Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Vladimir T Manchev"'
Autor:
Francesca Basso-Valentina, Alessandro Donada, Vladimir T Manchev, Manuel Lisetto, Nathalie Balayn, Jean Edouard Martin, Delphine Muller, Cecilia Paola Marin Oyarzun, Hélène Duparc, Brahim Arkoun, Alessandro Cumin, Lionel Faivre, Nathalie Droin, Ida Biunno, Alessandro Pecci, Alessandra Balduini, Najet Debili, Iléana Antony-Debré, Caroline Marty, William Vainchenker, Isabelle Plo, Remi Favier, Hana Raslova
Publikováno v:
Haematologica, Vol 108, Iss 8 (2023)
Sustained ANKRD26 expression associated with germline ANKRD26 mutations causes thrombocytopenia 2 (THC2), an inherited platelet disorder associated with a predisposition to leukemia. Some patients also present with erythrocytosis and/or leukocytosis.
Externí odkaz:
https://doaj.org/article/ea73fe6f815643c19db0d298819699a2
Autor:
Francesca Basso-Valentina, Alessandro Donada, Vladimir T Manchev, Manuel Lisetto, Nathalie Balayn, Jean Edouard Martin, Delphine Muller, Cecilia Paola Marin Oyarzun, Hélène Duparc, Brahim Arkoun, Alessandro Cumin, Lionel Faivre, Nathalie Droin, Ida Biunno, Alessandra Balduini, Najet Debili, Iléana Antony-Debré, Caroline Marty, William Vainchenker, Isabelle Plo, Remi Favier, Hana Raslova
Publikováno v:
bioRxiv
Sustained ANKRD26 expression associated with germline ANKRD26 mutations causes Thrombocytopenia 2 (THC2), an inherited platelet disorder associated with leukemia predisposition. Some of those patients present also erythrocytosis and/or leukocytosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0557b431e826cb53002ad45c084f18d6
https://doi.org/10.1101/2022.09.01.506160
https://doi.org/10.1101/2022.09.01.506160
Autor:
Vladimir T, Manchev, Hind, Bouzid, Iléana, Antony-Debré, Betty, Leite, Guillaume, Meurice, Nathalie, Droin, Thomas, Prebet, Régis T, Costello, William, Vainchenker, Isabelle, Plo, M'boyba, Diop, Elizabeth, Macintyre, Vahid, Asnafi, Rémi, Favier, Véronique, Baccini, Hana, Raslova
Publikováno v:
Journal of Cellular and Molecular Medicine
Familial platelet disorder with predisposition to acute myeloid leukaemia (FPD/AML) is characterized by germline RUNX1 mutations, thrombocytopaenia, platelet dysfunction and a risk of developing acute myeloid and in rare cases lymphoid T leukaemia. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::02ab643fb9be85598b797b3931b99d05
https://pubmed.ncbi.nlm.nih.gov/27997762
https://pubmed.ncbi.nlm.nih.gov/27997762
Autor:
Julian M. Ketley, Michael Jones, Jean-Philippe Grossier, Karl G. Wooldridge, Michael V. Tretyakov, Paul A. Barrow, Christopher Bayliss, Vladimir T. Manchev, Fadil A. Bidmos, Rebecca L . Richards, A. A. Anjum
Publikováno v:
Nucleic Acids Research
Phase variation of surface structures occurs in diverse bacterial species due to stochastic, high frequency, reversible mutations. Multiple genes of Campylobacter jejuni are subject to phase variable gene expression due to mutations in polyC/G tracts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b66108f4c290d2d2d2e5930057133336
https://doi.org/10.1093/nar/gks246
https://doi.org/10.1093/nar/gks246
Autor:
Mitchell J. Weiss, Eric Solary, Deborah L. French, Thierry Langlois, Olivia Bawa, Lucie Tosca, Vladimir T. Manchev, Cécile Tomowiak, Gérard Tachdjian, Nathalie Balayn, William Vainchenker, Jason A. Mills, Iléana Antony-Debré, Rémi Favier, Isabelle Plo, Hana Raslova, Najet Debili, Dominique Bluteau, Bruno Leheup, Céline Legrand
Publikováno v:
Blood
Blood, American Society of Hematology, 2015, pp.930-940. ⟨10.1182/blood-2014-06-585513⟩
Blood, American Society of Hematology, 2015, pp.930-940. ⟨10.1182/blood-2014-06-585513⟩
International audience; A half loss of RUNX1 activity leads to defects in primitive erythropoiesis, megakaryopoiesis, and proplatelet formation. • An almost complete loss of RUNX1 activity leads to the amplification of the granulomonocytic compartm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34a1a534960f26b7e44753b88be85847
https://hal.univ-lorraine.fr/hal-01681166
https://hal.univ-lorraine.fr/hal-01681166
Autor:
Morgane Hilpert, Gérard Pierron, François Lanza, Sylvie Souquere, Robert K. Andrews, Siham Boukour, Hana Raslova, Philippe Rameau, Achille Aouba, Jean Phillppe Rosa, Marijke Bryckaert, Najet Debili, Regis Bobe, Ziane Elaib, Vladimir T. Manchev, Eliane Berrou, William Vainchenker, Rémi Favier
Publikováno v:
Blood. 124(16)
Macrothrombocytopenias are the most important subgroup of inherited thrombocytopenias. This subgroup is particularly heterogeneous because the affected genes are involved in various functions such as cell signaling, cytoskeleton organization, and gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09ceaee11c73b90b14fc3b1cb70e89c5
https://pubmed.ncbi.nlm.nih.gov/25323684
https://pubmed.ncbi.nlm.nih.gov/25323684