Uirá Souto Melo

5PUBLICATIONS
32CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Rehabilitation engineeringTissue engineeringGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseases
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Publications (5)

|Apr 20, 2024
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.

Manon Baudic, Hiroshige Murata, Fernanda M Bosada

|Oct 09, 2023
Author Correction: Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation.

Uirá Souto Melo, Jerome Jatzlau, Cesar A Prada-Medina

|Apr 11, 2023
Enhancer hijacking at the ARHGAP36 locus is associated with connective tissue to bone transformation.

Uirá Souto Melo, Jerome Jatzlau, Cesar A Prada-Medina

|Jan 09, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay.

Uirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd

|Sep 11, 2018
Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations.

U S Melo, F Freua, D S Lynch

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