Published in Neuroendocrinology on January 01, 1983
Electrophysiological evidence for facilitatory control of oxytocin neurones by oxytocin during suckling in the rat. J Physiol (1984) 1.32
Paired recordings from supraoptic and paraventricular oxytocin cells in suckled rats: recruitment and synchronization. J Physiol (1986) 1.19
Electrophysiology of guinea-pig supraoptic neurones: role of a hyperpolarization-activated cation current in phasic firing. J Physiol (1993) 1.17
Oxytocin and Major Depressive Disorder: Experimental and Clinical Evidence for Links to Aetiology and Possible Treatment. Pharmaceuticals (Basel) (2010) 0.77
Enhanced responsiveness to selective serotonin reuptake inhibitors during lactation. PLoS One (2015) 0.77
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nat Genet (1995) 2.52
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
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
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
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy. Neurology (2002) 1.23
Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins. Brain (2006) 1.23
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
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
Vasopressin-induced intracellular Ca2+ increase in isolated rat supraoptic cells. J Physiol (1996) 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
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
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
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
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
Deletion in the cardiac troponin I gene in a family from northern Sweden with hypertrophic cardiomyopathy. J Mol Cell Cardiol (2000) 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
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7. J Neurol (2009) 0.93
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
[Limbic encephalitis with severe sleep disorder associated with voltage-gated potassium channels (VGKCs) antibodies]. Rev Neurol (Paris) (2008) 0.92
Excitatory effects of intraventricular injections of oxytocin on the milk ejection reflex in the rat. Neurosci Lett (1981) 0.92
Postprandial metabolic profiles following meals and snacks eaten during simulated night and day shift work. Chronobiol Int (2004) 0.92
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
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
Prevalence of L. loa and M. perstans filariasis in southern Cameroon. Trop Geogr Med (1995) 0.89
[Management of a giant paraovarian cyst]. Gynecol Obstet Fertil (2006) 0.88
Identification and quantitation of phosphorus metabolites in yeast neutral pH extracts by nuclear magnetic resonance spectroscopy. Anal Biochem (1999) 0.88
Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations. Circulation (2001) 0.88
Genetic epidemiology of host predisposition microfilaraemia in human loiasis. Trop Med Int Health (1999) 0.88
The V1a and V1b, but not V2, vasopressin receptor genes are expressed in the supraoptic nucleus of the rat hypothalamus, and the transcripts are essentially colocalized in the vasopressinergic magnocellular neurons. Endocrinology (1998) 0.88
Dynamic non-invasive measurements of arterial diameter and wall thickness. J Hypertens Suppl (1992) 0.87
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene. Muscle Nerve (2005) 0.87
Erve virus, a probable member of Bunyaviridae family isolated from shrews (Crocidura russula) in France. Acta Virol (1989) 0.87
An adult form of L-2-hydroxyglutaric aciduria revealed by tremor. Eur Neurol (2000) 0.86
Coexistence of competing orders with two energy gaps in real and momentum space in the high temperature superconductor Bi_{2}Sr_{2-x}La_{x}CuO_{6+delta}. Phys Rev Lett (2008) 0.86
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern. Neuromuscul Disord (2010) 0.86
Evolution of a pairing-induced pseudogap from the superconducting gap of (Bi,Pb)2Sr2CuO6. Phys Rev Lett (2009) 0.86
Increased incidence of moderate stenosis among patients with diabetes: substrate for myocardial infarction? Am Heart J (1997) 0.86
PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy. J Med Genet (1998) 0.86
A precise method for visualizing dispersive features in image plots. Rev Sci Instrum (2011) 0.86
The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder. J Med Genet (2004) 0.85
Evidence for connections between a discrete hypothalamic dorsochiasmatic area and the supraoptic and paraventricular nuclei. Brain Res Bull (1994) 0.85
Synchronized heat flux oscillations in yeast cell populations. J Biol Chem (1996) 0.85
Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy. Hum Mutat (1998) 0.85
Unconventional anisotropic s-wave superconducting gaps of the LiFeAs iron-pnictide superconductor. Phys Rev Lett (2012) 0.85
New aspects of firing pattern autocontrol in oxytocin and vasopressin neurones. Adv Exp Med Biol (1998) 0.85
A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia. J Med Genet (2004) 0.85
Density inversion in rapid granular flows: the supported regime. Eur Phys J E Soft Matter (2007) 0.85
Experimental compaction of anisotropic granular media. Eur Phys J E Soft Matter (2005) 0.85
V1a- and V2-type vasopressin receptors mediate vasopressin-induced Ca2+ responses in isolated rat supraoptic neurones. J Physiol (1999) 0.84
Electronic structure of optimally doped pnictide Ba0.6K0.4Fe2As2: a comprehensive angle-resolved photoemission spectroscopy investigation. J Phys Condens Matter (2011) 0.84
Heart involvement in lamin A/C related diseases. Arch Mal Coeur Vaiss (2006) 0.84
[Level of oxytocin release induced by vaginal dilatation (Ferguson reflex) and vagal stimulation (vago-pituitary reflex) in lactating rats (author's transl)]. J Physiol (Paris) (1975) 0.84
Suicide in patients hospitalized for schizophrenia: 1913-1940. J Nerv Ment Dis (1999) 0.84
Long-term bone marrow culture in Fanconi's anaemia. Br J Haematol (1993) 0.84
Activation of N-methyl-D-aspartate receptors regulates basal electrical activity of oxytocin and vasopressin neurons in lactating rats. Neuroscience (1997) 0.84
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations. Neuromuscul Disord (2011) 0.84
Stable isotopes document the trophic structure of a deep-sea cephalopod assemblage including giant octopod and giant squid. Biol Lett (2009) 0.83
Angle-resolved photoemission spectroscopy of the iron-chalcogenide superconductor Fe1.03Te0.7Se0.3: strong coupling behavior and the universality of interband scattering. Phys Rev Lett (2010) 0.83
Activation of multiple intracellular transduction signals by vasopressin in vasopressin-sensitive neurones of the rat supraoptic nucleus. J Physiol (1998) 0.83