High-density genomewide linkage analysis of exceptional human longevity identifies multiple novel loci.

by Steven E Boyden, Louis M Kunkel
Published 2010-08-01

Skeletal muscle regeneration and muscle progenitor cells

by Norio Motohashi, Matthew S. Alexander, Louis M. Kunkel
Published 2012-08-01

To dystrophin and beyond: an interview with Louis Kunkel

by Louis M. Kunkel, Annemieke Aartsma-Rus, James Dowling, Maaike van Putten
Published 2020-02-01

An open source microcontroller based flume for evaluating swimming performance of larval, juvenile, and adult zebrafish.

by Jeffrey J Widrick, Devin E Gibbs, Benjamin Sanchez, Vandana A Gupta, Anna Pakula, Christian Lawrence, Alan H Beggs, Louis M Kunkel
Published 2018-01-01

Molecular classification of nemaline myopathies: “nontyping” specimens exhibit unique patterns of gene expression

by Despina Sanoudou, Leslie A. Frieden, Judith N. Haslett, Alvin T. Kho, Steven A. Greenberg, Isaac S. Kohane, Louis M. Kunkel, Alan H. Beggs
Published 2004-04-01

Effect of serotonin modulation on dystrophin-deficient zebrafish

by Janelle M. Spinazzola, Matthias R. Lambert, Devin E. Gibbs, James R. Conner, Georgia L. Krikorian, Prithu Pareek, Carlo Rago, Louis M. Kunkel
Published 2020-08-01

A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish.

by Vandana A Gupta, Genri Kawahara, Jennifer A Myers, Aye T Chen, Thomas E Hall, M Chiara Manzini, Peter D Currie, Yi Zhou, Leonard I Zon, Louis M Kunkel, Alan H Beggs
Published 2012-01-01

Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease.

by Nathan P Palmer, Jocelyn A Silvester, Jessica J Lee, Andrew L Beam, Inbar Fried, Vladimir I Valtchinov, Fedik Rahimov, Sek Won Kong, Saum Ghodoussipour, Helen C Hood, Athos Bousvaros, Richard J Grand, Louis M Kunkel, Isaac S Kohane
Published 2019-01-01

Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.

by Sek Won Kong, Christin D Collins, Yuko Shimizu-Motohashi, Ingrid A Holm, Malcolm G Campbell, In-Hee Lee, Stephanie J Brewster, Ellen Hanson, Heather K Harris, Kathryn R Lowe, Adrianna Saada, Andrea Mora, Kimberly Madison, Rachel Hundley, Jessica Egan, Jillian McCarthy, Ally Eran, Michal Galdzicki, Leonard Rappaport, Louis M Kunkel, Isaac S Kohane
Published 2012-01-01

POLRMT mutations impair mitochondrial transcription causing neurological disease

by Monika Oláhová, Bradley Peter, Zsolt Szilagyi, Hector Diaz-Maldonado, Meenakshi Singh, Ewen W. Sommerville, Emma L. Blakely, Jack J. Collier, Emily Hoberg, Viktor Stránecký, Hana Hartmannová, Anthony J. Bleyer, Kim L. McBride, Sasigarn A. Bowden, Zuzana Korandová, Alena Pecinová, Hans-Hilger Ropers, Kimia Kahrizi, Hossein Najmabadi, Mark A. Tarnopolsky, Lauren I. Brady, K. Nicole Weaver, Carlos E. Prada, Katrin Õunap, Monica H. Wojcik, Sander Pajusalu, Safoora B. Syeda, Lynn Pais, Elicia A. Estrella, Christine C. Bruels, Louis M. Kunkel, Peter B. Kang, Penelope E. Bonnen, Tomáš Mráček, Stanislav Kmoch, Gráinne S. Gorman, Maria Falkenberg, Claes M. Gustafsson, Robert W. Taylor
Published 2021-02-01

Small RNA and A-to-I editing in Autism Spectrum Disorders

by Eran, Alal
Published 2013