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Items: 15

1.

Assigning function to natural allelic variation via dynamic modeling of gene network induction.

Richard M, Chuffart F, Duplus-Bottin H, Pouyet F, Spichty M, Fulcrand E, Entrevan M, Barthelaix A, Springer M, Jost D, Yvert G.

Mol Syst Biol. 2018 Jan 15;14(1):e7803. doi: 10.15252/msb.20177803.

2.

Nutrient shortage triggers the hexosamine biosynthetic pathway via the GCN2-ATF4 signalling pathway.

Chaveroux C, Sarcinelli C, Barbet V, Belfeki S, Barthelaix A, Ferraro-Peyret C, Lebecque S, Renno T, Bruhat A, Fafournoux P, Manié SN.

Sci Rep. 2016 Jun 3;6:27278. doi: 10.1038/srep27278.

3.

Natural sequence variants of yeast environmental sensors confer cell-to-cell expression variability.

Fehrmann S, Bottin-Duplus H, Leonidou A, Mollereau E, Barthelaix A, Wei W, Steinmetz LM, Yvert G.

Mol Syst Biol. 2013 Oct 8;9:695. doi: 10.1038/msb.2013.53.

4.

Diagnostic value of minor salivary glands biopsy for the detection of Lewy pathology.

Folgoas E, Lebouvier T, Leclair-Visonneau L, Cersosimo MG, Barthelaix A, Derkinderen P, Letournel F.

Neurosci Lett. 2013 Sep 13;551:62-4. doi: 10.1016/j.neulet.2013.07.016. Epub 2013 Jul 21.

PMID:
23880024
5.

Axonal regeneration is compromised in NFH-LacZ transgenic mice but not in NFH-GFP mice.

Cassereau J, Nicolas G, Lonchampt P, Pinier M, Barthelaix A, Eyer J, Letournel F.

Neuroscience. 2013 Jan 3;228:101-8. doi: 10.1016/j.neuroscience.2012.10.011. Epub 2012 Oct 16.

PMID:
23079625
6.

[The directory of French biological resources centres/biobanks].

Jadeau F, Barthelaix A, Burgun A, Deleval C, Garcelon N, Gelé P, Libersa C, Savonnet M, Tabone E, Combet C.

Med Sci (Paris). 2011 Oct;27(10):895-7. doi: 10.1051/medsci/20112710019. Epub 2011 Oct 21. French. No abstract available.

7.

[Preanalytical guidelines for clinical proteomics investigation of biological fluids].

Lehmann S, Roche S, Allory Y, Barthelaix A, Beaudeux JL, Berger F, Betsou F, Borg J, Dupuy A, Garin J, Quillard M, Lizard G, Peoc'h K, Riviere M, Ducoroy P.

Ann Biol Clin (Paris). 2009 Nov-Dec;67(6):629-39. doi: 10.1684/abc.2009.0374. French.

8.

A RasGAP SH3 peptide aptamer inhibits RasGAP-Aurora interaction and induces caspase-independent tumor cell death.

Pamonsinlapatham P, Hadj-Slimane R, Raynaud F, Bickle M, Corneloup C, Barthelaix A, Lepelletier Y, Mercier P, Schapira M, Samson J, Mathieu AL, Hugo N, Moncorgé O, Mikaelian I, Dufour S, Garbay C, Colas P.

PLoS One. 2008 Aug 6;3(8):e2902. doi: 10.1371/journal.pone.0002902.

9.

An autopsy case of acute multiple sclerosis (Marburg's type) during pregnancy.

Letournel F, Cassereau J, Scherer-Gagou C, Bernard I, Mercat A, Gray F, Tanguy JY, Richard-Crémieux I, Jeanfaivre T, Barthelaix A, Dubas F.

Clin Neurol Neurosurg. 2008 May;110(5):514-7. doi: 10.1016/j.clineuro.2008.01.011. Epub 2008 Mar 14.

PMID:
18342435
10.

Bioinformatic screening of human ESTs for differentially expressed genes in normal and tumor tissues.

Aouacheria A, Navratil V, Barthelaix A, Mouchiroud D, Gautier C.

BMC Genomics. 2006 Apr 26;7:94.

11.

Neurofilament high molecular weight-green fluorescent protein fusion is normally expressed in neurons and transported in axons: a neuronal marker to investigate the biology of neurofilaments.

Letournel F, Bocquet A, Perrot R, Dechaume A, Guinut F, Eyer J, Barthelaix A.

Neuroscience. 2006;137(1):103-11. Epub 2005 Nov 11.

PMID:
16289584
12.

[Malignant non-Hodgkin lymphoma presenting with Garcin's syndrome].

Letournel F, Lejeune P, Josselin N, Barthelaix A, Dubas F.

Rev Neurol (Paris). 2004 Oct;160(10):952-5. French.

PMID:
15492725
13.

Stable tubule only polypeptides (STOP) proteins co-aggregate with spheroid neurofilaments in amyotrophic lateral sclerosis.

Letournel F, Bocquet A, Dubas F, Barthelaix A, Eyer J.

J Neuropathol Exp Neurol. 2003 Dec;62(12):1211-9.

PMID:
14692697
14.

Two clinicopathological cases of a dominantly inherited, adult onset orthochromatic leucodystrophy.

Letournel F, Etcharry-Bouyx F, Verny C, Barthelaix A, Dubas F.

J Neurol Neurosurg Psychiatry. 2003 May;74(5):671-3.

15.

Central sympathetic dysregulation and immunological abnormalities in a case of progressive facial hemiatrophy (Parry-Romberg disease).

Lonchampt P, Emile J, Pélier-Cady MC, Cadou B, Barthelaix A.

Clin Auton Res. 1995 Sep;5(4):199-204.

PMID:
8520214

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