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Phospholipase that hydrolyzes phosphatidic acid. Additionally we are shipping DDHD1 Antibodies (6) and DDHD1 Proteins (4) and many more products for this protein.
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A novel homozygous mutation in DDHD1 was identified in a patient with hereditary spastic paraplegia, retinal dystrophy (show MERTK ELISA Kits) and a pattern of neurodegeneration with brain iron accumulation.
the novel mutation in DDHD1 is the causative variant for the SPG28 patient that is the first record of the disease in Japanese population.
Two novel heterozygous mutations in DDHD1 were found in the affected members of one family, with clinical features overlapping the SPG28 subtype.
a possible mechanism of PA regulation of the mitochondrial membrane and demonstrate an in vivo function of PA-PLA1 in the organization of mitochondria during spermiogenesis.
DDHD1-LPI (show Slc7a7 ELISA Kits)-GPR55 (show GPR55 ELISA Kits) axis to be involved in functions in the brain.
Phospholipase that hydrolyzes phosphatidic acid.
, DDHD domain containing 1
, DDHD domain-containing protein 1
, phosphatidic acid-preferring phospholipase A1 homolog
, phosphatidic acid-preferring phospholipase A1-like protein
, spastic paraplegia 28 (autosomal recessive)
, phosphatidic acid-preferring phospholipase A1