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1. Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disorders

3. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

4. Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2

5. Spinocerebellar ataxia type 6

6. Latitude-correlated genetic polymorphisms: selection or gene flow?

7. CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci

8. Human succinic semialdehyde dehydrogenase. Molecular cloning and chromosomal localization

9. Allele and haplotype frequency distribution of the EcoRI, RsaI, and MspI COL1A2 RFLPs among various human populations

10. Subject Index Vol. 100, 2003

11. The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus

12. HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds

13. The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds

14. Contents Vol. 100, 2003

15. The AXH module: an independently folded domain common to ataxin-1 and HBP1

16. Complete Loss of P/Q Calcium Channel Activity Caused by a CACNA1A Missense Mutation Carried by Patients with Episodic Ataxia Type 2

17. Autosomal dominant pure cerebellar ataxia: Neurological and genetic study

18. Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations

19. The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias

20. Genetic fitness in Huntington's disease and spinocerebellar ataxia 1: A population genetics model for CAG repeat expansions

21. Variation of the 3'RR1 HS1.2 Enhancer and Its Genomic Context.

22. DNA Damage Stress Response and Follicle Activation: Signaling Routes of Mammalian Ovarian Reserve.

23. Signs of continental ancestry in urban populations of Peru through autosomal STR loci and mitochondrial DNA typing.

24. Enlarging the gene-geography of Europe and the Mediterranean area to STR loci of common forensic use: longitudinal and latitudinal frequency gradients.

25. Alcohol use disorder and GABA B receptor gene polymorphisms in an Italian sample: haplotype frequencies, linkage disequilibrium and association studies.

26. Spatially Explicit Models to Investigate Geographic Patterns in the Distribution of Forensic STRs: Application to the North-Eastern Mediterranean.

27. Toxic effects of expanded ataxin-1 involve mechanical instability of the nuclear membrane.

28. Dramatically different levels of Cacna1a gene expression between pre-weaning wild type and leaner mice.

29. Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia.

30. Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2.

31. The AXH module: an independently folded domain common to ataxin-1 and HBP1.

32. Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disorders.

33. Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro.

34. Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.

35. Latitude-correlated genetic polymorphisms: selection or gene flow?

36. Are (CTG)n expansions at the SCA8 locus rare polymorphisms?

37. A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome.

38. CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci.

39. Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1.

40. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.

41. Population variation analysis at nine loci containing expressed trinucleotide repeats.

42. Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homology.

43. Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13.

44. Human succinic semialdehyde dehydrogenase. Molecular cloning and chromosomal localization.

45. Construction of a YAC contig covering human chromosome 6p22.

46. Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions.

47. Ordering of 44 genetic markers in the 6p22 cytogenetic band.

48. Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations.

49. Allele and haplotype frequency distribution of the EcoRI, RsaI, and MspI COL1A2 RFLPs among various human populations.

50. The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias.

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