LADEVEZE Véronique

Maître de conférence à l’Université de Poitiers, HDR

SFA, Biochimie Biologie Moléculaire

Publications à partir de 2011

Ladeveze V, Farhat R, El Seedy A and Kitzis A, 2016, Multi-Functional Consequences of a Single Mutation of CFTR of the Importance to Analyze Mutations by Functional Tests Single Cell Biol. 5:2. http://dx.doi.org/10.4172/2168-9431.1000142

El-Seedy A, Pasquet MC , Shafiek H, Morsi T, Kitzis A, Ladevèze V, 2016, Cystic Fibrosis Transmembrane  Conductance Regulator (CFTR) gene mutations in North Egyptian population: implications for the genetic diagnosis in Egypt. Cell. Mol. Biol. 2016, 62 (13): 21-28. ISSN: 1165-158X doi: 10.14715/cmb/2016.62.13.5

Farhat R, Puissesseau G, El-Seedy A, Pasquet M-C, Adolphe C, Corbani S, Megarbane A, Kitzis A, Ladeveze V. 2015. N1303K (c.3909C>G) Mutation and Splicing: Implication of Its c.[744-33GATT(6); 869+11C>T] Complex Allele in CFTR Exon 7 Aberrant Splicing, BioMed Research International, vol. 2015, Article ID 138103, 8 pages, 2015. doi:10.1155/2015/138103.

El-Seedy A, Girodon E, Norez C, Pajaud J, Pasquet M-C, De Becdelievre A, Bienvenu T, Des Georges M, Cabet F, Lalau G, Bieth E, Blayau M, Becq F, Kitzis A, Fanen P, Ladeveze V, 2012. CFTR mutation combinations producing frequent complex alleles with different clinical and functional outcomes. Human Mutation, 33(11):1557-1565. Highlight video Demande du journal Human Mutation (youtube)

Ladeveze V, Chaminade N, Lemeunier F, Periquet G, Aulard S, 2012. General survey of hAT transposon superfamily with highlight on hobo element in Drosophila. Genetica, 140 7-9:375-392.

El-Seedy A, Pasquet M-C, .Bienvenu T, Bieth E, Audrezet M-P, Kitzis A, Ladeveze V, 2013. Consequences of partial duplications of the human CFTR gene on CF diagnosis: mutations or ectopic variations. J. of cystic fibrosis;12(4):407-410.

El-Seedy A, Farhat R, Pasquet M-C, Kitzis A, Ladeveze V, 2014. Minigene analysis of the c.743+40A>G intronic variant in the CFTR gene. Health, 6:1352-1360.

 

Revue à partir de 2011

Sarrouilhe D, Ladeveze V, 2012. When the curtain goes up on spinophilin’s tumor suppressor function. Med Sci (Paris). 2012 Jan;28(1):26-28. doi: 10.1051/medsci/2012281009

Sarrouilhe D, Ladeveze V, 2014. The tumour suppressor function of the scaffolding protein spinophilin. Atlas Genet Cytogent Oncol Haematol. Free online version URL : http://AtlasGeneticsOncology.org/Deep/SpinophilinID20133.html

Communications colloques européens et/ou nationaux

Farhat R, El-Moussaoui K, Pasquet M-C, Adolphe C, Bieth E, Kitzis A, Ladeveze V, 2012. Etude de la mutation c.3903G>T dans la population libanaise et son impact sur l’épissage et la protéine. 13ème colloque des jeunes chercheurs en mucoviscidose, Paris. (*)

El-Seedy A, Pasquet M.C, .Bienvenu T, Bieth E, Audrezet Mp, Kitzis A, Ladeveze V. Consequences of partial duplications of the human CFTR gene on CF diagnosis: mutations or ectopic variations. 35th European Cystic Fibrosis Conference, Dublin. (Irlande). J. of cystic fibrosis, 11 :sup1, S16-WS8.4. (°)

Farhat R, El-Seedy A, El-Moussaoui K, Pasquet M.C, Adolphe C, Sermetgaudelus I, Kitzis A, Ladeveze V. Co-implication of the 5’ and 3’ regions of CFTR exon 10 in its alternative splicing : prediction to pathology. 35th European Cystic Fibrosis Conference, Dublin. (Irlande). J. of cystic fibrosis, 11 :sup1, S16-WS8.3. (°)

Farhat R, Puissesseau G, Pasquet Mc, Adolphe C, Kitzis A, Ladeveze V. Evolution of CFTR exon 10 and duplications in primates. 36th European Cystic Fibrosis Conference, Lisbonne (Portugal). J of Cystic Fibrosis, 12:1, WS21.5 S44.

Farhat R, Puissesseau G, Pasquet Mc, Adolphe C, Megarbane A, Kitzis A, Ladeveze V, 2013. Detection of a novel complex allele c.[869+11C>T;3909C>G] in CFTR gene. 36th European Cystic Fibrosis Society, Lisbonne (Portugal).J of Cystic Fibrosis, 12:1, S50.

El-Seedy A, Pasquet M-C, Shafiek H, El-Komy M, Kitzis A, Ladeveze V. 2013. Cystic Fibrosis in Egypt: New mutational detection of the CFTR gene in patients from Alexandria, Northern Egypt. J of Cystic Fibrosis, 12:1, S53.

Farhat R, El-Seedy A, Sari Aip, Pasquet Mc, C. Adolphe C, Kitzis A, Ladeveze V. 2014. In vivo and in silico analyses of impact of the p.Val322Ala mutation on CFTR protein in a Brittany family. European Human Genetics Conference, Milan

 

 

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