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S Gesk

Explore the profile of S Gesk including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 28
Citations 458
Followers 0
Related Specialties
Hematology
Oncology
Molecular Biology
Top 10 Co-Authors
R Siebert
L Harder
B Schlegelberger
W Grote
J I Martin-Subero
M J Calasanz
D Steinemann
M J Dyer
I Vater
T Sonoki
Published In
Leukemia
Blood
Cancer Genet Cytogenet
Genes Chromosomes Cancer
J Invest Dermatol
Affiliations
Soon will be listed here.
Recent Articles
1.
Maternal uniparental disomy 15 in a fetus resulting from a balanced familial translocation t(2;15)(p11;q11.2)
Heidemann S, Plendl H, Vater I, Gesk S, Exeler-Telker J, Grote W, et al.
Prenat Diagn . 2010 Jan; 30(2):183-5. PMID: 20063327
No abstract available.
2.
A 439 kb-sized homozygous deletion in 17p13.3 leading to biallelic loss of the ASPA as cause of Canavan disease detected by SNP-array analysis
Caliebe A, Vater I, Plendl H, Gesk S, Siebert R, Cremer F, et al.
Mol Genet Metab . 2009 Nov; 99(2):184-5. PMID: 19932039
No abstract available.
3.
Biallelic inactivation of TRAF3 in a subset of B-cell lymphomas with interstitial del(14)(q24.1q32.33)
Nagel I, Bug S, Tonnies H, Ammerpohl O, Richter J, Vater I, et al.
Leukemia . 2009 Aug; 23(11):2153-5. PMID: 19693093
No abstract available.
4.
Chromosomal imbalances and partial uniparental disomies in primary central nervous system lymphoma
Schwindt H, Vater I, Kreuz M, Montesinos-Rongen M, Brunn A, Richter J, et al.
Leukemia . 2009 Jun; 23(10):1875-84. PMID: 19494841
To determine the pattern of genetic alterations in primary central nervous system lymphomas (PCNSL), 19 PCNSL were studied by high-density single-nucleotide polymorphism arrays. Recurrent losses involved 6p21.32, 6q21, 8q12-12.2, 9p21.3,...
5.
Inv(11)(q21q23) fuses MLL to the Notch co-activator mastermind-like 2 in secondary T-cell acute lymphoblastic leukemia
Metzler M, Staege M, Harder L, Mendelova D, Zuna J, Fronkova E, et al.
Leukemia . 2008 Mar; 22(9):1807-11. PMID: 18337764
No abstract available.
6.
A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation
Martin-Subero J, Ibbotson R, Klapper W, Michaux L, Callet-Bauchu E, Berger F, et al.
Leukemia . 2007 May; 21(7):1532-44. PMID: 17495977
The biologic and pathologic features of B-cell malignancies bearing a translocation t(14;19)(q32;q13) leading to a fusion of IGH and BCL3 are still poorly described. Herein we report the results of...
7.
Gains of the proto-oncogene BCL11A and nuclear accumulation of BCL11A(XL) protein are frequent in primary mediastinal B-cell lymphoma
Weniger M, Pulford K, Gesk S, Ehrlich S, Banham A, Lyne L, et al.
Leukemia . 2006 Jul; 20(10):1880-2. PMID: 16871282
No abstract available.
8.
ALK-positive diffuse large B-cell lymphoma with ALK-Clathrin fusion belongs to the spectrum of pediatric lymphomas
Gesk S, Gascoyne R, Schnitzer B, Bakshi N, Janssen D, Klapper W, et al.
Leukemia . 2005 Aug; 19(10):1839-40. PMID: 16107887
No abstract available.
9.
Extramedullary manifestation of a donor-derived acute myeloid leukemia in a liver transplant patient
Subklewe M, Nagy M, Schoch C, Jenisch S, Siebert R, Gesk S, et al.
Leukemia . 2004 Oct; 18(12):2050-3. PMID: 15470493
No abstract available.
10.
Molecular cytogenetic analysis of chromosomal breakpoints in the IGH, MYC, BCL6, and MALT1 gene loci in primary cutaneous B-cell lymphomas
Hallermann C, Kaune K, Gesk S, Martin-Subero J, Gunawan B, Griesinger F, et al.
J Invest Dermatol . 2004 Jun; 123(1):213-9. PMID: 15191563
Chromosomal translocations affecting the IGH locus and various oncogene loci are recurrent in many types of systemic B-cell lymphomas. Hardly any data exist, however, on such translocations in primary cutaneous...