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A STAT3-decoy oligonucleotide induces cell death in a human colorectal carcinoma cell line by blocking nuclear transfer of STAT3 and STAT3-bound NF-κB.

Souissi I, Najjar I, Ah-Koon L, Schischmanoff PO, Lesage D, Le Coquil S, Roger C, Dusanter-Fourt I, Varin-Blank N, Cao A, Metelev V, Baran-Marszak F, Fagard R.

BMC Cell Biol. 2011 Apr 12;12:14. doi: 10.1186/1471-2121-12-14.


Prognostic impact of microsatellite instability in colorectal cancer patients treated with adjuvant FOLFOX.

Des Guetz G, Lecaille C, Mariani P, Bennamoun M, Uzzan B, Nicolas P, Boisseau A, Sastre X, Cucherousset J, Lagorce C, Schischmanoff PO, Morere JF.

Anticancer Res. 2010 Oct;30(10):4297-301.


STAT1-dependent IgG cell-surface expression in a human B cell line derived from a STAT1-deficient patient.

Najjar I, Deglesne PA, Schischmanoff PO, Fabre EE, Boisson-Dupuis S, Nimmerjahn F, Bornkamm GW, Dusanter-Fourt I, Fagard R.

J Leukoc Biol. 2010 Jun;87(6):1145-52. doi: 10.1189/jlb.1109714. Epub 2010 Mar 3.


Monocyte chemoattractant protein-1 (MCP-1)/CCL2 secreted by hepatic myofibroblasts promotes migration and invasion of human hepatoma cells.

Dagouassat M, Suffee N, Hlawaty H, Haddad O, Charni F, Laguillier C, Vassy R, Martin L, Schischmanoff PO, Gattegno L, Oudar O, Sutton A, Charnaux N.

Int J Cancer. 2010 Mar 1;126(5):1095-108. doi: 10.1002/ijc.24800.


Novel function of STAT1beta in B cells: induction of cell death by a mechanism different from that of STAT1alpha.

Najjar I, Schischmanoff PO, Baran-Marszak F, Deglesne PA, Youlyouz-Marfak I, Pampin M, Feuillard J, Bornkamm GW, Chelbi-Alix MK, Fagard R.

J Leukoc Biol. 2008 Dec;84(6):1604-12. doi: 10.1189/jlb.0508287. Epub 2008 Sep 11.


[Haemolysis and turbidity influence on three analysis methods of quantitative determination of total and conjugated bilirubin on ADVIA 1650].

Gobert De Paepe E, Munteanu G, Schischmanoff PO, Porquet D.

Ann Biol Clin (Paris). 2008 Mar-Apr;66(2):175-82. doi: 10.1684/abc.2008.0198. French.


Liver iron, HFE gene mutations, and hepatocellular carcinoma occurrence in patients with cirrhosis.

Nahon P, Sutton A, Rufat P, Ziol M, Thabut G, Schischmanoff PO, Vidaud D, Charnaux N, Couvert P, Ganne-Carrie N, Trinchet JC, Gattegno L, Beaugrand M.

Gastroenterology. 2008 Jan;134(1):102-10. Epub 2007 Oct 26.


Association between myeloid malignancies and acquired deficit in protein 4.1R: a retrospective analysis of six patients.

Alanio-Bréchot C, Schischmanoff PO, Fénéant-Thibault M, Cynober T, Tchernia G, Delaunay J, Garçon L.

Am J Hematol. 2008 Apr;83(4):275-8.


Progressive pulmonary sarcoidosis is associated with over-expression of TYK2 and p21Waf1/Cip1.

Schischmanoff PO, Naccache JM, Carrere A, Richardson S, Kambouchner M, Raphael M, Valeyre D, Fagard R.

Sarcoidosis Vasc Diffuse Lung Dis. 2006 Jun;23(2):101-7.


Microsatellite instability and sensitivitiy to FOLFOX treatment in metastatic colorectal cancer.

des Guetz G, Mariani P, Cucherousset J, Benamoun M, Lagorce C, Sastre X, Le Toumelin P, Uzzan B, Perret GY, Morere JF, Breau JL, Fagard R, Schischmanoff PO.

Anticancer Res. 2007 Jul-Aug;27(4C):2715-9. Erratum in: Anticancer Res. 2007 Sep-Oct;27(5b):3667.


A novel S115G mutation of CGI-58 in a Turkish patient with Dorfman-Chanarin syndrome.

Ben Selma Z, Yilmaz S, Schischmanoff PO, Blom A, Ozogul C, Laroche L, Caux F.

J Invest Dermatol. 2007 Sep;127(9):2273-6. Epub 2007 May 10. No abstract available.


Incidence of hereditary spherocytosis in a population of jaundiced neonates.

Saada V, Cynober T, Brossard Y, Schischmanoff PO, Sender A, Cohen H, Delaunay J, Tchernia G.

Pediatr Hematol Oncol. 2006 Jul-Aug;23(5):387-97.


Increasing level of CD56+ T-cells in peripheral blood in sarcoidosis.

Naccache JM, Kambouchner M, Schischmanoff PO, Baran-Marszak F, Raphaël M, Fagard R, Valeyre D.

Eur Respir J. 2006 Mar;27(3):654. No abstract available.


[Chemotherapy and MSI status].

des Guetz G, Schischmanoff PO.

Gastroenterol Clin Biol. 2005 Oct;29(10):1040. French. No abstract available.


[Hereditary non polyposis colon cancer: diagnosis and management].

Schischmanoff PO, Lagorce C, Wind P, Benamouzig R.

Gastroenterol Clin Biol. 2005 Oct;29(10):1028-34. Review. French. No abstract available.


Different impacts of alleles alphaLEPRA and alphaLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans.

Delaunay J, Nouyrigat V, Proust A, Schischmanoff PO, Cynober T, Yvart J, Gaillard C, Danos O, Tchernia G.

Br J Haematol. 2004 Oct;127(1):118-22.


Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation Ig.

Zdebska E, Bader-Meunier B, Schischmanoff PO, Dupré T, Seta N, Tchernia G, Kościelak J, Delaunay J.

Pediatr Res. 2003 Aug;54(2):224-9. Epub 2003 May 7.


Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.

Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H.

Am J Hum Genet. 2002 Dec;71(6):1467-74. Epub 2002 Nov 14.


A splicing alteration of 4.1R pre-mRNA generates 2 protein isoforms with distinct assembly to spindle poles in mitotic cells.

Delhommeau F, Vasseur-Godbillon C, Leclerc P, Schischmanoff PO, Croisille L, Rince P, Morinière M, Benz EJ Jr, Tchernia G, Tamagnini G, Ribeiro L, Delaunay J, Baklouti F.

Blood. 2002 Oct 1;100(7):2629-36.


Congenital dyserythropoietic anemia, type 1, in a polynesian patient: response to interferon alpha2b.

Roda L, Pasche J, Fournier A, Terorotua V, Wickramasinghe SN, Tamary H, Schischmanoff PO, Tchernia G, Delaunay J.

J Pediatr Hematol Oncol. 2002 Aug-Sep;24(6):503-6.


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