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D Nicholls

Showing results (111-120 of 228) with videos related to

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Nature|November 16, 1989
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndromeR D Nicholls, J H Knoll, M G Butler, et al.
American Journal of Human Genetics|September 26, 2003
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)Shirley Rainier, Jing-Hua Chai, Debra Tokarz, et al.
European Journal of Clinical Nutrition|December 13, 2005
Family-based behavioural treatment of obesity: acceptability and effectiveness in the UKC Edwards, D Nicholls, H Croker, et al.
The Journal of Biological Chemistry|January 24, 2002
Biogenesis of p53 involves cotranslational dimerization of monomers and posttranslational dimerization of dimers. Implications on the dominant negative effectChris D Nicholls, Kevin G McLure, Michael A Shields, et al.
Human Molecular Genetics|October 1, 1994
A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical regionJ Gabriel, W Gottlieb, A Garcia, et al.
The British Journal of Ophthalmology|September 1, 1980
Fungal retinitis: a case of Torulopsis glabrata infection treated with miconazoleR B Fitzsimons, M D Nicholls, F A Billson, et al.
Brain Research|November 22, 2002
Anorexigenic melanocortin signaling in the hypothalamus is augmented in association with failure-to-thrive in a transgenic mouse model for Prader-Willi syndromeYin- Lin Ge, Tohru Ohta, Daniel J Driscoll, et al.
Plos One|May 25, 2012
In vivo evolution of tumor-derived endothelial cellsTerence F McGuire, Gangadharan B Sajithlal, Jie Lu, et al.
British Journal of Haematology|January 1, 1984
Late onset pyridoxine-responsive sideroblastic anaemia after allogeneic bone marrow transplantationM D Nicholls, K Atkinson, J C Biggs, et al.
British Journal of Haematology|August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African populationS Vandenplas, D R Higgs, R D Nicholls, et al.
Pageof 23

Showing results (111-120 of 228) with videos related to

Sort By:
Pageof 23
Nature|November 16, 1989
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndromeR D Nicholls, J H Knoll, M G Butler, et al.
American Journal of Human Genetics|September 26, 2003
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)Shirley Rainier, Jing-Hua Chai, Debra Tokarz, et al.
European Journal of Clinical Nutrition|December 13, 2005
Family-based behavioural treatment of obesity: acceptability and effectiveness in the UKC Edwards, D Nicholls, H Croker, et al.
The Journal of Biological Chemistry|January 24, 2002
Biogenesis of p53 involves cotranslational dimerization of monomers and posttranslational dimerization of dimers. Implications on the dominant negative effectChris D Nicholls, Kevin G McLure, Michael A Shields, et al.
Human Molecular Genetics|October 1, 1994
A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical regionJ Gabriel, W Gottlieb, A Garcia, et al.
The British Journal of Ophthalmology|September 1, 1980
Fungal retinitis: a case of Torulopsis glabrata infection treated with miconazoleR B Fitzsimons, M D Nicholls, F A Billson, et al.
Brain Research|November 22, 2002
Anorexigenic melanocortin signaling in the hypothalamus is augmented in association with failure-to-thrive in a transgenic mouse model for Prader-Willi syndromeYin- Lin Ge, Tohru Ohta, Daniel J Driscoll, et al.
Plos One|May 25, 2012
In vivo evolution of tumor-derived endothelial cellsTerence F McGuire, Gangadharan B Sajithlal, Jie Lu, et al.
British Journal of Haematology|January 1, 1984
Late onset pyridoxine-responsive sideroblastic anaemia after allogeneic bone marrow transplantationM D Nicholls, K Atkinson, J C Biggs, et al.
British Journal of Haematology|August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African populationS Vandenplas, D R Higgs, R D Nicholls, et al.
Pageof 23