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J Pohlenz

Showing results (81-90 of 115) with videos related to

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Human Mutation|January 1, 1996
New point mutation (R243W) in the hormone binding domain of the c-erbA beta 1 gene in a family with generalized resistance to thyroid hormoneJ Pohlenz, W Schönberger, H Wemme, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 29, 2006
Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literatureC-J Partsch, F G Riepe, N Krone, et al.
Endocrinology|September 1, 1997
Thyrotropin regulation by thyroid hormone in thyroid hormone receptor beta-deficient miceR E Weiss, D Forrest, J Pohlenz, et al.
DTW. Deutsche Tierarztliche Wochenschrift|February 24, 1999
Total serum bile acid concentrations in dairy cows with fatty liver and liver failureJ Rehage, K Qualmann, C Meier, et al.
Archives of Virology. Supplementum|January 1, 1993
Distribution of cytopathogenic and noncytopathogenic bovine virus diarrhea virus in tissues from a calf with experimentally induced mucosal disease using antigenic and genetic markersI Greiser-Wilke, E Liebler, L Haas, et al.
Berliner Und Munchener Tierarztliche Wochenschrift|November 1, 1992
[Use of an immunoenzyme histochemical method for the improvement of the etiologic diagnosis of Aujeszky's disease in swine]P Wohlsein, A Klimke, G Matschullat, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 21, 2013
Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutationsK Altmann, P Hermanns, R Mühlenberg, et al.
The Journal of Clinical Endocrinology and Metabolism|July 21, 2000
Failure of membrane targeting causes the functional defect of two mutant sodium iodide symportersJ Pohlenz, L Duprez, R E Weiss, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 4, 2011
Clinical and metabolic findings in a 6-year-old boy with a Leydig cell tumourS Lignitz, C J Partsch, S A Wudy, et al.
Veterinary Microbiology|May 1, 1995
Pathomorphological and immunohistological findings in cattle experimentally infected with rinderpest virus isolates of different pathogenicityP Wohlsein, H M Wamwayi, G Trautwein, et al.
Pageof 12

Showing results (81-90 of 115) with videos related to

Sort By:
Pageof 12
Human Mutation|January 1, 1996
New point mutation (R243W) in the hormone binding domain of the c-erbA beta 1 gene in a family with generalized resistance to thyroid hormoneJ Pohlenz, W Schönberger, H Wemme, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 29, 2006
Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literatureC-J Partsch, F G Riepe, N Krone, et al.
Endocrinology|September 1, 1997
Thyrotropin regulation by thyroid hormone in thyroid hormone receptor beta-deficient miceR E Weiss, D Forrest, J Pohlenz, et al.
DTW. Deutsche Tierarztliche Wochenschrift|February 24, 1999
Total serum bile acid concentrations in dairy cows with fatty liver and liver failureJ Rehage, K Qualmann, C Meier, et al.
Archives of Virology. Supplementum|January 1, 1993
Distribution of cytopathogenic and noncytopathogenic bovine virus diarrhea virus in tissues from a calf with experimentally induced mucosal disease using antigenic and genetic markersI Greiser-Wilke, E Liebler, L Haas, et al.
Berliner Und Munchener Tierarztliche Wochenschrift|November 1, 1992
[Use of an immunoenzyme histochemical method for the improvement of the etiologic diagnosis of Aujeszky's disease in swine]P Wohlsein, A Klimke, G Matschullat, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 21, 2013
Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutationsK Altmann, P Hermanns, R Mühlenberg, et al.
The Journal of Clinical Endocrinology and Metabolism|July 21, 2000
Failure of membrane targeting causes the functional defect of two mutant sodium iodide symportersJ Pohlenz, L Duprez, R E Weiss, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 4, 2011
Clinical and metabolic findings in a 6-year-old boy with a Leydig cell tumourS Lignitz, C J Partsch, S A Wudy, et al.
Veterinary Microbiology|May 1, 1995
Pathomorphological and immunohistological findings in cattle experimentally infected with rinderpest virus isolates of different pathogenicityP Wohlsein, H M Wamwayi, G Trautwein, et al.
Pageof 12