Riccardo Sangermano

Riccardo Sangermano

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Riccardo Sangermano

Riccardo Sangermano

Publications by authors named "Riccardo Sangermano"

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14Publications

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Lactoferrin and oral pathologies: a therapeutic treatment.

Biochem Cell Biol 2020 Mar 26. Epub 2020 Mar 26.

Universita degli Studi di Roma La Sapienza, 9311, Public Health and Infectious Deseases , P.le Aldo Moro 5 , Roma, Italy , 00185 ;

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http://dx.doi.org/10.1139/bcb-2020-0052DOI Listing
March 2020

In or Out? New Insights on Exon Recognition through Splice-Site Interdependency.

Int J Mol Sci 2020 Mar 26;21(7). Epub 2020 Mar 26.

Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.

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http://dx.doi.org/10.3390/ijms21072300DOI Listing
March 2020

A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families.

Hum Mol Genet 2020 Feb 3. Epub 2020 Feb 3.

Ocular Genomics Institute, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA, 02114, USA.

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http://dx.doi.org/10.1093/hmg/ddaa016DOI Listing
February 2020

Identification and Rescue of Splice Defects Caused by Two Neighboring Deep-Intronic ABCA4 Mutations Underlying Stargardt Disease.

Am J Hum Genet 2018 04 8;102(4):517-527. Epub 2018 Mar 8.

Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, 6525 EN Nijmegen, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.02.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985352PMC
April 2018

midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease.

Genome Res 2018 01 21;28(1):100-110. Epub 2017 Nov 21.

Department of Human Genetics and Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.

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http://dx.doi.org/10.1101/gr.226621.117DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5749174PMC
January 2018

Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease.

Ophthalmology 2016 06 12;123(6):1375-85. Epub 2016 Mar 12.

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Radboud Institute of Molecular Life Sciences, Nijmegen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2016.01.053DOI Listing
June 2016

Autosomal dominant Ménétrier-like disease.

J Pediatr Gastroenterol Nutr 2012 Dec;55(6):717-20

Department of Pediatrics, Federico II University of Naples, Naples, Italy.

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http://dx.doi.org/10.1097/MPG.0b013e3182645c2fDOI Listing
December 2012