(Q31162611)

14 September 2017

Integrating genotypic data with transcriptomic and proteomic data (English)

1 reference

14 September 2017

0 references

Denis C Shields

1

1 reference

PMCID

2447235

14 September 2017

Aisling M O'Halloran

series ordinal

2

1 reference

14 September 2017

1 January 2002

1 reference

Comparative and Functional Genomics

14 September 2017

1 reference

14 September 2017

3

1 reference

14 September 2017

1

1 reference

14 September 2017

22-27

1 reference

Creative Commons Attribution 3.0 Unported

14 September 2017

start time

1 January 2002

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Proteomics: a link between genomics, genetics and physiology.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Protein function in the post-genomic era.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

The future of genetic studies of complex human diseases

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Combined segregation and linkage analysis of Graves disease with a thyroid autoantibody diathesis.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Identification of a heritable deficiency of the folate-dependent enzyme 10-formyltetrahydrofolate dehydrogenase in mice

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Identification of the cystic fibrosis gene: genetic analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

High resolution two-dimensional electrophoresis of human plasma proteins

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Insertion/deletion polymorphism of the angiotensin I-converting enzyme gene is not associated with restenosis after coronary stent placement

14 July 2018

1 reference

Factor V Leiden: a clinical review

21 January 2018

1 reference

Angiotensin-converting enzyme (ACE) I/D genotype and renal ACE gene expression

21 January 2018

1 reference

Genetical genomics: the added value from segregation.

21 January 2018

1 reference

Gene-Expression Profiles in Hereditary Breast Cancer

21 January 2018

1 reference

Platelet glycoprotein receptor IIIa polymorphism PLA1/PLA2 and coronary risk: a meta-analysis.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447235

Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5

31 October 2018

1 reference

Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators

21 January 2018

1 reference

Effect of the interleukin-1 genotype on monocyte IL-1beta expression in subjects with adult periodontitis

21 January 2018

1 reference

Relation between the insertion/deletion polymorphism of the angiotensin I converting enzyme gene and restenosis after coronary stenting

21 January 2018

1 reference

12 December 2020

Heterogeneity of glutathione S-transferase enzyme and gene expression in ovarian carcinoma

1 reference

12 December 2020

Mapping factors controlling genetic expression

1 reference

12 December 2020

Identification of the amino acid mutations associated with human erythrocyte spectrin alpha II domain polymorphisms

1 reference

12 December 2020

Identifiers

DOI

10.1002/CFG.135

1 reference

14 September 2017

1 reference

14 September 2017

1 reference

PMCID

2447235