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MRPL40 gene

Known as: MRPL40, NUCLEAR LOCALIZATION SIGNAL DELETED IN VELOCARDIOFACIAL SYNDROME, MRPL22 
National Institutes of Health

Related topics

Related topics

20 relations
MRPL41 geneMRPL42 geneMRPL43 geneMRPL48 gene
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia
Schizophrenia (SZ) is a highly heterogeneous disorder in both its symptoms and risk factors. One of the most prevalent genetic… 
2014
2014
Predicting the potential ankylosing spondylitis-related genes utilizing bioinformatics approaches
Given that ankylosing spondylitis (AS) occurs in approximately 5 out of 1,000 adults of European descent and the unclear… 
Highly Cited
2012
Highly Cited
2012
Mitochondria “fuel” breast cancer metabolism: Fifteen markers of mitochondrial biogenesis label epithelial cancer cells, but are excluded from adjacent stromal cells
Here, we present new genetic and morphological evidence that human tumors consist of two distinct metabolic compartments. First… 
2011
2011
The Mitospecific Region of Mrp20 and its Importance for the Assembly of Mitochondrial Ribosomes in Saccharomyces cerevisiae
THE MITOSPECIFIC REGION OF MRP20 AND ITS IMPORTANCE FOR THE ASSEMBLY OF MITOCHONDRIAL RIBOSOMES IN Saccharomyces cerevisiae… 
2009
2009
Mapping of the Saccharomyces cerevisiae Oxa1-Mitochondrial Ribosome Interface and Identification of MrpL40, a Ribosomal Protein in Close Proximity to Oxa1 and Critical for Oxidative Phosphorylation…
ABSTRACT The Oxa1 protein plays a central role in facilitating the cotranslational insertion of the nascent polypeptide chains… 
2004
2004
High levels of the mitochondrial large ribosomal subunit protein 40 prevent loss of mitochondrial DNA in null mmf1 Saccharomyces cerevisiae cells
Members of the YERO57c/YJGFc/UK114 protein family have been identified in bacteria and eukaryotes. The budding yeast… 
1998
1998
Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.
Velo-cardio-facial syndrome (VCFS) and DiGeorge syndrome are congenital disorders characterized by craniofacial anomalies… 
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