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A Ballabio

Showing results (41-50 of 200) with videos related to

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Genomics|October 1, 1990
Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this regionA Ballabio, B Bardoni, S Guioli, et al.
Trends in Genetics : TIG|February 1, 1997
DRES search engine: of flies, men and ESTsA Guffanti, S Banfi, G Simon, et al.
European Journal of Pediatrics|September 1, 1984
Steroid sulphatase deficiency and hypogonadismG Andria, A Ballabio, G Parenti, et al.
Human Molecular Genetics|March 7, 2001
WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor networkS Cairo, G Merla, F Urbinati, et al.
Bioinformatics (Oxford, England)|March 25, 1999
TargetFinder: searching annotated sequence databases for target genes of transcription factorsG Lavorgna, A Guffanti, G Borsani, et al.
Glycobiology|November 24, 1999
Expression of a novel human sialidase encoded by the NEU2 geneE Monti, A Preti, C Nesti, et al.
FEBS Letters|November 24, 1986
On the primary site of control in the spontaneous development of small-intestinal sucrase-isomaltase after birthG Sebastio, W Hunziker, A Ballabio, et al.
Genomics|April 7, 1999
Cloning and characterization of NEU2, a human gene homologous to rodent soluble sialidasesE Monti, A Preti, E Rossi, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Steroid sulphatase deficiency is present in patients with the syndrome 'ichthyosis and male hypogonadism' and with 'Rud syndrome'G Andria, A Ballabio, G Parenti, et al.
Human Genetics|January 1, 1985
Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiencyA Ballabio, G Parenti, E Napolitano, et al.
Pageof 20

Showing results (41-50 of 200) with videos related to

Sort By:
Pageof 20
Genomics|October 1, 1990
Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this regionA Ballabio, B Bardoni, S Guioli, et al.
Trends in Genetics : TIG|February 1, 1997
DRES search engine: of flies, men and ESTsA Guffanti, S Banfi, G Simon, et al.
European Journal of Pediatrics|September 1, 1984
Steroid sulphatase deficiency and hypogonadismG Andria, A Ballabio, G Parenti, et al.
Human Molecular Genetics|March 7, 2001
WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor networkS Cairo, G Merla, F Urbinati, et al.
Bioinformatics (Oxford, England)|March 25, 1999
TargetFinder: searching annotated sequence databases for target genes of transcription factorsG Lavorgna, A Guffanti, G Borsani, et al.
Glycobiology|November 24, 1999
Expression of a novel human sialidase encoded by the NEU2 geneE Monti, A Preti, C Nesti, et al.
FEBS Letters|November 24, 1986
On the primary site of control in the spontaneous development of small-intestinal sucrase-isomaltase after birthG Sebastio, W Hunziker, A Ballabio, et al.
Genomics|April 7, 1999
Cloning and characterization of NEU2, a human gene homologous to rodent soluble sialidasesE Monti, A Preti, E Rossi, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Steroid sulphatase deficiency is present in patients with the syndrome 'ichthyosis and male hypogonadism' and with 'Rud syndrome'G Andria, A Ballabio, G Parenti, et al.
Human Genetics|January 1, 1985
Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiencyA Ballabio, G Parenti, E Napolitano, et al.
Pageof 20