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Hereditary Coproporphyria

Known as: CPO DEFICIENCY, hereditary coproporphyria porphyria, Coproporphyrinogen Oxidase Deficiency 
An autosomal dominant porphyria that is due to a deficiency of COPROPORPHYRINOGEN OXIDASE in the LIVER, the sixth enzyme in the 8-enzyme biosynthetic… 
National Institutes of Health

Papers overview

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Highly Cited
2017
Highly Cited
2017
We report a hafnium-containing MOF, hcp UiO-67(Hf), which is a ligand-deficient layered analogue of the face-centered cubic fcu… 
Review
2011
Review
2011
This report updates the previously published summary of recommendations for vaccinating health-care personnel (HCP) in the United… 
Review
2009
Review
2009
Highly Cited
2005
Highly Cited
2005
Highly Cited
2005
Highly Cited
2005
Bacterial response to nitric oxide (NO) is of major importance since NO is an obligatory intermediate of the nitrogen cycle… 
Review
2005
Review
2005
Key Summary Points Early Diagnosis of Acute Porphyria Consider in all adults with unexplained symptoms seen in acute porphyrias… 
Highly Cited
2000
Highly Cited
2000
Species‐sensitivity distribution methods assemble single‐species toxicity data to predict hazardous concentrations (HCps… 
Highly Cited
1998
Highly Cited
1998
ABSTRACT The CpxA/R two-component signal transduction system ofEscherichia coli can combat a variety of extracytoplasmic protein…