Advanced search

Filter By:

Journal Check one or more journals to show results from those journals only.

Choose more journals

Article type Check one or more article types to show results from those article types only.
Subject Check one or more subjects to show results from those subjects only.
Date Choose a date option to show results from those dates only.

Custom date range

Clear all filters
Sort by:
Showing 1–18 of 18 results
Advanced filters: Author: Guillaume Charron Clear advanced filters

  • Natural populations of Saccharomyces paradoxus in which rapid evolution of chromosome architecture and contact between nascent species drove the formation of a new species through homoploid hybrid speciation.

    • Jean-Baptiste Leducq
    • Lou Nielly-Thibault
    • Christian R. Landry
    Research
    Nature Microbiology
    Volume: 1, P: 1-10

  • Hybridization can contribute to diversity from the genomic to the species level. Here, Eberlein, Hénault et al. investigate genomic, transcriptomic and phenotypic variation among wild lineages of the yeast Saccharomyces paradoxus and suggest that an incipient species has formed by recurrent hybridization.

    • Chris Eberlein
    • Mathieu Hénault
    • Christian R. Landry
    ResearchOpen Access
    Nature Communications
    Volume: 10, P: 1-14

  • Hybridization across species can lead to offspring with reduced fertility. Here, the authors experimentally evolve yeast and show that whole-genome duplication during asexual reproduction can restore fertility in hybrids over a relatively short evolutionary timespan.

    • Guillaume Charron
    • Souhir Marsit
    • Christian R. Landry
    ResearchOpen Access
    Nature Communications
    Volume: 10, P: 1-10

  • Proteomic analysis in dendritic cells identifies three palmitoylation sites within IFITM3, an innate immunity protein involved in inhibition of early replication of several viruses. Palmitoylation of IFITM3 regulates its clustering in membranes and is crucial for inhibition of influenza virus infection.

    • Jacob S Yount
    • Bruno Moltedo
    • Howard C Hang
    Research
    Nature Chemical Biology
    Volume: 6, P: 610-614

  • Biogenesis of small nucleolar RNAs ribonucleoproteins (snoRNPs) requires dedicated assembly machinery. Here, the authors show that a subset of snoRNP assembly factors interacts, genetically or directly, with factors modulating chromatin architecture, suggesting a link between ribosome formation and chromatin functions.

    • Benoît Bragantini
    • Christophe Charron
    • Bruno Charpentier
    ResearchOpen Access
    Nature Communications
    Volume: 12, P: 1-17

  • Here, the authors describe the geographies, hosts, substrates, and phylogenetic relationships for 1,794 Saccharomyces strains. They provide insight into the genetic and phenotypic diversity in the genus, not seen through prior work focused on the model species Saccharomyces cerevisiae.

    • David Peris
    • Emily J. Ubbelohde
    • Chris Todd Hittinger
    ResearchOpen Access
    Nature Communications
    Volume: 14, P: 1-19

  • The use of metal nanostructures for surface colourization has attracted considerable interest following recent developments in plasmonics. Here, Guayet al. use a bottom-up approach where picosecond laser pulses can produce a full palette of non-iridescent colours on silver, gold, copper, and aluminium.

    • Jean-Michel Guay
    • Antonino Calà Lesina
    • Arnaud Weck
    ResearchOpen Access
    Nature Communications
    Volume: 8, P: 1-12

  • The sirtuin family of enzymes are known as NAD-dependent deacetylases, although some of them have very weak deacetylase activity; here human SIRT6, an enzyme important for DNA repair and transcription, is shown to remove long-chain fatty acyl groups from protein lysine residues, and to have a function in promoting tumour necrosis factor alpha secretion.

    • Hong Jiang
    • Saba Khan
    • Hening Lin
    Research
    Nature
    Volume: 496, P: 110-113

  • 1. Name of the Disease (Synonyms):

    Aortic aneurysm, familial thoracic (AAT); aneurysm, thoracic aortic; aortic dissection, familial; thoracic aortic aneurysm and dissection, familial; Alport syndrome, X-linked (ATS); aortic valve disease 1 (AOVD1); bicuspid aortic valve; arterial tortuosity syndrome (ATS); contractural arachnodactyly, congenital, Beals syndrome (CCA); cutis laxa, autosomal dominant 1 (ADCL1); cutis laxa, autosomal recessive, type 1B (ARCL1B); Ehlers–Danlos syndrome, classical type/type I (EDS I); Ehlers–Danlos syndrome, classical type/type II (EDS II); Ehlers–Danlos syndrome, vascular type/type IV (EDS IV); Ehlers–Danlos syndrome, kyphoskoliotic type/type VI (EDS VI); Ehlers–Danlos syndrome, arthrochalasic type/type VIIA (EDS VIIA); familial thoracic aortic aneurysm and aortic dissection; Furlong syndrome (FS); heterotopia, periventricular, Ehlers–Danlos variant (PVNH4); juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome (JPHT); Loeys–Dietz syndrome type 1 (LDS1/AAT5); Loeys–Dietz syndrome type 2, Marfan syndrome type 2 (LDS2/MFS2/AAT3); Loeys–Dietz syndrome type 3, Aneurysm osteoarthritis syndrome (LDS3/AOS); Loeys–Dietz syndrome type 4 (LDS4); Marfan syndrome (MFS); Moyamoya disease 5 (MYMY5); Shprintzen–Goldberg craniosynostosis syndrome (SGS).

    2. OMIM# of the Disease:

    109730, 121050, 123700, 130000, 130010, 130010, 130050, 130060, 132900, 154700, 175050, 182212, 208050, 225400, 300537, 301050, 609192, 610168, 611788, 613780, 613795, 614042, 614437, 614816, 615436.

    3. Name of the Analysed Genes or DNA/Chromosome Segments:

    ACTA2, COL1A1, COL3A1, COL4A5, COL5A1, COL5A2, EFEMP2, ELN, FBN1, FBN2, FLNA, GATA5, MAT2A, MFAP5, MYH11, MYLK, NOTCH1, PLOD1, PRKG1, SKI, SLC2A10, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR2.

    4. OMIM# of the Gene(s):

    102620, 120150, 120180, 120190, 120215, 130160, 134797, 153454, 160745, 164780, 176894, 190181, 190182, 190198, 190220, 190230, 300017, 303630, 600922, 600993, 601103, 601468, 603109, 604633, 606145, 611496, 612570.

    Review of the analytical and clinical validity as well as of the clinical utility of DNA-based testing in diagnostic, predictive and prenatal settings and for risk assessment in relatives.

    • Mine Arslan-Kirchner
    • Eloisa Arbustini
    • Jörg Schmidtke
    Research
    European Journal of Human Genetics
    Volume: 24, P: 146-150