Zobrazeno 1 - 10
of 84
pro vyhledávání: '"R. Chater"'
Publikováno v:
Science & Sports. 33:58-62
Summary Objectives The present study was designed to assess physical activity, sedentary behaviors and dietary habits among adolescents in Morocco and to define the correlates of physical inactivity (PI). Summary of facts and results This school-base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1dfe90d5bcb5c7c80973112d1a1e130
https://doi.org/10.1016/j.scispo.2017.07.012
https://doi.org/10.1016/j.scispo.2017.07.012
Publikováno v:
Journal of Superconductivity and Novel Magnetism. 29:1583-1592
Nanostructured Fe1−x Ni x and Fe1−x−y Ni x Cr y (x = 30, 40; y = 10) powders were obtained by mechanical alloying technique (MA) from elemental powders using a planetary ball mill. The evolution of structure, microstructure and magnetic propert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54100a59b2fca18729df757f0c2d34d3
https://doi.org/10.1007/s10948-016-3433-2
https://doi.org/10.1007/s10948-016-3433-2
Publikováno v:
Materials Characterization. 100:21-30
Nanostructured Fe–20Al–2Cr (wt.%) powders have been prepared using high energy planetary ball-mill. Changes in structural, morphological and magnetic properties of the powders during mechanical alloying (MA) and during subsequent annealing have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b70d090c4f5d481b29967fbe3287d31a
https://doi.org/10.1016/j.matchar.2014.12.010
https://doi.org/10.1016/j.matchar.2014.12.010
Publikováno v:
Journal of Solid State Chemistry. 201:317-323
Nanocrystalline Fe1−x−yNixCry (x=20, y=10% in Wt)) alloy samples were prepared by mechanical alloying process. Fe, Ni and Cr elemental powders have been ball milled in a planetary mill for various periods of time, up to 27 h. XRD analysis allowed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21eb71551933c13a3367fbd3e6a34897
https://doi.org/10.1016/j.jssc.2013.02.028
https://doi.org/10.1016/j.jssc.2013.02.028
Autor:
Cortney R. Kreller, T. J. McDonald, Stuart B. Adler, Ethan J. Crumlin, Eva Mutoro, Sung Jin Ahn, G. J. la O', Yang Shao-Horn, Michael D. Biegalski, Hans M. Christen, Richard R. Chater, John A. Kilner
Publikováno v:
Journal of The Electrochemical Society. 160:F931-F942
This work was supported in part by National Science Foundation Division of Chemical, Bioengineering, Environmental, and Transport Systems (CBET) under award numbers 0829171 and 0844526, the U.S. Department of Energy (SISGR DE-SC0002633) and King Abdu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b07116bf75c73bc0dad42c7b6e8a1f6c
https://doi.org/10.1149/2.021309jes
https://doi.org/10.1149/2.021309jes
Publikováno v:
Sensor Letters. 9:2236-2240
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31b1cf4dfdf091801544790c4ef34c22
https://doi.org/10.1166/sl.2011.1770
https://doi.org/10.1166/sl.2011.1770
Autor:
Anas Drissi, R. Chater, Ahmed Adlouni, Philippe Giral, Eric Bruckert, Jean-Louis Beaudeux, M. John Chapman, Mariame El Messal
Publikováno v:
Clinica Chimica Acta. 366:185-189
Familial hypercholesterolemia (FH) is a common inherited disorder of lipoprotein metabolism, whose origin involves mutations in the gene coding for the low-density lipoprotein receptor protein. Although FH is monogenic, wide variation occurs in the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96ba1d9d1b0637f32f25ff48aeb1b3d6
https://doi.org/10.1016/j.cca.2005.09.027
https://doi.org/10.1016/j.cca.2005.09.027
Autor:
R. Chater, A. Adlouni, Karima Aït Chihab, Josep Ribalta, Joan-Carles Vallvé, Mohammed Loutfi, Catherine Boileau, Faiza Bennis, Luis Masana, Mariame El Messal, Jean-Pierre Rabès, Mathilde Varret, Anass Kettani, A. Hafidi
Publikováno v:
Journal of Human Genetics. 48:199-203
Familial hypercholesterolemia (FH) is a genetic disorder mainly caused by defects in the low-density lipoprotein receptor (LDLR) gene, although it can also be due to alterations in the gene encoding apolipoprotein B (familial defective apoB or FDB) o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9ddd426922f079b3b60650b87fc440
https://doi.org/10.1007/s10038-003-0010-x
https://doi.org/10.1007/s10038-003-0010-x
Autor:
C R, Schlegel, M L, Georgiou, M B, Misterek, S, Stöcker, E R, Chater, C E, Munro, O E, Pardo, M J, Seckl, A P, Costa-Pereira
Publikováno v:
Cell Death & Disease
Death-associated protein kinase (DAPK) 2 is a serine/threonine kinase that belongs to the DAPK family. Although it shows significant structural differences from DAPK1, the founding member of this protein family, DAPK2 is also thought to be a putative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5806807af3295d69ad277f99f19fa79
https://pubmed.ncbi.nlm.nih.gov/25741596
https://pubmed.ncbi.nlm.nih.gov/25741596
Autor:
A. Hafidi, Karima Aït Chihab, A. Adlouni, R. Chater, Mariame El Messal, Anas Kettani, Mohamed Loutfi
Publikováno v:
Acta cardiologica. 61(5)
Familial hypercholesterolaemia (FH) is an autosomal dominant disorder characterized by high levels of low-density lipoprotein cholesterol (LDL-C) as a result of mutations that impair their removal from plasma.The clinical consequence is a high risk o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7343b5d4c70f2c6d90046535bf6dfac
https://pubmed.ncbi.nlm.nih.gov/17117756
https://pubmed.ncbi.nlm.nih.gov/17117756