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RNU1-18P gene
Known as:
RNA, U1 small nuclear 18, pseudogene
, RNU1-18P
National Institutes of Health
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2018
2018
Prediction of mechanical response for 5000-Series aluminum alloy coupling visco-plastic self-consistent approach with finite element method
A. Ruggiero
,
M. Colliander
,
+4 authors
Gabriel Testa
Journal of Physics: Conference Series
2018
Corpus ID: 58944686
In the present work, a hybrid micro macro-approach was adopted to investigate the material behavior of the A5XXX-O object of the…
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2016
2016
Soft drink makers consider legal challenge against sugar tax
N. Hawkes
British medical journal
2016
Corpus ID: 206909919
The government’s plans to tax soft drinks containing sugar may be challenged in court by manufacturers who say that they are…
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2015
2015
Computational design of a mechanical test for material characterization by inverse analysis
N. Souto
2015
Corpus ID: 113988911
With the development of full-field measurements methods, recent material parameters identification strategies call upon the use…
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2013
2013
Mechanical behavior of mild steel up to rupture : characterization and validation
N. Souto
,
A. Andrade-Campos
,
S. Thuillier
2013
Corpus ID: 16465496
In this work, the initial anisotropy and its evolution with strain, hardening and rupture of DC04 mild steel are characterized by…
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2012
2012
Tetrasomie 18p und Innenohrschwerhörigkeit
Dr. C. Schwemmle
,
M. Arslan-Kirchner
,
B. Pabst
,
M. Ptok
HNO (Berlin. Print)
2012
Corpus ID: 25709700
ZusammenfassungDie Tetrasomie 18p ist eine seltene chromosomale Störung (1:140.000 Lebendgeborene), die Mädchen und Jungen…
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2012
2012
Tetrasomie 18p und Innenohrschwerhörigkeit Ein ungewöhnlicher Fall
C. Matthias
2012
Corpus ID: 89305772
2008
2008
Tetrasomie 18p
A. Kujat
,
M. Bernhard
,
W. Hirsch
,
A. Merkenschlager
,
U. Froster
Monatsschrift Kinderheilkunde Zeitschrift für…
2008
Corpus ID: 44671857
ZusammenfassungDie Tetrasomie 18p ist eine seltene numerische Chromosomenstörungen. Der Phänotyp resultiert aus dem Vorliegen…
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2003
2003
Monosomy of the short arm of chromosome 18
I. Petković
,
I. Barišić
,
I. Sansović
2003
Corpus ID: 80436481
Monosomija 18p je jedna od najcescih delecija autosoma. Klinicko pojavljivanje 18p je veoma varijabilno. U vecini opisanih…
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1983
1983
Pernicious anemia, 18q deletion syndrome, and IgA deficiency.
J. Hasen
Journal of the American Medical Association (JAMA…
1983
Corpus ID: 40697643
To the Editor.— Reading the CASE REPORT entitled "Pernicious Anemia, 18q Deletion Syndrome, and IgA Deficiency" (1982;248:1359…
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1975
1975
佐伯富編 宋代文集索引, 京都大學東洋史硏究會刊 1970年 3月 發行, 菊版 845p, 檢字表 18p
申採湜
1975
Corpus ID: 147138992
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