Ultrastructural study of electrophysiologically identified neurones in the paraventricular nucleus of the rat.

PubWeight™: 0.79‹?›

🔗 View Article (PMID 7237518)

Published in Cell Tissue Res on January 01, 1981

Authors

M J Freund-Mercier, M E Stoeckel, F Moos, A Porte, P Richard

Articles by these authors

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nat Genet (1995) 2.52

Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy. Circ Res (1997) 2.25

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children. Eur Heart J (1998) 2.20

Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene. Circulation (1998) 2.04

Familial hypertrophic cardiomyopathy: from mutations to functional defects. Circ Res (1998) 1.92

Whisker isotopic signature depicts migration patterns and multi-year intra- and inter-individual foraging strategies in fur seals. Biol Lett (2009) 1.85

Absence of a holelike fermi surface for the iron-based K0.8F1.7Se2 superconductor revealed by angle-resolved photoemission spectroscopy. Phys Rev Lett (2011) 1.81

Biogenesis and intranuclear trafficking of human box C/D and H/ACA RNPs. Cold Spring Harb Symp Quant Biol (2006) 1.80

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome. Circ Res (1999) 1.70

Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue. Brain (2008) 1.65

Fermi surface dichotomy of the superconducting gap and pseudogap in underdoped pnictides. Nat Commun (2011) 1.63

Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism? Neurology (2007) 1.59

The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein. Hum Mol Genet (1994) 1.47

Interference effect in electron emission in heavy ion collisions with h2 detected by comparison with the measured electron spectrum from atomic hydrogen. Phys Rev Lett (2004) 1.45

Visual neurophysiological dysfunction in infants exposed to hydroxychloroquine in utero. Acta Paediatr (2009) 1.43

Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk. Cardiovasc Res (2000) 1.42

[Oculopharyngeal muscular dystrophy: study of patients from seven Spanish families with different GCG expansions in PABP2 gene]. Neurologia (2004) 1.42

Electrophysiological evidence for facilitatory control of oxytocin neurones by oxytocin during suckling in the rat. J Physiol (1984) 1.32

A rise in the intracellular Ca2+ concentration of isolated rat supraoptic cells in response to oxytocin. J Physiol (1994) 1.32

Vasopressin regularizes the phasic firing pattern of rat hypothalamic magnocellular vasopressin neurons. J Neurosci (1998) 1.28

The interaction of caffeine with ultra-violet-light-irradiated DNA. Int J Radiat Biol Relat Stud Phys Chem Med (1970) 1.27

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy. J Mol Med (Berl) (1998) 1.27

Accelerated telomere shortening and telomerase activation in Fanconi's anaemia. Br J Haematol (1999) 1.26

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence. Circulation (1999) 1.26

Central effects of oxytocin. Physiol Rev (1991) 1.25

The steroidogenic acute regulatory protein homolog MLN64, a late endosomal cholesterol-binding protein. J Biol Chem (2000) 1.23

Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins. Brain (2006) 1.23

Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy. Neurology (2002) 1.23

Distribution of oxytocin- and vasopressin-binding sites in the rat extended amygdala: a histoautoradiographic study. J Comp Neurol (1997) 1.22

Release of oxytocin and vasopressin by magnocellular nuclei in vitro: specific facilitatory effect of oxytocin on its own release. J Endocrinol (1984) 1.21

Agonist action of taurine on glycine receptors in rat supraoptic magnocellular neurones: possible role in osmoregulation. J Physiol (1997) 1.20

Release of oxytocin within the supraoptic nucleus during the milk ejection reflex in rats. Exp Brain Res (1989) 1.20

Paired recordings from supraoptic and paraventricular oxytocin cells in suckled rats: recruitment and synchronization. J Physiol (1986) 1.19

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy. Circulation (1996) 1.18

GABA- and peptide-immunoreactivities co-localize in the rat central extended amygdala. Neuroreport (1997) 1.14

Paraventricular and supraoptic bursting oxytocin cells in rat are locally regulated by oxytocin and functionally related. J Physiol (1989) 1.13

Intrathoracic gossypiboma: magnetic resonance features. Int J Cardiol (1999) 1.11

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population. Circulation (1997) 1.10

Synchronization of oxytocin cells in the hypothalamic paraventricular and supraoptic nuclei in suckled rats: direct proof with paired extracellular recordings. Exp Brain Res (1984) 1.06

Excitatory effect of dopamine on oxytocin and vasopressin reflex releases in the rat. Brain Res (1982) 1.06

Pharmacological characteristics and anatomical distribution of [3H]oxytocin-binding sites in the Wistar rat brain studied by autoradiography. Neuroscience (1987) 1.06

Vasopressin-induced intracellular Ca2+ increase in isolated rat supraoptic cells. J Physiol (1996) 1.06

Brain inflammatory response induced by intracerebroventricular infusion of lipopolysaccharide: an immunohistochemical study. Brain Res (1998) 1.05

Frequencies of HPRT- lymphocytes and glycophorin A variants erythrocytes in Fanconi anemia patients, their parents and control donors. Mutat Res (1993) 1.03

Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene. Neuromuscul Disord (2008) 1.02

Oxytocin receptors on oxytocin neurones: histoautoradiographic detection in the lactating rat. J Physiol (1994) 1.01

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience. J Med Genet (2002) 1.01

Splicing mutations in KCNQ1: a mutation hot spot at codon 344 that produces in frame transcripts. Circulation (1999) 1.00

Biochemical and ultrastructural studies of cultured rat astroglial cells: effect of brain extract and dibutyryl cyclic AMP on glial fibrillary acidic protein and glial filaments. Differentiation (1980) 1.00

An unusual familial cardiomyopathy characterized by aberrant accumulations of desmin-type intermediate filaments. Virchows Arch A Pathol Anat Histol (1981) 1.00

Oxytocin modulates glutamatergic synaptic transmission between cultured neonatal spinal cord dorsal horn neurons. J Neurosci (1998) 0.99

Fermi surface nesting induced strong pairing in iron-based superconductors. Proc Natl Acad Sci U S A (2009) 0.98

Heart-hand syndrome of Slovenian type: a new kind of laminopathy. J Med Genet (2008) 0.98

Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes. Neuromuscul Disord (2005) 0.98

Electrical stimulations of perifused magnocellular nuclei in vitro elicit Ca2+-dependent, tetrodotoxin-insensitive release of oxytocin and vasopressin. Neurosci Lett (1987) 0.98

On the existence of stationary states during granular compaction. Eur Phys J E Soft Matter (2007) 0.97

Electrophysiological properties of cultured neonatal rat dorsal horn neurons containing GABA and met-enkephalin-like immunoreactivity. J Neurophysiol (1998) 0.97

Action of endogenous oxytocin within the paraventricular or supraoptic nuclei: a powerful link in the regulation of the bursting pattern of oxytocin neurons during the milk-ejection reflex in rats. Neuroscience (1993) 0.97

Oxytocinergic innervation of autonomic nuclei controlling penile erection in the rat. Neuroscience (1999) 0.96

Deletion in the cardiac troponin I gene in a family from northern Sweden with hypertrophic cardiomyopathy. J Mol Cell Cardiol (2000) 0.96

Intrinsic and extrinsic connections of the rat central extended amygdala: an in vivo electrophysiological study of the central amygdaloid nucleus. Brain Res (1998) 0.96

[Congenital long QT syndrome. The value of genetics in prognostic evaluation]. Arch Mal Coeur Vaiss (1999) 0.95

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey. Heart (2004) 0.94

Sexually dimorphic expression of oxytocin binding sites in forebrain and spinal cord of the rat. Neuroscience (2005) 0.94

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7. J Neurol (2009) 0.93

The fine structure of the conducting system of the monkey heart (Macaca mulatta). I. The sino-atrial node and the internodal connections. Z Zellforsch Mikrosk Anat (1973) 0.93

Excitatory effects of intraventricular injections of oxytocin on the milk ejection reflex in the rat. Neurosci Lett (1981) 0.92

[Ultrastructural studies on the mouse parathyroid gland. 1. Studies in the normal mouse]. Z Zellforsch Mikrosk Anat (1966) 0.92

[Limbic encephalitis with severe sleep disorder associated with voltage-gated potassium channels (VGKCs) antibodies]. Rev Neurol (Paris) (2008) 0.92

L-, N- and T- but neither P- nor Q-type Ca2+ channels control vasopressin-induced Ca2+ influx in magnocellular vasopressin neurones isolated from the rat supraoptic nucleus. J Physiol (1997) 0.92

Postprandial metabolic profiles following meals and snacks eaten during simulated night and day shift work. Chronobiol Int (2004) 0.92

Ultrastructure of anaplastic bronchial carcinomas. Cancer (1967) 0.91

Penetrance of familial hypertrophic cardiomyopathy. Genet Couns (1997) 0.91

Towards a theoretical picture of dense granular flows down inclines. Nat Mater (2007) 0.90

Hypervascularization in the magnocellular nuclei of the rat hypothalamus: relationship with the distribution of aquaporin-4 and markers of energy metabolism. J Neuroendocrinol (2000) 0.90

Transplantation for Fanconi's anaemia: long-term follow-up of fifty patients transplanted from a sibling donor after low-dose cyclophosphamide and thoraco-abdominal irradiation for conditioning. Br J Haematol (1998) 0.90

Localization of oxytocin binding sites in the thoracic and upper lumbar spinal cord of the adult and postnatal rat: a histoautoradiographic study. Eur J Neurosci (1994) 0.89

Subcellular localization of calcium in the mouse hypophysis. I. Calcium distribution in the adeno- and neurohypophysis under normal conditions. Cell Tissue Res (1975) 0.89

Histoautoradiographic detection of oxytocin- and vasopressin-binding sites in the telencephalon of the rat. J Comp Neurol (1993) 0.89

Prevalence of L. loa and M. perstans filariasis in southern Cameroon. Trop Geogr Med (1995) 0.89

Identification and quantitation of phosphorus metabolites in yeast neutral pH extracts by nuclear magnetic resonance spectroscopy. Anal Biochem (1999) 0.88