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Cell
|
October 2, 2012
A validated regulatory network for Th17 cell specification
Maria Ciofani, Aviv Madar, Carolina Galan, et al.
G3 (Bethesda, Md.)
|
February 10, 2022
Genome assembly of the Australian black tiger shrimp (Penaeus monodon) reveals a novel fragmented IHHNV EVE sequence
Roger Huerlimann, Jeff A Cowley, Nicholas M Wade, et al.
Plos One
|
October 13, 2021
Cohort profile: The UK COVID-19 Public Experiences (COPE) prospective longitudinal mixed-methods study of health and well-being during the SARSCoV2 coronavirus pandemic
Rhiannon Phillips, Khadijeh Taiyari, Anna Torrens-Burton, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 20, 2022
Improved T-cell Immunity Following Neoadjuvant Chemotherapy in Ovarian Cancer
Min Liu, Nabihah Tayob, Livius Penter, et al.
American Journal of Human Genetics
|
February 14, 2017
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy
Daniel P S Osborn, Heather L Pond, Neda Mazaheri, et al.
Human Mutation
|
July 26, 2019
Iranome: A catalog of genomic variations in the Iranian population
Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
March 10, 2021
European Federation of Societies for Ultrasound in Medicine and Biology (EFSUMB): An Update on the Pediatric CEUS Registry on Behalf of the "EFSUMB Pediatric CEUS Registry Working Group"
Christoph F Dietrich, Rasa Augustiniene, Tomasz Batko, et al.
International Journal of Environmental Research and Public Health
|
July 2, 2021
Community Engagement Practices at Research Centers in U.S. Minority Institutions: Priority Populations and Innovative Approaches to Advancing Health Disparities Research
Tabia Henry Akintobi, Payam Sheikhattari, Emma Shaffer, et al.
American Journal of Medical Genetics. Part A
|
May 1, 2014
Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum
Kim M Keppler-Noreuil, Julie C Sapp, Marjorie J Lindhurst, et al.
Human Molecular Genetics
|
October 18, 2017
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
Yanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.
Page
of 44
Search research articles
Search
Showing results (421-430 of 437) with videos related to
Sort By:
Page
of 44
Cell
|
October 2, 2012
A validated regulatory network for Th17 cell specification
Maria Ciofani, Aviv Madar, Carolina Galan, et al.
G3 (Bethesda, Md.)
|
February 10, 2022
Genome assembly of the Australian black tiger shrimp (Penaeus monodon) reveals a novel fragmented IHHNV EVE sequence
Roger Huerlimann, Jeff A Cowley, Nicholas M Wade, et al.
Plos One
|
October 13, 2021
Cohort profile: The UK COVID-19 Public Experiences (COPE) prospective longitudinal mixed-methods study of health and well-being during the SARSCoV2 coronavirus pandemic
Rhiannon Phillips, Khadijeh Taiyari, Anna Torrens-Burton, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 20, 2022
Improved T-cell Immunity Following Neoadjuvant Chemotherapy in Ovarian Cancer
Min Liu, Nabihah Tayob, Livius Penter, et al.
American Journal of Human Genetics
|
February 14, 2017
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy
Daniel P S Osborn, Heather L Pond, Neda Mazaheri, et al.
Human Mutation
|
July 26, 2019
Iranome: A catalog of genomic variations in the Iranian population
Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
March 10, 2021
European Federation of Societies for Ultrasound in Medicine and Biology (EFSUMB): An Update on the Pediatric CEUS Registry on Behalf of the "EFSUMB Pediatric CEUS Registry Working Group"
Christoph F Dietrich, Rasa Augustiniene, Tomasz Batko, et al.
International Journal of Environmental Research and Public Health
|
July 2, 2021
Community Engagement Practices at Research Centers in U.S. Minority Institutions: Priority Populations and Innovative Approaches to Advancing Health Disparities Research
Tabia Henry Akintobi, Payam Sheikhattari, Emma Shaffer, et al.
American Journal of Medical Genetics. Part A
|
May 1, 2014
Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum
Kim M Keppler-Noreuil, Julie C Sapp, Marjorie J Lindhurst, et al.
Human Molecular Genetics
|
October 18, 2017
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy
Yanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.
Page
of 44