1. Activation of serum/glucocorticoid‐induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy. Issue 1 (19th November 2012) Authors: Andres‐Mateos, Eva; Brinkmeier, Heinrich; Burks, Tyesha N.; Mejias, Rebeca; Files, Daniel C.; Steinberger, Martin; Soleimani, Arshia; Marx, Ruth; Simmers, Jessica L.; Lin, Benjamin; Finanger Hedderick, Erika; Marr, Tom G.; Lin, Brian M.; Hourdé, Christophe; Leinwand, Leslie A.; Kuhl, Dietmar; Föl... Journal: EMBO molecular medicine Issue: Volume 5:Issue 1(2013:Jan.) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Activation of serum/glucocorticoid‐induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy. Issue 1 (19th November 2012) Authors: Andres‐Mateos, Eva; Brinkmeier, Heinrich; Burks, Tyesha N.; Mejias, Rebeca; Files, Daniel C.; Steinberger, Martin; Soleimani, Arshia; Marx, Ruth; Simmers, Jessica L.; Lin, Benjamin; Finanger Hedderick, Erika; Marr, Tom G.; Lin, Brian M.; Hourdé, Christophe; Leinwand, Leslie A.; Kuhl, Dietmar; Föl... Journal: EMBO molecular medicine Issue: Volume 5:Issue 1(2013:Jan.) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Development of therapeutic genome engineering in laminin-α2-deficient congenital muscular dystrophy. Issue 1 (14th March 2019) Authors: Kemaladewi, Dwi U.; Cohn, Ronald D. Editors: MacKenzie, Alex; Groft, Stephen; Justice, Monica; van Karnebeek, Clara Journal: Emerging topics in life sciences Issue: Volume 3:Issue 1(2019) Page Start: 11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. ERCC6L2‐associated inherited bone marrow failure syndrome. Issue 3 (6th April 2018) Authors: Shabanova, Iren; Cohen, Elisa; Cada, Michaela; Vincent, Ajoy; Cohn, Ronald D.; Dror, Yigal Journal: Molecular genetics & genomic medicine Issue: Volume 6:Issue 3(2018) Page Start: 463 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Exon Snipping in Duchenne Muscular Dystrophy. Issue 3 (March 2016) Authors: Kemaladewi, Dwi U.; Cohn, Ronald D. Journal: Trends in molecular medicine Issue: Volume 22:Issue 3(2016) Page Start: 187 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genome sequencing among children with medical complexity: What constitutes value from parents' perspective?. Issue 2 (21st October 2021) Authors: Lee, Whiwon; Luca, Stephanie; Costain, Gregory; Snell, Meaghan; Marano, Maria; Curtis, Meredith; Dunsmore, Kourtney; Veenma, Danielle; Walker, Susan; Cohn, Ronald D.; Marshall, Christian R.; Cohen, Eyal; Meyn, M. Stephen; Orkin, Julia; Hayeems, Robin Z. Journal: Journal of genetic counseling Issue: Volume 31:Issue 2(2022) Page Start: 523 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Letter to the Editor. (March 2019) Authors: Cohn, Ronald D. Journal: Forensic science international Issue: Volume 296(2019) Page Start: 144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Maintaining skeletal muscle mass: lessons learned from hibernation. Issue 4 (17th January 2014) Authors: Ivakine, Evgueni A.; Cohn, Ronald D. Journal: Experimental physiology Issue: Volume 99:Issue 4(2014:Apr.) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Maintaining skeletal muscle mass: lessons learned from hibernation. Issue 4 (24th February 2014) Authors: Ivakine, Evgueni A.; Cohn, Ronald D. Journal: Experimental physiology Issue: Volume 99:Issue 4(2014:Apr.) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. MEF2C-related epilepsy: Delineating the phenotypic spectrum from a novel mutation and literature review. (April 2019) Authors: Borlot, Felippe; Whitney, Robyn; Cohn, Ronald D.; Weiss, Shelly K. Journal: Seizure Issue: Volume 67(2019) Page Start: 86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗