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PCSK9 wt Allele

Known as: Proprotein Convertase Subtilisin/Kexin Type 9 wt Allele, PC9, NARC-1 
Human PCSK9 wild-type allele is located in the vicinity of 1p32.3 and is approximately 25 kb in length. This allele, which encodes proprotein… 
National Institutes of Health

Related topics

Related topics

4 relations
1p32.3Cholesterol HomeostasisHydrolysisProteolysis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Early emergence of de novo EGFR T790M gatekeeper mutations during erlotinib treatment in PC9 non-small cell lung cancer cells.
2016
2016
Language, Power, and Ideology in High School EFL Textbooks in Saudi Arabia
Using critical discourse analysis (CDA) as a research method, I investigated in the present study the discursive intersections… 
2013
2013
Norcantharidin suppresses cell growth and migration with enhanced anticancer activity of gefitinib and cisplatin in human non-small cell lung cancer cells.
Norcantharidin is the demethylated analog of cantharidin isolated from blister beetles (Mylabris phalerata Pall.). In… 
2013
2013
Structure and Stability of Chemically Modified DNA Bases: Quantum Chemical Calculations on 16 Isomers of Diphosphocytosine
We studied for the first time 16 tautomers/rotamers of diphosphocytosine by four computational methods. Some of these tautomers… 
2012
2012
Co-localisation of host plant resistance QTLs affecting the performance and feeding behaviour of the aphid Myzus persicae in the peach tree
The architecture and action of quantitative trait loci (QTL) contributing to plant resistance mechanisms against aphids, the… 
2009
2009
Tragverhalten von gebogenen Glasscheiben im Bauwesen : Abschlussbericht ; im Rahmen des Programmes: FH3 - Angewandte Forschung an Fachhochschulen im Verbund mit der Wirtschaft ; Bewilligungszeitraum…
2001
2001
A Comparison of Neural, Fuzzy, Evolutionary, and Adaptive Approaches for Carrier Landing
Abstract : This paper compares in simulation six control approaches for an automated carrier landing design problem. The key… 
2001
2001
Visual Quality of Service Programming for Distributed Heterogeneous Systems
" $#% & ' ( ) $ * + ' , . /#0 1 23 ! 54167 . -8 & 9#0 :,; ",< (,;# & . , =#0 $ '5#> ? @ % ' 5#0 $ 2A 5 . B C . !D -E D & 5 . F… 
Highly Cited
1999
Highly Cited
1999
A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32.
Autosomal dominant hypercholesterolemia (ADH), one of the most frequent hereditary disorders, is characterized by an isolated… 
1998
1998
Familial hypercholesterolemia: potential diagnostic value of mutation screening in a pediatric population of South Africa
Three founder‐related low‐density lipoprotein receptor (LDLR) gene mutations, D154N, D206E and V408M, cause familial… 
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