OpenURL Connection Search

Select item for more details and to access through your institution.

No evidence of somatic FGFR3 mutation in various types of carcinoma.
Published in:
Oncogene, 2001, v. 20, n. 36, p. 5059, doi. 10.1038/sj.onc.1204651
By:
- Karoui, Mehdi;
- Hofmann-Radvanyi, Hélène;
- Zimmermann, Ute;
- Couvelard, Anne;
- Degott, Claude;
- Faridoni-Laurens, Laetitia;
- Ahomadegbe, Jean-Charles;
- Gazzeri, Sylvie;
- Brambilla, Elisabeth;
- Clerici, Thierry;
- Charbonnier, Peggy;
- Tresallet, Christophe;
- Mitry, Emmanuel;
- Penna, Christophe;
- Rougier, Philippe;
- Boileau, Catherine;
- Thiery, Jean-Paul;
- Nordlinger, Bernard;
- Franc, Brigitte;
- Radvanyi, François
Publication type:
Article
MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1.
Published in:
Journal of Neurology, 2013, v. 260, n. 4, p. 998, doi. 10.1007/s00415-012-6740-y
By:
- Huin, Vincent;
- Vasseur, Francis;
- Schraen-Maschke, Susanna;
- Dhaenens, Claire-Marie;
- Devos, Patrick;
- Dupont, Kathy;
- Sergeant, Nicolas;
- Buée, Luc;
- Lacour, Arnaud;
- Hofmann-Radvanyi, Hélène;
- Sablonnière, Bernard
Publication type:
Article
Evaluation of predictive models in daily practice for the identification of patients with Lynch syndrome.
Published in:
International Journal of Cancer, 2012, v. 130, n. 6, p. 1367, doi. 10.1002/ijc.26144
By:
- Tresallet, Christophe;
- Brouquet, Antoine;
- Julié, Catherine;
- Beauchet, Alain;
- Vallot, Céline;
- Ménégaux, Fabrice;
- Mitry, Emmanuel;
- Radvanyi, François;
- Malafosse, Robert;
- Rougier, Philippe;
- Nordlinger, Bernard;
- Laurent-Puig, Pierre;
- Boileau, Catherine;
- Emile, Jean-François;
- Muti, Christine;
- Penna, Christophe;
- Hofmann-Radvanyi, Hélène
Publication type:
Article
Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities.
Published in:
Human Molecular Genetics, 1998, v. 7, n. 8, p. 1285, doi. 10.1093/hmg/7.8.1285
By:
- Lia, Anne‐Sophie;
- Seznec, Hervé;
- Hofmann‐Radvanyi, Hélène;
- Radvanyi, François;
- Duros, Chantal;
- Saquet, Céline;
- Blanche, Martine;
- Junien, Claudine;
- Gourdon, Geneviève
Publication type:
Article
Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele.
Published in:
Human Molecular Genetics, 1993, v. 2, n. 8, p. 1263
By:
- Hofmann-Radvanyi, Hélène;
- Lavedan, Christian;
- Rabès, Jean-Pierre;
- Savoy, Daniel;
- Duros, Chantal;
- Johnson, Keith;
- Junien, Claudine
Publication type:
Article
Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based Approach Versus Molecular Screening.
Published in:
American Journal of Gastroenterology (Springer Nature), 2008, v. 103, n. 11, p. 2825, doi. 10.1111/j.1572-0241.2008.02084.x
By:
- Julié, Catherine;
- Trésallet, Christophe;
- Brouquet, Antoine;
- Vallot, Céline;
- Zimmermann, Ute;
- Mitry, Emmanuel;
- Radvanyi, François;
- Rouleau, Etienne;
- Lidereau, Rosette;
- Coulet, Florence;
- Olschwang, Sylviane;
- Frébourg, Thierry;
- Rougier, Philippe;
- Nordlinger, Bernard;
- Laurent-Puig, Pierre;
- Penna, Christophe;
- Boileau, Catherine;
- Franc, Brigitte;
- Muti, Christine;
- Hofmann-Radvanyi, Hélène
Publication type:
Article

Found: 6

No evidence of somatic FGFR3 mutation in various types of carcinoma.

MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1.

Evaluation of predictive models in daily practice for the identification of patients with Lynch syndrome.

Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities.

Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele.

Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based Approach Versus Molecular Screening.