Corinne Kostic Bensadoun

Publications | Phd and Masters theses

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55 publications

2024 | 2023 | 2022 | 2021 | 2020 | 2019 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011 | 2010 | 2009 | 2008 | 2006 | 2005 | 2003 | 2001 | 2000 | 1996 |
2024
Fine-tuning FAM161A gene augmentation therapy to restore retinal function.
Arsenijevic Y., Chang N., Mercey O., El Fersioui Y., Koskiniemi-Kuendig H., Joubert C., Bemelmans A.P., Rivolta C., Banin E., Sharon D. et al., 2024/04. EMBO molecular medicine, 16 (4) pp. 805-822. Peer-reviewed.
[DOI][Pmid][serval:BIB_1D2B15A51CB3]
2023
 
Fine-tuning FAM161A gene augmentation therapy to restore retinal function
Arsenijevic Yvan, Chang Ning, Mercey Olivier, Fersioui Younes El, Koskiniemi-Kuendig Hanna, Joubert Caroline, Bemelmans Alexis-Pierre, Rivolta Carlo, Banin Eyal, Sharon Dror et al., 2023/10/06..
[DOI][serval:BIB_F4BD07C58D84]
 
Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa.
Matsevich C., Gopalakrishnan P., Chang N., Obolensky A., Beryozkin A., Salameh M., Kostic C., Sharon D., Arsenijevic Y., Banin E., 2023/10/04. Molecular therapy, 31 (10) pp. 2948-2961. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_219699766F24]
2022
 
Occipital cortex activity in response to melanopsin in healthy humans
Minier Astrid, Kostic Corinne, Murray Micah, Kawasaki Aki, 2022/12. dans Acta Ophthalmologica. Peer-reviewed.
[DOI][serval:BIB_E108BF14649E]
Lentiviral Vectors for Ocular Gene Therapy.
Arsenijevic Y., Berger A., Udry F., Kostic C., 2022/07/31. Pharmaceutics, 14 (8) p. 1605. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_CB4F66C51B64]
The connecting cilium inner scaffold provides a structural foundation that protects against retinal degeneration.
Mercey O., Kostic C., Bertiaux E., Giroud A., Sadian Y., Gaboriau DCA, Morrison C.G., Chang N., Arsenijevic Y., Guichard P. et al., 2022/06. PLoS biology, 20 (6) pp. e3001649. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_CB6312C7BDA5]
2021
Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy.
Mbefo M., Berger A., Schouwey K., Gérard X., Kostic C., Beryozkin A., Sharon D., Dolfuss H., Munier F., Tran H.V. et al., 2021/08/28. International journal of molecular sciences, 22 (17) p. 9331. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_CD3CAE19D3B7]
Quantification of the early pupillary dilation kinetic to assess rod and cone activity.
Kostic C., Crippa S.V., Leon L., Hamel C., Meunier I., Kawasaki A., 2021/05/05. Scientific reports, 11 (1) p. 9549. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8331002DACE5]
 
A new mouse model for retinal degeneration due to Fam161a deficiency.
Beryozkin A., Matsevich C., Obolensky A., Kostic C., Arsenijevic Y., Wolfrum U., Banin E., Sharon D., 2021/01/21. Scientific reports, 11 (1) p. 2030. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_56AD3917FBE0]
2020
Lentiviral mediated RPE65 gene transfer in healthy hiPSCs-derived retinal pigment epithelial cells markedly increased RPE65 mRNA, but modestly protein level.
Udry F., Decembrini S., Gamm D.M., Déglon N., Kostic C., Arsenijevic Y., 2020/06/01. Scientific reports, 10 (1) p. 8890. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_4962E58BA82D]
 
An in vitro Model of Human Retinal Detachment Reveals Successive Death Pathway Activations.
Potic J., Mbefo M., Berger A., Nicolas M., Wanner D., Kostic C., Matet A., Behar-Cohen F., Moulin A., Arsenijevic Y., 2020. Frontiers in neuroscience, 14 p. 571293. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_BB8A3A871929]
2019
Maturation of the Pupil Light Reflex Occurs Until Adulthood in Mice.
Kircher N., Crippa S.V., Martin C., Kawasaki A., Kostic C., 2019. Frontiers in neurology, 10 p. 56. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8F7689A2DBF9]
2017
Evaluation of tolerance to lentiviral LV-RPE65 gene therapy vector after subretinal delivery in non-human primates.
Matet A., Kostic C., Bemelmans A.P., Moulin A., Rosolen S.G., Martin S., Mavilio F., Amirjanians V., Stieger K., Lorenz B. et al., 2017/10. Translational research, 188 pp. 40-57.e4. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_BA0EF611C7C2]
Rai1 frees mice from the repression of active wake behaviors by light.
Diessler S., Kostic C., Arsenijevic Y., Kawasaki A., Franken P., 2017. eLife, 6 pp. e23292. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_2A7CEC2344D6]
2016
Adamts18 deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development.
Ataca D., Caikovski M., Piersigilli A., Moulin A., Benarafa C., Earp S.E., Guri Y., Kostic C., Arsenivic Y., Soininen R. et al., 2016/11/15. Biology open, 5 (11) pp. 1585-1594. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_BD206DF55CF5]
Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
Dinet V., Ciccotosto G.D., Delaunay K., Borras C., Ranchon-Cole I., Kostic C., Savoldelli M., El Sanharawi M., Jonet L., Pirou C. et al., 2016/06/08. Molecular brain, 9 (1) p. 64. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8DB27D0809EA]
Determination of Rod and Cone Influence to the Early and Late Dynamic of the Pupillary Light Response.
Kostic C., Crippa S.V., Martin C., Kardon R.H., Biel M., Arsenijevic Y., Kawasaki A., 2016/05. Investigative Ophthalmology and Visual Science, 57 (6) pp. 2501-2508. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_A52A9EB92208]
Animal modelling for inherited central vision loss.
Kostic C., Arsenijevic Y., 2016. Journal of Pathology, 238 (2) pp. 300-310. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_55559404111F]
2015
Multigenic lentiviral vectors for combined and tissue-specific expression of miRNA- and protein-based antiangiogenic factors.
Askou A.L., Aagaard L., Kostic C., Arsenijevic Y., Hollensen A.K., Bek T., Jensen T.G., Mikkelsen J.G., Corydon T.J., 2015. Molecular Therapy. Methods and Clinical Development, 2 p. 14064. Peer-reviewed.
[URN][DOI][Pmid][serval:BIB_4CD7D795B26A]
2014
 
Notch signaling in the pigmented epithelium of the anterior eye segment promotes ciliary body development at the expense of iris formation.
Sarode B., Nowell C.S., Ihm J., Kostic C., Arsenijevic Y., Moulin A.P., Schorderet D.F., Beermann F., Radtke F., 2014. Pigment Cell and Melanoma Research, 27 (4) pp. 580-589. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_399E479FDEF0]
2013
Hyperactivation of retina by light in mice leads to photoreceptor cell death mediated by VEGF and retinal pigment epithelium permeability.
Cachafeiro M., Bemelmans A.P., Samardzija M., Afanasieva T., Pournaras J.A., Grimm C., Kostic C., Philippe S., Wenzel A., Arsenijevic Y., 2013. Cell Death and Disease, 4 pp. e781. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_C3B47D2E3C0C]
Rapid cohort generation and analysis of disease spectrum of large animal model of cone dystrophy.
Kostic C., Lillico S.G., Crippa S.V., Grandchamp N., Pilet H., Philippe S., Lu Z., King T.J., Mallet J., Sarkis C. et al., 2013. Plos One, 8 (8) pp. e71363. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_A9CD5A3261C0]
2012
 
Analysis of photoreceptor abnormality in GUCY2D E837D/R838S transgenic pigs
Kostic C., King T., Crippa S., Philippe S., Lillico S., Sarkis C., Mallet J., Arsenijevic Y., Whitelaw B., 2012., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 6462/A388. Peer-reviewed.
[serval:BIB_726D7A980A1B]
 
FAM161A, associated with autosomal recessive retinitis pigmentosa,localizes at the level of the photoreceptor cilium and interacts with proteins involved in ciliopathies
Di Gioia S.A., Kostic C., Letteboer S.J.F., Hetterschijt L., Arsenijevic Y., Roepman R., Rivolta C., 2012., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 1732. Peer-reviewed.
[serval:BIB_8C0C3B682635]
FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies.
Di Gioia S.A., Letteboer S.J., Kostic C., Bandah-Rozenfeld D., Hetterschijt L., Sharon D., Arsenijevic Y., Roepman R., Rivolta C., 2012. Human Molecular Genetics, 21 (23) pp. 5174-5184. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8220F56B55C8]
 
Lentiviral-directed transgenesis in swine is an efficient tool to study human dominant genetic diseases
Kostic C., Grandchamp N., King T., Crippa S., Philippe S., Lillico S., Sarkis C., Mallet J., Arsenijevic Y., Whitelaw B., 2012. pp. A147 dans Collaborative Congress of the European Society of Gene and Cell Therapy/French Society of Cell and Gene Therapy, Human Gene Therapy.
[WoS][serval:BIB_45FEC99682C9]
 
Reduction of choroidal neovascularization in mice by adeno-associated virus-delivered anti-vascular endothelial growth factor short hairpin RNA.
Askou A.L., Pournaras J.A., Pihlmann M., Svalgaard J.D., Arsenijevic Y., Kostic C., Bek T., Dagnaes-Hansen F., Mikkelsen J.G., Jensen T.G. et al., 2012. Journal of Gene Medicine, 14 (11) pp. 632-641. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_D55541D29D4B]
 
Use of a short hPDE6b promoter for rod gene transfer in a model of severe retinal cystrophy, the Rd10 mouse
Arsenijevic Y., Kostic C., Auricchio A., Ihm J., 2012., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 1925/D742. Peer-reviewed.
[serval:BIB_5F067CFCB6D4]
2011
Gene therapy regenerates protein expression in cone photoreceptors in Rpe65(R91W/R91W) mice.
Kostic C., Crippa S.V., Pignat V., Bemelmans A.P., Samardzija M., Grimm C., Wenzel A., Arsenijevic Y., 2011. Plos One, 6 (2) pp. e16588. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_B59505CFD57B]
 
Mice Transgenic For Human Dominant Mutations Of The GUCY2D Gene
Kostic C., Pignat V., Whitelaw B., Pilet H., Ursulet S., Dussaud S., Arsenijevic Y., Sarkis C., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 4343/D1087. Peer-reviewed.
[serval:BIB_36A00276F224]
 
Pigs Transgenic For Human Dominant Mutations Of The GUCY2D Gene
Arsenijevic Y., King T., Crippa S.V., Lillico S., Sarkis C., Mallet J., Kostic C., Whitelaw B., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 4340/D1084. Peer-reviewed.
[serval:BIB_A57907D11DCA]
 
Reduced choroidal neovascularization by AAV-anti-VEGF shRNA delivery
Askou A. L., Pihlmann M., Pournaras J. C., Arsenijevic Y., Kostic C., Bek T., Dagnaes-Hansen F., Mikkelsen J. G., Jensen T. G., Corydon T. J., 2011. pp. A75 dans European Society of Gene and Cell Therapy British Society for Gene Therapy Collaborative Congress 2011, Human gene therapy. Peer-reviewed.
[WoS][serval:BIB_B60DF1C9B82D]
Retinal degeneration progression changes lentiviral vector cell targeting in the retina.
Calame M., Cachafeiro M., Philippe S., Schouwey K., Tekaya M., Wanner D., Sarkis C., Kostic C., Arsenijevic Y., 2011. Plos One, 6 (8) pp. e23782.
[URN][DOI][WoS][Pmid][serval:BIB_750EC38D5FB4]
 
Use of human MAR elements to improve retroviral vector production.
Buceta M., Galbete J.L., Kostic C., Arsenijevic Y., Mermod N., 2011. Gene Therapy, 18 (1) pp. 7-13. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_970D20965719]
2010
 
Lentiviral Vector Tropism In Degenerating Retinas
Calame M., Tekaya M., Maillard A., Cachafeiro M., Philippe S., Sarkis C., Mallet J., Kostic C., Arsenijevic Y., 2010., ARVO E-Abstract 4502/A474 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
[serval:BIB_42178D68503E]
Remaining rod activity mediates visual behavior in adult Rpe65-/- mice.
Cachafeiro M., Bemelmans A.P., Canola K., Pignat V., Crippa S.V., Kostic C., Arsenijevic Y., 2010. Investigative Ophthalmology and Visual Science, 51 (12) pp. 6835-6842. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_DE0563D3C273]
 
Rpe65-Gene Transfer Using an Integration-Deficient Lentiviral Vector
Kostic C., Philippe S., Crippa S., Samardzija M., Pignat V., Wanner D., Grimm C., Sarkis C., Mallet J., Arsenijevic Y., 2010., ARVO E-Abstract 4498/A470 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
[serval:BIB_EA2084982B75]
2009
 
Comparison of visual preservation after transplantation of BDNF or GDNF secreting mesenchymal stem cells in glaucomatous rat eyes
Harper M.M., Sakaguchi D.S., Kuehn M.H., Kwon Y.H., Kardon R.H., Bemelmans A., Kostic C., Arsenijevic Y., Grozdanic S.C., 2009., ARVO E-Abstract 2754 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
[serval:BIB_3C7BECCBE71D]
In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death.
Samardzija M., Tanimoto N., Kostic C., Beck S., Oberhauser V., Joly S., Thiersch M., Fahl E., Arsenijevic Y., von Lintig J. et al., 2009. Human molecular genetics, 18 (7) pp. 1266-75. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_FFCE10CC2F55]
 
Increased therapeutic window for the R91W mutant form of Rpe65 compared to Rpe65 null backgroud
Kostic C., Bemelmans A.P., Crippa S., Samardzija M., Pignat V., Tekaya M., Wanner D., Wenzel A., Arsenijevic Y., 2009., ARVO E-Abstract 1743 dans Investigative ophthalmology and visual science. Peer-reviewed.
[serval:BIB_6D632DC82D99]
 
Non integrative lentiviral vactors for gene transfer in the retina
Philippe S., Arsenijevic Y., Kostic C., Serguera C., Mallet J., Sarkis C., 2009., ARVO E-Abstract 3024 dans Investigative ophthalmology and visual science. Peer-reviewed.
[serval:BIB_953FD56B6752]
 
Novel relationship between Vegf expression and retinal pigmented epithelium permeability following light damage in the mouse retina
Cachafeiro M., Bemelmans A.P., Kostic C., Samardzija M., Tekaya M., Wanner D., Wenzel A., Arsenijevic Y., 2009., ARVO E-Abstract 3524 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
[serval:BIB_2B2B0967F09C]
Ophtalmologie. Thérapie génique des rétinopathies héréditaires: premiers résultats [Gene therapy for hereditary eye diseases: where are we?]
Viet Tran H., Schorderet D.F., Kostic C., Munier F.L., Arsenijevic Y., 2009. Revue Médicale Suisse, 5 (186) pp. 118-123.
[URN][Pmid][serval:BIB_12D02EB80388]
2008
 
Lentiviral gene transfer-mediated cone vision restoration in RPE65 knockout mice.
Bemelmans A.P., Kostic C., Cachafeiro M., Crippa S.V., Wanner D., Tekaya M., Wenzel A., Arsenijevic Y., 2008. Advances In Experimental Medicine and Biology, 613 pp. 89-95. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_3AFF440BCB72]
When green algae give light to blind mice
Arsenijevic Y., Kostic C., 2008. p. 55 dans Abstract, Cellscience. Peer-reviewed.
[URN][serval:BIB_49EBD3CB108E]
2006
 
High yield of cells committed to the photoreceptor fate from expanded mouse retinal stem cells
Merhi-Soussi F., Angenieux B., Canola K., Kostic C., Tekaya M., Hornfeld D., Arsenijevic Y., 2006/09. Stem Cells, 24 (9) pp. 2060-70.
[DOI][WoS][Pmid][serval:BIB_EA56EB4EF5B1]
Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosis.
Bemelmans A.P., Kostic C., Crippa S.V., Hauswirth W.W., Lem J., Munier F.L., Seeliger M.W., Wenzel A., Arsenijevic Y., 2006. PLoS Medicine, 3 (10) pp. e347. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_B54F8E1C9922]
2005
Bmi1 loss produces an increase in astroglial cells and a decrease in neural stem cell population and proliferation
Zencak D., Lingbeek M., Kostic C., Tekaya M., Tanger E., Hornfeld D., Jaquet M., Munier F. L., Schorderet D. F., van Lohuizen M. et al., 2005/06. Journal of Neuroscience, 25 (24) pp. 5774-83.
[URN][DOI][WoS][Pmid][serval:BIB_2007EBF82C8C]
 
Lentiviral vector-mediated gene transfer in adult mouse photoreceptors is impaired by the presence of a physical barrier.
Grüter O., Kostic C., Crippa S.V., Perez M.T., Zografos L., Schorderet D.F., Munier F.L., Arsenijevic Y., 2005. Gene therapy, 12 (11) pp. 942-947. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_FBF2D4888723]
2003
 
Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retina.
Kostic C., Chiodini F., Salmon P., Wiznerowicz M., Deglon N., Hornfeld D., Trono D., Aebischer P., Schorderet D.F., Munier F.L. et al., 2003. Gene Therapy, 10 (9) pp. 818-821.
[DOI][WoS][Pmid][serval:BIB_09B86DC7497E]
 
Delivery of ciliary neurotrophic factor via lentiviral-mediated transfer protects axotomized retinal ganglion cells for an extended period of time.
van Adel B.A., Kostic C., Déglon N., Ball A.K., Arsenijevic Y., 2003. Human Gene Therapy, 14 (2) pp. 103-115.
[DOI][WoS][Pmid][serval:BIB_BFDF3CF1FEB8]
 
Non-neural regions of the adult human eye: a potential source of neurons?
Arsenijevic Y., Taverney N., Kostic C., Tekaya M., Riva F., Zografos L., Schorderet D., Munier F., 2003. Investigative Ophthalmology and Visual Science, 44 (2) pp. 799-807. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_28652]
2001
 
Isolation of multipotent neural precursors residing in the cortex of the adult human brain
Arsenijevic Y., Villemure J. G., Brunet J. F., Bloch J. J., Deglon N., Kostic C., Zurn A., Aebischer P., 2001/07. Experimental Neurology, 170 (1) pp. 48-62. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_A5313C94B214]
2000
 
Isolation and characterization of sixteen novel p53 response genes
Kostic C., Shaw P. H., 2000. Oncogene, 19 (35) pp. 3978-3987.
[DOI][WoS][Pmid][serval:BIB_FE15879F82D0]
1996
Hunchback-independent silencing of late Ubx enhancers by a Polycomb Group Response Element.
Poux S., Kostic C., Pirrotta V., 1996. Embo Journal, 15 (17) pp. 4713-4722. Peer-reviewed.
[Pmid][serval:BIB_DDEC1BD92884]
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