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D Nicholls

Showing results (141-150 of 228) with videos related to

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Infection|December 13, 2002
Ciclopiroxolamine cream for treating seborrheic dermatitis: a double-blind parallel group comparisonA Unholzer, G Varigos, D Nicholls, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|November 26, 1998
Patterns of abnormality on bone scans in acute childhood leukemiaE J Bernard, W D Nicholls, R B Howman-Giles, et al.
The Medical Journal of Australia|July 20, 1992
Transfusion of frozen thawed blood stored at -20 degrees C to -25 degrees CM D Nicholls, V J Davies, D Au-Yeung, et al.
The Journal of Biological Chemistry|April 7, 2004
UV-dependent alternative splicing uncouples p53 activity and PIG3 gene function through rapid proteolytic degradationChris D Nicholls, Michael A Shields, Patrick W K Lee, et al.
European Journal of Clinical Nutrition|April 1, 2004
Validation of the Dutch Eating Behaviour Questionnaire parent version (DEBQ-P) in the Italian population: a screening tool to detect differences in eating behaviour among obese, overweight and normal-weight preadolescentsR Caccialanza, D Nicholls, H Cena, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 7B C Holdener, S D Brown, J M Angel, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
American Journal of Medical Genetics|July 15, 1992
Pericentric inversion of chromosome 16 in a large kindred: spectrum of morbidity and mortality in offspringD W Bianchi, R D Nicholls, K A Russell, et al.
American Journal of Medical Genetics|February 1, 1989
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionJ H Knoll, R D Nicholls, R E Magenis, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 9, 1998
A model system to study genomic imprinting of human genesJ M Gabriel, M J Higgins, T C Gebuhr, et al.
Pageof 23

Showing results (141-150 of 228) with videos related to

Sort By:
Pageof 23
Infection|December 13, 2002
Ciclopiroxolamine cream for treating seborrheic dermatitis: a double-blind parallel group comparisonA Unholzer, G Varigos, D Nicholls, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|November 26, 1998
Patterns of abnormality on bone scans in acute childhood leukemiaE J Bernard, W D Nicholls, R B Howman-Giles, et al.
The Medical Journal of Australia|July 20, 1992
Transfusion of frozen thawed blood stored at -20 degrees C to -25 degrees CM D Nicholls, V J Davies, D Au-Yeung, et al.
The Journal of Biological Chemistry|April 7, 2004
UV-dependent alternative splicing uncouples p53 activity and PIG3 gene function through rapid proteolytic degradationChris D Nicholls, Michael A Shields, Patrick W K Lee, et al.
European Journal of Clinical Nutrition|April 1, 2004
Validation of the Dutch Eating Behaviour Questionnaire parent version (DEBQ-P) in the Italian population: a screening tool to detect differences in eating behaviour among obese, overweight and normal-weight preadolescentsR Caccialanza, D Nicholls, H Cena, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 7B C Holdener, S D Brown, J M Angel, et al.
Human Molecular Genetics|February 1, 1993
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomyA Mutirangura, F Greenberg, M G Butler, et al.
American Journal of Medical Genetics|July 15, 1992
Pericentric inversion of chromosome 16 in a large kindred: spectrum of morbidity and mortality in offspringD W Bianchi, R D Nicholls, K A Russell, et al.
American Journal of Medical Genetics|February 1, 1989
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionJ H Knoll, R D Nicholls, R E Magenis, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 9, 1998
A model system to study genomic imprinting of human genesJ M Gabriel, M J Higgins, T C Gebuhr, et al.
Pageof 23