Search Results - Willer, Jason

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  1. 1
    snow white, a Zebrafish Model of Hermansky-Pudlak Syndrome Type 5

    snow white, a Zebrafish Model of Hermansky-Pudlak Syndrome Type 5 by Daly, Christina M. S., Willer, Jason, Gregg, Ronald, Gross, Jeffrey M.

    Published 2013
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  2. 2
    Whole Exome Sequencing of a Dominant Retinitis Pigmentosa Family Identifies a Novel Deletion in PRPF31

    Whole Exome Sequencing of a Dominant Retinitis Pigmentosa Family Identifies a Novel Deletion in PRPF31 by Villanueva, Adda, Willer, Jason R., Bryois, Julien, Dermitzakis, Emmanouil T., Katsanis, Nicholas, Davis, Erica E.

    Published 2014
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  3. 3
    Muscle Contractions Guide Rohon–Beard Peripheral Sensory Axons

    Muscle Contractions Guide Rohon–Beard Peripheral Sensory Axons by Paulus, Jeremiah D., Willer, Gregory B., Willer, Jason R., Gregg, Ronald G., Halloran, Mary C.

    Published 2009
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  4. 4
    Zebrafish blowout provides genetic evidence for Patched1 mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye

    Zebrafish blowout provides genetic evidence for Patched1 mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye by Lee, Jiwoon, Willer, Jason R., Willer, Gregory B., Smith, Kierann, Gregg, Ronald G., Gross, Jeffrey M.

    Published 2008
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  5. 5
    Rapid identification of kidney cyst mutations by whole exome sequencing in zebrafish

    Rapid identification of kidney cyst mutations by whole exome sequencing in zebrafish by Ryan, Sean, Willer, Jason, Marjoram, Lindsay, Bagwell, Jennifer, Mankiewicz, Jamie, Leshchiner, Ignaty, Goessling, Wolfram, Bagnat, Michel, Katsanis, Nicholas

    Published 2013
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  6. 6
    The GARP Domain of the Rod CNG Channel's β1-Subunit Contains Distinct Sites for Outer Segment Targeting and Connecting to the Photoreceptor Disk Rim

    The GARP Domain of the Rod CNG Channel's β1-Subunit Contains Distinct Sites for Outer Segment Targeting and Connecting to the Photoreceptor Disk Rim by Pearring, Jillian N., Martínez-Márquez, Jorge, Willer, Jason R., Lieu, Eric C., Salinas, Raquel Y., Arshavsky, Vadim Y.

    Published 2021
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  7. 7
    Transient laminin beta 1a Induction Defines the Wound Epidermis during Zebrafish Fin Regeneration

    Transient laminin beta 1a Induction Defines the Wound Epidermis during Zebrafish Fin Regeneration by Chen, Chen-Hui, Merriman, Alexander F., Savage, Jeremiah, Willer, Jason, Wahlig, Taylor, Katsanis, Nicholas, Yin, Viravuth P., Poss, Kenneth D.

    Published 2015
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  8. 8
    Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome

    Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome by Helm, Benjamin M., Willer, Jason R., Sadeghpour, Azita, Golzio, Christelle, Crouch, Eric, Vergano, Samantha Schrier, Katsanis, Nicholas, Davis, Erica E.

    Published 2017
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  9. 9
    Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular Degeneration

    Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular Degeneration by Tan, Perciliz L., Garrett, Melanie E., Willer, Jason R., Campochiaro, Peter A., Campochiaro, Betsy, Zack, Donald J., Ashley-Koch, Allison E., Katsanis, Nicholas

    Published 2017
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  10. 10
    Neural and Synaptic Defects in slytherin, a Zebrafish Model for Human Congenital Disorders of Glycosylation

    Neural and Synaptic Defects in slytherin, a Zebrafish Model for Human Congenital Disorders of Glycosylation by Song, Yuanquan, Willer, Jason R., Scherer, Paul C., Panzer, Jessica A., Kugath, Amy, Skordalakes, Emmanuel, Gregg, Ronald G., Willer, Gregory B., Balice-Gordon, Rita J.

    Published 2010
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  11. 11
    A Novel Ribosomopathy Caused by Dysfunction of RPL10 Disrupts Neurodevelopment and Causes X-Linked Microcephaly in Humans

    A Novel Ribosomopathy Caused by Dysfunction of RPL10 Disrupts Neurodevelopment and Causes X-Linked Microcephaly in Humans by Brooks, Susan S., Wall, Alissa L., Golzio, Christelle, Reid, David W., Kondyles, Amalia, Willer, Jason R., Botti, Christina, Nicchitta, Christopher V., Katsanis, Nicholas, Davis, Erica E.

    Published 2014
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  12. 12
    Elution Profile Analysis of SDS-induced Subcomplexes by Quantitative Mass Spectrometry

    Elution Profile Analysis of SDS-induced Subcomplexes by Quantitative Mass Spectrometry by Texier, Yves, Toedt, Grischa, Gorza, Matteo, Mans, Dorus A., van Reeuwijk, Jeroen, Horn, Nicola, Willer, Jason, Katsanis, Nicholas, Roepman, Ronald, Gibson, Toby J., Ueffing, Marius, Boldt, Karsten

    Published 2014
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  13. 13
    rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA

    rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA by Haud, Noémie, Kara, Firat, Diekmann, Simone, Henneke, Marco, Willer, Jason R., Hillwig, Melissa S., Gregg, Ronald G., MacIntosh, Gustavo C., Gärtner, Jutta, Alia, A., Hurlstone, Adam F. L.

    Published 2011
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  14. 14
    KCTD13 is a major driver of mirrored neuroanatomical phenotypes associated with the 16p11.2 CNV

    KCTD13 is a major driver of mirrored neuroanatomical phenotypes associated with the 16p11.2 CNV by Golzio, Christelle, Willer, Jason, Talkowski, Michael E, Oh, Edwin C, Taniguchi, Yu, Jacquemont, Sébastien, Reymond, Alexandre, Sun, Mei, Sawa, Akira, Gusella, James F, Kamiya, Atsushi, Beckmann, Jacques S, Katsanis, Nicholas

    Published 2012
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  15. 15
    Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome

    Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome by Ta-Shma, Asaf, Khan, Tahir N., Vivante, Asaf, Willer, Jason R., Matak, Pavle, Jalas, Chaim, Pode-Shakked, Ben, Salem, Yishay, Anikster, Yair, Hildebrandt, Friedhelm, Katsanis, Nicholas, Elpeleg, Orly, Davis, Erica E.

    Published 2017
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  16. 16
    Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

    Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion by Spataro, Rossella, Kousi, Maria, Farhan, Sali M. K., Willer, Jason R., Ross, Jay P., Dion, Patrick A., Rouleau, Guy A., Daly, Mark J., Neale, Benjamin M., La Bella, Vincenzo, Katsanis, Nicholas

    Published 2019
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  17. 17
    Maternal topoisomerase II alpha, not topoisomerase II beta, enables embryonic development of zebrafish top2a(-/- )mutants

    Maternal topoisomerase II alpha, not topoisomerase II beta, enables embryonic development of zebrafish top2a(-/- )mutants by Sapetto-Rebow, Beata, McLoughlin, Sarah C, O'Shea, Lynne C, O'Leary, Olivia, Willer, Jason R, Alvarez, Yolanda, Collery, Ross, O'Sullivan, Jacintha, Van Eeden, Freek, Hensey, Carmel, Kennedy, Breandán N

    Published 2011
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  18. 18
    Mutations in Zebrafish lrp2 Result in Adult-Onset Ocular Pathogenesis That Models Myopia and Other Risk Factors for Glaucoma

    Mutations in Zebrafish lrp2 Result in Adult-Onset Ocular Pathogenesis That Models Myopia and Other Risk Factors for Glaucoma by Veth, Kerry N., Willer, Jason R., Collery, Ross F., Gray, Matthew P., Willer, Gregory B., Wagner, Daniel S., Mullins, Mary C., Udvadia, Ava J., Smith, Richard S., John, Simon W. M., Gregg, Ronald G., Link, Brian A.

    Published 2011
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  19. 19
    Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain development

    Loss of Lrp2 in zebrafish disrupts pronephric tubular clearance but not forebrain development by Kur, Esther, Christa, Anna, Veth, Kerry N., Gajera, Chandresh R., Andrade-Navarro, Miguel A., Zhang, Jingjing, Willer, Jason R., Gregg, Ronald G., Abdelilah-Seyfried, Salim, Bachmann, Sebastian, Link, Brian A., Hammes, Annette, Willnow, Thomas E.

    Published 2011
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  20. 20
    Epigenetic control of intestinal barrier function and inflammation in zebrafish

    Epigenetic control of intestinal barrier function and inflammation in zebrafish by Marjoram, Lindsay, Alvers, Ashley, Deerhake, M. Elizabeth, Bagwell, Jennifer, Mankiewicz, Jamie, Cocchiaro, Jordan L., Beerman, Rebecca W., Willer, Jason, Sumigray, Kaelyn D., Katsanis, Nicholas, Tobin, David M., Rawls, John F., Goll, Mary G., Bagnat, Michel

    Published 2015
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