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Summary Expression Phenotypes Gene Literature (531) GO Terms (11) Nucleotides (79) Proteins (47) Interactants (1198) Wiki
XB-GENEPAGE-487168

Papers associated with nodal1



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Effects of ionic concentration on permeability properties of nodal membrane in myelinated nerve fibres of Xenopus laevis. Potential clamp experiments., Brismar T., Acta Physiol Scand. April 1, 1973; 87 (4): 474-84.

The rate of action of tetrodotoxin on myelinated nerve fibres of Xenopus laevis and Rana esculenta., Schwarz JR, Ulbricht W, Wagner HH., J Physiol. August 1, 1973; 233 (1): 167-94.

Effect of lanthanum at the nodal membrane., Vogel W., Experientia. December 1, 1973; 29 (12): 1517.

Calcium and lanthanum effects at the nodal membrane., Vogel W., Pflugers Arch. January 1, 1974; 350 (1): 25-39.

Local anesthetics: effects on permeability properties of nodal membrane in myelinated nerve fibres from xenopus. Potential clamp experiments., Arhem P, Frankenhaeuser B., Acta Physiol Scand. May 1, 1974; 91 (1): 11-21.

Effects of ionic concentration on sodium permeability properties of myelinated nerve fibres of Xenopus laevis., Brismar T, Frankenhaeuser B., J Physiol. August 1, 1975; 249 (3): 549-59.

Tetanic hyperpolarization of single medullated nerve fibers in sodium and lithium., Schoepfle GM., Am J Physiol. October 1, 1976; 231 (4): 1033-8.

Slow action of Ca on myelinated nerve fibres of Xenopus laevis., Brismar T., Acta Physiol Scand. March 1, 1977; 99 (3): 361-7.

Slow mechanism for sodium permeability inactivation in myelinated nerve fibre of Xenopus laevis., Brismar T., J Physiol. September 1, 1977; 270 (2): 283-97.

Effect of the nonionic detergent triton X-100 on sodium permeability of the myelinated nerve fibre of Xenopus laevis., Brismar T, Rydqvist B., Acta Physiol Scand. April 1, 1978; 102 (4): 425-33.

Delayed development of sodium permeability inactivation in the nodal membrane [proceedings]., Kniffki KD, Siemen D, Vogel W., J Physiol. November 1, 1978; 284 92P-93P.

Development of sodium permeability inactivation in nodal membranes., Kniffki KD, Siemen D, Vogel W., J Physiol. January 1, 1981; 313 37-48.

Computer simulation of the effect of the nodal gap resistance on ionic current measurements in the Ranvier node membrane., Zaciu C, Tripa M, Vasilescu V., Biophys J. December 1, 1981; 36 (3): 797-802.

Potassium permeability in thin amphibian myelinated fibres., Brismar T., Pflugers Arch. June 1, 1982; 393 (4): 348-50.

Tetrabutylammonium affects the nodal nerve membrane from inside only., Kristbjarnarson H, Arhem P., Acta Physiol Scand. November 1, 1982; 116 (3): 303-4.

On the capacity current in myelinated nerve fibres., Wiese H, Koppenhöfer E., Gen Physiol Biophys. August 1, 1983; 2 (4): 297-312.

The strength-duration relationship for excitation of myelinated nerve: computed dependence on membrane parameters., Bostock H., J Physiol. August 1, 1983; 341 59-74.

The distribution of sodium and potassium channels in single demyelinated axons of the frog., Shrager P., J Physiol. November 1, 1987; 392 587-602.

Minimizing the influence of the series resistance in potential clamped Ranvier nodes., Wiese H, Koppenhöfer E., Gen Physiol Biophys. April 1, 1988; 7 (2): 143-56.

Single-channel recording in myelinated nerve fibers reveals one type of Na channel but different K channels., Jonas P, Bräu ME, Hermsteiner M, Vogel W., Proc Natl Acad Sci U S A. September 1, 1989; 86 (18): 7238-42.

A K+ channel in Xenopus nerve fibres selectively blocked by bee and snake toxins: binding and voltage-clamp experiments., Bräu ME, Dreyer F, Jonas P, Repp H, Vogel W., J Physiol. January 1, 1990; 420 365-85.

Control by asparagine residues of calcium permeability and magnesium blockade in the NMDA receptor., Burnashev N, Schoepfer R, Monyer H, Ruppersberg JP, Günther W, Seeburg PH, Sakmann B., Science. September 4, 1992; 257 (5075): 1415-9.

Single-channel conductances of NMDA receptors expressed from cloned cDNAs: comparison with native receptors., Stern P, Béhé P, Schoepfer R, Colquhoun D., Proc Biol Sci. December 22, 1992; 250 (1329): 271-7.

Developmental switch in the expression of NMDA receptors occurs in vivo and in vitro., Williams K, Russell SL, Shen YM, Molinoff PB., Neuron. February 1, 1993; 10 (2): 267-78.

Nodal is a novel TGF-beta-like gene expressed in the mouse node during gastrulation., Zhou X, Sasaki H, Lowe L, Hogan BL, Kuehn MR., Nature. February 11, 1993; 361 (6412): 543-7.

Subunit-specific block of cloned NMDA receptors by argiotoxin636., Raditsch M, Ruppersberg JP, Kuner T, Günther W, Schoepfer R, Seeburg PH, Jahn W, Witzemann V., FEBS Lett. June 7, 1993; 324 (1): 63-6.

Splice variants of the N-methyl-D-aspartate receptor NR1 identify domains involved in regulation by polyamines and protein kinase C., Durand GM, Bennett MV, Zukin RS., Proc Natl Acad Sci U S A. July 15, 1993; 90 (14): 6731-5.

Axonal coding of action potentials in demyelinated nerve fibers., Shrager P., Dev Biol. August 13, 1993; 619 (1-2): 278-90.

Preferential co-assembly of recombinant NMDA receptors composed of three different subunits., Wafford KA, Bain CJ, Le Bourdelles B, Whiting PJ, Kemp JA., Neuroreport. September 30, 1993; 4 (12): 1347-9.

Ifenprodil discriminates subtypes of the N-methyl-D-aspartate receptor: selectivity and mechanisms at recombinant heteromeric receptors., Williams K., Mol Pharmacol. October 1, 1993; 44 (4): 851-9.

Expression of a minimal K+ channel protein in mammalian cells and immunolocalization in guinea pig heart., Freeman LC, Kass RS., Circ Res. November 1, 1993; 73 (5): 968-73.

Glycine-glutamate interactions at the NMDA receptor: role of cysteine residues., Laube B, Kuryatov A, Kuhse J, Betz H., FEBS Lett. December 13, 1993; 335 (3): 331-4.

Sensitivity of the N-methyl-D-aspartate receptor to polyamines is controlled by NR2 subunits., Williams K, Zappia AM, Pritchett DB, Shen YM, Molinoff PB., Mol Pharmacol. May 1, 1994; 45 (5): 803-9.

Cloning, functional coexpression, and pharmacological characterisation of human cDNAs encoding NMDA receptor NR1 and NR2A subunits., Le Bourdellès B, Wafford KA, Kemp JA, Marshall G, Bain C, Wilcox AS, Sikela JM, Whiting PJ., J Neurochem. June 1, 1994; 62 (6): 2091-8.

Subunit-specific potentiation of recombinant N-methyl-D-aspartate receptors by histamine., Williams K., Mol Pharmacol. September 1, 1994; 46 (3): 531-41.

Na(+)-activated K+ channels localized in the nodal region of myelinated axons of Xenopus., Koh DS, Jonas P, Vogel W., J Physiol. September 1, 1994; 479 ( Pt 2) 183-97.

Spermine potentiation of recombinant N-methyl-D-aspartate receptors is affected by subunit composition., Zhang L, Zheng X, Paupard MC, Wang AP, Santchi L, Friedman LK, Zukin RS, Bennett MV., Proc Natl Acad Sci U S A. November 8, 1994; 91 (23): 10883-7.

Identification of amino acids in the N-methyl-D-aspartate receptor NR1 subunit that contribute to the glycine binding site., Wafford KA, Kathoria M, Bain CJ, Marshall G, Le Bourdellès B, Kemp JA, Whiting PJ., Mol Pharmacol. February 1, 1995; 47 (2): 374-80.

Recombinant human NMDA homomeric NR1 receptors expressed in mammalian cells form a high-affinity glycine antagonist binding site., Grimwood S, Le Bourdellès B, Whiting PJ., J Neurochem. February 1, 1995; 64 (2): 525-30.

Dimensions of the narrow portion of a recombinant NMDA receptor channel., Villarroel A, Burnashev N, Sakmann B., Biophys J. March 1, 1995; 68 (3): 866-75.

Control of proton sensitivity of the NMDA receptor by RNA splicing and polyamines., Traynelis SF, Hartley M, Heinemann SF., Science. May 12, 1995; 268 (5212): 873-6.

A nodal-related gene defines a physical and functional domain within the Spemann organizer., Smith WC, McKendry R, Ribisi S, Harland RM., Cell. July 14, 1995; 82 (1): 37-46.              

Glycine modulates ethanol inhibition of heteromeric N-methyl-D-aspartate receptors expressed in Xenopus oocytes., Buller AL, Larson HC, Morrisett RA, Monaghan DT., Mol Pharmacol. October 1, 1995; 48 (4): 717-23.

Nodal-related signals induce axial mesoderm and dorsalize mesoderm during gastrulation., Jones CM, Kuehn MR, Hogan BL, Smith JC, Wright CV., Development. November 1, 1995; 121 (11): 3651-62.                

Determination of NMDA NR1 subunit copy number in recombinant NMDA receptors., Béhé P, Stern P, Wyllie DJ, Nassar M, Schoepfer R, Colquhoun D., Proc Biol Sci. November 22, 1995; 262 (1364): 205-13.

An acidic amino acid in the N-methyl-D-aspartate receptor that is important for spermine stimulation., Williams K, Kashiwagi K, Fukuchi J, Igarashi K., Mol Pharmacol. December 1, 1995; 48 (6): 1087-98.

A novel TGF-beta-like gene, fugacin, specifically expressed in the Spemann organizer of Xenopus., Ecochard V, Cayrol C, Foulquier F, Zaraisky A, Duprat AM., Dev Biol. December 1, 1995; 172 (2): 699-703.      

Differential contribution of the NR1- and NR2A-subunits to the selectivity filter of recombinant NMDA receptor channels., Wollmuth LP, Kuner T, Seeburg PH, Sakmann B., J Physiol. March 15, 1996; 491 ( Pt 3) 779-97.

The 5'-untranslated region of the N-methyl-D-aspartate receptor NR2A subunit controls efficiency of translation., Wood MW, VanDongen HM, VanDongen AM., J Biol Chem. April 5, 1996; 271 (14): 8115-20.

Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus., Lowe LA, Supp DM, Sampath K, Yokoyama T, Wright CV, Potter SS, Overbeek P, Kuehn MR., Nature. May 9, 1996; 381 (6578): 158-61.

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