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

D Nicholls

Showing results (121-130 of 228) with videos related to

Pageof 23
Sort By:
Genomics|March 20, 1995
Organization and sequence of the human P gene and identification of a new family of transport proteinsS T Lee, R D Nicholls, M T Jong, et al.
American Journal of Medical Genetics|January 11, 1996
DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi regionP A Mowery-Rushton, D J Driscoll, R D Nicholls, et al.
Australian and New Zealand Journal of Medicine|April 1, 1984
Current management of aplastic anemiaM D Nicholls, J C Biggs, K Atkinson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 15, 2002
Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion siteJ H Chai, D P Locke, T Ohta, et al.
Genomics|October 13, 2001
Phylogenetic conservation of the makorin-2 gene, encoding a multiple zinc-finger protein, antisense to the RAF1 proto-oncogeneT A Gray, K Azama, K Whitmore, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 24, 1998
Structure and function correlations at the imprinted mouse Snrpn locusJ M Gabriel, T A Gray, L Stubbs, et al.
Human Molecular Genetics|December 1, 1993
Functional imprinting and epigenetic modification of the human SNRPN geneC C Glenn, K A Porter, M T Jong, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouseR D Nicholls, W Gottlieb, L B Russell, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|January 15, 2016
The impact of a dedicated patent ductus arteriosus ligation team on neonatal health-care outcomesM H F Resende, K More, D Nicholls, et al.
Medical and Pediatric Oncology|April 17, 1998
Misleading leads. Thallium-201 uptake in rebound thymic hyperplasiaD J Roebuck, W D Nicholls, E J Bernard, et al.
Pageof 23

Showing results (121-130 of 228) with videos related to

Sort By:
Pageof 23
Genomics|March 20, 1995
Organization and sequence of the human P gene and identification of a new family of transport proteinsS T Lee, R D Nicholls, M T Jong, et al.
American Journal of Medical Genetics|January 11, 1996
DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi regionP A Mowery-Rushton, D J Driscoll, R D Nicholls, et al.
Australian and New Zealand Journal of Medicine|April 1, 1984
Current management of aplastic anemiaM D Nicholls, J C Biggs, K Atkinson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 15, 2002
Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion siteJ H Chai, D P Locke, T Ohta, et al.
Genomics|October 13, 2001
Phylogenetic conservation of the makorin-2 gene, encoding a multiple zinc-finger protein, antisense to the RAF1 proto-oncogeneT A Gray, K Azama, K Whitmore, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 24, 1998
Structure and function correlations at the imprinted mouse Snrpn locusJ M Gabriel, T A Gray, L Stubbs, et al.
Human Molecular Genetics|December 1, 1993
Functional imprinting and epigenetic modification of the human SNRPN geneC C Glenn, K A Porter, M T Jong, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouseR D Nicholls, W Gottlieb, L B Russell, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|January 15, 2016
The impact of a dedicated patent ductus arteriosus ligation team on neonatal health-care outcomesM H F Resende, K More, D Nicholls, et al.
Medical and Pediatric Oncology|April 17, 1998
Misleading leads. Thallium-201 uptake in rebound thymic hyperplasiaD J Roebuck, W D Nicholls, E J Bernard, et al.
Pageof 23