Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R Hanke

Showing results (31-40 of 49) with videos related to

Pageof 5
Sort By:
Clinical Laboratory|June 19, 2001
The determination of free and protein-bound haemoglobin in plasma using a combination of HPLC and absorption spectrometryW G Wood, M Kress, D Meissner, et al.
Journal of Medicinal Chemistry|February 15, 2001
seco-Cyclothialidines: new concise synthesis, inhibitory activity toward bacterial and human DNA topoisomerases, and antibacterial propertiesJ Rudolph, H Theis, R Hanke, et al.
Journal of Medical Genetics|November 1, 1993
Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin geneU Lenk, R Hanke, U Kräft, et al.
Analytical Biochemistry|August 15, 1987
Use of cyanuric chloride-activated paper for detection of subpicogram quantities of specific DNA sequences and its application to linked restriction fragment length polymorphism analysis in a Duchenne muscular dystrophy affected familyH D Hunger, A Speer, C Flachmeier, et al.
Acta Biologica Et Medica Germanica|January 1, 1979
Pre-mRNA from erythroid enriched bone marrow cells of the rabbitH D Hunger, H Grützmann, A Speer, et al.
Der Urologe. Ausg. A|May 8, 1999
[Improved tumor stent for internal palliative urinary diversion]R W Schlick, E Seidl, J Küster, et al.
Clinical Genetics|June 1, 1986
Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLPA Speer, H H Dahl, O Riess, et al.
Biomedica Biochimica Acta|January 1, 1990
Mapping and sequencing in two intron regions of the human dystrophin geneA Speer, H Billwitz, A Huth, et al.
Nucleic Acids Research|June 26, 1989
DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screeningA Speer, A Rosenthal, H Billwitz, et al.
Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysisA Speer, R Bollman, A Michel, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Clinical Laboratory|June 19, 2001
The determination of free and protein-bound haemoglobin in plasma using a combination of HPLC and absorption spectrometryW G Wood, M Kress, D Meissner, et al.
Journal of Medicinal Chemistry|February 15, 2001
seco-Cyclothialidines: new concise synthesis, inhibitory activity toward bacterial and human DNA topoisomerases, and antibacterial propertiesJ Rudolph, H Theis, R Hanke, et al.
Journal of Medical Genetics|November 1, 1993
Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin geneU Lenk, R Hanke, U Kräft, et al.
Analytical Biochemistry|August 15, 1987
Use of cyanuric chloride-activated paper for detection of subpicogram quantities of specific DNA sequences and its application to linked restriction fragment length polymorphism analysis in a Duchenne muscular dystrophy affected familyH D Hunger, A Speer, C Flachmeier, et al.
Acta Biologica Et Medica Germanica|January 1, 1979
Pre-mRNA from erythroid enriched bone marrow cells of the rabbitH D Hunger, H Grützmann, A Speer, et al.
Der Urologe. Ausg. A|May 8, 1999
[Improved tumor stent for internal palliative urinary diversion]R W Schlick, E Seidl, J Küster, et al.
Clinical Genetics|June 1, 1986
Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLPA Speer, H H Dahl, O Riess, et al.
Biomedica Biochimica Acta|January 1, 1990
Mapping and sequencing in two intron regions of the human dystrophin geneA Speer, H Billwitz, A Huth, et al.
Nucleic Acids Research|June 26, 1989
DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screeningA Speer, A Rosenthal, H Billwitz, et al.
Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysisA Speer, R Bollman, A Michel, et al.
Pageof 5