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Chamberlin

Showing results (861-870 of 1,103) with videos related to

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Frontiers in Psychology|May 19, 2023
Chronic pain and problematic substance use for veterans during COVID-19: the moderating role of psychological flexibilityErin D Reilly, Noah R Wolkowicz, Alicia Heapy, et al.
American Journal of Human Genetics|April 15, 2025
Integration of protein stability and AlphaMissense scores improves bioinformatic impact prediction for p53 missense and in-frame amino acid deletion variantsNitsan Rotenberg, Cristina Fortuno, Matthew J Varga, et al.
The New England Journal of Medicine|June 26, 1986
Fluosol-DA as a red-cell substitute in acute anemiaS A Gould, A L Rosen, L R Sehgal, et al.
Natural Product Research|June 9, 2005
Identifying bryostatins and potential precursors from the bryozoan Bugula neritinaThomas J Manning, Michael Land, Emily Rhodes, et al.
Headache|November 24, 2020
Spatial aspects of pain modulation are not disrupted in adolescents with migraineHadas Nahman-Averbuch, Priya L Thomas, Victor J Schneider, et al.
Plos One|March 17, 2016
Genomic Instability Associated with p53 Knockdown in the Generation of Huntington's Disease Human Induced Pluripotent Stem CellsAndrew M Tidball, M Diana Neely, Reed Chamberlin, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association|February 11, 2018
Goal Attainment and Goal Adjustment of Older Adults During Person-Directed Cancer RehabilitationKathleen Doyle Lyons, Robin M Newman, Peter A Kaufman, et al.
JACC. Basic to Translational Science|November 12, 2019
First-in-Man Study of a Cardiac Extracellular Matrix Hydrogel in Early and Late Myocardial Infarction PatientsJay H Traverse, Timothy D Henry, Nabil Dib, et al.
International Journal of Pediatric Otorhinolaryngology|December 4, 2003
GJB2 gene mutations causing familial hereditary deafness in TurkeyYildirim A Bayazit, Benjamin B Cable, Osman Cataloluk, et al.
Human Mutation|September 15, 2004
GJB2: the spectrum of deafness-causing allele variants and their phenotypeHela Azaiez, G Parker Chamberlin, Stephanie M Fischer, et al.
Pageof 111

Showing results (861-870 of 1,103) with videos related to

Sort By:
Pageof 111
Frontiers in Psychology|May 19, 2023
Chronic pain and problematic substance use for veterans during COVID-19: the moderating role of psychological flexibilityErin D Reilly, Noah R Wolkowicz, Alicia Heapy, et al.
American Journal of Human Genetics|April 15, 2025
Integration of protein stability and AlphaMissense scores improves bioinformatic impact prediction for p53 missense and in-frame amino acid deletion variantsNitsan Rotenberg, Cristina Fortuno, Matthew J Varga, et al.
The New England Journal of Medicine|June 26, 1986
Fluosol-DA as a red-cell substitute in acute anemiaS A Gould, A L Rosen, L R Sehgal, et al.
Natural Product Research|June 9, 2005
Identifying bryostatins and potential precursors from the bryozoan Bugula neritinaThomas J Manning, Michael Land, Emily Rhodes, et al.
Headache|November 24, 2020
Spatial aspects of pain modulation are not disrupted in adolescents with migraineHadas Nahman-Averbuch, Priya L Thomas, Victor J Schneider, et al.
Plos One|March 17, 2016
Genomic Instability Associated with p53 Knockdown in the Generation of Huntington's Disease Human Induced Pluripotent Stem CellsAndrew M Tidball, M Diana Neely, Reed Chamberlin, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association|February 11, 2018
Goal Attainment and Goal Adjustment of Older Adults During Person-Directed Cancer RehabilitationKathleen Doyle Lyons, Robin M Newman, Peter A Kaufman, et al.
JACC. Basic to Translational Science|November 12, 2019
First-in-Man Study of a Cardiac Extracellular Matrix Hydrogel in Early and Late Myocardial Infarction PatientsJay H Traverse, Timothy D Henry, Nabil Dib, et al.
International Journal of Pediatric Otorhinolaryngology|December 4, 2003
GJB2 gene mutations causing familial hereditary deafness in TurkeyYildirim A Bayazit, Benjamin B Cable, Osman Cataloluk, et al.
Human Mutation|September 15, 2004
GJB2: the spectrum of deafness-causing allele variants and their phenotypeHela Azaiez, G Parker Chamberlin, Stephanie M Fischer, et al.
Pageof 111