Glypicans: proteoglycans with a surprise

Por Filmus, Jorge, Selleck, Scott B.
Publicado em 2001

The Elusive Functions of Proteoglycans: In Vivo Veritas

Por Lander, Arthur D., Selleck, Scott B.
Publicado em 2000

Cell Type-Specific Requirements for Heparan Sulfate Biosynthesis at the Drosophila Neuromuscular Junction: Effects on Synapse Function, Membrane Trafficking, and Mitochondrial Loca...

Por Ren, Yi, Kirkpatrick, Catherine A., Rawson, Joel M., Sun, Mu, Selleck, Scott B.
Publicado em 2009

Alterations in Heparan Sulfate in the Vessel in Response to Vascular Injury in the Mouse

Por Adhikari, Neeta, Rusch, Melissa, Mariash, Ami, Li, Qinglu, Selleck, Scott B., Hall, Jennifer L.
Publicado em 2008

Akt regulates glutamate receptor trafficking and postsynaptic membrane elaboration at the Drosophila neuromuscular junction

Por Lee, Hyun-Gwan, Zhao, Na, Campion, Bridget K, Nguyen, Michelle M, Selleck, Scott B
Publicado no Dev Neurobiol (2013)

Heparan sulfate proteoglycans regulate autophagy in Drosophila

Por Reynolds-Peterson, Claire E., Zhao, Na, Xu, Jie, Serman, Taryn M., Xu, Jielin, Selleck, Scott B.
Publicado no Autophagy (2017)

Sulfatase 1 Is an Inhibitor of Ductal Morphogenesis with Sexually Dimorphic Expression in the Urogenital Sinus

Por Buresh, Rita A., Kuslak, Sheri L., Rusch, Melissa A., Vezina, Chad M., Selleck, Scott B., Marker, Paul C.
Publicado em 2010

Regulation of Zebrafish Skeletogenesis by ext2/dackel and papst1/pinscher

Por Clément, Aurélie, Wiweger, Malgorzata, von der Hardt, Sophia, Rusch, Melissa A., Selleck, Scott B., Chien, Chi-Bin, Roehl, Henry H.
Publicado em 2008

sqv-3, -7, and -8, a set of genes affecting morphogenesis in Caenorhabditis elegans, encode enzymes required for glycosaminoglycan biosynthesis

Por Bulik, Dorota A., Wei, Ge, Toyoda, Hidenao, Kinoshita-Toyoda, Akiko, Waldrip, W. Ross, Esko, Jeffrey D., Robbins, Phillips W., Selleck, Scott B.
Publicado em 2000

Diet and Energy-Sensing Inputs Affect TorC1-Mediated Axon Misrouting but Not TorC2-Directed Synapse Growth in a Drosophila Model of Tuberous Sclerosis

Por Dimitroff, Brian, Howe, Katie, Watson, Adrienne, Campion, Bridget, Lee, Hyun-Gwan, Zhao, Na, O'Connor, Michael B., Neufeld, Thomas P., Selleck, Scott B.
Publicado em 2012

Functional abnormalities of heparan sulfate in mucopolysaccharidosis-I are associated with defective biologic activity of FGF-2 on human multipotent progenitor cells

Por Pan, Chendong, Nelson, Matthew S., Reyes, Morayma, Koodie, Lisa, Brazil, Joseph J., Stephenson, Elliot J., Zhao, Robert C., Peters, Charles, Selleck, Scott B., Stringer, Sally E., Gupta, Pankaj
Publicado em 2005

Mechanisms of TSC-mediated Control of Synapse Assembly and Axon Guidance

Por Knox, Sarah, Ge, Hong, Dimitroff, Brian D., Ren, Yi, Howe, Katie A., Arsham, Andrew M., Easterday, Mathew C., Neufeld, Thomas P., O'Connor, Michael B., Selleck, Scott B.
Publicado em 2007

Heparan Sulfate Ndst1 Regulates Vascular Smooth Muscle Cell Proliferation, Vessel Size and Vascular Remodeling

Por Adhikari, Neeta, Basi, David L., Townsend, DeWayne, Rusch, Melissa, Mariash, Ami, Mullegama, Sureni, Watson, Adrienne, Larson, Jon, Tan, Sara, Lerman, Ben, Esko, Jeffrey D., Selleck, Scott B., Hall, Jennifer L.
Publicado em 2010

Effect of Genetic Variation in a Drosophila Model of Diabetes-Associated Misfolded Human Proinsulin

Por He, Bin Z., Ludwig, Michael Z., Dickerson, Desiree A., Barse, Levi, Arun, Bharath, Vilhjálmsson, Bjarni J., Jiang, Pengyao, Park, Soo-Young, Tamarina, Natalia A., Selleck, Scott B., Wittkopp, Patricia J., Bell, Graeme I., Kreitman, Martin
Publicado em 2014

Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors

Por Ciesielski, Timothy H, Pendergrass, Sarah A, White, Marquitta J, Kodaman, Nuri, Sobota, Rafal S, Huang, Minjun, Bartlett, Jacquelaine, Li, Jing, Pan, Qinxin, Gui, Jiang, Selleck, Scott B, Amos, Christopher I, Ritchie, Marylyn D, Moore, Jason H, Williams, Scott M
Publicado em 2014

Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities

Por Balciuniene, Jorune, Feng, Ningping, Iyadurai, Kelly, Hirsch, Betsy, Charnas, Lawrence, Bill, Brent R., Easterday, Mathew C., Staaf, Johan, Oseth, LeAnn, Czapansky-Beilman, Desiree, Avramopoulos, Dimitri, Thomas, George H., Borg, Åke, Valle, David, Schimmenti, Lisa A., Selleck, Scott B.
Publicado em 2007

Global increases in both common and rare copy number load associated with autism

Por Girirajan, Santhosh, Johnson, Rebecca L., Tassone, Flora, Balciuniene, Jorune, Katiyar, Neerja, Fox, Keolu, Baker, Carl, Srikanth, Abhinaya, Yeoh, Kian Hui, Khoo, Su Jen, Nauth, Therese B., Hansen, Robin, Ritchie, Marylyn, Hertz-Picciotto, Irva, Eichler, Evan E., Pessah, Isaac N., Selleck, Scott B.
Publicado em 2013

The phenotype of recurrent 10q22q23 deletions and duplications

Por van Bon, Bregje W M, Balciuniene, Jorune, Fruhman, Gary, Nagamani, Sandesh Chakravarthy Sreenath, Broome, Diane L, Cameron, Elizabeth, Martinet, Danielle, Roulet, Eliane, Jacquemont, Sebastien, Beckmann, Jacques S, Irons, Mira, Potocki, Lorraine, Lee, Brendan, Cheung, Sau Wai, Patel, Ankita, Bellini, Melissa, Selicorni, Angelo, Ciccone, Roberto, Silengo, Margherita, Vetro, Annalisa, Knoers, Nine V, de Leeuw, Nicole, Pfundt, Rolph, Wolf, Barry, Jira, Petr, Aradhya, Swaroop, Stankiewicz, Pawel, Brunner, Han G, Zuffardi, Orsetta, Selleck, Scott B, Lupski, James R, de Vries, Bert B A
Publicado em 2011