Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Alexandre Atkinson"'
Autor:
Camille Aucouturier, Nicolas Soirat, Laurent Castéra, Denis Bertrand, Alexandre Atkinson, Thibaut Lavolé, Nicolas Goardon, Céline Quesnelle, Julien Levilly, Sosthène Barbachou, Angelina Legros, Olivier Caron, Louise Crivelli, Philippe Denizeau, Pascaline Berthet, Agathe Ricou, Flavie Boulouard, Dominique Vaur, Sophie Krieger, Raphael Leman
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-13 (2024)
Abstract Background Solving the structure of mRNA transcripts is a major challenge for both research and molecular diagnostic purposes. Current approaches based on short-read RNA sequencing and RT-PCR techniques cannot fully explore the complexity of
Externí odkaz:
https://doaj.org/article/a050435307744b7baf273c3a085e00d7
Autor:
Antoine Gilbert, Mihaela Tudor, Amandine Delaunay, Raphaël Leman, Julien Levilly, Alexandre Atkinson, Laurent Castéra, Anca Dinischiotu, Diana Iulia Savu, Samuel Valable, François Chevalier
Publikováno v:
Biomolecules, Vol 14, Iss 9, p 1071 (2024)
Chondrosarcoma is a rare malignant tumor that forms in bone and cartilage. The primary treatment involves surgical removal of the tumor with a margin of healthy tissue. Especially if complete surgical removal is not possible, radiation therapy and ch
Externí odkaz:
https://doaj.org/article/ea03a70df7ab485dbde011ce8e1c3eff
Autor:
Hager Jaouadi, Valérie Delague, Sonia Abdelhak, Rym Benkhalifa, Ridha Mrad, Lilia Chaker, Lilia Kraoua, Alexandre Atkinson, Nicolas Lévy, Stéphane Zaffran
Publikováno v:
Journal of Human Genetics
Journal of Human Genetics, Nature Publishing Group, 2018, 63, pp.1077--1082. ⟨10.1038/s10038-018-0492-1⟩
Journal of Human Genetics, 2018, 63, pp.1077--1082. ⟨10.1038/s10038-018-0492-1⟩
Journal of Human Genetics, Nature Publishing Group, 2018, 63, pp.1077--1082. ⟨10.1038/s10038-018-0492-1⟩
Journal of Human Genetics, 2018, 63, pp.1077--1082. ⟨10.1038/s10038-018-0492-1⟩
International audience; Pediatric cardiomyopathy is a complex disease with clinical and genetic heterogeneity. Recently, the ALPK3 gene was described as a new hereditary cardiomyopathy gene underlying pediatric cardiomyopathies. Only eight patients c
Autor:
Marc Bartoli, Salam Koussa, Nathalie Bernard-Marissal, Rosette Jabbour, Khalil Rihan, Christel Castro, André Mégarbané, Valérie Delague, Nicolas Lévy, Lara El-Bazzal, Alexandre Atkinson, Jean-Pierre Desvignes, Eliane Chouery-Khoury, Karine Bertaux
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2019, ⟨10.1093/hmg/ddz060⟩
Human Molecular Genetics, Oxford University Press (OUP), 2019, ⟨10.1093/hmg/ddz060⟩
Distal hereditary motor neuropathies (dHMNs) are a heterogeneous group of diseases, resembling Charcot–Marie–Tooth syndromes, but characterized by an exclusive involvement of the motor part of the peripheral nervous system. Here, we describe two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::379ad8ce8f9b1eb0c81979c36fc1c62a
https://hal-amu.archives-ouvertes.fr/hal-02152040/document
https://hal-amu.archives-ouvertes.fr/hal-02152040/document
Autor:
Bertrand Napoleon, Vincent Valantin, Romina Urena-Campos, Philippe Grandval, L. Lecomte, Arnaud Lagarde, Laurence Curel, Raphael Bourdariat, Gianfranco Donatelli, Jean Pascal Buono, B. Pol, Alexandre Atkinson, A. Laquière, Sylviane Olschwang, François Mithieux, T. Helbert
Publikováno v:
World Journal of Gastroenterology
BACKGROUND: DNA mutational analysis of pancreatic cystic fluid (CF) is a useful adjunct to the evaluation of pancreatic cysts. KRAS/GNAS or RAF/PTPRD/CTNNB1/RNF43 mutations are highly specific to precancerous or advanced neoplasia. Several studies re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae7a99c4aee7820c27e37419e20d4ff9
http://hdl.handle.net/11588/885812
http://hdl.handle.net/11588/885812
Autor:
Marc Obeid, Valérie Delague, Anne-Celine Gillart, Lara El-Bazzal, Alexandre Atkinson, André Mégarbané
Publikováno v:
European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2018, 62 (4), pp.259-264. ⟨10.1016/j.ejmg.2018.07.025⟩
European Journal of Medical Genetics, Elsevier, 2018, 62 (4), pp.259-264. ⟨10.1016/j.ejmg.2018.07.025⟩
International audience; We report a consanguineous family where 2 boys presented with developmental delay, hypotonia, microcephaly, seizures, gastro-intestinal abnormalities, osteopenia, and neurological regression. Whole exome sequencing performed i
Autor:
Alexandre Atkinson, Céline Jeziorski, Patricia Bonin, Cécile Militon, Valérie Michotey, Robert Duran, Cristiana Cravo-Laureau, Philippe Cuny
Publikováno v:
Marine Genomics
Marine Genomics, Elsevier, 2016, 29, pp.55-59. 〈10.1016/j.margen.2016.06.006〉
Marine Genomics, Elsevier, 2016, 29, pp.55-59. ⟨10.1016/j.margen.2016.06.006⟩
Marine Genomics, 2016, 29, pp.55-59. ⟨10.1016/j.margen.2016.06.006⟩
Marine Genomics, Elsevier, 2016, 29, pp.55-59. 〈10.1016/j.margen.2016.06.006〉
Marine Genomics, Elsevier, 2016, 29, pp.55-59. ⟨10.1016/j.margen.2016.06.006⟩
Marine Genomics, 2016, 29, pp.55-59. ⟨10.1016/j.margen.2016.06.006⟩
In coastal marine sediment, oxygen fluctuations induced by bioturbating activities are widespread and exert a great influence, not only on the structure and diversity of the microbenthic communities, but also on their activities. Thus, the activity o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e29a0f5768bd70cc3737262d8aef4c1
https://hal.archives-ouvertes.fr/hal-01408732
https://hal.archives-ouvertes.fr/hal-01408732
Autor:
Corinne Bouvier, Alexandre Atkinson, Florence Duffaud, Sylviane Olschwang, Elise Lavit, Anne Brouchet, Jean-Claude Gentet, Sébastien Salas, Arnaud Lagarde, Aurélie Fabre
Publikováno v:
Journal of Clinical Oncology. 36:e24235-e24235
e24235Background: : Conventional osteosarcoma is the most frequent malignant tumor in adolescents. Treatment is based on neoadjuvant chemotherapy, surgery and adjuvant chemotherapy. Histological re...
Publikováno v:
Proteins. 82(10)
Structural and theoretical studies on the geometrical features of a hydrogen-bond network occurring in the binding site of nicotinic acetylcholine receptors (nAChRs) and composed of interconnected WxPD (Trp-x-Pro-Asp) and SWyz (Ser-Trp-yz) sequences
Publikováno v:
Malaria Journal
Malaria Journal, 2012, 11 (1), pp.108. ⟨10.1186/1475-2875-11-108⟩
Malaria Journal, BioMed Central, 2012, 11 (1), pp.108. ⟨10.1186/1475-2875-11-108⟩
Malaria Journal, Vol 11, Iss 1, p 108 (2012)
Malaria Journal, 2012, 11 (1), pp.108. ⟨10.1186/1475-2875-11-108⟩
Malaria Journal, BioMed Central, 2012, 11 (1), pp.108. ⟨10.1186/1475-2875-11-108⟩
Malaria Journal, Vol 11, Iss 1, p 108 (2012)
Background There is accumulating evidence that host heparan sulphate proteoglycans play an important role in the life cycle of Plasmodium through their heparan sulphate chains, suggesting that genetic variations in genes involved in heparan sulphate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc1d6b67ce138668079476727476bdd9
https://www.hal.inserm.fr/inserm-00703058/file/1475-2875-11-108.pdf
https://www.hal.inserm.fr/inserm-00703058/file/1475-2875-11-108.pdf