标题
Recent Advances in Imprinting Disorders
作者
关键词
-
出版物
CLINICAL GENETICS
Volume 91, Issue 1, Pages 3-13
出版商
Wiley
发表日期
2016-07-01
DOI
10.1111/cge.12827
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Regulatory links between imprinted genes: evolutionary predictions and consequences
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- Genes, assisted reproductive technology and trans-illumination
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- DNA-binding motif and target genes of the imprinted transcription factor PEG3
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- In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions
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- Mechanisms of imprint dysregulation
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- Clinical utility gene card for: Silver–Russell syndrome
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- The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers
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- H19 acts as a trans regulator of the imprinted gene network controlling growth in mice
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- Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells
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- Maternal Uniparental Disomy 14 Syndrome Demonstrates Prader-Willi Syndrome-Like Phenotype
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- Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome)
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- Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9
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- A Maternal-Zygotic Effect Gene, Zfp57, Maintains Both Maternal and Paternal Imprints
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- Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
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