New insights reveal complex mechanisms involved in genomic imprinting.

Por Nicholls, R. D.
Publicado em 1994

Three allele TaqI RFLP for probe 3-21 [D15S10] on chromosome 15q.

Por Nicholls, R D, Lalande, M
Publicado em 1989

Diverse splicing mechanisms fuse the evolutionarily conserved bicistronic MOCS1A and MOCS1B open reading frames.

Por Gray, T A, Nicholls, R D
Publicado em 2000

RFLPs for beta 2-microglobulin.

Por Nicholls, R D, Glatt, K, Latt, S A
Publicado em 1989

Long range genome structure around the human alpha-globin complex analysed by PFGE.

Por Fischel-Ghodsian, N, Nicholls, R D, Higgs, D R
Publicado em 1987

Unusual features of CpG-rich (HTF) islands in the human alpha globin complex: association with non-functional pseudogenes and presence within the 3' portion of the zeta gene.

Por Fischel-Ghodsian, N, Nicholls, R D, Higgs, D R
Publicado em 1987

Reply to Engel

Por Knoll, J. H. M., Nicholls, R. D., Malcolm, S., Lalande, M.
Publicado em 1991

Direct cloning of specific genomic DNA sequences in plasmid libraries following fragment enrichment.

Por Nicholls, R D, Hill, A V, Clegg, J B, Higgs, D R
Publicado em 1985

Non-methylated CpG-rich islands at the human alpha-globin locus: implications for evolution of the alpha-globin pseudogene.

Por Bird, A P, Taggart, M H, Nicholls, R D, Higgs, D R
Publicado em 1987

Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.

Por Knoll, J H, Glatt, K A, Nicholls, R D, Malcolm, S, Lalande, M
Publicado em 1991

A model system to study genomic imprinting of human genes

Por Gabriel, J. M., Higgins, M. J., Gebuhr, T. C., Shows, T. B., Saitoh, S., Nicholls, R. D.
Publicado em 1998

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.

Por Nicholls, R D, Gottlieb, W, Russell, L B, Davda, M, Horsthemke, B, Rinchik, E M
Publicado em 1993

Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster.

Por Jarman, A P, Nicholls, R D, Weatherall, D J, Clegg, J B, Higgs, D R
Publicado em 1986

Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.

Por White, L. M., Rogan, P. K., Nicholls, R. D., Wu, B. L., Korf, B., Knoll, J. H.
Publicado em 1996

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

Por Glenn, C. C., Saitoh, S., Jong, M. T., Filbrandt, M. M., Surti, U., Driscoll, D. J., Nicholls, R. D.
Publicado em 1996

Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptor.

Por Culiat, C T, Stubbs, L, Nicholls, R D, Montgomery, C S, Russell, L B, Johnson, D K, Rinchik, E M
Publicado em 1993

Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.

Por Knoll, J H, Nicholls, R D, Magenis, R E, Glatt, K, Graham, J M, Kaplan, L, Lalande, M
Publicado em 1990

High resolution gene mapping of the human alpha globin locus.

Por Nicholls, R D, Jonasson, J A, McGee, J O, Patil, S, Ionasescu, V V, Weatherall, D J, Higgs, D R
Publicado em 1987

The mechanisms involved in formation of deletions and duplications of 15q11-q13.

Por Robinson, W P, Dutly, F, Nicholls, R D, Bernasconi, F, Peñaherrera, M, Michaelis, R C, Abeliovich, D, Schinzel, A A
Publicado em 1998

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.

Por Ohta, T, Buiting, K, Kokkonen, H, McCandless, S, Heeger, S, Leisti, H, Driscoll, D J, Cassidy, S B, Horsthemke, B, Nicholls, R D
Publicado em 1999