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Items where Author is "Arsenijevic, Yvan"

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Jump to: 2016 | 2015 | 2012 | 2010
Number of items: 4.

2016

Nikopoulos, Konstantinos and Farinelli, Pietro and Giangreco, Basilio and Tsika, Chrysanthi and Royer-Bertrand, Beryl and Mbefo, Martial K. and Bedoni, Nicola and Kjellström, Ulrika and El Zaoui, Ikram and Di Gioia, Silvio Alessandro and Balzano, Sara and Cisarova, Katarina and Messina, Andrea and Decembrini, Sarah and Plainis, Sotiris and Blazaki, Styliani V. and Khan, Muhammad Imran and Micheal, Shazia and Boldt, Karsten and Ueffing, Marius and Moulin, Alexandre P. and Cremers, Frans P. M. and Roepman, Ronald and Arsenijevic, Yvan and Tsilimbaris, Miltiadis K. and Andréasson, Sten and Rivolta, Carlo. (2016) Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects. American Journal of Human Genetics, 99 (3). pp. 770-776.

2015

Di Gioia, Silvio Alessandro and Farinelli, Pietro and Letteboer, Stef J. F. and Arsenijevic, Yvan and Sharon, Dror and Roepman, Ronald and Rivolta, Carlo. (2015) Interactome analysis reveals that FAM161A, deficient in recessive retinitis pigmentosa, is a component of the Golgi-centrosomal network. Human Molecular Genetics, 24 (12). pp. 3359-3371.

2012

Di Gioia, Silvio Alessandro and Letteboer, Stef J. F. and Kostic, Corinne and Bandah-Rozenfeld, Dikla and Hetterschijt, Lisette and Sharon, Dror and Arsenijevic, Yvan and Roepman, Ronald and Rivolta, Carlo. (2012) FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies. Human Molecular Genetics, 21 (23). pp. 5174-5184.

2010

Langmann, Thomas and Di Gioia, Silvio Alessandro and Rau, Isabella and Stöhr, Heidi and Maksimovic, Nela S. and Corbo, Joseph C. and Renner, Agnes B. and Zrenner, Eberhart and Kumaramanickavel, Govindasamy and Karlstetter, Marcus and Arsenijevic, Yvan and Weber, Bernhard H. F. and Gal, Andreas and Rivolta, Carlo. (2010) Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa. American Journal of Human Genetics, 87 (3). pp. 376-381.

This list was generated on Tue Nov 30 10:14:58 2021 CET.