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Morphological variability of lymphohistiocytic variant of anaplastic large cell lymphoma (former lymphohistiocytic lymphoma according to the Kiel classification).
- Published in:
- 2008
- By:
- Publication type:
- journal article
Expression of ELF1, a lymphoid ETS domain‐containing transcription factor, is recurrently lost in classical Hodgkin lymphoma.
- Published in:
- Angewandte Chemie, 2019, v. 131, n. 15, p. 79, doi. 10.1111/bjh.15757
- By:
- Publication type:
- Article
Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 8, p. 586, doi. 10.1002/gcc.22954
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- Publication type:
- Article
Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome.
- Published in:
- Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 602, doi. 10.1002/gcc.22728
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- Publication type:
- Article
Non‐leukemic pediatric mixed phenotype acute leukemia/lymphoma: Genomic characterization and clinical outcome in a prospective trial for pediatric lymphoblastic lymphoma.
- Published in:
- Genes, Chromosomes & Cancer, 2019, v. 58, n. 6, p. 365, doi. 10.1002/gcc.22726
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- Publication type:
- Article
Array‐based profiling of the lymphoma cell DNA methylome does not unequivocally distinguish primary lymphomas of the central nervous system from non‐CNS diffuse large B‐cell lymphomas.
- Published in:
- Genes, Chromosomes & Cancer, 2019, v. 58, n. 1, p. 66, doi. 10.1002/gcc.22687
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- Publication type:
- Article
Multiple DICER1‐related tumors in a child with a large interstitial 14q32 deletion.
- Published in:
- Genes, Chromosomes & Cancer, 2018, v. 57, n. 5, p. 223, doi. 10.1002/gcc.22523
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- Publication type:
- Article
Novel IGH and MYC Translocation Partners in Diffuse Large B-Cell Lymphomas.
- Published in:
- Genes, Chromosomes & Cancer, 2016, v. 55, n. 12, p. 932, doi. 10.1002/gcc.22391
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- Publication type:
- Article
Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3).
- Published in:
- Genes, Chromosomes & Cancer, 2016, v. 55, n. 9, p. 677, doi. 10.1002/gcc.22369
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- Publication type:
- Article
Alterations of the CD58 gene in classical Hodgkin lymphoma.
- Published in:
- Genes, Chromosomes & Cancer, 2015, v. 54, n. 10, p. 638, doi. 10.1002/gcc.22276
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- Publication type:
- Article
Recurrent RHOA mutations in pediatric Burkitt lymphoma treated according to the NHL-BFM protocols.
- Published in:
- Genes, Chromosomes & Cancer, 2014, v. 53, n. 11, p. 911, doi. 10.1002/gcc.22202
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- Publication type:
- Article
Recurrent mutation of JAK3 in T-cell prolymphocytic leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2014, v. 53, n. 4, p. 309, doi. 10.1002/gcc.22141
- By:
- Publication type:
- Article
Breakpoint characterization of the der(19)t(11;19)(q13;p13) in the ovarian cancer cell line SKOV-3.
- Published in:
- Genes, Chromosomes & Cancer, 2013, v. 52, n. 5, p. 512, doi. 10.1002/gcc.22048
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- Publication type:
- Article
High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas.
- Published in:
- Genes, Chromosomes & Cancer, 2013, v. 52, n. 2, p. 150, doi. 10.1002/gcc.22014
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- Publication type:
- Article
High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors.
- Published in:
- Genes, Chromosomes & Cancer, 2013, v. 52, n. 2, p. 185, doi. 10.1002/gcc.22018
- By:
- Publication type:
- Article
The CBFA2T3/ACSF3 locus is recurrently involved in IGH chromosomal translocation t(14;16)(q32;q24) in pediatric B-cell lymphoma with germinal center phenotype.
- Published in:
- Genes, Chromosomes & Cancer, 2012, v. 51, n. 4, p. 338, doi. 10.1002/gcc.21919
- By:
- Publication type:
- Article
A putative 'hepitype' in the ATM gene associated with chronic lymphocytic leukemia risk.
- Published in:
- Genes, Chromosomes & Cancer, 2011, v. 50, n. 11, p. 887, doi. 10.1002/gcc.20912
- By:
- Publication type:
- Article
High resolution ArrayCGH and expression profiling identifies PTPRD and PCDH17/PCH68 as tumor suppressor gene candidates in laryngeal squamous cell carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 2011, v. 50, n. 3, p. 154, doi. 10.1002/gcc.20840
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- Publication type:
- Article
Rare occurrence of biallelic CYLD gene mutations in classical Hodgkin lymphoma.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 9, p. 803, doi. 10.1002/gcc.20789
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- Publication type:
- Article
Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 5, p. 439, doi. 10.1002/gcc.20754
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- Publication type:
- Article
Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 176, doi. 10.1002/gcc.20729
- By:
- Publication type:
- Article
PVRL2 is translocated to the TRA@ locus in t(14;19)(q11;q13)-positive peripheral T-cell lymphomas.
- Published in:
- Genes, Chromosomes & Cancer, 2007, v. 46, n. 11, p. 1011, doi. 10.1002/gcc.20490
- By:
- Publication type:
- Article
Gains of REL in primary mediastinal B-cell lymphoma coincide with nuclear accumulation of REL protein.
- Published in:
- Genes, Chromosomes & Cancer, 2007, v. 46, n. 4, p. 406, doi. 10.1002/gcc.20420
- By:
- Publication type:
- Article
A novel fusion of the MALT1 gene and the microtubule‐associated protein 4 (MAP4) gene occurs in diffuse large B‐cell lymphoma.
- Published in:
- Genes, Chromosomes & Cancer, 2006, v. 45, n. 9, p. 863, doi. 10.1002/gcc.20350
- By:
- Publication type:
- Article
X-linked Dystonia-Parkinsonism manifesting in a female patient due to atypical turner syndrome.
- Published in:
- Movement Disorders, 2013, v. 28, n. 5, p. 675, doi. 10.1002/mds.25369
- By:
- Publication type:
- Article
Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.
- Published in:
- Movement Disorders, 2010, v. 25, n. 11, p. 1577, doi. 10.1002/mds.22857
- By:
- Publication type:
- Article
Clinical, biological, and molecular genetic features of Richter syndrome and prognostic significance: A study of the French Innovative Leukemia Organization.
- Published in:
- American Journal of Hematology, 2021, v. 96, n. 9, p. E311, doi. 10.1002/ajh.26239
- By:
- Publication type:
- Article
LINC00892 Is an lncRNA Induced by T Cell Activation and Expressed by Follicular Lymphoma-Resident T Helper Cells.
- Published in:
- Non-Coding RNA, 2022, v. 8, n. 3, p. 40, doi. 10.3390/ncrna8030040
- By:
- Publication type:
- Article
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12–q13.
- Published in:
- Human Genetics, 2000, v. 106, n. 1, p. 58, doi. 10.1007/s004399900227
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- Publication type:
- Article
Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2.
- Published in:
- International Journal of Cancer, 2003, v. 103, n. 4, p. 489, doi. 10.1002/ijc.10845
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- Publication type:
- Article
Interphase FISH assays for the detection of translocations with breakpoints in immunoglobulin light chain loci.
- Published in:
- International Journal of Cancer, 2002, v. 98, n. 3, p. 470, doi. 10.1002/ijc.10169
- By:
- Publication type:
- Article
The novel human beta-defensin-3 is widely expressed in oral tissues.
- Published in:
- European Journal of Oral Sciences, 2002, v. 110, n. 2, p. 121, doi. 10.1034/j.1600-0722.2002.11186.x
- By:
- Publication type:
- Article
Primary Bilateral Burkitt Lymphoma of the Lactating Breast.
- Published in:
- Molecular Diagnosis & Therapy, 2010, v. 14, n. 4, p. 243, doi. 10.1007/BF03256380
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- Publication type:
- Article
Preimplantation genetic diagnosis (polar body biopsy) and trisomy 21.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
The master-code of DNA: epigenetic mechanisms and their role for the development of diseases.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Der Über-Code der DNA: epigenetische Mechanismen und deren Bedeutung für die Entstehung von Krankheiten.
- Published in:
- Journal of Laboratory Medicine / Laboratoriums Medizin, 2013, v. 37, n. 6, p. 317, doi. 10.1515/labmed-2013-0048
- By:
- Publication type:
- Article
Homeobox NKX2-3 promotes marginal-zone lymphomagenesis by activating B-cell receptor signalling and shaping lymphocyte dynamics.
- Published in:
- Nature Communications, 2016, v. 7, n. 6, p. 11889, doi. 10.1038/ncomms11889
- By:
- Publication type:
- Article
Points-to-consider on the return of results in epigenetic research.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0646-6
- By:
- Publication type:
- Article
Clinical utility gene card for: Transient Neonatal Diabetes Mellitus, 6q24-related.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 9, p. -1, doi. 10.1038/ejhg.2014.27
- By:
- Publication type:
- Article
Frequency and characterization of DNA methylation defects in children born SGA.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 8, p. 838, doi. 10.1038/ejhg.2012.262
- By:
- Publication type:
- Article
Fast Approach for Clarification of Chromosomal Aberrations by Using LM-PCR and FT-CGH in Leukaemic Sample.
- Published in:
- Acta Haematologica, 2011, v. 127, n. 1, p. 16, doi. 10.1159/000330519
- By:
- Publication type:
- Article
Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5.
- Published in:
- Medizinische Genetik, 2024, v. 36, n. 1, p. 59, doi. 10.1515/medgen-2024-2005
- By:
- Publication type:
- Article
Overview on WHO-HAEM5 and the diagnostic relevance of genetic alterations for the classification.
- Published in:
- Medizinische Genetik, 2024, v. 36, n. 1, p. 3, doi. 10.1515/medgen-2024-2008
- By:
- Publication type:
- Article
Appraisal of current technologies for the study of genetic alterations in hematologic malignancies with a focus on chromosome analysis and structural variants.
- Published in:
- Medizinische Genetik, 2024, v. 36, n. 1, p. 13, doi. 10.1515/medgen-2024-2001
- By:
- Publication type:
- Article
Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5.
- Published in:
- Medizinische Genetik, 2024, v. 36, n. 1, p. 47, doi. 10.1515/medgen-2024-2006
- By:
- Publication type:
- Article
Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas.
- Published in:
- 2024
- By:
- Publication type:
- Editorial
Staffelübergabe in der Redaktionsleitung.
- Published in:
- 2022
- By:
- Publication type:
- Editorial
Pränataldiagnostik.
- Published in:
- 2019
- By:
- Publication type:
- Editorial
Bericht 2017 des GfH-Beauftragten für Ausbildung und Lehre zum Nationalen Kompetenzbasierten Lernzielkatalog Medizin (NKLM).
- Published in:
- Medizinische Genetik, 2018, v. 30, n. 1, p. 57, doi. 10.1007/s11825-018-0177-3
- By:
- Publication type:
- Article
Seltene Tumordispositionssyndrome.
- Published in:
- 2017
- By:
- Publication type:
- Editorial