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126 results on '"Hinzmann B"'

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1. Increased risk of severe clinical course of COVID-19 in carriers of HLA-C*04:01

3. 1800P Concordance between treatment-naive tissue and circulating tumour DNA (ctDNA) in late stage non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC)

4. 1356P Disease monitoring and TKI resistance mutations of EGFR mutation-positive NSCLC patients via circulating tumour DNA

5. P2.03-25 Assessing the Impact of Clonal Hematopoiesis in Disease Monitoring Using Targeted Cell-Free DNA (cfDNA) Sequencing Technology

6. P1.01-34 Early Assessment of Therapy Response in Non-Small Cell Lung Cancer (NSCLC) via Longitudinal ctDNA Analysis

7. Mutational profiling of tumour tissue and sequential plasma illustrates emergent clones during treatment in late stage small cell lung cancer (SCLC)

8. Ecological diversity indices as measurements of tumor heterogeneity correlates with clinical outcomes in late stage small cell lung cancer (SCLC)

10. P1.15-011 Longitudinal Mutation Monitoring in Plasma Without Matching Tumor Tissue by Deep Sequencing in Small Cell Lung Cancer (SCLC)

12. Identification of Novel Tumor-Associated Genes in 11q12-q23

15. The DNA sequence of the human X chromosome

17. Measurement of the cross section for production of bb¯X decaying to muons in pp collisions at √s = 7 TeV

18. Study of W boson production in PbPb and pp collisions at √sNN=2.76 TeV

22. Mutation Status of KRAS, BRAF, PIK3CA and Expression Level of AREG and EREG Identify Responders to Cetuximab in a Large Panel of Patient Derived Colorectal Carcinoma Xenografts of All Four UICC Stages

23. Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy

28. KRAS- and BRAF-Mutations and their clinical correlates in a prospective, multi-center, diagnostic clinical trial „molecular signatures in colorectal cancer“ (MSKK)

30. Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X; autosome translocations

31. Positional cloning of the gene for X-linked retinitis pigmentosa 2

32. Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5 , in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia

33. Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations

36. Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations.

38. Comparative genome sequence analysis of the Bpa/Str region in mouse and Man.

40. Genome-wide expression patterns of invasion front, inner tumor mass and surrounding normal epithelium of colorectal tumors

41. A genome-wide map of aberrantly expressed chromosomal islands in colorectal cancer

42. Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy

44. Highly multiplexed immune repertoire sequencing links multiple lymphocyte classes with severity of response to COVID-19.

45. Quantitative PCR-Based Method to Assess Cell-Free DNA Quality, Adjust Input Mass, and Improve Next-Generation Sequencing Assay Performance.

46. Increased risk of severe clinical course of COVID-19 in carriers of HLA-C*04:01.

47. Innovative Tumor Tissue Dissection Tool for Molecular Oncology Diagnostics.

48. Patient perception of disease burden in diffuse cutaneous systemic sclerosis.

49. Factors influencing early referral, early diagnosis and management in patients with diffuse cutaneous systemic sclerosis.

50. [Adenocarcinoma of the mamma in a Göttingen minipig].

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