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Arginine vasopressin controls p27(KiP1) protein expression by PKC activation and irreversibly inhibits the proliferation of K-Ras-dependent mouse Y1 adrenocortical malignant cells
(ELSEVIER SCIENCE BV, 2011)
The neurohypophyseal hormone arginine vasopressin (AVP) is a classic mitogen in many cells. In K-Ras-dependent mouse Y1 adrenocortical malignant cells, AVP elicits antagonistic responses such as the activation of the PKC ...
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family
(Sociedade Brasileira de Endocrinologia e Metabologia, 2008)
Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is a rare autosomal dominant disorder characterized by polyuria and polydipsia due to deficiency of arginine vasopressin (AVP). More than 50 mutations ...
[Mutations in the arginine vasopressin neurophysin-II gene in familial neurohypophyseal diabetes insipidus patients]
(2008)
Neurogenic diabetes insipidus (NDI) is a rare condition characterized by polyuria and polydipsia caused by deficient arginine vasopressin hormone production. More than a 50 mutations have been identified for familial ...
[Mutations in the arginine vasopressin neurophysin-II gene in familial neurohypophyseal diabetes insipidus patients]
(2008)
Neurogenic diabetes insipidus (NDI) is a rare condition characterized by polyuria and polydipsia caused by deficient arginine vasopressin hormone production. More than a 50 mutations have been identified for familial ...
Hyponatremia resulting from Arginine Vasopressin Receptor 2 gene mutation
(Springer, 2007-03)
Chronic hyponatremia, unless associated with extracellular fluid volume expansion, is an infrequent electrolyte imbalance in pediatrics. We report an infant with chronic hyponatremia suggestive of a syndrome of inappropriate ...
Mutations in the arginine vasopressin neurophysin-II gene in familial neurohypophyseal diabetes insipidus patients [Mutaciones en el gen de arginina vasopresina neurofisina II en pacientes con diabetes insípida neurohipofisiaria familiar]
(2008)
Neurogenic diabetes insipidus (NDI) is a rare condition characterized by polyuria and polydipsia caused by deficient arginine vasopressin hormone production. More than a 50 mutations have been identified for familial ...
Mutations in the arginine vasopressin neurophysin-II gene in familial neurohypophyseal diabetes insipidus patients [Mutaciones en el gen de arginina vasopresina neurofisina II en pacientes con diabetes insípida neurohipofisiaria familiar]
(2008)
Neurogenic diabetes insipidus (NDI) is a rare condition characterized by polyuria and polydipsia caused by deficient arginine vasopressin hormone production. More than a 50 mutations have been identified for familial ...
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus
(Soc Neuroscience, 2014-03-12)
Arginine vasopressin (AVP) is a neurohypophysial hormone regulating hydromineral homeostasis. Here we show that the mRNA encoding cAMP responsive element-binding protein-3 like-1 (CREB3L1), a transcription factor of the ...
Transcription Factor CREB3L1 Regulates Vasopressin Gene Expression in the Rat Hypothalamus
(Soc Neuroscience, 2014)
Clinical features and molecular analysis of arginine-vasopressin neurophysin II gene in long-term follow-up patients with idiopathic central diabetes insipidus
(Sociedade Brasileira de Endocrinologia e Metabologia, 2010)
INTRODUCTION: Central diabetes insipidus (DI) characterized by polyuria, polydipsia and inability to concentrate urine, has different etiologies including genetic, autoimmune, post-traumatic, among other causes. Autosomal ...