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Publications by Thomas Büchner
Isolated Trisomy 13 Defines a Homogeneous AML Subgroup With High Frequency of Mutations in Spliceosome Genes and Poor Prognosis
Blood
Biochemistry
Immunology
Cell Biology
Hematology
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Mutations in Rb1 Pathway-Related Genes Are Associated With Poor Prognosis in Anaplastic Astrocytomas
British Journal of Cancer
Cancer Research
Oncology
PIK3CA Mutations Frequently Coexist With EGFR/KRAS Mutations in Non-Small Cell Lung Cancer and Suggest Poor Prognosis in EGFR/KRAS Wildtype Subgroup
PLoS ONE
Multidisciplinary
Better Prognosis in Newborns With Trisomy 13 Who Received Intensive Treatments: A Retrospective Study of 16 Patients
Cell Biochemistry and Biophysics
Medicine
Biochemistry
Cell Biology
Biophysics
Heterogeneity Within AML With CEBPA Mutations; Only CEBPA Double Mutations, but Not Single CEBPA Mutations Are Associated With Favourable Prognosis
British Journal of Cancer
Cancer Research
Oncology
Transformation of MDS/MPN-RS-T to AML: Trisomy 13, Resistant Thrombocytosis and Transient Disease Control With Oral Busulfan Therapy
American Journal of Hematology
Hematology
MB4-2 Breakpoint in MMSET Combined With Del(17p) Defines a Subset of T(4;14) Multiple Myeloma With Very Poor Prognosis
Haematologica
Hematology
BRCAness Combined With Family History of Cancer Is Associated With Poor Prognosis in Breast Cancer Patients With High Risk of BRCA Mutations
Clinical Breast Cancer
Cancer Research
Oncology
AB245. Down-Regulation of C12orf59 Is Associated With a Poor Prognosis and VHL Mutations in Renal Cell Carcinoma
Translational Andrology and Urology
Reproductive Medicine
Urology
Loss of Tumor Suppressors KAI1 and P27 Identifies a Unique Subgroup of Primary Melanoma Patients With Poor &Shy;­prognosis
Oncotarget
Oncology