Genomic imprinting in human placentation
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DOI: 10.1002/rmb2.12490
Abstract: Genomic imprinting (GI) is a mammalian‐specific epigenetic phenomenon that has been implicated in the evolution of the placenta in mammals. read more here.
Keywords: imprinting; human placentation; genomic imprinting; imprinting human ... See more keywords
Conserved non-coding sequences and de novo Mutator insertion alleles are imprinted in maize.
Sign Up to like & getrecommendations! Published in 2022 at "Plant physiology"
DOI: 10.1093/plphys/kiac459
Abstract: Genomic imprinting is an epigenetic phenomenon in which differential allele expression occurs in a parent-of-origin dependent manner. Imprinting in plants is tightly linked to transposable elements (TEs), and it has been hypothesized that genomic imprinting… read more here.
Keywords: imprinting; coding sequences; conserved non; mutator ... See more keywords
Canonical and Non-canonical Genomic Imprinting in Rodents
Sign Up to like & getrecommendations! Published in 2021 at "Frontiers in Cell and Developmental Biology"
DOI: 10.3389/fcell.2021.713878
Abstract: Genomic imprinting is an epigenetic phenomenon that results in unequal expression of homologous maternal and paternal alleles. This process is initiated in the germline, and the parental epigenetic memories can be maintained following fertilization and… read more here.
Keywords: imprinted genes; genomic imprinting; non canonical; canonical genomic ... See more keywords
Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network
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DOI: 10.3390/genes12040585
Abstract: Intrauterine and postnatal growth disturbances are major clinical features of imprinting disorders, a molecularly defined group of congenital syndromes caused by molecular alterations affecting parentally imprinted genes. These genes are expressed monoallelically and in a… read more here.
Keywords: restriction genomic; growth restriction; imprinting disorders; genomic imprinting ... See more keywords
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders: Characterization of Basic Mechanisms to Improve Clinical Management
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DOI: 10.3390/ijms20174219
Abstract: Silver–Russell and Beckwith–Wiedemann syndromes (SRS, BWS) are rare congenital human disorders characterized by opposite growth disturbances. With the increasing knowledge on the molecular basis of SRS and BWS, it has become obvious that the disorders… read more here.
Keywords: srs bws; molecular clinical; imprinting disorders; clinical opposite ... See more keywords