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Showing results (521-530 of 1,336) with videos related to

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European Journal of Pediatrics|July 1, 1996
Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuriaP Burgard, A Rupp, D S Konecki, et al.
Clinical Pharmacology and Therapeutics|April 17, 2020
Interventional Pharmacoeconomics: A Novel Mechanism for Unlocking ValueAnthony V Serritella, Garth W Strohbehn, Daniel A Goldstein, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2014
Father's brain is sensitive to childcare experiencesEyal Abraham, Talma Hendler, Irit Shapira-Lichter, et al.
The American Journal of Medicine|June 17, 1998
Blood thrombopoietin levels in clonal thrombocytosis and reactive thrombocytosisJ C Wang, C Chen, A D Novetsky, et al.
Human Genetics|April 1, 1988
Linkage disequilibrium between mutation and RFLP haplotype at the phenylalanine hydroxylase locus in the German populationU Lichter-Konecki, M Schlotter, D S Konecki, et al.
Cancer Genetics and Cytogenetics|May 15, 2007
Cytogenetic and molecular genetic analyses of giant cell glioblastoma multiforme reveal distinct profiles in giant cell and non-giant cell subpopulationsRamon Martinez, Wolfgang Roggendorf, Gustavo Baretton, et al.
Experimental Cell Research|December 2, 2004
Characterization of a nuclear compartment shared by nuclear bodies applying ectopic protein expression and correlative light and electron microscopyKarsten Richter, Michaela Reichenzeller, Sabine M Görisch, et al.
The American Journal of Pathology|October 28, 2003
Gene expression patterns in ependymomas correlate with tumor location, grade, and patient ageAndrey Korshunov, Kai Neben, Gunnar Wrobel, et al.
Nature Communications|January 11, 2022
Association of mutation signature effectuating processes with mutation hotspots in driver genes and non-coding regionsJohn K L Wong, Christian Aichmüller, Markus Schulze, et al.
Journal of Pediatric Orthopedics|September 17, 1999
An orthopaedic scoring system for nail-patella syndrome and application to a kindred with variable expressivity and glaucomaF A Farley, P R Lichter, C A Downs, et al.
Pageof 134

Showing results (521-530 of 1,336) with videos related to

Sort By:
Pageof 134
European Journal of Pediatrics|July 1, 1996
Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuriaP Burgard, A Rupp, D S Konecki, et al.
Clinical Pharmacology and Therapeutics|April 17, 2020
Interventional Pharmacoeconomics: A Novel Mechanism for Unlocking ValueAnthony V Serritella, Garth W Strohbehn, Daniel A Goldstein, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2014
Father's brain is sensitive to childcare experiencesEyal Abraham, Talma Hendler, Irit Shapira-Lichter, et al.
The American Journal of Medicine|June 17, 1998
Blood thrombopoietin levels in clonal thrombocytosis and reactive thrombocytosisJ C Wang, C Chen, A D Novetsky, et al.
Human Genetics|April 1, 1988
Linkage disequilibrium between mutation and RFLP haplotype at the phenylalanine hydroxylase locus in the German populationU Lichter-Konecki, M Schlotter, D S Konecki, et al.
Cancer Genetics and Cytogenetics|May 15, 2007
Cytogenetic and molecular genetic analyses of giant cell glioblastoma multiforme reveal distinct profiles in giant cell and non-giant cell subpopulationsRamon Martinez, Wolfgang Roggendorf, Gustavo Baretton, et al.
Experimental Cell Research|December 2, 2004
Characterization of a nuclear compartment shared by nuclear bodies applying ectopic protein expression and correlative light and electron microscopyKarsten Richter, Michaela Reichenzeller, Sabine M Görisch, et al.
The American Journal of Pathology|October 28, 2003
Gene expression patterns in ependymomas correlate with tumor location, grade, and patient ageAndrey Korshunov, Kai Neben, Gunnar Wrobel, et al.
Nature Communications|January 11, 2022
Association of mutation signature effectuating processes with mutation hotspots in driver genes and non-coding regionsJohn K L Wong, Christian Aichmüller, Markus Schulze, et al.
Journal of Pediatric Orthopedics|September 17, 1999
An orthopaedic scoring system for nail-patella syndrome and application to a kindred with variable expressivity and glaucomaF A Farley, P R Lichter, C A Downs, et al.
Pageof 134