Morpholino Publication Database

Chang H-W, Wang W-D, Chiu C-C, Chen C-H, Wang Y-S, Chen Z-Y, Liu W, Tai M-H, Wen Z-H, Wu C-Y. Ftr82 Is Critical for Vascular Patterning during Zebrafish Development. Int J Mol Sci. 2017;18(1):156. doi:10.3390/ijms18010156.

Macia MS, Halbritter J, Delous M, Bredrup C, Gutter A, Filhol E, Mellgren AEC, Leh S, Bizet A, Braun DA, Gee HY, Silbermann F, Henry C, Krug P, Bole-Feysot C, Nitschké P, Joly D, Nicoud P, Paget A, Haugland H, Brackmann D, Ahmet N, Sandford R, Cengiz N, Knappskog PM, Boman H, Linghu B, Yang F, Oakeley EJ, Mézard SP, Sailer AW, Johansson S, Rødah E, Saunier S, Hildebrandt F, Benmerah A. Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis. Am J Hum Genet. 2017;[Epub ahead of print] doi:10.1016/j.ajhg.2016.12.011.

Sun TY, Wang HY, Kwon JW, Yuan B, Lee IW, Cui XS, Kim NH. Centriolin, a centriole-appendage protein, regulates peripheral spindle migration and asymmetric division in mouse meiotic oocytes. Cell Cycle. 2017 Jan 11:0. doi: 10.1080/15384101.2016.1264544. [Epub ahead of print].

Zhang Y, O’Leary MN, Peri S, Wang M, Zha J, Melov S, Kappes DJ, Feng Q, Rhodes J, Amieux PS, Morris DR, Kennedy BK, Wiest DL. Ribosomal Proteins Rpl22 and Rpl22l1 Control Morphogenesis by Regulating Pre-mRNA Splicing. Cell Rep. 2017;18:545-556. doi:10.1016/j.celrep.2016.12.034.

Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, <authors removed - database limit>, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME. SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nat Genet. 2017 Jan 9. doi: 10.1038/ng.3743. [Epub ahead of print].

Wild R, Klems A, Takamiya M0, Hayashi Y, Strähle U, Ando K, Mochizuki N, van Impel A, Schulte-Merker S, Krueger J, Preau L, le Noble F. Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization. Nat Comm. 2017;8:13991. doi:10.1038/ncomms13991.

Dzieciolowska S, Larroque AL, Kranjec EA, Drapeau P, Samarut E. The larvicide pyriproxyfen blamed during the Zika virus outbreak does not cause microcephaly in zebrafish embryos. Sci Rep. 2017 Jan 4;7:40067. doi: 10.1038/srep40067.

Mesquita FS, Brito C, Mazon Moya MJ, Pinheiro JC, Mostowy S, Cabanes D, Sousa S. Endoplasmic reticulum chaperone Gp96 controls actomyosin dynamics and protects against pore-forming toxins. EMBO Rep. 2016 Dec 30. pii: e201642833. doi: 10.15252/embr.201642833. [Epub ahead of print].

Li RA, Traver D, Matthes T, Bertrand JY. Ndrg1b and fam49ab modulate the PTEN pathway to control T-cell lymphopoiesis in the zebrafish. Blood. 2016 Dec 29;128(26):3052-3060. doi: 10.1182/blood-2016-09-742502.

Harata A, Nishida H, Nishihara A, Hashimoto C. Purinergic P2Y Receptors Are Involved in Xenopus Head Formation. CellBio. 2016;5(4):49-65. doi:10.4236/cellbio.2016.54004.