supported by the National Institutes of Health R01-AR053643;Veterans Research Administration Merit Award I01BX00515;a Research Support Funds Grant(RSFG),Indiana University Purdue University Indianapolis-Office of the Vice Chancellor for Research,Indianapolis to LIP.;supported by ASBMR Fund for Research and Education Research and Collaborative Grant Program;supported by the National Institutes of Health R01AG067997 to CJH;supported by the IUPUI Diversity Scholars Research Program(DSRP);Diversity Summer Undergraduate Research Opportunity Program(DS-UROP);Indiana CTSI Student Summer Research Program;IUPUI work study program;supported by the Life Health Science Internship(LHSI)。
Fragile X Messenger Ribonucleoprotein 1(FMR1)gene mutations lead to fragile X syndrome,cognitive disorders,and,in some individuals,scoliosis and craniofacial abnormalities.Four-month-old(mo)male mice with deletion of ...