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D Nicholls

Showing results (131-140 of 228) with videos related to

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Research in Veterinary Science|July 1, 1988
Hypergastrinaemia of sheep infected with Haemonchus contortusC D Nicholls, D L Lee, T E Adrian, 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.
Schizophrenia Research|January 20, 2026
Trauma and hallucinations across the sensory modalities: the importance of considering experiences in childhood and adulthoodMikaela Bere, Susan L Rossell, Denny Meyer, et al.
Biochimica Et Biophysica Acta|June 30, 1988
Phorbol ester translocation of protein kinase C in guinea-pig synaptosomes and the potentiation of calcium-dependent glutamate releaseM J Díaz-Guerra, J Sánchez-Prieto, L Bosca, 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.
American Journal of Physiology. Endocrinology and Metabolism|February 24, 2011
Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndromeMihaela Stefan, Rebecca A Simmons, Suzanne Bertera, et al.
American Journal of Medical Genetics|February 11, 1997
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15S B Cassidy, M Forsythe, S Heeger, et al.
Pageof 23

Showing results (131-140 of 228) with videos related to

Sort By:
Pageof 23
Research in Veterinary Science|July 1, 1988
Hypergastrinaemia of sheep infected with Haemonchus contortusC D Nicholls, D L Lee, T E Adrian, 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.
Schizophrenia Research|January 20, 2026
Trauma and hallucinations across the sensory modalities: the importance of considering experiences in childhood and adulthoodMikaela Bere, Susan L Rossell, Denny Meyer, et al.
Biochimica Et Biophysica Acta|June 30, 1988
Phorbol ester translocation of protein kinase C in guinea-pig synaptosomes and the potentiation of calcium-dependent glutamate releaseM J Díaz-Guerra, J Sánchez-Prieto, L Bosca, 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.
American Journal of Physiology. Endocrinology and Metabolism|February 24, 2011
Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndromeMihaela Stefan, Rebecca A Simmons, Suzanne Bertera, et al.
American Journal of Medical Genetics|February 11, 1997
Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15S B Cassidy, M Forsythe, S Heeger, et al.
Pageof 23