HnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies

Authors: Alexander, Matthew S., Hightower, Rylie M., Reid, Andrea L., Bennett, Alexis H., Iyer, Lakshmanan, Slonim, Donna K., Saha, Madhurima, Kawahara, Genri, Kunkel, Louis M., Kopin, Alan S., Gupta, Vandana A., Kang, Peter B., Draper, Isabelle

Source: Muscle & nerve. 63(6):928-940

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100130984500.0x000001&indx=1&recIds=ETOCvdc_100130984500.0x000001

The SINE Compound KPT-350 Blocks Dystrophic Pathologies in DMD Zebrafish and Mice

Authors: Hightower, Rylie M. ^{1, 2}, Reid, Andrea L. ¹, Gibbs, Devin E. ³, Wang, Yimin ¹, Widrick, Jeffrey J. ³, Kunkel, Louis M. ^{3, 4, 5, 6}, Kastenschmidt, Jenna M. ^{7, 8}, Villalta, S. Armando ^{7, 8}, van Groen, Thomas ⁹, Chang, Hua ¹⁰, Gornisiewicz, Savanna ¹⁰, Landesman, Yosef ¹⁰, Tamir, Sharon ¹⁰, Alexander, Matthew S. ^{1, 2, 11, 12, ∗}

Source: In Molecular Therapy 8 January 2020 28(1):189-201

Mouse genotyping in an hour

Authors: Reid, Andrea L., Alexander, Matthew S.

Source: Muscle & nerve. 61(6):679-680

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100152446175.0x000001&indx=1&recIds=ETOCvdc_100152446175.0x000001

Next-Generation SINE Compound KPT−8602 Ameliorates Dystrophic Pathology in Zebrafish and Mouse Models of DMD.

Authors: English, Katherine G., Reid, Andrea L., Samani, Adrienne, Coulis, Gerald J. F., Villalta, S. Armando, Walker, Christopher J., Tamir, Sharon, Alexander, Matthew S.

Source: Biomedicines; Oct2022, Vol. 10 Issue 10, pN.PAG-N.PAG, 13p

Subject Terms: PATHOLOGY, LABORATORY mice, DUCHENNE muscular dystrophy, BRACHYDANIO, DYSTROPHIN genes

miR-486 is essential for muscle function and suppresses a dystrophic transcriptome.

Authors: Samani, Adrienne, Hightower, Rylie M., Reid, Andrea L., English, Katherine G., Lopez, Michael A., Doyle, J. Scott, Conklin, Michael J., Schneider, David A., Bamman, Marcas M., Widrick, Jeffrey J., Crossman, David K., Min Xie, Jee, David, Lai, Eric C., Alexander, Matthew S.

Source: Life Science Alliance; Sep2022, Vol. 5 Issue 9, p1-15, 15p

DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies.

Authors: Reid, Andrea L, Wang, Yimin, Samani, Adrienne, Hightower, Rylie M, Lopez, Michael A, Gilbert, Shawn R, Ianov, Lara, Crossman, David K, Dell'Italia, Louis J, Millay, Douglas P, Groen, Thomas van, Halade, Ganesh V, Alexander, Matthew S

Source: Human Molecular Genetics; Sep2020, Vol. 29 Issue 17, p2855-2871, 17p

What are the perceptions of runners and healthcare professionals on footwear and running injury risk?

Authors: Dhillon, Gurmeet K., Hunt, Michael A., Reid, Andrea L., Esculier, Jean-Francois

Source: BMJ Open Sport & Exercise Medicine; 6/30/2020, Vol. 6, p1-7, 7p

The Interplay of Mitophagy and Inflammation in Duchenne Muscular Dystrophy.

Authors: Reid, Andrea L.¹ (AUTHOR) areid01@uab.edu, Alexander, Matthew S.^1,2,3,4 (AUTHOR) malexander@peds.uab.edu

Source: Life (2075-1729). Jul2021, Vol. 11 Issue 7, p648. 1p.

Subject Terms: *DUCHENNE muscular dystrophy, *PATHOLOGY, *DRUG target, *DYSTROPHIN genes, *ARRHYTHMIA, *MYOFIBROBLASTS, *MUSCLE growth