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SAR1B wt Allele

Known as: SAR1 Homolog B (S. cerevisiae) Gene, GTBPB, ANDD 
Human SAR1B wild-type allele is located in the vicinity of 5q31.1 and is approximately 48 kb in length. This allele, which encodes GTP-binding… 
National Institutes of Health

Related topics

Related topics

6 relations
5q31.1GTP BindingHomo sapiensIntracellular Transport

Papers overview

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Highly Cited
2011
Highly Cited
2011
Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease)
BackgroundAnderson's disease (AD) or chylomicron retention disease (CMRD) is a very rare hereditary lipid malabsorption syndrome… 
Highly Cited
2008
Highly Cited
2008
Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein.
2008
2008
Anderson’s disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities
Anderson’s disease (AD) or chylomicron retention disease (CMRD) is a rare hereditary lipid malabsorption syndrome linked to SARA2… 
Review
2007
Review
2007
Review of Monetary Policy in South Africa Since 1994
This paper reviews the design and performance of monetary policy in South Africa since 1994. Quantitative indexes of transparency… 
Highly Cited
1998
Highly Cited
1998
Partial Purification of the Sec 13 – 31 Complex from Rat Liver Cytosol
Cargo is selectively exported from the ER in COPII vesicles. To analyze the role of COPII in selective transport from the ER, we… 
Highly Cited
1998
Highly Cited
1998
Transcriptional Analysis of Different Promoters in the sar Locus in Staphylococcus aureus
ABSTRACT The expression of extracellular virulence determinants inStaphylococcus aureus is controlled by a 510-nucleotide RNA… 
Highly Cited
1998
Highly Cited
1998
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.
Human synpolydactyly (SPD) is an inherited congenital limb malformation caused by mutations in the HOXD13 gene. Heterozygotes are… 
Highly Cited
1998
Highly Cited
1998
Salmonella virulence plasmid. Modular acquisition of the spv virulence region by an F-plasmid in Salmonella enterica subspecies I and insertion into the chromosome of subspecies II, IIIa, IV and VII…
The spv operon is common to all Salmonella virulence plasmids. DNA hybridization analysis indicates that the spv region is… 
Highly Cited
1996
Highly Cited
1996
The molecular architecture of the sar locus in Staphylococcus aureus
The global regulator sar in Staphylococcus aureus controls the synthesis of a variety of cell wall and extracellular proteins… 
Highly Cited
1990
Highly Cited
1990
Conformational restriction of angiotensin II: cyclic analogues having high potency.
Cyclic analogues of angiotensin II (AII) were synthesized by connecting the side chains of residues 3 and 5 via a disulfide… 
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