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Agne Larsson

Showing results (11-20 of 18) with videos related to

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Human Mutation|November 25, 2003
Diagnostics in patients with glutathione synthetase deficiency but without mutations in the exons of the GSS geneRuna Njålsson, Katarina Carlsson, Andreas Winkler, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 2002
Sex-typed toy play behavior correlates with the degree of prenatal androgen exposure assessed by CYP21 genotype in girls with congenital adrenal hyperplasiaAnna Nordenström, Anna Servin, Gunilla Bohlin, et al.
Ophthalmology|December 30, 2008
Rod-cone dystrophy with maculopathy in genetic glutathione synthetase deficiency: a morphologic and electrophysiologic studyMarie S I Burstedt, Ellinor Ristoff, Agne Larsson, et al.
Drug and Alcohol Dependence|April 1, 2008
Long-term outcomes of adolescents treated for substance misusePeter Larm, Sheilagh Hodgins, Agne Larsson, et al.
Human Genetics|February 18, 2005
Genotype, enzyme activity, glutathione level, and clinical phenotype in patients with glutathione synthetase deficiencyRuna Njålsson, Ellinor Ristoff, Katarina Carlsson, et al.
Human Genetics|April 6, 2002
Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidismBodil Edman Ahlbom, Muhammad Yaqoob, Peter Gustavsson, et al.
The Biochemical Journal|April 2, 2004
Human hereditary glutathione synthetase deficiency: kinetic properties of mutant enzymesRuna Njålsson, Katarina Carlsson, Vikas Bhansali, et al.
Biochemical and Biophysical Research Communications|August 2, 2011
Glutathione is essential for early embryogenesis--analysis of a glutathione synthetase knockout mouseAndreas Winkler, Runa Njålsson, Katarina Carlsson, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Human Mutation|November 25, 2003
Diagnostics in patients with glutathione synthetase deficiency but without mutations in the exons of the GSS geneRuna Njålsson, Katarina Carlsson, Andreas Winkler, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 2002
Sex-typed toy play behavior correlates with the degree of prenatal androgen exposure assessed by CYP21 genotype in girls with congenital adrenal hyperplasiaAnna Nordenström, Anna Servin, Gunilla Bohlin, et al.
Ophthalmology|December 30, 2008
Rod-cone dystrophy with maculopathy in genetic glutathione synthetase deficiency: a morphologic and electrophysiologic studyMarie S I Burstedt, Ellinor Ristoff, Agne Larsson, et al.
Drug and Alcohol Dependence|April 1, 2008
Long-term outcomes of adolescents treated for substance misusePeter Larm, Sheilagh Hodgins, Agne Larsson, et al.
Human Genetics|February 18, 2005
Genotype, enzyme activity, glutathione level, and clinical phenotype in patients with glutathione synthetase deficiencyRuna Njålsson, Ellinor Ristoff, Katarina Carlsson, et al.
Human Genetics|April 6, 2002
Linkage analysis identifies the thyroglobulin gene region as a major locus for familial congenital hypothyroidismBodil Edman Ahlbom, Muhammad Yaqoob, Peter Gustavsson, et al.
The Biochemical Journal|April 2, 2004
Human hereditary glutathione synthetase deficiency: kinetic properties of mutant enzymesRuna Njålsson, Katarina Carlsson, Vikas Bhansali, et al.
Biochemical and Biophysical Research Communications|August 2, 2011
Glutathione is essential for early embryogenesis--analysis of a glutathione synthetase knockout mouseAndreas Winkler, Runa Njålsson, Katarina Carlsson, et al.
Pageof 2