Rezultati - Matthew Ellinwood
- Showing 1 - 13 results of 13
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Quantitative diffusion tensor imaging analysis does not distinguish pediatric canines with mucopolysaccharidosis I from control canines od Middleton, Dana M, Li, Jonathan Y, Chen, Steven D, White, Leonard E, Dickson, Patricia I, Matthew Ellinwood, N, Provenzale, James M
Izdano 2017Text -
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Differential Transcriptomic Profiles Following Stimulation with Lipopolysaccharide in Intestinal Organoids from Dogs with Inflammatory Bowel Disease and Intestinal Mast Cell Tumor od Dipak Kumar Sahoo, Dana C. Borcherding, Lawrance C. Chandra, Albert E. Jergens, Todd Atherly, Agnes Bourgois‐Mochel, N. Matthew Ellinwood, Elizabeth Snella, Andrew Severin, Martin Martin, Karin Allenspach, Jonathan P. Mochel
Izdano 2022Artigo -
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A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus) od Markus H. Kuehn, Koren Lipsett, Marilyn Menotti‐Raymond, S. Scott Whitmore, Todd E. Scheetz, Victor A. David, Stephen J. O’Brien, Zhongyuan Zhao, Jackie K. Jens, Elizabeth Snella, N. Matthew Ellinwood, Gillian J. McLellan
Izdano 2016Artigo -
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Not All SCID Pigs Are Created Equally: Two Independent Mutations in the <i>Artemis</i> Gene Cause SCID in Pigs od Emily H. Waide, Jack C. M. Dekkers, Jason W. Ross, Raymond R. R. Rowland, Carol R. Wyatt, Catherine Ewen, Alyssa B. Evans, Dinesh M. Thekkoot, Nicholas J. Boddicker, Nick V. L. Serão, N. Matthew Ellinwood, Christopher K. Tuggle
Izdano 2015Artigo -
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O39: The ClinGen Lysosomal Diseases Variant Curation Expert Panel’s guidance on classification of IDUA variants for mucopolysaccharidosis type I od Jenny Goldstein, Amber Waddell, Carlos Alberto de Moura Aschoff, Xiangwen Chen‐Deutsch, Matthew Ellinwood, Roberto Méndez, Raquel Fernández, Deeksha Bali, Troy C. Lund, Laura Pollard, Richard Steet, Filippo Pinto e Vairo, Timothy C. Wood, Lorne A. Clarke, Catherine Rehder
Izdano 2024Artigo -
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Therapeutic neonatal hepatic gene therapy in mucopolysaccharidosis VII dogs od Katherine P. Ponder, John R. Melniczek, Lingfei Xu, Margaret A. Weil, Thomas O’Malley, Patricia A. O’Donnell, Van W. Knox, Gustavo D. Aguirre, Hamutal Mazrier, N. Matthew Ellinwood, Meg M. Sleeper, Albert M. Maguire, Susan W. Volk, Robert L. Mango, Jean Zweigle, John H. Wolfe, Mark E. Haskins
Izdano 2002Artigo -
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Derivation of adult canine intestinal organoids for translational research in gastroenterology od Lawrance C. Chandra, Dana C. Borcherding, Dawn D. Kingsbury, Todd Atherly, Yoko M. Ambrosini, Agnes Bourgois‐Mochel, Yuan Wang, Michael J. Kimber, Yijun Qi, Qun Wang, Michael J. Wannemuehler, N. Matthew Ellinwood, Elizabeth Snella, Martin Martin, Melissa C. Skala, David K. Meyerholz, Mary K. Estes, Martín E. Fernández-Zapico, Albert E. Jergens, Jonathan P. Mochel, Karin Allenspach
Izdano 2019Artigo -
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Safe, Efficient, and Reproducible Gene Therapy of the Brain in the Dog Models of Sanfilippo and Hurler Syndromes od N. Matthew Ellinwood, Jérôme Ausseil, Nathalie Desmaris, Stéphanie Bigou, Song Liu, Jackie K. Jens, Elizabeth Snella, Eman Mohammed, Chris Thomson, Sylvie Raoul, Béatrice Joussemet, Françoise Roux, Yan Chérel, Y Lajat, Monique Piraud, Rachid Benchaouir, Stephan Hermening, Harald Petry, Roseline Froissart, Marc Tardieu, Carine Ciron, Philippe Moullier, J. Parkes, Karen L. Kline, Irène Maire, Marie‐Thérèse Vanier, Jean‐Michel Heard, Marie-Anne Colle
Izdano 2010Artigo -
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Replacing the Enzyme α- <scp>l</scp> -Iduronidase at Birth Ameliorates Symptoms in the Brain and Periphery of Dogs with Mucopolysaccharidosis Type I od Ashley D. Dierenfeld, Michael F. McEntee, Carole Vogler, Charles H. Vite, Agnes H. Chen, Merry Passage, Steven Q. Le, Sahil Shah, Jackie K. Jens, Elizabeth Snella, Karen L. Kline, J. Parkes, Wendy A. Ware, Lori E. Moran, Amanda J. Fales‐Williams, Jane A. Wengert, R. David Whitley, Daniel M. Betts, Amy M. Boal, Elizabeth A. Riedesel, W Gross, N. Matthew Ellinwood, Patricia Dickson
Izdano 2010Artigo -
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Precision Medicine in Cats: Novel Niemann‐Pick Type C1 Diagnosed by Whole‐Genome Sequencing od Mauler, D.A., Gandolfi, B., Reinero, C.R., O'Brien, D.P., Spooner, J.L., Lyons, L.A., Aberdein, Danielle, Alves, Paulo C., Barsh, Gregory S., Beale, Holly C., Boyko, Adam R., Brockman, Jeffrey A., Castelhano, Marta G., Chan, Patricia P., Matthew Ellinwood, N., Fogle, Jonathan E., Garrick, Dorian J., Helps, Christopher R., Hytönen, Marjo K., Kaukonen, Maria, Kaelin, Christopher B., Leclerc, Emilie, Leeb, Tosso, Lohi, Hannes, Longeri, Maria, Malik, Richard, Montague, Michael J., Munday, John S., Murphy, William J., Pedersen, Niels C., Rothschild, Max F., Stern, Joshua A., Swanson, William F., Terio, Karen A., Todhunter, Rory J., Ueda, Yu, Warren, Wesley C., Wilcox, Elizabeth A., Wildschutte, Julia H.
Izdano 2017Text -
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Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy od Benjamin Cogné, Xénia Latypova, Lokuliyanage Dona Samudita Senaratne, Ludovic Martin, Daniel C. Koboldt, Georgios Kellaris, Lorraine Fievet, Guylène Le Meur, D. Caldari, Dominique Debray, Mathilde Nizon, Eirik Frengen, Sara J. Bowne, Elizabeth L. Cadena, Stephen P. Daiger, Kinga M. Bujakowska, Eric A. Pierce, Michael B. Gorin, Nicholas Katsanis, Stéphane Bézieau, Simon M. Petersen‐Jones, Laurence M. Occelli, Leslie A. Lyons, Laurence Legeai‐Mallet, Lori S. Sullivan, Erica E. Davis, Bertrand Isidor, Reuben M. Buckley, Danielle Aberdein, Paulo C. Alves, Gregory S. Barsh, Rebecca R. Bellone, Tomas F. Bergström, Adam R. Boyko, Jeffrey A. Brockman, Margret L. Casal, Marta G. Castelhano, O. Distl, Nicholas H. Dodman, N. Matthew Ellinwood, Jonathan E. Fogle, Oliver P. Forman, Dorian J. Garrick, Edward I. Ginns, Jens Häggström, Victoria L. Harvey, Daisuke Hasegawa, Bianca Haase, Chris R. Helps, Isabel Hernández, Marjo K. Hytönen, Maria Kaukonen, Christopher B. Kaelin, Tomoki Kosho, Emilie Leclerc, T.L. Lear, Tosso Leeb, Ronald H. L. Li, Hannes Lohi, M. Longeri, Mark A. Magnuson, Richard Malík, Shrinivasrao P. Mane, John S. Munday, William J. Murphy, Niels C. Pedersen, Max F. Rothschild, Clare Rusbridge, Beth Shapiro, Joshua A. Stern, William F. Swanson, Karen A. Terio, Rory J. Todhunter, Wesley C. Warren, Elizabeth A. Wilcox, Julia H Wildschutte, Yoshihiko Yu
Izdano 2020Artigo
Iskalna orodja:
Sorodne teme
Biology
Medicine
Gene
Biochemistry
Disease
Enzyme replacement therapy
Internal medicine
Mucopolysaccharidosis
Endocrinology
Genetics
Lysosomal storage disease
Pathology
Cell biology
Chemistry
Enzyme
Genetic enhancement
Hurler syndrome
Immune system
Immunology
Mucopolysaccharidosis I
Mucopolysaccharidosis type I
Phenotype
Receptor
Alkaline phosphatase
Biotechnology
Cancer research
Cancer stem cell
Candidate gene
Ciliary body
Ciliopathy