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The carboxyl-terminal nucleoplasmic region of MAN1 exhibits a DNA binding winged helix domain. [electronic resource] by
- Caputo, Sandrine
- Couprie, Joël
- Duband-Goulet, Isabelle
- Kondé, Emilie
- Lin, Feng
- Braud, Sandrine
- Gondry, Muriel
- Gilquin, Bernard
- Worman, Howard J
- Zinn-Justin, Sophie
Producer: 20060818
In:
The Journal of biological chemistry vol. 281
Availability: No items available.
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9.
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The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophy. [electronic resource] by
- Vadrot, Nathalie
- Duband-Goulet, Isabelle
- Cabet, Eva
- Attanda, Wikayatou
- Barateau, Alice
- Vicart, Patrick
- Gerbal, Fabien
- Briand, Nolwenn
- Vigouroux, Corinne
- Oldenburg, Anja R
- Lund, Eivind G
- Collas, Philippe
- Buendia, Brigitte
Producer: 20160113
In:
Human molecular genetics vol. 24
Availability: No items available.
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10.
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Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins. [electronic resource] by
- Duband-Goulet, Isabelle
- Woerner, Stephanie
- Gasparini, Sylvaine
- Attanda, Wikayatou
- Kondé, Emilie
- Tellier-Lebègue, Carine
- Craescu, Constantin T
- Gombault, Aurélie
- Roussel, Pascal
- Vadrot, Nathalie
- Vicart, Patrick
- Ostlund, Cecilia
- Worman, Howard J
- Zinn-Justin, Sophie
- Buendia, Brigitte
Producer: 20120307
In:
Experimental cell research vol. 317
Availability: No items available.
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The checkpoint Saccharomyces cerevisiae Rad9 protein contains a tandem tudor domain that recognizes DNA. [electronic resource] by
- Lancelot, Nathalie
- Charier, Gaëlle
- Couprie, Joël
- Duband-Goulet, Isabelle
- Alpha-Bazin, Béatrice
- Quémeneur, Eric
- Ma, Emilie
- Marsolier-Kergoat, Marie-Claude
- Ropars, Virginie
- Charbonnier, Jean-Baptiste
- Miron, Simona
- Craescu, Constantin T
- Callebaut, Isabelle
- Gilquin, Bernard
- Zinn-Justin, Sophie
Producer: 20071105
In:
Nucleic acids research vol. 35
Availability: No items available.
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The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease. [electronic resource] by
- Davignon, Laurianne
- Chauveau, Claire
- Julien, Cédric
- Dill, Corinne
- Duband-Goulet, Isabelle
- Cabet, Eva
- Buendia, Brigitte
- Lilienbaum, Alain
- Rendu, John
- Minot, Marie Christine
- Guichet, Agnès
- Allamand, Valérie
- Vadrot, Nathalie
- Fauré, Julien
- Odent, Sylvie
- Lazaro, Leïla
- Leroy, Jean Paul
- Marcorelles, Pascale
- Dubourg, Odile
- Ferreiro, Ana
Producer: 20161213
In:
Human molecular genetics vol. 25
Availability: No items available.
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13.
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ASC-1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of Myopathy. [electronic resource] by
- Villar-Quiles, Rocío N
- Catervi, Fabio
- Cabet, Eva
- Juntas-Morales, Raul
- Genetti, Casie A
- Gidaro, Teresa
- Koparir, Asuman
- Yüksel, Adnan
- Coppens, Sandra
- Deconinck, Nicolas
- Pierce-Hoffman, Emma
- Lornage, Xavière
- Durigneux, Julien
- Laporte, Jocelyn
- Rendu, John
- Romero, Norma B
- Beggs, Alan H
- Servais, Laurent
- Cossée, Mireille
- Olivé, Montse
- Böhm, Johann
- Duband-Goulet, Isabelle
- Ferreiro, Ana
Producer: 20200518
In:
Annals of neurology vol. 87
Availability: No items available.
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The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress. [electronic resource] by
- Verstraeten, Valerie L R M
- Caputo, Sandrine
- van Steensel, Maurice A M
- Duband-Goulet, Isabelle
- Zinn-Justin, Sophie
- Kamps, Miriam
- Kuijpers, Helma J H
- Ostlund, Cecilia
- Worman, Howard J
- Briedé, Jacob J
- Le Dour, Caroline
- Marcelis, Carlo L M
- van Geel, Michel
- Steijlen, Peter M
- van den Wijngaard, Arthur
- Ramaekers, Frans C S
- Broers, Jos L V
Producer: 20090928
In:
Journal of cellular and molecular medicine vol. 13
Availability: No items available.
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