Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Analyse mutationnelle"'
Autor:
Hoffmann, Anais
Les maladies amyloïdes sont des affections sévères caractérisées par la présence de dépôts extracellulaires fibreux susceptibles de toucher un ou plusieurs tissus du corps humain. Au cours de ma thèse, je me suis intéressée au peptide β a
Externí odkaz:
http://www.theses.fr/2015PA066442/document
Autor:
Hoffmann, Anais
Publikováno v:
Biophysics. Université Pierre et Marie Curie-Paris VI, 2015. English. ⟨NNT : 2015PA066442⟩
Amyloid diseases, including Alzheimer's (AD), Parkinson's, Prion diseases and type 2 diabetes mellitus (T2DM), are characterized by the accumulation of insoluble fibrillar aggregates in tissues. These diseases are the result of the aberrant folding o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::85bbecd95c7f5f238df3e4efbc85587c
https://tel.archives-ouvertes.fr/tel-01372204/file/2015PA066442.pdf
https://tel.archives-ouvertes.fr/tel-01372204/file/2015PA066442.pdf
Autor:
Feldhammer, Matthew
L’acétylation des résidus de glucosamine terminaux par la N-acétyltransférase lysosomale (HGSNAT) est une étape essentielle de la dégradation catabolique de l’héparan sulfate. Des défauts dans cette réaction causent une maladie de surcha
Externí odkaz:
http://hdl.handle.net/1866/3729
Autor:
Foo, Eloise, Bullier, Erika, Goussot, Magali, Foucher, Fabrice, Rameau, Catherine, Beveridge, Christine Anne
Publikováno v:
The Plant cell
The Plant cell, American Society of Plant Biologists (ASPB), 2005, 17 (2), pp.464-474. ⟨10.1105/tpc.104.026716⟩
The Plant cell, American Society of Plant Biologists (ASPB), 2005, 17 (2), pp.464-474. ⟨10.1105/tpc.104.026716⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::555e35b98f86bcf8ffb57e62bff3c79d
https://hal.inrae.fr/hal-02682807
https://hal.inrae.fr/hal-02682807
Autor:
Kerkeni E; Research Unit 01/UR/08-14, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia. Electronic address: emnakerkeni@gmail.com., Boubaker S; Research Unit 01/UR/08-14, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia., Sfar S; Research Unit 01/UR/08-14, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia., Bizid M; Research Unit 01/UR/08-14, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of Intensive care and Neonatal Medicine, CHU Fattouma Bourguiba, Monastir, Tunisia., Besbes H; Research Unit 01/UR/08-14, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of Intensive care and Neonatal Medicine, CHU Fattouma Bourguiba, Monastir, Tunisia., Bouaziz S; Research Unit 01/UR/08-14, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia., Ghedira N; Research Unit 01/UR/08-14, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia., Amara A; Laboratory of Human Cytogenetics, Molecular Genetics and Reproductive Biology, Farhat Hached University Hospital, Sousse, Tunisia., Manoubi W; Laboratory of Human Cytogenetics, Molecular Genetics and Reproductive Biology, Farhat Hached University Hospital, Sousse, Tunisia., Gribaa M; Laboratory of Human Cytogenetics, Molecular Genetics and Reproductive Biology, Farhat Hached University Hospital, Sousse, Tunisia., Monastiri K; Research Unit 01/UR/08-14, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia; Department of Intensive care and Neonatal Medicine, CHU Fattouma Bourguiba, Monastir, Tunisia.
Publikováno v:
Pathologie-biologie [Pathol Biol (Paris)] 2015 Jun; Vol. 63 (3), pp. 113-6. Date of Electronic Publication: 2015 Apr 21.
