Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maryam Ghalandary"'
Autor:
Maryam Ghalandary, Yue Li, Thomas Fröhlich, Thomas Magg, Yanshan Liu, Meino Rohlfs, Sebastian Hollizeck, Raffaele Conca, Tobias Schwerd, Holm H. Uhlig, Philip Bufler, Sibylle Koletzko, Aleixo M. Muise, Scott B. Snapper, Fabian Hauck, Christoph Klein, Daniel Kotlarz
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract NOD2 polymorphisms may affect sensing of the bacterial muramyl dipeptide (MDP) and trigger perturbed inflammatory responses. Genetic screening of a patient with immunodeficiency and enteropathy revealed a rare homozygous missense mutation in
Externí odkaz:
https://doaj.org/article/dc2f306c826c406ba1811dcfaa3f2007
Autor:
Maryam Ghalandary, Yuqiao Gao, Diana Amend, Ginte Kutkaite, Binje Vick, Karsten Spiekermann, Maja Rothenberg-Thurley, Klaus H. Metzeler, Anetta Marcinek, Marion Subklewe, Michael P. Menden, Vindi Jurinovic, Ehsan Bahrami, Irmela Jeremias
Publikováno v:
Blood 141, 955-960 (2023)
Autor:
Scott B. Snapper, Veit Hornung, Hans Clevers, Moritz M. Gaidt, Nadine Yazbeck, Fabian Hauck, Rima Hanna-Wakim, Katja Lammens, Philip Bufler, Yue Li, Aleixo M. Muise, Maryam Ghalandary, Birgitta E. Michels, Anna S. Lehle, Henner F. Farin, Raffaele Conca, Thomas Magg, Batia Weiss, Yanshan Liu, Sibylle Koletzko, Atar Lev, Neil Warner, Olaf Groß, Daniel Kotlarz, Amos J. Simon, Christoph Walz, Christoph Klein, Sebastian Hollizeck, Benjamin Marquardt, Raz Somech, Dror S. Shouval, Meino Rohlfs
Publikováno v:
Gastroenterology, 156(1), 275-278. W.B. Saunders Ltd
Gastroenterology, 156(1), 275. W.B. Saunders Ltd
Gastroenterology, 156(1), 275. W.B. Saunders Ltd
Caspase-8 (CASP8) is a protease that initiates apoptosis and regulates inflammation and immune responses. We identified germline mutations in CASP8 in 3 unrelated patients with infant-onset inflammatory bowel disease: 2 patients were homozygous for t
Autor:
Maryam Ghalandary, Yuqiao Gao, Martin Becker, Diana Amend, Klaus H. Metzeler, Maja Rothenberg-Thurley, Irmela Jeremias
Publikováno v:
Blood. 138:377-377
Background: The prognosis of patients with acute myeloid leukemia (AML) remains poor and novel therapeutic options are intensively needed. Targeted therapies specifically address molecules with essential function for AML and deciphering novel essenti
Autor:
Parvin, Rostami, Sahar, Valizadegan, Maryam, Ghalandary, Mana M, Mehrjouy, Giti, Esmail-Nia, Soheila, Khalili, Shahrzad Sadat, Shahmoradi, Hashem, Imanian, Valeh, Hadavi, Siavash, Ghaderi-Sohi, Navid, Almadani, Fariba, Afroozan, Ariana, Kariminejad, Roxana, Kariminejad, Hossein, Najmabadi
Publikováno v:
Archives of Iranian medicine. 18(5)
We have investigated the efficacy of QF-PCR for the prenatal recognition of common aneuploidy and compared our findings with cytogenetic results in our laboratories.A total of 4058 prenatal samples (4031 amniotic fluid and 27 chorionic villous sample
Autor:
Houra, Loghmani Khouzani, Ariana, Kariminejad, Gholamreza, Zamani, Maryam, Ghalandary, Bita, Bozorgmehr, Susan, Amirsalari, Faezeh, Mojahedi, Sayed Hassan, Tonekaboni, Roxana, Kariminejad, Hossein, Najmabadi
Publikováno v:
Archives of Iranian medicine. 17(7)
Intellectual Disabilities (ID), defined as a state of developmental deficit, result in significant limitation of intellect and poor adaptation behavior. A number of genetic factors can result in ID, such as chromosomal abnormalities, copy number vari