References in periodicals archive

Genetic testing was performed on the mother and the infant, and they were both confirmed to have a novel heterozygous mutation in the ACTG2 gene (C632G>A, p.R211Q) on chromosome 2p13.1.

Visceral myopathy is a rare condition that has recently been attributed to mutations in the ACTG2 gene.

A Novel Mutation in ACTG2 Gene in Mother with Chronic Intestinal Pseudoobstruction and Fetus with Megacystis Microcolon Intestinal Hypoperistalsis Syndrome

Primers for electron transfer flavoprotein subunit alpha, mitochondrial (ETFa), actin (ACTG2), transgelin (TAGLN), cofilin-1 (CFL1), cyclophilin A (PPIA), myosin (MYL6), galectin-1 (LGALS1), apolipoprotein A-I (APOA), and control genes ([sz]-actin) were obtained from Shanghai Sangon Company, China.

Proteomic Analysis of the Uterosacral Ligament in Postmenopausal Women with and without Pelvic Organ Prolapse

The primary antibodies used were rabbit anti-yactin (ACTG2) (GeneTex, GTX101794, 100-fold dilution); rabbit anti-myosin light chain kinase (MYLK) (Origene, TA347970, 400-fold dilution); rabbit anti-PP1[delta] (PPP1CB) (EMD Millipore, 07-1217, 100-fold dilution), Santa Cruz Biotechnology, Santa Cruz, CA, USA; rabbit anti-ROCK2 (sc-5561, 100-fold dilution); rabbit anti-CPI-17 (PPP1R14A) (sc-48406, 100-fold dilution); rabbit anti-pT38-CPI-17 (sc17560-R, 50-fold dilution); rabbit anti-myosin light chain (MYL9) (sc-15370, 500-fold dilution); anti-pS19-MYL9 (sc19849-R, 500-fold dilution); rabbit anti-MYPT1 (PPP1R12A) (sc-25618, 100-fold dilution); rabbit anti-pT853-MYPT1 (sc17432-R; 100-fold dilution); and rabbit anti pT696/MYPT1 (sc-.017556; 200-fold dilution).

Contractile Protein Expression and Phosphorylation and Contractility of Gastric Smooth Muscles from Obese Patients and Patients with Obesity and Diabetes