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Human Mutation
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September 28, 2011
Enhancer-adoption as a mechanism of human developmental disease
Laura A Lettice, Sarah Daniels, Elizabeth Sweeney, et al.
Human Genetics
|
October 18, 2002
A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolved
M Elizabeth McCready, Elizabeth Sweeney, Allan E Fryer, et al.
Journal of Virology
|
June 3, 2011
Protection against rectal transmission of an emtricitabine-resistant simian/human immunodeficiency virus SHIV162p3M184V mutant by intermittent prophylaxis with Truvada
Mian-Er Cong, Ae S Youngpairoj, Qi Zheng, et al.
Journal of Medical Primatology
|
January 15, 2013
Evaluation of the lymphocyte trafficking drug FTY720 in vaginal tissues
Ai Tsuiki, Wei Luo, Tara Henning, et al.
Frontiers in Aging Neuroscience
|
September 26, 2022
Higher body mass index is associated with worse hippocampal vasoreactivity to carbon dioxide
Lidia Glodzik, Henry Rusinek, Tracy Butler, et al.
Journal of Medical Primatology
|
July 26, 2011
Development of a pigtail macaque model of sexually transmitted infection/HIV coinfection using Chlamydia trachomatis, Trichomonas vaginalis, and SHIV(SF162P3)
Tara Henning, Yetunde Fakile, Christi Phillips, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
January 20, 2022
Dimethyl Fumarate Reduces Inflammation in Chronic Active Multiple Sclerosis Lesions
Nicole Zinger, Gerald Ponath, Elizabeth Sweeney, et al.
Epilepsia
|
February 23, 2023
A pharmacokinetic model of antiseizure medication load to guide care in the epilepsy monitoring unit
Nina J Ghosn, Kevin Xie, Akash R Pattnaik, et al.
Scientific Reports
|
March 16, 2022
Disease correlates of rim lesions on quantitative susceptibility mapping in multiple sclerosis
Melanie Marcille, Sandra Hurtado Rúa, Charles Tyshkov, et al.
American Journal of Human Genetics
|
December 19, 2012
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex
Sandra M Pasternack, Melanie Refke, Elham Paknia, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 59) with videos related to
Sort By:
Page
of 6
Human Mutation
|
September 28, 2011
Enhancer-adoption as a mechanism of human developmental disease
Laura A Lettice, Sarah Daniels, Elizabeth Sweeney, et al.
Human Genetics
|
October 18, 2002
A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolved
M Elizabeth McCready, Elizabeth Sweeney, Allan E Fryer, et al.
Journal of Virology
|
June 3, 2011
Protection against rectal transmission of an emtricitabine-resistant simian/human immunodeficiency virus SHIV162p3M184V mutant by intermittent prophylaxis with Truvada
Mian-Er Cong, Ae S Youngpairoj, Qi Zheng, et al.
Journal of Medical Primatology
|
January 15, 2013
Evaluation of the lymphocyte trafficking drug FTY720 in vaginal tissues
Ai Tsuiki, Wei Luo, Tara Henning, et al.
Frontiers in Aging Neuroscience
|
September 26, 2022
Higher body mass index is associated with worse hippocampal vasoreactivity to carbon dioxide
Lidia Glodzik, Henry Rusinek, Tracy Butler, et al.
Journal of Medical Primatology
|
July 26, 2011
Development of a pigtail macaque model of sexually transmitted infection/HIV coinfection using Chlamydia trachomatis, Trichomonas vaginalis, and SHIV(SF162P3)
Tara Henning, Yetunde Fakile, Christi Phillips, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
January 20, 2022
Dimethyl Fumarate Reduces Inflammation in Chronic Active Multiple Sclerosis Lesions
Nicole Zinger, Gerald Ponath, Elizabeth Sweeney, et al.
Epilepsia
|
February 23, 2023
A pharmacokinetic model of antiseizure medication load to guide care in the epilepsy monitoring unit
Nina J Ghosn, Kevin Xie, Akash R Pattnaik, et al.
Scientific Reports
|
March 16, 2022
Disease correlates of rim lesions on quantitative susceptibility mapping in multiple sclerosis
Melanie Marcille, Sandra Hurtado Rúa, Charles Tyshkov, et al.
American Journal of Human Genetics
|
December 19, 2012
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex
Sandra M Pasternack, Melanie Refke, Elham Paknia, et al.
Page
of 6