Fibrogenesis in LAMA2-Related Muscular Dystrophy Is a Central Tenet of Disease Etiology

מאת Accorsi, Anthony, Cramer, Megan L., Girgenrath, Mahasweta
הוצא לאור ב Front Mol Neurosci (2020)

Diseased muscles that lack dystrophin or laminin-α2 have altered compositions and proliferation of mononuclear cell populations

מאת Girgenrath, Mahasweta, Kostek, Christine A, Miller, Jeffrey Boone
יצא לאור 2005

Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2(Dy-w) mice, a model for congenital muscular dystrophy type 1A

מאת Kumar, Ajay, Yamauchi, Jenny, Girgenrath, Tanya, Girgenrath, Mahasweta
יצא לאור 2011

Do's and Don'ts in the Preparation of Muscle Cryosections for Histological Analysis

מאת Kumar, Ajay, Accorsi, Anthony, Rhee, Younghwa, Girgenrath, Mahasweta
הוצא לאור ב J Vis Exp (2015)

Prdm1 (Blimp-1) and the Expression of Fast and Slow Myosin Heavy Chain Isoforms during Avian Myogenesis In Vitro

מאת Beermann, Mary Lou, Ardelt, Magdalena, Girgenrath, Mahasweta, Miller, Jeffrey Boone
יצא לאור 2010

Magnetic Resonance Imaging Is Sensitive to Pathological Amelioration in a Model for Laminin-Deficient Congenital Muscular Dystrophy (MDC1A)

מאת Vohra, Ravneet, Accorsi, Anthony, Kumar, Ajay, Walter, Glenn, Girgenrath, Mahasweta
הוצא לאור ב PLoS One (2015)

Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy

מאת Girgenrath, Mahasweta, Dominov, Janice A., Kostek, Christine A., Boone Miller, Jeffrey
יצא לאור 2004

Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy

מאת Mehuron, Thomas, Kumar, Ajay, Duarte, Lina, Yamauchi, Jenny, Accorsi, Anthony, Girgenrath, Mahasweta
יצא לאור 2014

Correction: dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy

מאת Mehuron, Thomas, Kumar, Ajay, Duarte, Lina, Yamauchi, Jenny, Accorsi, Anthony, Girgenrath, Mahasweta
יצא לאור 2014

Pathology is alleviated by doxycycline in a laminin-α2-null model of congenital muscular dystrophy

מאת Girgenrath, Mahasweta, Beermann, Mary Lou, Vishnudas, Vivek K., Homma, Sachiko, Miller, Jeffrey Boone
יצא לאור 2009

miR-410 and miR-495 Are Dynamically Regulated in Diverse Cardiomyopathies and Their Inhibition Attenuates Pathological Hypertrophy

מאת Clark, Amanda L., Maruyama, Sonomi, Sano, Soichi, Accorsi, Anthony, Girgenrath, Mahasweta, Walsh, Kenneth, Naya, Francisco J.
הוצא לאור ב PLoS One (2016)

Immortalization of mouse myogenic cells can occur without loss of p16(INK4a), p19(ARF), or p53 and is accelerated by inactivation of Bax

מאת Nowak, Jonathan A, Malowitz, Jonathan, Girgenrath, Mahasweta, Kostek, Christine A, Kravetz, Amanda J, Dominov, Janice A, Miller, Jeffrey Boone
יצא לאור 2004

Report on the Myomatrix Conference April 22–24, 2012, University of Nevada, Reno, Nevada, USA

מאת Rutkowski, Anne, Bönnemann, Carsten, Brown, Susan, Sólveig, Thorsteinsdóttir, Dominov, Janice, Ruegg, Markus A., Matter, Michelle L., Guttridge, Denis, Crosbie-Watson, Rachelle H., Kardon, Gabrielle, Nagaraju, Kanneboyina, Girgenrath, Mahasweta, Burkin, Dean J.
הוצא לאור ב Neuromuscul Disord (2012)

Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy

מאת Willmann, Raffaella, Gordish-Dressman, Heather, Meinen, Sarina, Rüegg, Markus A., Yu, Qing, Nagaraju, Kanneboyina, Kumar, Ayar, Girgenrath, Mahasweta, Coffey, Caroline B.M., Cruz, Vivian, Van Ry, Pam M., Bogdanik, Laurent, Lutz, Cathleen, Rutkowski, Anne, Burkin, Dean J.
הוצא לאור ב J Neuromuscul Dis (2017)

TWEAK, via its receptor Fn14, is a novel regulator of mesenchymal progenitor cells and skeletal muscle regeneration

מאת Girgenrath, Mahasweta, Weng, Shawn, Kostek, Christine A, Browning, Beth, Wang, Monica, Brown, Sharron AN, Winkles, Jeffrey A, Michaelson, Jennifer S, Allaire, Norm, Schneider, Pascal, Scott, Martin L, Hsu, Yen-ming, Yagita, Hideo, Flavell, Richard A, Miller, Jeffrey Boone, Burkly, Linda C, Zheng, Timothy S
יצא לאור 2006

“Of Mice and Measures”: A Project to Improve How We Advance Duchenne Muscular Dystrophy Therapies to the Clinic: First Workshop Report: Examining current findings and opportunities...

מאת Gordish-Dressman, Heather, Willmann, Raffaella, Dalle Pazze, Laura, Kreibich, Arati, van Putten, Maaike, Heydemann, Ahlke, Bogdanik, Laurent, Lutz, Cathleen, Davies, Kay, Demonbreun, Alexis R., Duan, Dongsheng, Elsey, David, Fukada, So-ichiro, Girgenrath, Mahasweta, Patrick Gonzalez, J., Grounds, Miranda D., Nichols, Andy, Partridge, Terry, Passini, Marco, Sanarica, Francesca, Schnell, Frederick J., Wells, Dominic J., Yokota, Toshifumi, Young, Courtney S., Zhong, Zhong, Spurney, Christopher, Spencer, Melissa, De Luca, Annamaria, Nagaraju, Kanneboyina, Aartsma-Rus, Annemieke
הוצא לאור ב J Neuromuscul Dis (2018)