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Nature
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November 16, 1989
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome
R 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 UK
C 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 effect
Chris 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 region
J 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 miconazole
R 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 syndrome
Yin- Lin Ge, Tohru Ohta, Daniel J Driscoll, et al.
Plos One
|
May 25, 2012
In vivo evolution of tumor-derived endothelial cells
Terence 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 transplantation
M 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 population
S Vandenplas, D R Higgs, R D Nicholls, et al.
Page
of 23
Search research articles
Search
Showing results (111-120 of 228) with videos related to
Sort By:
Page
of 23
Nature
|
November 16, 1989
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome
R 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 UK
C 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 effect
Chris 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 region
J 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 miconazole
R 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 syndrome
Yin- Lin Ge, Tohru Ohta, Daniel J Driscoll, et al.
Plos One
|
May 25, 2012
In vivo evolution of tumor-derived endothelial cells
Terence 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 transplantation
M 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 population
S Vandenplas, D R Higgs, R D Nicholls, et al.
Page
of 23