(Q37429188)

English

Severe insulin resistance and intrauterine growth deficiency associated with haploinsufficiency for INSR and CHN2: new insights into synergistic pathways involved in growth and metabolism

scientific article published on 31 August 2009

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scholarly article

1 reference

Europe PubMed Central

20 August 2017

Severe insulin resistance and intrauterine growth deficiency associated with haploinsufficiency for INSR and CHN2: new insights into synergistic pathways involved in growth and metabolism (English)

1 reference

Europe PubMed Central

20 August 2017

haploinsufficiency

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1 reference

based on heuristic

inferred from title

insulin resistance

1 reference

based on heuristic

inferred from title

Emanuela V Volpi

object named as

Emanuela V Volpi

12

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object named as

Anna L Gloyn

14

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object named as

Sian Ellard

11

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author name string

Sara G I Suliman

1

1 reference

Europe PubMed Central

20 August 2017

Juraj Stanik

2

1 reference

Europe PubMed Central

20 August 2017

Laura J McCulloch

3

1 reference

Europe PubMed Central

20 August 2017

Natalie Wilson

4

1 reference

Europe PubMed Central

20 August 2017

Emma L Edghill

5

1 reference

Europe PubMed Central

20 August 2017

Nadezda Misovicova

6

1 reference

Europe PubMed Central

20 August 2017

Daniela Gasperikova

7

1 reference

Europe PubMed Central

20 August 2017

Vilja Sandrikova

8

1 reference

Europe PubMed Central

20 August 2017

Katherine S Elliott

9

1 reference

Europe PubMed Central

20 August 2017

Lubomir Barak

10

1 reference

Europe PubMed Central

20 August 2017

Iwar Klimes

13

1 reference

Europe PubMed Central

20 August 2017

language of work or name

0 references

publication date

31 August 2009

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

58

1 reference

Europe PubMed Central

20 August 2017

2954-2961

1 reference

Europe PubMed Central

20 August 2017

12

1 reference

Europe PubMed Central

20 August 2017

copyright license

Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

28 August 2021

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Diabetes risk begins in utero

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

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23 August 2017

Role of chimaerins, a group of Rac-specific GTPase activating proteins, in T-cell receptor signaling

1 reference

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23 August 2017

The genetic aetiology of Silver-Russell syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Critical nodes in signalling pathways: insights into insulin action

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Growth retardation and abnormal maternal behavior in mice lacking testicular orphan nuclear receptor 4.

1 reference

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23 August 2017

A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Microarray Analysis of Gene‐expression Profiles in Diffuse Large B‐cell Lymphoma: Identification of Genes Related to Disease Progression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Digenic inheritance of severe insulin resistance in a human pedigree

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Genotype-phenotype correlation in inherited severe insulin resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Role of insulin receptors and IGF receptors in growth and development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Role of insulin-like growth factors in embryonic and postnatal growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Molecular genetics of severe insulin resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Mutant insulin receptors in syndromes of insulin resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

The syndromes of insulin resistance and acanthosis nigricans. Insulin-receptor disorders in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

23 August 2017

Prenatal screening for mutations in the insulin receptor gene. How reliably does genotype predict phenotype?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

26 June 2018

Beta2-chimaerin in cancer signaling: connecting cell adhesion and MAP kinase activation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

2 September 2018

Elevated plasma adiponectin in humans with genetically defective insulin receptors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

2 September 2018

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

2 September 2018

Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor-4alpha (HNF4A) gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

2 September 2018

Homozygous nonsense mutation in the insulin receptor gene in infant with leprechaunism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2780873

2 September 2018

Early neonatal death in mice homozygous for a null allele of the insulin receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19720790

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of a novel polygenic model of NIDDM in mice heterozygous for IR and IRS-1 null alleles

1 reference

https://pubmed.ncbi.nlm.nih.gov/19720790

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.2337/DB09-0787

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

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0 references

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