Works matching DE "NEUROPHYSINS"

Results: 28

Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 1, p. 44, doi. 10.1038/sj.ejhg.5201086

By:

Christensen, Jane H.;
Siggaard, Charlotte;
Corydon, Thomas J.;
deSanctis, Luisa;
Kovacs, Laszlo;
Robertson, Gary L.;
Gregersen, Niels;
Rittig, Søren

Publication type:

Article

Genetic characterization of the oxytocin-neurophysin I gene (OXT) and its regulatory regions analysis in domestic Old and New World camelids.

Published in:

PLoS ONE, 2018, v. 13, n. 4, p. 1, doi. 10.1371/journal.pone.0195407

By:

Pauciullo, Alfredo;
Ogah, Danlami Moses;
Iannaccone, Marco;
Erhardt, Georg;
Di Stasio, Liliana;
Cosenza, Gianfranco

Publication type:

Article

Molecular characterisation, genetic variability and detection of a functional polymorphism influencing the promoter activity of OXT gene in goat and sheep.

Published in:

Journal of Dairy Research, 2017, v. 84, n. 2, p. 165, doi. 10.1017/S0022029917000097

By:

Cosenza, Gianfranco;
Iannaccone, Marco;
Pico, Boipuso Alpheus;
Gallo, Daniela;
Capparelli, Rosanna;
Pauciullo, Alfredo

Publication type:

Article

Variation of the oxytocin/neurophysin I ( OXT) gene in four human populations.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 7, p. 637, doi. 10.1007/s10038-008-0292-0

By:

Yang Xu;
Yali Xue;
Daly, Allan;
Lijie Wu;
Tyler-Smith, Chris

Publication type:

Article

Impact of copeptin on diagnosis of acute coronary syndrome.

Published in:

Egyptian Journal of Medical Human Genetics, 2014, v. 15, n. 3, p. 241, doi. 10.1016/j.ejmhg.2014.02.005

By:

El Sayed, Zeinab H.;
Mahmoud, Hala A.;
El Shall, Layla Y.;
El Sheshtawey, Fawzia A.;
Mohamed, Manal A.

Publication type:

Article

Familial neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin–neurophysin II gene.

Published in:

European Journal of Endocrinology, 2011, v. 165, n. 1, p. 161, doi. 10.1530/EJE-11-0048

By:

M de Fost

Publication type:

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.

Published in:

European Journal of Endocrinology, 2011, v. 164, n. 2, p. 179, doi. 10.1530/EJE-10-0823

By:

Cécile Brachet

Publication type:

Article

Copeptin as a stress marker prior and after a written examination - the CoEXAM study.

Published in:

Stress: The International Journal on the Biology of Stress, 2015, v. 18, n. 1, p. 134, doi. 10.3109/10253890.2014.993966

By:

Urwyler, Sandrine A.;
Schuetz, Philipp;
Sailer, Clara;
Christ-Crain, Mirjam

Publication type:

Article

Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family.

Published in:

Annals of Pediatric Endocrinology & Metabolism, 2014, v. 19, n. 4, p. 220, doi. 10.6065/apem.2014.19.4.220

By:

Myo-Jing Kim;
Young-Eun Kim;
Chang-Seok Ki;
Jae-Ho Yoo

Publication type:

Article

Kinetics of precursor cleavage at the dibasic sites: Involvement of peptide dynamics

Published in:

FEBS Letters, 2002, v. 516, n. 1-3, p. 75, doi. 10.1016/S0014-5793(02)02505-X

By:

Glandieres, Jean-Marie;
Hertzog, Maud;
Lazar, Noureddine;
Brakch, Noureddine;
Cohen, Paul;
Alpert, Bernard;
Rholam, Mohamed

Publication type:

Article

Oxytocin, oxytocin-associated neurophysin and the oxytocin receptor in the human prostate.

Published in:

Cell & Tissue Research, 2004, v. 318, n. 2, p. 375, doi. 10.1007/s00441-004-0968-5

By:

Whittington, Kate;
Assinder, Steve;
Gould, Maree;
Nicholson, Helen

Publication type:

Article

Null Mutation of the Arginine-Vasopressin Gene in Rats Slows Attentional Engagement and Facilitates Response Accuracy in a Lateralized Reaction Time Task.

Published in:

Neuropsychopharmacology, 2003, v. 28, n. 9, p. 1597, doi. 10.1038/sj.npp.1300194

By:

Jentsch, J. David;
Arguello, P. Alexander;
Anzivino, Luigi A.

Publication type:

Article

Visualization of local afferent inputs to magnocellular oxytocin neurons in vitro.

Published in:

European Journal of Neuroscience, 1999, v. 11, n. 6, p. 1960, doi. 10.1046/j.1460-9568.1999.00620.x

By:

Jourdain, P.;
Dupouy, B.;
Bonhomme, R.;
Poulain, D. A.;
Israel, J. M.;
Theodosis, D. T.

Publication type:

Article

Permeability of rat neurohypophysial blood vessels for neurophysins and ferritin in acute hyperoxia.

Published in:

Biology Bulletin, 2008, v. 35, n. 3, p. 243, doi. 10.1134/S1062359008030035

By:

Sinichkin, A. S.;
Bardahchyan, E. A.;
Sagakyants, A. B.;
Vnukov, V. V.

Publication type:

Article

Neurohormonal Regulation of Tumor Growth.

Published in:

Russian Journal of Genetics, 2018, v. 54, n. 1, p. 36, doi. 10.1134/S1022795418010064

By:

Khegai, I.

Publication type:

Article

Expression of Hypothalamic Peptides in Mice Lacking Neuronal Nitric Oxide Synthase: Reduced β-END Immunoreactivity in the Arcuate Nucleus.

Published in:

Neuroendocrinology, 1998, v. 68, n. 6, p. 403, doi. 10.1159/000054390

By:

Bernstein, Hans-Gert;
Keilhoff, Gerburg;
Seidel, Bertolt;
Stanarius, Andreas;
Huang, Paul L.;
Fishman, Mark C.;
Reiser, Michael;
Bogerts, Bernhard;
Wolf, Gerald

Publication type:

Article

The Release of Oxytocin, Vasopressin and Associated Neurophysins after Electroconvulsive Therapy.

Published in:

Human Psychopharmacology: Clinical & Experimental, 1991, v. 6, n. 2, p. 161, doi. 10.1002/hup.470060211

By:

Scott, Allan I. F.;
Shering, P. Anne;
Lightman, Stafford L.;
Legros, Jean-Jacques;
Whalley, Lawrence J.

Publication type:

Article

Comparison of ex vivo stability of copeptin and vasopressin.

Published in:

Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 7, p. 948, doi. 10.1515/cclm-2016-0559

By:

Heida, Judith E.;
Boesten, Lianne S. M.;
Ettema, Esmée M.;
Muller Kobold, Anneke C.;
Franssen, Casper F. M.;
Gansevoort, Ron T.;
Zittema, Debbie

Publication type:

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.

Published in:

2012

By:

Luo, Yongfeng;
Wang, Binbin;
Qiu, Yu;
Zhang, Chuan;
Jin, Chengluo;
Zhao, Yakun;
Zhu, Qingguo;
Ma, Xu

Publication type:

Letter

Abnormal hypothalamic oxytocin system in fibroblast growth factor 8-deficient mice.

Published in:

Endocrine (1355008X), 2010, v. 38, n. 2, p. 174, doi. 10.1007/s12020-010-9366-9

By:

Brooks, Leah R.;
Chung, Wilson C. J.;
Pei-San Tsai

Publication type:

Article

MOLECULAR GENETICS STRATEGIES TO IDENTIFY VASOTOCIN CODING SEQUENCES IN HUMANS: FAMILY-SPECIFIC APPROACH USING GENOMIC DNA AND FETAL TISSUES mRNAs.

Published in:

Acta Endocrinologica (1841-0987), 2005, v. 1, n. 2, p. 131, doi. 10.4183/aeb.2005.131

By:

Radian, S.;
Bensaada, M.;
Lautier, Corinne;
Molés, J. P.;
Grigorescu, F.;
Gussi, Ilinca;
Badiu, C.;
Nastasia, S.;
Hudita, D.;
Leonte, Laura;
Marinescu, B.;
Coculescu, M.

Publication type:

Article

The human endolymphatic sac expresses natriuretic peptides.

Published in:

2017

By:

Møller, Martin Nue;
Kirkeby, Svend;
Vikeså, Jonas;
Nielsen, Finn Cilius;
Cayé‐Thomasen, Per

Publication type:

journal article

PROTEIN SYNTHESIS CHANGE IN BRAIN SUB CELLULAR PARTICLES AND SOLUBLE FRACTION AT THE CRUSH SYNDROME.

Published in:

Electronic Journal of Natural Sciences, 2006, v. 6, n. 1, p. 3

By:

Kevorkian, G. A.;
Kanayan, A. S.;
Guevorkian, A. G.;
Hayrapetyan, H. L.;
Galoyan, A. A.

Publication type:

Article

Comparative sequences of the canine and feline vasopressin prohormones.

Published in:

Comparative Clinical Pathology, 2007, v. 16, n. 3, p. 173, doi. 10.1007/s00580-007-0684-0

By:

Santos, Andrea P.;
Biondo, Alexander W.;
Sisson, David D.;
Lopes, Sonia T. A.;
Souza, Cleverson;
Solter, Philip F.

Publication type:

Article

Progressive decline of vasopressin secretion in familial autosomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene.

Published in:

Clinical Endocrinology, 2003, v. 59, n. 4, p. 511, doi. 10.1046/j.1365-2265.2003.01834.x

By:

Elias, Paula C. L.;
Elias, Lucila L. K.;
Torres, Natalia;
Moreira, Ayrton C.;
Antunes-Roddrigues, Jose;
Castro, Margaret

Publication type:

Article

The accessory magnocellular neurosecretory system of the rostral human hypothalamus.

Published in:

Cell & Tissue Research, 2018, v. 373, n. 2, p. 487, doi. 10.1007/s00441-018-2818-x

By:

Møller, Morten;
Busch, Johannes R.;
Jacobsen, Christina;
Lundemose, Sissel B.;
Lynnerup, Niels;
Rath, Martin F.;
Banner, Jytte

Publication type:

Article

Akt Induces Apoptosis in Neuroblastoma Cells Expressing a C98X Vasopressin Mutant Following Autophagy Suppression.

Published in:

Journal of Neuroendocrinology, 2008, v. 20, n. 10, p. 1165, doi. 10.1111/j.1365-2826.2008.01769.x

By:

Castino, R.;
Thepparit, C.;
Bellio, N.;
Murphy, D.;
Isidoro, C.

Publication type:

Article

The Hormone Domain of the Vasopressin Prohormone is Required for the Correct Prohormone Trafficking Through the Secretory Pathway.

Published in:

Journal of Neuroendocrinology, 2003, v. 15, n. 12, p. 1156, doi. 10.1111/j.1365-2826.2003.01114.x

By:

de Bree, F.M.;
van der Kleij, A.A.M.;
Nijenhuis, M.;
Zalm, R.;
Murphy, D.;
Burbach, J.P.H.

Publication type:

Article