Search Results - Feldman, Benjamin

The Second European Conference on Zebrafish Genetics and Development by Feldman, Benjamin

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Identification of common and unique modifiers of zebrafish midline bifurcation and cyclopia by Pei, Wuhong, Feldman, Benjamin

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Environmental and Genetic Modifiers of squint Penetrance during Zebrafish Embryogenesis by Pei, Wuhong, Williams, P. Huw, Clark, Matthew D., Stemple, Derek L., Feldman, Benjamin

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An Early Requirement for Maternal FoxH1 during Zebrafish Gastrulation by Pei, Wuhong, Noushmehr, Houtan, Costa, Justin, Ouspenskaia, Maia V., Elkahloun, Abdel G., Feldman, Benjamin

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Embryonic mesoderm and endoderm induction requires the actions of non-embryonic Nodal-related ligands and Mxtx2 by Hong, Sung-Kook, Jang, Moon Kyoo, Brown, Jamie L., McBride, Alison A., Feldman, Benjamin

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Transcriptional profiling of endogenous germ layer precursor cells identifies dusp4 as an essential gene in zebrafish endoderm specification by Brown, Jamie L., Snir, Mirit, Noushmehr, Houtan, Kirby, Martha, Hong, Sung-Kook, Elkahloun, Abdel G., Feldman, Benjamin

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Visualizing heavy fermion confinement and Pauli-limited superconductivity in layered CeCoIn(5) by Gyenis, András, Feldman, Benjamin E., Randeria, Mallika T., Peterson, Gabriel A., Bauer, Eric D., Aynajian, Pegor, Yazdani, Ali

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Increased functional protein expression using nucleotide sequence features enriched in highly expressed genes in zebrafish by Horstick, Eric J., Jordan, Diana C., Bergeron, Sadie A., Tabor, Kathryn M., Serpe, Mihaela, Feldman, Benjamin, Burgess, Harold A.

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Pre-gastrula expression of zebrafish extraembryonic genes by Hong, Sung-Kook, Levin, Carly S, Brown, Jamie L, Wan, Haiyan, Sherman, Brad T, Huang, Da Wei, Lempicki, Richard A, Feldman, Benjamin

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OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondria by Huizing, Marjan, Dorward, Heidi, Ly, Lien, Klootwijk, Enriko, Kleta, Robert, Skovby, Flemming, Pei, Wuhong, Feldman, Benjamin, Gahl, William A., Anikster, Yair

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The role of Niemann–Pick type C2 in zebrafish embryonic development by Tseng, Wei-Chia, Johnson Escauriza, Ana J., Tsai-Morris, Chon-Hwa, Feldman, Benjamin, Dale, Ryan K., Wassif, Christopher A., Porter, Forbes D.

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Mutations in the human SIX3 gene in holoprosencephaly are loss of function by Domené, Sabina, Roessler, Erich, El-Jaick, Kenia B., Snir, Mirit, Brown, Jamie L., Vélez, Jorge I., Bale, Sherri, Lacbawan, Felicitas, Muenke, Maximilian, Feldman, Benjamin

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The X-linked acrogigantism-associated gene gpr101 is a regulator of early embryonic development and growth in zebrafish by Trivellin, Giampaolo, Tirosh, Amit, Hernández-Ramírez, Laura C., Gupta, Tripti, Tsai-Morris, Chon Hwa, Faucz, Fabio R., Burgess, Harold A., Feldman, Benjamin, Stratakis, Constantine A.

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SUN-038 Role Of The Satb 1 Gene In Growth Across Species: Findings In A Cohort Of Patients With Short Stature And In A Knockout Zebrafish Model by Gutierrez Maria, Andrea, Hernandez-Ramirez, Laura, Trivellin, Giampaolo, Chasseloup, Fanny, Dionysiou, Margarita, Vasques, Gabriela, Feldman, Benjamin, Tsai-Morris, Chon-Hwa, Faucz, Fabio, Jorge, Alexander, Stratakis, Constantine

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A model of Costeff Syndrome reveals metabolic and protective functions of mitochondrial OPA3 by Pei, Wuhong, Kratz, Lisa E., Bernardini, Isa, Sood, Raman, Yokogawa, Tohei, Dorward, Heidi, Ciccone, Carla, Kelley, Richard I., Anikster, Yair, Burgess, Harold A., Huizing, Marjan, Feldman, Benjamin

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Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly by Roessler, Erich, Ouspenskaia, Maia V., Karkera, Jayaprakash D., Vélez, Jorge I., Kantipong, Amy, Lacbawan, Felicitas, Bowers, Peter, Belmont, John W., Towbin, Jeffrey A., Goldmuntz, Elizabeth, Feldman, Benjamin, Muenke, Maximilian

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Unique Alterations of an Ultraconserved Non-Coding Element in the 3′UTR of ZIC2 in Holoprosencephaly by Roessler, Erich, Hu, Ping, Hong, Sung-Kook, Srivastava, Kshitij, Carrington, Blake, Sood, Raman, Petrykowska, Hanna, Elnitski, Laura, Ribeiro, Lucilene A., Richieri-Costa, Antonio, Feldman, Benjamin, Odenwald, Ward F., Muenke, Maximilian

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Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for in vivo screening of candidate therapeutic compounds by Tseng, Wei-Chia, Loeb, Hannah E., Pei, Wuhong, Tsai-Morris, Chon-Hwa, Xu, Lisha, Cluzeau, Celine V., Wassif, Christopher A., Feldman, Benjamin, Burgess, Shawn M., Pavan, William J., Porter, Forbes D.

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Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly by Roessler, Erich, Pei, Wuhong, Ouspenskaia, Maia V., Karkera, Jayaprakash D., Veléz, Jorge Ivan, Banerjee-Basu, Sharmilla, Gibney, Gretchen, Lupo, Philip J., Mitchell, Laura E., Towbin, Jeffrey A., Bowers, Peter, Belmont, John W., Goldmuntz, Elizabeth, Baxevanis, Andreas D., Feldman, Benjamin, Muenke, Maximilian

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Characterization of GPR101 transcript structure and expression patterns by Trivellin, Giampaolo, Bjelobaba, Ivana, Daly, Adrian F., Larco, Darwin O., Palmeira, Leonor, Faucz, Fabio R., Thiry, Albert, Leal, Letícia F., Rostomyan, Liliya, Quezado, Martha, Schernthaner-Reiter, Marie Helene, Janjic, Marija M., Villa, Chiara, Wu, T. John, Stojilkovic, Stanko S., Beckers, Albert, Feldman, Benjamin, Stratakis, Constantine A.

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