Long noncoding RNAs (lncRNAs) are emerging as potential key regulators in gene
expression networks and exhibit a surprising range of shapes and sizes. Several distinct …

Prader-Willi syndrome (PWS) is characterized by severe hypotonia and feeding difficulties in
early infancy, followed in later infancy or early childhood by excessive eating and gradual …

El trastorno del espectro autista (TEA) fue descrito por primera vez en 1943 por Leo Kanner,
y desde entonces se han publicado 18 490 artículos, los cuales han sido citados 48 416 …

Prader-Willi syndrome (PWS) is caused by a loss of paternally expressed genes in an
imprinted region of chromosome 15q. Among the canonical PWS phenotypes are …

Prader–Willi syndrome (PWS) is an imprinting disorder caused by a deficiency of paternally
expressed gene (s) in the 15q11–q13 chromosomal region. The regulation of imprinted …

C/D box snoRNAs (SNORDs) are an abundantly expressed class of short, non‐coding
RNAs that have been long known to perform 2′‐O‐methylation of rRNAs. However …

The nucleolus of mammalian cells contains hundreds of box C/D small nucleolar RNAs
(SNORDs). Through their ability to base pair with ribosomal RNA precursors, most play …

Recent studies have indicated that long noncoding RNAs (lncRNAs) play important roles in
multiple processes, such as epigenetic regulation, gene expression regulation …

Chromosomal microarray (CMA) testing, used to identify DNA copy number variations
(CNVs), has helped advance knowledge about genetics of human neurodevelopmental …

Cancer is the second leading cause of death in the United States and is a major public
health concern worldwide. Basic, clinical and epidemiological research is leading to …