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 Siebert

Showing results (321-330 of 332) with videos related to

Pageof 34
Sort By:
The Journal of Clinical Endocrinology and Metabolism|September 2, 2016
Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR ActivityN C Hornig, M Ukat, H U Schweikert, et al.
Human Genetics|September 12, 2000
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13M Takahashi, E Rapley, P J Biggs, et al.
Nature Genetics|June 3, 2000
Identification of the familial cylindromatosis tumour-suppressor geneG R Bignell, W Warren, S Seal, et al.
Acta Neuropathologica|August 4, 2021
Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformationParthiv Haldipur, Silvia Bernardo, Kimberly A Aldinger, et al.
Leukemia|May 15, 2007
A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocationJ I Martín-Subero, R Ibbotson, W Klapper, et al.
Leukemia|February 16, 2017
Genomic profiling of Acute lymphoblastic leukemia in ataxia telangiectasia patients reveals tight link between ATM mutations and chromothripsisM Ratnaparkhe, M Hlevnjak, T Kolb, et al.
Leukemia|August 26, 2014
A B-cell epigenetic signature defines three biologic subgroups of chronic lymphocytic leukemia with clinical impactA C Queirós, N Villamor, G Clot, et al.
Science (New York, N.Y.)|October 18, 2017
Early spectra of the gravitational wave source GW170817: Evolution of a neutron star mergerB J Shappee, J D Simon, M R Drout, et al.
Science (New York, N.Y.)|October 18, 2017
Light curves of the neutron star merger GW170817/SSS17a: Implications for r-process nucleosynthesisM R Drout, A L Piro, B J Shappee, et al.
Human Mutation|March 19, 2013
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domainPartha Sen, Yaping Yang, Colby Navarro, et al.
Pageof 34

Showing results (321-330 of 332) with videos related to

Sort By:
Pageof 34
The Journal of Clinical Endocrinology and Metabolism|September 2, 2016
Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR ActivityN C Hornig, M Ukat, H U Schweikert, et al.
Human Genetics|September 12, 2000
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13M Takahashi, E Rapley, P J Biggs, et al.
Nature Genetics|June 3, 2000
Identification of the familial cylindromatosis tumour-suppressor geneG R Bignell, W Warren, S Seal, et al.
Acta Neuropathologica|August 4, 2021
Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformationParthiv Haldipur, Silvia Bernardo, Kimberly A Aldinger, et al.
Leukemia|May 15, 2007
A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocationJ I Martín-Subero, R Ibbotson, W Klapper, et al.
Leukemia|February 16, 2017
Genomic profiling of Acute lymphoblastic leukemia in ataxia telangiectasia patients reveals tight link between ATM mutations and chromothripsisM Ratnaparkhe, M Hlevnjak, T Kolb, et al.
Leukemia|August 26, 2014
A B-cell epigenetic signature defines three biologic subgroups of chronic lymphocytic leukemia with clinical impactA C Queirós, N Villamor, G Clot, et al.
Science (New York, N.Y.)|October 18, 2017
Early spectra of the gravitational wave source GW170817: Evolution of a neutron star mergerB J Shappee, J D Simon, M R Drout, et al.
Science (New York, N.Y.)|October 18, 2017
Light curves of the neutron star merger GW170817/SSS17a: Implications for r-process nucleosynthesisM R Drout, A L Piro, B J Shappee, et al.
Human Mutation|March 19, 2013
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domainPartha Sen, Yaping Yang, Colby Navarro, et al.
Pageof 34