626 results on '"Rathkolb, Birgit"'
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2. Knockout mouse models as a resource for the study of rare diseases
3. Knockout of the Complex III subunit Uqcrh causes bioenergetic impairment and cardiac contractile dysfunction
4. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
5. Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain
6. AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease
7. Maternal hyperglycemia induces alterations in hepatic amino acid, glucose and lipid metabolism of neonatal offspring: Multi-omics insights from a diabetic pig model
8. Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
9. Glutathione peroxidase 4 and vitamin E control reticulocyte maturation, stress erythropoiesis and iron homeostasis.
10. GPR101 loss promotes insulin resistance and diet-induced obesity risk
11. Co-expression of prepulse inhibition and schizophrenia genes in the mouse and human brain
12. New C3H KitN824K/WT cancer mouse model develops late-onset malignant mammary tumors with high penetrance
13. Dietary intervention improves health metrics and life expectancy of the genetically obese Titan mouse
14. Monitoring longitudinal disease progression in a novel murine Kit tumor model using high-field MRI
15. Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice
16. Comparative Phenotyping of Mice Reveals Canonical and Noncanonical Physiological Functions of TRα and TRβ.
17. Identification of genetic elements in metabolism by high-throughput mouse phenotyping
18. Characterization of liver-pancreas crosstalk following beta-cell loss reveals a role for the molybdenum cofactor in beta-cell regeneration
19. eATP/P2X7R axis drives nanoparticle induced neutrophil recruitment in the pulmonary microcirculation
20. A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse
21. Examining the liver–pancreas crosstalk reveals a role for the molybdenum cofactor in β-cell regeneration.
22. Functional changes of the liver in the absence of growth hormone (GH) action – Proteomic and metabolomic insights from a GH receptor deficient pig model
23. In-depth phenotyping reveals common and novel disease symptoms in a hemizygous knock-in mouse model (Mut-ko/ki) of mut-type methylmalonic aciduria
24. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
25. Comparative phenotyping of mice reveals canonical and noncanonical physiological functions of TRα and TRβ
26. Congenic expression of poly-GA but not poly-PR in mice triggers selective neuron loss and interferon responses found in C9orf72 ALS
27. A mouse model for intellectual disability caused by mutations in the X-linked 2′‑O‑methyltransferase Ftsj1 gene
28. Multi-omics insights into functional alterations of the liver in insulin-deficient diabetes mellitus
29. Dilution correction for dynamically influenced urinary analyte data
30. Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice
31. Growth hormone receptor-deficient pigs resemble the pathophysiology of human Laron syndrome and reveal altered activation of signaling cascades in the liver
32. The Role of Fibroblast Growth Factor-Binding Protein 1 in Skin Carcinogenesis and Inflammation
33. Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria
34. Bezafibrate ameliorates diabetes via reduced steatosis and improved hepatic insulin sensitivity in diabetic TallyHo mice
35. PAX6 mutation alters circadian rhythm and β cell function in mice without affecting glucose tolerance
36. Irp2 regulates insulin production through iron-mediated Cdkal1-catalyzed tRNA modification
37. LncRNA U90926 is dispensable for the development of obesity‐associated phenotypes in vivo.
38. TXNIP overexpression in mice enhances streptozotocin-induced diabetes severity
39. Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
40. Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria
41. Implication ofFOXD2dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
42. Knockout of the Complex III subunit Uqcrh causes bioenergetic impairment and cardiac contractile dysfunction
43. Dietary digestible carbohydrates are associated with higher prevalence of asthma in humans and with aggravated lung allergic inflammation in mice
44. Identifying causal serum protein–cardiometabolic trait relationships using whole genome sequencing
45. A novel biological function of soluble biglycan: Induction of erythropoietin production and polycythemia
46. Cardioprotection and lifespan extension by the natural polyamine spermidine
47. Serum Response Factor (SRF) Ablation Interferes with Acute Stress-Associated Immediate and Long-Term Coping Mechanisms
48. Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation
49. Mouse Genetics and Metabolic Mouse Phenotyping
50. The German Mouse Clinic – Running an Open Access Platform
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