Search Results - "Main, Martin J."

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  1. 1

    RAMPs regulate the transport and ligand specificity of the calcitonin-receptor-like receptor by Foord, Steven M, McLatchie, Linda M, Fraser, Neil J, Main, Martin J, Wise, Alan, Brown, Jason, Thompson, Nicola, Solari, Roberto, Lee, Melanie G

    Published in Nature (London) (28-05-1998)
    “…Calcitonin-gene-related peptide (CGRP) and adrenomedullin are related peptides with distinct pharmacological profiles. Here we show that a receptor with seven…”
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    Journal Article
  2. 2

    Advanced molecular imaging for the characterisation of complex medicines by Yilmaz, Duygu, Sharp, Paul S., Main, Martin J., Simpson, Peter B.

    Published in Drug discovery today (01-06-2022)
    “…•Complex medicines with a novel delivery mechanism or chemistry are growing in clinical impact.•New chemistry and carrier technology will take complex…”
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  3. 3

    Functional expression of the voltage-gated Na⁺-channel Nav1.7 is necessary for EGF-mediated invasion in human non-small cell lung cancer cells by Campbell, Thomas M, Main, Martin J, Fitzgerald, Elizabeth M

    Published in Journal of cell science (01-11-2013)
    “…Various ion channels are expressed in human cancers where they are intimately involved in proliferation, angiogenesis, invasion and metastasis. Expression of…”
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    Journal Article
  4. 4

    Heterologous expression and functional analysis of rat Nav1.8 (SNS) voltage-gated sodium channels in the dorsal root ganglion neuroblastoma cell line ND7-23 by John, Victoria H, Main, Martin J, Powell, Andrew J, Gladwell, Zoe M, Hick, Caroline, Sidhu, Harjeet S, Clare, Jeff J, Tate, Simon, Trezise, Derek J

    Published in Neuropharmacology (01-03-2004)
    “…The voltage-gated sodium channel NaV1.8 (SNS, PN3) is thought to be a molecular correlate of the dorsal root ganglion (DRG) tetrodotoxin resistant (TTX-R) Na+…”
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    Journal Article
  5. 5

    Positioning High-Throughput CETSA in Early Drug Discovery through Screening against B-Raf and PARP1 by Shaw, Joseph, Dale, Ian, Hemsley, Paul, Leach, Lindsey, Dekki, Nancy, Orme, Jonathan P, Talbot, Verity, Narvaez, Ana J, Bista, Michal, Martinez Molina, Daniel, Dabrowski, Michael, Main, Martin J, Gianni, Davide

    Published in SLAS discovery (01-02-2019)
    “…Methods to measure cellular target engagement are increasingly being used in early drug discovery. The Cellular Thermal Shift Assay (CETSA) is one such method…”
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    Journal Article
  6. 6

    Use of escin as a perforating agent on the IonWorks quattro automated electrophysiology platform by Morton, Michael J, Main, Martin J

    Published in Journal of biomolecular screening (01-01-2013)
    “…The automated electrophysiology platform IonWorks has facilitated the medium-throughput study of ion channel biology and pharmacology. Electrical and chemical…”
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    Journal Article
  7. 7

    Functional expression of the voltage-gated sodium channel, Nav1.7, underlies epidermal growth factor-mediated invasion in human [R1.S1] non-small cell lung cancer cells by Campbell, Thomas M., Main, Martin J., Fitzgerald, Elizabeth M.

    Published in Journal of cell science (01-01-2013)
    “…Various ion channels are expressed in human cancers where they are intimately involved in proliferation, angiogenesis, invasion and metastasis. Expression of…”
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    Journal Article
  8. 8

    Multiple amylin receptors arise from receptor activity-modifying protein interaction with the calcitonin receptor gene product by Christopoulos, G, Perry, K J, Morfis, M, Tilakaratne, N, Gao, Y, Fraser, N J, Main, M J, Foord, S M, Sexton, P M

    Published in Molecular pharmacology (01-07-1999)
    “…Receptor activity-modifying proteins (RAMPs) are single-transmembrane proteins that transport the calcitonin receptor-like receptor (CRLR) to the cell surface…”
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    Journal Article
  9. 9

    Modulation of KCNQ2/3 potassium channels by the novel anticonvulsant retigabine by Main, M J, Cryan, J E, Dupere, J R, Cox, B, Clare, J J, Burbidge, S A

    Published in Molecular pharmacology (01-08-2000)
    “…Retigabine is a novel anticonvulsant with an unknown mechanism of action. It has recently been reported that retigabine modulates a potassium channel current…”
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    Journal Article
  10. 10

    The CGRP receptor can couple via pertussis toxin sensitive and insensitive G proteins by Main, Martin J, Brown, Jason, Brown, Susan, Fraser, Neil J, Foord, Steven M

    Published in FEBS letters (11-12-1998)
    “…Swiss 3T3 cell lines were constructed co-expressing receptor activity modifying protein (RAMP) 1 with the calcitonin receptor-like receptor (CRLR), and showed…”
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    Journal Article
  11. 11

    The amino terminus of receptor activity modifying proteins is a critical determinant of glycosylation state and ligand binding of calcitonin receptor-like receptor by Fraser, N J, Wise, A, Brown, J, McLatchie, L M, Main, M J, Foord, S M

    Published in Molecular pharmacology (01-06-1999)
    “…The calcitonin receptor-like receptor (CRLR) can function as either a receptor for calcitonin gene-related peptide (CGRP) or for adrenomedullin (ADM),…”
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    Journal Article
  12. 12

    Heterodimerization is required for the formation of a functional GABAB receptor by WHITE, J. H, WISE, A, MAIN, M. J, GREEN, A, FRASER, N. J, DISNEY, G. H, BARNES, A. A, EMSON, P, FOORD, S. M, MARSHALL, F. H

    Published in Nature (London) (17-12-1998)
    “…GABA (gamma-aminobutyric acid) is the main inhibitory neurotransmitter in the mammalian central nervous system, where it exerts its effects through ionotropic…”
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    Journal Article
  13. 13

    An industrial perspective on utilizing functional ion channel assays for high throughput screening by Worley, 3rd, Jennings F, Main, Martin J

    Published in Receptors & channels (2002)
    “…The ability to apply large-scale screening formats to measures of ion channel function offers immense opportunities for drug discovery and academic research…”
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    Journal Article
  14. 14

    Heterodimerization is required for the formation of a functional GABA(B) receptor by White, J H, Wise, A, Main, M J, Green, A, Fraser, N J, Disney, G H, Barnes, A A, Emson, P, Foord, S M, Marshall, F H

    Published in Nature (London) (17-12-1998)
    “…GABA (gamma-aminobutyric acid) is the main inhibitory neurotransmitter in the mammalian central nervous system, where it exerts its effects through ionotropic…”
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    Journal Article
  15. 15

    Calcium sensing properties of the GABA(B) receptor by Wise, A, Green, A, Main, M J, Wilson, R, Fraser, N, Marshall, F H

    Published in Neuropharmacology (01-11-1999)
    “…The GABA(B) receptor has been shown to consist of a heterodimer of two related 7-transmembrane receptors GABAB-R1 and GABA(B)-R2. These receptors share close…”
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    Journal Article
  16. 16

    Heterologous expression and functional analysis of rat Na V1.8 (SNS) voltage-gated sodium channels in the dorsal root ganglion neuroblastoma cell line ND7–23 by John, Victoria H., Main, Martin J., Powell, Andrew J., Gladwell, Zoe M., Hick, Caroline, Sidhu, Harjeet S., Clare, Jeff J., Tate, Simon, Trezise, Derek J.

    Published in Neuropharmacology (2004)
    “…The voltage-gated sodium channel Na V1.8 (SNS, PN3) is thought to be a molecular correlate of the dorsal root ganglion (DRG) tetrodotoxin resistant (TTX-R) Na…”
    Get full text
    Journal Article
  17. 17

    Calcium sensing properties of the GABA B receptor by Wise, Alan, Green, Andrew, Main, Martin J, Wilson, Richard, Fraser, Neil, Marshall, Fiona H

    Published in Neuropharmacology (1999)
    “…The GABA B receptor has been shown to consist of a heterodimer of two related 7-transmembrane receptors GABA B-R1 and GABA B-R2. These receptors share close…”
    Get full text
    Journal Article
  18. 18

    Heterodimerization is required for the formation of a functional GABA B receptor by Marshall, Fiona H, White, Julia H, Wise, Alan, Main, Martin J, Green, Andrew, Fraser, Neil J, Disney, Graham H, Barnes, Ashley A, Emson, Piers, Foord, Steven M

    Published in Nature (London) (17-12-1998)
    “…GABA (γ-aminobutyric acid) is the main inhibitory neurotransmitter in the mammalian central nervous system, where it exerts its effects through ionotropic…”
    Get full text
    Journal Article
  19. 19

    Differences in the effects of tachykinin NK1 receptor antagonists: neuronal versus smooth muscle tissues by Seabrook, G R, Main, M J, Razzaque, Z, Longmore, J

    Published in European journal of pharmacology (30-11-1993)
    “…The effects of three tachykinin NK1 receptor antagonists (L-668,169, (+/-)-RP 67580, and (+/-)-CP 96.345) were examined for their ability to antagonise…”
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  20. 20

    Heterodimerization is required for the formation of a functional GABA sub(B) receptor by White, J H, Wise, A, Main, MJ, Green, A, Fraser, N J, Disney, G H, Barnes, A A, Emson, P, Foord, S M, Marshall, F H

    Published in Nature (London) (17-12-1998)
    “…GABA ( gamma -aminobutyric acid) is the main inhibitory neurotransmitter in the mammalian central nervous system, where it exerts its effects through…”
    Get full text
    Journal Article