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RNA, Messenger, Paternal
Known as:
mRNA, Paternal
, Paternal Messenger RNA
, RNA, Paternal Messenger
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Messenger RNA derived from the paternal genome during spermatogenesis. It is stored in a masked state for translation in the early stages of…
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National Institutes of Health
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RNA, Messenger, Stored
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Chinese Siblings with Prader-Willi Syndrome Inherited from Their Paternal Grandmother
Y. Dai
,
H. Ke
,
Chao-chun Zou
,
Guan-ping Dong
Indian Pediatrics
2019
Corpus ID: 204833790
Prader-Willi syndrome (PWS) is a complex neurobehavioral disorder caused by failure of expression of paternally inherited genes…
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2009
2009
Diagnostic complication and molecular characteristics of Hb SC-Chicago disease with α-thal-2 (-α3.7 deletion): effects of multiple variant on patient’s phenotype
Heather Y. Hughes
,
K. Mckie
,
Harris Carmichael
,
Komal Bora
,
A. Kutlar
,
F. Kutlar
Annals of Hematology
2009
Corpus ID: 26546579
Dear Editor, Co-inheritance of α and β chain variants are not uncommon and mostly influence the molecular interactions of…
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2009
2009
Honfoglalás kori, valamint magyar és székely populációk apai ági genetikai kapcsolatrendszerének vizsgálata
K. Bernadett
2009
Corpus ID: 82725842
Review
2008
Review
2008
Paternal environmental exposures and gene expression during spermatogenesis: research review to research framework.
D. Hansen
Birth Defects Research Part C Embryo Today…
2008
Corpus ID: 28342131
The primary objective is to review Dioxin toxicity, the potential impact on spermatogenesis, what is known and unknown about…
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Review
2003
Review
2003
Comprehensive microsatellite marker analysis contradicts previous report of segmental maternal heterodisomy of chromosome 14
K. Coveler
,
V. Sutton
,
C. Knox-DuBois
,
L. Shaffer
Journal of Medical Genetics
2003
Corpus ID: 32300886
Uniparental disomy of chromosome 14 (UPD(14)) results in one of two distinct abnormal phenotypes depending upon the parent of…
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2001
2001
Deletion of a direct repeat element has no effect on Igf2 and H19 imprinting
M. R. Reed
,
A. Riggs
,
J. Mann
Mammalian Genome
2001
Corpus ID: 37318719
Genomic imprinting is a mammalian epigenetic system that determines the parent-of-origin dependent or monoallelic expression of a…
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1994
1994
EFFECTS OF SPERMATOGENIC CELL TYPE ON QUANTITY AND QUALITY OF MUTATIONS
L. B. Russell
1994
Corpus ID: 82477293
It is probable that most instances of male-mediated developmental toxicity will be traceable to damage induced in male germ cells…
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1983
1983
A variant of von Willebrand's disease characterized by recessive inheritance and missing triplet structure of von Willebrand factor multimers
P. Mannucci
,
R. Lombardi
,
F. Pareti
,
S. Solinas
,
M. Mazzucconi
,
G. Mariani
1983
Corpus ID: 209181728
A 10-yr-old girl had bleeding symptoms of moderate severity; her mother and maternal aunt had milder bleeding symptoms, and other…
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1980
1980
Estimation of singular spectrum of boundary values for some semihyperbolic operators : To the memory of the late professor Mikio ISE, with a paternal reverence.
Akira Kaneko
1980
Corpus ID: 117866587
1974
1974
Chromosomal inactivation and reactivation in mealy bugs.
L. Berlowitz
Genetics
1974
Corpus ID: 8455008
UNDERSTANDING genetic inactivation and reactivation in a developing organism is the key to understanding cytodifferentiation. One…
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