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156 results on '"Hrabĕ de Angelis, Martin"'

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1. EchoVisuAL: Efficient Segmentation of Echocardiograms Using Deep Active Learning

3. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

4. Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain

5. AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease

7. Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

8. Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans

9. Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome

11. Costs of Implementing Quality in Research Practice

21. The calcium-sensing receptor has only a parathyroid hormone-dependent role in the acute response of renal phosphate transporters to phosphate intake.

23. Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse Clinic

25. Genome-wide analysis of PDX1 target genes in human pancreatic progenitors

26. The Role of Fibroblast Growth Factor-Binding Protein 1 in Skin Carcinogenesis and Inflammation

27. Roquin Suppresses the PI3K-mTOR Signaling Pathway to Inhibit T Helper Cell Differentiation and Conversion of Treg to Tfr Cells

29. The Role of Eif6 in Skeletal Muscle Homeostasis Revealed by Endurance Training Co-expression Networks

31. Molecular Integration of Incretin and Glucocorticoid Action Reverses Immunometabolic Dysfunction and Obesity

35. N-acyl Taurines and Acylcarnitines Cause an Imbalance in Insulin Synthesis and Secretion Provoking β Cell Dysfunction in Type 2 Diabetes

38. Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic Disease

41. Calcineurin Links Mitochondrial Elongation with Energy Metabolism

43. MIM-Induced Membrane Bending Promotes Dendritic Spine Initiation

44. The German Mouse Clinic – Running an Open Access Platform

45. Simulation of Finnish Population History, Guided by Empirical Genetic Data, to Assess Power of Rare-Variant Tests in Finland

46. Mitochondrial Dysfunction and Decrease in Body Weight of a Transgenic Knock-in Mouse Model for TDP-43

48. Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome

50. An ENU Mutagenesis-Derived Mouse Model with a Dominant Jak1 Mutation Resembling Phenotypes of Systemic Autoimmune Disease

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