Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection (Q40408816)

20 September 2017

Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection (English)

1 reference

20 September 2017

Rust S

1

1 reference

PMCID

309856

20 September 2017

Funke H

series ordinal

2

1 reference

PMCID

309856

20 September 2017

Assmann G

series ordinal

3

1 reference

20 September 2017

1 August 1993

1 reference

20 September 2017

7

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inferred from page(s)

published in

Nucleic Acids Research

1 reference

20 September 2017

21

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20 September 2017

16

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20 September 2017

3623-3629

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Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease

20 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Human lecithin-cholesterol acyltransferase gene: complete gene sequence and sites of expression

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

The complete cDNA and amino acid sequence of human apolipoprotein B-100

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Structure and expression of the human apolipoprotein A-IV gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Nucleotide sequence and structure of the human apolipoprotein E gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Detection of single DNA base differences by competitive oligonucleotide priming

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Multiple mutations in HIV-1 reverse transcriptase confer high-level resistance to zidovudine (AZT)

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Isothermal, in vitro amplification of nucleic acids by a multienzyme reaction modeled after retroviral replication

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Effects of primer-template mismatches on the polymerase chain reaction: human immunodeficiency virus type 1 model studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Genetic disease detection and DNA amplification using cloned thermostable ligase

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Nonsynonymous polymorphic sites in the apolipoprotein (apo) A-IV gene are associated with changes in the concentration of apo B- and apo A-I-containing lipoproteins in a normal population

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Is relationship between serum cholesterol and risk of premature death from coronary heart disease continuous and graded? Findings in 356,222 primary screenees of the Multiple Risk Factor Intervention Trial (MRFIT).

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Detection of ras point mutations by polymerase chain reaction using mutation-specific, inosine-containing oligonucleotide primers

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Oncogene detection at the single cell level

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309856

Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases

15 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8367277

12 December 2020

inferred from PubMed ID database lookup

Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8367277

12 December 2020

inferred from PubMed ID database lookup

Using mutagenic polymerase chain reaction primers to detect carriers of familial defective apolipoprotein B-100

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8367277

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1093/NAR/21.16.3623

1 reference

20 September 2017

1 reference

20 September 2017

1 reference

PMCID

309856