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Items: 1 to 20 of 21

1.

Calpain-mediated cleavage of collapsin response mediator protein(CRMP)-2 during neurite degeneration in mice.

Touma E, Kato S, Fukui K, Koike T.

Eur J Neurosci. 2007 Dec;26(12):3368-81. Epub 2007 Dec 4.

PMID:
18052987
2.

TP508 accelerates fracture repair by promoting cell growth over cell death.

Li X, Wang H, Touma E, Qi Y, Rousseau E, Quigg RJ, Ryaby JT.

Biochem Biophys Res Commun. 2007 Dec 7;364(1):187-93. Epub 2007 Aug 22.

PMID:
17942078
3.

Genetic network and pathway analysis of differentially expressed proteins during critical cellular events in fracture repair.

Li X, Wang H, Touma E, Rousseau E, Quigg RJ, Ryaby JT.

J Cell Biochem. 2007 Feb 1;100(2):527-43.

PMID:
16960878
4.

Molecular characterization of G6PD deficiency in Cyprus.

Drousiotou A, Touma EH, Andreou N, Loiselet J, Angastiniotis M, Verrelli BC, Tishkoff SA.

Blood Cells Mol Dis. 2004 Jul-Aug;33(1):25-30.

PMID:
15223006
5.

Mitochondrial acetoacetyl-CoA thiolase (T2) deficiency: T2-deficient patients with "mild" mutation(s) were previously misinterpreted as normal by the coupled assay with tiglyl-CoA.

Zhang GX, Fukao T, Rolland MO, Zabot MT, Renom G, Touma E, Kondo M, Matsuo N, Kondo N.

Pediatr Res. 2004 Jul;56(1):60-4. Epub 2004 May 5.

PMID:
15128923
6.

Oligodeoxyribonucleotide probe accessibility on a three-dimensional DNA microarray surface and the effect of hybridization time on the accuracy of expression ratios.

Dorris DR, Nguyen A, Gieser L, Lockner R, Lublinsky A, Patterson M, Touma E, Sendera TJ, Elghanian R, Mazumder A.

BMC Biotechnol. 2003 Jun 11;3:6. Epub 2003 Jun 11.

7.

An assessment of Motorola CodeLink microarray performance for gene expression profiling applications.

Ramakrishnan R, Dorris D, Lublinsky A, Nguyen A, Domanus M, Prokhorova A, Gieser L, Touma E, Lockner R, Tata M, Zhu X, Patterson M, Shippy R, Sendera TJ, Mazumder A.

Nucleic Acids Res. 2002 Apr 1;30(7):e30.

8.

Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance.

Tishkoff SA, Varkonyi R, Cahinhinan N, Abbes S, Argyropoulos G, Destro-Bisol G, Drousiotou A, Dangerfield B, Lefranc G, Loiselet J, Piro A, Stoneking M, Tagarelli A, Tagarelli G, Touma EH, Williams SM, Clark AG.

Science. 2001 Jul 20;293(5529):455-62. Epub 2001 Jun 21.

9.

A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency.

Touma EH, Rashed MS, Vianey-Saban C, Sakr A, Divry P, Gregersen N, Andresen BS.

Arch Dis Child. 2001 Jan;84(1):58-60.

10.

Competitive antagonism of recombinant P2X(2/3) receptors by 2', 3'-O-(2,4,6-trinitrophenyl) adenosine 5'-triphosphate (TNP-ATP).

Burgard EC, Niforatos W, van Biesen T, Lynch KJ, Kage KL, Touma E, Kowaluk EA, Jarvis MF.

Mol Pharmacol. 2000 Dec;58(6):1502-10.

11.

Unusual presentation of Kearns-Sayre syndrome in early childhood.

Simaan EM, Mikati MA, Touma EH, Rötig A.

Pediatr Neurol. 1999 Nov;21(5):830-1.

PMID:
10593676
12.

Molecular and functional characterization of human P2X(2) receptors.

Lynch KJ, Touma E, Niforatos W, Kage KL, Burgard EC, van Biesen T, Kowaluk EA, Jarvis MF.

Mol Pharmacol. 1999 Dec;56(6):1171-81.

13.

P2X receptor-mediated ionic currents in dorsal root ganglion neurons.

Burgard EC, Niforatos W, van Biesen T, Lynch KJ, Touma E, Metzger RE, Kowaluk EA, Jarvis MF.

J Neurophysiol. 1999 Sep;82(3):1590-8.

14.

Pharmacological characterization of recombinant human and rat P2X receptor subtypes.

Bianchi BR, Lynch KJ, Touma E, Niforatos W, Burgard EC, Alexander KM, Park HS, Yu H, Metzger R, Kowaluk E, Jarvis MF, van Biesen T.

Eur J Pharmacol. 1999 Jul 2;376(1-2):127-38.

PMID:
10440098
15.

Holocarboxylase synthetase deficiency: report of a case with onset in late infancy.

Touma E, Suormala T, Baumgartner ER, Gerbaka B, Ogier de Baulny H, Loiselet J.

J Inherit Metab Dis. 1999 Apr;22(2):115-22.

PMID:
10234606
16.

Gain of function mutation of the alpha7 nicotinic receptor: distinct pharmacology of the human alpha7V274T variant.

Briggs CA, McKenna DG, Monteggia LM, Touma E, Roch JM, Arneric SP, Gopalakrishnan M, Sullivan JP.

Eur J Pharmacol. 1999 Feb 5;366(2-3):301-8.

PMID:
10082212
17.

Stable expression and pharmacological properties of the human alpha 7 nicotinic acetylcholine receptor.

Gopalakrishnan M, Buisson B, Touma E, Giordano T, Campbell JE, Hu IC, Donnelly-Roberts D, Arneric SP, Bertrand D, Sullivan JP.

Eur J Pharmacol. 1995 Aug 15;290(3):237-46.

PMID:
7589218
18.

Positive interference from homocystinuria urine in a spot test for molybdenum cofactor deficiency.

Habbal ZM, Touma EH.

Clin Chem. 1995 Jul;41(7):1056-7. No abstract available.

19.

Cloning and transient expression of genes encoding the human alpha 4 and beta 2 neuronal nicotinic acetylcholine receptor (nAChR) subunits.

Monteggia LM, Gopalakrishnan M, Touma E, Idler KB, Nash N, Arneric SP, Sullivan JP, Giordano T.

Gene. 1995 Apr 3;155(2):189-93.

PMID:
7721089
20.

Medium chain acyl-CoA dehydrogenase deficiency.

Touma EH, Charpentier C.

Arch Dis Child. 1992 Jan;67(1):142-5. Review.

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