Pages that link to "Q35538234"

The following pages link to Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction (Q35538234):

Displaying 20 items.

• Testing the role of predicted gene knockouts in human anthropometric trait variation (Q28597672) (← links)
• Towards Increasing the Clinical Relevance of In Silico Methods to Predict Pathogenic Missense Variants (Q36015435) (← links)
• Systematic evaluation of underlying defects in DNA repair as an approach to case-only assessment of familial prostate cancer (Q36545434) (← links)
• The use of targeted exome sequencing in genetic diagnosis of young patients with severe hypercholesterolemia (Q37405756) (← links)
• When is it MODY? Challenges in the Interpretation of Sequence Variants in MODY Genes (Q38816600) (← links)
• Aggregate penetrance of genomic variants for actionable disorders in European and African Americans (Q39199102) (← links)
• Systematic Cell-Based Phenotyping of Missense Alleles (Q39282863) (← links)
• Reduction of TMEM97 increases NPC1 protein levels and restores cholesterol trafficking in Niemann-pick type C1 disease cells (Q39732986) (← links)
• Correction: systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction (Q43190943) (← links)
• Whole genome sequencing of extreme phenotypes identifies variants in CD101 and UBE2V1 associated with increased risk of sexually acquired HIV-1. (Q45812682) (← links)
• Caffeine Mitigates the Locomotor Hyperactivity in Middle-aged Low-density Lipoprotein Receptor (LDLr)-Knockout Mice. (Q53139562) (← links)
• Bioinformatic Analysis of the Possible Regulative Network of miR-30a/e in Cardiomyocytes 2 Days Post Myocardial Infarction. (Q55289464) (← links)
• Validation of LDLr Activity as a Tool to Improve Genetic Diagnosis of Familial Hypercholesterolemia: A Retrospective on Functional Characterization of LDLr Variants. (Q55607061) (← links)
• Systematic RNA-interference in primary human monocyte-derived macrophages: A high-throughput platform to study foam cell formation. (Q55692468) (← links)
• Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (Q56333979) (← links)
• The complex molecular genetics of familial hypercholesterolaemia (Q58046669) (← links)
• p.(Asp47Asn) and p.(Thr62Met): non deleterious LDL receptor missense variants functionally characterized in vitro (Q58571259) (← links)
• Heterozygous familial hypercholesterolaemia in a pair of identical twins: a case report and updated review (Q64053643) (← links)
• Interdisciplinary Models for Research and Clinical Endeavors in Genomic Medicine: A Scientific Statement From the American Heart Association (Q88909731) (← links)
• Wikidata:WikiProject Mathematics/Wikidata lists/Methods used (P4510) by people with a zbMATH author ID (P1556) (← links | edit)