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NHP2 gene

Known as: NOLA2, NHP2 ribonucleoprotein, FLJ20479 
National Institutes of Health

Related topics

Related topics

1 relation
GAR1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Downregulation of NHP2 promotes proper cyst formation in Drosophila ovary
In Drosophila ovary, germline stem cells (GSCs) divide to produce two daughter cells. One daughter is maintained as a GSC… 
2016
2016
Dyskératose congénitale : à propos d’un cas d’aplasie médullaire constitutionnelle☆
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.
Dyskeratosis congenita (DC) is an inherited disorder that implicates defects in the biology of telomeres, which are maintained by… 
2009
2009
E008 Study on the mechanism of human telomerase assembly
2009
2009
[Mutation in the telomerase complex component NHP2 in dyskeratosis congenita].
2007
2007
Hippocampal CA1 cell loss in a non-human primate model of transient global ischemia: A pilot study
2005
2005
[The NOLA2 and RPS3A genes as highly informative markers for human squamous cell lung cancer].
cDNA libraries enriched with sequences that are differentially transcribed in normal and tumor tissues were prepared using the… 
2002
2002
Expression of the human homologue of the small nucleolar RNA-binding protein NHP2 gene during monocytic differentiation of U937 cells.
1991
1991
Sequence and genetic analysis of NHP2: A moderately abundant high mobility group‐like nuclear protein with an essential function in Saccharomyces cerevisiae
In order to determine the biological functions of moderately abundant, high mobility group (HMG)‐like nuclear proteins, a genetic… 
1991
1991
Studies on low molecular weight nuclear protein of tumour and normal cells.
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