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R D Nicholls

Showing results (41-50 of 107) with videos related to

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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.
The EMBO Journal|August 1, 1986
Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene clusterA P Jarman, R D Nicholls, D J Weatherall, et al.
The New England Journal of Medicine|February 24, 1994
Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinismS T Lee, R D Nicholls, S Bundey, et al.
Nature Genetics|April 1, 1995
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15K Buiting, S Saitoh, S Gross, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1999
Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting centerJ M Greally, T A Gray, J M Gabriel, et al.
Human Molecular Genetics|April 1, 1996
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patientY Sun, R D Nicholls, M G Butler, et al.
Pageof 11

Showing results (41-50 of 107) with videos related to

Sort By:
Pageof 11
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.
The EMBO Journal|August 1, 1986
Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene clusterA P Jarman, R D Nicholls, D J Weatherall, et al.
The New England Journal of Medicine|February 24, 1994
Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinismS T Lee, R D Nicholls, S Bundey, et al.
Nature Genetics|April 1, 1995
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15K Buiting, S Saitoh, S Gross, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 10, 1999
Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting centerJ M Greally, T A Gray, J M Gabriel, et al.
Human Molecular Genetics|April 1, 1996
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patientY Sun, R D Nicholls, M G Butler, et al.
Pageof 11