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S Rondot

Showing results (1-10 of 10) with videos related to

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Nature Biotechnology|January 3, 2001
A helper phage to improve single-chain antibody presentation in phage displayS Rondot, J Koch, F Breitling, et al.
Journal of Microscopy|November 25, 2016
Effect of nanoclay concentration level on the electrical properties of polypropylene under electron irradiation in a SEML Ben Ammar, S Fakhfakh, O Jbara, et al.
Science (New York, N.Y.)|March 25, 1994
Following ion diffusion in solutionS Rondot, J Cazaux, O Aaboubi, et al.
Deutsche Medizinische Wochenschrift (1946)|September 15, 2011
[Hereditary variants of primary hyperparathyroidism--MEN1, MEN2, HPT-JT, FHH, FIHPT]K Frank-Raue, G Leidig-Bruckner, A Lorenz, et al.
European Journal of Endocrinology|July 27, 2006
Long-term outcome in 46 gene carriers of hereditary medullary thyroid carcinoma after prophylactic thyroidectomy: impact of individual RET genotypeK Frank-Raue, H Buhr, H Dralle, et al.
Thyroid : Official Journal of the American Thyroid Association|December 17, 2005
Primary hyperparathyroidism as the leading symptom in a patient with a Y791F RET mutationH Vierhapper, S Rondot, E Schulze, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 17, 2009
New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumourK Frank-Raue, J Döhring, G Scheumann, et al.
Journal of Molecular Biology|June 26, 1998
Epitopes fused to F-pilin are incorporated into functional recombinant piliS Rondot, K G Anthony, S Dübel, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
Mutational spectrum of the steroid 21-hydroxylase gene in Austria: identification of a novel missense mutationS M Baumgartner-Parzer, E Schulze, W Waldhäusl, et al.
Deutsche Medizinische Wochenschrift (1946)|September 26, 2003
[Hereditary medullary thyroid carcinoma--genotype-phenotype characterization]K Frank-Raue, C Heimbach, S Rondot, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Nature Biotechnology|January 3, 2001
A helper phage to improve single-chain antibody presentation in phage displayS Rondot, J Koch, F Breitling, et al.
Journal of Microscopy|November 25, 2016
Effect of nanoclay concentration level on the electrical properties of polypropylene under electron irradiation in a SEML Ben Ammar, S Fakhfakh, O Jbara, et al.
Science (New York, N.Y.)|March 25, 1994
Following ion diffusion in solutionS Rondot, J Cazaux, O Aaboubi, et al.
Deutsche Medizinische Wochenschrift (1946)|September 15, 2011
[Hereditary variants of primary hyperparathyroidism--MEN1, MEN2, HPT-JT, FHH, FIHPT]K Frank-Raue, G Leidig-Bruckner, A Lorenz, et al.
European Journal of Endocrinology|July 27, 2006
Long-term outcome in 46 gene carriers of hereditary medullary thyroid carcinoma after prophylactic thyroidectomy: impact of individual RET genotypeK Frank-Raue, H Buhr, H Dralle, et al.
Thyroid : Official Journal of the American Thyroid Association|December 17, 2005
Primary hyperparathyroidism as the leading symptom in a patient with a Y791F RET mutationH Vierhapper, S Rondot, E Schulze, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 17, 2009
New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumourK Frank-Raue, J Döhring, G Scheumann, et al.
Journal of Molecular Biology|June 26, 1998
Epitopes fused to F-pilin are incorporated into functional recombinant piliS Rondot, K G Anthony, S Dübel, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
Mutational spectrum of the steroid 21-hydroxylase gene in Austria: identification of a novel missense mutationS M Baumgartner-Parzer, E Schulze, W Waldhäusl, et al.
Deutsche Medizinische Wochenschrift (1946)|September 26, 2003
[Hereditary medullary thyroid carcinoma--genotype-phenotype characterization]K Frank-Raue, C Heimbach, S Rondot, et al.
Pageof 1