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8. The DNA sequence of human chromosome 21

12. Amyloid-PET and (18)F-FDG-PET in the diagnostic investigation of Alzheimer's disease and other dementias

15. Contributors

19. Genetics of Parkinson's Disease

22. The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts

26. The need for standardization and larger clinical studies in emerging indications to [18F]FDG PET brain PET: autoimmune encephalitis

27. Recommendations of the 2006 Human Variome Project meeting

28. Initial sequencing and analysis of the human genome

30. MutationView: A Graphical Database System for Mutations and Polymorphisms in Human Disease Genes

35. Systematic gene identification based on the genomic sequence of human chromosome 21

36. Evolution of the human immunoglobulin [V.sub.[Kappa]] gene locus

38. Isolation and characterization of a novel gene encoding a protein with UBA and SH3 domains on Human Chromosome 21q22.3; its exclusion for the autosomal recessive deafness locus, DFNB10

40. A novel mutation mechanism, insertion of [Beta]-satellite repeats, in a transmembrane protease gene causes the autosomal recessive deafness DFNB10

42. Multicenter standardized FDG-PET diagnosis of mild cognitive impairment, Alzheimer's disease and other dementias

44. 18F-FDG kinetics in locally advanced breast cancer: correlation with tumor blood flow and changes in response to neoadjuvant chemotherapy

45. Integrative Annotation of 21,037 Human Genes\ud Validated by Full-Length cDNA Clones

46. SNM practice guideline for dopamine transporter imaging with 123I-ioflupane SPECT 1.0

47. A prioritization analysis of disease association by data-mining of functional annotation of human genes

48. Effets de l’âge et du genre sur la perfusion cérébrale régionale étudiée par deux méthodes d’analyse statistique voxel-par-voxel

49. Initial sequencing and analysis of the human genome

50. The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts.

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