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J Dopazo

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The Pharmacogenomics Journal|August 3, 2010

Functional analysis of multiple genomic signatures demonstrates that classification algorithms choose phenotype-related genesW Shi, M Bessarabova, D Dosymbekov, et al.

Translational Psychiatry|January 20, 2016

Human DNA methylomes of neurodegenerative diseases show common epigenomic patternsJ V Sanchez-Mut, H Heyn, E Vidal, et al.

The British Journal of Dermatology|January 30, 2019

Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatosesE Chacón-Solano, C León, F Díaz, et al.

Scientific Reports|October 14, 2016

Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis PigmentosaM Corton, A Avila-Fernández, L Campello, et al.

Pageof 8

Search research articles

Showing results (71-80 of 74) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 74 results.

The Pharmacogenomics Journal|August 3, 2010

Functional analysis of multiple genomic signatures demonstrates that classification algorithms choose phenotype-related genesW Shi, M Bessarabova, D Dosymbekov, et al.

Translational Psychiatry|January 20, 2016

Human DNA methylomes of neurodegenerative diseases show common epigenomic patternsJ V Sanchez-Mut, H Heyn, E Vidal, et al.

The British Journal of Dermatology|January 30, 2019

Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatosesE Chacón-Solano, C León, F Díaz, et al.

Scientific Reports|October 14, 2016

Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis PigmentosaM Corton, A Avila-Fernández, L Campello, et al.

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