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1. Distinct Phenotypes of Shank2 Mouse Models Reflect Neuropsychiatric Spectrum Disorders of Human Patients With SHANK2 Variants

2. Fetal mesenchymal stromal cells differentiating towards chondrocytes acquire a gene expression profile resembling human growth plate cartilage.

3. The homeobox transcription factor HOXA9 is a regulator of SHOX in U2OS cells and chicken micromass cultures.

4. Alternative splicing and nonsense-mediated RNA decay contribute to the regulation of SHOX expression.

5. Evidence for a role of srGAP3 in the positioning of commissural axons within the ventrolateral funiculus of the mouse spinal cord.

6. Serotonin type 3 receptor subunit gene polymorphisms associated with psychosomatic symptoms in irritable bowel syndrome: A multicenter retrospective study

7. Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in

8. Distinct Phenotypes of

9. The Human Serotonin Type 3 Receptor Gene (HTR3A-E) Allelic Variant Database

10. Lesch-Nyhan Variant

11. Leukemia, Chronic Lymphocytic

12. Limbic Epilepsy

13. Undescended Testis

14. Legg-Calvé-Perthes' Disease

15. Lattice Corneal Dystrophy Type I

16. Lewy Body Dementia

17. Usher Syndrome

18. Lactose Intolerance

19. Legasthenia

20. Lesion-associated Partial Epilepsies

21. Linear IgA Bullous Dermatosis

22. Leukocyte Adhesion Deficiency Syndromes

23. Urolithiasis, Calcium Phosphate

24. Léri-Weill Dyschondrosteosis

25. Limb Girdle Muscular Dystrophy, Autosomal Dominant Type 1B

26. Launois-Bensaude Syndrome

27. Lobular Glomerulonephritis

28. Limb Girdle Muscular Dystrophy Type 2G

29. Uremia

30. Liver Cancer

31. Lewy Body Variant of Alzheimer’s Disease

32. Ureteral Obstruction

33. Uridine Monophosphate Hydrolase-1 Deficiency

34. β-UP

35. Uveal Melanoma

36. Late Onset Immunoglobulin Deficiency

37. Lymphedema and Ptosis

38. Late-Onset Multiple Carboxylase Deficiency

39. Lenarduzzi-Cacchi-Ricci Disease

40. Lipogranuloma of the Mesentery

41. Lyell’s Syndrome

42. Lysosomal Alpha-D-Mannosidase Deficiency

43. Leucocytoclastic Angiitis

44. Lattice Corneal Dystrophy Type I and Variants

45. Liver Fibrosis

46. Urate Gout

47. Lambert Eaton Myasthenic Syndrome

48. Lung Disease, Environmental

49. LGMD 2B

50. Leukoencephalopathy with Vanishing White Matter

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