Schraen-Maschke S - Search Results

1

The novel retinoid 6-[3-(1-adamantyl)-4-hydroxyphenyl]-2-naphtalene carboxylic acid can trigger apoptosis through a mitochondrial pathway independent of the nucleus.

Marchetti P, Zamzami N, Joseph B, Schraen-Maschke S, Méreau-Richard C, Costantini P, Métivier D, Susin SA, Kroemer G, Formstecher P. Marchetti P, et al. Cancer Res. 1999 Dec 15;59(24):6257-66. Cancer Res. 1999. PMID: 10626821

2

The novel retinoid AHPN/CD437 induces a rapid but incomplete apoptotic response in human myeloma cells.

Joseph B, Marchetti P, Lefebvre O, Schraen-Maschke S, Méreau-Richard C, Formstecher P. Joseph B, et al. Biochim Biophys Acta. 2003 Feb 17;1593(2-3):277-82. doi: 10.1016/s0167-4889(02)00399-3. Biochim Biophys Acta. 2003. PMID: 12581872 Free article.

3

Real time RT-PCR shows correlation between retinoid-induced apoptosis and NGF-R mRNA levels.

Vuillaume I, Schraen-Maschke S, Formstecher P, Sablonnière B. Vuillaume I, et al. Biochem Biophys Res Commun. 2001 Dec 7;289(3):647-52. doi: 10.1006/bbrc.2001.6028. Biochem Biophys Res Commun. 2001. PMID: 11726196

4

ETR-3 represses Tau exons 2/3 inclusion, a splicing event abnormally enhanced in myotonic dystrophy type I.

Leroy O, Dhaenens CM, Schraen-Maschke S, Belarbi K, Delacourte A, Andreadis A, Sablonnière B, Buée L, Sergeant N, Caillet-Boudin ML. Leroy O, et al. J Neurosci Res. 2006 Sep;84(4):852-9. doi: 10.1002/jnr.20980. J Neurosci Res. 2006. PMID: 16862542

5

Dysregulation of human brain microtubule-associated tau mRNA maturation in myotonic dystrophy type 1.

Sergeant N, Sablonnière B, Schraen-Maschke S, Ghestem A, Maurage CA, Wattez A, Vermersch P, Delacourte A. Sergeant N, et al. Hum Mol Genet. 2001 Sep 15;10(19):2143-55. doi: 10.1093/hmg/10.19.2143. Hum Mol Genet. 2001. PMID: 11590131

6

Absence of unidentified CAG repeat expansion in patients with Huntington's disease-like phenotype.

Vuillaume I, Meynieu P, Schraen-Maschke S, Destée A, Sablonnière B. Vuillaume I, et al. J Neurol Neurosurg Psychiatry. 2000 May;68(5):672-5. doi: 10.1136/jnnp.68.5.672. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766906 Free PMC article.

7

[Triplet expansion diseases].

Sablonnière B, Vuillaume I, Schraen-Maschke S. Sablonnière B, et al. Ann Biol Clin (Paris). 2000 May-Jun;58(3):356-60. Ann Biol Clin (Paris). 2000. PMID: 10846241 Free article. Review. French. No abstract available.

8

Altered splicing of Tau in DM1 is different from the foetal splicing process.

Ghanem D, Tran H, Dhaenens CM, Schraen-Maschke S, Sablonnière B, Buée L, Sergeant N, Caillet-Boudin ML. Ghanem D, et al. FEBS Lett. 2009 Feb 18;583(4):675-9. doi: 10.1016/j.febslet.2008.12.065. Epub 2009 Jan 21. FEBS Lett. 2009. PMID: 19166838 Free article.

9

The first identified French family with dentatorubral-pallidoluysian atrophy.

Destée A, Delalande I, Vuillaume I, Schraen-Maschke S, Defebvre L, Sablonnière B. Destée A, et al. Mov Disord. 2000 Sep;15(5):996-9. doi: 10.1002/1531-8257(200009)15:5<996::aid-mds1036>3.0.co;2-9. Mov Disord. 2000. PMID: 11009212

10

Clinical features and genetic analysis of a new form of spinocerebellar ataxia.

Devos D, Schraen-Maschke S, Vuillaume I, Dujardin K, Nazé P, Willoteaux C, Destée A, Sablonnière B. Devos D, et al. Neurology. 2001 Jan 23;56(2):234-8. doi: 10.1212/wnl.56.2.234. Neurology. 2001. PMID: 11160961

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