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

P Lohse

Showing results (11-20 of 90) with videos related to

Pageof 9
Sort By:
Human Reproduction (Oxford, England)|December 1, 2000
The number of dichorionic twin pregnancies is reduced by the common MTHFR 677C-->T mutationU Hasbargen, P Lohse, C J Thaler
The Journal of Biological Chemistry|July 15, 1992
Heterozygosity for apolipoprotein E-4Philadelphia(Glu13----Lys, Arg145----Cys) is associated with incomplete dominance of type III hyperlipoproteinemiaP Lohse, D J Rader, H B Brewer
Deutsche Medizinische Wochenschrift (1946)|May 16, 2003
[Persistent polyclonal B-cell lymphocytosis]U Schönermarck, H Diem, P Lohse, et al.
Der Internist|February 9, 2000
[47-year-old patient with resistant pulmonary embolism in congenital hemodynamic disorder]J Tischer, R Forstpointner, P Lohse, et al.
Infection|March 3, 2017
Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome: differential diagnosis of septic arthritis by regular detection of exceedingly high synovial cell countsW Löffler, P Lohse, T Weihmayr, et al.
Clinical Chemistry|April 28, 2001
Fluorescence-based detection of the CETP TaqIB polymorphism: false positives with the TaqMan-based exonuclease assay attributable to a previously unknown gene variantD Teupser, W Rupprecht, P Lohse, et al.
Beitrage Zur Infusionstherapie = Contributions to Infusion Therapy|January 1, 1993
[The genetics of factor XII deficiency]B Kempter, S Rüth, I Epple, et al.
Der Internist|September 15, 2001
[19-year old Turkish female patient with recurrent abdominal pains and fever. Molecular genetics investigation yields a definitive diagnosis ]J Ascherl, W Schmidbaur, M Wienbeck, et al.
European Journal of Biochemistry|December 1, 1988
A novel human myosin alkali light chain is developmentally regulated. Expression in fetal cardiac and skeletal muscle and in adult atriaH H Arnold, P Lohse, U Seidel, et al.
The Journal of Biological Chemistry|May 25, 1989
The alkali light chains of human smooth and nonmuscle myosins are encoded by a single gene. Tissue-specific expression by alternative splicing pathwaysS Lenz, P Lohse, U Seidel, et al.
Pageof 9

Showing results (11-20 of 90) with videos related to

Sort By:
Pageof 9
Human Reproduction (Oxford, England)|December 1, 2000
The number of dichorionic twin pregnancies is reduced by the common MTHFR 677C-->T mutationU Hasbargen, P Lohse, C J Thaler
The Journal of Biological Chemistry|July 15, 1992
Heterozygosity for apolipoprotein E-4Philadelphia(Glu13----Lys, Arg145----Cys) is associated with incomplete dominance of type III hyperlipoproteinemiaP Lohse, D J Rader, H B Brewer
Deutsche Medizinische Wochenschrift (1946)|May 16, 2003
[Persistent polyclonal B-cell lymphocytosis]U Schönermarck, H Diem, P Lohse, et al.
Der Internist|February 9, 2000
[47-year-old patient with resistant pulmonary embolism in congenital hemodynamic disorder]J Tischer, R Forstpointner, P Lohse, et al.
Infection|March 3, 2017
Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome: differential diagnosis of septic arthritis by regular detection of exceedingly high synovial cell countsW Löffler, P Lohse, T Weihmayr, et al.
Clinical Chemistry|April 28, 2001
Fluorescence-based detection of the CETP TaqIB polymorphism: false positives with the TaqMan-based exonuclease assay attributable to a previously unknown gene variantD Teupser, W Rupprecht, P Lohse, et al.
Beitrage Zur Infusionstherapie = Contributions to Infusion Therapy|January 1, 1993
[The genetics of factor XII deficiency]B Kempter, S Rüth, I Epple, et al.
Der Internist|September 15, 2001
[19-year old Turkish female patient with recurrent abdominal pains and fever. Molecular genetics investigation yields a definitive diagnosis ]J Ascherl, W Schmidbaur, M Wienbeck, et al.
European Journal of Biochemistry|December 1, 1988
A novel human myosin alkali light chain is developmentally regulated. Expression in fetal cardiac and skeletal muscle and in adult atriaH H Arnold, P Lohse, U Seidel, et al.
The Journal of Biological Chemistry|May 25, 1989
The alkali light chains of human smooth and nonmuscle myosins are encoded by a single gene. Tissue-specific expression by alternative splicing pathwaysS Lenz, P Lohse, U Seidel, et al.
Pageof 9