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pro vyhledávání: '"Xavier, Gerard"'
The aim of this note is to show how the introduction of certain tableaux, called Catalan alternative tableaux, provides a very simple and elegant description of the product in the Hopf algebra of binary trees defined by Loday and Ronco. Moreover, we
Externí odkaz:
http://arxiv.org/abs/0912.0798
Autor:
Viennot, Xavier Gérard
Publikováno v:
FPSAC 2007, Formal Power Series and Algebraic Combinatorics, Tianjiin : Chine (2007)
The purpose of this paper is twofold. First we answer to a question asked by Steingrimsson and Williams about certain permutation tableaux: we construct a bijection between binary trees and the so-called Catalan tableaux. These tableaux are certain F
Externí odkaz:
http://arxiv.org/abs/0905.3081
Autor:
Xavier Gerard, Isabelle Perrault, Sylvain Hanein, Eduardo Silva, Karine Bigot, Sabine Defoort-Delhemmes, Marlèene Rio, Arnold Munnich, Daniel Scherman, Josseline Kaplan, Antoine Kichler, Jean-Michel Rozet
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 1, Iss C (2012)
Leber congenital amaurosis (LCA) is a severe hereditary retinal dystrophy responsible for congenital or early-onset blindness. The most common disease-causing mutation (>10%) is located deep in intron 26 of the CEP290 gene (c.2991+1655A>G). It create
Externí odkaz:
https://doaj.org/article/4c6ac99f7bf04c2eb9a5d0e5fd83e9c1
Autor:
Iris, Barny, Isabelle, Perrault, Marlène, Rio, Hélène, Dollfus, Sabine, Defoort-Dhellemmes, Josseline, Kaplan, Jean-Michel, Rozet, Xavier, Gerard
Publikováno v:
Advances in experimental medicine and biology. 1185
CEP290 mutations cause a spectrum of ciliopathies, including Leber congenital amaurosis. Milder retinal diseases have been ascribed to exclusion of CEP290 mutant exons through basal exon skipping (BES) and/or nonsense-associated altered splicing (NAS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ee46e57f0e83e0682cd45014263f126
https://pubmed.ncbi.nlm.nih.gov/31884610
https://pubmed.ncbi.nlm.nih.gov/31884610
Autor:
Iris, Barny, Isabelle, Perrault, Christel, Michel, Nicolas, Goudin, Sabine, Defoort-Dhellemmes, Imad, Ghazi, Josseline, Kaplan, Jean-Michel, Rozet, Xavier, Gerard
Publikováno v:
Genes
Mutations in CEP290 encoding a centrosomal protein important to cilia formation cause a spectrum of diseases, from isolated retinal dystrophies to multivisceral and sometimes embryo–lethal ciliopathies. In recent years, endogenous and/or selective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a868b258d0af3baea4fd529e6cc7146f
https://pubmed.ncbi.nlm.nih.gov/31091803
https://pubmed.ncbi.nlm.nih.gov/31091803
Autor:
Lech Wojtasik, Krzysztof Cichocki, Jarosław Kołodziej, Błażej Przychocki, Jakub Bednarek, Józef Jasiczak, Rene-Xavier Gerard
Publikováno v:
IOP Conference Series: Materials Science and Engineering. 471:022040
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::517710b0e05ec7cb892ab9fb83a75e51
https://doi.org/10.1088/1757-899x/471/2/022040
https://doi.org/10.1088/1757-899x/471/2/022040
Publikováno v:
Journal of Asset Management. 14:140-161
Alpha modelling typically refers to the selection and weighting of various information sources, which when combined are used by active portfolio managers to forecast security returns. It is traditionally seen as an exogenous input in the construction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e391299a8ee7f456f2a2647379de80b
https://doi.org/10.1057/jam.2013.12
https://doi.org/10.1057/jam.2013.12
Publikováno v:
Venture Capital. 11:87-105
Using a dataset of French IPOs over the period 1996–2000 we provide a test of the certification ability of venture capitalists (VCs). We do this in two ways. First we compare forecast publication between VC- and non-VC-backed IPOs. Secondly, condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb0a2bc2ee59808a6968cf44d3bfe715
https://doi.org/10.1080/13691060802525296
https://doi.org/10.1080/13691060802525296
Publikováno v:
Advances in experimental medicine and biology. 854
Inherited retinal dystrophies (IRDs) are an extremely heterogeneous group of genetic diseases for which currently no effective treatment strategies exist. Over the last decade, significant progress has been made utilizing gene augmentation therapy fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad6a60192ab58223cecb845b598fb74f
https://pubmed.ncbi.nlm.nih.gov/26427454
https://pubmed.ncbi.nlm.nih.gov/26427454