH3149 3 Blackfan Circle Boston, MA 02115
Country: United States
Phone: 617-919-2751
Fax: 6177304834
Line Designation: cl


GENOMIC FEATURES ORIGINATING FROM THIS LAB
Show all 1 genomic features


STATEMENT OF RESEARCH INTERESTS
Zebrafish modeling of cranial motor neuron and cranial muscle development


LAB MEMBERS
Di Gioia, Silvio Alessandro Post-Doc Gilette, Nicole Technical Staff Chan, Wai-Man Administrative Staff


ZEBRAFISH PUBLICATIONS OF LAB MEMBERS
Frints, S.G.M., Hennig, F., Colombo, R., Jacquemont, S., Terhal, P., Zimmerman, H.H., Hunt, D., Mendelsohn, B.A., Kordaß, U., Webster, R., Sinnema, M., Abdul-Rahman, O., Suckow, V., Deciphering Developmental Disorders (DDD) Study, Fernández-Jaén, A., van Roozendaal, K., Stevens, S.J.C., Macville, M.V.E., Al-Nasiry, S., van Gassen, K., Utzig, N., Koudijs, S.M., McGregor, L., Maas, S.M., Baralle, D., Dixit, A., Wieacker, P., Lee, M., Lee, A.S., Engle, E.C., Houge, G., Gradek, G.A., Douglas, A.G.L., Longman, C., Joss, S., Velasco, D., Hennekam, R.C., Hirata, H., Kalscheuer, V.M. (2019) Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita. Human Mutation. 40(12):2270-2285
Di Gioia, S.A., Connors, S., Matsunami, N., Cannavino, J., Rose, M.F., Gilette, N.M., Artoni, P., de Macena Sobreira, N.L., Chan, W.M., Webb, B.D., Robson, C.D., Cheng, L., Van Ryzin, C., Ramirez-Martinez, A., Mohassel, P., Leppert, M., Scholand, M.B., Grunseich, C., Ferreira, C.R., Hartman, T., Hayes, I.M., Morgan, T., Markie, D.M., Fagiolini, M., Swift, A., Chines, P.S., Speck-Martins, C.E., Collins, F.S., Jabs, E.W., Bönnemann, C.G., Olson, E.N., Carey, J.C., Robertson, S.P., Manoli, I., Engle, E.C. (2017) A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome. Nature communications. 8:16077