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P Di Natale

Showing results (61-70 of 72) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1993
Biochemical diagnosis of mucopolysaccharidoses: experience of 297 diagnoses in a 15-year period (1977-1991)P Di Natale, T Annella, A Daniele, et al.
Biochimica Et Biophysica Acta|March 23, 2000
Heparan N-sulfatase gene: two novel mutations and transient expression of 15 defectsS Esposito, N Balzano, A Daniele, et al.
European Journal of Cell Biology|August 1, 1997
Echistatin induces decrease of pp125FAK phosphorylation, disassembly of actin cytoskeleton and focal adhesions, and detachment of fibronectin-adherent melanoma cellsN Staiano, C Garbi, C Squillacioti, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Bone marrow transplantation in Hunter syndromeG V Coppa, O Gabrielli, L Zampini, et al.
European Journal of Biochemistry|August 10, 2000
Echistatin inhibits pp125FAK autophosphorylation, paxillin phosphorylation and pp125FAK-paxillin interaction in fibronectin-adherent melanoma cellsR Della Morte, C Squillacioti, C Garbi, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
Journal of Inherited Metabolic Disease|September 19, 2007
Effect of 'attenuated' mutations in mucopolysaccharidosis IVA on molecular phenotypes of N-acetylgalactosamine-6-sulfate sulfataseA M Montaño, K Sukegawa, Z Kato, et al.
Genomics|January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndromeG Palmieri, V Capra, G Romano, et al.
Journal of Medical Genetics|June 1, 1991
Sanfilippo syndrome type D in two adolescent sistersL Siciliano, A Fiumara, L Pavone, et al.
Gene Therapy|May 1, 1997
In vitro correction of iduronate-2-sulfatase deficiency by adenovirus-mediated gene transferC Di Francesco, C Cracco, R Tomanin, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
Journal of Inherited Metabolic Disease|January 1, 1993
Biochemical diagnosis of mucopolysaccharidoses: experience of 297 diagnoses in a 15-year period (1977-1991)P Di Natale, T Annella, A Daniele, et al.
Biochimica Et Biophysica Acta|March 23, 2000
Heparan N-sulfatase gene: two novel mutations and transient expression of 15 defectsS Esposito, N Balzano, A Daniele, et al.
European Journal of Cell Biology|August 1, 1997
Echistatin induces decrease of pp125FAK phosphorylation, disassembly of actin cytoskeleton and focal adhesions, and detachment of fibronectin-adherent melanoma cellsN Staiano, C Garbi, C Squillacioti, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Bone marrow transplantation in Hunter syndromeG V Coppa, O Gabrielli, L Zampini, et al.
European Journal of Biochemistry|August 10, 2000
Echistatin inhibits pp125FAK autophosphorylation, paxillin phosphorylation and pp125FAK-paxillin interaction in fibronectin-adherent melanoma cellsR Della Morte, C Squillacioti, C Garbi, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
Journal of Inherited Metabolic Disease|September 19, 2007
Effect of 'attenuated' mutations in mucopolysaccharidosis IVA on molecular phenotypes of N-acetylgalactosamine-6-sulfate sulfataseA M Montaño, K Sukegawa, Z Kato, et al.
Genomics|January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndromeG Palmieri, V Capra, G Romano, et al.
Journal of Medical Genetics|June 1, 1991
Sanfilippo syndrome type D in two adolescent sistersL Siciliano, A Fiumara, L Pavone, et al.
Gene Therapy|May 1, 1997
In vitro correction of iduronate-2-sulfatase deficiency by adenovirus-mediated gene transferC Di Francesco, C Cracco, R Tomanin, et al.
Pageof 8