LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis (Q34650934)

3 August 2017

title

LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis (English)

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ORCID Public Data File 2021

3 August 2017

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author name string

Varret M

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3 August 2017

Rabés JP

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3 August 2017

Thiart R

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3 August 2017

Kotze MJ

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3 August 2017

Baron H

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3 August 2017

Cenarro A

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3 August 2017

Descamps O

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3 August 2017

Ebhardt M

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3 August 2017

Hondelijn JC

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3 August 2017

Kostner GM

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3 August 2017

Miyake Y

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3 August 2017

Pocovi M

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3 August 2017

Schmidt H

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3 August 2017

Schuster H

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3 August 2017

Stuhrmann M

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3 August 2017

Yamamura T

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3 August 2017

Junien C

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3 August 2017

Béroud C

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3 August 2017

Boileau C

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3 August 2017

language of work or name

English

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publication date

1 January 1998

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3 August 2017

published in

Nucleic Acids Research

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3 August 2017

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3 August 2017

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3 August 2017

page(s)

248-252

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CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolemia among South African Indians

3 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

A double mutant LDL receptor allele in a Cypriot family with heterozygous familial hypercholesterolemia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Software and database for the analysis of mutations in the human LDL receptor gene

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

The human LDL receptor: a cysteine-rich protein with multiple Alu sequences in its mRNA

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Cassette of eight exons shared by genes for LDL receptor and EGF precursor

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Human genes involved in cholesterol metabolism: chromosomal mapping of the loci for the low density lipoprotein receptor and 3-hydroxy-3-methylglutaryl-coenzyme A reductase with cDNA probes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Receptor-mediated endocytosis: concepts emerging from the LDL receptor system

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

The low density lipoprotein receptor in Xenopus laevis. I. Five domains that resemble the human receptor

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Detection of the Pro664-Leu mutation in the low-density lipoprotein receptor and its relation to lipoprotein(a) levels in patients with familial hypercholesterolemia of Dutch ancestry from The Netherlands and Canada

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Molecular genetics of the LDL receptor gene in familial hypercholesterolemia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Two novel point mutations causing receptor-negative familial hypercholesterolemia in a South African Indian homozygote.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish population.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147253

Identification of a double mutation in the low-density lipoprotein receptor gene causing familial hypercholesterolemia

26 October 2018

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12 December 2020

Molecular genetics of familial hypercholesterolaemia in Norway

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12 December 2020

A novel point mutation (Pro84-->Ser) of the low density lipoprotein receptor gene in a family with moderate hypercholesterolemia

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12 December 2020

Two mutations in the same low-density lipoprotein receptor allele act in synergy to reduce receptor function in heterozygous familial hypercholesterolemia

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12 December 2020

A novel V415A mutation in exon 9 of the low density lipoprotein receptor gene causing familial hypercholesterolemia

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12 December 2020

Identification of two novel LDL receptor gene defects in French-Canadian pediatric population: mutational analysis and biochemical studies

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12 December 2020

High prevalence of a novel mutation in the exon 4 of the low‐density lipoprotein receptor gene causing familial hypercholesterolemia in Belgium

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12 December 2020

Familial Moderate Hypercholesterolemia Caused by Asp235→Glu Mutation of the LDL Receptor Gene and Co-occurrence of a De Novo Deletion of the LDL Receptor Gene in the Same Family

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12 December 2020

A novel complex mutation in the LDL receptor gene probably caused by the simultaneous occurrence of deletion and insertion in the same region

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12 December 2020

An efficient screening procedure detecting six novel mutations in the LDL receptor gene in Swedish children with hypercholesterolemia

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12 December 2020

Screening for mutations in exon 4 of the LDL receptor gene in a German population with severe hypercholesterolemia

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12 December 2020

Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemia

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12 December 2020

Ten LDL receptor mutants explain one third of familial hypercholesterolemia in a German sample

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12 December 2020

High sensitivity of the single-strand conformation polymorphism method for detecting sequence variations in the low-density lipoprotein receptor gene validated by DNA sequencing

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12 December 2020

Mutation analysis reveals an insertional hotspot in exon 4 of the LDL receptor gene

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12 December 2020

Molecular genetics of familial hypercholesterolemia in Israel

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12 December 2020

A high incidence of mutations in exon 6 of the low-density lipoprotein receptor gene in Greek familial hypercholesterolemia patients, including a novel mutation

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12 December 2020

Identifiers

DOI

10.1093/NAR/26.1.248

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journals/nar/VarretRTKBCDEHKMPSSSSYJBB98

3 August 2017

DBLP publication ID

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DBLP Dataset 2021-01-02

28 January 2021

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3 August 2017

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