Zobrazeno 1 - 10
of 668
pro vyhledávání: '"Balabanian A"'
Autor:
Lilian Roland, Chi Huu Nguyen, Katarina Zmajkovicova, Mélanie Khamyath, Maria Kalogeraki, Bérénice Schell, Vanessa Gourhand, Vincent Rondeau, Zeina Abou Nader, Halenya Monticelli, Barbara Maierhofer, Robert Johnson, Arthur Taveras, Marion Espéli, Karl Balabanian
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundWHIM (Warts, Hypogammaglobulinemia, Infections, and Myelokathexis) syndrome is an ultra-rare, combined primary immunodeficiency and chronic neutropenic disorder characterized by a range of clinical presentations, including peripheral neutro
Externí odkaz:
https://doaj.org/article/0dce767235e54235a04e512a4f02e6e0
Autor:
Balabanian, Cinthia1 cinthia.balabanian@gmail.com, Lemos, Viviana1 viviananoemilemos@gmail.com
Publikováno v:
Revista Iberoamericana de Diagncstico y Evaluacicn Psicolcgica. 2024, Vol. 3 Issue 73, p83-92. 10p.
Autor:
David Fandrei, Tony Huynh, Marie Sébert, Lorea Aguinaga, Valeria Bisio, Rathana Kim, Emmanuelle Clappier, Marion Espéli, Karl Balabanian, Hélène Moins-Teisserenc, Antoine Toubert, Nicolas Dulphy, Pierre Fenaux, Lionel Adès, Lin-Pierre Zhao
Publikováno v:
Blood Cancer Journal, Vol 13, Iss 1, Pp 1-5 (2023)
Externí odkaz:
https://doaj.org/article/88c7fccd841544b4a98e51be7f98109a
Publikováno v:
In Current Opinion in Immunology June 2024 88
Autor:
Dyikanov, Daniiar, Zaitsev, Aleksandr, Vasileva, Tatiana, Wang, Iris, Sokolov, Arseniy A., Bolshakov, Evgenii S., Frank, Alena, Turova, Polina, Golubeva, Olga, Gantseva, Anna, Kamysheva, Anna, Shpudeiko, Polina, Krauz, Ilya, Abdou, Mary, Chasse, Madison, Conroy, Tori, Merriam, Nicholas R., Alesse, Julia E., English, Noel, Shpak, Boris, Shchetsova, Anna, Tikhonov, Evgenii, Filatov, Ivan, Radko, Anastasia, Bolshakova, Anastasiia, Kachalova, Anastasia, Lugovykh, Nika, Bulahov, Andrey, Kilina, Anastasiia, Asanbekov, Syimyk, Zheleznyak, Irina, Skoptsov, Pavel, Alekseeva, Evgenia, Johnson, Jennifer M., Curry, Joseph M., Linnenbach, Alban J., South, Andrew P., Yang, EnJun, Morozov, Kirill, Terenteva, Anastasiya, Nigmatullina, Lira, Fastovetz, Dmitry, Bobe, Anatoly, Balabanian, Linda, Nomie, Krystle, Yong, Sheila T., Davitt, Christopher J.H., Ryabykh, Alexander, Kudryashova, Olga, Tazearslan, Cagdas, Bagaev, Alexander, Fowler, Nathan, Luginbuhl, Adam J., Ataullakhanov, Ravshan I., Goldberg, Michael F.
Publikováno v:
In Cancer Cell 13 May 2024 42(5):759-779
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Adrienne Anginot, Julie Nguyen, Zeina Abou Nader, Vincent Rondeau, Amélie Bonaud, Maria Kalogeraki, Antoine Boutin, Julia P. Lemos, Valeria Bisio, Joyce Koenen, Lea Hanna Doumit Sakr, Amandine Picart, Amélie Coudert, Sylvain Provot, Nicolas Dulphy, Michel Aurrand-Lions, Stéphane J. C. Mancini, Gwendal Lazennec, David H. McDermott, Fabien Guidez, Claudine Blin-Wakkach, Philip M. Murphy, Martine Cohen-Solal, Marion Espéli, Matthieu Rouleau, Karl Balabanian
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-20 (2023)
Abstract WHIM Syndrome is a rare immunodeficiency caused by gain-of-function CXCR4 mutations. Here we report a decrease in bone mineral density in 25% of WHIM patients and bone defects leading to osteoporosis in a WHIM mouse model. Imbalanced bone ti
Externí odkaz:
https://doaj.org/article/71e743108c284ff4a7d508b10f487735
Autor:
Maxime Boy, Valeria Bisio, Lin-Pierre Zhao, Fabien Guidez, Bérénice Schell, Emilie Lereclus, Guylaine Henry, Juliette Villemonteix, Fernando Rodrigues-Lima, Katia Gagne, Christelle Retiere, Lise Larcher, Rathana Kim, Emmanuelle Clappier, Marie Sebert, Arsène Mekinian, Olivier Fain, Anne Caignard, Marion Espeli, Karl Balabanian, Antoine Toubert, Pierre Fenaux, Lionel Ades, Nicolas Dulphy
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)
Myelodysplastic syndromes are characterised by clonal haematopoiesis, with the affected cells often harbouring mutations in the TET2 gene, an important regulator of DNA methylation state. Here authors show that the same mutations are also found in NK
Externí odkaz:
https://doaj.org/article/e6f10687f44445c184e49bfa3bcfcf30
Autor:
Pierre-Edouard Debureaux, Nathalie Forgeard, Dikelele Elessa, Stéphanie Harel, Laurent Frenzel, Bruno Royer, Alexis Talbot, Sylvain Choquet, Frederic Davi, Florence Nguyen-Khac, Wendy Cuccuini, Morgane Cheminant, Clotilde Bravetti, Gregory Lazarian, Sophie Kaltenbach, Olivier Hermine, Damien Roos-Weil, Marion Espéli, Karl Balabanian, Bertrand Arnulf
Publikováno v:
Haematologica, Vol 109, Iss 1 (2023)
Externí odkaz:
https://doaj.org/article/ab84babbb7c54bb5a1d146187514f7eb