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NOP10 gene
Known as:
NOP10P
, NOP10 ribonucleoprotein
, NOP10
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Arabidopsis thaliana NOP10 is required for gametophyte formation.
Lin-xiao Li
,
Hong-Ze Liao
,
Li-xi Jiang
,
Qing Tan
,
D. Ye
,
Xueqin Zhang
Journal of Integrative Plant Biology
2018
Corpus ID: 37511819
The female gametophyte is crucial for sexual reproduction of higher plants, yet little is known about the molecular mechanisms…
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2015
2015
Differential requirements for H/ACA ribonucleoprotein components in cell proliferation and response to DNA damage
P. Lin
,
Maral E. Mobasher
,
+4 authors
F. Alawi
Histochemistry and Cell Biology
2015
Corpus ID: 253891651
H/ACA ribonucleoproteins (RNPs) are comprised of four conserved proteins, dyskerin, NHP2, NOP10, and GAR1, and a function…
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2015
2015
[Genotype analysis and telomere length measure in patients with dyskeratosis congenita].
Jia-yuan Zhang
,
W. An
,
+7 authors
Xiao-Fan Zhu
Zhongguo shi yan xue ye xue za zhi
2015
Corpus ID: 26125682
OBJECTIVE To analysze genotype and measure telomere length in two Chinese patients with dyskeratosis congenita(DC). METHODS The…
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2014
2014
The Clinical and Genetic Features of Dyskeratosis Congenita, Cryptic Dyskeratosis Congenita, and Hoyeraal-Hreidarsson Syndrome in Japan
H. Yamaguchi
,
H. Sakaguchi
,
+9 authors
S. Kojima
2014
Corpus ID: 208288727
Background: Dyskeratosis congenita (DKC) is an inherited bone marrow failure syndrome typified by reticulated skin pigmentation…
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2014
2014
Abstract IA19: Dyskeratosis congenita and related syndromes
I. Dokal
2014
Corpus ID: 58809481
Dyskeratosis Congenita (DC) is a heterogeneous multi-system syndrome exhibiting marked clinical and genetic heterogeneity. In its…
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Highly Cited
2009
Highly Cited
2009
Dyskeratosis congenita mutations in the H/ACA domain of human telomerase RNA affect its assembly into a pre-RNP.
C. Trahan
,
F. Dragon
RNA: A publication of the RNA Society
2009
Corpus ID: 38926700
Dyskeratosis congenita (DC) is an inherited disorder that implicates defects in the biology of telomeres, which are maintained by…
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2009
2009
E008 Study on the mechanism of human telomerase assembly
A. Huttin
,
F. Schlotter
,
S. Massenet
,
B. Charpentier
,
C. Branlant
2009
Corpus ID: 73144263
2007
2007
Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP
Osama A. Youssef
,
R. Terns
,
M. Terns
Nucleic Acids Research
2007
Corpus ID: 8262713
H/ACA RNP complexes change uridines to pseudouridines in target non-coding RNAs in eukaryotes and archaea. H/ACA RNPs are…
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2007
2007
NOP10 Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome
F. M. Sonmez
,
A. Aksoy
,
A. Sarı
2007
Corpus ID: 72419970
2003
2003
Etude des modes d'assemblage des particules ribonucléoprotéiques de type H/ACA et des ribosomes
Christophe Dez
2003
Corpus ID: 190503239
Les particules ribonucleoproteiques de type H/ACA (snoRNP de type H/ACA) sont impliquees dans plusieurs etapes de maturation du…
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