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1. Metabolic pathway-based subtypes associate glycan biosynthesis and treatment response in head and neck cancer

3. Kind mit gefäßreichem „Kloß“ im Hals

4. Xenografts Show Signs of Concentric Hypertrophy and Dynamic Left Ventricular Outflow Tract Obstruction After Orthotopic Pig-to-baboon Heart Transplantation

5. BACH: Grand Challenge on Breast Cancer Histology Images

6. Assessment of Breast Cancer Histology using Densely Connected Convolutional Networks

8. A transcriptomic map of EGFR-induced epithelial-to-mesenchymal transition identifies prognostic and therapeutic targets for head and neck cancer

10. Molecular biomarkers for personalised medicine in patients with head and neck cancer

11. 414.7: The Perioperative Cardiac Xenograft Dysfunction (PCXD) Has A Major Impact in (Life-Supporting) Orthotopic (oXTx) Cardiac Xenotransplantation, but Not in the Heterotopic Thoracic (htXTx) Xenotransplantation

12. Pig-to-non-human primate heart transplantation: The final step toward clinical xenotransplantation?

13. Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases

14. BACH: Grand challenge on breast cancer histology images

15. Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 Deficiency

16. Molecular characterization of the evolution of premalignant lesions in the upper aerodigestive tract.

17. Essential role for Stat5a/b in myeloproliferative neoplasms induced by BCR-ABL1 and JAK2(V617F) in mice.

18. No NLRP3 inflammasome activity in kidney epithelial cells, not even when the NLRP3-A350V Muckle-Wells variant is expressed in podocytes of diabetic mice

19. Comparison of mutated JAK2 and ABL1 as oncogenes and drug targets in myeloproliferative disorders

21. NOX1 Regulates Collective and Planktonic Cell Migration: Insights From Patients With Pediatric-Onset IBD and NOX1 Deficiency

22. Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy

23. Supplementary Figure from Therapy-Related Transcriptional Subtypes in Matched Primary and Recurrent Head and Neck Cancer

24. Supplementary Data from Therapy-Related Transcriptional Subtypes in Matched Primary and Recurrent Head and Neck Cancer

25. Supplementary Table from Therapy-Related Transcriptional Subtypes in Matched Primary and Recurrent Head and Neck Cancer

26. Human MD2 deficiency—an inborn error of immunity with pleiotropic features

29. Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency

31. Comparative proteomics reveals a diagnostic signature for pulmonary head‐and‐neck cancer metastasis

32. Analysis of genetic variants of frequently mutated genes in human papillomavirus‐negative primary head and neck squamous cell carcinoma, resection margins, local recurrences and corresponding circulating cell‐free DNA

34. Comprehensive mutational profiling in advanced systemic mastocytosis

36. Liquid BIOpsy for MiNimal RESidual DiSease Detection in Head and Neck Squamous Cell Carcinoma (LIONESS) – A personalised analysis of circulating cell-free tumour DNA

37. Gain-of-function IKZF1 variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation

38. Therapy-Related Transcriptional Subtypes in Matched Primary and Recurrent Head and Neck Cancer

39. Additional file 1 of A transcriptomic map of EGFR-induced epithelial-to-mesenchymal transition identifies prognostic and therapeutic targets for head and neck cancer

40. Additional file 4 of A transcriptomic map of EGFR-induced epithelial-to-mesenchymal transition identifies prognostic and therapeutic targets for head and neck cancer

42. The Neurokinin-1 Receptor Is a Target in Pediatric Rhabdoid Tumors

43. Rubella Virus Infected Macrophages and Neutrophils Define Patterns of Granulomatous Inflammation in Inborn and Acquired Errors of Immunity

48. Abstract 553: Personalized circulating tumor DNA analysis in head and neck squamous cell carcinoma: Preliminary results of the Liquid BIOpsy for MiNimal RESidual DiSease Detection in Head and NeckSquamous Cell Carcinoma (LIONESS) study

49. Heterozygous OAS1 gain-of-function variants cause an autoinflammatory immunodeficiency

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