(Q39938787)

15 September 2017

Diabetes susceptibility in the Canadian Oji-Cree population is moderated by abnormal mRNA processing of HNF1A G319S transcripts (English)

1 reference

15 September 2017

Sian Ellard

5

0 references

Andrew Tym Hattersley

series ordinal

4

object named as

Andrew T Hattersley

1 reference

15 September 2017

Lorna W Harries

1

1 reference

15 September 2017

Melissa J Sloman

series ordinal

2

1 reference

15 September 2017

Elizabeth A C Sellers

series ordinal

3

1 reference

15 September 2017

language of work or name

English

0 references

publication date

1 July 2008

1 reference

15 September 2017

1 reference

15 September 2017

57

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15 September 2017

7

1 reference

15 September 2017

1978-1982

1 reference

A periodic pattern of mRNA secondary structure created by the genetic code

15 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Hearing silence: non-neutral evolution at synonymous sites in mammals

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Evidence for selection on synonymous mutations affecting stability of mRNA secondary structure in mammals

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndrome.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Messenger RNA transcripts of the hepatocyte nuclear factor-1alpha gene containing premature termination codons are subject to nonsense-mediated decay

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Mfold web server for nucleic acid folding and hybridization prediction

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Evidence for haploinsufficiency of the human HNF1alpha gene revealed by functional characterization of MODY3-associated mutations

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

The prevalence of the HNF-1alpha G319S mutation in Canadian aboriginal youth with type 2 diabetes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Abnormal splicing of hepatocyte nuclear factor 1 alpha in maturity-onset diabetes of the young.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

HNF-1alpha G319S, a transactivation-deficient mutant, is associated with altered dynamics of diabetes onset in an Oji-Cree community

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Maturity-onset diabetes of the young: from clinical description to molecular genetic characterization

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Nonsense-mediated mRNA decay in health and disease

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2453634

Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstream

2 December 2018

1 reference

12 December 2020

The hepatic nuclear factor-1alpha G319S variant is associated with early-onset type 2 diabetes in Canadian Oji-Cree

1 reference

12 December 2020

Hepatocyte nuclear factor-1 alpha G319S. A private mutation in Oji-Cree associated with type 2 diabetes

1 reference

12 December 2020

Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes

1 reference

12 December 2020

Functional dissection of the HNF-1alpha transcription factor: a study on nuclear localization and transcriptional activation

1 reference

12 December 2020

Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations

1 reference

12 December 2020

Gender, obesity, hepatic nuclear factor-1alpha G319S and the age-of-onset of type 2 diabetes in Canadian Oji-Cree

1 reference

12 December 2020

Identifiers

DOI

10.2337/DB07-1633

1 reference

15 September 2017

1 reference

15 September 2017

PubMed publication ID

18586913

1 reference