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Paul Piccinelli

Researcher at National Institute for Medical Research

Publications -  6
Citations -  759

Paul Piccinelli is an academic researcher from National Institute for Medical Research. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 4, co-authored 4 publications receiving 689 citations. Previous affiliations of Paul Piccinelli include Medical Research Council.

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Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution

J. Joshua Smith, +59 more
- 01 Apr 2013 - 
TL;DR: Analyses of the assembly indicate that two whole-genome duplications likely occurred before the divergence of ancestral lamprey and gnathostome lineages, and help define key evolutionary events within vertebrate lineages.
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In Vivo T-Box Transcription Factor Profiling Reveals Joint Regulation of Embryonic Neuromesodermal Bipotency

TL;DR: In vivo genome-wide regulatory inputs of the T-box proteins Brachyury, Eomesodermin, and VegT, which together maintain neuromesodermal stem cells and determine their bipotential fates in frog embryos, are defined to ensure the continuous formation of correctly proportioned neural and mesodermal tissues in vertebrate embryos during axial elongation.
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Ancient Pbx-Hox signatures define hundreds of vertebrate developmental enhancers

TL;DR: This work identifies ancient functional signatures within vertebrate conserved non-coding elements (CNEs) through a combination of phylogenetic footprinting and functional assay, using genomic sequence from the sea lamprey as a reference, and reveals a striking enrichment within vertebrates for conserved binding-site motifs of the Pbx-Hox hetero-dimer.
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Insights into the Global Microbial Community Structure Associated with Iron Oxyhydroxide Minerals Deposited in the Aerobic Biogeosphere

TL;DR: In this paper, the authors focus on the microbial community structure of iron oxyhydroxide minerals that often occur in tight association with microbial life, referred to as Biogenic Iron Oxyhydroxides (BIOS).
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Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation.

TL;DR: In this article , a prospective pilot study including eleven children with profound bilateral hearing loss who underwent cochlear implant surgery was performed with whole exome sequencing (WES) complemented with XONarray to identify copy number variants, using a manually curated gene panel incorporating 179 genes associated with non-syndromic and syndromic SNHL.