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Search Results - Florence Ribierre
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Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells
by
de Dieuleveult, Maud
,
Yen, Kuangyu
,
Hmitou, Isabelle
,
Depaux, Arnaud
,
Boussouar, Fayçal
,
Bou Dargham, Daria
,
Jounier, Sylvie
,
Humbertclaude, Hélène
,
Ribierre, Florence
,
Baulard, Céline
,
Farrell, Nina P
,
Park, Bongsoo
,
Keime, Céline
,
Carrière, Lucie
,
Berlivet, Soizick
,
Gut, Marta
,
Gut, Ivo
,
Werner, Michel
,
Deleuze, Jean-François
,
Olaso, Robert
,
Aude, Jean-Christophe
,
Chantalat, Sophie
,
Pugh, B Franklin
,
Gérard, Matthieu
Published in
Nature (London)
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Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans
by
Radner, Franz P W
,
Marrakchi, Slaheddine
,
Kirchmeier, Peter
,
Kim, Gwang-Jin
,
Ribierre, Florence
,
Kamoun, Bourane
,
Abid, Leila
,
Leipoldt, Michael
,
Turki, Hamida
,
Schempp, Werner
,
Heilig, Roland
,
Lathrop, Mark
,
Fischer, Judith
Published in
PLoS genetics
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Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans
by
Radner, Franz P. W.
,
Marrakchi, Slaheddine
,
Kirchmeier, Peter
,
Kim, Gwang-Jin
,
Ribierre, Florence
,
Kamoun, Bourane
,
Abid, Leila
,
Leipoldt, Michael
,
Turki, Hamida
,
Schempp, Werner
,
Heilig, Roland
,
Lathrop, Mark
,
Fischer, Judith
Published in
PLoS genetics
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Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state
by
Velasco, Guillaume
,
Grillo, Giacomo
,
Touleimat, Nizar
,
Ferry, Laure
,
Ivkovic, Ivana
,
Ribierre, Florence
,
Deleuze, Jean-François
,
Chantalat, Sophie
,
Picard, Capucine
,
Francastel, Claire
Published in
Human molecular genetics
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Correction: Mutations in Cause Autosomal Recessive Congenital Ichthyosis in Humans
by
Franz P. W. Radner
,
Slaheddine Marrakchi
,
Peter Kirchmeier
,
Gwang-Jin Kim
,
Florence Ribierre
,
Bourane Kamoun
,
Leila Abid
,
Michael Leipoldt
,
Hamida Turki
,
Werner Schempp
,
Roland Heilig
,
Mark Lathrop
,
Judith Fischer
Published in
PLoS genetics
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Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans: e1003536
by
Radner, Franz PW
,
Marrakchi, Slaheddine
,
Kirchmeier, Peter
,
Kim, Gwang-Jin
,
Ribierre, Florence
,
Kamoun, Bourane
,
Abid, Leila
,
Leipoldt, Michael
,
Turki, Hamida
,
Schempp, Werner
,
Heilig, Roland
,
Lathrop, Mark
,
Fischer, Judith
Published in
PLoS genetics
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Vacuoliting Megalencephalic Leukoencephalopathy with Subcortical Cysts, Mapped to Chromosome 22q tel
by
Topçu, Meral
,
Gartioux, Corine
,
Ribierre, Florence
,
Yalçinkaya, Cengiz
,
Tokus, Erem
,
Öztekin, Nese
,
Beckmann, Jacques S.
,
Ozguc, Meral
,
Seboun, Eric
Published in
American journal of human genetics
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A Causative Relationship between Mutant IFNgR1 Alleles and Impaired Cellular Response to IFNγ in a Compound Heterozygous Child
by
Altare, Frédéric
,
Jouanguy, Emmanuelle
,
Lamhamedi-Cherradi, Salma
,
Fondanèche, Marie-Claude
,
Fizame, Cécile
,
Ribiérre, Florence
,
Merlin, Gilles
,
Dembic, Zlatko
,
Schreiber, Robert
,
Lisowska-Grospierre, Barbara
,
Fischer, Alain
,
Seboun, Eric
,
Casanova, Jean-Laurent
Published in
American journal of human genetics
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Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtel
by
TOPCU, M
,
GARTIOUX, C
,
RIBIERRE, F
,
YALCINKAYA, C
,
TOKUS, E
,
ÖZTEKIN, N
,
BECKMANN, J. S
,
OZGUC, M
,
SEBOUN, E
Published in
American journal of human genetics
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