Zobrazeno 1 - 10
of 19
pro vyhledávání: '"S. K. Bohlander"'
Autor:
M Rothenberg-Thurley, S Amler, D Goerlich, T Köhnke, N P Konstandin, S Schneider, M C Sauerland, T Herold, M Hubmann, B Ksienzyk, E Zellmeier, S K Bohlander, M Subklewe, A Faldum, W Hiddemann, J Braess, K Spiekermann, K H Metzeler
Publikováno v:
Leukemia.
Some patients with acute myeloid leukemia (AML) who are in complete remission after induction chemotherapy harbor persisting pre-leukemic clones, carrying a subset of leukemia-associated somatic mutations. There is conflicting evidence on the prognos
Publikováno v:
Monatsschrift Kinderheilkunde. 147:22-26
Wir berichten uber 2 verwandte Patienten mit einer partiellen Trisomie des langen Arms von Chromosom 7 und einer partiellen Monosomie des kurzen Arms von Chromosom 17. Eine Stammbaumanalyse zeigt eine familiare balancierte Translokation mit Beteiligu
Autor:
P. Langer, A. Machens, S. K. Bohlander, W. Höppner, Oliver Gimm, Detlef K. Bartsch, Caroline L. Lopez, Henning Dralle, V. Fendrich
Publikováno v:
Praxis der Viszeralchirurgie ISBN: 9783642142840
Multiple endokrine Neoplasien (MEN) stellen vererbte, neoplastische Veranderungen dar, die auf bekannte, definieriegenetischeVeranderungen zuruckzufuhren sind. Haufig sind mehrere endokrine Organe desselben Patienten von der MEN betroffen, aber auch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80d5e7ad0b7ab95c75d0071d23739839
https://doi.org/10.1007/978-3-642-14285-7_6
https://doi.org/10.1007/978-3-642-14285-7_6
Autor:
H, Kobayashi, K T, Montgomery, S K, Bohlander, C N, Adra, B L, Lim, R S, Kucherlapati, H, Donis-Keller, M S, Holt, M M, Le Beau, J D, Rowley
Publikováno v:
Blood. 84:3473-3482
Translocations and deletions of the short arm of chromosome 12 [t(12p) and del(12p)] are common recurring abnormalities in a broad spectrum of hematologic malignant diseases. We studied 20 patients and one cell line whose cells contained 12p13 transl
Publikováno v:
Human reproduction (Oxford, England). 16(1)
Karyotyping of a malformed male newborn revealed the unbalanced karyotype of 46,XY, psudic(5;21)(q12;p13), +5 resulting in trisomy for the short arm of chromosome 5 and partial trisomy for 5q. Both parents had normal karyotypes in their peripheral bl
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
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
Autor:
Y, Sato, S K, Bohlander, H, Kobayashi, S, Reshmi, Y, Suto, E M, Davis, R, Espinosa, R, Hoopes, K T, Montgomery, R S, Kucherlapati, M M, Le Beau, J D, Rowley
Publikováno v:
Blood. 90(12)
Using fluorescence in situ hybridization (FISH) and probes located on 12p12.1 to 13.3, we studied the breakpoints of 23 patients who had various hematologic malignant diseases and who had 12p13-balanced translocations (21 patients), inversion (1 pati
Publikováno v:
Genes, chromosomescancer. 18(4)
ETV6 (TEL) is rearranged in various types of hematologic malignancies. The B-cell precursor acute lymphoblastic leukemia (ALL) cell line SUP-B2 has a t(6;12)(q23;p13) involving ETV6 at 12p13 and a submicroscopic deletion of the other ETV6 allele. The
Autor:
S, Tanabe, S K, Bohlander, C V, Vignon, R, Espinosa, N, Zhao, P L, Strissel, N J, Zeleznik-Le, J D, Rowley
Publikováno v:
Blood. 88(9)
Invins(10;11)(p12;q23q12) is one of the rare but recurring chromosome rearrangements seen in acute monoblastic leukemia. We cloned the proximal 10p breakpoint from one patient and showed that the MLL gene at 11q23 was fused to the 3' portion of AF10