Prader–Willi syndrome (PWS) is a neurodevelopmental disorder that arises from lack of
expression of paternally inherited genes known to be imprinted and located in the …

Skeletal myofibers are injured due to mechanical stresses experienced during physical
activity, or due to myofiber fragility caused by genetic diseases. The injured myofiber needs …

Objective. To determine whether phenotypic differences exist among individuals with Prader-
Willi syndrome with either type I or type II deletions of chromosome 15 or maternal disomy …

Metal response element-binding transcription factor-1 (MTF-1) is a six-zinc finger protein that
plays an essential role in activating metallothionein expression in response to the heavy …

Small nucleolar RNAs (snoRNAs) are a group of noncoding RNAs that perform various
biological functions, including biochemical modifications of other RNAs, precursors of …

Prader–Willi syndrome (PWS) is a complex neurodevelopmental disorder characterized by
hypotonia, suck and feeding difficulties, hypogonadism, small hands and feet …

Objective: To screen cDNA for NLGN3 and NLGN4 from lymphoblastoid cells from autistic
subjects. Methods and results: 10 young autistic females and 30 non-autistic subjects were …

Background—The importance of noncoding RNAs (ncRNA), especially microRNAs
(miRNAs), for maintaining stability in the developing vertebrate heart has recently become …

Background: X-chromosome inactivation (XCI) is the mechanism by which gene dosage
uniformity is achieved between female mammals with two X chromosomes and male …

Prader-Willi syndrome is a neurodevelopmental disorder that is characterized by infantile
hypotonia, feeding difficulties, hypogonadism, mental deficiency, hyperphagia (leading to …