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David Adams

Showing results (271-280 of 370) with videos related to

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Orphanet Journal of Rare Diseases|July 10, 2020
A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosisTeresa Coelho, David Adams, Isabel Conceição, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 8, 2013
1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of NephrolithiasisGalina Nesterova, May Christine Malicdan, Kaori Yasuda, et al.
Journal of Pathology Informatics|December 1, 2025
The comparative pathology workbench: An updateMichael N Wicks, Michael Glinka, Bill Hill, et al.
American Journal of Medical Genetics. Part A|March 10, 2020
A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung diseaseElizabeth A Burke, Kyle E Reichard, Lynne A Wolfe, et al.
Disease Models & Mechanisms|March 23, 2013
Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screeningDavid Adams, Richard Baldock, Shoumo Bhattacharya, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|January 12, 2019
Cause of death analysis and temporal trends in survival after liver transplantation for transthyretin familial amyloid polyneuropathyVincent Algalarrondo, Teresa Antonini, Marie Théaudin, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2024
Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viabilityDebdeep Dutta, Oguz Kanca, Rishi V Shridharan, et al.
JAMA Cardiology|March 17, 2019
Association of Patisiran, an RNA Interference Therapeutic, With Regional Left Ventricular Myocardial Strain in Hereditary Transthyretin Amyloidosis: The APOLLO StudyMasatoshi Minamisawa, Brian Claggett, David Adams, et al.
Molecular Genetics and Metabolism|January 27, 2012
Sensitive quantification of mosaicism using high density SNP arrays and the cumulative distribution functionThomas C Markello, Hannah Carlson-Donohoe, Murat Sincan, et al.
Blood|July 21, 2007
CCR1/CCL5 (RANTES) receptor-ligand interactions modulate allogeneic T-cell responses and graft-versus-host disease following stem-cell transplantationSung W Choi, Gerhard C Hildebrandt, Krystyna M Olkiewicz, et al.
Pageof 37

Showing results (271-280 of 370) with videos related to

Sort By:
Pageof 37
Orphanet Journal of Rare Diseases|July 10, 2020
A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosisTeresa Coelho, David Adams, Isabel Conceição, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 8, 2013
1,25-(OH)2D-24 Hydroxylase (CYP24A1) Deficiency as a Cause of NephrolithiasisGalina Nesterova, May Christine Malicdan, Kaori Yasuda, et al.
Journal of Pathology Informatics|December 1, 2025
The comparative pathology workbench: An updateMichael N Wicks, Michael Glinka, Bill Hill, et al.
American Journal of Medical Genetics. Part A|March 10, 2020
A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung diseaseElizabeth A Burke, Kyle E Reichard, Lynne A Wolfe, et al.
Disease Models & Mechanisms|March 23, 2013
Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screeningDavid Adams, Richard Baldock, Shoumo Bhattacharya, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|January 12, 2019
Cause of death analysis and temporal trends in survival after liver transplantation for transthyretin familial amyloid polyneuropathyVincent Algalarrondo, Teresa Antonini, Marie Théaudin, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2024
Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viabilityDebdeep Dutta, Oguz Kanca, Rishi V Shridharan, et al.
JAMA Cardiology|March 17, 2019
Association of Patisiran, an RNA Interference Therapeutic, With Regional Left Ventricular Myocardial Strain in Hereditary Transthyretin Amyloidosis: The APOLLO StudyMasatoshi Minamisawa, Brian Claggett, David Adams, et al.
Molecular Genetics and Metabolism|January 27, 2012
Sensitive quantification of mosaicism using high density SNP arrays and the cumulative distribution functionThomas C Markello, Hannah Carlson-Donohoe, Murat Sincan, et al.
Blood|July 21, 2007
CCR1/CCL5 (RANTES) receptor-ligand interactions modulate allogeneic T-cell responses and graft-versus-host disease following stem-cell transplantationSung W Choi, Gerhard C Hildebrandt, Krystyna M Olkiewicz, et al.
Pageof 37