Laminin-111 Protein Therapy Reduces Muscle Pathology and Improves Viability of a Mouse Model of Merosin-Deficient Congenital Muscular Dystrophy
Rooney, Jachinta E, Knapp, Jolie R, Hodges, Bradley L, Wuebbles, Ryan D, Burkin, Dean J
Published in The American journal of pathology (01.04.2012)
Published in The American journal of pathology (01.04.2012)
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Collagen VIα2 chain deficiency causes trabecular bone loss by potentially promoting osteoclast differentiation through enhanced TNFα signaling
Pham, Hai T., Kram, Vardit, Dar, Qurratul-Ain, Komori, Taishi, Ji, Youngmi, Mohassel, Payam, Rooney, Jachinta, Li, Li, Kilts, Tina M., Bonnemann, Carsten, Lamande, Shireen, Young, Marian F.
Published in Scientific reports (13.08.2020)
Published in Scientific reports (13.08.2020)
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Transgenic overexpression of the α7 integrin reduces muscle pathology and improves viability in the dy(W) mouse model of merosin-deficient congenital muscular dystrophy type 1A
Doe, Jinger A, Wuebbles, Ryan D, Allred, Erika T, Rooney, Jachinta E, Elorza, Margaret, Burkin, Dean J
Published in Journal of cell science (01.07.2011)
Published in Journal of cell science (01.07.2011)
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Myotendinous Junction Defects and Reduced Force Transmission in Mice that Lack α7 Integrin and Utrophin
Welser, Jennifer V, Rooney, Jachinta E, Cohen, Nicolette C, Gurpur, Praveen B, Singer, Cherie A, Evans, Rebecca A, Haines, Bryan A, Burkin, Dean J
Published in The American journal of pathology (2009)
Published in The American journal of pathology (2009)
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Transgenic overexpression of the α7 integrin reduces muscle pathology and improves viability in the dyW mouse model of merosin-deficient congenital muscular dystrophy type 1A
Doe, Jinger A., Wuebbles, Ryan D., Allred, Erika T., Rooney, Jachinta E., Elorza, Margaret, Burkin, Dean J.
Published in Journal of cell science (01.07.2011)
Published in Journal of cell science (01.07.2011)
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GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome
Foley, A. Reghan, Zou, Yaqun, Dunford, James E., Rooney, Jachinta, Chandra, Goutam, Xiong, Hui, Straub, Volker, Voit, Thomas, Romero, Norma, Donkervoort, Sandra, Hu, Ying, Markello, Thomas, Horn, Adam, Qebibo, Leila, Dastgir, Jahannaz, Meilleur, Katherine G., Finkel, Richard S., Fan, Yanbin, Mamchaoui, Kamel, Duguez, Stephanie, Nelson, Isabelle, Laporte, Jocelyn, Santi, Mariarita, Malfatti, Edoardo, Maisonobe, Thierry, Touraine, Philippe, Hirano, Michio, Hughes, Imelda, Bushby, Kate, Oppermann, Udo, Böhm, Johann, Jaiswal, Jyoti K., Stojkovic, Tanya, Bönnemann, Carsten G.
Published in Annals of neurology (01.08.2020)
Published in Annals of neurology (01.08.2020)
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Successfully Navigating Food and Drug Administration Orphan Drug and Rare Pediatric Disease Designations for AAV9-hPCCA Gene Therapy: The National Institutes of Health Platform Vector Gene Therapy Experience
Lomash, Richa Madan, Shchelochkov, Oleg, Chandler, Randy J, Venditti, Charles P, Pariser, Anne R, Ottinger, Elizabeth A
Published in Human gene therapy (01.03.2023)
Published in Human gene therapy (01.03.2023)
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Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family
Zukosky, Kristen, Meilleur, Katherine, Traynor, Bryan J, Dastgir, Jahannaz, Medne, Livija, Devoto, Marcella, Collins, James, Rooney, Jachinta, Zou, Yaqun, Yang, Michele L, Gibbs, J Raphael, Meier, Markus, Stetefeld, Joerg, Finkel, Richard S, Schessl, Joachim, Elman, Lauren, Felice, Kevin, Ferguson, Toby A, Ceyhan-Birsoy, Ozge, Beggs, Alan H, Tennekoon, Gihan, Johnson, Janel O, Bönnemann, Carsten G
Published in JAMA neurology (01.06.2015)
Published in JAMA neurology (01.06.2015)
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Role for the α7β1 integrin in vascular development and integrity
Flintoff‐Dye, Nichole L., Welser, Jennifer, Rooney, Jachinta, Scowen, Paul, Tamowski, Susan, Hatton, William, Burkin, Dean J.
Published in Developmental dynamics (01.09.2005)
Published in Developmental dynamics (01.09.2005)
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199th ENMC international workshop: FHL1 related myopathies, June 7–9, 2013, Naarden, The Netherlands
Bertrand, Anne T, Bönnemann, Carsten G, Bonne, Gisèle
Published in Neuromuscular disorders : NMD (01.05.2014)
Published in Neuromuscular disorders : NMD (01.05.2014)
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Conference Proceeding
Transgenic overexpression of the alpha 7 integrin reduces muscle pathology and improves viability in the dyW mouse model of merosin-deficient congenital muscular dystrophy type 1A
Doe, Jinger A, Wuebbles, Ryan D, Allred, Erika T, Rooney, Jachinta E, Elorza, Margaret, Burkin, Dean J
Published in Journal of cell science (01.07.2011)
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Published in Journal of cell science (01.07.2011)
Journal Article
Collagen type VI regulates TGFβ bioavailability in skeletal muscle
Mohassel, Payam, Rooney, Jachinta, Zou, Yaqun, Johnson, Kory, Norato, Gina, Hearn, Hailey, Nalls, Matthew A, Yun, Pomi, Ogata, Tracy, Silverstein, Sarah, Sleboda, David A, Roberts, Thomas J, Rifkin, Daniel B, Bönnemann, Carsten G
Published in bioRxiv : the preprint server for biology (24.06.2023)
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Published in bioRxiv : the preprint server for biology (24.06.2023)
Journal Article
Role for the alpha7beta1 integrin in vascular development and integrity
Flintoff-Dye, Nichole L, Welser, Jennifer, Rooney, Jachinta, Scowen, Paul, Tamowski, Susan, Hatton, William, Burkin, Dean J
Published in Developmental dynamics (01.09.2005)
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Published in Developmental dynamics (01.09.2005)
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