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

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

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

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

6. GPR101 loss promotes insulin resistance and diet-induced obesity risk

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

10. Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice

11. Costs of Implementing Quality in Research Practice

12. Creld1 regulates myocardial development and function

13. In-depth phenotyping reveals common and novel disease symptoms in a hemizygous knock-in mouse model (Mut-ko/ki) of mut-type methylmalonic aciduria

14. A mouse model for intellectual disability caused by mutations in the X-linked 2′‑O‑methyltransferase Ftsj1 gene

15. Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice

16. Noncanonical thyroid hormone signaling mediates cardiometabolic effects in vivo

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

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

21. Cognitive impairment and autistic-like behaviour in SAPAP4-deficient mice

22. Costs of Implementing Quality in Research Practice

24. Offspring born to influenza A virus infected pregnant mice show increased vulnerability to viral and bacterial infections in early life

25. Knockout of the Complex III subunit Uqcrh causes bioenergetic impairment and cardiac contractile dysfunction

27. Mouse Genetics and Metabolic Mouse Phenotyping

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

30. Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in mice

31. Mutations within the cGMP-binding domain of CNGA1 causing autosomal recessive retinitis pigmentosa in human and animal model

33. Modeling hepatic osteodystrophy in Abcb4 deficient mice

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

35. Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

37. Deep Phenotyping and Lifetime Trajectories Reveal Limited Effects of Longevity Regulators on the Aging Process in C57BL/6J Mice

39. Immune modulation by Fas ligand reverse signaling: lymphocyte proliferation is attenuated by the intracellular Fas ligand domain

41. MiR-34a deficiency accelerates medulloblastoma formation in vivo

42. Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project

43. Innovations in phenotyping of mouse models in the German Mouse Clinic

44. Long-term proteasomal inhibition in transgenic mice by UBB+1 expression results in dysfunction of central respiration control reminiscent of brainstem neuropathology in Alzheimer patients

46. Rapamycin extends murine lifespan but has limited effects on aging

48. Systemic First-Line Phenotyping

49. Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines

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