Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

MRPL40 gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Schizophrenia (SZ) is a highly heterogeneous disorder in both its symptoms and risk factors. One of the most prevalent genetic… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
2014
2014
Given that ankylosing spondylitis (AS) occurs in approximately 5 out of 1,000 adults of European descent and the unclear… Expand
  • table 1
  • table 2
  • figure 1
  • table 3
Highly Cited
2012
Highly Cited
2012
Here, we present new genetic and morphological evidence that human tumors consist of two distinct metabolic compartments. First… Expand
2011
2011
THE MITOSPECIFIC REGION OF MRP20 AND ITS IMPORTANCE FOR THE ASSEMBLY OF MITOCHONDRIAL RIBOSOMES IN Saccharomyces cerevisiae… Expand
2009
2009
ABSTRACT The Oxa1 protein plays a central role in facilitating the cotranslational insertion of the nascent polypeptide chains… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
2004
2004
Members of the YERO57c/YJGFc/UK114 protein family have been identified in bacteria and eukaryotes. The budding yeast… Expand
1998
1998
Velo-cardio-facial syndrome (VCFS) and DiGeorge syndrome are congenital disorders characterized by craniofacial anomalies… Expand