Works matching DE "NEUROPHYSINS"
Results: 28
PROTEIN SYNTHESIS CHANGE IN BRAIN SUB CELLULAR PARTICLES AND SOLUBLE FRACTION AT THE CRUSH SYNDROME.
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- Electronic Journal of Natural Sciences, 2006, v. 6, n. 1, p. 3
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- Article
Comparative sequences of the canine and feline vasopressin prohormones.
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- Comparative Clinical Pathology, 2007, v. 16, n. 3, p. 173, doi. 10.1007/s00580-007-0684-0
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- Article
Null Mutation of the Arginine-Vasopressin Gene in Rats Slows Attentional Engagement and Facilitates Response Accuracy in a Lateralized Reaction Time Task.
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- Neuropsychopharmacology, 2003, v. 28, n. 9, p. 1597, doi. 10.1038/sj.npp.1300194
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- Article
Kinetics of precursor cleavage at the dibasic sites: Involvement of peptide dynamics
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- FEBS Letters, 2002, v. 516, n. 1-3, p. 75, doi. 10.1016/S0014-5793(02)02505-X
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- Article
Neurohormonal Regulation of Tumor Growth.
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- Russian Journal of Genetics, 2018, v. 54, n. 1, p. 36, doi. 10.1134/S1022795418010064
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- Article
The Release of Oxytocin, Vasopressin and Associated Neurophysins after Electroconvulsive Therapy.
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- Human Psychopharmacology: Clinical & Experimental, 1991, v. 6, n. 2, p. 161, doi. 10.1002/hup.470060211
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- Article
Variation of the oxytocin/neurophysin I ( OXT) gene in four human populations.
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- Journal of Human Genetics, 2008, v. 53, n. 7, p. 637, doi. 10.1007/s10038-008-0292-0
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- Article
The human endolymphatic sac expresses natriuretic peptides.
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- 2017
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- journal article
Oxytocin, oxytocin-associated neurophysin and the oxytocin receptor in the human prostate.
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- Cell & Tissue Research, 2004, v. 318, n. 2, p. 375, doi. 10.1007/s00441-004-0968-5
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- Article
The accessory magnocellular neurosecretory system of the rostral human hypothalamus.
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- Cell & Tissue Research, 2018, v. 373, n. 2, p. 487, doi. 10.1007/s00441-018-2818-x
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- Article
Progressive decline of vasopressin secretion in familial autosomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene.
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- Clinical Endocrinology, 2003, v. 59, n. 4, p. 511, doi. 10.1046/j.1365-2265.2003.01834.x
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- Article
Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis.
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- European Journal of Human Genetics, 2004, v. 12, n. 1, p. 44, doi. 10.1038/sj.ejhg.5201086
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- Article
Impact of copeptin on diagnosis of acute coronary syndrome.
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- Egyptian Journal of Medical Human Genetics, 2014, v. 15, n. 3, p. 241, doi. 10.1016/j.ejmhg.2014.02.005
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- Article
Permeability of rat neurohypophysial blood vessels for neurophysins and ferritin in acute hyperoxia.
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- Biology Bulletin, 2008, v. 35, n. 3, p. 243, doi. 10.1134/S1062359008030035
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- Article
Molecular characterisation, genetic variability and detection of a functional polymorphism influencing the promoter activity of OXT gene in goat and sheep.
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- Journal of Dairy Research, 2017, v. 84, n. 2, p. 165, doi. 10.1017/S0022029917000097
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- Article
Visualization of local afferent inputs to magnocellular oxytocin neurons in vitro.
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- European Journal of Neuroscience, 1999, v. 11, n. 6, p. 1960, doi. 10.1046/j.1460-9568.1999.00620.x
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- Article
MOLECULAR GENETICS STRATEGIES TO IDENTIFY VASOTOCIN CODING SEQUENCES IN HUMANS: FAMILY-SPECIFIC APPROACH USING GENOMIC DNA AND FETAL TISSUES mRNAs.
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- Acta Endocrinologica (1841-0987), 2005, v. 1, n. 2, p. 131, doi. 10.4183/aeb.2005.131
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- Article
Familial neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin–neurophysin II gene.
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- European Journal of Endocrinology, 2011, v. 165, n. 1, p. 161, doi. 10.1530/EJE-11-0048
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- Article
Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene.
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- European Journal of Endocrinology, 2011, v. 164, n. 2, p. 179, doi. 10.1530/EJE-10-0823
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- Article
Akt Induces Apoptosis in Neuroblastoma Cells Expressing a C98X Vasopressin Mutant Following Autophagy Suppression.
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- Journal of Neuroendocrinology, 2008, v. 20, n. 10, p. 1165, doi. 10.1111/j.1365-2826.2008.01769.x
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- Article
The Hormone Domain of the Vasopressin Prohormone is Required for the Correct Prohormone Trafficking Through the Secretory Pathway.
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- Journal of Neuroendocrinology, 2003, v. 15, n. 12, p. 1156, doi. 10.1111/j.1365-2826.2003.01114.x
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- Article
Expression of Hypothalamic Peptides in Mice Lacking Neuronal Nitric Oxide Synthase: Reduced β-END Immunoreactivity in the Arcuate Nucleus.
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- Neuroendocrinology, 1998, v. 68, n. 6, p. 403, doi. 10.1159/000054390
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- Article
Comparison of ex vivo stability of copeptin and vasopressin.
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- Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 7, p. 948, doi. 10.1515/cclm-2016-0559
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- Article
Genetic characterization of the oxytocin-neurophysin I gene (OXT) and its regulatory regions analysis in domestic Old and New World camelids.
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- PLoS ONE, 2018, v. 13, n. 4, p. 1, doi. 10.1371/journal.pone.0195407
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- Article
Copeptin as a stress marker prior and after a written examination - the CoEXAM study.
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- Stress: The International Journal on the Biology of Stress, 2015, v. 18, n. 1, p. 134, doi. 10.3109/10253890.2014.993966
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- Article
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family.
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- Annals of Pediatric Endocrinology & Metabolism, 2014, v. 19, n. 4, p. 220, doi. 10.6065/apem.2014.19.4.220
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- Article
Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin-neurophysin II gene.
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- 2012
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- Publication type:
- Letter
Abnormal hypothalamic oxytocin system in fibroblast growth factor 8-deficient mice.
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- Endocrine (1355008X), 2010, v. 38, n. 2, p. 174, doi. 10.1007/s12020-010-9366-9
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- Article