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Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene

El Matri, Leila ; Ambresin, Aude ; Schorderet, Daniel ; Kawasaki, Aki ; Seeliger, Mathias ; Wenzel, Andreas ; Arsenijevic, Yvan ; Borruat, François‐Xavier ; Munier, Francis

In: Graefe's Archive for Clinical and Experimental Ophthalmology, 2006, vol. 244, no. 9, p. 1104-1112

Consortium of Swiss Academic Libraries

Mammalian neural stem-cell renewal : Nature versus nurture

Arsenijevic, Yvan

In: Molecular Neurobiology, 2003, vol. 27, no. 1, p. 73-98

Consortium of Swiss Academic Libraries

Retinal stem cells: promising candidates for retina transplantation

Djojosubroto, Meta ; Arsenijevic, Yvan

In: Cell and Tissue Research, 2008, vol. 331, no. 1, p. 347-357

Consortium of Swiss Academic Libraries

Caveolin-1 opens endothelial cell junctions by targeting catenins

Kronstein, Romy ; Seebach, Jochen ; Großklaus, Sylvia ; Minten, Carsten ; Engelhardt, Britta ; Drab, Marek ; Liebner, Stefan ; Arsenijevic, Yvan ; Taha, Abdallah Abu ; Afanasieva, Tatiana ; Schnittler, Hans-Joachim

In: Cardiovascular Research, 2012, vol. 93, no. 1, p. 130-140

Consortium of Swiss Academic Libraries

FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies

Di Gioia, Silvio Alessandro ; Letteboer, Stef J.F. ; Kostic, Corinne ; Bandah-Rozenfeld, Dikla ; Hetterschijt, Lisette ; Sharon, Dror ; Arsenijevic, Yvan ; Roepman, Ronald ; Rivolta, Carlo

In: Human Molecular Genetics, 2012, vol. 21, no. 23, p. 5174-5184

Consortium of Swiss Academic Libraries

In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death

Samardzija, Marijana ; Tanimoto, Naoyuki ; Kostic, Corinne ; Beck, Susanne ; Oberhauser, Vitus ; Joly, Sandrine ; Thiersch, Markus ; Fahl, Edda ; Arsenijevic, Yvan ; von Lintig, Johannes ; Wenzel, Andreas ; Seeliger, Mathias W. ; Grimm, Christian

In: Human Molecular Genetics, 2009, vol. 18, no. 7, p. 1266-1275

Consortium of Swiss Academic Libraries

Interactome analysis reveals that FAM161A, deficient in recessive retinitis pigmentosa, is a component of the Golgi-centrosomal network

Di Gioia, Silvio Alessandro ; Farinelli, Pietro ; Letteboer, Stef J.F. ; Arsenijevic, Yvan ; Sharon, Dror ; Roepman, Ronald ; Rivolta, Carlo

In: Human Molecular Genetics, 2015, vol. 24, no. 12, p. 3359-3371

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