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Ivan Conte

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The EMBO Journal|May 2, 2021

The TBC1D31/praja2 complex controls primary ciliogenesis through PKA-directed OFD1 ubiquitylationEmanuela Senatore, Francesco Chiuso, Laura Rinaldi, et al.

The EMBO Journal|July 28, 2020

MiT/TFE factors control ER-phagy via transcriptional regulation of FAM134BLaura Cinque, Chiara De Leonibus, Maria Iavazzo, et al.

Journal of Medical Genetics|August 21, 2020

Pathogenic variants in <i>IMPG1</i> cause autosomal dominant and autosomal recessive retinitis pigmentosaGuillaume Olivier, Marta Corton, Daniela Intartaglia, et al.

American Journal of Human Genetics|December 3, 2013

Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.

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Search research articles

Showing results (51-60 of 54) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 54 results.

The EMBO Journal|May 2, 2021

The TBC1D31/praja2 complex controls primary ciliogenesis through PKA-directed OFD1 ubiquitylationEmanuela Senatore, Francesco Chiuso, Laura Rinaldi, et al.

The EMBO Journal|July 28, 2020

MiT/TFE factors control ER-phagy via transcriptional regulation of FAM134BLaura Cinque, Chiara De Leonibus, Maria Iavazzo, et al.

Journal of Medical Genetics|August 21, 2020

Pathogenic variants in <i>IMPG1</i> cause autosomal dominant and autosomal recessive retinitis pigmentosaGuillaume Olivier, Marta Corton, Daniela Intartaglia, et al.

American Journal of Human Genetics|December 3, 2013

Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.

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