Pages that link to "Q28200129"

The following pages link to Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin C gene (Q28200129):

Displaying 26 items.

• Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndrome (Q24793749) (← links)
• (Q28158665) (redirect page) (← links)
• Papillon-Lefèvre syndrome: a successful outcome (Q28280753) (← links)
• CTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update (Q33726087) (← links)
• Identification of novel mutation in cathepsin C gene causing Papillon-Lefèvre Syndrome in Mexican patients. (Q34545787) (← links)
• Functional significance of the perforin/granzyme cell death pathway (Q34931863) (← links)
• Mendelian diseases and conditions in Croatian island populations: historic records and new insights (Q36147760) (← links)
• Novel cathepsin C mutation in a Brazilian family with Papillon-Lefèvre syndrome: case report and mutation update (Q36197268) (← links)
• Mendelian forms of periodontitis (Q36938531) (← links)
• The novel CTSC homozygous nonsense mutation p.Lys106X in a patient with Papillon-Lefèvre syndrome with all permanent teeth remaining at over 40 years of age. (Q43844985) (← links)
• A novel mutation of the cathepsin C gene in Papillon-Lefèvre syndrome (Q43939164) (← links)
• Ligand activation of peroxisome proliferator-activated receptor delta suppresses cathepsin B expression in human endothelial cells in a posttranslational manner. (Q44374642) (← links)
• Novel mutations in the cathepsin C gene in patients with pre-pubertal aggressive periodontitis and Papillon-Lefèvre syndrome (Q44865926) (← links)
• A homozygous cathepsin C mutation associated with Haim-Munk syndrome (Q45280047) (← links)
• Orthodontic treatment in a patient with Papillon-Lefèvre syndrome. (Q46460026) (← links)
• The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitis. (Q47195914) (← links)
• Cytokine production by leukocytes of Papillon-Lefèvre syndrome patients in whole blood cultures. (Q51496212) (← links)
• [Gene mutational analyses of the cathepsin C gene in families with Papillon-Lefèvre syndrome]. (Q54196343) (← links)
• One mutation, two phenotypes: a single nonsense mutation of the CTSC gene causes two clinically distinct phenotypes. (Q55059216) (← links)
• Papillon-Lefèvre syndrome: report of six patients and identification of a novel mutation. (Q55059664) (← links)
• Cathepsin C Gene Variants in Aggressive Periodontitis (Q57338115) (← links)
• Cathepsin C Gene 5'-Untranslated Region Mutation in Papillon-Lefèvre Syndrome (Q57715650) (← links)
• A Rare Presentation of Psychotic Depression with Suicidality in a Case of Papillon-Lefèvre Syndrome. (Q64916678) (← links)
• Identification of a novel cathepsin C mutation (p.W185X) in a Brazilian kindred with Papillon-Lefèvre syndrome (Q74361160) (← links)
• Pyogenic liver abscess and peritonitis due to Rhizopus oryzae in a child with Papillon-Lefevre syndrome (Q82928604) (← links)
• [Gene mutational analyses of cathepsin C gene in a family with Papillon-Lefèvre syndrome] (Q92260769) (← links)