نتایج جستجو برای: genomic imprinting

تعداد نتایج: 122074  

Journal: :iranian biomedical journal 0
marzieh derakhshan-horeh department of anatomy, school of medicine, tehran university of medical sciences, tehran, iran farid abolhassani department of anatomy, school of medicine, tehran university of medical sciences, tehran, iran farnoosh jafarpour department of reproductive biotechnology, reproductive biomedicine research center, royan institute for biotechnology, academic center for education, culture and research (acecr), isfahan, iran ashraf moini department of endocrinology and female infertility, reproductive biomedicine research centre, royan institute for reproductive biomedicine, acecr, tehran, iran khadijeh karbalaie department of cellular biotechnology, cell science research center, royan institute for biotechnology, acecr, isfahan, iran sayyed morteza hosseini department of reproductive biotechnology, reproductive biomedicine research center, royan institute for biotechnology, academic center for education, culture and research (acecr), isfahan, iran

backgrund: imprinted genes are a unique subset of few genes, which have been differentially methylated region (dmr) in a parental origin-dependent manner during gametogenesis, and these genes are highly protected during pre-implantation epigenetic reprogramming. several studies heve shown that the particular vulnerability of imprinting genes during suboptimal pre- and peri-conception microenvir...

Background Genomic imprinting is a heritable and developmentally essential phenomenon by which gene expression occurs in an allele-specific manner1. While the imprinted alleles are primarily silenced by DNA methylation, it remains largely unknown how methylation is targeted to imprinting control region (ICR), also called differentially methylated region (DMR), and maintained. Here we show that ...

Journal: :Open Access Macedonian Journal of Medical Sciences 2016

Journal: :Briefings in Functional Genomics 2010

Journal: :Cold Spring Harbor Perspectives in Biology 2011

Journal: :The Journal of reproduction and development 2011
Yayoi Obata

In mammals, both parental genomes are essential for normal ontogeny because epigenetic modifications imposed in the parents' gametes lead to parent-of-origin specific gene expression in their offspring. These phenomena are referred to as genomic imprinting. It has been shown that maternal imprinting is established during oocyte growth, lack of maternal imprinting in zygotes leads to early embry...

Journal: :Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2013
Marilyn B Renfree Shunsuke Suzuki Tomoko Kaneko-Ishino

Genomic imprinting is widespread in eutherian mammals. Marsupial mammals also have genomic imprinting, but in fewer loci. It has long been thought that genomic imprinting is somehow related to placentation and/or viviparity in mammals, although neither is restricted to mammals. Most imprinted genes are expressed in the placenta. There is no evidence for genomic imprinting in the egg-laying mono...

Journal: :Genetics 2004
Francisco Ubeda David Haig

We present a one-locus model that breaks two symmetries of Mendelian genetics. Whereas symmetry of transmission is breached by allowing sex-specific segregation distortion, symmetry of expression is breached by allowing genomic imprinting. Simple conditions for the existence of at least one polymorphic stable equilibrium are provided. In general, population mean fitness is not maximized at poly...

2016
Emirjeta Bajrami Mirko Spiroski

BACKGROUND Genomic imprinting is the inheritance out of Mendelian borders. Many of inherited diseases and human development violates Mendelian law of inheritance, this way of inheriting is studied by epigenetics. AIM The aim of this review is to analyze current opinions and options regarding to this way of inheriting. RESULTS Epigenetics shows that gene expression undergoes changes more com...

2016
Stefania Benonisdottir Asmundur Oddsson Agnar Helgason Ragnar P Kristjansson Gardar Sveinbjornsson Arna Oskarsdottir Gudmar Thorleifsson Olafur B Davidsson Gudny A Arnadottir Gerald Sulem Brynjar O Jensson Hilma Holm Kristjan F Alexandersson Laufey Tryggvadottir G Bragi Walters Sigurjon A Gudjonsson Lucas D Ward Jon K Sigurdsson Paul D Iordache Michael L Frigge Thorunn Rafnar Augustine Kong Gisli Masson Hannes Helgason Unnur Thorsteinsdottir Daniel F Gudbjartsson Patrick Sulem Kari Stefansson

Adult height is a highly heritable trait. Here we identified 31.6 million sequence variants by whole-genome sequencing of 8,453 Icelanders and tested them for association with adult height by imputing them into 88,835 Icelanders. Here we discovered 13 novel height associations by testing four different models including parent-of-origin (|β|=0.4-10.6 cm). The minor alleles of three parent-of-ori...

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