Zobrazeno 1 - 10
of 628
pro vyhledávání: '"W. Wlodarski"'
Autor:
Maria Angeles Lillo Osuna, Lei Han, Jon P. Connelly, Shondra Miller-Preutt, Mitchell J. Weiss, Marcin W. Wlodarski, Senthil Velan Bhoopalan
Publikováno v:
Stem Cell Research, Vol 79, Iss , Pp 103479- (2024)
Diamond-Blackfan anemia syndrome (DBAS) is an inherited bone marrow failure disorder that typically presents in infancy as hypoplastic anemia and developmental abnormalities in approximately 50% of cases. DBAS is caused by haploinsufficiency in one o
Externí odkaz:
https://doaj.org/article/f21789a5250943979693ee10e4025149
Autor:
Majd Khiami, Yan Ju, Lei Han, Jonathan Klein, Min-Joon Han, Shondra M. Pruett-Miller, Marcin W. Wlodarski
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103532- (2024)
Induced pluripotent stem cells (iPSCs) harboring patient derived SAMD9 mutation offer a unique platform to study the multi-organ involvement observed in this rare disease, referred to as myelodysplasia, infections, restriction of growth, adrenal hypo
Externí odkaz:
https://doaj.org/article/0c12dce7c9574b02bd12643e74df49a5
Publikováno v:
Proceedings, Vol 1, Iss 4, p 327 (2017)
Hybrid SnS2-SnO2−x flaked nanostructures were obtained from 2D-SnS2 flakes deposited as a thin sensing film onto a conductometric transducing platform and annealed in air. The formation of 2D-SnS2/SnO2−x mixed phases and the materials morphologie
Externí odkaz:
https://doaj.org/article/5fca674b8c154a56ac7d49e6833a94d7
Autor:
Amr Qudeimat, Shruthi Suryaprakash, Renee Madden, Ashok Srinivasan, Marcin W. Wlodarski, Senthil Velan Bhoopalan
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/2d242d8505ca4e6db42c19c7a2359a2c
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Diamond-Blackfan anemia (DBA) is one of the most common inherited causes of bone marrow failure in children. DBA typically presents with isolated erythroid hypoplasia and anemia in infants. Congenital anomalies are seen in 50% of the patients. Over t
Externí odkaz:
https://doaj.org/article/2a5a14e542f246d5bfe1c691f2f52e1a
Autor:
Miriam Erlacher, Felicia Andresen, Martina Sukova, Jan Stary, Barbara de Moerloose, Jutte van der Werff Ten Bosch, Michael Dworzak, Markus G. Seidel, Sophia Polychronopoulou, Rita Beier, Christian P. Kratz, Michaela Nathrath, Michael C. Frühwald, Gudrun Göhring, Anke K. Bergmann, Christina Mayerhofer, Dirk Lebrecht, Senthilkumar Ramamoorthy, Ayami Yoshimi, Brigitte Strahm, Marcin W. Wlodarski, Charlotte M. Niemeyer
Publikováno v:
Haematologica, Vol 109, Iss 2 (2023)
Monosomy 7 is the most common cytogenetic abnormality in pediatric myelodysplastic syndrome (MDS) and associated with a high risk of disease progression. However, in young children, spontaneous loss of monosomy 7 with concomitant hematologic recovery
Externí odkaz:
https://doaj.org/article/6e53529cf46a4b9fadc250cce7c36618
Autor:
Oskar Marin-Bejar, Damia Romero-Moya, Javier Rodriguez-Ubreva, Maximiliano Distefano, Francesca Lessi, Paolo Aretini, Alessandro Liquori, Julio Castaño, Emilia Kozyra, Lili Kotmayer, Clara Bueno, José Cervera, José Carlos Rodriguez-Gallego, Josep F Nomdedeu, Laura Murillo-Sanjuán, Cristina Díaz de Heredia, Antonio Pérez-Martinez, Félix López-Cardenas, Carolina Martínez-Laperche, Nieves Dorado-Herrero, Francisco M Marco, Felipe Prósper, Pablo Menendez, David Valcárcel, Esteban Ballestar, Csaba Bödör, Anna Bigas, Albert Catalá, Marcin W Wlodarski, Alessandra Giorgetti
Publikováno v:
HemaSphere, Vol 7, p e891194b (2023)
Externí odkaz:
https://doaj.org/article/73cdfb6289c94ebfa4e147d1498cc8f1
Autor:
Damia Romero-Moya, Oskar Marin-Bejar, Maximiliano Distefano, Joan Pera, Julio Castaño, Jessica Gonzalez, Lili Kotmayer, Csaba Bödör, Albert Català, Marcin W Wlodarski, Anna Bigas, Alessandra Giorgetti
Publikováno v:
HemaSphere, Vol 7, p e83481ae (2023)
Externí odkaz:
https://doaj.org/article/97f62a70f6314b658d5e88da7fef8376
Autor:
Oskar Marin-Bejar, Damia Romero-Moya, Javier Rodriguez-Ubreva, Maximiliano Distefano, Francesca Lessi, Paolo Aretini, Alessandro Liquori, Julio Castaño, Emilia Kozyra, Lili Kotmayer, Clara Bueno, José Cervera, José Carlos Rodriguez-Gallego, Josep F Nomdedeu, Laura Murillo-Sanjuán, Cristina Díaz de Heredia, Antonio Pérez-Martinez, Félix López-Cadenas, Carolina Martínez-Laperche, Nieves Dorado-Herrero, Francisco M Marco, Felipe Prósper, Pablo Menendez, David Valcárcel, Esteban Ballestar, Csaba Bödör, Anna Bigas, Albert Catalá, Marcin W Wlodarski, Alessandra Giorgetti
Publikováno v:
Haematologica, Vol 108, Iss 9 (2023)
Externí odkaz:
https://doaj.org/article/64a9f674d5c1431a8af78aa2de7d0937
Autor:
Senthil Velan Bhoopalan, Jonathan S. Yen, Thiyagaraj Mayuranathan, Kalin D. Mayberry, Yu Yao, Maria Angeles Lillo Osuna, Yoonjeong Jang, Janaka S.S. Liyanage, Lionel Blanc, Steven R. Ellis, Marcin W. Wlodarski, Mitchell J. Weiss
Publikováno v:
JCI Insight, Vol 8, Iss 1 (2023)
Diamond-Blackfan anemia (DBA) is a genetic blood disease caused by heterozygous loss-of-function mutations in ribosomal protein (RP) genes, most commonly RPS19. The signature feature of DBA is hypoplastic anemia occurring in infants, although some ol
Externí odkaz:
https://doaj.org/article/954998aac9b04c778272299720472298