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W Krone

Showing results (151-160 of 235) with videos related to

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Human Genetics|July 1, 1988
Increased amounts of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TS)C Neidlinger, G Assum, W Krone, et al.
Human Genetics|June 10, 1977
Frequency of Ag-stained nucleolus organizer regions in the acrocentric chromosomes of manA V Mikelsaar, M Schmid, W Krone, et al.
The Journal of Investigative Dermatology|March 1, 1997
Post-transcriptional regulation of neurofibromin level in cultured human melanocytes in response to growth factorsJ Griesser, D Kaufmann, B Maier, et al.
The New England Journal of Medicine|October 1, 1998
Obesity associated with a mutation in a genetic regulator of adipocyte differentiationM Ristow, D Müller-Wieland, A Pfeiffer, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 20, 2006
Association of the promoter polymorphism -232C/G of the phosphoenolpyruvate carboxykinase gene (PCK1) with Type 2 diabetes mellitusI Gouni-Berthold, E Giannakidou, M Faust, et al.
Endocrinology|November 1, 1976
Concentration of cyclic AMP in rat liver as a function of the insulin/glucagon ratio in blood under standardized physiological conditionsH J Seitz, M J Müller, P Nordmeyer, et al.
Nuklearmedizin. Nuclear Medicine|May 7, 2002
[Assessment of endocrine disorders of the hypothalamic-pituitary axis by nuclear medicine techniques]M Schmidt, F Jockenhövel, P Theissen, et al.
Physiology (Bethesda, Md.)|May 13, 2005
Transgenic and knockout mice in diabetes research: novel insights into pathophysiology, limitations, and perspectivesL Plum, F T Wunderlich, S Baudler, et al.
Human Molecular Genetics|August 1, 1995
On unequal allelic expression of the neurofibromin gene in neurofibromatosis type 1S Hoffmeyer, G Assum, J Griesser, et al.
Biochemical and Biophysical Research Communications|September 25, 1995
Reduced neurofibromin content but normal GAP activity in a patient with neurofibromatosis type 1 caused by a five base pair duplication in exon 12b of the NF1 geneA Böddrich, J Griesser, D Horn, et al.
Pageof 24

Showing results (151-160 of 235) with videos related to

Sort By:
Pageof 24
Human Genetics|July 1, 1988
Increased amounts of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TS)C Neidlinger, G Assum, W Krone, et al.
Human Genetics|June 10, 1977
Frequency of Ag-stained nucleolus organizer regions in the acrocentric chromosomes of manA V Mikelsaar, M Schmid, W Krone, et al.
The Journal of Investigative Dermatology|March 1, 1997
Post-transcriptional regulation of neurofibromin level in cultured human melanocytes in response to growth factorsJ Griesser, D Kaufmann, B Maier, et al.
The New England Journal of Medicine|October 1, 1998
Obesity associated with a mutation in a genetic regulator of adipocyte differentiationM Ristow, D Müller-Wieland, A Pfeiffer, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 20, 2006
Association of the promoter polymorphism -232C/G of the phosphoenolpyruvate carboxykinase gene (PCK1) with Type 2 diabetes mellitusI Gouni-Berthold, E Giannakidou, M Faust, et al.
Endocrinology|November 1, 1976
Concentration of cyclic AMP in rat liver as a function of the insulin/glucagon ratio in blood under standardized physiological conditionsH J Seitz, M J Müller, P Nordmeyer, et al.
Nuklearmedizin. Nuclear Medicine|May 7, 2002
[Assessment of endocrine disorders of the hypothalamic-pituitary axis by nuclear medicine techniques]M Schmidt, F Jockenhövel, P Theissen, et al.
Physiology (Bethesda, Md.)|May 13, 2005
Transgenic and knockout mice in diabetes research: novel insights into pathophysiology, limitations, and perspectivesL Plum, F T Wunderlich, S Baudler, et al.
Human Molecular Genetics|August 1, 1995
On unequal allelic expression of the neurofibromin gene in neurofibromatosis type 1S Hoffmeyer, G Assum, J Griesser, et al.
Biochemical and Biophysical Research Communications|September 25, 1995
Reduced neurofibromin content but normal GAP activity in a patient with neurofibromatosis type 1 caused by a five base pair duplication in exon 12b of the NF1 geneA Böddrich, J Griesser, D Horn, et al.
Pageof 24