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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.
2020
2020
NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndrome.
M. Benyelles
,
M. O'Donohue
,
+21 authors
P. Revy
Human Molecular Genetics
2020
Corpus ID: 210923663
Telomeres are nucleoprotein structures at the end of chromosomes. The telomerase complex, constituted of the catalytic subunit…
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2017
2017
Acute telomerase components depletion triggers oxidative stress as an early event previous to telomeric shortening
J. S. Ibañez-Cabellos
,
Giselle Pérez-Machado
,
M. Seco-Cervera
,
E. Berenguer-Pascual
,
J. García-Giménez
,
F. Pallardó
Redox Biology
2017
Corpus ID: 55038
2013
2013
Pulmonary fibrosis in dyskeratosis congenita with TINF2 gene mutation
A. Fukuhara
,
Y. Tanino
,
+8 authors
M. Munakata
European Respiratory Journal
2013
Corpus ID: 737839
To the Editor: Dyskeratosis congenita is a rare inherited disorder of ectodermal dysplasia characterised by the classical…
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2011
2011
Structure of the Shq1–Cbf5–Nop10–Gar1 complex and implications for H/ACA RNP biogenesis and dyskeratosis congenita
Shuang Li
,
Jingqi Duan
,
Dandan Li
,
Shoucai Ma
,
K. Ye
EMBO Journal
2011
Corpus ID: 15600996
Shq1 is a conserved protein required for the biogenesis of eukaryotic H/ACA ribonucleoproteins (RNPs), including human telomerase…
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Highly Cited
2010
Highly Cited
2010
Effects of dyskeratosis congenita mutations in dyskerin, NHP2 and NOP10 on assembly of H/ACA pre-RNPs.
C. Trahan
,
C. Martel
,
F. Dragon
Human Molecular Genetics
2010
Corpus ID: 23765572
Dyskeratosis congenita (DC) is a rare genetic syndrome that gives rise to a variety of disorders in affected individuals…
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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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2006
2006
Structural study of the H/ACA snoRNP components Nop10p and the 3' hairpin of U65 snoRNA.
M. Khanna
,
Haihong Wu
,
C. Johansson
,
M. Caizergues-Ferrer
,
J. Feigon
RNA: A publication of the RNA Society
2006
Corpus ID: 1125573
The H/ACA small nucleolar ribonucleoprotein (snoRNP) complexes guide the modification of uridine to pseudouridine at conserved…
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Highly Cited
2002
Highly Cited
2002
Immunopurified Small Nucleolar Ribonucleoprotein Particles Pseudouridylate rRNA Independently of Their Association with Phosphorylated Nopp140
chen wang
,
C. Query
,
U. Meier
Molecular and Cellular Biology
2002
Corpus ID: 14334919
ABSTRACT The isomerization of up to 100 uridines to pseudouridines (Ψs) in eukaryotic rRNA is guided by a similar number of box H…
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Highly Cited
2001
Highly Cited
2001
Stable expression in yeast of the mature form of human telomerase RNA depends on its association with the box H/ACA small nucleolar RNP proteins Cbf5p, Nhp2p and Nop10p.
C. Dez
,
Anthony K. Henras
,
B. Faucon
,
D. Lafontaine
,
M. Caizergues-Ferrer
,
Y. Henry
Nucleic Acids Research
2001
Corpus ID: 14083973
Telomerase is a ribonucleoprotein (RNP) particle required for the replication of telomeres. The RNA component, termed hTR, of…
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1999
1999
The Bradyrhizobium japonicum nolA Gene Encodes Three Functionally Distinct Proteins
J. Loh
,
M. Stacey
,
M. Sadowsky
,
G. Stacey
Journal of Bacteriology
1999
Corpus ID: 34306053
ABSTRACT Examination of nolA revealed that NolA can be uniquely translated from three ATG start codons. Translation from the…
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