Zobrazeno 1 - 10
of 25
pro vyhledávání: '"M H, Dreyling"'
Autor:
Bao, Mengni1,2,3, Hua, Xiumeng1,2,4,5, Chen, Xiao1,2,4,5, An, Tao1,6, Mo, Han3, Sun, Zhe3, Tao, Menghao2, Yue, Guangxin1, Song, Jiangping1,2,3,4,5 songjiangping@fuwaihospital.org
Publikováno v:
Advanced Science. 8/27/2024, Vol. 11 Issue 32, p1-16. 16p.
Autor:
L, Sanz-Vaqué, D, Colomer, F, Bosch, A, López-Guillermo, M H, Dreyling, E, Montserrat, E, Campo
Publikováno v:
Haematologica. 86(2)
Microsatellite instability (MSI) is characterized by tumor-associated alterations in the germline size of microsatellite repeats caused by a reduced efficacy of the DNA mismatch repair machinery. The aim of this study was to investigate the presence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::75067e5f76033b2f68abe5c8107bb990
https://pubmed.ncbi.nlm.nih.gov/11224488
https://pubmed.ncbi.nlm.nih.gov/11224488
Autor:
C. Fonatsch, Detlef Haase, C. Schoch, M. H. Dreyling, W. Hiddemann, W.-D. Ludwig, Stefan K. Bohlander, K. Schrader, Brigitte Schlegelberger, V. Muschinsky
Publikováno v:
Haematology and Blood Transfusion / Hämatologie und Bluttransfusion ISBN: 9783642621093
The t(10,11)(pl3;ql4) is a recurring translocation that has been observed in acute lymphoblastic as well as acute myeloid leukemia. A previous study revealed a MLL/AF10fusion in all cases of AML with t(10;11) and various breakpoints on chromosome 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0167779b7d4e6d7be310e44ba3f51308
https://doi.org/10.1007/978-3-642-18156-6_4
https://doi.org/10.1007/978-3-642-18156-6_4
Autor:
A, Rosenwald, G, Ott, A K, Krumdiek, M H, Dreyling, T, Katzenberger, J, Kalla, S, Roth, M M, Ott, H K, Müller-Hermelink
Publikováno v:
Genes, chromosomescancer. 26(3)
Structural aberrations of chromosomal band 13q14 are frequent in B-cell chronic lymphocytic leukemia (B-CLL) and target a putative tumor suppressor gene in the genomic region between the RB1 gene and the genetic marker D13S25. Recently, it has been s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a0d76ebae8261558e1aaaba507ba3e70
https://pubmed.ncbi.nlm.nih.gov/10502318
https://pubmed.ncbi.nlm.nih.gov/10502318
Autor:
M H, Dreyling, K, Schrader, C, Fonatsch, B, Schlegelberger, D, Haase, C, Schoch, W, Ludwig, H, Löffler, T, Büchner, B, Wörmann, W, Hiddemann, S K, Bohlander
Publikováno v:
Blood. 91(12)
The translocation t(10;11)(p13;q14) has been observed in acute lymphoblastic leukemia (ALL) as well as acute myeloid leukemia (AML). A recent study showed a MLL/AF10 fusion in all cases of AML with t(10;11) and various breakpoints on chromosome 11 ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d4c938459525941eeec0d5970e6052e3
https://pubmed.ncbi.nlm.nih.gov/9616163
https://pubmed.ncbi.nlm.nih.gov/9616163
Publikováno v:
Genes, chromosomescancer. 22(1)
Identifying the various genetic alterations that contribute to lymphomagenesis is key to our improved understanding of the biological behavior of the disease. Recently, we and others have defined a tumor suppressor region on the short arm of chromoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::845a053b02303603907e37d0ecec552b
https://pubmed.ncbi.nlm.nih.gov/9591637
https://pubmed.ncbi.nlm.nih.gov/9591637
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 2(12)
The tumor suppressor p16(INK4a) has been shown to be inactivated in numerous cancer lines and primary tumors. Recently, we reported loss of heterozygosity of the region in which p16(INK4a) is located in more than one-half of primary breast tumors. Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::954c91ab0d0f28f68358de8c82bf0939
https://pubmed.ncbi.nlm.nih.gov/9816158
https://pubmed.ncbi.nlm.nih.gov/9816158
Publikováno v:
Blood. 86(5)
Deletions of chromosomal band 9p21 have been detected in various tumor types as well as in more than 20% of acute lymphoblastic leukemia (ALL). These deletions frequently include the entire interferon (IFN) gene cluster as well as the methylthioadeno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4af90091a2f9ffe0a1956b3f610e6dc3
https://pubmed.ncbi.nlm.nih.gov/7544647
https://pubmed.ncbi.nlm.nih.gov/7544647
Publikováno v:
Cancer research. 55(5)
Deletions of chromosomal band 9p21 have been detected in various tumor types including melanoma, glioma, lung cancer, mesothelioma, and bladder cancer. Recently, the CDKN2 gene (p16INK4A, MTS I, CDK41) has been proposed as a candidate tumor suppresso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c9d5c0b2081d18aebb0181b73310780
https://pubmed.ncbi.nlm.nih.gov/7867008
https://pubmed.ncbi.nlm.nih.gov/7867008
Publikováno v:
Case Reports in Hematology. 2012, p1-4. 4p.