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Paper Details

Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator.
Nature
62
2021
300 kilobases upstream, EN1, En1, Long non-coding RNAs, Maenli, Maenli lncRNA, Maenli locus, Mendelian disease, complex limb malformation, congenital limb malformation, dorsal dimelia, double dorsal-limb, engrailed-1 gene, four-exon-long non-coding transcript, human, human chromosome 2, human deletions, limb, limb-specific En1 regulator, lncRNA loci, lncRNA locus, lncRNAs, mesomelic shortening, mice, mouse, patients, syndactyly, ventral nails
Author NameAffiliation
Mathieu QuinodozUniversity of Lausanne
Mathieu QuinodozInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Mathieu QuinodozUniversity of Basel
Daniel R CarvalhoSARAH Network of Rehabilitation Hospitals
Malte SpielmannMax Planck Institute for Molecular Genetics
Malte SpielmannInstitute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Malte SpielmannInstitut fur Humangenetik Lubeck, Universitat zu Lubeck
Carlo RivoltaUniversity of Lausanne
Carlo RivoltaUniversity of Leicester
Carlo RivoltaUniversity of Basel
Carlo RivoltaInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Carlo RivoltaUniversity of Lausanne
Carlo RivoltaInstitute of Molecular and Clinical Ophthalmology Basel (IOB)
Carlo RivoltaUniversity of Basel
Carlo RivoltaUniversity of Leicester
Stefan MundlosMax Planck Institute for Molecular Genetics
Stefan MundlosInstitute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Stefan MundlosBerlin-Brandenburg Center for Regenerative Therapies, Charite-Universitatsmedizin Berlin
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