Year |
Citation |
Score |
2020 |
Eggenschwiler JT. Elucidating CCRK’s function in ciliary assembly and cilium‐dependent signaling The Faseb Journal. 34: 1-1. DOI: 10.1096/Fasebj.2020.34.S1.00396 |
0.519 |
|
2017 |
Lupu FI, Burnett JB, Eggenschwiler JT. Cell cycle-related kinase regulates mammalian eye development through positive and negative regulation of the Hedgehog pathway. Developmental Biology. PMID 29166577 DOI: 10.1016/J.Ydbio.2017.10.022 |
0.474 |
|
2017 |
Snouffer A, Brown D, Lee H, Walsh J, Lupu F, Norman R, Lechtreck K, Ko HW, Eggenschwiler J. Cell Cycle-Related Kinase (CCRK) regulates ciliogenesis and Hedgehog signaling in mice. Plos Genetics. 13: e1006912. PMID 28817564 DOI: 10.1371/Journal.Pgen.1006912 |
0.687 |
|
2017 |
Burnett JB, Lupu FI, Eggenschwiler JT. Proper ciliary assembly is critical for restricting Hedgehog signaling during early eye development in mice. Developmental Biology. PMID 28778798 DOI: 10.1016/J.Ydbio.2017.07.012 |
0.518 |
|
2014 |
Fuller K, O'Connell JT, Gordon J, Mauti O, Eggenschwiler J. Rab23 regulates Nodal signaling in vertebrate left-right patterning independently of the Hedgehog pathway. Developmental Biology. 391: 182-95. PMID 24780629 DOI: 10.1016/J.Ydbio.2014.04.012 |
0.772 |
|
2014 |
Liu A, Eggenschwiler J. Identifying essential genes in mouse development via an ENU-based forward genetic approach. Methods in Molecular Biology (Clifton, N.J.). 1092: 95-118. PMID 24318816 DOI: 10.1007/978-1-60327-292-6_7 |
0.326 |
|
2013 |
Eggenschwiler J. Hedgehog signaling and the cilium: in the zone. Developmental Cell. 23: 677-8. PMID 23079593 DOI: 10.1016/J.Devcel.2012.10.001 |
0.626 |
|
2012 |
Nishio M, Hamada K, Kawahara K, Sasaki M, Noguchi F, Chiba S, Mizuno K, Suzuki SO, Dong Y, Tokuda M, Morikawa T, Hikasa H, Eggenschwiler J, Yabuta N, Nojima H, et al. Cancer susceptibility and embryonic lethality in Mob1a/1b double-mutant mice. The Journal of Clinical Investigation. 122: 4505-18. PMID 23143302 DOI: 10.1172/Jci63735 |
0.432 |
|
2011 |
Ocbina PJ, Eggenschwiler JT, Moskowitz I, Anderson KV. Complex interactions between genes controlling trafficking in primary cilia. Nature Genetics. 43: 547-53. PMID 21552265 DOI: 10.1038/Ng.832 |
0.475 |
|
2011 |
Qin J, Lin Y, Norman RX, Ko HW, Eggenschwiler JT. Intraflagellar transport protein 122 antagonizes Sonic Hedgehog signaling and controls ciliary localization of pathway components. Proceedings of the National Academy of Sciences of the United States of America. 108: 1456-61. PMID 21209331 DOI: 10.1073/Pnas.1011410108 |
0.611 |
|
2010 |
Walczak-Sztulpa J, Eggenschwiler J, Osborn D, Brown DA, Emma F, Klingenberg C, Hennekam RC, Torre G, Garshasbi M, Tzschach A, Szczepanska M, Krawczynski M, Zachwieja J, Zwolinska D, Beales PL, et al. Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene. American Journal of Human Genetics. 86: 949-56. PMID 20493458 DOI: 10.1016/J.Ajhg.2010.04.012 |
0.6 |
|
2010 |
Ko HW, Norman RX, Tran J, Fuller KP, Fukuda M, Eggenschwiler JT. Broad-minded links cell cycle-related kinase to cilia assembly and hedgehog signal transduction. Developmental Cell. 18: 237-47. PMID 20159594 DOI: 10.1016/J.Devcel.2009.12.014 |
0.789 |
|
2009 |
Ko HW, Liu A, Eggenschwiler JT. Analysis of hedgehog signaling in mouse intraflagellar transport mutants. Methods in Cell Biology. 93: 347-69. PMID 20409825 DOI: 10.1016/S0091-679X(08)93017-X |
0.589 |
|
2009 |
Norman RX, Ko HW, Huang V, Eun CM, Abler LL, Zhang Z, Sun X, Eggenschwiler JT. Tubby-like protein 3 (TULP3) regulates patterning in the mouse embryo through inhibition of Hedgehog signaling. Human Molecular Genetics. 18: 1740-54. PMID 19286674 DOI: 10.1093/Hmg/Ddp113 |
0.667 |
|
2009 |
Eggenschwiler JT, Norman RX. Tubby-like 3 (TULP3) and mammalian Sonic Hedgehog signaling Developmental Biology. 331: 485. DOI: 10.1016/J.Ydbio.2009.05.371 |
0.61 |
|
2008 |
Cho A, Ko HW, Eggenschwiler JT. FKBP8 cell-autonomously controls neural tube patterning through a Gli2- and Kif3a-dependent mechanism. Developmental Biology. 321: 27-39. PMID 18590716 DOI: 10.1016/J.Ydbio.2008.05.558 |
0.753 |
|
2008 |
Norman RA, Ikeda A, Eggenschwiler JT. A role for TULP3 in mouse hedgehog signaling and neural patterning Developmental Biology. 319: 526. DOI: 10.1016/J.Ydbio.2008.05.215 |
0.714 |
|
2007 |
Eggenschwiler JT, Anderson KV. Cilia and developmental signaling. Annual Review of Cell and Developmental Biology. 23: 345-73. PMID 17506691 DOI: 10.1146/Annurev.Cellbio.23.090506.123249 |
0.676 |
|
2006 |
Eggenschwiler JT, Bulgakov OV, Qin J, Li T, Anderson KV. Mouse Rab23 regulates hedgehog signaling from smoothened to Gli proteins. Developmental Biology. 290: 1-12. PMID 16364285 DOI: 10.1016/J.Ydbio.2005.09.022 |
0.655 |
|
2005 |
García-García MJ, Eggenschwiler JT, Caspary T, Alcorn HL, Wyler MR, Huangfu D, Rakeman AS, Lee JD, Feinberg EH, Timmer JR, Anderson KV. Analysis of mouse embryonic patterning and morphogenesis by forward genetics. Proceedings of the National Academy of Sciences of the United States of America. 102: 5913-9. PMID 15755804 DOI: 10.1073/Pnas.0501071102 |
0.425 |
|
2004 |
Bulgakov OV, Eggenschwiler JT, Hong DH, Anderson KV, Li T. FKBP8 is a negative regulator of mouse sonic hedgehog signaling in neural tissues. Development (Cambridge, England). 131: 2149-59. PMID 15105374 DOI: 10.1242/Dev.01122 |
0.629 |
|
2002 |
Caspary T, García-García MJ, Huangfu D, Eggenschwiler JT, Wyler MR, Rakeman AS, Alcorn HL, Anderson KV. Mouse Dispatched homolog1 is required for long-range, but not juxtacrine, Hh signaling. Current Biology : Cb. 12: 1628-32. PMID 12372258 DOI: 10.1016/S0960-9822(02)01147-8 |
0.583 |
|
2001 |
Eggenschwiler JT, Espinoza E, Anderson KV. Rab23 is an essential negative regulator of the mouse Sonic hedgehog signalling pathway. Nature. 412: 194-8. PMID 11449277 DOI: 10.1038/35084089 |
0.606 |
|
2000 |
Eggenschwiler JT, Anderson KV. Dorsal and lateral fates in the mouse neural tube require the cell-autonomous activity of the open brain gene. Developmental Biology. 227: 648-60. PMID 11071781 DOI: 10.1006/Dbio.2000.9918 |
0.538 |
|
1996 |
Ludwig T, Eggenschwiler J, Fisher P, D'Ercole AJ, Davenport ML, Efstratiadis A. Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds. Developmental Biology. 177: 517-35. PMID 8806828 DOI: 10.1006/Dbio.1996.0182 |
0.317 |
|
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