Zobrazeno 1 - 10
of 90
pro vyhledávání: '"F. Morle"'
Autor:
A. Pamart, F. Ponchio, V. Abergel, A. Alaoui M'Darhri, M. Corsini, M. Dellepiane, F. Morlet, R. Scopigno, L. De Luca
Publikováno v:
The International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol XLII-2-W9, Pp 573-580 (2019)
Close-Range Photogrammetry (CRP) and Reflectance Transformation Imaging (RTI) are two of the most used image-based techniques when documenting and analyzing Cultural Heritage (CH) objects. Nevertheless, their potential impact in supporting study and
Externí odkaz:
https://doaj.org/article/7a357a28933b47e29ab76de370f40742
Publikováno v:
The International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol XLII-2-W9, Pp 565-571 (2019)
Image based-modeling practices in the field of Cultural Heritage studies are nowadays no longer seen as one-shot applications but as various and complex multimodal scenarios. Current use of SFM and photogrammetric methods implies their extensions to
Externí odkaz:
https://doaj.org/article/06e0263890cb42009e02f72dcbf058f0
Autor:
P. Jarrier, Vladimir Lazar, Ali G. Turhan, Jean-Francois Geay, Hana Raslova, F. Morle, Dorothee Buet, William Vainchenker, Fawzia Louache
Publikováno v:
Leukemia
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (5), pp.917-25. ⟨10.1038/sj.leu.2404600⟩
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (5), pp.917-25. ⟨10.1038/sj.leu.2404600⟩
International audience; The BCR-ABL oncoprotein exhibits deregulated protein tyrosine kinase activity and is implicated in the pathogenesis of Philadelphia chromosome (Ph)-positive human leukemias. Here, we report that ectopic expression of p210(BCR-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefec3cb931e4955b455faaf55534151
https://hal.archives-ouvertes.fr/hal-00176495
https://hal.archives-ouvertes.fr/hal-00176495
Autor:
A. Khelif, Georges Uzan, C. Grenier, Christine Vinciguerra, F. Morle, Claude Negrier, M. Alemany, Marc Dechavanne, D. Gulino
Publikováno v:
British journal of haematology. 95(2)
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder, caused by a quantitative or qualitative defect of the GPIIb-IIIa integrin (alpha IIb beta 3), which functions as the platelet fibrinogen receptor. We report a case of type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48ff0ef34692e6888f2c5ba3ed568d8d
https://pubmed.ncbi.nlm.nih.gov/8904900
https://pubmed.ncbi.nlm.nih.gov/8904900
Akademický článek
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Publikováno v:
Blood. 79(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9222c6edcd722cd47d0904deda3975c7
https://pubmed.ncbi.nlm.nih.gov/1586753
https://pubmed.ncbi.nlm.nih.gov/1586753
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
D, Seigneurin, P, Champelovier, G, Mouchiroud, R, Berthier, D, Leroux, M, Prenant, J, McGregor, J, Starck, F, Morle, C, Micouin
Publikováno v:
Experimental hematology. 15(8)
A cell line (LAMA-84) has been established from the blood of a patient with chronic myeloid leukemia in acute phase. LAMA-84 cells retained the patient's chromosome abnormalities, i.e., triplication of all chromosomes except chromosome 18, the presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::67419ae514c6272c1dde7cffa9e598f9
https://pubmed.ncbi.nlm.nih.gov/3476310
https://pubmed.ncbi.nlm.nih.gov/3476310
Publikováno v:
Human genetics. 62(2)
The organization of the alpha-globin genes was studied by restriction endonuclease mapping, in subjects carrying the alpha variant Hb J Mexico. A subject homozygous for Hb J synthesized both Hb J (about 55%) and Hb A and had two alpha loci per chromo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7ba9028b39b1f8332f316af098339c77
https://pubmed.ncbi.nlm.nih.gov/6298095
https://pubmed.ncbi.nlm.nih.gov/6298095
Publikováno v:
European journal of haematology. 40(4)
G gamma to A gamma globin ratios, haplotypes at the beta globin gene cluster and the C----T substitution at -158 5' to the G gamma globin gene were studied in three Algerian families that include SS or S-beta(0) thal patients. G gamma to A gamma rati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e25a090697d83111265399e1ea53e262
https://pubmed.ncbi.nlm.nih.gov/3366225
https://pubmed.ncbi.nlm.nih.gov/3366225