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Nicholas Silver

Showing results (21-30 of 31) with videos related to

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Blood|July 25, 2006
cMYB is involved in the regulation of fetal hemoglobin production in adultsJie Jiang, Steve Best, Stephan Menzel, et al.
Blood|August 23, 2007
The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humansStephan Menzel, Jie Jiang, Nicholas Silver, et al.
British Journal of Haematology|May 18, 2006
Alpha-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta-thalassaemiaMei I Lai, Jie Jiang, Nicholas Silver, et al.
AIDS Research and Therapy|November 10, 2018
Characterization of minority HIV-1 drug resistant variants in the United Kingdom following the verification of a deep sequencing-based HIV-1 genotyping and tropism assayNicholas Silver, Mary Paynter, Georgina McAllister, et al.
Cephalalgia : an International Journal of Headache|December 13, 2017
Non-invasive vagus nerve stimulation for the acute treatment of episodic and chronic cluster headache: A randomized, double-blind, sham-controlled ACT2 studyPeter J Goadsby, Ilse F de Coo, Nicholas Silver, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2007
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adultsSwee Lay Thein, Stephan Menzel, Xu Peng, et al.
Cephalalgia : an International Journal of Headache|September 17, 2019
Non-invasive vagus nerve stimulation (nVNS) for the preventive treatment of episodic migraine: The multicentre, double-blind, randomised, sham-controlled PREMIUM trialHans-Christoph Diener, Peter J Goadsby, Messoud Ashina, et al.
Annals of Human Genetics|July 30, 2014
Global genetic architecture of an erythroid quantitative trait locus, HMIP-2Stephan Menzel, Helen Rooks, Diana Zelenika, et al.
Plos Genetics|December 5, 2014
Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular diseaseMichelle D Johnson, Michael Mueller, Martyna Adamowicz-Brice, et al.
Blood Advances|February 14, 2018
<i>g(HbF)</i>: a genetic model of fetal hemoglobin in sickle cell diseaseKate Gardner, Tony Fulford, Nicholas Silver, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Blood|July 25, 2006
cMYB is involved in the regulation of fetal hemoglobin production in adultsJie Jiang, Steve Best, Stephan Menzel, et al.
Blood|August 23, 2007
The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humansStephan Menzel, Jie Jiang, Nicholas Silver, et al.
British Journal of Haematology|May 18, 2006
Alpha-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta-thalassaemiaMei I Lai, Jie Jiang, Nicholas Silver, et al.
AIDS Research and Therapy|November 10, 2018
Characterization of minority HIV-1 drug resistant variants in the United Kingdom following the verification of a deep sequencing-based HIV-1 genotyping and tropism assayNicholas Silver, Mary Paynter, Georgina McAllister, et al.
Cephalalgia : an International Journal of Headache|December 13, 2017
Non-invasive vagus nerve stimulation for the acute treatment of episodic and chronic cluster headache: A randomized, double-blind, sham-controlled ACT2 studyPeter J Goadsby, Ilse F de Coo, Nicholas Silver, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2007
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adultsSwee Lay Thein, Stephan Menzel, Xu Peng, et al.
Cephalalgia : an International Journal of Headache|September 17, 2019
Non-invasive vagus nerve stimulation (nVNS) for the preventive treatment of episodic migraine: The multicentre, double-blind, randomised, sham-controlled PREMIUM trialHans-Christoph Diener, Peter J Goadsby, Messoud Ashina, et al.
Annals of Human Genetics|July 30, 2014
Global genetic architecture of an erythroid quantitative trait locus, HMIP-2Stephan Menzel, Helen Rooks, Diana Zelenika, et al.
Plos Genetics|December 5, 2014
Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular diseaseMichelle D Johnson, Michael Mueller, Martyna Adamowicz-Brice, et al.
Blood Advances|February 14, 2018
<i>g(HbF)</i>: a genetic model of fetal hemoglobin in sickle cell diseaseKate Gardner, Tony Fulford, Nicholas Silver, et al.
Pageof 4