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RNA, Messenger, Paternal

Known as: mRNA, Paternal, Paternal Messenger RNA, RNA, Paternal Messenger 
Messenger RNA derived from the paternal genome during spermatogenesis. It is stored in a masked state for translation in the early stages of… 
National Institutes of Health

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RNA, Messenger, Stored

Papers overview

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Review
2018
Review
2018
Developmental Programming of Obesity and Diabetes in Mouse, Monkey, and Man in 2018: Where Are We Headed?
Childhood obesity and its comorbidities continue to accelerate across the globe. Two-thirds of pregnant women are obese… 
Highly Cited
2014
Highly Cited
2014
Central precocious puberty in a girl and early puberty in her brother caused by a novel mutation in the MKRN3 gene.
CONTEXT Central precocious puberty (CPP), defined as the development of secondary sex characteristics prior to age 8 years in… 
Highly Cited
2012
Highly Cited
2012
Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies.
BACKGROUND There is an increased incidence of rare imprinting disorders associated with assisted reproduction technologies (ARTs… 
Review
2007
Review
2007
Paternal kin discrimination: the evidence and likely mechanisms
One of the most important assumptions of kin selection theory is that individuals behave differently towards kin than non‐kin. In… 
Highly Cited
2004
Highly Cited
2004
Psychopathology in the adolescent and young adult offspring of a community sample of mothers and fathers with major depression
Background. There is a large literature indicating that the offspring of mothers with Major Depressive Disorder (MDD) are at… 
Highly Cited
1998
Highly Cited
1998
Nuclear Inclusions in Glutamine Repeat Disorders Are They Pernicious, Coincidental, or Beneficial?
Review
1998
Review
1998
Voles and vasopressin: a review of molecular, cellular, and behavioral studies of pair bonding and paternal behaviors.
Highly Cited
1998
Highly Cited
1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.
The Prader-Willi syndrome (PWS) and the Angelman syndrome (AS) are caused by the loss of function of imprinted genes in proximal… 
Highly Cited
1998
Highly Cited
1998
Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene.
A very large cervical tumor that extended to the upper mediastinum was seen in a newborn after an uneventful pregnancy. The… 
Highly Cited
1992
Highly Cited
1992
Mutational analysis of SRY: nonsense and missense mutations in XY sex reversal
SummaryXY females (n=17) were analysed for mutations in SRY (sex-determining region Y gene), a gene that has recently been… 
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