Genetische Erkrankungen der Neurohypophyse

Alves SE et al. (1998) Differential colocalization of estrogen receptor beta (ERbeta) with oxytocin and vasopressin in the paraventricular and supraoptic nuclei of the female rat brain: an immunocytochemical study.

None (2003) Dominant-negative diabetes insipidus and other endocrinopathies.

Russell TA et al. (2003) A murine model of autosomal dominant neurohypophyseal diabetes insipidus reveals progressive loss of vasopressin-producing neurons.

Christensen JH et al. (2004) Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis.

Wahlstrom JT et al. (2004) A novel mutation in the preprovasopressin gene identified in a kindred with autosomal dominant neurohypophyseal diabetes insipidus.

Rao VV et al. (1992) The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridization.

Summar ML et al. (1990) Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20.

Sausville E et al. (1985) The human vasopressin gene is linked to the oxytocin gene and is selectively expressed in a cultured lung cancer cell line.

Brownstein MJ et al. (1980) Synthesis, transport, and release of posterior pituitary hormones.

Marini JC et al. (1993) The pituitary hormones arginine vasopressin-neurophysin II and oxytocin-neurophysin I show close linkage with interleukin-1 on mouse chromosome 2.

None (1959) Familial diabetes insipidus.

Ferguson JN et al. (2000) Social amnesia in mice lacking the oxytocin gene.

Kosfeld M et al. (2005) Oxytocin increases trust in humans.

Kavaliers M et al. (2006) Inadvertent social information and the avoidance of parasitized male mice: a role for oxytocin.

Tyzio R et al. (2006) Maternal oxytocin triggers a transient inhibitory switch in GABA signaling in the fetal brain during delivery.

Jin D et al. (2007) CD38 is critical for social behaviour by regulating oxytocin secretion.

None (2007) Comment on "Maternal oxytocin triggers a transient inhibitory switch in GABA signaling in the fetal brain during delivery".

De Dreu CK et al. (2010) The neuropeptide oxytocin regulates parochial altruism in intergroup conflict among humans.

Viviani D et al. (2011) Oxytocin selectively gates fear responses through distinct outputs from the central amygdala.

Majzoub JA et al. (1984) Vasopressin gene is expressed at low levels in the hypothalamus of the Brattleboro rat.

Laing RB et al. (1991) Facial dysmorphism: a marker of autosomal dominant cranial diabetes insipidus.

Repaske DR et al. (1990) Molecular analysis of autosomal dominant neurohypophyseal diabetes insipidus.

Pedersen EB et al. (1985) Familial cranial diabetes insipidus: a report of five families. Genetic, diagnostic and therapeutic aspects.

Sokol HW et al. (1965) Morphology of the neurosecretory system in rats homozygous and heterozygous for hypothalamic diabetes insipidus (Brattleboro strain).

Valtin H et al. (1965) Neurohypophysial principles in rats homozygous and heterozygous for hypothalamic diabetes insipidus (Brattleboro strain).

None (1967) Hereditary hypothalamic diabetes insipidus in rats (Brattleboro strain). A useful experimental model.

Nagai I et al. (1984) Two cases of hereditary diabetes insipidus, with an autopsy finding in one.

Toth EL et al. (1984) Hereditary central diabetes insipidus: plasma levels of antidiuretic hormone in a family with a possible osmoreceptor defect.

Schmale H et al. (1984) The mutant vasopressin gene from diabetes insipidus (Brattleboro) rats is transcribed but the message is not efficiently translated.

Jirikowski GF et al. (1992) Reversal of diabetes insipidus in Brattleboro rats: intrahypothalamic injection of vasopressin mRNA.

Blackett PR et al. () Familial central diabetes insipidus: vasopressin and nicotine stimulated neurophysin deficiency with subnormal oxytocin and estrogen stimulated neurophysin.

Pivonello R et al. (1998) Impairment of bone status in patients with central diabetes insipidus.

Willcutts MD et al. (1999) Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin.

Leger J et al. (1999) Thickened pituitary stalk on magnetic resonance imaging in children with central diabetes insipidus.

Pivonello R et al. (1999) Effect of a short-term treatment with alendronate on bone density and bone markers in patients with central diabetes insipidus.

Pivonello R et al. (2003) Central diabetes insipidus and autoimmunity: relationship between the occurrence of antibodies to arginine vasopressin-secreting cells and clinical, immunological, and radiological features in a large cohort of patients with central diabetes insipidus of known and unknown etiology.

PENDER CB et al. (1953) Dominant inheritance of diabetes insipidus; a family study.

BRAVERMAN LE et al. (1965) HEREDITARY IDIOPATHIC DIABETES INSIPIDUS. A CASE REPORT WITH AUTOPSY FINDINGS.