Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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.

PMID:
12801425
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

PMID:
11917036
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

PMID:
11423617
[PubMed - indexed for MEDLINE]
Free Article
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.

PMID:
11124787
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

PMID:
11093790
[PubMed - indexed for MEDLINE]
Free Article
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
[PubMed - indexed for MEDLINE]
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.

PMID:
10570044
[PubMed - indexed for MEDLINE]
Free Article
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.

PMID:
10482772
[PubMed - indexed for MEDLINE]
Free Article
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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.

PMID:
7600694
[PubMed - indexed for MEDLINE]
Free Article
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
[PubMed - indexed for MEDLINE]
20.

Medium chain acyl-CoA dehydrogenase deficiency.

Touma EH, Charpentier C.

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

PMID:
1739332
[PubMed - indexed for MEDLINE]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk