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H Schuster

Showing results (171-180 of 272) with videos related to

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Nuklearmedizin. Nuclear Medicine|July 1, 1977
Bone-to-bone, joint-to-bone and joint-to-joint ratios in normal and diseased skeletal states using region-of-interest technique and bone-seeking radiopharmaceuticalsU Büll, H Schuster, J P Pfeifer, et al.
European Journal of Biochemistry|March 1, 1979
Association of the prophage P1ban protein with the dnaB protein of Escherichia coli. Overproduction of ban protein by a P1bac crr mutantC Edelbluth, E Lanka, W von der Hude, et al.
Klinische Wochenschrift|May 3, 1991
Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100G Rauh, H Schuster, J Fischer, et al.
American Heart Journal|April 1, 1980
Multiple coronary thromboses in previously normal coronary arteries: a rare cause of acute myocardial infarctionE H Schuster, S C Achuff, W R Bell, et al.
Analytical Biochemistry|July 1, 1992
Allele-specific and asymmetric polymerase chain reaction amplification in combination: a one step polymerase chain reaction protocol for rapid diagnosis of familial defective apolipoprotein B-100H Schuster, G Rauh, S Müller, et al.
Clinical and Experimental Dermatology|July 13, 2004
Severe sporotrichoid infection with Mycobacterium szulgaiN Kapur, H Schuster, N Parker, et al.
Klinische Wochenschrift|August 16, 1991
Identification of a silent point mutation in the LDL-receptor gene by direct DNA sequencingH Schuster, S Richter, G Stratmann, et al.
Medical & Biological Engineering & Computing|November 1, 1982
External fixation of unstable pelvic ring fractures: comparative rigidity of some current frame configurationsT D Brown, J P Stone, J H Schuster, et al.
Organic Letters|September 18, 2020
Ruthenium-Catalyzed Enantioselective Hydrogenation of HydrazonesChristopher H Schuster, James F Dropinski, Michael Shevlin, et al.
The British Journal of Ophthalmology|February 4, 1999
Absence of hypertensive retinopathy in a Turkish kindred with autosomal dominant hypertension and brachydactylyL O Hattenbach, H R Toka, O Toka, et al.
Pageof 28

Showing results (171-180 of 272) with videos related to

Sort By:
Pageof 28
Nuklearmedizin. Nuclear Medicine|July 1, 1977
Bone-to-bone, joint-to-bone and joint-to-joint ratios in normal and diseased skeletal states using region-of-interest technique and bone-seeking radiopharmaceuticalsU Büll, H Schuster, J P Pfeifer, et al.
European Journal of Biochemistry|March 1, 1979
Association of the prophage P1ban protein with the dnaB protein of Escherichia coli. Overproduction of ban protein by a P1bac crr mutantC Edelbluth, E Lanka, W von der Hude, et al.
Klinische Wochenschrift|May 3, 1991
Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100G Rauh, H Schuster, J Fischer, et al.
American Heart Journal|April 1, 1980
Multiple coronary thromboses in previously normal coronary arteries: a rare cause of acute myocardial infarctionE H Schuster, S C Achuff, W R Bell, et al.
Analytical Biochemistry|July 1, 1992
Allele-specific and asymmetric polymerase chain reaction amplification in combination: a one step polymerase chain reaction protocol for rapid diagnosis of familial defective apolipoprotein B-100H Schuster, G Rauh, S Müller, et al.
Clinical and Experimental Dermatology|July 13, 2004
Severe sporotrichoid infection with Mycobacterium szulgaiN Kapur, H Schuster, N Parker, et al.
Klinische Wochenschrift|August 16, 1991
Identification of a silent point mutation in the LDL-receptor gene by direct DNA sequencingH Schuster, S Richter, G Stratmann, et al.
Medical & Biological Engineering & Computing|November 1, 1982
External fixation of unstable pelvic ring fractures: comparative rigidity of some current frame configurationsT D Brown, J P Stone, J H Schuster, et al.
Organic Letters|September 18, 2020
Ruthenium-Catalyzed Enantioselective Hydrogenation of HydrazonesChristopher H Schuster, James F Dropinski, Michael Shevlin, et al.
The British Journal of Ophthalmology|February 4, 1999
Absence of hypertensive retinopathy in a Turkish kindred with autosomal dominant hypertension and brachydactylyL O Hattenbach, H R Toka, O Toka, et al.
Pageof 28