A single amino acid change, A91V, leads to conformational changes that can impair processing to the active form of perforin
Mutations in the perforin gene have been found in patients with hemophagocytic
lymphohistiocytosis (HLH), a rare autosomal recessive disease. We describe a patient …
lymphohistiocytosis (HLH), a rare autosomal recessive disease. We describe a patient …
[引用][C] A single amino acid change, A91V, leads to conformational changes that can impair processing to the active form of perforin
C TRAMBAS, F GALLO, D PENDE, S MARCENARO… - Blood, 2005 - pascal-francis.inist.fr
A single amino acid change, A91V, leads to conformational changes that can impair
processing to the active form of perforin CNRS Inist Pascal-Francis CNRS Pascal and …
processing to the active form of perforin CNRS Inist Pascal-Francis CNRS Pascal and …
[PDF][PDF] A single amino acid change, A91V, leads to conformational changes that can impair processing to the active form of perforin
C Trambas, F Gallo, D Pende, S Marcenaro, L Moretta… - BLOOD, 2005 - researchgate.net
Perforin plays a key role in the cytotoxicity of natural killer (NK) cells and cytotoxic T
lymphocytes (CTLs). 1 Perforin is stored as an active protein in specialized secretory …
lymphocytes (CTLs). 1 Perforin is stored as an active protein in specialized secretory …
A single amino acid change, A91V, leads to conformational changes that can impair processing to the active form of perforin.
C Trambas, F Gallo, D Pende, S Marcenaro, L Moretta… - Blood, 2005 - europepmc.org
Mutations in the perforin gene have been found in patients with hemophagocytic
lymphohistiocytosis (HLH), a rare autosomal recessive disease. We describe a patient …
lymphohistiocytosis (HLH), a rare autosomal recessive disease. We describe a patient …
[HTML][HTML] A single amino acid change, A91V, leads to conformational changes that can impair processing to the active form of perforin
C Trambas, F Gallo, D Pende, S Marcenaro, L Moretta… - Blood, 2005 - Elsevier
Mutations in the perforin gene have been found in patients with hemophagocytic
lymphohistiocytosis (HL7777), a rare autosomal recessive disease. We describe a patient …
lymphohistiocytosis (HL7777), a rare autosomal recessive disease. We describe a patient …
A single amino acid change, A91V, leads to conformational changes that can impair processing to the active form of perforin
C Trambas, F Gallo, D Pende, S Marcenaro… - …, 2005 - pubmed.ncbi.nlm.nih.gov
Mutations in the perforin gene have been found in patients with hemophagocytic
lymphohistiocytosis (HLH), a rare autosomal recessive disease. We describe a patient …
lymphohistiocytosis (HLH), a rare autosomal recessive disease. We describe a patient …