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A Roscher

Showing results (51-60 of 186) with videos related to

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The Journal of Pharmacology and Experimental Therapeutics|February 1, 1981
Changes in beta adrenergic receptors in submaxillary glands of chronically reserpine- or isoproterenol-treated ratsA A Roscher, U N Wiesmann, U E Honegger
The Journal of Biological Chemistry|May 25, 1991
Solubilization and characterization of B2 bradykinin receptors from cultured human fibroblastsA Faussner, P Heinz-Erian, C Klier, et al.
Pflugers Archiv : European Journal of Physiology|August 1, 1993
A linear 16 pS Cl- channel in the apical membrane of Caco-2 cellsS Huber, D Költgen, A A Roscher, et al.
Human Mutation|August 14, 1999
A novel frameshift mutation (141delT) in exon 1 of the 21-hydroxylase gene (CYP21) in a patient with the salt wasting form of congenital adrenal hyperplasia. Mutation in brief no. 255. OnlineN Krone, A Braun, A A Roscher, et al.
Biochemical and Biophysical Research Communications|February 25, 1998
B1 bradykinin receptors and carboxypeptidase M are both upregulated in the aorta of pigs after LPS infusionE Schremmer-Danninger, A Offner, M Siebeck, et al.
The Journal of Cardiovascular Surgery|December 1, 1996
Intra-atrial myxomas, clinical-pathologic correlation based on two case studies including historical reviewA A Roscher, N S Kato, H Quan, et al.
European Journal of Pediatrics|August 1, 1980
Elevated CSF cyclic AMP concentrations in patients with inflammatory diseases of cerebral and extracerebral originA A Roscher, A Thetter, U N Wiesmann, et al.
Molecular Cancer|February 13, 2014
RNAi-mediated silencing of MLL-AF9 reveals leukemia-associated downstream targets and processesKatrin K Fleischmann, Philipp Pagel, Irene Schmid, et al.
Clinical Chemistry|October 7, 1998
Comprehensive analytical strategy for mutation screening in 21-hydroxylase deficiencyN Krone, A A Roscher, H P Schwarz, et al.
Klinische Padiatrie|September 1, 1987
[Blood propionic acid with hyperammonemic coma]S Stöckler, U Kastner, B Pokits, et al.
Pageof 19

Showing results (51-60 of 186) with videos related to

Sort By:
Pageof 19
The Journal of Pharmacology and Experimental Therapeutics|February 1, 1981
Changes in beta adrenergic receptors in submaxillary glands of chronically reserpine- or isoproterenol-treated ratsA A Roscher, U N Wiesmann, U E Honegger
The Journal of Biological Chemistry|May 25, 1991
Solubilization and characterization of B2 bradykinin receptors from cultured human fibroblastsA Faussner, P Heinz-Erian, C Klier, et al.
Pflugers Archiv : European Journal of Physiology|August 1, 1993
A linear 16 pS Cl- channel in the apical membrane of Caco-2 cellsS Huber, D Költgen, A A Roscher, et al.
Human Mutation|August 14, 1999
A novel frameshift mutation (141delT) in exon 1 of the 21-hydroxylase gene (CYP21) in a patient with the salt wasting form of congenital adrenal hyperplasia. Mutation in brief no. 255. OnlineN Krone, A Braun, A A Roscher, et al.
Biochemical and Biophysical Research Communications|February 25, 1998
B1 bradykinin receptors and carboxypeptidase M are both upregulated in the aorta of pigs after LPS infusionE Schremmer-Danninger, A Offner, M Siebeck, et al.
The Journal of Cardiovascular Surgery|December 1, 1996
Intra-atrial myxomas, clinical-pathologic correlation based on two case studies including historical reviewA A Roscher, N S Kato, H Quan, et al.
European Journal of Pediatrics|August 1, 1980
Elevated CSF cyclic AMP concentrations in patients with inflammatory diseases of cerebral and extracerebral originA A Roscher, A Thetter, U N Wiesmann, et al.
Molecular Cancer|February 13, 2014
RNAi-mediated silencing of MLL-AF9 reveals leukemia-associated downstream targets and processesKatrin K Fleischmann, Philipp Pagel, Irene Schmid, et al.
Clinical Chemistry|October 7, 1998
Comprehensive analytical strategy for mutation screening in 21-hydroxylase deficiencyN Krone, A A Roscher, H P Schwarz, et al.
Klinische Padiatrie|September 1, 1987
[Blood propionic acid with hyperammonemic coma]S Stöckler, U Kastner, B Pokits, et al.
Pageof 19