Mechanistic Insights into Axenfeld-Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants von French, Curtis R.

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Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling von Havrylov, Serhiy, Chrystal, Paul, van Baarle, Suey, French, Curtis R., MacDonald, Ian M., Avasarala, Jagannadha, Rogers, R. Curtis, Berry, Fred B., Kume, Tsutomu, Waskiewicz, Andrew J., Lehmann, Ordan J.

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foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish von Whitesell, Thomas R., Chrystal, Paul W., Ryu, Jae-Ryeon, Munsie, Nicole, Grosse, Ann, French, Curtis R., Workentine, Matthew L., Li, Rui, Zhu, Lihua Julie, Waskiewicz, Andrew, Lehmann, Ordan J., Lawson, Nathan D., Childs, Sarah J.

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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease von French, Curtis R, Seshadri, Sudha, Destefano, Anita L, Fornage, Myriam, Arnold, Corey R, Gage, Philip J, Skarie, Jonathan M, Dobyns, William B, Millen, Kathleen J, Liu, Ting, Dietz, William, Kume, Tsutomu, Hofker, Marten, Emery, Derek J, Childs, Sarah J, Waskiewicz, Andrew J, Lehmann, Ordan J

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Phytocannabinoids Reduce Seizures in Larval Zebrafish and Affect Endocannabinoid Gene Expression von Kollipara, Roshni, Langille, Evan, Tobin, Cameron, French, Curtis R.

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Gdf6a is required for the initiation of dorsal–ventral retinal patterning and lens development von French, Curtis R., Erickson, Timothy, French, Danielle V., Pilgrim, David B., Waskiewicz, Andrew J.

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Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies von Asai-Coakwell, Mika, March, Lindsey, Dai, Xiao Hua, Duval, Michele, Lopez, Irma, French, Curtis R, Famulski, Jakub, De Baere, Elfride, Francis, Peter J, Sundaresan, Periasamy, Sauvé, Yves, Koenekoop, Robert K, Berry, Fred B, Allison, W Ted, Waskiewicz, Andrew J, Lehmann, Ordan J

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GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies von Asai-Coakwell, Mika, French, Curtis R., Berry, Karyn M., Ye, Ming, Koss, Ron, Somerville, Martin, Mueller, Rosemary, van Heyningen, Veronica, Waskiewicz, Andrew J., Lehmann, Ordan J.

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Meis1 specifies positional information in the retina and tectum to organize the zebrafish visual system von Erickson, Timothy, French, Curtis R, Waskiewicz, Andrew J

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Aberrant forebrain signaling during early development underlies the generation of holoprosencephaly and coloboma von Gongal, Patricia A., French, Curtis R., Waskiewicz, Andrew J.

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Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer von Umali, Jurgienne, Hawkey-Noble, Alexia, French, Curtis R.

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Protein fucosylation is required for Notch dependent vascular integrity in zebrafish von Fowler, Gerissa, French, Danielle V., Rose, April, Squires, Paige, Aniceto da Silva, Catarina, Ohata, Shinya, Okamoto, Hitoshi, French, Curtis R.

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Expression of three P4-phospholipid flippases—atp11a, atp11b, and atp11c in zebrafish (Danio rerio) von Hawkey-Noble, Alexia, Umali, Jurgienne, Fowler, Gerissa, French, Curtis R.

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Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene von Pater, Justin A., Penney, Cindy, O’Rielly, Darren D., Griffin, Anne, Kamal, Lara, Brownstein, Zippora, Vona, Barbara, Vinkler, Chana, Shohat, Mordechai, Barel, Ortal, French, Curtis R., Singh, Sushma, Werdyani, Salem, Burt, Taylor, Abdelfatah, Nelly, Houston, Jim, Doucette, Lance P., Squires, Jessica, Glaser, Fabian, Roslin, Nicole M., Vincent, Daniel, Marquis, Pascale, Woodland, Geoffrey, Benoukraf, Touati, Hawkey-Noble, Alexia, Avraham, Karen B., Stanton, Susan G., Young, Terry-Lynn

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A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene von Abdelfatah, Nelly, Mostafa, Ahmed A., French, Curtis R., Doucette, Lance P., Penney, Cindy, Lucas, Matthew B., Griffin, Anne, Booth, Valerie, Rowley, Christopher, Besaw, Jessica E., Tranebjærg, Lisbeth, Rendtorff, Nanna Dahl, Hodgkinson, Kathy A., Little, Leichelle A., Agrawal, Sumit, Parnes, Lorne, Batten, Tony, Moore, Susan, Hu, Pingzhao, Pater, Justin A., Houston, Jim, Galutira, Dante, Benteau, Tammy, MacDonald, Courtney, French, Danielle, O’Rielly, Darren D., Stanton, Susan G., Young, Terry-Lynn

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Comparison of multifrequency bioelectrical impedance analysis with dual-energy X-ray absorptiometry for assessment of percentage body fat in a large, healthy population von Sun, G, French, C.R, Martin, G.R, Younghusband, B, Green, R.C, Xie, Y.G, Mathews, M

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Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis von Hawkey-Noble, Alexia, Pater, Justin A., Kollipara, Roshni, Fitzgerald, Meriel, Maekawa, Alexandre S., Kovacs, Christopher S., Young, Terry-Lynn, French, Curtis R.

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Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies von Ye, Ming, Berry-Wynne, Karyn M., Asai-Coakwell, Mika, Sundaresan, Periasamy, Footz, Tim, French, Curtis R., Abitbol, Marc, Fleisch, Valerie C., Corbett, Nathan, Allison, W. Ted, Drummond, Garry, Walter, Michael A., Underhill, T. Michael, Waskiewicz, Andrew J., Lehmann, Ordan J.

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Pbx homeodomain proteins pattern both the zebrafish retina and tectum von French, Curtis R, Erickson, Timothy, Callander, Davon, Berry, Karyn M, Koss, Ron, Hagey, Daniel W, Stout, Jennifer, Wuennenberg-Stapleton, Katrin, Ngai, John, Moens, Cecilia B, Waskiewicz, Andrew J

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Apoptotic and proliferative defects characterize ocular development in a microphthalmic BMP model von French, Curtis R, Stach, Tara R, March, Lindsey D, Lehmann, Ordan J, Waskiewicz, Andrew J

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