Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ramin Monajemi"'
Autor:
Shadi Darvish Shafighi, Szymon M. Kiełbasa, Julieta Sepúlveda-Yáñez, Ramin Monajemi, Davy Cats, Hailiang Mei, Roberta Menafra, Susan Kloet, Hendrik Veelken, Cornelis A.M. van Bergen, Ewa Szczurek
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-16 (2021)
Abstract Background Drawing genotype-to-phenotype maps in tumors is of paramount importance for understanding tumor heterogeneity. Assignment of single cells to their tumor clones of origin can be approached by matching the genotypes of the clones to
Externí odkaz:
https://doaj.org/article/3d2fdb3a359f473fa50be1499b8e526d
Autor:
Bharati Jadhav, Ramin Monajemi, Kristina K. Gagalova, Daniel Ho, Harmen H. M. Draisma, Mark A. van de Wiel, Lude Franke, Bastiaan T. Heijmans, Joyce van Meurs, Rick Jansen, GoNL Consortium, BIOS Consortium, Peter A. C. ‘t Hoen, Andrew J. Sharp, Szymon M. Kiełbasa
Publikováno v:
BMC Biology, Vol 17, Iss 1, Pp 1-20 (2019)
Abstract Background Identification of imprinted genes, demonstrating a consistent preference towards the paternal or maternal allelic expression, is important for the understanding of gene expression regulation during embryonic development and of the
Externí odkaz:
https://doaj.org/article/ac49695a15374f9b92412458d4082fc2
Autor:
Kyra J. Fuchs, M. Willy Honders, Edith D. van der Meijden, Alwin E. Adriaans, Dyantha I. van der Lee, Margot J. Pont, Ramin Monajemi, Szymon M. Kielbasa, Peter A. C. ’t Hoen, Cornelis A. M. van Bergen, J. H. Frederik Falkenburg, Marieke Griffioen
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Patients undergoing allogeneic stem cell transplantation as treatment for hematological diseases face the risk of Graft-versus-Host Disease as well as relapse. Graft-versus-Host Disease and the favorable Graft-versus-Leukemia effect are mediated by d
Externí odkaz:
https://doaj.org/article/637c84af066b418ab1a4cb4789bd764f
Autor:
Szymon M. Kielbasa, Ramin Monajemi, Hailiang Mei, Cornelis A.M. van Bergen, Hendrik Veelken, Shadi Darvish Shafighi, Susan L. Kloet, Ewa Szczurek, Julieta Sepulveda-Yanez, Davy Cats, Roberta Menafra
Publikováno v:
Genome Medicine
Genome Medicine, 13(1). BMC
Genome Medicine, Vol 13, Iss 1, Pp 1-16 (2021)
bioRxiv
Genome Medicine, 13(1). BMC
Genome Medicine, Vol 13, Iss 1, Pp 1-16 (2021)
bioRxiv
Background Drawing genotype-to-phenotype maps in tumors is of paramount importance for understanding tumor heterogeneity. Assignment of single cells to their tumor clones of origin can be approached by matching the genotypes of the clones to the muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12ec842631b07229188811e860351dc4
https://doi.org/10.1101/2020.06.05.134452
https://doi.org/10.1101/2020.06.05.134452
Autor:
Roberta Menafra, Edwin Quinten, Marcelo Navarrete Signorile, Cornelis A.M. van Bergen, Susan L. Kloet, Ramin Monajemi, Szymon M. Kielbasa, Juleta H. Sepulveda-Yanez, Hendrik Veelken, Diego Alvarez-Saravia
Publikováno v:
Blood. 138:1151-1151
Introduction Follicular Lymphoma (FL) is one of the most prevalent B-cell neoplasms and despite recent advances remains incurable in most cases. FL cells are malignant counterparts of normal germinal center B-cells. At molecular level FL are characte
Autor:
Marvyn T. Koning, Ramin Monajemi, Szymon M. Kielbasa, Marcelo A. Navarrete, Joost S.P. Vermaat, Agnieszka Mykowiecka, Edwin Quinten, Hendrik Veelken, Julieta Sepulveda, Ruben A.L. de Groen, Cornelis A.M. van Bergen, Susan L. Kloet, Paweł Górecki
Publikováno v:
Blood. 134:298-298
Objectives: Follicular lymphoma (FL) typically originates from premalignant mature B cells that carry the founder t(14;18) BCL2 translocation. Mutations in epigenetic modifiers and acquisition of N-glycosylation sites in CDR regions of the B-cell rec
Autor:
Bharati Jadhav, Ramin Monajemi, Kristina K. Gagalova, Daniel Ho, Harmen H.M. Draisma, Mark A. van de Wiel, Lude Franke, Bastiaan T. Heijmans, Joyce van Meurs, Rick Jansen, GoNL Consortium, BIOS Consortium, Peter A.C. ‘t Hoen, Andrew J. Sharp, Szymon M. Kiełbasa
Combining allelic analysis of RNA-Seq data with phased genotypes in family trios provides a powerful method to detect parent-of-origin biases in gene expression. We report findings in 296 family trios from two large studies: 165 lymphoblastoid cell l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2c88f0cd61be634cd45d1b6d722b0fa
Autor:
Alwin E Adriaans, W. Honders, D. van der Lee, E. van der Meijden, Margot J. Pont, Szymon M. Kielbasa, P.A.C. ’t Hoen, Frederik Falkenburg, C.A.M. van Bergen, K. Fuchs, Marieke Griffioen, Ramin Monajemi
Publikováno v:
HemaSphere. 3:400-401
Autor:
Jhf Falkenburg, Wilhelmina G. M. Kroes, R. G. Vries, Maria W. Honders, C. Out, A. S. Al Hinai, Martine J. Jager, Pieter S. Hiemstra, Eva Schmelzer, Jelle J. Goeman, C. van Kooten, W.A.F. Marijt, Marieke Griffioen, Stefan Böhringer, Margot J. Pont, Ramin Monajemi, Anita N. Kremer, H.C. de Boer
Publikováno v:
PLoS Medicine, 11, 155
PLoS ONE [E], 11(5). Public Library of Science
PLoS ONE, Vol 11, Iss 5, p e0155165 (2016)
PLoS ONE, 11(5)
PLoS ONE
PLoS ONE [E], 11(5). Public Library of Science
PLoS ONE, Vol 11, Iss 5, p e0155165 (2016)
PLoS ONE, 11(5)
PLoS ONE
Cellular immunotherapy has proven to be effective in the treatment of hematological cancers by donor lymphocyte infusion after allogeneic hematopoietic stem cell transplantation and more recently by targeted therapy with chimeric antigen or T-cell re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44df62fb1a72e37097b212106d057c39
https://hdl.handle.net/1887/113973
https://hdl.handle.net/1887/113973
Autor:
Harold Snieder, Jelle J. Goeman, Brenda W.J.H. Penninx, Tineke van Veen, Klaas J. Wardenaar, Catharina A. Hartman, Ilja M. Nolte, Frans G. Zitman, Ramin Monajemi
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(5), 519-528. Wiley-Liss Inc.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 159B(5), 519-528. Wiley
van Veen, T, Goeman, J J, Monajemi, R, Wardenaar, K J, Hartman, C A, Snieder, H, Nolte, I M, Penninx, B W J H & Zitman, F G 2012, ' Different gene sets contribute to different symptom dimensions of depression and anxiety ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 159B, no. 5, pp. 519-528 . https://doi.org/10.1002/ajmg.b.32058
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(5), 519-528
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 159B(5), 519-528. Wiley
van Veen, T, Goeman, J J, Monajemi, R, Wardenaar, K J, Hartman, C A, Snieder, H, Nolte, I M, Penninx, B W J H & Zitman, F G 2012, ' Different gene sets contribute to different symptom dimensions of depression and anxiety ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 159B, no. 5, pp. 519-528 . https://doi.org/10.1002/ajmg.b.32058
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(5), 519-528
Although many genetic association studies have been carried out, it remains unclear which genes contribute to depression. This may be due to heterogeneity of the DSM-IV category of depression. Specific symptom-dimensions provide a more homogenous phe