Putting It All Together: Postmortem Diagnosis of a Rare Ichthyosis Syndrome

por Jain, Pragya Virendrakumar, Maxey, Jauntea, W Lawlor, Michael, Parsons, Lauren N
Publicado 2023

Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature

por Kilbourn, Kent J., Green, Jaquise, Zacharewski, Nicholas, Aferzon, Joseph, Lawlor, Michael, Jaffa, Matthew
Publicado 2022

Duchenne muscular dystrophy (DMD) cardiomyocyte-secreted exosomes promote the pathogenesis of DMD-associated cardiomyopathy

por Gartz, Melanie, Lin, Chien-Wei, Sussman, Mark A., Lawlor, Michael W., Strande, Jennifer L.
Publicado 2020

Effects of Regulatory T Cell Depletion in BALB/c Mice Infected with Low Doses of Borrelia burgdorferi

por Santiago, Kaitlyn N., Kozlik, Tanya, Liedhegner, Elizabeth S., Slick, Rebecca A., Lawlor, Michael W., Nardelli, Dean T.
Publicado 2023

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy

por Konersman, Chamindra G., Freyermuth, Fernande, Winder, Thomas L., Lawlor, Michael W., Lagier‐Tourenne, Clotilde, Patel, Shailendra B.
Publicado 2017

Cardioprotective effect of nicorandil on isoproterenol induced cardiomyopathy in the Mdx mouse model

por Sullivan, Rachel T., Lam, Ngoc T., Haberman, Margaret, Beatka, Margaret J., Afzal, Muhammad Z., Lawlor, Michael W., Strande, Jennifer L.
Publicado 2021

One-Year Results of a Community-Based Translation of the Diabetes Prevention Program: Healthy-Living Partnerships to Prevent Diabetes (HELP PD) Project

por Katula, Jeffrey A., Vitolins, Mara Z., Rosenberger, Erica L., Blackwell, Caroline S., Morgan, Timothy M., Lawlor, Michael S., Goff, David C.
Publicado 2011

Novel mutations in NEB cause abnormal nebulin expression and markedly impaired muscle force generation in severe nemaline myopathy

por Lawlor, Michael W, Ottenheijm, Coen A, Lehtokari, Vilma-Lotta, Cho, Kiyomi, Pelin, Katarina, Wallgren-Pettersson, Carina, Granzier, Henk, Beggs, Alan H
Publicado 2011

Mechanosensory and ATP Release Deficits following Keratin14-Cre-Mediated TRPA1 Deletion Despite Absence of TRPA1 in Murine Keratinocytes

por Zappia, Katherine J., Garrison, Sheldon R., Palygin, Oleg, Weyer, Andy D., Barabas, Marie E., Lawlor, Michael W., Staruschenko, Alexander, Stucky, Cheryl L.
Publicado 2016

Loss of Mtm1 causes cholestatic liver disease in a model of X-linked myotubular myopathy

por Karolczak, Sophie, Deshwar, Ashish R., Aristegui, Evangelina, Kamath, Binita M., Lawlor, Michael W., Andreoletti, Gaia, Volpatti, Jonathan, Ellis, Jillian L., Yin, Chunyue, Dowling, James J.
Publicado 2023

Effect of the Look AHEAD Study Intervention on Medication Use and Related Cost to Treat Cardiovascular Disease Risk Factors in Individuals With Type 2 Diabetes

por Redmon, J. Bruce, Bertoni, Alain G., Connelly, Stephanie, Feeney, Patricia A., Glasser, Stephen P., Glick, Henry, Greenway, Frank, Hesson, Louise A., Lawlor, Michael S., Montez, Maria, Montgomery, Brenda
Publicado 2010

Muscle‐directed gene therapy corrects Pompe disease and uncovers species‐specific GAA immunogenicity

por Eggers, Michelle, Vannoy, Charles H, Huang, Jianyong, Purushothaman, Pravinkumar, Brassard, Jacqueline, Fonck, Carlos, Meng, Hui, Prom, Mariah J, Lawlor, Michael W, Cunningham, Justine, Sadhu, Chanchal, Mavilio, Fulvio
Publicado 2021

Skeletal Muscle Pathology in X-Linked Myotubular Myopathy: Review With Cross-Species Comparisons

por Lawlor, Michael W., Beggs, Alan H., Buj-Bello, Ana, Childers, Martin K., Dowling, James J., James, Emma S., Meng, Hui, Moore, Steven A., Prasad, Suyash, Schoser, Benedikt, Sewry, Caroline A.
Publicado 2016

Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function

por Hall, Arielle, Fontelonga, Tatiana, Wright, Alec, Bugda Gwilt, Katlynn, Widrick, Jeffrey, Pasut, Alessandra, Villa, Francesco, Miranti, Cynthia K., Gibbs, Devin, Jiang, Evan, Meng, Hui, Lawlor, Michael W., Gussoni, Emanuela
Publicado 2020

rAAV-related therapy fully rescues myonuclear and myofilament function in X-linked myotubular myopathy

por Ross, Jacob A., Tasfaout, Hichem, Levy, Yotam, Morgan, Jennifer, Cowling, Belinda S., Laporte, Jocelyn, Zanoteli, Edmar, Romero, Norma B., Lowe, Dawn A., Jungbluth, Heinz, Lawlor, Michael W., Mack, David L., Ochala, Julien
Publicado 2020

Tissue Triage and Freezing for Models of Skeletal Muscle Disease

por Meng, Hui, Janssen, Paul M.L., Grange, Robert W., Yang, Lin, Beggs, Alan H., Swanson, Lindsay C., Cossette, Stacy A., Frase, Alison, Childers, Martin K., Granzier, Henk, Gussoni, Emanuela, Lawlor, Michael W.
Publicado 2014

Troponin activator augments muscle force in nemaline myopathy patients with nebulin mutations

por de Winter, Josine Marieke, Buck, Danielle, Hidalgo, Carlos, Jasper, Jeffrey R, Malik, Fady I, Clarke, Nigel F, Stienen, Ger J M, Lawlor, Michael W, Beggs, Alan H, Ottenheijm, Coen A C, Granzier, Henk
Publicado 2013

Whole-thorax irradiation induces hypoxic respiratory failure, pleural effusions and cardiac remodeling

por Medhora, Meetha, Gao, Feng, Glisch, Chad, Narayanan, Jayashree, Sharma, Ashish, Harmann, Leanne M., Lawlor, Michael W., Snyder, Laura A., Fish, Brian L., Down, Julian D., Moulder, John E., Strande, Jennifer L., Jacobs, Elizabeth R.
Publicado 2015

Intrahepatic Cholestasis Is a Clinically Significant Feature Associated with Natural History of X-Linked Myotubular Myopathy (XLMTM): A Case Series and Biopsy Report

por Molera, Cristina, Sarishvili, Tinatin, Nascimento, Andrés, Rtskhiladze, Irakli, Muñoz Bartolo, Gema, Fernández Cebrián, Santiago, Valverde Fernández, Justo, Muñoz Cabello, Beatriz, Graham, Robert J., Miller, Weston, Sepulveda, Bryan, Kamath, Binita M., Meng, Hui, Lawlor, Michael W.
Publicado 2022

Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency

por Nagree, Murtaza S., Rybova, Jitka, Kleynerman, Annie, Ahrenhoerster, Carissa J., Saville, Jennifer T., Xu, TianMeng, Bachochin, Maxwell, McKillop, William M., Lawlor, Michael W., Pshezhetsky, Alexey V., Isaeva, Olena, Budde, Matthew D., Fuller, Maria, Medin, Jeffrey A.
Publicado 2023