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Nature Communications
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September 20, 2017
Uncontrolled angiogenic precursor expansion causes coronary artery anomalies in mice lacking Pofut1
Yidong Wang, Bingruo Wu, Pengfei Lu, et al.
Nature
|
March 21, 2008
Thyrotrophin in the pars tuberalis triggers photoperiodic response
Nobuhiro Nakao, Hiroko Ono, Takashi Yamamura, et al.
Brain : a Journal of Neurology
|
July 2, 2025
Biomarker evidence of neurodegeneration in mid-life former rugby players
Neil S N Graham, Karl A Zimmerman, Jessica Hain, et al.
Bioinformatics (Oxford, England)
|
March 24, 2019
ORE identifies extreme expression effects enriched for rare variants
F Richter, G E Hoffman, K B Manheimer, et al.
BMJ Public Health
|
August 12, 2025
Are there inequalities in the attendance at and effectiveness of behavioural weight management interventions for adults in the UK? An individual participant data meta-analysis
Jack M Birch, Julia Mueller, Sarah Damery, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disability
Bharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
BMJ (Clinical Research Ed.)
|
June 8, 2012
Facilitated physical activity as a treatment for depressed adults: randomised controlled trial
Melanie Chalder, Nicola J Wiles, John Campbell, et al.
The Journal of Organic Chemistry
|
March 25, 2008
Asymmetric synthesis of an N-acylpyrrolidine for inhibition of HCV polymerase
Armel A Agbodjan, Bob E Cooley, Royston C B Copley, et al.
Human Molecular Genetics
|
March 16, 2007
Characterization of a recurrent 15q24 microdeletion syndrome
Andrew J Sharp, Rebecca R Selzer, Joris A Veltman, et al.
Journal of Medical Genetics
|
June 14, 2008
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
F D Hannes, A J Sharp, H C Mefford, et al.
Page
of 142
Search research articles
Search
Showing results (1281-1290 of 1,414) with videos related to
Sort By:
Page
of 142
Nature Communications
|
September 20, 2017
Uncontrolled angiogenic precursor expansion causes coronary artery anomalies in mice lacking Pofut1
Yidong Wang, Bingruo Wu, Pengfei Lu, et al.
Nature
|
March 21, 2008
Thyrotrophin in the pars tuberalis triggers photoperiodic response
Nobuhiro Nakao, Hiroko Ono, Takashi Yamamura, et al.
Brain : a Journal of Neurology
|
July 2, 2025
Biomarker evidence of neurodegeneration in mid-life former rugby players
Neil S N Graham, Karl A Zimmerman, Jessica Hain, et al.
Bioinformatics (Oxford, England)
|
March 24, 2019
ORE identifies extreme expression effects enriched for rare variants
F Richter, G E Hoffman, K B Manheimer, et al.
BMJ Public Health
|
August 12, 2025
Are there inequalities in the attendance at and effectiveness of behavioural weight management interventions for adults in the UK? An individual participant data meta-analysis
Jack M Birch, Julia Mueller, Sarah Damery, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disability
Bharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
BMJ (Clinical Research Ed.)
|
June 8, 2012
Facilitated physical activity as a treatment for depressed adults: randomised controlled trial
Melanie Chalder, Nicola J Wiles, John Campbell, et al.
The Journal of Organic Chemistry
|
March 25, 2008
Asymmetric synthesis of an N-acylpyrrolidine for inhibition of HCV polymerase
Armel A Agbodjan, Bob E Cooley, Royston C B Copley, et al.
Human Molecular Genetics
|
March 16, 2007
Characterization of a recurrent 15q24 microdeletion syndrome
Andrew J Sharp, Rebecca R Selzer, Joris A Veltman, et al.
Journal of Medical Genetics
|
June 14, 2008
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
F D Hannes, A J Sharp, H C Mefford, et al.
Page
of 142