Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration

Por Murphy, Malea M., Lawson, Jennifer A., Mathew, Sam J., Hutcheson, David A., Kardon, Gabrielle
Publicado em 2011

Transiently Active Wnt/β-Catenin Signaling Is Not Required but Must Be Silenced for Stem Cell Function during Muscle Regeneration

Por Murphy, Malea M., Keefe, Alexandra C., Lawson, Jennifer A., Flygare, Steven D., Yandell, Mark, Kardon, Gabrielle
Publicado no Stem Cell Reports (2014)

Naturally Arising Human CD4 T-Cells That Recognize Islet Autoantigens and Secrete Interleukin-10 Regulate Proinflammatory T-Cell Responses via Linked Suppression

Por Tree, Timothy I.M., Lawson, Jennifer, Edwards, Hannah, Skowera, Ania, Arif, Sefina, Roep, Bart O., Peakman, Mark
Publicado em 2010

Muscle connective tissue controls development of the diaphragm and is a source of congenital diaphragmatic hernias

Por Merrell, Allyson J., Ellis, Benjamin J., Fox, Zachary D., Lawson, Jennifer A., Weiss, Jeffrey A., Kardon, Gabrielle
Publicado no Nat Genet (2015)

Muscle stem cells contribute to myofibers in sedentary adult mice

Por Keefe, Alexandra C., Lawson, Jennifer A., Flygare, Steven D., Fox, Zachary D., Colasanto, Mary P., Mathew, Sam J., Yandell, Mark, Kardon, Gabrielle
Publicado no Nat Commun (2015)

Connective tissue fibroblasts and Tcf4 regulate myogenesis

Por Mathew, Sam J., Hansen, Jody M., Merrell, Allyson J., Murphy, Malea M., Lawson, Jennifer A., Hutcheson, David A., Hansen, Mark S., Angus-Hill, Melinda, Kardon, Gabrielle
Publicado em 2011

Evolutionarily conserved morphogenetic movements at the vertebrate head–trunk interface coordinate the transport and assembly of hypopharyngeal structures

Por Lours-Calet, Corinne, Alvares, Lucia E., El-Hanfy, Amira S., Gandesha, Saniel, Walters, Esther H., Sobreira, Débora Rodrigues, Wotton, Karl R., Jorge, Erika C., Lawson, Jennifer A., Kelsey Lewis, A., Tada, Masazumi, Sharpe, Colin, Kardon, Gabrielle, Dietrich, Susanne
Publicado em 2014

Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies

Por Schueler, Markus, Halbritter, Jan, Phelps, Ian G., Braun, Daniela A., Otto, Edgar A., Porath, Jonathan D., Gee, Heon Yung, Shendure, Jay, O’Roak, Brian J., Lawson, Jennifer A., Soliman, Neveen A., Nabhan, Marwa M., Doherty, Dan, Hildebrandt, Friedhelm
Publicado no J Med Genet (2015)

Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis

Por Braun, Daniela Anne, Lawson, Jennifer Ashley, Gee, Heon Yung, Halbritter, Jan, Shril, Shirlee, Tan, Weizhen, Stein, Deborah, Wassner, Ari J., Ferguson, Michael A., Gucev, Zoran, Fisher, Brittany, Spaneas, Leslie, Varner, Jennifer, Sayer, John A., Milosevic, Danko, Baum, Michelle, Tasic, Velibor, Hildebrandt, Friedhelm
Publicado no Clin J Am Soc Nephrol (2016)

Mutations in SLC26A1 Cause Nephrolithiasis

Por Gee, Heon Yung, Jun, Ikhyun, Braun, Daniela A., Lawson, Jennifer A., Halbritter, Jan, Shril, Shirlee, Nelson, Caleb P., Tan, Weizhen, Stein, Deborah, Wassner, Ari J., Ferguson, Michael A., Gucev, Zoran, Sayer, John A., Milosevic, Danko, Baum, Michelle, Tasic, Velibor, Lee, Min Goo, Hildebrandt, Friedhelm
Publicado no Am J Hum Genet (2016)

Strategies to assess the validity of recommendations: a study protocol

Por Martínez García, Laura, Sanabria, Andrea Juliana, Araya, Ignacio, Lawson, Jennifer, Haynes, R Brian, Rigau, David, Solà, Ivan, Díaz del Campo, Petra, Estrada, Maria Dolors, Etxeandia-Ikobaltzeta, Itziar, García Álvarez, Elvira, Gracia, Javier, Kotzeva, Anna, Louro-González, Arturo, Salcedo-Fernandez, Flavia, Trujillo-Martín, Maria Mar, Alonso-Coello, Pablo
Publicado em 2013

The validity of recommendations from clinical guidelines: a survival analysis

Por García, Laura Martínez, Sanabria, Andrea Juliana, Álvarez, Elvira García, Trujillo-Martín, Maria Mar, Etxeandia-Ikobaltzeta, Itziar, Kotzeva, Anna, Rigau, David, Louro-González, Arturo, Barajas-Nava, Leticia, del Campo, Petra Díaz, Estrada, Maria-Dolors, Solà, Ivan, Gracia, Javier, Salcedo-Fernandez, Flavia, Lawson, Jennifer, Haynes, R. Brian, Alonso-Coello, Pablo
Publicado em 2014

IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype

Por Perrault, Isabelle, Halbritter, Jan, Porath, Jonathan D, Gérard, Xavier, Braun, Daniela A, Gee, Heon Yung, Fathy, Hanan M, Saunier, Sophie, Cormier-Daire, Valérie, Thomas, Sophie, Attié-Bitach, Tania, Boddaert, Nathalie, Taschner, Michael, Schueler, Markus, Lorentzen, Esben, Lifton, Richard P, Lawson, Jennifer A, Garfa-Traore, Meriem, Otto, Edgar A, Bastin, Philippe, Caillaud, Catherine, Kaplan, Josseline, Rozet, Jean-Michel, Hildebrandt, Friedhelm
Publicado no J Med Genet (2015)

Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity

Por Braun, Daniela A., Schueler, Markus, Halbritter, Jan, Gee, Heon Yung, Porath, Jonathan D., Lawson, Jennifer A., Airik, Rannar, Shril, Shirlee, Allen, Susan J., Stein, Deborah, Al Kindy, Adila, Beck, Bodo B., Cengiz, Nurcan, Moorani, Khemchand N., Ozaltin, Fatih, Hashmi, Seema, Sayer, John A., Bockenhauer, Detlef, Soliman, Neveen A., Otto, Edgar A., Lifton, Richard P., Hildebrandt, Friedhelm
Publicado no Kidney Int (2016)

Mutations in nuclear pore genes NUP93, NUP205, and XPO5 cause steroid resistant nephrotic syndrome

Por Braun, Daniela A., Sadowski, Carolin E., Kohl, Stefan, Lovric, Svjetlana, Astrinidis, Susanne A., Pabst, Werner L., Gee, Heon Yung, Ashraf, Shazia, Lawson, Jennifer A., Shril, Shirlee, Airik, Merlin, Tan, Weizhen, Schapiro, David, Rao, Jia, Choi, Won-Il, Hermle, Tobias, Kemper, Markus J., Pohl, Martin, Ozaltin, Fatih, Konrad, Martin, Bogdanovic, Radovan, Büscher, Rainer, Helmchen, Udo, Serdaroglu, Erkin, Lifton, Richard P., Antonin, Wolfram, Hildebrandt, Friedhelm
Publicado no Nat Genet (2016)