Search Results - "Ray, Catherine A"

Transcriptomic, proteomic, and metabolomic landscape of positional memory in the caudal fin of zebrafish by Rabinowitz, Jeremy S., Robitaille, Aaron M., Wang, Yuliang, Ray, Catherine A., Thummel, Ryan, Gu, Haiwei, Djukovic, Danijel, Raftery, Daniel, Berndt, Jason D., Moon, Randall T.

“…Regeneration requires cells to regulate proliferation and patterning according to their spatial position. Positional memory is a property that enables…”
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Hesr1 and Hesr2 may act as early effectors of Notch signaling in the developing cochlea by Hayashi, Toshinori, Kokubo, Hiroki, Hartman, Byron H., Ray, Catherine A., Reh, Thomas A., Bermingham-McDonogh, Olivia

“…In cochlear development, the Notch signaling pathway is required for both the early prosensory phase and a later lateral inhibition phase. While it is known…”
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Acheate‐scute like 1 (Ascl1) is required for normal delta‐like (Dll) gene expression and notch signaling during retinal development by Nelson, Branden R., Hartman, Byron H., Ray, Catherine A., Hayashi, Toshinori, Bermingham‐McDonogh, Olivia, Reh, Thomas A.

“…Delta gene expression in Drosophila is regulated by proneural basic helix–loop–helix (bHLH) transcription factors, such as acheate‐scute. In vertebrates,…”
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Expression patterns of FGF receptors in the developing mammalian cochlea by Hayashi, Toshinori, Ray, Catherine A., Younkins, Christa, Bermingham‐McDonogh, Olivia

“…Many studies have shown the importance of the fibroblast growth factor (FGF) family of factors in the development of the mammalian cochlea. There are four…”
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CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development by Geller, Scott F, Guerin, Karen I, Visel, Meike, Pham, Aaron, Lee, Edwin S, Dror, Amiel A, Avraham, Karen B, Hayashi, Toshinori, Ray, Catherine A, Reh, Thomas A, Bermingham-McDonogh, Olivia, Triffo, William J, Bao, Shaowen, Isosomppi, Juha, Västinsalo, Hanna, Sankila, Eeva-Marja, Flannery, John G

“…Mutations in the CLRN1 gene cause Usher syndrome type 3 (USH3), a human disease characterized by progressive blindness and deafness. Clarin 1, the protein…”
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Wnt/β-catenin signaling promotes regeneration after adult zebrafish spinal cord injury by Strand, Nicholas S., Hoi, Kimberly K., Phan, Tien M.T., Ray, Catherine A., Berndt, Jason D., Moon, Randall T.

“…Unlike mammals, zebrafish can regenerate their injured spinal cord and regain control of caudal tissues. It was recently shown that Wnt/β-catenin signaling is…”
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Fgf20 Is Required for Sensory Epithelial Specification in the Developing Cochlea by Hayashi, Toshinori, Ray, Catherine A, Bermingham-McDonogh, Olivia

“…Tissue-specific deletion of Fgfr1 results in severe defects in the development of both hair cells and support cells (Pirvola et al., 2002). Despite the…”
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Effects of 3,3′-Iminodipropionitrile on Hair Cell Numbers in Cristae of CBA/CaJ and C57BL/6J Mice by Wilkerson, Brent A., Artoni, Filippo, Lea, Colby, Ritchie, Kayla, Ray, Catherine A., Bermingham-McDonogh, Olivia

“…This study examines absolute hair cell numbers in the cristae of C57BL/6J mice and CBA/CaJ mice from weaning to adulthood as well as the dose required for…”
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Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation by Geng, Ruishuang, Geller, Scott F., Hayashi, Toshinori, Ray, Catherine A., Reh, Thomas A., Bermingham-McDonogh, Olivia, Jones, Sherri M., Wright, Charles G., Melki, Sami, Imanishi, Yoshikazu, Palczewski, Krzysztof, Alagramam, Kumar N., Flannery, John G.

“…Usher syndrome 3A (USH3A) is an autosomal recessive disorder characterized by progressive loss of hearing and vision due to mutation in the clarin-1 (CLRN1)…”
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Acheate‐scute like 1 (Ascl1) is required for normal delta‐like (Dll) gene expression and notch signaling during retinal development by Nelson, Branden R., Hartman, Byron H., Ray, Catherine A., Hayashi, Toshinori, Bermingham‐McDonough, Olivia, Reh, Thomas A.

“…Retinascape: Multiphoton microscopy was used to look deep into the retina, at the dawn of neurogenesis in the embryonic mouse eye: mitotic progenitors…”
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CLRN1 Is Nonessential in the Mouse Retina but Is Required for Cochlear Hair Cell Development: e1000607 by Geller, Scott F, Guerin, Karen I, Visel, Meike, Pham, Aaron, Lee, Edwin S, Dror, Amiel A, Avraham, Karen B, Hayashi, Toshinori, Ray, Catherine A, Reh, Thomas A, Bermingham-McDonogh, Olivia, Triffo, William J, Bao, Shaowen, Isosomppi, Juha, Västinsalo, Hanna, Sankila, Eeva-Marja, Flannery, John G

“…Mutations in the CLRN1 gene cause Usher syndrome type 3 (USH3), a human disease characterized by progressive blindness and deafness. Clarin 1, the protein…”
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Regional cerebral glucose metabolism compared in rodents and humans by Blin, J, Ray, C A, Chase, T N, Piercey, M F

“…In order to compare regional brain glucose metabolism in rats and humans, this parameter was measured using Sokoloff's deoxyglucose method in rats, and…”
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