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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Drug Development
Wenyan Lu, Thomas R Caulfield, Suren Jeevaratnam, et al.
Neuron
|
June 4, 2024
Cryo-EM structures of pathogenic fibrils and their impact on neurodegenerative disease research
Tiffany W Todd, Naeyma N Islam, Casey N Cook, et al.
Human Genome Variation
|
April 13, 2018
Protein molecular modeling shows residue T599 is critical to wild-type function of POLG and description of a novel variant associated with the SANDO phenotype
John E Richter, Hector G Robles, Elizabeth Mauricio, et al.
Molecular Pharmacology
|
December 16, 2011
Inhibition of prohormone convertases PC1/3 and PC2 by 2,5-dideoxystreptamine derivatives
Mirella Vivoli, Thomas R Caulfield, Karina Martínez-Mayorga, et al.
The Journal of Biological Chemistry
|
February 23, 2013
Long-range electrostatic complementarity governs substrate recognition by human chymotrypsin C, a key regulator of digestive enzyme activation
Jyotica Batra, András Szabó, Thomas R Caulfield, et al.
Cancer Genetics
|
January 25, 2021
Clinical description & molecular modeling of novel MAX pathogenic variant causing pheochromocytoma in family, supports paternal parent-of-origin effect
John E Richter, S Hines, Pavalan Selvam, et al.
Molecular Genetics & Genomic Medicine
|
January 30, 2019
Protein informatics combined with multiple data sources enriches the clinical characterization of novel TRPV4 variant causing an intermediate skeletal dysplasia
Stephanie L Hines, John E Richter, Ahmed N Mohammad, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
Discovery of a CI-994 derivative as a dual modulator of class I HDACs and Wnt/β-catenin signaling for Alzheimer's disease therapy
Wenyan Lu, Thomas R Caulfield, Eunmi Lee, et al.
Molecular Genetics & Genomic Medicine
|
April 28, 2018
Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family
Thomas R Caulfield, John E Richter, Emily E Brown, et al.
Molecular Genetics & Genomic Medicine
|
November 28, 2017
A novel splice site variant in CYP11A1 in trans with the p.E314K variant in a male patient with congenital adrenal insufficiency
Montserrat Lara-Velazquez, Alexander Perdomo-Pantoja, Patrick R Blackburn, et al.
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Search research articles
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Showing results (11-20 of 69) with videos related to
Sort By:
Page
of 7
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Drug Development
Wenyan Lu, Thomas R Caulfield, Suren Jeevaratnam, et al.
Neuron
|
June 4, 2024
Cryo-EM structures of pathogenic fibrils and their impact on neurodegenerative disease research
Tiffany W Todd, Naeyma N Islam, Casey N Cook, et al.
Human Genome Variation
|
April 13, 2018
Protein molecular modeling shows residue T599 is critical to wild-type function of POLG and description of a novel variant associated with the SANDO phenotype
John E Richter, Hector G Robles, Elizabeth Mauricio, et al.
Molecular Pharmacology
|
December 16, 2011
Inhibition of prohormone convertases PC1/3 and PC2 by 2,5-dideoxystreptamine derivatives
Mirella Vivoli, Thomas R Caulfield, Karina Martínez-Mayorga, et al.
The Journal of Biological Chemistry
|
February 23, 2013
Long-range electrostatic complementarity governs substrate recognition by human chymotrypsin C, a key regulator of digestive enzyme activation
Jyotica Batra, András Szabó, Thomas R Caulfield, et al.
Cancer Genetics
|
January 25, 2021
Clinical description & molecular modeling of novel MAX pathogenic variant causing pheochromocytoma in family, supports paternal parent-of-origin effect
John E Richter, S Hines, Pavalan Selvam, et al.
Molecular Genetics & Genomic Medicine
|
January 30, 2019
Protein informatics combined with multiple data sources enriches the clinical characterization of novel TRPV4 variant causing an intermediate skeletal dysplasia
Stephanie L Hines, John E Richter, Ahmed N Mohammad, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
Discovery of a CI-994 derivative as a dual modulator of class I HDACs and Wnt/β-catenin signaling for Alzheimer's disease therapy
Wenyan Lu, Thomas R Caulfield, Eunmi Lee, et al.
Molecular Genetics & Genomic Medicine
|
April 28, 2018
Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family
Thomas R Caulfield, John E Richter, Emily E Brown, et al.
Molecular Genetics & Genomic Medicine
|
November 28, 2017
A novel splice site variant in CYP11A1 in trans with the p.E314K variant in a male patient with congenital adrenal insufficiency
Montserrat Lara-Velazquez, Alexander Perdomo-Pantoja, Patrick R Blackburn, et al.
Page
of 7