276 results on '"Kruse, Roland"'
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2. Arctic Coastline Erosion: Novel Experimental Avenues Help Understand Its Response To A Changing Climate
3. Tumorassoziierte Genodermatosen
4. Cancer-Associated Genodermatoses
5. Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata
6. Manfred Schroeder and Acoustical Impedance
7. On the anisotropy of skeletal muscle tissue under compression
8. Tumorassoziierte Genodermatosen
9. An omnidirectional loudspeaker based on a ring-radiator
10. On a staggered iFEM approach to account for friction in compression testing of soft materials
11. A phase-field model for ductile fracture at finite strains and its experimental verification
12. Experimental Analysis of Residual Stresses in CFRPs through Hole-Drilling Method: The Role of Stacking Sequence, Thickness, and Defects
13. Compressive properties of passive skeletal muscle—The impact of precise sample geometry on parameter identification in inverse finite element analysis
14. The influence of environmental conditions on estimation of source distance and height using a single vertical array
15. Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
16. Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
17. Manfred Schroeder and Acoustical Impedance
18. A Novel Missense Mutation in the DNA Mismatch Repair Gene hMLH1 Present among East Asians but Not among Europeans
19. Effect and minimization of errors in in situ ground impedance measurements
20. Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair
21. Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26
22. Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease
23. Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia
24. Tumorassoziierte Genodermatosen
25. Familial aggregation of alopecia areata
26. Neues zu genetischen Hautkrankheiten
27. Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified
28. Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
29. Hautkrankheiten und genetische Instabilität Teil II: Genodermatosen mit genetischer Instabilität: Teil II: Genodermatosen mit genetischer Instabilität
30. Hautkrankheiten und genetische Instabilität Teil I: Grundlagen genetischer Instabilität: Teil I: Grundlagen genetischer Instabilität
31. WAARDENBURG SYNDROME TYPE I WITH HETEROCHROMIA IRIDIS AND CIRCUMSCRIBED HYPOPIGMENTATION OF THE SKIN
32. Loss of the PLA2G2A gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAP
33. Richner–Hanhart Syndrome Detected by Expanded Newborn Screening
34. Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?
35. Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria
36. A gene for the universal congenital alopecia maps to chromosome 8p21-22
37. Painful rash and swelling of the limbs after recurrent infections in a teenager: Polyarteritis nodosa
38. Thelalgia in Man: Successful Treatment With Botulinum Toxin
39. Birt-Hogg-Dubé Syndrome: Germline Mutation in the (C)8 Mononucleotide Tract of the BHD Gene in a German Patient
40. DNA mismatch repair and the significance of a sebaceous skin tumor for visceral cancer prevention
41. Frequency of Microsatellite Instability in Unselected Sebaceous Gland Neoplasias and Hyperplasias
42. Intolerance Reactions due to the Selective Cyclooxygenase Type II Inhibitors Rofecoxib and Celecoxib: Results of Oral Provocation Tests in Patients with NSAID Hypersensitivity
43. "Second Hit" in Sebaceous Tumors from Muir-Torre Patients with Germline Mutations in MSH2: Allele Loss is Not the Preferred Mode of Inactivation
44. Settling the Score on Hairless
45. Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
46. Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue
47. A Novel Germline Mutation in the hMLH1 DNA Mismatch Repair Gene in a Patient with an Isolated Cystic Sebaceous Tumor
48. Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2
49. Towards multiscale modeling of the interaction between transport and fracture in concrete
50. Variant 1859G [right arrow] A (Arg620Gln) of the 'Hairless' Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
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