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ADELE SOUTAR, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1174152243Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Mechanisms of disease: genetic causes of familial hypercholesterolemia.
PMID 17380167·Nat Clin Pract Cardiovasc Med·2007
6-review
Genetics, clinical phenotype, and molecular cell biology of autosomal recessive hypercholesterolemia.
PMID 12958046·Arterioscler Thromb Vasc Biol·2003
6-review
Degradation of LDLR protein mediated by 'gain of function' PCSK9 mutants in normal and ARH cells.
PMID 19081568·Atherosclerosis·2009
8-other
Genetic diagnosis of familial hypercholesterolaemia: the importance of functional analysis of potential splice-site mutations.
PMID 19411563·J Med Genet·2009
8-other
Effects of ezetimibe and/or simvastatin on LDL receptor protein expression and on LDL receptor and HMG-CoA reductase gene expression: a randomized trial in healthy men.
PMID 17980884·Atherosclerosis·2008
2-rct
Adaptor protein disabled-2 modulates low density lipoprotein receptor synthesis in fibroblasts from patients with autosomal recessive hypercholesterolaemia.
PMID 17761685·Hum Mol Genet·2007
4-observational
Genetic defects causing familial hypercholesterolaemia: identification of deletions and duplications in the LDL-receptor gene and summary of all mutations found in patients attending the Hammersmith Hospital Lipid Clinic.
PMID 17094996·Atherosclerosis·2007
8-other
A rare polymorphism in the low density lipoprotein (LDL) gene that affects mRNA splicing.
PMID 17335829·Atherosclerosis·2007
5-case
A single point mutation in the low-density lipoprotein receptor switches the degradation of its mature protein from the proteasome to the lysosome.
PMID 16530458·Int J Biochem Cell Biol·2006
7-preclinical
Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk.
PMID 17142622·J Med Genet·2006
8-other
Evidence for effect of mutant PCSK9 on apolipoprotein B secretion as the cause of unusually severe dominant hypercholesterolaemia.
PMID 15772090·Hum Mol Genet·2005
4-observational
Characterisation of a duplex TiO2/CaP coating on Ti6Al4V for hard tissue replacement.
PMID 15451628·Biomaterials·2005
8-other
The ecological validity of the "who said what?" technique: an examination of the role of self-involvement, cognitive interference and acquaintanceship.
PMID 15660637·Scand J Psychol·2005
8-other
Severe hypercholesterolemia in four British families with the D374Y mutation in the PCSK9 gene: long-term follow-up and treatment response.
PMID 16224054·Arterioscler Thromb Vasc Biol·2005
4-observational
Sorting motifs in the intracellular domain of the low density lipoprotein receptor interact with a novel domain of sorting nexin-17.
PMID 14739284·J Biol Chem·2004
7-preclinical
Autosomal recessive hypercholesterolaemia: long-term follow up and response to treatment.
PMID 15135266·Atherosclerosis·2004
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2131 S 17TH ST
WILMINGTON, NC 28401 - Phone
- (910) 667-7000
Quick Facts
- NPI
- 1174152243
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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