Expression of <it>KCNQ1OT1</it>, <it>CDKN1C</it>, <it>H19</it>, and <it>PLAGL1</it> and the methylation patterns at the KvDMR1 and <it>H19/IGF2</it> imprinting control regions is conserved between human and bovine
<p>Abstract</p> <p>Background</p> <p>Beckwith-Wiedemann syndrome (BWS) is a loss-of-imprinting pediatric overgrowth syndrome. The primary features of BWS include macrosomia, macroglossia, and abdominal wall defects. Secondary features that are frequently observed in BWS...
Main Authors: | Robbins Katherine, Chen Zhiyuan, Wells Kevin, Rivera Rocío |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2012-11-01
|
Series: | Journal of Biomedical Science |
Subjects: | |
Online Access: | http://www.jbiomedsci.com/content/19/1/95 |
Similar Items
-
Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases
by: Maria Francesca Bedeschi, et al.
Published: (2017-10-01) -
Reduced DNA methylation at the PEG3 DMR and KvDMR1 loci in children exposed to alcohol in utero: A South African Fetal Alcohol Syndrome cohort study
by: Michele eRamsay, et al.
Published: (2015-03-01) -
Identification of a novel ANK1 mutation in hereditary spherocytosis co‐existing with BWS
by: Qinghua Zhang, et al.
Published: (2022-04-01) -
Downregulation of Long Non-Coding RNA Kcnq1ot1: An Important Mechanism of Arsenic Trioxide-Induced Long QT Syndrome
by: Yanan Jiang, et al.
Published: (2018-01-01) -
Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of <i>CDKN1C</i>
by: Angela Sparago, et al.
Published: (2021-05-01)