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A Wedell

Showing results (21-30 of 54) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 1, 1992
Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutationsA Wedell, E M Ritzén, B Haglund-Stengler, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1994
Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestationA Wedell, A Thilén, E M Ritzén, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 1994
Regulation of human insulin receptor RNA splicing in vivoS Norgren, J Zierath, A Wedell, et al.
Lakartidningen|January 31, 1998
[Prenatal diagnosis and treatment of adrenogenital syndrome. Prevent virilization of female fetuses]S Lajic, T H Bui, M Holst, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
CYP21 mutations in simple virilizing congenital adrenal hyperplasiaS Lajić, T Robins, N Krone, et al.
The Journal of Clinical Endocrinology and Metabolism|April 13, 1999
Failure of cortisone acetate treatment in congenital adrenal hyperplasia because of defective 11beta-hydroxysteroid dehydrogenase reductase activityA Nordenström, C Marcus, M Axelson, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasiaS Lajic, A Wedell, T H Bui, et al.
Human Genetics|June 1, 1997
A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interactionS Lajic, A Levo, A Nikoshkov, et al.
Advances in Experimental Medicine and Biology|January 1, 1993
Molecular genetics of NIDDM and the genes for insulin and insulin receptorH Luthman, I Delin, A Glaser, et al.
Clinical Endocrinology|August 6, 1999
No overrepresentation of congenital adrenal hyperplasia in patients with adrenocortical tumoursM Kjellman, M Holst, M Bäckdahl, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1992
Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutationsA Wedell, E M Ritzén, B Haglund-Stengler, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1994
Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestationA Wedell, A Thilén, E M Ritzén, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 1994
Regulation of human insulin receptor RNA splicing in vivoS Norgren, J Zierath, A Wedell, et al.
Lakartidningen|January 31, 1998
[Prenatal diagnosis and treatment of adrenogenital syndrome. Prevent virilization of female fetuses]S Lajic, T H Bui, M Holst, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
CYP21 mutations in simple virilizing congenital adrenal hyperplasiaS Lajić, T Robins, N Krone, et al.
The Journal of Clinical Endocrinology and Metabolism|April 13, 1999
Failure of cortisone acetate treatment in congenital adrenal hyperplasia because of defective 11beta-hydroxysteroid dehydrogenase reductase activityA Nordenström, C Marcus, M Axelson, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasiaS Lajic, A Wedell, T H Bui, et al.
Human Genetics|June 1, 1997
A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interactionS Lajic, A Levo, A Nikoshkov, et al.
Advances in Experimental Medicine and Biology|January 1, 1993
Molecular genetics of NIDDM and the genes for insulin and insulin receptorH Luthman, I Delin, A Glaser, et al.
Clinical Endocrinology|August 6, 1999
No overrepresentation of congenital adrenal hyperplasia in patients with adrenocortical tumoursM Kjellman, M Holst, M Bäckdahl, et al.
Pageof 6