|1.||Laterre, Pierre-François: 1 article (10/2015)|
|2.||Castanares-Zapatero, Diego: 1 article (10/2015)|
|3.||Collienne, Christine: 1 article (10/2015)|
|4.||Wittebole, Xavier: 1 article (10/2015)|
|5.||Lienart, Daphné: 1 article (10/2015)|
|6.||Laribi, Said: 1 article (10/2015)|
|7.||Struck, Joachim: 1 article (03/2012)|
|8.||Bergmann, Andreas: 1 article (03/2012)|
|9.||Hedblad, Bo: 1 article (03/2012)|
|10.||Belting, Mattias: 1 article (03/2012)|
03/01/2012 - "We measured midregional proatrial natriuretic peptide (MR-proANP), proadrenomedullin (MR-proADM), and C-terminal preprovasopressin (copeptin) in fasting plasma from participants of the Malmö Diet and Cancer Study that were free from cancer prior to the baseline exam in 1991 to 1994 (1,768 males and 2,293 females). "
01/01/1997 - "Genotype analysis of prepro-vasopressin signal peptide in vasopressin-producing and -non-producing lung tumors."
10/01/2015 - "The primary objective of this study was to determine if patients dead or with sustained vasopressor need at day 7 had a relative arginine vasopressin (AVP) deficiency as compared with vasopressor-free patients at day 7. Another objective was to explore if plasma CT-proAVP (C terminal part of preprovasopressin) measured within 24 h of sepsis onset could predict patient severity. "
|3.||Neurogenic Diabetes Insipidus (Central Diabetes Insipidus)
04/01/2004 - "A novel mutation in the preprovasopressin gene identified in a kindred with autosomal dominant neurohypophyseal diabetes insipidus."
10/01/2001 - "Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II)."
05/01/1999 - "A novel mutation (R97C) in the neurophysin moiety of prepro-vasopressin-neurophysin II associated with autosomal-dominant neurohypophyseal diabetes insipidus."
06/01/1993 - "Possible involvement of inefficient cleavage of preprovasopressin by signal peptidase as a cause for familial central diabetes insipidus."
07/02/1999 - "Autosomal dominant neurohypophyseal diabetes insipidus is caused by mutations in the gene encoding the vasopressin precursor protein, prepro-vasopressin-neurophysin II. We analyzed the molecular consequences of a mutation (DeltaG227) recently identified in a Swiss kindred that destroys the translation initiation codon. "
|4.||Small Cell Lung Carcinoma (Small Cell Lung Cancer)
|1.||Arginine Vasopressin (Argipressin)
|4.||Neurophysins (Neurophysin I)
|7.||Protein Sorting Signals (Signal Peptide)
|8.||Initiator Codon (Start Codon)
|9.||Complementary DNA (cDNA)
|10.||type I signal peptidase (signal peptidase)