about
Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family.Whole Exome Sequencing and Molecular Modeling of a Missense Variant in TNFAIP3 That Segregates with Disease in a Family with Chronic Urticaria and Angioedema.Protein informatics combined with multiple data sources enriches the clinical characterization of novel TRPV4 variant causing an intermediate skeletal dysplasiaCharacterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular ModelingFAM111A protects replication forks from protein obstacles via its trypsin-like domainPersonalized molecular modeling for pinpointing associations of protein dysfunction and variants associated with hereditary cancer syndromesProtein modeling and clinical description of a novel in-frame GLB1 deletion causing GM1 gangliosidosis type IIMolecular Dynamics Simulations Suggest a Non-Doublet Decoding Model of -1 Frameshifting by tRNASer3Genomic Observations of a Rare/Pathogenic SMAD3 Variant in Loeys⁻Dietz Syndrome 3 Confirmed by Protein Informatics and Structural InvestigationsApolipoprotein E and Alzheimer disease: pathobiology and targeting strategies
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description
researcher
@en
name
Thomas R Caulfield
@en
type
label
Thomas R Caulfield
@en
prefLabel
Thomas R Caulfield
@en
P31
P496
0000-0002-1055-3069