Gabrielle Kardon

Publication Activity (10 Years)

Years Active: 2016-2022
Publications (10 Years): 6

Top Topics

Dna Methylation

Skeletal Muscle

Top Venues

Disease models & mechanisms

Science advances

Development (Cambridge, England)

This page only lists publications with an associated author ORCID identifier.

Publications

Elizabeth M Sefton, Mirialys Gallardo, Claire E Tobin, Brittany C Collins, Mary P Colasanto, Allyson J Merrell, Gabrielle Kardon
Fibroblast-derived Hgf controls recruitment and expansion of muscle during morphogenesis of the mammalian diaphragm. eLife 11 (2022)
Brittany C Collins, Gabrielle Kardon
It takes all kinds: heterogeneity among satellite cells and fibro-adipogenic progenitors during skeletal muscle regeneration. Development (Cambridge, England) 148 (21) (2021)
Glenda Evangelina Comai, Eglantine Heude, Sebastian Mella, Sylvain Paisant, Francesca Pala, Mirialys Gallardo, Francina Langa, Gabrielle Kardon, Swetha Gopalakrishnan, Shahragim Tajbakhsh
A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle. eLife 8 (2019)
Timothy D Heden, Jordan M Johnson, Patrick J Ferrara, Hiroaki Eshima, Anthony R P Verkerke, Edward J Wentzler, Piyarat Siripoksup, Tara M Narowski, Chanel B Coleman, Chien-Te Lin, Terence E Ryan, Paul T Reidy, Lisandra E de Castro Brás, Courtney M Karner, Charles F Burant, J Alan Maschek, James Eric Cox, Douglas G Mashek, Gabrielle Kardon, Sihem Boudina, Tonya N Zeczycki, Jared Rutter, Saame Raza Shaikh, Jean E Vance, Micah J Drummond, P Darrell Neufer, Katsuhiko Funai
Mitochondrial PE potentiates respiratory enzymes to amplify skeletal muscle aerobic capacity. Science advances 5 (9) (2019)
Gabrielle Kardon, Kate G Ackerman, David J McCulley, Yufeng Shen, Julia Wynn, Linshan Shang, Eric Bogenschutz, Xin Sun, Wendy K Chung
Congenital diaphragmatic hernias: from genes to mechanisms to therapies. Disease models & mechanisms 10 (8) (2018)
Mary P Colasanto, Shai Eyal, Payam Mohassel, Michael Bamshad, Carsten G Bonnemann, Elazar Zelzer, Anne M Moon, Gabrielle Kardon
Development of a subset of forelimb muscles and their attachment sites requires the ulnar-mammary syndrome gene Tbx3. Disease models & mechanisms 9 (11) (2016)