Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Anna, Djos"'
Autor:
Medha Suman, Maja Löfgren, Susanne Fransson, Jewahri Idris Yousuf, Johanna Svensson, Anna Djos, Tommy Martinsson, Per Kogner, Teresia Kling, Helena Carén
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-25 (2024)
Abstract Background Neuroblastoma (NB) is a complex disease, and the current understanding of NB biology is limited. Deregulation in genomic imprinting is a common event in malignancy. Since imprinted genes play crucial roles in early fetal growth an
Externí odkaz:
https://doaj.org/article/4d33e6752f68449d9e475c908b6d3e32
Autor:
Se Whee Sammy Park, Susanne Fransson, Fredrik Sundquist, Joachim N. Nilsson, Per Grybäck, Sandra Wessman, Jacob Strömgren, Anna Djos, Henrik Fagman, Helene Sjögren, Kleopatra Georgantzi, Nikolas Herold, Per Kogner, Dan Granberg, Mark N. Gaze, Tommy Martinsson, Kasper Karlsson, Jakob J. E. Stenman
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
In this case report, we present the treatment outcomes of the first patient enrolled in the LuDO-N trial. The patient is a 21-month-old girl diagnosed with high-risk neuroblastoma (NB) and widespread skeletal metastasis. The patient initially underwe
Externí odkaz:
https://doaj.org/article/41ba518bf7834ac3b8d9e8df52b0b021
Autor:
Angela Martinez-Monleon, Hanna Kryh Öberg, Jennie Gaarder, Ana P. Berbegall, Niloufar Javanmardi, Anna Djos, Marek Ussowicz, Sabine Taschner-Mandl, Inge M. Ambros, Ingrid Øra, Bengt Sandstedt, Klaus Beiske, Ruth Ladenstein, Rosa Noguera, Peter F. Ambros, Lena Gordon Murkes, Gustaf Ljungman, Per Kogner, Susanne Fransson, Tommy Martinsson
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-17 (2022)
Abstract In neuroblastoma, MYCN amplification and 11q-deletion are important, although incomplete, markers of high-risk disease. It is therefore relevant to characterize additional alterations that can function as prognostic and/or predictive markers
Externí odkaz:
https://doaj.org/article/be646e3979c84617bde833d6925092df
Publikováno v:
PLoS ONE, Vol 17, Iss 11, p e0277524 (2022)
Vesicoureteral reflux (VUR) is a common urological problem in children and its hereditary nature is well recognised. However, despite decades of research, the aetiological factors are poorly understood and the genetic background has been elucidated i
Externí odkaz:
https://doaj.org/article/135b6eeff7df4b81903b350d72a0ebd8
Autor:
Anna Djos, Diana Treis, Susanne Fransson, Lena Gordon Murkes, Sandra Wessman, Jurate Ásmundsson, Agneta Markström, Per Kogner, Tommy Martinsson
Publikováno v:
Diagnostics, Vol 12, Iss 9, p 2260 (2022)
A preterm infant with central hypoventilation was diagnosed with multifocal neuroblastoma. Congenital anomalies of the autonomic nervous system in association with neuroblastoma are commonly associated with germline mutations in PHOX2B. Further, the
Externí odkaz:
https://doaj.org/article/adca38d569f04e61bc19932c66f1b595
Autor:
Joachim Tetteh Siaw, Niloufar Javanmardi, Jimmy Van den Eynden, Dan Emil Lind, Susanne Fransson, Angela Martinez-Monleon, Anna Djos, Rose-Marie Sjöberg, Malin Östensson, Helena Carén, Gunhild Trøen, Klaus Beiske, Ana P. Berbegall, Rosa Noguera, Wei-Yun Lai, Per Kogner, Ruth H. Palmer, Bengt Hallberg, Tommy Martinsson
Publikováno v:
Cell Reports, Vol 32, Iss 12, Pp 108171- (2020)
Summary: High-risk neuroblastomas typically display an undifferentiated or poorly differentiated morphology. It is therefore vital to understand molecular mechanisms that block the differentiation process. We identify an important role for oncogenic
Externí odkaz:
https://doaj.org/article/01191b05e5974287a9be5d2989de4d0a
Autor:
Roshan Vaid, Ketan Thombare, Akram Mendez, Rebeca Burgos-Panadero, Anna Djos, Daniel Jachimowicz, Christoph Bartenhagen, Navinder Kumar, Carina Sihlbom, Susanne Fransson, John Inge Johnsen, Per Kogner, Tommy Martinsson, Matthias Fischer, Tanmoy Mondal
Telomerase-negative tumors can maintain telomere length by alternative lengthening of telomeres (ALT) but the mechanism behind ALT is poorly understood. Aggressive Neuroblastoma (NB), in particular, relapsed tumors are positive for ALT (ALT+) which s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3716f1cd65f6d81580409536fb0877b
https://doi.org/10.1101/2022.12.09.519591
https://doi.org/10.1101/2022.12.09.519591
Autor:
Diana, Treis, Ganesh, Umapathy, Susanne, Fransson, Jikui, Guan, Patricia, Mendoza-García, Joachim T, Siaw, Sandra, Wessman, Lena, Gordon Murkes, Jakob J E, Stenman, Anna, Djos, Lotta H M, Elfman, John Inge, Johnsen, Bengt, Hallberg, Ruth H, Palmer, Tommy, Martinsson, Per, Kogner
Publikováno v:
JCO precision oncology. 6
Publikováno v:
International journal of oncology. 62(2)
Neuroblastoma (NB) is a childhood malignancy of the sympathetic nervous system. NB is mainly driven by copy number alterations, such as
Autor:
Angela Martinez-Monleon, Hanna Kryh Öberg, Jennie Gaarder, Ana P. Berbegall, Niloufar Javanmardi, Anna Djos, Marek Ussowicz, Sabine Taschner-Mandl, Inge M. Ambros, Ingrid Øra, Bengt Sandstedt, Klaus Beiske, Ruth Ladenstein, Rosa Noguera, Peter F. Ambros, Lena Gordon Murkes, Gustaf Ljungman, Per Kogner, Susanne Fransson, Tommy Martinsson
Publikováno v:
Scientific reports. 12(1)
In neuroblastoma, MYCN amplification and 11q-deletion are important, although incomplete, markers of high-risk disease. It is therefore relevant to characterize additional alterations that can function as prognostic and/or predictive markers. Using S