PMC Links for Protein (Select 1054487227) - PMC

Select item 60756181.

Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy

Andreia M. Nunes, Ryan D. Wuebbles, Apurva Sarathy, Tatiana M. Fontelonga, Marianne Deries, Dean J. Burkin, Sólveig Thorsteinsdóttir

Hum Mol Genet. 2017 Jun 1; 26(11): 2018–2033. Published online 2017 Mar 7. doi: 10.1093/hmg/ddx083

PMCID:: PMC6075618

Abstract Article PDF–2.8M

Select item 60755082.

PTRH2 gene mutation causes progressive congenital skeletal muscle pathology

Jinger Doe, Angela M. Kaindl, Mayumi Jijiwa, Michelle de la Vega, Hao Hu, Genevieve S. Griffiths, Tatiana M. Fontelonga, Pamela Barraza, Vivian Cruz, Pam Van Ry, Joe W. Ramos, Dean J. Burkin, Michelle L. Matter

Hum Mol Genet. 2017 Apr 15; 26(8): 1458–1464. Published online 2017 Feb 8. doi: 10.1093/hmg/ddx048

PMCID:: PMC6075508

Abstract Article PDF–513K

Select item 54515183.

α₇β₁ Integrin regulation of gene transcription in skeletal muscle following an acute bout of eccentric exercise

Ziad S. Mahmassani, Kook Son, Yair Pincu, Michael Munroe, Jenny Drnevich, Jie Chen, Marni D. Boppart

Am J Physiol Cell Physiol. 2017 May 1; 312(5): C638–C650. Published online 2017 Mar 8. doi: 10.1152/ajpcell.00106.2016

PMCID:: PMC5451518

Abstract Article

Select item 52888534.

Deletion of the Ste20-like kinase SLK in skeletal muscle results in a progressive myopathy and muscle weakness

Benjamin R. Pryce, Khalid N. Al-Zahrani, Sébastien Dufresne, Natalya Belkina, Cédrik Labrèche, Genaro Patino-Lopez, Jérôme Frenette, Stephen Shaw, Luc A. Sabourin

Skelet Muscle. 2017; 7: 3. Published online 2017 Feb 2. doi: 10.1186/s13395-016-0119-1