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HYPEROXALURIA, PRIMARY, TYPE III

Known as: HP3, Primary Hyperoxaluria Type III 
Recessively inherited primary hyperoxaluria due to mitochondrial 4-hydroxy-2-oxoglutarate aldolase (HOGA1) gene mutations.(NICHD)
National Institutes of Health

Papers overview

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2019
2019
Protamine 1 (P1) and protamine 2 family (P2) are extremely basic sperm-specific proteins, packing 85-95% of the paternal DNA. P1… 
2011
2011
Antioxidant activities of polyphenolic compounds extracted (PPEs) from ripe fruits of oil palms are investigated by studying… 
2003
2003
Summary. Experimental and clinical studies have shown that HAp granules and powder may be successfully applied in reconstruction… 
Highly Cited
1993
Highly Cited
1993
We synthesized and evaluated four hydrazino nicotinamide (HYNIC) derivatized chemotactic peptide analogs: For-NleLFK-HYNIC (HP1… 
Review
1992
Review
1992
Antibody to Borrelia burgdorferi was examined in 380 healthy and 38 clinical cases of cows from Hokkaido and Shizuoka in Japan… 
1990
1990
The largest intermediate basic protein HPI1 (101 residues) from human sperm chromatin was isolated and characterized. The amino… 
1977
1977
Bacteriophage phi 29 mutation sus8(22) has been mapped by two-factor crosses between markers sus8(769) and ts8(93). Whe sus8(22…