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M Stuhrmann

Showing results (41-50 of 60) with videos related to

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Human Mutation|January 1, 1995
Pancreatic insufficiency and pulmonary disease in German and Slavic cystic fibrosis patients with the R347P mutationR Varon, M Stuhrmann, M Macek, et al.
Human Genetics|September 1, 1990
Frequency of the F508 deletion in the CFTR gene in Turkish cystic fibrosis patientsJ Hundrieser, S Bremer, F Peinemann, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Genotype-phenotype correlations in cystic fibrosis patientsM Stuhrmann, T Dörk, M Krawczak, et al.
Journal of Medical Genetics|January 16, 1998
Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosisE A el-Harith, T Dörk, M Stuhrmann, et al.
Pediatric Nephrology (Berlin, Germany)|May 11, 2000
Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuriaH Langen, D von Kietzell, D Byrd, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1995
Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor geneE Schipani, L S Weinstein, C Bergwitz, et al.
Gynecologic Oncology|March 4, 1999
Frequency of BRCA1 mutation 5382insC in German breast cancer patientsJ Backe, S Hofferbert, B Skawran, et al.
The Journal of Clinical Endocrinology and Metabolism|June 17, 1998
Delayed low density lipoprotein (LDL) catabolism despite a functional intact LDL-apolipoprotein B particle and LDL-receptor in a subject with clinical homozygous familial hypercholesterolemiaH H Schmidt, M Stuhrmann, R Shamburek, et al.
Cancer Research|October 19, 2001
Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patientsT Dörk, R Bendix, M Bremer, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|August 16, 2014
Vascular endothelial growth factor A polymorphism and risk of Kaposi's sarcoma herpesvirus viremia in kidney allograft recipientsK R Alkharsah, A J Alzahrani, O E Obeid, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Human Mutation|January 1, 1995
Pancreatic insufficiency and pulmonary disease in German and Slavic cystic fibrosis patients with the R347P mutationR Varon, M Stuhrmann, M Macek, et al.
Human Genetics|September 1, 1990
Frequency of the F508 deletion in the CFTR gene in Turkish cystic fibrosis patientsJ Hundrieser, S Bremer, F Peinemann, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Genotype-phenotype correlations in cystic fibrosis patientsM Stuhrmann, T Dörk, M Krawczak, et al.
Journal of Medical Genetics|January 16, 1998
Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosisE A el-Harith, T Dörk, M Stuhrmann, et al.
Pediatric Nephrology (Berlin, Germany)|May 11, 2000
Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuriaH Langen, D von Kietzell, D Byrd, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1995
Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor geneE Schipani, L S Weinstein, C Bergwitz, et al.
Gynecologic Oncology|March 4, 1999
Frequency of BRCA1 mutation 5382insC in German breast cancer patientsJ Backe, S Hofferbert, B Skawran, et al.
The Journal of Clinical Endocrinology and Metabolism|June 17, 1998
Delayed low density lipoprotein (LDL) catabolism despite a functional intact LDL-apolipoprotein B particle and LDL-receptor in a subject with clinical homozygous familial hypercholesterolemiaH H Schmidt, M Stuhrmann, R Shamburek, et al.
Cancer Research|October 19, 2001
Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patientsT Dörk, R Bendix, M Bremer, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|August 16, 2014
Vascular endothelial growth factor A polymorphism and risk of Kaposi's sarcoma herpesvirus viremia in kidney allograft recipientsK R Alkharsah, A J Alzahrani, O E Obeid, et al.
Pageof 6